LISA D. HAMILTON-FIELDMAN, Special Master.
This is an action by Olivia Meylor ("Petitioner")
Petitioner was born on May 8, 1994, without complications. Pet'r's Ex. 3 at 5-22, ECF No. 8-4.
Following the first vaccination, Petitioner experienced headaches, cramping, and joint pain. Tr. at 36, Madelyn Meylor v. Sec'y of HHS, No. 10-770V, ECF No. 60, 62, 66 (hereinafter "Meylor Tr."). Additionally, she complained "of general symptoms such as depression and sleep disturbances" and had "episodes of lightheadedness and tremulousness, anxiety, panic attacks, and difficulties in focusing/concentrating in her school work." Pet'r's Ex. 31 at 2, ECF No. 50-3 (Serena Colafrancesco et al., Human Papilloma Virus Vaccine and Primary Ovarian Failure: Another Facet of the Autoimmune/Inflammatory Syndrome Induced by Adjuvants, Am. J. Reproductive Immunology (2013)).
Petitioner received the second dose of the HPV vaccine on November 15, 2007, Pet'r's Ex. 4a at 71, and the third dose on August 1, 2008, id. at 62. On September 28, 2009, Mrs. Meylor telephoned the office of Petitioner's gynecologist to inquire about testing for menstrual problems, since Petitioner's older sister was undergoing such testing. Id. at 44. Mrs. Meylor was advised to contact Petitioner's primary provider if she was "not getting periods." Id.
On October 8, 2009, Mrs. Meylor called the office of Petitioner's pediatrician to express her concern that Petitioner might be depressed. Id. at 43. She described Petitioner as "tearful, withdrawn, not motivated, and [unable to] sleep." Id. She was referred to make an appointment for behavioral counseling. Id.
On November 27, 2009, Petitioner presented to her pediatrician for an evaluation of swelling around her eyes and hives on her abdomen. Id. at 38. Following an examination, she was diagnosed with acute urticaria of likely viral etiology and advised to treat with an anti-inflammatory and an antihistamine. Id. at 39. There was no discussion of her lack of menses noted, nor any mention of the behavioral issues.
On January 29, 2010, Petitioner was evaluated for an upper respiratory infection ("URI"). Id. at 34. She reported symptoms of cough, chest tightness, and intermittent fever. Id. The physician diagnosed viral URI with bronchospasm, and prescribed Prednisone (an albuterol inhaler) and cough syrup with codeine. Id.
On February 10, 2010, Petitioner saw her primary physician for fever, cough, and body aches, including some headaches, and lethargy, all of which had been ongoing for two months. Id. at 29. Physical examination was "basically normal." Id. at 30. She was diagnosed with sinusitis and prescribed a high-dose of amoxicillin. Pet'r's Ex. 4a at 30. The physician noted that he was "not sure" all of Petitioner's symptoms were due to the sinusitis and suspected possible anxiety or depression. Id.
On March 30, 2010, Petitioner returned for an evaluation of cold symptoms. Id. at 24. She was diagnosed with chronic sinusitis and prescribed another course of amoxicillin. Id.
On April 28, 2010, Petitioner's mother called the primary care physician's after-hours service to report that Petitioner had a fever and was vomiting. Id. at 20. Based on the symptoms, the nurse assessed probable viral gastritis and provided instructions on proper care. Id. In response to a question asked during the call, Petitioner's mother stated that Petitioner's menses were irregular, with her only menstrual period occurring in December 2009. Id.
In early May 2010, Petitioner's mother telephoned the primary care physician's office to express concern about Petitioner having had only one period to date and to request an evaluation for possible primary ovarian insufficiency ("POI").
On July 6, 2010, Petitioner presented for her evaluation with Ms. Gamoke. Petitioner reported that she had had only two menstrual periods—the first in November 2009 and a second in December—and was thereafter amenorrheic. Id. at 13-17. Physical examination was unremarkable and she appeared to be in good health. Id. Blood was drawn for testing, and depending on the results, a pelvic ultrasound and additional screening would be ordered. Id.
On July 8, 2010, Ms. Gamoke left a message for Petitioner's mother to call regarding Petitioner's results. Id. at 11. The following day, Petitioner's mother was informed that the testing showed Petitioner had "high FSH and LH with undetectable estradiol," results that were consistent with ovarian failure. Id. On July 12, 2010, Petitioner underwent a pelvic ultrasound, which reflected a normal appearing uterus, but did not convincingly identify her ovaries. Id. at 136. Subsequent genetic testing was negative for Fragile-X syndrome. Id. at 126.
