VICP Registry Case Source Bundle
Canonical URL: https://vicp-registry.org/case/USCOURTS-cofc-1_17-vv-01112
Package ID: USCOURTS-cofc-1_17-vv-01112
Petitioner: Eileen Schmigel
Filed: 2017-08-18
Decided: 2025-05-09
Vaccine: influenza
Vaccination date: 2015-10-21
Condition: chronic inflammatory demyelinating polyneuropathy
Outcome: dismissed
Award amount USD: 

AI-assisted case summary:
Eileen Schmigel filed a petition alleging that she suffered from Chronic Inflammatory Demyelinating Polyneuropathy (CIDP) following an influenza vaccination on October 21, 2015. The court found that CIDP is not a Table injury and that Ms. Schmigel would need to prove causation-in-fact under the Althen test. The court previously found that Ms. Schmigel experienced numbness and tingling in her extremities around late November 2015, approximately five weeks after her vaccination, but did not experience weakness until July 2016, about nine months later. Respondent argued that Ms. Schmigel's symptoms were better explained by diabetic neuropathy, a condition she had a history of. Petitioner's expert, Dr. Chen, argued that Ms. Schmigel's condition was an atypical presentation of CIDP, potentially triggered by the vaccine, and that diabetes was not the primary cause. Respondent's expert, Dr. Donofrio, maintained that Ms. Schmigel's symptoms were consistent with diabetic neuropathy and that her condition did not meet the diagnostic criteria for CIDP, nor was there sufficient evidence to link it to the flu vaccine. The court found that the evidence preponderated in favor of Ms. Schmigel suffering from both diabetic neuropathy and later CIDP, but that the timing of the CIDP onset (around July 2016) was too distant from the vaccination to infer causation. Furthermore, the court noted that none of Ms. Schmigel's treating physicians opined that her vaccination caused her condition, and that her pre-existing diabetes was a significant factor. Ultimately, the court concluded that Ms. Schmigel failed to meet her burden of proof under the Althen test for both a logical sequence of cause and effect and a proximate temporal relationship. Therefore, her petition was dismissed.

Theory of causation field:
Influenza vaccine on October 21, 2015, adult exact age not stated, alleged to cause chronic inflammatory demyelinating polyneuropathy, with numbness/tingling around five weeks later and weakness months later. DISMISSED/DENIED. Petitioner Eileen Schmigel relied on Dr. Chen's atypical CIDP theory. Respondent's Dr. Peter Donofrio argued the presentation fit diabetic neuropathy and did not meet CIDP criteria. Special Master Horner found petitioner did not prove vaccine causation and dismissed the petition May 9, 2025.

Public staged source text:

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DOCUMENT 1: USCOURTS-cofc-1_17-vv-01112-0
Date issued/filed: 2021-12-14
Pages: 16
Docket text: PUBLIC ORDER/RULING (Originally filed: 11/19/2021) regarding 74 Findings of Fact & Conclusions of Law. Signed by Special Master Daniel T. Horner. (mly) Service on parties made.
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Case 1:17-vv-01112-UNJ Document 75 Filed 12/14/21 Page 1 of 16
In the United States Court of Federal Claims
OFFICE OF SPECIAL MASTERS
No. 17-1112V
Filed: November 19, 2021
PUBLISHED
Special Master Horner
EILEEN SCHMIGEL,
Petitioner,
Finding of Fact; Onset; Chronic
v.
Inflammatory Demyelinating
Polyneuropathy (CIDP);
SECRETARY OF HEALTH AND
Influenza (Flu) Vaccine
HUMAN SERVICES,
Respondent.
Paul R. Brazil, Muller Brazil, LLP, Dresher, PA, for petitioner.
Wei Kit Tai, U.S. Department of Justice, Washington, DC, for respondent.
Finding of Fact1
On August 18, 2017, petitioner, Eileen Schmigel, filed a petition under the
National Childhood Vaccine Injury Act, 42 U.S.C. § 300aa-10-34 (2012), alleging that
she suffered chronic inflammatory demyelinating polyneuropathy (“CIDP”) resulting
from the adverse effects of the influenza (“Flu”) vaccine that she received on October
21, 2015. (ECF No. 1, p. 1.) Upon review of petitioner’s medical records, respondent
concluded that onset of petitioner’s condition was likely in March of 2016, approximately
five months after her vaccination, which he indicates is “well outside the accepted
timeframe to demonstrate vaccine causation.” (ECF No. 28, p. 11.) Petitioner now
moves for a finding of fact that her symptoms began “between one (1) and five (5)
weeks of vaccination.” (ECF No. 72, p. 1.) For the reasons discussed below, I find that
petitioner experienced numbness, tingling, and fatigue, no later than late November of
2015.
1 Because this decision contains a reasoned explanation for the special master’s action in this case, it will
be posted on the United States Court of Federal Claims’ website in accordance with the E-Government
Act of 2002. See 44 U.S.C. § 3501 note (2012) (Federal Management and Promotion of Electronic
Government Services). This means the decision will be available to anyone with access to the
Internet. In accordance with Vaccine Rule 18(b), petitioner has 14 days to identify and move to redact
medical or other information the disclosure of which would constitute an unwarranted invasion of privacy.
If the special master, upon review, agrees that the identified material fits within this definition, it will be
redacted from public access.
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Case 1:17-vv-01112-UNJ Document 75 Filed 12/14/21 Page 2 of 16
I. Procedural History
This petition was initially assigned to Special Master Sanders. (ECF No. 6.)
Petitioner filed a Statement of Completion on February 28, 2018 (ECF No. 22) and
respondent filed his Rule 4(c) Report recommending against compensation on June 11,
2018. (ECF No. 28.) Respondent’s report primarily raised the issue of the timing of
onset of petitioner’s alleged CIDP and also noted that none of petitioner’s physicians
had attributed her CIDP to her flu vaccine. (Id.)
Petitioner subsequently filed additional medical records and affidavits by Kristin
Johnson, a coworker (Ex. 23), Ginger Williams, a friend (Ex. 24), herself (Ex. 26), Lina
Robertson, a former supervisor (Ex. 25), and Kathleen Sorensen, her sister (Ex. 34).
(ECF Nos. 30-31, 33-34, 56.) Petitioner filed an expert report by neurologist Nizar
Souayah, M.D., on January 9, 2019. (ECF No. 40; Ex. 30.) Dr. Souayah opined that
petitioner’s CIDP was caused by her October 21, 2015 flu vaccine. (Ex. 30.) His
opinion was premised on his assessment that onset of petitioner’s CIDP symptoms
occurred within five weeks of her vaccination. (Ex. 30, p. 16.) Respondent filed a
competing expert opinion by neurologist Peter Donofrio, M.D., on May 23, 2019. (ECF
No. 42; Ex. A.) Based on the contemporaneous medical records, Dr. Donofrio
assessed onset of neurologic symptoms as occurring approximately four and a half
months following vaccination. (Ex. A, p. 10.)
The case was then reassigned to me on August 29, 2019. (ECF No. 46.) In a
status conference held November 26, 2019, I advised the parties that, given the
differing assumptions of the parties’ experts regarding onset, a fact hearing and fact
finding would be necessary to resolve this case. (ECF No. 47.) A fact hearing was held
September 25, 2020. (Transcript of Proceedings at ECF No. 67 (hereinafter (“Tr.”).)
Petitioner testified along with two other witnesses, Ms. Robertson and Ms. Sorensen.
On April 19, 2021, petitioner filed the instant motion for a finding of fact as to the timing
of onset of her CIDP. (ECF No. 72.) Respondent filed his response on June 21, 2021.
(ECF No. 73.) No reply was filed. Petitioner’s motion is now ripe for resolution.2
II. Factual History3
A. As reflected in petitioner’s medical records
At the time of vaccination, petitioner was located in Ridgecrest, California. (See,
e.g., Ex. 1, p. 1.) Prior to vaccination her medical history included, inter alia, attention
2 That is, the record is sufficiently developed and the parties have had a full and fair opportunity to present
their respective cases. Vaccine Rule 8(d); Vaccine Rule 3(b)(2); see also Kreizenbeck v. Sec’y of Health
& Human Servs., 945 F.3d 1362, 1366 (Fed. Cir. 2020).
3 Although I have reviewed the entirety of the record compiled to date, including petitioner’s complete
medical history, the factual history discussed in this decision is limited to describing the evidence most
relevant to identifying the date of onset of petitioner’s symptoms.
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deficit disorder, diabetes and atrial fibrillation (“afib”). (Ex. 2, pp. 1-2; Ex. 3, p. 1.) She
had established care with her primary care physician in March of 2014. (Ex. 16, p. 21.)
Just prior to receiving the flu vaccine at issue, petitioner presented to an
orthopedist with a comminuted fracture to her right distal radius. (Ex. 21, p. 1.) She
underwent a closed reduction and her arm was splinted. (Id.) Petitioner received the flu
vaccination at issue in this case on October 21, 2015, during a primary care follow up
regarding her broken arm. (Ex. 1, p. 1.)
Petitioner had several follow up encounters with her orthopedist in California on
October 27, 2015,4 November 3, 2015,5 and November 17, 2015. (Ex. 22, pp. 1-4.)
Respondent stresses that petitioner had no pain or complaints at these follow up
encounters and that the November 3 and November 17 encounters explicitly record that
petitioner had no numbness or tingling. (ECF No. 73, p. 4.) Importantly, these
observations were recorded in the context of an examination of petitioner’s right wrist
status post fracture. (Ex. 22, pp. 1-2.) Numbness and tingling in petitioner’s right hand
were among her presenting symptoms prior to the resetting of her broken arm. (Id. at
6.)
Petitioner did not seek any medical care again until March of 2016, after she had
relocated from California to Missouri. (Ex. 2, p. 1.) She established care with Eric
Vonholten, D.O., on March 18, 2016. (Id.; see also Tr. at 46.) Petitioner provided a
broad medical history of attention deficit disorder, atrial fibrillation, and diabetes. (Id. at
1-2.) Although petitioner is characterized as seeking care “mainly” for her attention
deficit disorder, she also reported that she had “some issues with peripheral numbness
and tingling that she’s had for quite a long time.” (Id.) Nothing in this record clarifies
how long “quite a long time” would be however. Her Review of Systems also recorded
pain in her back, hands, and feet. (Id. at 2.) On physical exam, petitioner was noted to
have normal gait and station and no focal neurological deficits. (Id. at 3.) Petitioner was
assessed with, inter alia, peripheral neuropathy. (Id.) Petitioner did not return to this
provider.
4 Respondent asserts in his Rule 4 Report and in his motion response that petitioner was also seen by
her orthopedist on October 29, 2015. (ECF No. 28, p. 2 (citing Ex. 22, p. 199); see also ECF No. 73, p.
4.) Respondent cites to a page 199 of Exhibit 22, but Exhibit 22 only has 33 pages. Upon my review of
Exhibit 22, I do not see any evidence that petitioner had an orthopedic office visit on October 29, 2015.
Petitioner presented for a follow up appointment on October 27, 2015, at which time x-rays appeared to
show “good alignment,” but petitioner’s orthopedist was concerned that no “true lateral” imaging was
performed and he recommended such imaging. (Ex. 22, p. 4.) Notably, requisition forms included in
petitioner’s medical records indicate that petitioner went to another facility for x-ray imaging. (Id. at 8-13.)
There is a record with a “visit date” of October 29, 2015; however, that record indicates only that
petitioner’s x-ray imaging was reviewed and that “a message was left for the patient regarding x-ray
findings.” (Id. at 3.) Thus, this record does not indicate that petitioner actually spoke to her orthopedist.
Accordingly, it does not support respondent’s assertion that petitioner “had no complaints when briefly
seen on October 29, 2015.” (ECF No. 28, p. 2; ECF No. 73, p. 4.)
5 Respondent misidentifies this encounter as occurring on November 5, 2015. (ECF No. 28, p. 2 (citing
Ex. 22, p. 2); see also ECF No. 73, p. 4.)
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Instead, on April 8, 2016, petitioner established care with a different primary care
provider, Rajamanickam Purushothaman, M.D. (Ex. 3, pp. 1-2.; see also Tr. at 47.)
Petitioner’s reported history again focused heavily on her history of attention deficit
disorder, diabetes, and atrial fibrillation. (Id. at 1.) However, she also reported that
“she’s recently been having [a] problem with left-sided numbness from face to lower
extremity.” (Id.) Nothing in this record further contextualizes the characterization of
“recently.” On physical exam, petitioner could move all of her extremities without
difficulty, but had “slightly impaired sensation for light touch and pinprick lower
extremity.” (Id. at 2.) A CAT scan of petitioner’s head was ordered, which was normal.
(Id. at 3, 12.)
On April 12, 2016, petitioner returned to the same primary care provider. (Ex. 3,
pp. 6-8.) This time, petitioner’s primary complaint was “multiple joint pains, tingling of
the left side of the body, and [n]umbness.” (Id. at 6.) The joint pain is recorded as
having been occurring “intermittently for the past 2-3 months”; however, no duration is
noted for the numbness and tingling. (Id.) Three months prior to April 12, 2016, would
be about mid-January of 2016. Petitioner received a rheumatology referral. (Id. at 8.)
The same day, petitioner contacted a third primary care physician seeking to
establish care. (Ex. 20, p. 30.) Petitioner spoke to a nurse on the phone. She reported
that she was having “numbness all over her body including hands, arms, legs, back,
mouth and tongue.” (Id.) She acknowledged that she had sought care from her current
primary care doctor but indicated that she was having difficulty getting in touch with him.
(Id.) Petitioner was given an appointment for the following September and was
encouraged to continue trying to contact her current doctor’s office and to go to the
emergency department if her condition worsened. (Id.)
Petitioner subsequently presented to the emergency department on April 17,
2016, complaining of numbness and tingling in both of her hands, feet, legs, and
shoulders, as well as in her tongue for “at least six weeks.”6 (Ex. 5, p. 1.) She felt she
had chronic fibromyalgia. (Id.) Six weeks prior to April 17, 2016, would be
approximately the first week of March. Petitioner also described diffuse neck and back
pain and indicated that she was feeling opposite touch sensations (i.e. things felt hot
when they were cold and vice versa). On physical exam, she had normal deep tendon
reflexes, normal gait, and normal strength; however, she had diminished light touch
sensation with secondary tingling diffusely. (Id. at 2.) Petitioner had an MRI of the brain
performed which was negative for any abnormality. (Id. at 8.) No cause was found for
petitioner’s diffuse numbness. (Id.)
On April 22, 2016, petitioner established care with another primary care
physician. (Ex. 6, pp. 1-4.) Initially, petitioner is recorded as reporting that “for the last
6 Other notations in this emergency department record state that petitioner’s symptoms began six weeks
ago rather than “at least” six weeks ago. (E.g. Ex. 5, p. 5 (11:02 Triage Assessment states “pain began
six weeks ago.”); Ex. 5, p. 6 (13:36 assessment states “pain began 6 weeks ago”).) Notably, however,
the notations are not consistent. During the 11:02 triage assessment, petitioner’s pain is noted to be
continuous and in the 13:36 assessment it is noted to be intermittent. (Compare Ex. 5, p. 5, and Ex. 5, p.
6.)
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7 weeks she’s had paresthesias all over.” (Id. at 1.) This is consistent with what she
reported at the emergency department five days earlier. She also reported tingling in
her face and tongue, burning sensations in her feet, and back pain, without a specific
reference to onset. (Id.) However, in the same history, petitioner is also reported as
indicating that “[s]he also feels very tired. It started after she lost her balance and fell
and broke her right wrist.” (Id.) Based on the contemporaneous record of petitioner’s
treatment for her right wrist injury, this places onset in October of 2015. (Ex. 21, p. 1.)