On July 28, 2010, Ms. Gamoke confirmed that Petitioner suffered from POI and recommended that she receive hormone replacement therapy and maintain adequate calcium intake for bone health. Pet'r's Ex. 4a at 9. She also recommended yearly screening for other autoimmune disorders. Id. She counseled that if Petitioner wished to conceive, she would need to see a reproductive endocrinologist. Id. However, the likelihood of a pregnancy was low. Id. Petitioner received a prescription for Ortho-Cept (desogestrel and ethinyl estradiol). Id.
On October 5, 2010, Petitioner's mother telephoned Ms. Gamoke's office to report that Petitioner was experiencing breakthrough bleeding and to request that a higher dose of hormones be prescribed. Id. at 8. A prescription for TriNessa (norgestimate and ethinyl estradiol), a different hormone medication, was provided. Id. On October 14, 2010, Petitioner's mother called to report that Petitioner continued to bleed heavily. Id. at 7. Ms. Gamoke advised that Petitioner stop the hormone treatment and retry the new pill after two months. Id. At a follow-up appointment on December 1, 2010, Petitioner was prescribed a new hormone therapy regimen consisting of Vivelle-Dot (estradiol) and Prometrium (progesterone). Id. at 2.
On November 8, 2010, Petitioner filed the present action, alleging that the Human Papillomavirus vaccinations ("Gardasil" or "HPV" vaccines) administered to her July 6 and November 15, 2007, and August 1, 2008 caused her to suffer from POI. Pet., ECF No. 1.
On December 15, 2010, the special master to whom the case was assigned held the initial status conference with the parties' counsel. See Minute Entry (Dec. 17, 2010). Thereafter, on December 23, 2010, Petitioner filed the required medical records and a statement of completion. See Statement of Completion, ECF No. 9.
On March 18, 2011, Respondent filed her Rule 4(c) Report, wherein she argued both that the claim was untimely filed and that Petitioner had failed to carry her burden of proof under Althen v. Sec'y of HHS, 418 F.3d 1274, 1278 (Fed. Cir. 2005). Resp't's Report at 4-8, ECF No. 11. Specifically, Respondent argued that Petitioner had not submitted an expert report or medical literature to support the assertion that the HPV vaccine caused Petitioner's POI, and "[n]one of her treating physicians attributed her problem to the vaccine." Id. at 6. Furthermore, "although Petitioner stopped menstruating after she had received three HPV vaccinations, her last menstrual period was in December 2009, two and a half years after the first vaccination and more than a year after the third." Id. Respondent asserted that there was "no basis" in the record to establish this as a temporally appropriate time frame to associate Petitioner's vaccinations and her illness. Resp't's Report at 6. Respondent additionally noted that Petitioner's sister suffered from the same condition, which "strongly suggests that there may be a genetic cause." Id. In Respondent's view, Petitioner's claim was "based entirely on a `post hoc ergo propter hoc' line of reasoning (i.e., her symptoms started after the vaccinations, therefore they were caused by the vaccinations)." Id.
Following a status conference on April 28, 2011, Petitioner was ordered to file a medical expert report. See Scheduling Order (Apr. 29, 2011), ECF No. 12. On February, 13, 2012, Petitioner filed the expert report of Dr. Shoenfeld, along with his CV and relevant medical literature. See Pet'r's Exs. 7-16, ECF Nos. 23-2 to 24-3. The report and CV of a second expert, Dr. Orit Pinhas-Hamiel ("Dr. Hamiel"), were filed on March 22, 2012. Pet'r's Exs. 17-18, ECF Nos. 24-2 to 24-3.
On March 28, 2012, the special master convened a status conference to discuss Petitioner's expert reports. See Minute Entry (Mar. 28, 2012). Due to certain deficiencies in the reports, Petitioner was ordered to file a supplemental report from Dr. Shoenfeld, and was given the option of filing a supplemental report from Dr. Hamiel. See Scheduling Order (Mar. 30, 2012) at 1-3, ECF No. 26.
On August 15, 2012, Petitioner filed Dr. Shoenfeld's supplemental report, along with supporting medical literature. See Pet'r's Exs. 21-26, ECF No. 31-2 to 31-7.
On October 22, 2012, Respondent filed responsive expert reports and CVs from Drs. Barry Bercu and Arnold Levinson. Resp't's Exs. A-D, ECF Nos. 32-1 to 32-4.
On February 20, 2013, the special master convened a status conference to discuss the parties' respective expert reports and to set deadlines. See Scheduling Order (Feb. 21, 2013), ECF No. 38. Among other things, the parties were ordered to identify dates for a two-day Entitlement Hearing. Id. at 3.
On February 21, 2013, Petitioner submitted a second supplemental expert report from Dr. Shoenfeld addressing the opinions of Drs. Bercu and Levinson. Pet'r's Ex. 27, ECF No. 36-2. Respondent's experts declined to respond to Dr. Shoenfeld's second supplemental report. See Resp't's Status Report (Mar. 8, 2013) at 1, ECF No. 42.