On physical exam, petitioner had normal strength but diminished sensation to
monofilament in her feet. (Ex. 6, p. 2.) She was referred to a neurologist. (Id.)
Petitioner received a cervical spine MRI on May 3, 2016, which showed mild
degenerative changes. (Ex. 21, p. 5-6.) At a massage clinic visit on May 6, 2016,
petitioner was observed to be experiencing “severe nerve pain” in all of her extremities
which she reported began in October of 2015. (Ex. 14, p. 3.) Petitioner reported to Dr.
Hankins on May 9, 2016 that her condition had deteriorated to the point that she could
no longer perform her job duties and that she had been experiencing severe numbness
and tingling for the past ten weeks, placing onset of these symptoms at around mid-
February of 2016. (Ex. 21, p. 9.)
Petitioner received an EMG/NCS study on her upper extremities on May 24,
2016. (Ex. 7, p. 1.) Petitioner reported that she was experiencing a sensation of pins
and needles in her upper extremities for around twelve weeks, or since February 2016.
(Id.) The NCS showed bilateral median sensory/motor neuropathy consistent with
moderate to severe carpal tunnel syndrome (“CTS”), and bilateral ulnar motor
neuropathy, lacking features of cubital tunnel syndrome. (Id.) The EMG was
unremarkable. (Id.) Neither study revealed evidence for cervical radiculopathy,
myopathy, or plexopathy. (Id.) A note on this record however indicates that the
providers suspected a possible underlying peripheral neuropathy and referred petitioner
to a neurologist and orthopedist. (Id. at 2.)
Petitioner began physical therapy for her left shoulder on May 25, 2016. (Ex. 8,
p. 6.) She reported that the “pins and needles” sensation in her hands and feet began
twelve weeks prior, or late February of 2016. (Id.)
On June 30, 2016 petitioner was seen by Dr. Martin Schudy for a consultation.
(Ex. 9, p. 1.) Petitioner reported that she had recently moved from California to Missouri
and that she had fractured her right wrist in October of 2015. (Id.) However, Dr.
Schudy’s note continued that “[o]n further questioning it is now clear that she was
already having balance and tingling issues.” (Id.) He further indicated that “[a]bout 4
months ago, she was trying to move a boat with her son’s assistance and felt a sudden
increase in sensation of generalized tingling followed by weakness.” (Id.) This event
would have taken place in late February of 2016. Notably, this record suggests that
petitioner was already experiencing sensations of tingling and weakness prior to
February of 2016, but that those sensations “increased” after she exerted herself while
moving this boat with her son.
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Petitioner next saw neurologist Dr. Tania Beltran Papsdorf on July 20, 2016
where she reported that onset of her neurological symptoms began four and a half
months prior, or early February 2016. (Ex. 10, p. 1.) She reported that onset of these
symptoms was “very quick . . . .” (Id. at 3.) Petitioner denied fatigue, weakness, and
ataxia, but reported issues with balance and strength in addition to constipation,
incontinence, sweating, dizziness, and lightheadedness. (Id.) Petitioner showed
normal reflexes, sensation, coordination, gait, and strength aside from a 4+ toe
extension and 5- toe flexion. (Id. at 3-4.) Dr. Papsdorf diagnosed petitioner with
diabetic peripheral neuropathy and ordered an additional EMG and NCS. (Ex. 10, p. 4.)
Dr. Papsdorf also observed “[e]vidence of both small and large fiber peripheral
neuropathy.” (Id.) Dr. Papsdorf did not suspect CIDP, changed petitioner’s medication
to Lyrica, and opined that petitioner would not benefit from IVIG due to the lack of
demyelination on her NCV testing which showed a greater likelihood of axonal loss. (Id.
at 5.)
Petitioner’s PCP, Dr. Schudy, wrote on July 26, 2016 that “Dr. Papsdorf is
concerned that [petitioner] developed an axonal sensorimotor demyelinating peripheral
neuropathy secondary to insulin neuritis, [due] to rapid decline in chronic
hyperglycemia.” (Ex. 9, p. 6.) Dr. Schudy scheduled an additional NCV test to
reassess for CIDP. (Id.) Petitioner reported that shortly after moving to Missouri, “a
local doctor discontinued many of her medications including Cardizem.” (Id.) Dr.
Schudy believed petitioner experienced infrequent paroxysmal atrial fibrillation and
scheduled a four-month follow up. (Id. at 8.)
The following day, petitioner underwent an EMG and NCS, the results of which
were:
[S]uggestive of a possible demyelinating diffuse peripheral neuropathy such
as CIDP, however, this study is not complete due to the patient’s intolerance
of the study. Proximal muscles should be tested to look for more
denervation and reinnervation patterns (in CIDP would expect worsening
proximally). The left hand should be tested as well to look for possible
conduction block. This study showed worsening from the study done in
June 2016 . . . . A diabetic amyotrophy [] cannot be ruled out complete[ly]
[and] needle study with proximal muscle testing should be recommended,
however, the upper extremity findings would not be expected in a diabetic
amyotrophy.
(Ex. 19, p. 65.)
An August 24, 2016 record from Dr. Schudy describes a visit by petitioner to the
ER on August 22, 2016, for “possible [CIDP] . . . onset 4.5 months ago,” with “fast”
progression and treatment with IVIG. (Ex. 20, p. 4.) This would place onset of
petitioner’s CIDP symptoms at mid-April 2016.
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Petitioner was next seen by neurologist Dr. Brennen Bittel on September 20,
2016 “for evaluation of CIDP.” (Ex. 4, p. 1.) Petitioner reported that, “[a]fter the flu shot,
she began to feel just extreme fatigue. She attributed it to moving [and] the stress of
that, but then by February, she had noticed some tingling in her feet.” (Id.) Petitioner
also reported that her PCP suspected CIDP, as did a neurology consult following an
EMG. (Id.) Dr. Bittel observed mild weakness in petitioner’s hip flexors and finger
abductors, absent reflexes of her brachioradialis and legs, reduced sensation in her
distal legs, and an antalgic gait. (Id. at 5.) Dr. Bittel’s impression was “CIDP with
symptom onset in Feb 2016.” (Id. at 5-6.) Dr. Bittel prescribed nortriptyline for
petitioner’s pain and recommended a seven-month follow up if needed. (Id. at 6.)
Dr. Bittel noted on April 10, 2017, that petitioner had received IVIG every three
weeks until January when she began receiving it every six weeks. (Ex. 17, pp. 20-21.)
Petitioner reported that her strength had completely returned and wondered why she
still needed IVIG considering she did not receive any further benefit from it. (Id.)
Petitioner reported that she had been to a pain specialist and was taking oxycodone
twice daily as well as Cellcept since that February. (Id.) Dr. Bittel believed that
petitioner may have monophasic CIDP and that she could stop taking Cellcept. (Id.) He
also recommended that petitioner taper off IVIG and scheduled a three-month follow up.
(Id.)
By May 12, 2017, petitioner’s IVIG had been tapered down to ten-week intervals
and she reported that her symptoms had returned after the fifth week off IVIG. (Ex. 17,
pp. 32-38.)
Petitioner next saw neurologist Dr. Dipika Aggarwal on August 9, 2017 to
establish care for her now diagnosed CIDP. (Ex. 17, pp. 32-38.) She reported an onset
date of February 2016, a diagnosis date of July 2016, and that she began IVIG in
September of 2016. (Id.)
On November 10, 2017, petitioner reported to neurologist Dr. Ruthanna Hunger
that her “[s]ymptoms started in Oct 2015 after flu shot – she had pain, fatigue. Pain in
back and shoulder. Then in Feb 2016 – developed drop foot – left. Had tingling in
extremities and muscle atrophy.” (Ex. 19, p. 2.) Dr. Hunger concurred with Drs. Bittel
and Aggarwal’s diagnoses and recommended that petitioner continue IVIG. (Id.)
B. As described in testimony and affidavits
1. Petitioner’s affidavit and testimony
Petitioner filed an affidavit signed July 27, 2018, detailing the progression of her
CIDP. (Ex. 26.) Petitioner averred that she began experiencing “muscle aches, fatigue,
and weakness,” in late November of 2015. (Id.) She also stated that she reported
feeling pain and fatigue, but not numbness or tingling at a November 17, 2015
appointment with Dr. Shah. (Id.) She explained that she also experienced “prickly
feeling[s] in her fingers and toes,” at this appointment, but that she did not report it to Dr.
Shah because she was concerned that she would not be released if she reported her
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sensory symptoms. (Id.) She also noted that she was under the impression that these
symptoms which she withheld from Dr. Shah were due to her wrist fracture. (Id.)
Petitioner offered substantially the same testimony during the fact hearing. (Tr. at 14-
15, 19.)
Petitioner additionally testified that prior to her vaccination she had no serious
health conditions, only a broken wrist in October of 2015 and evidence of atrial
fibrillation in March of the same year. (Tr. at 7.) She never experienced any numbness,
tingling, or weakness prior to her vaccination and had no issues with walking or
balance. (Tr. at 8.) Petitioner had a physically demanding job as a real estate agent
prior to onset of her condition which required her to be on her feet for a majority of the
day walking, painting, staging furniture, and doing other tasks to prepare her properties
for showings. (Tr. at 7-8.)
In her affidavit, petitioner averred that “[b]y Christmas 2015, I was experiencing
muscle aches, fatigue, foggy brain, muscle weakness, pain in my back, shoulder, and
hips, and soreness in my wrists, which increased in intensity [as] time went on.” (Ex.
26, p. 2.) She explained that her hand symptoms gradually progressed to numbness
and tingling which eventually spread to her feet as well. (Id.) She stated that she was
unable to walk, but believed her symptoms were caused by a pinched nerve that
occurred during the fall that fractured her wrist. (Id.) Petitioner noted that by January of
2016, she was experiencing “unbearable” pain. She also noted that she began to feel
unstable on her feet and odd sensations such as dry clothes feeling damp or having
“hot and cold sensations” all over her body. (Id.)
In testimony, petitioner indicated that in January of 2016, her symptoms
drastically changed, progressing from a feeling of “pins and needles” to pain, as if she
were “holding a cactus.” (Tr. at 26.) Petitioner also experienced inconsistent sensations
associated with temperatures, and sensations in her feet. (Id.) Petitioner indicated that
she was not having difficulty walking in January 2016, but that it was nonetheless
painful to do so. (Tr. at 28.) Petitioner testified that in February of 2016 she developed
drop foot and her symptoms became significantly worse, spreading to both sides of her
body. (Tr. at 32-33.)
Although she reported February 2016 as the date of onset to most of her care
providers, petitioner testified that she did so because she thought she was only
suffering from a pinched nerve before February 2016. (Tr. at 53-54.) She explained
that because her condition changed so drastically in February of 2016, she thought this
drastic change signaled the onset of her condition. (Id.) However, she now believes
that her onset occurred much earlier in the form of numbness and tingling in her
extremities around the time she moved to Missouri in November of 2015. (Tr. at 18-19.)
Petitioner testified that some of her medical records contained inaccuracies
regarding her weight, certain dates, family medical history, neurological exam results,
and history of neck pain, however, she did not know why or how these inaccuracies
occurred. (Tr. at 11-12.)
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2. Kathleen Sorensen’s affidavit and testimony
Petitioner’s sister, Kathleen Sorensen, submitted an affidavit dated April 7, 2020,
and also testified in support of petitioner. (Ex. 34.) Ms. Sorensen testified that
petitioner told her in November of 2015 that she was experiencing some “funky
numbness or tingling or something going on, but it was in her feet.” (Tr. at 70-71.) She
also testified that petitioner mentioned numbness in her feet, tingling in her hands,
soreness in her shoulders and back, and significant fatigue during her move in
November 2015. (Tr. at 74-75.) Ms. Sorenson also testified that she noticed petitioner
had trouble walking during the move. (Tr. at 76-77.) In her affidavit, Ms. Sorensen
recounted that she went to petitioner’s home in Missouri on November 20, 2015, and
observed in person for the first time that petitioner was experiencing fatigue and
reduced strength while unpacking. (Ex. 34, pp. 1-2.)
3. Lina Robertson’s affidavit and testimony
Petitioner also filed an affidavit from her supervisor at Re/Max, Lina Robertson.
(Ex. 25.) Ms. Robertson avers that she first met petitioner as her real estate agent while
petitioner was searching for a house in Missouri. (Id. at 1.) According to Ms.
Robertson’s affidavit, petitioner “didn’t mention any health issues, appeared well, and
spoke of activities with her kids and grandkids.” (Id.) Ms. Robertson writes that shortly
after Thanksgiving, petitioner reported that she was feeling extremely tired, had back
and shoulder pain, and experiencing “prickly feelings,” which she believed was caused
by a pinched nerve. (Id. at 1.) In mid-December of 2015 however, Ms. Robertson
observed petitioner at the office noting that she “looked tired and . . . walked
unbalanced.” (Id.) Ms. Robertson also testified at the fact hearing. She provided
testimony substantially similar to her affidavit. (Tr. at 93-94, 97.) Ms. Robertson
testified that in mid-December of 2015, she observed petitioner walking into her office
and distinctly observed an abnormal gait that she described as “twitchy,” “guarded”, and
“slow.” (Tr. at 98-100.) Ms. Robertson also confirmed that her relationship with
petitioner was professional rather than personal and that they no longer work together.
(Tr. at 93, 105.)
4. Kristin Johnson’s affidavit
Petitioner filed an affidavit from her coworker, Kristin Johnson on July 13, 2018.
(Ex. 23.) Ms. Johnson avers that in January of 2016, petitioner confessed to her that
she had not been coming into the office because was not feeling well and unable to
work. (Id. at 1.) Petitioner asked Ms. Johnson not to tell anybody at their workplace
about petitioner’s inability to work because she was “new to RE/Max.” (Id.)
5. Ginger Williams’s affidavit
Petitioner filed an affidavit from her close friend Ginger Williams on July 17,
2018. (Ex. 24.) Ms. Williams avers that at the end of October of 2015, she called
9

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petitioner who reported that she was experiencing muscle aches and pains. (Id. at 1.)
Ms. Williams also avers that in early November of 2015, petitioner reported that she was
experiencing constant fatigue, brain fog, increased muscle aches, and new pain in her
shoulders, back, and arms. (Id.) Finally, Ms. Williams avers that she visited petitioner
in January of 2017 and at that point petitioner explained her complete history, including
that she was experiencing a “pins and needles” sensation in her arms, hands, and feet,
extreme back and shoulder pain, and extreme sensation to different temperatures. (Id.
at 1-2.) Ms. Williams avers that at that time she observed that petitioner could not walk,
drive or stand. (Id.)
C. Petitioner’s journal
Around March of 2016, petitioner began documenting her visits to various
doctors including the various treatments and therapies she received and the test results
that were relayed to her by her specialists. (Ex. 33.) The first entry occurs in March of
2016. (Ex. 33, p. 1.) Petitioner writes that she was not having success getting an
appointment by describing the symptoms she was experiencing, so she instead asked
for an appointment to address her ADD which was scheduled for March 18, 2016 with
Dr. Vonholten. (Id.) Petitioner writes on March 18, 2016 that she told Dr. Vonholten
she had experienced numbness in both of her feet and hands for several months.7 She
writes that “hand and feet problems started months ago,” and that she “[t]old him
[m]uscle and nerves for many months.” (Id.)
On April 17, 2016, petitioner wrote that she began carrying a card of her
symptoms to present to doctors and nurses. (Id. at 4.) She notes that her medical
records “show different eruptation [sic] and errors of my communication with the
[d]octors and nurses . . . .” (Id.) Petitioner wrote on April 22, 2016 that she “[told] most
doctors onset was January – February 2016 because that’s when it was at its [sic]
worse [sic] muscle and nerves both sides and got dropped [sic] foot.”8 (Id. at 6.)
The remainder of petitioner’s journal documents her struggles securing prompt
treatment and diagnosis but does not bear directly on the issue of onset.
D. Expert opinion relevant to onset
a. Petitioner’s expert, Dr. Nizar Souayah
Petitioner’s expert, Dr. Nizar Souyah writes that CIDP is “characterized clinically
by a presence of symmetric weakness that involves proximal and distal muscles
progressing over a period of two months,” but notes that “its clinical presentation and
course are variable.” (Ex. 30, p. 6.) Dr. Souyah also writes that “[t]he disease usually
7 In this entry, petitioner later crossed out “several months,” wrote “a long time,” and added “He wouldn’t
listen” in her own writing.
8 Petitioner later added to this entry in her own handwriting, “[p]rior to Feb tired, pinch nerve pain back
shoulders.”
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starts with distal arm weakness,” and that he believed that “[petitioner’s] [CIDP]
symptoms started approximately 5 weeks after influenza vaccination and progressed
over the next several months.” (Id. at 7.) This would place her onset at around late
November or early-December of 2015.
b. Respondent’s expert, Dr. Peter Donofrio
Respondent’s expert, Dr. Peter Donofrio cites several diagnostic criteria for CIDP
in his expert report. (Ex. A, p. 9.) The criteria note that typical onset is recognized by
progressive, stepwise, or recurrent symmetric proximal and distal weakness, sensory
dysfunction in all extremities developing over two months, potential cranial nerve
effects, and absent reduced tendon reflexes in all extremities. (Id.; see also Ex. D, p.
3.) Atypical CIDP is recognized by the same criteria, except that tendon reflexes may
be normal in unaffected limbs, and additional symptoms may include pure motor or
sensory presentations, and asymmetric or focal presentations. (Ex. D, p. 3.) Dr.
Donofrio writes that “[i]f one chooses to use the onset of numbness and tingling as the
first feature of [CIDP], it began in late February or early March 2016.” (Ex. A. p. 8.) The
remainder of his report however focuses on the medical theory linking the flu vaccine to
CIDP and not onset of petitioner’s condition.
III. Legal Standard
The process for making determinations in Vaccine Program cases regarding
factual issues begins with consideration of the medical records. § 11(c)(2). The special
master is required to consider “all [ ] relevant medical and scientific evidence contained
in the record,” including “any diagnosis, conclusion, medical judgment, or autopsy or
coroner's report which is contained in the record regarding the nature, causation, and
aggravation of the petitioner's illness, disability, injury, condition, or death,” as well as
“the results of any diagnostic or evaluative test which are contained in the record and
the summaries and conclusions.” § 13(b)(1)(A). The special master is then required to
weigh the evidence presented, including contemporaneous medical records and
testimony. See Burns v. Sec'y of Health & Human Servs., 3 F.3d 415, 417 (Fed. Cir.
1993). Pursuant to Vaccine Act § 13(a)(1)(A), a petitioner must prove their claim by a
preponderance of the evidence. A special master must consider the record as a whole,
but is not bound by any diagnosis, conclusion, judgment, test result, report, or summary
concerning the nature, causation, and aggravation of petitioner’s injury or illness that is
contained in a medical record. § 13(b)(1).
Medical records generally constitute trustworthy evidence. Cucuras v. Sec’y of
Health & Human Servs., 993 F.2d 1525, 1528 (Fed. Cir. 1993). “The records contain
information supplied to or by health professionals to facilitate diagnosis and treatment of
medical conditions. With proper treatment hanging in the balance, accuracy has an
extra premium.” Id. However, it must also be noted that there is no presumption that
medical records are accurate or complete as to all of a patient’s conditions. Kirby v.
Sec’y of Health & Human Servs., 997 F.3d 1378, 1382-83 (Fed. Cir. 2021). Afterall,
“[m]edical records are only as accurate as the person providing the information.”
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Parcells v. Sec’y of Health & Human Servs., No. 03-1192V, 2006 WL 2252749, at *2
(Fed. Cl. Spec. Mstr. July 18, 2006). Nonetheless, “the absence of a reference to a
condition or circumstance is much less significant than a reference which negates the
existence of the condition or circumstance.” Murphy v. Sec’y of Health & Human
Servs., 23 Cl. Ct. 726, 733 (1991) (quoting the decision below), aff’d per curiam, 968
F.2d 1226 (Fed. Cir. 1992). Where medical records are clear, consistent, and complete,
they ordinarily receive substantial weight.9 Lowrie v. Sec’y of Health & Human Servs.,
No. 03-1585V, 2005 WL 6117475, at *19 (Fed. Cl. Spec. Mstr. Dec. 12, 2005).
There are situations in which compelling testimony may be more persuasive than
written records, such as where records are deemed to be incomplete or inaccurate.
Campbell v. Sec'y of Health & Human Servs., 69 Fed. Cl. 775, 779 (2006) (“like any
norm based upon common sense and experience, this rule should not be treated as an
absolute and must yield where the factual predicates for its application are weak or
lacking”); Lowrie, 2005 WL 6117475, at *19 (“[w]ritten records which are, themselves,
inconsistent, should be accorded less deference than those which are internally
consistent”) (quoting Murphy, 23 Cl. Ct. at 733). When witness testimony is offered to
overcome the presumption of accuracy afforded to contemporaneous medical records,
such testimony must be “consistent, clear, cogent, and compelling.” Camery v. Sec'y of
Health & Human Servs., 42 Fed. Cl. 381, 391 (1998) (citing Blutstein v. Sec'y of Health
& Human Servs., No. 90–2808V, 1998 WL 408611, at *5 (Fed. Cl. Spec. Mstr. June 30,
1998)). Further, the Special Master must consider the credibility of the individual
offering the testimony. Andreu v. Sec’y of Health & Human Servs., 569 F.3d 1367,
1379 (Fed. Cir. 2009); Bradley v. Sec’y of Health & Human Servs., 991 F.2d 1570, 1575
(Fed. Cir. 1993). In making a determination regarding whether to afford greater weight
to contemporaneous medical records or other evidence, such as testimony at hearing,
there must be evidence that this decision was the result of a rational determination.
Burns v. Sec’y of Health & Human Servs., 3 F.3d 415, 417 (Fed. Cir. 1993).
IV. Party Contentions
a. Petitioner
In support of her position, petitioner argues that the lay testimony offered in this
case supports a finding that onset of her symptoms occurred between October 28, 2015
and November 22, 2015. First, she argues that each fact witness testified that they
noticed a change in petitioner’s strength and energy in either late November of 2015 or
early December of 2015. (ECF No. 72, p. 7.) Petitioner points to the testimony of Lina
Robertson, who testified that she witnessed petitioner arrive at the office in December of
9 For example, the Court of Federal Claims has listed four possible explanations for inconsistencies
between contemporaneously created medical records and later testimony: (1) a person's failure to
recount to the medical professional everything that happened during the relevant time period; (2) the
medical professional's failure to document everything reported to her or him; (3) a person's faulty
recollection of the events when presenting testimony; or (4) a person's purposeful recounting of
symptoms that did not exist. La Londe v. Sec'y Health & Human Servs., 110 Fed. Cl. 184, 203–04
(2013), aff'd, 746 F.3d 1334 (Fed. Cir. 2014).
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2015 with a noticeable gait abnormality. (Id.) Next, petitioner cites her sister’s
testimony that petitioner was unable to help in her move to Missouri at the end of
November 2015 and instead sat in a chair giving directions. (Id.) Petitioner notes that
her sister testified that petitioner’s gait was unsure, as if her “foot was asleep.” (Id.)
Petitioner also argues that the medical records corroborate her own testimony.
However, she does not cite any actual records that corroborate her own testimony, and
instead, recites the testimony itself, noting that “[t]he only records within petitioner’s
alleged onset window pertained to petitioner’s wrist treatment in October and November
of 2015. However, as petitioner explained, she was not yet concerned about her
symptoms at that time,” and that “[s]ome subsequent medical records, which are even
further removed from the onset, point to February 2016 at the start date. However,
petitioner explained that it was around February when she noted a worsening of her
condition. In fact, she noticed her symptoms worsening in January.” (Id. at 7-8.)
Finally, petitioner explains that she reported that the weakness in her arms and legs
“suddenly increased approximately four months prior, which would have been February
of 2016,” to Dr. Schudy. (Id. at 8.) Petitioner argues that this specific report that her
symptoms increased in February of 2016 necessarily means they occurred prior to that
time. (Id.)
b. Respondent
Respondent urges the Court to disregard petitioner’s post vaccination fatigue as
the point of onset for her CIDP symptoms, explaining that petitioner’s medical records
do not document any reports of fatigue that began following her broken wrist. (ECF No.
73, p. 15.) Respondent notes that although petitioner’s sister testified that petitioner
appeared weak and unable to assist during her move to Missouri, she also testified that
she did not really “remember [tiredness] being a huge issue. [She] just figured it was
from the wrist or whatever,” and that “[people say] ‘I’m tired’ all the time,” figuring that
petitioner was simply tired on account of the move and her recently broken wrist. (Id.)
Respondent also argues that petitioner’s fatigue following her vaccination is nonspecific
and not neurologic in nature, and that petitioner’s first report of neurological
symptomology began roughly four months after vaccination in February of 2016. (Id. at
16.) The remainder of respondent’s argument focuses on the issue of entitlement as
opposed to onset. (See id. at 16-18.)
V. Discussion
The inconsistencies between the contemporaneous medical records, affidavits,
testimony, and other documentation present a significant challenge when evaluating the
record as a whole. However, in spite of these inconsistencies, several pieces of
evidence, including several medical records and the testimony of petitioner’s former
employer, Ms. Lina Robertson, carry significant weight in favor of finding that at least
some of petitioner’s neurological symptoms began in late November of 2015.
Specifically, the evidence preponderates in favor of a finding that petitioner experienced
onset of numbness and tingling beginning in late November 2015. There is also
13

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preponderant evidence she also experienced fatigue at that time; however, onset of
weakness is not demonstrated until July of 2016.
Petitioner’s medical records suggest at least five different periods of onset for her
peripheral numbness and tingling: October of 2015 shortly after her flu shot (Ex. 14, p.
3), February of 2016 (Ex. 8, p. 6; Ex. 9, p. 1; Ex. 10, p. 1; Ex. 17, pp. 32-39; Ex. 19, p.
2), during the first week of March 2016 (Ex. 5, p. 1; Ex. 6, p. 1), “quite a long time”
before March 18 (Ex. 2, p. 2), and “recently” relative to April 8 (Ex. 3, p. 1). Accordingly,
taken as a whole, the medical records are not clear and consistent, reducing their
weight.10 Lowrie, 2005 WL 6117475, at *19. Notably, petitioner’s initial treatment record
of March 18, 2016 confirms as of that date that petitioner was experiencing peripheral
numbness and tingling “for quite a long time,” strongly suggesting that those later
records placing onset in early March or later are unlikely to be accurate.11 (Ex. 5, p. 1;
Ex. 6, p. 1; Ex. 3, p. 1.)
Additionally, although February of 2016 is the most frequently referenced period
of onset in the medical records, there are several reasons why this fact alone should not
control. First, initial onset occurring in February of 2016 is also not necessarily
consistent with petitioner’s initial treatment record indicating that petitioner was
experiencing peripheral numbness and tingling “for quite a long time.” (Ex. 2, p. 2.)
Furthermore, one among these records placing onset in February of 2016 actually
explains that what petitioner experienced at that time was an “increase” in symptoms
she associated with a specific incident she experienced while trying to move a boat with
her son. (Ex. 9, p. 1.) Dr. Schudy’s June 30, 2016 record explains that he questioned
petitioner with respect to the details of her history and that “[o]n further questioning it is
now clear that she was already having balance and tingling issues” before her move to
Missouri and that she experienced an “increase” in symptoms in February of 2016.12
10 Petitioner also submitted an electronic journal documenting the progress of her disease and treatment.
(See Ex. 33.) However, I do not find petitioner’s journal particularly useful in determining the date of
onset because it was started in March of 2016 and largely restates the medical records with regard to
onset. Petitioner’s testimony and journal both indicate that she had difficulty communicating with her
physicians, felt frustrated with her access to care and the quality of care she received, and may not have
been entirely forthcoming with her physicians in all instances. This presents a further challenge in
weighing both petitioner’s medical records and her testimony.
11 However, there is no evidence of record to suggest that “quite a long time” refers to any time prior to
the period of onset alleged by petitioner. As respondent stressed, petitioner’s prior encounters in
California in late October and the first half of November 2015 showed no evidence of numbness or
tingling. (ECF No. 73, p. 4; Ex. 22, pp. 1-4.)
12 Petitioner similarly testified that in February of 2016, she developed drop foot and at that time became
certain she was experiencing a serious neurological issue and not a pinched nerve as she previously
thought. (Tr. at 54.) Because drop foot was the condition that made petitioner realize she was suffering
from a serious condition, she anchored the date of onset to that event in subsequent visits to her
physicians. (Id.) Notably, several of the visits placing onset in February occurred consecutively and
within a few months of each other. It is not necessarily surprising that petitioner would consistently report
the same onset at encounters happening around the same time, reducing the significance of the multiple
instances of such reports. Upon learning that CIDP may begin with numbness and tingling in the
14

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(Id.) This harmonizes with the “quite a long time” description of peripheral numbness
and tingling provided in petitioner’s initial March 18 treatment record. (Ex. 2, p. 2.)
There is also significant fact witness testimony supporting onset of numbness,
tingling, and fatigue occurring in late November of 2015.13 First, petitioner’s sister
testified that when she spoke to petitioner shortly before her move to Missouri, petitioner
reported that “[s]he had some funky numbness or tingling or something going on, but it
was in her feet . . . .” (Tr. at 71.) She also testified that when she arrived to help
petitioner move around November 24, 2016, petitioner reported having numbness in her
feet and tingling in her hands as well as other nonspecific symptoms such as myalgias
and arthralgias. (Tr. at 74.)
The testimony of Ms. Lina Robertson is perhaps the most helpful in that Ms.
Robertson is neither related to petitioner, nor a close friend, and is therefore the most
arms-length witness who testified in this case. (See Tr 93.) Ms. Robertson testified that
she received a report from petitioner in late November of experiencing fatigue as well as
“prickly” sensations she at that time attributed to a pinched nerve. (Tr. at 97; Ex. 25, p.
1.) Ms. Robertson was also able to recall a distinct and readily observable difference in
petitioner’s health prior to and after her vaccination due to their limited contact during
that period. (See Tr. at 94, 98-100.) Prior to petitioner’s vaccination, Ms. Robertson
worked as petitioner’s real estate agent, showing petitioner houses in Missouri before
her move. (Tr. at 93.) She testified that while viewing houses, petitioner had no trouble
walking or using her hands and seemed to be a very energetic person. (Id. at 94-95.)
However, Ms. Robertson testified, when she next saw petitioner in person in mid-
December, she noticed a marked difference in her condition. (Tr. at 98-100.) Ms.
Robertson testified that petitioner no longer seemed to have the energy she did when
they first met, and most importantly, that petitioner seemed to have significant difficulty
ambulating, walking in a way that she described as twitchy, guarded, and slow. (Id. at
99.) Combined with the other evidence in the record, Ms. Robertson’s testimony is
consistent with a finding that petitioner began experiencing numbness and tingling in
her extremities around late November of 2015.14
In her affidavit, petitioner also averred that she experienced weakness as early
as November of 2015. (Ex. 26.) However, despite many physical examinations during
the course of petitioner’s care, weakness was not documented in petitioner’s medical
extremities, petitioner now believes that her onset began long before February 2016, closer to
Thanksgiving of 2015. (Id. at 53-54.)
13 The two affidavits provided by non-testifying witnesses are less helpful in resolving this motion. Ms.
Williams’ affidavit only describes nonspecific symptoms during the alleged period of onset and states that
she was not made aware of petitioner’s neurologic symptoms until January of 2017. Thus, it is largely
unhelpful in determining the date of onset. (Ex. 24.) Ms. Johnson’s affidavit is likewise nonspecific as to
symptoms occurring in December and January. Ms. Johnson’s affidavit would tend to support the
conclusion that petitioner’s condition further deteriorated in February but is less helpful with respect to the
initial onset of symptoms. (Ex. 25.)
14 Petitioner testified that through January of 2016 she had no difficulty walking, though walking was
painful. (Tr. 28.)
15

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records until June 30, 2016, when petitioner first saw Dr. Schudy. (Ex. 9, pp. 1-3.) At
that time, however, Dr. Schudy’s physical examination found “adequate” strength and
muscle tone. (Id. at 2.) At least two prior physical examinations during petitioner’s April
17, 2016, and April 22, 2016, encounters had confirmed that she had normal strength at
that time. (Ex. 5, p. 2; Ex. 6, p. 2.) Petitioner’s July 27, 2016 encounter with Dr.
Papsdorf is the first time that weakness of any degree was found on physical
examination. (Ex. 10, p. 4.) Especially in light of these findings on physical examination,
the observations included in the lay witness testimony are inadequate to distinguish
weakness as a neurologic sign from the effects of deteriorated health attributable to
generalized pain and fatigue. Accordingly, there is not preponderant evidence that
petitioner experienced weakness at or prior to Dr. Schudy’s June 30, 2016 encounter.
VI. Conclusion
Considering petitioner’s medical records, her testimony, the expert reports, and
the testimony and affidavits of petitioner’s fact witnesses, the record as a whole
preponderates in favor of finding that petitioner experienced numbness and tingling in
her extremities along with fatigue beginning in late November 2015; however, there is
not preponderant evidence on the current record that she suffered weakness until July
of 2016. At this time I do not reach the question of whether or how these symptoms,
coupled with the overall medical course reflected in the treatment records, support
petitioner’s allegation of vaccine-caused CIDP. The experts shall have an opportunity
to submit additional reports in light of this fact finding.
IT IS SO ORDERED.
s/Daniel T. Horner
Daniel T. Horner
Special Master
16

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DOCUMENT 2: USCOURTS-cofc-1_17-vv-01112-1
Date issued/filed: 2025-06-06
Pages: 22
Docket text: PUBLIC DECISION (Originally filed: 05/09/2025) regarding 101 DECISION of Special Master. Signed by Special Master Daniel T. Horner. (cd) Service on parties made.
--------------------------------------------------------------------------------
Case 1:17-vv-01112-UNJ Document 105 Filed 06/06/25 Page 1 of 22
In the United States Court of Federal Claims
OFFICE OF SPECIAL MASTERS
No. 17-1112V
Filed: May 9, 2025
Special Master Horner
EILEEN SCHMIGEL,
Petitioner,
v.
SECRETARY OF HEALTH AND
HUMAN SERVICES,
Respondent.
Paul R. Brazil, Muller Brazil, LLP, Dresher, PA, for petitioner.
Dorian Hurley, U.S. Department of Justice, Washington, DC, for respondent.
DECISION1
On August 18, 2017, petitioner filed a petition under the National Childhood
Vaccine Injury Act, 42 U.S.C. § 300aa-10, et seq. (2012),2 alleging that she suffered
chronic inflammatory demyelinating polyneuropathy (“CIDP”) following receipt of an
influenza (“flu”) vaccination on October 21, 2015. (ECF No. 1.) For the reasons
discussed below, I find that petitioner is not entitled to an award of compensation.
I. Applicable Statutory Scheme
Under the National Vaccine Injury Compensation Program, compensation
awards are made to individuals who have suffered injuries after receiving vaccines. In
general, to gain an award, a petitioner must make a number of factual demonstrations,
including showing that an individual received a vaccination covered by the statute;
1 Because this document contains a reasoned explanation for the action taken in this case, it must be
made publicly accessible and will be posted on the United States Court of Federal Claims' website, and/or
at https://www.govinfo.gov/app/collection/uscourts/national/cofc, in accordance with the E-Government
Act of 2002. 44 U.S.C. § 3501 note (2018) (Federal Management and Promotion of Electronic
Government Services). This means the document will be available to anyone with access to the
internet. In accordance with Vaccine Rule 18(b), Petitioner has 14 days to identify and move to redact
medical or other information, the disclosure of which would constitute an unwarranted invasion of privacy.
If, upon review, I agree that the identified material fits within this definition, I will redact such material from
public access.
2 All references to “§ 300aa” below refer to the relevant section of the Vaccine Act at 42 U.S.C. § 300aa-
10, et seq.
1

Case 1:17-vv-01112-UNJ Document 105 Filed 06/06/25 Page 2 of 22
received it in the United States; suffered a serious, long-standing injury; and has
received no previous award or settlement on account of the injury. Finally – and the key
question in most cases under the Program – the petitioner must also establish a causal
link between the vaccination and the injury.
In some cases, the petitioner may simply demonstrate the occurrence of what
has been called a “Table Injury.” That is, it may be shown that the vaccine recipient
suffered an injury of the type enumerated in the “Vaccine Injury Table,” corresponding to
the vaccination in question, within an applicable time period following the vaccination
also specified in the Table. If so, the Table Injury is presumed to have been caused by
the vaccination unless it is affirmatively shown that the injury was caused by some
factor other than the vaccination. § 300aa-13(a)(1)(A); § 300aa-11(c)(1)(C)(i);
§ 300aa-14(a); § 300aa-13(a)(1)(B). In many cases, however, the vaccine recipient
may have suffered an injury not of the type covered in the Vaccine Injury Table. In such
instances, an alternative means exists to demonstrate entitlement to a Program award.
That is, the petitioner may gain an award by showing that the recipient’s injury was
“caused-in-fact” by the vaccination in question. § 300aa-13(a)(1)(B);
§ 300aa-11(c)(1)(C)(ii). In that context, the presumptions available under the Vaccine
Injury Table are inoperative. The burden is on the petitioner to introduce evidence
demonstrating that the vaccination actually caused the injury in question. Althen v.
Sec’y of Health & Human Servs., 418 F.3d 1274, 1278 (Fed. Cir. 2005); Hines ex rel.
Sevier v. Sec’y of Health & Human Servs., 940 F.2d 1518, 1525 (Fed. Cir. 1991).
CIDP is not an injury listed on the Vaccine Injury Table relative to any
vaccination. Guillain-Barre Syndrome (“GBS”), which petitioner’s expert invokes as
partial support for his theory of causation, is a Table injury if onset occurs 3-42 days
following receipt of a flu vaccine. 42 C.F.R. § 100.3(a)(XIV)(D). However, a diagnosis
of CIDP is listed among the exclusionary criteria for a Table Injury of GBS. 42 C.F.R.
§ 100.3(c)(15)(vi). To succeed on a claim that petitioner’s flu vaccine caused CIDP,
petitioner must satisfy the burden of proof for “causation-in-fact.”
The showing of “causation-in-fact” must satisfy the “preponderance of the
evidence” standard, the same standard ordinarily used in tort litigation.
§ 300aa-13(a)(1)(A); see also Althen, 418 F.3d at 1279; Hines, 940 F.2d at 1525.
Under that standard, the petitioner must show that it is “more probable than not” that the
vaccination was the cause of the injury. Althen, 418 F.3d at 1279. The petitioner need
not show that the vaccination was the sole cause but must demonstrate that the
vaccination was at least a “substantial factor” in causing the condition, and was a “but
for” cause. Shyface v. Sec’y of Health & Human Servs., 165 F.3d 1344, 1352 (Fed. Cir.
1999). Thus, the petitioner must supply “proof of a logical sequence of cause and effect
showing that the vaccination was the reason for the injury[,]” with the logical sequence
being supported by “reputable medical or scientific explanation.” Althen, 418 F.3d at
1278; Grant v. Sec’y of Health & Human Servs., 956 F.2d 1144, 1148 (Fed. Cir. 1992).
Ultimately, petitioner must satisfy what has come to be known as the Althen test, which
requires: (1) a medical theory causally connecting the vaccination and the injury; (2) a
logical sequence of cause and effect showing that the vaccination was the reason for
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Case 1:17-vv-01112-UNJ Document 105 Filed 06/06/25 Page 3 of 22
the injury; and (3) a showing of proximate temporal relationship between vaccination
and injury. Id.
A petitioner may not receive a Vaccine Program award based solely on his or her
assertions, but may support the petition with either medical records or by the opinion of
a competent physician. § 300aa-13(a)(1). Medical records are generally viewed as
particularly trustworthy evidence, because they are created contemporaneously with the
treatment of the patient. Cucuras v. Sec’y of Health & Human Servs., 993 F.2d 1525,
1528 (Fed. Cir. 1993). However, medical records and/or statements of a treating
physician’s views do not per se bind the special master to adopt the conclusions of such
an individual, even if they must be considered and carefully evaluated.
§ 300aa-13(b)(1). A petitioner may also rely upon circumstantial evidence. Althen, 418
F.3d at 1280. In that regard, the Althen court noted that a petitioner need not
necessarily supply evidence from medical literature supporting petitioner’s causation
contention, so long as the petitioner supplies the medical opinion of an expert. Id. at
1279-80. While scientific certainty is not required, that expert’s opinion must be based
on “sound and reliable” medical or scientific explanation. Boatmon v. Sec’y of Health &
Human Servs., 941 F.3d 1351, 1359 (Fed. Cir. 2019).
Cases in the Vaccine Program are assigned to special masters who are
responsible for “conducting all proceedings, including taking such evidence as may be
appropriate, making the requisite findings of fact and conclusions of law, preparing a
decision, and determining the amount of compensation, if any, to be awarded.” Vaccine
Rule 3. Special masters must ensure each party has had a “full and fair opportunity” to
develop the record but are empowered to determine the format for taking evidence
based on the circumstances of each case. Vaccine Rule 3(b)(2); Vaccine Rule 8(a);
Vaccine Rule 8(d). Special masters are not bound by common law or statutory rules of
evidence but must consider all relevant and reliable evidence in keeping with
fundamental fairness to both parties. Vaccine Rule 8(b)(1). The special master is
required to consider “all . . . relevant medical and scientific evidence contained in the
record,” including “any diagnosis, conclusion, medical judgment, or autopsy or coroner’s
report which is contained in the record regarding the nature, causation, and aggravation
of the petitioner’s illness, disability, injury, condition, or death,” as well as the “results of
any diagnostic or evaluative test which are contained in the record and the summaries
and conclusions.” § 300aa-13(b)(1). The special master is required to consider the
entirety of the record, draw plausible inferences, and articulate a rational basis for the
decision. Winkler v. Sec’y of Health & Human Servs., 88 F.4th 958, 963 (Fed. Cir.
2023) (citing Hines, 940 F.2d at 1528).
II. Procedural History
This case was reassigned to the undersigned in August of 2019. (ECF No. 46.)
By that time, respondent had already filed his Rule 4 Report, recommending against
compensation (ECF No. 28), and the parties had filed expert reports, with neurologist
Nizar Souayah, M.D., opining on petitioner’s behalf and neurologist Peter Donofrio,
M.D., opining on respondent’s behalf. (ECF Nos. 40, 42; Exs. 30, A.) After the case
was reassigned, I held a fact hearing on September 25, 2020 (see Transcript of
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Proceedings (“Tr.”) at ECF No. 67), and issued a finding of fact regarding onset of
petitioner’s symptoms on November 19, 2021. (ECF No 74; see also Schmigel v. Sec’y
of Health & Human Servs., No. 17-1112V, 2021 WL 5905687 (Fed. Cl. Spec. Mstr. Nov.
19, 2021).)
The parties subsequently filed several additional rounds of expert reports to
account for the facts as I had found them. Petitioner filed three reports by neurologist
and virologist Maria Fangchun Chen, M.D., Ph.D. (ECF Nos. 79, 86, 95; Exs. 47, 67,
131) and respondent filed three further reports by Dr. Donofrio (ECF Nos. 84, 88, 96;
Exs. N, W, Y). Respondent also filed a report by immunologist William Hawse, Ph.D.
(ECF No. 96; Ex. DD.) Petitioner then filed a motion for a ruling on the written record on
February 27, 2024. (ECF No. 97.) That motion is fully briefed. (ECF Nos. 98, 100.)
I have concluded that the parties have had a full and fair opportunity to develop
the record and that it is appropriate to resolve this case on the existing record. See
Kreizenbeck v. Sec’y of Health & Human Servs., 945 F.3d 1362, 1366 (Fed. Cir. 2020)
(citing Simanski v. Sec’y of Health & Human Servs., 671 F.3d 1368, 1385 (Fed. Cir.
2012)); see also Vaccine Rule 8(d); Vaccine Rule 3(b)(2).
III. Factual Summary
The pertinent facts regarding onset of petitioner’s symptoms are set forth in
greater detail in the prior Finding of Fact. (ECF No. 74, pp. 2-10; 2021 WL 5905687, at
*2-8.) Petitioner, who had a relevant prior history of insulin-dependent diabetes,
received a flu vaccination on October 21, 2015. For the reasons discussed throughout
the Finding of Fact, I resolved conflicting evidence to conclude that she subsequently
experienced numbness and tingling in her extremities around late November of 2015.
Schmigel, 2021 WL 5905687, at *12. However, although there was evidence to suggest
petitioner was also experiencing generalized pain and fatigue, the medical records
documented normal strength up to a June 30, 2016 medical encounter at which
“adequate” strength and muscle tone were noted. Id. (discussing Ex. 9, pp. 1-3; Ex. 5,
p. 2; Ex. 6, p. 2). Thereafter, weakness “of any degree” was first detected on physical
exam on July 20, 2016, about nine months post-vaccination.3 Id. at *12 (discussing Ex.
10, p. 4). At that encounter, petitioner had full strength in all four extremities but had 4+
toe extension and 5- toe flexion. Id. at *4 (discussing Ex. 10, p. 4). Petitioner’s treating
physicians had difficulty determining whether her condition was better explained by
CIDP or diabetic neuropathy. Id. at *4-5 (discussing Ex. 10, p. 4; Ex. 9, p. 6; Ex. 19, p.
65). However, she was ultimately diagnosed with CIDP, id. at *5 (discussing Ex. 17, pp.
32-38), though respondent disputes the accuracy of that diagnosis. (ECF No. 98, pp.
24-31.)
3 In one location within the analysis portion of the Finding of Fact, petitioner’s encounter with Dr. Papsdorf
is incorrectly stated as being July 27, rather than July 20. 2021 WL 5905687, at *12. However, the
encounter is correctly dated in the explanation of petitioner’s medical history, id. at *4, and the
typographic error does not affect the analysis.
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Petitioner sought care from a number of different physicians during the first half
of 2016. She established care with a primary care provider, Dr. Schudy, on June 30,
2016. (Ex. 9, p. 1.) By that time, petitioner had undergone an EMG/NCS of her upper
extremities4 in May of 2016 and a lower extremity EMG/NCS in June of 2016.5 (Ex. 7,
p. 1; Ex. 19, p. 54.) Dr. Schudy was the first physician to become concerned that
petitioner may have CIDP. (Ex. 9, pp. 2-3.) In particular, he felt that petitioner’s June
NCS was “highly suggestive” of CIDP. (Id. at 3.)
Petitioner first presented to a neurologist, Dr. Papsdorf, on July 20, 2016, for an
evaluation of possible CIDP as suspected by Dr. Schudy. (Ex. 10, p. 1.) Petitioner
reported that her neuropathy was “very fast” in onset, and she was concerned it was
related to her flu vaccination. (Id. at 3.) However, she also reported a 1.5 year history
of diabetes, which was by then “[v]ery controlled.” (Id.) She explained that her A1C
started at 8.8% when she was diagnosed, but that she had lost weight and brought it
down to 5.6%. (Id.) Thus, Dr. Papsdorf was concerned that petitioner had both diabetic
neuropathy, which she noted to be the most common peripheral neuropathy in the
United States, as well as “insulin neuritis,” which is a sudden onset of neuropathy that
appears during the treatment of diabetes. (Id. at 4-5.) She noted that petitioner also
had gait issues, but explained that the gait issues could be secondary to the
neuropathy. (Id.) She found that petitioner had a length-dependent, symmetrical
peripheral neuropathy with evidence of both small and large fiber involvement. (Id. at
4.) At this encounter, petitioner’s strength was normal throughout her proximal and
distal muscles in all four extremities, and she had normal reflexes. (Id.) Dr. Papsdorf
ordered an NCS/EMG to rule out CIDP, though CIDP was not suspected “by exam or by
history.” (Id. at 5.) In particular, Dr. Papsdorf felt petitioner’s prior NCS was more
consistent with axonal loss than demyelination. (Id.)
Petitioner underwent a follow up electrodiagnostic study on July 27, 2016. (Ex.
10, p. 6.) However, the study was incomplete due to petitioner not being able to tolerate
the needle portion of the study. (Id.; see also Ex. 19, p. 65.) This study showed a
worsening of petitioner’s condition as compared to her prior June study. (Ex. 19, p. 65.)
The study was “suggestive of a possible demyelinating diffuse peripheral neuropathy
such as [CIDP].” (Ex. 10, p. 6.) However, the study did not rule out diabetic
amyotrophy without a complete needle study. (Ex. 19, p. 65.) The parties’ experts
disagree as to the diagnostic significance of petitioner’s NCS/EMG studies, as
discussed in greater detail below. Petitioner also underwent a lumbar puncture, which
showed protein of 126 and glucose of 61. (Ex. 4, p. 2.)
Petitioner self-referred to another neurologist, Dr. Bittle, in September of 2016.
(Ex. 4, p. 1.) Dr. Bittle concluded that petitioner was suffering CIDP, though he noted
4 The EMG was normal, but the NCS showed bilateral median sensory/motor neuropathy consistent with
carpal tunnel syndrome, as well as bilateral ulnar motor neuropathy. (Ex. 7, p. 1.)
5 The June study showed peroneal and tibial motor neuropathy, as well as sural and superficial peroneal
sensory neuropathy with evidence of sensorimotor axonopathic and demyelinating peripheral neuropathy.
(Ex. 19, p. 54.)
5

Case 1:17-vv-01112-UNJ Document 105 Filed 06/06/25 Page 6 of 22
that her strength was “fairly good” relative to her EMG/NCS findings and also noted that
her neuropathic pain was less common for CIDP (reported in less than 20% of patients).
(Id. at 6.) Dr. Bittle’s assessment also noted petitioner’s CSF protein of 126. (Id.)
Thereafter, petitioner continued to seek treatment for CIDP, including IVIG. As
discussed below, the parties’ experts disagree as to whether petitioner’s condition
responded to IVIG.
Petitioner consulted a third neurologist, Dr. Aggarwal, in August of 2017, who
maintained the impression of CIDP. (Ex. 17, pp. 32-38.) She consulted a fourth
neurologist, Dr. Hunter, beginning in November of 2017. Dr. Hunter also recorded an
impression of CIDP. (Ex. 19, pp. 2-3.) These encounters appear to have been primarily
focused on management of petitioner’s CIDP, rather than revisiting diagnosis. Although
petitioner’s prior neurology evaluations were reviewed, no further electrodiagnostic
studies were performed.
Although petitioner repeatedly reported to her physicians that her condition arose
post-vaccination, none of the physicians specifically addressed whether her condition
was casually related to her vaccination.
IV. Expert Opinions
a. Nizar Souayah, M.D., for petitioner6
Dr. Souayah prepared a single report for this case, which was filed prior to
issuance of my finding of fact regarding onset. (Ex. 30.) Dr. Souayah’s opinion as to
specific causation assumed that, within five weeks of her vaccination, petitioner
experienced onset of a constellation of symptoms consistent with CIDP, including
diffuse muscle pain, numbness and tingling, and weakness. (Id. at 5, 7, 16-17.)
Accordingly, because this assumption is inconsistent with my findings of fact, Dr.
Souayah’s opinion is not informative with regard to specific causation. Dr. Souayah’s
opinion remains relevant with respect to general causation; however, for the reasons
discussed below, I do not find it necessary to reach that question. Important to the
discussion that follows, Dr. Souayah opines that CIDP can be causally linked to flu
vaccinations occurring up to eight weeks prior to onset of the condition. (Id. at 10 (citing
Karissa L. Gable et al., Distal Acquired Demyelinating Symmetric Neuropathy After
Vaccination, 14 J. CLINICAL NEUROMUSCULAR DISEASE 117 (2013) (Ex. 111)).)
6 Dr. Souayah is board certified in neurology with a subspecialty in neuromuscular medicine, and he
maintains an active medical license in New Jersey. (Ex. 30, p. 1.) He currently works as a professor of
neurology at Rutgers-New Jersey Medical School. In his medical practice, he regularly diagnoses and
treats patients with neurological conditions, including CIDP. In his research capacity, he investigates the
causal relationship between vaccines and adverse events with a particular interest in the incidence of
neurological adverse reactions related to vaccination. (Id.)
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Case 1:17-vv-01112-UNJ Document 105 Filed 06/06/25 Page 7 of 22
b. Maria Fangchun Chen, M.D., Ph.D., for petitioner7
Dr. Chen describes CIDP as an under-diagnosed “cousin” of Guillain-Barre
Syndrome (“GBS”), stressing in particular that it is difficult to diagnose due to a
heterogeneous presentation. (Ex. 47, p. 11 (citing Yhojan Rodríguez et al., Chronic
Inflammatory Demyelinating Polyneuropathy as an Autoimmune Disease, 102 J.
AUTOIMMUNITY 8 (2019) (Ex. 49); Kelly Gwathmey, Chronic Inflammatory Demyelinating
Polyradiculoneuropathy and Its Variants, 26 CONTINUUM (MINNEAPOLIS MINN.) 1205
(2020) (Ex. 50); Y. A. Rajabally et al., Clinical Heterogeneity in Mild Chronic
Inflammatory Demyelinating Polyneuropathy, 13 EUR. J. NEUROLOGY 958 (2006) (Ex.
51); Francisco T. Rotta et al., The Spectrum of Chronic Inflammatory Demyelinating
Polyneuropathy, 173 J. NEUROLOGICAL SCIS. 129 (2000) (Ex. 52); Umair J. Chaudhary &
Yusuf A. Rajabally, Underdiagnosis and Diagnostic Delay in Chronic Inflammatory
Demyelinating Polyneuropathy, 268 J. NEUROLOGY 1366 (2021) (Ex. 54); Filip Eftimov et
al., Diagnostic Challenges in Chronic Inflammatory Demyelinating
Polyradiculoneuropathy, 143 BRAIN 3214 (2020) (Ex. 55)).) It often takes years to reach
a CIDP diagnosis. (Id. (citing Rotta et al., supra, at Ex. 52).) Dr. Chen acknowledges
that weakness and numbness are “core” features that are required for a diagnosis of
typical forms of CIDP, but suggests that other symptoms can be diagnostic of “atypical”
forms of the condition. (Id.) She cites several sources for the proposition that fatigue
can be an initial presenting symptom of CIDP. (Id. (citing Rajabally et al., supra, at Ex.
51; S. R. M. Bus et al., Clinical Outcome of CIDP One Year After Start of Treatment: A
Prospective Cohort Study, 269 J. NEUROLOGY 945 (2022) (Ex. 56); Antonino Uncini et
al., Minimal and Asymptomatic Chronic Inflammatory Demyelinating Polyneuropathy,
110 CLINICAL NEUROPHYSIOLOGY 694 (1999) (Ex. 57); S. Boukhris et al., Pain as the
Presenting Symptom of Chronic Inflammatory Demyelinating Polyradiculoneuropathy
(CIDP), 254 J. NEUROLOGICAL SCIS. 33 (2007) (Ex. 58); Sami Boukhris et al., Fatigue as
the Main Presenting Symptom of Chronic Inflammatory Demyelinating
Polyradiculoneuropathy: A Study of 11 Cases, 10 J. PERIPHERAL NERVOUS SYSTEM 329
(2005) (Ex. 59); Andrew Lawley et al., Clinical Correlates of Fatigue in Chronic
Inflammatory Demyelinating Polyneuropathy, 62 MUSCLE & NERVE 226 (2020) (Ex. 60);
Karissa L. Gable et al., Fatigue in Chronic Inflammatory Demyelinating Polyneuropathy,
62 MUSCLE & NERVE 673 (2020) (Ex. 61)).) She further notes a particular case report of
an electrodiagnostically confirmed case of CIDP where the primary symptom was
7 Dr. Chen received her Ph.D. in molecular virology and medical degree from the University of
Pennsylvania School of Medicine in 2005 and 2007, respectively, before moving to the Hospital of the
University of Pennsylvania to complete an internship in 2008 and a neurology residency in 2011. (Ex. 48,
p. 1; Ex. 47, p. 1.) From there, Dr. Chen briefly worked as an attending neurologist at the Albert Einstein
Healthcare Network; however, in 2013, she transitioned to a faculty position as an assistant professor of
clinical neurology at Penn Medicine. (Ex. 48, p. 1; Ex. 47, p. 1.) She currently works as Associate
Director of Clinical Development, Neurology and Psychiatry at Teva Pharmaceuticals Industries. (Ex. 48,
p. 1.) Dr. Chen is board certified in neurology, and she maintains an active medical license in
Pennsylvania. (Id. at 2; Ex. 47, p. 1.) In her clinical practice, Dr. Chen saw patients and supervised
neurology resident physicians and medical students. (Ex. 47, p. 1.) Although she no longer sees
patients, she oversees clinical research at a pharmaceutical company. (Id.) She has also authored four
publications and researched mechanisms for how viruses, and specifically HIV, injure the nervous
system. (Id.; Ex. 48, pp. 2-3.)
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Case 1:17-vv-01112-UNJ Document 105 Filed 06/06/25 Page 8 of 22
disabling fatigue without frank weakness or sensory symptoms. (Id. (citing Véronique
Bissay et al., Fatigue as the Presenting Symptoms of Chronic Inflammatory
Demyelinating Polyneuropathy, 38 MUSCLE & NERVE 1653 (2008) (Ex. 62)).) She opines
that neuropathic pain, including painful paresthesia and muscle pain, are not uncommon
features of CIDP. (Id. at 12 (citing Athena Michaelides et al., Pain in Chronic
Inflammatory Demyelinating Polyradiculoneuropathy: A Systematic Review and Meta-
Analysis, 8 PAIN & THERAPY 177 (2019) (Ex. 64); Andreas Goebel et al., Pain Intensity
and Distribution in Chronic Inflammatory Demyelinating Polyneuropathy, 46 MUSCLE &
NERVE 294 (2012) (Ex. 65); Peter Y. K. Van den Bergh et al., European Academy of
Neurology/Peripheral Nerve Society Guideline on Diagnosis and Treatment of Chronic
Inflammatory Demyelinating Polyradiculoneuropathy: Report of a Joint Task Force–
Second Revision, 28 EUR. J. NEUROLOGY 3556 (2021) (Ex. 66)).) However, she is less
clear as to whether these symptoms would be expected to herald the condition.
With respect to petitioner’s own condition, Dr. Chen notes that petitioner at a
September 21, 2016 encounter with her second neurologist, Dr. Bittle, reported
“extreme fatigue” following her flu vaccination. (Ex. 47, p. 12 (citing Ex. 17, p. 5).) At
that same encounter, Dr. Bittle attributed petitioner’s neuropathic pain to CIDP. (Id.
(citing Ex. 17, p. 10).) Because Dr. Chen places the onset of petitioner’s CIDP within
weeks of her flu vaccination based on fatigue and neuropathic pain, she opines that
petitioner’s CIDP can be causally linked to her flu vaccination based on Dr. Souayah’s
theory of causation. (Id. at 13 (citing Ex. 30).) However, she acknowledges this would
be an atypical presentation. (Id.)
Regarding respondent’s expert’s competing view, Dr. Chen cites Dr. Donofrio’s
strict application of the European Federation Neurologic Society/Peripheral Nerve
Society (“EFNS/PNS”) diagnostic criteria for CIDP, by which Dr. Donofrio seeks to
require hyporeflexia or areflexia, as exemplary of how CIDP is under-diagnosed. (Ex.
67, pp. 2-3 (discussing Joint Task Force of the EFNS and the PNS, EFNS/PNS CIDP
Guidelines: European Federation of Neurological Societies/Peripheral Nerve Society
Guideline on Management of Chronic Inflammatory Demyelinating
Polyradiculoneuropathy. Report of a Joint Task Force of the European Federation of
Neurological Societies and the Peripheral Nerve Society, 10 J. PERIPHERAL NERVOUS
SYS. 220 (2005) [hereinafter 2005 EFNS/PNS CIDP Guideline] (Ex. O; see also Ex. D);
Joint Task Force of the EFNS and the PNS, EFNS/PNS CIDP Guidelines, European
Federation of Neurological Societies/Peripheral Nerve Society Guideline on
Management of Choric Inflammatory Demyelinating Polyradiculoneuropathy: Report of
a Joint Task Force of the European Federation of Neurological Societies and the
Peripheral Nerve Society – First Revision, 15 J. PERIPHERAL NERVOUS SYS. 1 (2010)
[hereinafter 2010 EFNS/PNS CIDP Guidelines] (Ex. P; see also Ex. E); Peter Y. K. Van
den Bergh et al., European Academy of Neurology/Peripheral Nerve Society Guideline
on Diagnosis and Treatment of Chronic Inflammatory Demyelinating
Polyradiculoneuropathy: Report of a Joint Task Force – Second Edition, 26 J.
PERIPHERAL NERVOUS SYS. 242 (2021) (Ex. Q)).) According to Dr. Chen, these criteria
have sensitivity ranging from 73-84%, meaning that the criteria fail to diagnose about 1
out of every 5 patients. (Id. (citing Pietro Emiliano Doneddu et al., Comparison of the
8

Case 1:17-vv-01112-UNJ Document 105 Filed 06/06/25 Page 9 of 22
Diagnostic Accuracy of the 2021 EAN/PNS and 2010 EFNS/PNS Diagnostic Criteria for
Chronic Inflammatory Demyelinating Polyradiculoneuropathy, 93 J. NEUROLOGY
NEUROSURGERY & PSYCHIATRY 1239 (2022) (Ex. 69); Satoshi Kuwabara & Tomoki
Suichi, Validation of the 2021 EAN/PNS Diagnostic Criteria for Chronic Inflammatory
Demyelinating Polyneuropathy, 93 J. NEUROLOGY NEUROSURGERY & PSYCHIATRY 1237
(2022) (Ex. 70)).) Moreover, she stresses that the criteria Dr. Donofrio cites do allow for
atypical presentations to include intact reflexes. (Id. at 3 (citing Van den Bergh et al.,
supra, at Ex. Q, p. 4, tbl.1).) With regard to electrodiagnostic testing, although Dr.
Donofrio indicates that nerve conduction velocities must be 70% or less than normal in
two or more nerves to be diagnostic, Dr. Chen asserts this is not required as it is only
one of seven electrodiagnostic abnormalities that will support a diagnosis. (Id. (citing
Van den Bergh et al., supra, at Ex. Q, p. 6, tbl.2).) The fact that petitioner’s nerve
conduction study demonstrated prolonged F-waves greater or equal to 20% of the
upper limit of normal for her left median and ulnar nerves is sufficient to be diagnostic of
CIDP. (Id. (citing Ex. 10, p. 10; Van den Bergh et al., supra, at Ex. Q, p. 6, tbl.2).)
Additionally, petitioner’s elevated CSF protein and response to immunotherapy are
further supportive of the CIDP diagnosis. (Id.)
Further, Dr. Chen seeks to rule out other explanations for petitioner’s initial
symptoms of numbness, tingling, and fatigue. First, she does not agree that petitioner
suffered diabetic neuropathy. (Ex. 67, pp. 3-4.) Without diagnostic testing (such as skin
or nerve biopsy or EMG), it is not possible to be more specific than to conclude that
petitioner’s numbness and tingling were consistent with peripheral neuropathy. (Ex.
131, p. 3.) However, Dr. Chen stressed that petitioner’s sensory symptoms did not
correlate to her glycemic control, which would ordinarily be expected. (Id. at 2-3.) That
is, while petitioner had documented high A1C of 8.3 in March of 2015, she was not
experiencing sensory symptoms at that time. (Id. at 2 (citing Ex. 16, p. 78).) Prior to
onset of numbness and tingling, petitioner’s A1C had improved, documented as 6.5 as
of September 15, 2015. (Id. (citing Ex. 16, p. 146).) An exception would be treatment-
induced neuropathy, which can occur from rapid and sudden control of diabetes. (Id. at
2-3 (citing Hideyuki Sasaki et al., Spectrum of Diabetic Neuropathies, 11 DIABETOLOGY
INT’L 87 (2020) (Ex. 134)).) This was expressed as a concern by Dr. Papsdorf (Ex. 9, p.
6); however, Dr. Chen opines that this was not petitioner’s presentation. (Ex. 67, p. 3.)
Additionally, petitioner’s nerve conduction studies showed conduction velocity slowing
without a drop in amplitude in the left ulnar motor conduction, as well as F-wave latency
delay that was not mild, which she indicates is not consistent with axonal neuropathy as
should be present if petitioner was suffering diabetic neuropathy. (Id. at 3-4 (citing Ex.
7, p. 4; Ex. 10, pp. 10, 12; Bruce Perkins & Vera Bril, Electrophysiologic Testing in
Diabetic Neuropathy, 126 HANDBOOK CLINICAL NEUROLOGY 235 (2014) (Ex. 72)).) In
contrast, Dr. Chen stresses that petitioner’s numbness and tingling are also consistent
with CIDP and that petitioner’s May 24, 2016 EMG included evidence of demyelination
consistent with CIDP that predated the onset of her symptom of weakness. (Ex. 131, p.
3 (citing Ex. 7, pp. 1-4).)
Petitioner’s symptoms also cannot be explained by vitamin deficiency, because
petitioner had a normal methylmalonic acid (MMA) level. (Ex. 67, p. 4 (citing Ex. 9, p.
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Case 1:17-vv-01112-UNJ Document 105 Filed 06/06/25 Page 10 of 22
4).) An elevated MMA level would be necessary before one could conclude that a low
normal Vitamin B level could be indicative of a functional deficiency. (Id. (citing Sally P.
Stabler, Vitamin B
12
Deficiency, 368 N. ENG. J. MED. 149 (2013) (Ex. U, p. 5)).)
Additionally, petitioner had normal vitamin D levels and no evidence of myopathy on
electrodiagnostic study. (Id. (citing Ex. 16, p. 144; Ex. 10, p. 9).) Therefore, there is no
evidence she had any vitamin D-related muscular disorder. (Id.) Dr. Chen also
disagrees that obstructive sleep apnea explains petitioner’s fatigue. She observes that
petitioner was diagnosed with obstructive sleep apnea in April of 2014 whereas her
reported fatigue did not begin until the autumn of 2015, more than a year later. (Id.
(citing Ex. 16, p. 34).) Moreover, petitioner’s fatigue occurred at a time when she was
losing weight and using a CPAP machine to treat her sleep apnea, suggesting that her
fatigue was not responsive to treatment for her sleep apnea. (Id.)
Prompted to discuss whether diabetes can cause CIDP, Dr. Chen initially
remarked that there is “not much” support for this in the relevant medical literature,
stressing that CIDP is immune mediated, whereas diabetes is primarily metabolic and
vascular. (Ex. 131, pp. 1-2 (citing Amanda C. Peltier & Peter R. Donofrio, Chronic
Inflammatory Demyelinating Polyradiculoneuropathy: From Bench to Bedside, 32
SEMINARS NEUROLOGY 187 (2012) (Ex. 132)).) However, she acknowledged that at least
some cohort studies support an increased risk of CIDP among diabetic patients. (Id. at
2 (citing Yan Chen & Xiangqi Tang, Chronic Inflammatory Demyelinating
Polyradiculoneuropathy in Association with Concomitant Disease: Identification and
Management, 13 FRONTIERS IMMUNOLOGY 890 (2022) (Ex. 133); J. Bradley Layton et al.,
Intravenous Immunoglobulin Initiation in Patients with Chronic Inflammatory
Demyelinating Polyradiculoneuropathy: A US Claims-Based Cohort Study, 12
NEUROLOGY & THERAPY 1171 (2023) (Ex. 135)).) On that point, she noted that it is
hypothesized that diabetes can cause injury to the nerve and thereby expose neuronal
antigens to the immune system, leading to an autoreactive immune response. (Id.
(citing Chen & Tang, supra, at Ex. 133).) She considers this hypothesis to be
unsupported and the epidemiology to be unconvincing. Thus, she considers the idea
that diabetes can lead to increased risk of CIDP to be “controversial.” (Id.)
However, Dr. Chen also opines that, even if onset of petitioner’s CIDP occurred
“months” after her flu vaccination, it would still be plausible for her flu vaccine to have
been the cause based on the above-discussed hypothesis. Specifically, she opines that
Proponents of the view that diabetes can increase the risk of CIDP note
that diabetes can injure nerves thereby exposing neuronal antigens to an
immune system that previously were not exposed and hence increase the
risk of autoimmunity. Notably, while CIDP is accepted to be an immune
mediated disease, there is not evidence for a single immune process. The
scientific literature points to a wide variety of immune processes at play for
the pathology of CIDP and it’s not clear which and if all of these processes
are required. Furthermore, the onset of typical CIDP is expected to be on
the chronic spectrum (symptoms lasting for at least 8 weeks) indicating
that the underlying pathology of CIDP is protracted and may require
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Case 1:17-vv-01112-UNJ Document 105 Filed 06/06/25 Page 11 of 22
repeated attacks on the peripheral nerves to result in the wide-spread
injury of sensory or motor nerves in a sufficient number and distribution of
nerves. The lack of the identification of an inciting event prior to the
occurrence of CIDP further supports that the immune mediated attack on
nerves may be a slow chronic process and hence supports the
presentation of symptoms months out from the inciting event.
(Ex. 131, p. 4 (footnotes omitted) (citing Peltier & Donofrio, supra, at Ex. 132; Emily K.
Mathey et al., Chronic Inflammatory Demyelinating Polyradiculoneuropathy, 86 J.
NEUROLOGY NEUROSURGERY & PSYCHIATRY 973 (2015) (Ex. 136)).)
Ultimately, though it is not her preferred explanation, Dr. Chen agrees that it is
plausible that petitioner’s initial symptoms of numbness and tingling represented
diabetic neuropathy and that she then experienced later manifesting CIDP. (Ex. 131, p.
2.) In general, Dr. Chen approximates that “the likelihood of a diagnosis with both
diabetic neuropathy and CIDP may be equivalent or 2-3 times more likely than an
atypical presentation of CIDP.” (Id. at 3.)
c. Peter Donofrio, M.D., for respondent8
Dr. Donofrio describes CIDP as chronic condition that presents either in a
progressive stepwise fashion or in a relapsing-remitting pattern. (Ex. A, p. 9.) Although
it is sometimes characterized as a chronic form of GBS, this is a misconception. (Id.)
There are some overlapping clinical features, but they are two distinct conditions. (Id.)
He disagrees that CIDP can be causally linked to flu vaccination, stressing the Institute
of Medicine’s 2012 conclusion that epidemiologic evidence is lacking and that
mechanistic evidence, which was limited to case reports, was weak. (Id. at 10.)
Whereas petitioner’s experts indicate CIDP is under-diagnosed, Dr. Donofrio suggests
that it is often misdiagnosed, indicating that nearly half (47%) of patients initially
diagnosed with CIDP will fail to meet the minimum diagnostic criteria after specialist
referral. (Id. at 9-10 (citing Jeffrey A. Allen & Richard A. Lewis, CIDP Diagnostic Pitfalls
8 Dr. Donofrio received his medical degree from Ohio State University School of Medicine in 1975, before
going on to complete a residency in internal medicine at Good Samaritan Hospital in Cincinnati, Ohio in
1978, a residency in neurology at the University of Michigan Medical Center in 1981, and a
neuromuscular fellowship at the University of Michigan in 1982. (Ex. B, pp. 1-2.) While completing his
fellowship, Dr. Donofrio worked as a neurology instructor at various institutions. (Id. at 3.) Thereafter, he
worked as an assistant professor of neurology at the University of Michigan Medical Center and Veterans
Administration Medical Center in Ann Arbor, Michigan. (Id.) In 1986, Dr. Donofrio accepted a position as
an assistant professor of neurology at Wake Forest University School of Medicine, and he was eventually
promoted to professor of neurology in 2005. (Id. at 2-3.) In 2006, Dr. Donofrio accepted a position as a
professor of neurology at Vanderbilt University School of Medicine, where he is currently employed. (Id.
at 2.) Dr. Donofrio is board certified in internal medicine, psychiatry and neurology, and electrodiagnostic
medicine, and he maintains an active medical license in Ohio, Michigan, and Tennessee. (Id.) In his
clinical capacity, he has evaluated a spectrum of neuropathies, including GBS and CIDP, and in his
research capacity, he has published in the areas of GBS, CIDP, and other neuropathies, as well as
reviewed literature and data on vaccine-related GBS, CIDP, and other neurologic conditions. (Ex. A, p.
1.) He has published several articles and book chapters, as well as a textbook title The Textbook of
Peripheral Neuropathy, which was published in 2012. (Id.; Ex. B, pp. 12-22.)
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and Perception of Treatment Benefit, 85 NEUROLOGY 498 (2015) (Ex. H; see also Ex.
R); Kenneth C. Gorson & Clifton L. Gooch, The (Mis)diagnosis of CIDP: The High Price
of Missing the Mark, 85 NEUROLOGY 488 (2015) (Ex. I)).) Dr. Donofrio suggests that
“atypical” presentations are correlated with “misdiagnosis.” (Id. at 10 (citing 2005
EFNS/PNS CIDP Guideline, supra, at Ex. D; 2010 EFNS/PNS CIDP Guidelines, supra,
at Ex. E).)
Citing the EFNS/PNS diagnostic criteria, Dr. Donofrio opines that petitioner’s
presentation cannot support a “probable,” let alone “definite” diagnosis of CIDP. (Ex. A,
p. 9.) He opines that she does not satisfy the clinical criteria given that she did not have
symmetrical proximal and distal weakness and sensory dysfunction of all extremities
when her condition first presented. (Id. (citing 2010 EFNS/PNS CIDP Guidelines,
supra, at Ex. E, p. 6, tbl.4).) Dr. Donofrio further noted that separate CIDP diagnostic
criteria by Koski et al. require documented weakness in all four limbs with proximal
weakness in at least one limb, which petitioner did not have. (Id. (citing C.L. Koski et
al., Derivation and Validation of Diagnostic Criteria for Chronic Inflammatory
Demyelinating Polyneuropathy, 277 J. NEUROLOGICAL SCIS. 1 (2009) (Ex. F)).) Dr.
Donofrio also disagrees with Dr. Chen’s assessment that petitioner’s condition improved
with IVIG treatment. (Ex. W, p. 3.) But in any event, he would not find such
improvement to be diagnostically informative. (Id.; Ex. A, p. 10; Ex. N, p. 4 (citing Allen
& Lewis, supra, at Ex. R).) Although petitioner’s CSF protein level could be used to help
support a CIDP diagnosis, this would also be a common finding in diabetes and diabetic
neuropathy. (Ex. W, pp. 4-5.)
Dr. Donofrio further opines that petitioner’s EMG and nerve conduction studies
did not satisfy the criteria for a demyelinating neuropathy. Dr. Donofrio expresses that
the electrodiagnostic criteria for CIDP are “strict and exact.” (Ex. N, p. 4.) As noted
above, Dr. Donofrio stresses that conduction velocities of less than 70% of the lower
limit of normal in two or more motor nerves is required for a CIDP diagnosis. (Id.)
However, none of petitioner’s studies demonstrated this abnormality. (Id. (citing Ex. 7,
pp. 1-5; Ex. 10, pp. 6-13; Ex. 30, p. 7).) Additionally, petitioner did not undergo
additional testing, such as MRI to rule out spinal nerve root issues. (Ex. A, p. 9.)
Although Dr. Chen suggested that petitioner demonstrated slowed conduction velocity
in her left ulnar nerve as some evidence of demyelination, Dr. Donofrio counters that
this result is only 1 m/s below the permitted lower limit and exceeds the lower limit once
the result is corrected for temperature. (Ex. W, p. 2.) Thus, this finding is not evidence
of demyelination. (Id.) Moreover, this particular finding is better explained as
compression neuropathy secondary to her diabetes, especially because the finding was
not symmetric (the opposite ulnar nerve study was normal). (Id.) Dr. Donofrio also
charges that Dr. Chen misinterprets petitioner’s F-wave data as evidence of
demyelination. Whereas Dr. Chen simply observed prolonged F-wave latency greater
than or equal to 20% of the upper limit for the left median nerve and the left ulnar nerve,
Dr. Donofrio indicates that these findings must be assessed in the setting of the results
of the left median and ulnar motor nerve distal latencies. (Id.) Because these motor
nerve distal latencies were also prolonged, the prolonged F-wave data cited by Dr.
Chen can be attributed to pathology at the wrist and forearm, rather than evidencing
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proximal demyelination. (Id.) Even if Dr. Chen were correct, evidence of abnormality in
only one nerve is only weak support for demyelination. (Id. at 3 (citing Van den Bergh
et al., supra, at Ex. Q, p. 6, tbl.2).)
Dr. Donofrio stresses that, while petitioner did receive a CIDP diagnosis, other
treating physicians were unwilling to reach that diagnosis, instead diagnosing peripheral
neuropathy, insulin neuritis superimposed on diabetic neuropathy, and paresthesias.
(Ex. A, p. 10 (citing Ex. 2, pp. 1-10; Ex. 10, pp. 1-5; Ex. 5, pp. 1-15).) He observes that
Dr. Bittle, the neurologist that initially diagnosed CIDP, did not explain what diagnostic
criteria were used to render the diagnosis and that preserved reflexes in the biceps and
triceps were documented, which does not support a CIDP diagnosis in the context of
petitioner’s nerve conduction studies under the EFNS/PNS criteria. (Ex. N, p. 4
(discussing Ex. 4, pp. 1, 6).) By contrast, Dr. Papsdorf did not believe that petitioner’s
May and June nerve conduction studies demonstrated demyelination and instead
opined that petitioner had diabetic neuropathy with superimposed insulin neuritis. (Ex.
W, p. 3.) Dr. Donofrio stresses that petitioner’s June NCS, which was never interpreted
as being consistent with CIDP, showed low amplitude CMAPs, which are expected in an
axonopathy. Thus, Dr. Donofrio opines that, in addition to being inconsistent with CIDP,
is consistent with diabetic neuropathy. (Id.)
Dr. Donofrio explains that he maintains his diagnostic opinion after accounting for
the finding of fact regarding symptom onset. (Ex. N, p. 3.) He also stresses that Dr.
Chen did not cite any specific criteria for her diagnosis of CIDP. (Id.) He is not
persuaded by Dr. Chen’s citation to the case report by Bissay et al. (Ex. 62), contending
that the failure of IVIG treatment in that case counsels against the CIDP diagnosis.9
(Id.) He stresses that even more recent revised criteria by the European Academy of
Neurology/Peripheral Nerve Society published in 2021, which accounts for variants
beyond “typical” CIDP, still do not include fatigue as diagnostic of CIDP. (Id. at 3-4
(citing Van den Bergh et al., supra, at Ex. Q).) Moreover, whereas Dr. Chen identified
numbness and weakness as the “core” features of CIDP, Dr. Donofrio counters that
numbness is not a core feature of CIDP, but that the core features of CIDP should also
include areflexia or hyporeflexia. (Id. at 4.) Dr. Donofrio disagrees that petitioner’s
presentation is consistent with any of the established “variants” of CIDP, which he
identifies as distal CIDP, multifocal CIDP, focal CIDP, pure motor CIDP, and sensory
CIDP. (Ex. W, p. 2.)
According to Dr. Donofrio, there are a number of other potential explanations for
petitioner’s various symptoms suggested within the medical records. (Ex. N, p. 5.)
Petitioner’s fatigue, in particular, might be explained by documented attention deficit
disorder, diabetes, atrial fibrillation, obesity, obstructive sleep apnea, low vitamin D, low
vitamin B12, insomnia, acid reflux, elevated cholesterol, periodic limb movement during
9 Notably, as explained above, Dr. Donofrio also conversely indicates that patients misdiagnosed with
CIDP frequently report improvement with immunotherapy despite not actually having CIDP, suggesting
that improvement after receiving IVIG does not necessarily support the diagnosis. (Ex. A, p. 10; Ex. N, p.
4 (citing Allen & Lewis, supra, at Ex. R).) Thus, Dr. Donofrio opines that, while CIDP should improve with
IVIG treatment, such improvement is not specific to CIDP. (Ex. N, p. 4.)
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sleep, anxiety and depression, and a thyroid nodule. (Id. (citing Ex. 16, pp. 20, 34, 51,
68, 77, 108, 169; Ex. 12, p. 11; Ex. 4, p. 3).) Dr. Donofrio also supports Dr. Papsdorf’s
diagnosis of insulin neuritis (Id. (citing Ex. 10, pp. 4-5)) and further stresses, contrary to
Dr. Chen’s assessment, that petitioner’s A1C remained elevated after onset of her
numbness and tingling. (Id. (citing Ex. 16, p. 69 (A1C of 8.3 as of March 13, 2015); Ex.
43, pp. 1-13 (A1C of 6.3 as of March 18, 2016); Ex. 10, p. 3 (A1C of 8.8 as of July 20,
2016)).) Numbness and tingling are common initial symptoms of diabetic neuropathy,
which will be experienced by 40-50% of diabetics within 10 years of diagnosis. (Id. at 5-
6 (citing Caitlin W. Hicks & Elizabeth Selvin, Epidemiology of Peripheral Neuropathy
and Lower Extremity Disease in Diabetes, 19 CURRENT DIABETES REPS. 86 (2019) (Ex.
V)).)
d. William Hawse, Ph.D., for respondent10
Dr. Hawse’s report is limited to seeking to rebut the general theory of causation
presented by Dr. Souayah. (Ex. DD.) Because the analysis that follows does not
address general causation, it is not necessary to explain Dr. Hawse’s opinion.
V. Party Contentions
Petitioner argues that her correct diagnosis is CIDP. (ECF No. 97, p. 6.) She
stresses that, despite a “windy” road to that diagnosis, it was the clinical judgment of
two neurologists. (Id.) In particular, petitioner argues that the fact that Dr. Papsdorf
initiated IVIG treatment following petitioner’s July 2016 electrodiagnostic study is
evidence that she changed her diagnosis from diabetic neuropathy to CIDP. (Id. at 7-8.)
Moreover, her expert explains that it is not unusual for CIDP patients to have difficulty in
getting properly diagnosed. (Id. at 6.) Acknowledging the finding of fact that onset of
weakness first occurred in July of 2016, petitioner argues that fatigue is a common
presenting symptom of CIDP and that onset of weakness in CIDP can occur “several
years” after the initial onset of other symptoms. (Id. at 7.) Therefore, petitioner argues
that the onset of her CIDP occurred at the time she first experienced numbness and
tingling, approximately five weeks post-vaccination. (Id. at 14.)
Petitioner cites numerous cases for the proposition that molecular mimicry has
been accepted as a sound a reliable theory of causation for vaccine-related GBS. (ECF
No. 97, pp. 8-9 (citing Conte v. Sec’y of Health & Human Servs., No. 17-403V, 2020 WL
5743696, at *23 (Fed. Cl. Spec. Mstr. July 27, 2020); Barone v. Sec’y of Health &
10 Dr. Hawse received his Ph.D. in biophysical chemistry from Johns Hopkins University in 2009, before
going on to complete two postdoctoral fellowships, one in structural immunology at the University of Notre
Dame in 2013 and another in immunology and signal transduction at the University of Pittsburgh in 2015.
(Ex. OO, p. 1.) His research focused on the biochemical basis for T cell receptor cross-reactivity and
CD4+ T cell differentiation and immune tolerance. (Ex. DD, p. 1.) From there, Dr. Hawse accepted a
faculty position as a research assistant professor at the University of Pittsburgh. (Ex. OO, p. 1; Ex. DD, p.
1.) He was subsequently promoted to assistant professor of immunology in 2019. (Ex. OO, p. 1; Ex. DD,
p. 1.) Dr. Hawse’s background is in basic immunological mechanisms focused on adaptive immune
response, and he has published nearly 30 peer-reviewed articles. (Ex. DD, p. 2; Ex. OO, pp. 2-5.)
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Human Servs., No. 11-707V, 2014 WL 6834557, at *8-9 (Fed. Cl. Spec. Mstr. Nov. 12,
2024); Koller v. Sec’y of Health & Human Servs., No. 16-439V, 2021 WL 5027947, at
*18 (Fed. Cl. Spec. Mstr. Oct. 8, 2021); Pierson v. Sec’y of Health & Human Servs., No.
17-1136V, 2022 WL 322836, at *31 (Fed. Cl. Spec. Mstr. Jan. 19, 2022); Deshler v.
Sec’y of Health & Human Servs., No. 16-1070V, 2020 WL 4593162, at *19 (Fed. Cl.
Spec. Mstr. July 1, 2020); Maloney v. Sec’y of Health & Human Servs., No. 19-1713V,
2022 WL 1074087 (Fed. Cl. Spec. Mstr. Mar. 17, 2022)).) Petitioner further cites Berg
v. Secretary of Health & Human Services to support the relevance of evidence
pertaining to GBS in cases alleging CIDP. (Id. at 9-10 (quoting No. 16-650V, 2021 WL
6883495, at *44 (Fed. Cl. Spec. Mstr. Dec. 14, 2021)).) In addition to citing several
case reports regarding CIDP arising after flu vaccination, Dr. Souayah explained the
pathophysiologic similarities between GBS and CIDP as relating to post-infectious
humeral and cellular dysfunction, including molecular mimicry and polyclonal activation.
(Id. at 10-11 (citing Ex. 30, pp. 8, 12-13, 15).) Although petitioner acknowledges that
“the degree of eventual T-cell dysfunction could be a differentiating factor,” both GBS
and CIDP are associated with antigen-presenting molecules from the HLA-DR/DQ
system. (Id. at 11 (citing Ex. 30, p. 8).) Petitioner argues that she is not required to
demonstrate “exactly which molecules reacted to the vaccination to incite her immune
system’s attack on her nerves.” (Id.)
Petitioner contends that there is no causal relationship between diabetes and
CIDP. (ECF No. 97, p. 12.) Thus, she argues that her flu vaccination is the only
potential cause of her CIDP. (Id.) However, petitioner does acknowledge that diabetes
may have played a contributory role in her development of CIDP. (Id.) Given the
difficulties petitioner’s treating physicians had in arriving at a diagnosis and pinpointing
onset of petitioner’s CIDP, the lack of any attribution of petitioner’s condition to her flu
vaccination should not be viewed as surprising. (Id.) Citing several prior cases,
petitioner contends that the onset of her CIDP occurred within a timeframe from which a
causal inference can be drawn based on the prior finding of fact. (Id. at 13-14 (citing
Nieves v. Sec’y of Health & Human Servs., No. 18-1602V, 2023 WL 3580148 (Fed. Cl.
Spec. Mstr. Apr. 17, 2023), mot. for rev. denied, 167 Fed. Cl. 422 (2023); Kelley v.
Sec’y of Health & Human Servs., 68 Fed. Cl. 84, 102 (1005); Daily v. Sec’y of Health &
Human Servs., No. 07-173V, 2011 WL 2174535, at *9 (Fed. Cl. Spec. Mstr. May 11,
2011); Patel v. Sec’y of Health & Human Servs., No. 16-848V, 2020 WL 2954950, at
*18-21 (Fed. Cl. Spec. Mstr. May 1, 2020); Strong v. Sec’y of Health & Human Servs.,
No. 15-1108V, 2018 WL 1125666, at *21 (Fed. Cl. Spec. Mstr. Jan. 12, 2018)).) In her
motion, petitioner did not cite any medical evidence establishing on this record what the
appropriate timeframe would be pursuant to the theory she advanced. (Id.) However,
in her reply, petitioner clarified that she relies on Dr. Souayah’s opinion that up to six
weeks is the appropriate timeframe within which CIDP could develop post-vaccination.
(ECF No. 100, p. 6 (citing Ex. 30, p. 7; P. A. McCombe et al., Chronic Inflammatory
Demyelinating Polyradiculoneuropathy: A Clinical and Electrophysiological Study of 92
Cases, 110 BRAIN 1617 (1987) (Ex. 79)).)11
11 While petitioner is correct that Dr. Souayah noted a six-week onset period on page 7 of his report, he
also separately identified an eight-week period on page 10 of his report, as noted above in the summary
of Dr. Souayah’s opinion.
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Preferring his own expert’s assessment, respondent argues first and foremost
that petitioner never actually suffered CIDP. (ECF No. 98, pp. 24-31.) Instead,
petitioner’s entire clinical history is more likely explained by diabetic neuropathy. (Id. at
30-31.) Respondent argues this alone is fatal to petitioner’s claim. (Id. at 31 (citing
Broekelschen v. Sec’y of Health & Human Servs., 618 F.3d 1339, 1346 (Fed. Cir.
2010); Lombardi v. Sec’y of Health & Human Servs., 656 F.3d 1343, 1352-53 (Fed. Cir.
2011)).) Addressing an Althen analysis for CIDP arguendo, respondent contends that
petitioner has presented no reliable evidence causally linking the flu vaccine to CIDP.
(Id. at 32-39.) The fact that molecular mimicry explains some autoimmune diseases
does not mean that it explains CIDP in particular, and it is insufficient for petitioner to
merely rely on prior cases or analogy to GBS. (Id.) Respondent stresses the lack of
any treating physician opinion supporting vaccine causation in this case and further
suggests that petitioner’s comorbidities cloud her attempted causal relationship. In
particular, respondent urges that the numbness and tingling that began in November
2015, as determined by the prior fact finding, are best explained by diabetic neuropathy.
(Id. at 40-41.) Moreover, respondent argues that there is a “strong” relationship
between diabetes and CIDP that supports a casual inference between petitioner’s
diabetes and any CIDP in preference to any causal relationship between petitioner’s flu
vaccination and her alleged CIDP. (Id.) Respondent disagrees that onset of CIDP
would have occurred five weeks post-vaccination as Dr. Chen opined; however, even if
that were the onset, petitioner has not presented a medical opinion sufficient to
establish the appropriate timeframe for the development of a post-vaccination CIDP.
(Id. at 43-45.)
VI. Analysis
For purposes of this decision, I will assume arguendo that CIDP can be caused
by the flu vaccine for purposes of Althen prong one. The question of whether CIDP can
be caused by the flu vaccine remains unsettled. Compare, e.g. Daily, 2011 WL
2174535, at *6-8 (concluding that petitioner had substantiated, and respondent had not
sufficiently rebutted, that the flu vaccine can cause CIDP via molecular mimicry based
on analogy to GBS) with Jacunski v. Sec’y of Health & Human Servs., No. 09-524V,
2014 WL 5168422, at *12, *16-17 (Fed. Cl. Spec. Mstr. Sept. 23, 2014) (concluding that
petitioner had not preponderantly proven that the flu vaccine can cause or significant
aggravate CIDP via molecular mimicry); see also Nieves, 2023 WL 3580148, at *36, *46
(explaining that whether the flu vaccine can cause CIDP is “an extremely close call” and
that “overlap between GBS and CIDP cannot be employed as a shortcut to entitlement,
simply because certain principles that have been preponderantly shown bearing on the
flu vaccine-GBS connection (like the mechanism of molecular mimicry) could plausibly
be extended” to flu vaccine-CIDP). However, this case has also presented significant
questions regarding petitioner’s own personal clinical history that are dispositive
regardless of the question of general causation. That is, even if flu vaccine can cause
CIDP, petitioner cannot meet her burden of proof under either Althen prongs two or
three.
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a. Althen prong two
The second Althen prong requires proof of a logical sequence of cause and
effect showing that the vaccine was the reason for the injury, usually supported by facts
derived from a petitioner’s medical records. Althen, 418 F.3d at 1278; Andreu v. Sec’y
of Health & Human Servs., 569 F.3d 1367, 1375-77 (Fed. Cir. 2009); Capizzano v.
Sec’y of Health & Human Servs., 440 F.3d 1317, 1326 (Fed. Cir. 2006); Grant, 956 F.2d
at 1148. However, petitioner may support her claim by presenting either medical
records or the opinion of a competent medical expert. § 300aa-13(a)(1). Medical
records and/or statements of a treating physician do not per se bind the special master
to adopt the conclusions of such an individual, even if they must be considered and
carefully evaluated. See § 300aa-13(b)(1) (providing that “[a]ny such diagnosis,
conclusion, judgment, test result, report, or summary shall not be binding on the special
master or court”); Snyder v. Sec’y of Health & Human Servs., 88 Fed. Cl. 706, 745 n.67
(2009) (“[T]here is nothing . . . that mandates that the testimony of a treating physician
is sacrosanct—that it must be accepted in its entirety and cannot be rebutted.”).
As noted above, I previously issued findings of fact in this case. Specifically, I
found that “the record as a whole preponderates in favor of finding that petitioner
experienced numbness and tingling in her extremities along with fatigue beginning in
late November 2015; however, there is not preponderant evidence on the current record
that she suffered weakness until July of 2016.” (ECF No. 74, p. 16; 2021 WL 5905687,
at *12.) Following review of the subsequently filed expert reports and the parties’
briefing, these findings stand and are applied within this analysis. Left unaddressed by
the prior fact finding, however, was the further question of “whether or how these
symptoms, coupled with the overall medical course reflected in the treatment records,
support petitioner’s allegation of vaccine-caused CIDP.” (ECF No. 74, p. 16; 2021 WL
5905687, at *12.)
Throughout the pendency of this case, Dr. Donofrio has been consistent on
respondent’s behalf in opining that petitioner’s condition is explained exclusively by
diabetic neuropathy, which he stresses is the most common form of peripheral
neuropathy worldwide. However, if petitioner did suffer CIDP, then Dr. Donofrio would
opine that petitioner initially suffered a months long course of diabetic neuropathy
followed by a later onset of CIDP heralded by the onset of weakness, which he places
in July based on the above-referenced finding of fact. (Ex. Y, pp. 3-4.) Dr. Chen agrees
on petitioner’s behalf that it is plausible that she suffered both diabetic neuropathy and a
later manifesting CIDP, but she prefers to invoke an atypical course of CIDP to explain
petitioner’s entire clinical history. (Ex. 131, pp. 2-3.)
Contrary to either party’s assessment, a review of petitioner’s medical history
confirms that she was diagnosed with both diabetic neuropathy and CIDP. See Sword
v. United States, 44 Fed. Cl. 183, 187-89 (1999) (explaining of special masters that “as
fact-finders, they may find that truth lies somewhere in between the opposing,
uncompromising views of the partisan experts”). Regarding respondent’s view, even if
Dr. Donofrio were correct that petitioner’s electrodiagnostic study is not diagnostic of
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CIDP under stringent application of the relevant criteria, he stands alone in drawing that
conclusion as a matter of clinical judgment. In addition to Dr. Chen, two treating
neurologists (Drs. Papsdorf and Bittle) felt that petitioner’s July 2016 electrodiagnostic
study was at least “suggestive” of CIDP and Dr. Bittle explicitly reached the diagnosis of
CIDP. (Ex. 10, p. 6; Ex. 4, p. 6.) Conversely, petitioner is not persuasive in contending
that Dr. Papsdorf retracted her initial diagnoses of diabetic neuropathy and insulin
neuritis. Although petitioner is correct to observe that Dr. Papsdorf initiated treatment
for CIDP following the July 2016 electrodiagnostic study, Dr. Papsdorf explicitly
indicated that the study had not ruled out diabetic amyotrophy because it was
incomplete. (Ex. 19, p. 65.) Indeed, petitioner specifically testified that she switched to
another neurologist because she was frustrated that Dr. Papsdorf remained insistent
that her condition was related to her diabetes. (Tr. 63-64.)
In rejecting petitioner’s diagnosis of diabetic neuropathy, Dr. Chen relied in part
on the fact that petitioner’s July 2016 electrodiagnostic study did not demonstrate
axonal nerve damage consistent with diabetic neuropathy. (Ex. 67, pp. 3-4.) However,
this is not reliable in light of Dr. Papsdorf’s explanation that the study was incomplete
and unable to rule out diabetic amyotrophy. (Ex. 19, p. 65.) Moreover, whereas CIDP
was not electrodiagnostically evidenced until petitioner’s July 2016 study, Dr. Donofrio
opined in agreement with Dr. Papsdorf’s opinion that petitioner’s earlier June 2016
nerve conduction study was consistent with axonal injury due to diabetic neuropathy.
(Ex. W, p. 3.) Dr. Chen also doubted petitioner’s diabetic neuropathy diagnosis
because diabetic neuropathy is “correlated with the degree of glycemic control.” (Ex.
131, p. 2 (citing Sasaki et al., supra, at Ex. 134).) She cited a September 15, 2015 A1C
reading of 6.5, from which she observes “[i]t would be odd for her to have sensory
symptoms of a diabetic neuropathy after she obtained glycemic control.” (Id.) Dr.
Donofrio observed, however, that subsequent A1C readings from March and July of
2016 showed that that it had become elevated again. (Ex. Y, p. 3 (citing Ex. 43, pp. 1-
13; Ex. 10, p. 3).) Especially in light of Dr. Donofrio’s observation, Dr. Chen is not
persuasive in using a single A1C reading to extrapolate petitioner’s degree of glycemic
control over time.
Accordingly, the evidence preponderates in favor of a finding that petitioner
suffered both diabetic neuropathy and later CIDP. In that regard, Dr. Donofrio noted
that there is a known association between diabetes and CIDP, though he acknowledges
that relevant studies have not been uniform in detecting an increased risk of CIDP
among diabetics. (Ex. Y, pp. 1-2.) Dr. Chen considers the association “controversial,”
but likewise acknowledges that an increased risk of CIDP among diabetics has been
detected epidemiologically. (Ex. 131, p. 2.) Although both experts stressed that
association alone does not equate to a causal relationship, Dr. Chen further explained
that the relevant literature hypothesizes that “diabetes causes injury to the nerve
resulting in exposure of neuronal antigens that were previously hidden from the immune
system . . . [which] may trigger autoreactive immune cells to recognize these self-
antigens as foreign.” (Id. (citing Chen & Tang, supra, at Ex. 133).) Dr. Donofrio agreed
that this hypothesis “makes pathological and immunological sense.” (Ex. Y, p. 3.) Such
a hypothesis, especially when coupled with the evidence indicating an increased risk of
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CIDP among diabetics, supports a direct causal relationship between diabetic nerve
damage and later manifesting CIDP.12
Even if an atypical form of CIDP is possible, Dr. Chen is not persuasive in
applying that concept to this case. Dr. Chen relies, in particular, on a case report by
Bissay et al., reporting on a patient who was diagnosed with CIDP based on
electrodiagnostic criteria despite his only symptom being fatigue. (Bissay et al., supra,
at Ex. 62.) Even setting aside Dr. Donofrio’s criticism of the Bissay subject’s CIDP
diagnosis (Ex. N, p. 3), the case report is not informative. As the case report authors
note, fatigue is “a nonspecific symptom, and the differential diagnosis is extensive.”
(Bissay et al., supra, at Ex. 62, p. 1.) The fact that the Bissay subject’s differential
diagnosis was ultimately narrowed to CIDP does not mean that fatigue necessarily
implicates CIDP. Rather, the Bissay subject was diagnosed based on electrodiagnostic
evidence, not the presence of fatigue. Moreover, the Bissay subject’s case was notable
as potentially representative of a minimal form of CIDP because he lacked any clinical
features of any other form of neuropathy. (Id. at 4.) Here, however, Dr. Donofrio
explained that petitioner’s May and June 2016 electrodiagnostic studies were more
consistent with diabetic neuropathy than CIDP and her treating neurologist (Dr.
Papsdorf) at the time felt that her differential diagnosis prior to onset of weakness
favored diabetic neuropathy as an explanation for her presentation. Indeed, Dr.
Donofrio observed that diabetic neuropathy can cause or worsen fatigue. (Ex. N, p. 5.)
Additionally, a significant finding among patients purportedly experiencing so-called
“minimal CIDP,” in which fatigue and sensory symptoms are the primary presentation, is
areflexia or hyporeflexia. (Bissay et al., supra, at Ex. 62, p. 3; Boukhris et al., supra, at
Ex. 59, p. 6.) Dr. Donofrio likewise explained that this is a “core” feature of CIDP.13 (Ex.
N, pp. 3-4.) However, prior to June of 2016, petitioner did not have either areflexia or
hyporeflexia. (Compare Ex. 5, p. 2 (emergency department record noting normal deep
tendon reflexes on physical examination as of April 17, 2016), with Ex. 9, p. 2 (Dr.
Schudy documenting reduced deep tendon reflexes as of June 30, 2016).) In citing the
concept of “minimal CIDP,” Dr. Chen does not adequately grapple with the fact that
there was a change in petitioner’s condition around June and July of 2016 wherein
12 Dr. Chen did state that she felt the hypothesis is “purely hypothetical,” but nonetheless sought to apply
it as a means of opining that the flu vaccine could, when combined with pre-existing diabetic neuropathy,
culminate in CIDP occurring “months” after vaccination. (Compare Ex. 131, p. 2, with id. at 4.) Notably,
however, though demonstrating her willingness to accept a causal relationship between diabetes and
CIDP, Dr. Chen did not adequately explain how this hypothesis would support the involvement of the flu
vaccine in manifesting CIDP “months” after exposure. (Id. at 4.)
13 Dr. Chen disputes the necessity of absent or reduced reflexes under the diagnostic criteria favored by
Dr. Donofrio because that criteria allows that reflexes may be present among CIDP variants. (Ex. 67, p. 3
(citing Van den Bergh et al., supra, at Ex. Q, p. 4, tbl.1).) However, Dr. Chen overstates the significance
of the CIDP variants. The Table that Dr. Chen cites first indicates that “typical” CIDP requires absent or
reduced tendon reflexes in all limbs. (Van den Bergh et al., supra, at Ex. Q, p. 4, tbl.1.) The list of CIDP
variants includes descriptions of various presentations, some of which do not affect all limbs. Regarding
these variants, the criteria states “otherwise as in typical CIDP (tendon reflexes may be normal in
unaffected limbs).” (Id.) Notably, the medical literature Dr. Chen herself cites for the concept of “minimal
CIDP” notes of these patients that areflexia or hyporeflexia are the “most constant feature.” (Boukhis et
al., supra, at Ex. 59, p. 6.)
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during the same period she saw onset of weakness, reduction in reflexes, and for the
first time had an electrodiagnostic study “suggestive” of CIDP. Ultimately,
notwithstanding her case-specific assessment, Dr. Chen agrees as a general matter
that it would be 2-3 times more likely for petitioner to have had both diabetic neuropathy
and CIDP as compared to the atypical presentation of CIDP that she proposes. (Ex.
131, p. 3.)
In sum, considering the record as a whole, the evidence preponderates in favor
of a finding that petitioner’s symptoms of numbness, tingling, and fatigue, which first
arose approximately five weeks post-vaccination, are more likely explained by Dr.
Papsdorf’s initial diagnoses of diabetic neuropathy and/or insulin neuritis. Although
petitioner was also later diagnosed with CIDP, there is not preponderant evidence that
onset of that condition occurred prior to about June or July of 2016. Ultimately, the
evidence weighs against any logical sequence of cause-and-effect implicating
petitioner’s flu vaccination as a cause of her CIDP for the following reasons:
• Although petitioner repeatedly reported her vaccine as a relevant part of her
history, none of her physicians, including those that diagnosed CIDP, opined that
her vaccination was a cause of her condition.
• Petitioner not only had a history of diabetes, which is associated with increased
risk of CIDP, but was also suffering diabetic neuropathy, which the experts
explain can help explain the development of CIDP. Even petitioner’s own expert
agrees that diabetes may have been at least a contributing factor in the
development of her CIDP.
• A typical presentation of CIDP would arise with demonstrated weakness and
reduced or absent reflexes, which in this case would place onset CIDP about 8-9
months post-vaccination. As discussed under Althen prong three, this timing of
onset does not support a casual inference relative to petitioner’s flu vaccination.
• In order to account for petitioner’s own presentation – a months long course of
numbness, tingling, pain, and fatigue only later followed by a separate onset of
weakness – petitioner’s expert suggests that she experienced an “atypical” or
“minimal” form of CIDP. However, respondent’s expert observes that petitioner’s
presentation does not fit any of the recognized variants of CIDP and none of
petitioner’s treating physicians diagnosed her as having any atypical
presentation.
• Separate and apart from whether diabetes or diabetic neuropathy would be the
cause of a subsequent presentation of CIDP, diabetic neuropathy would be
sufficient to explain petitioner’s symptoms of numbness, tingling, pain, and
fatigue during the months prior to the onset of weakness, which is consistent with
the treating neurologist’s (Dr. Papsdorf’s) impression and further undercuts any
suspicion of an atypical form of CIDP in preference to a typical, but later
manifesting, CIDP.
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• Dr. Chen acknowledges that a presentation of diabetic neuropathy and
subsequent CIDP would be 2-3 times more likely than an atypical presentation of
CIDP.
Thus, considering the record as a whole, petitioner has not met her preponderant
burden of proof under Althen prong two.
b. Althen prong three
The third Althen prong requires establishing a “proximate temporal relationship”
between the vaccination and the injury alleged. Althen, 418 F.3d at 1278. A petitioner
must offer “preponderant proof that the onset of symptoms occurred within a timeframe
which, given the medical understanding of the disorder’s etiology, it is medically
acceptable to infer causation-in-fact.” de Bazan v. Sec’y of Health & Human Servs.,
539 F.3d 1347, 1352 (Fed. Cir. 2008).
Here, petitioner cites Dr. Souayah’s opinion that CIDP can be causally related to
a flu vaccination occurring up to six (or eight) weeks earlier. (ECF No. 100, p. 6 (citing
Ex. 30, p. 7; McCombe et al., supra, at Ex. 79); see also Ex. 30, p. 10 (citing Gable et
al., supra, at Ex. 111).) Thus, petitioner argues that she has met her burden of proof
under Althen prong three based on the prior finding of fact, which found that petitioner
experienced onset of numbness and tingling approximately five weeks post-vaccination.
(ECF No. 97, p. 14.) However, for the reasons discussed above relative to Althen prong
two, the onset of numbness and tingling is not indicative of the initial onset of CIDP in
this case. Petitioner has not demonstrated that the onset of CIDP occurred within the
six or eight weeks that Dr. Souayah identifies as the period within which a causal
inference can be drawn.14 Therefore, petitioner has not met her burden of proof under
Althen prong three.
VII. Conclusion
There is no question that petitioner has suffered, and she has my sympathy.
However, for all the reasons discussed above, I find that petitioner has not met her
burden of proof in this case. Therefore, this case is dismissed.15
14 Dr. Chen also opined that in the context of pre-existing diabetic neuropathy the flu vaccine could be the
cause of CIDP manifesting “months” later. (Ex. 131, p. 4.) However, Dr. Chen did not adequately
address the expected timing of this theory, stating only that the expected course would be “protracted.”
(Id.)
15 In the absence of a timely-filed motion for review of this Decision, the Clerk of the Court shall enter
judgment accordingly.
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IT IS SO ORDERED.
s/Daniel T. Horner
Daniel T. Horner
Special Master
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