In response to the parties' input, an Entitlement Hearing was scheduled for November 7-8, 2013, in Washington, D.C., before the undersigned. See Hearing Order (Apr. 8, 2013); see also Order Reassigning Case, ECF No. 39. A status conference was held on May 2, 2013, to discuss the pending hearing and to set additional deadlines. See Scheduling Order (May 23, 2013), ECF No. 45. Another status conference was held on September 17, 2013, to further discuss the hearing and to establish a schedule for pre-hearing submissions.
The Entitlement Hearing was held as scheduled, see Minute Entry (Nov. 8, 2013), with additional testimony heard on February 6, 2014, see Minute Entry (Feb. 6, 2014). Petitioner filed her post-hearing brief on March 14, 2014, and Respondent filed hers on April 4, 2014. Pet'r's Post Hr'g Br., ECF No. 64; Resp't's Post Hr'g Br., ECF No. 70.
In November 2014, this case was identified for inclusion with other POI cases in an "omnibus proceeding" established to address the question of what constitutes the first symptom or manifestation of POI. See Pet'r's Status Report (Oct. 1, 2014), Culligan, ECF No. 23. The answer to this question is integral to the undersigned's determination of whether each petitioner had filed her claim within the statute of limitations. See 42 U.S.C. § 300aa-16(a)(2) (2012) (requiring that petitions be filed prior to "the expiration of 36 months after the date of the occurrence of the first symptom or manifestation of onset . . . of injury").
The lead case in the proceeding was Culligan.
At a Culligan status conference held on September 23, 2014, the undersigned discussed with the parties the necessity of establishing the date that the statute of limitations began to run in Culligan and other cases alleging an injury of POI caused by Gardasil in order to assess the timeliness of the claims. See Scheduling Order (Sept. 25, 2014) at 1, Culligan, ECF No. 22. The undersigned directed the petitioner in Culligan's counsel, Mark Krueger, who is also counsel in the instant case, to begin the process of identifying other POI claimants for inclusion in an omnibus proceeding focused on the question of timeliness.
On October 1, 2014, Mr. Krueger filed a status report in which he identified eight POI cases
Another status conference was held on November 20, 2014, during which the parties agreed that "in all pending [POI] cases . . . an expert hearing [would] be held to address the question of what constitutes `the first symptom or manifestation of [POI] onset recognized as such by the medical profession at large.'" Scheduling Order (Nov. 24, 2014) at 1, Culligan, ECF No. 26 (citing Cloer v. Sec'y of HHS, 654 F.3d 1322, 1340 (Fed. Cir. 2011) (en banc)). The undersigned explained that a timeliness determination would be made on the basis of the evidence presented at the Culligan hearing; similar hearings would not be conducted in the other POI cases, all of which would trail Culligan for purposes of timeliness determinations. Id. The undersigned added four additional POI cases
The parties and the undersigned proceeded to identify questions for the experts (to be researched and answered before the hearing) regarding the nature and timing of the first symptom or manifestation of onset of POI in the aforementioned cases. See, e.g., Order (Feb. 18, 2015) at 1, Culligan, ECF No. 37; Scheduling Order (Jan. 30, 2015) at 1, Culligan, ECF No. 36; Pet'r's Status Report (Dec. 29, 2014) at 1, Culligan, ECF No. 31; Scheduling Order (Nov. 24, 2014) at 2, Culligan; Resp't's Status Report (Oct. 28, 2014) at 1, Culligan, ECF No. 24. The parties and their experts ultimately agreed that, except in Culligan, in which the entire medical record would be considered by the experts, the experts would "offer opinions regarding the onset issues in the trailing cases by considering the facts of those cases as hypotheticals." Joint Status Report (Jan. 20, 2015) at 1, Culligan, ECF No. 33. To facilitate this process, Petitioner filed summaries of the facts of all twelve POI cases. See Pet'r's Ex. 9, Culligan, ECF No. 34-2.
At a status conference held on January 28, 2015, the undersigned set deadlines for the parties' expert reports regarding timeliness. See Order (Jan. 30, 2015) at 2, Culligan. The experts were directed to address all of the identified timeliness questions separately, "on a question-by-question basis." Id. at 1.
On February 19 and March 3, 2015, three additional cases,
On March 12, March 13, and April 29, 2015, Petitioner filed expert reports and supporting medical literature, all of which were purportedly limited to the issue of timeliness. See Pet'r's Ex. 13, Culligan, ECF Nos. 47-2 to 51-6; Pet'r's Ex. 15, Culligan, ECF Nos. 53-1 to 54-3; Pet'r's Ex. 17, Culligan, ECF Nos. 76-78. The expert reports were authored by Dr. Felice Gersh and Dr. Hamiel. See Pet'r's Ex. 13, Tab 1, Culligan; Pet'r's Ex. 15, Tab 1, Culligan. The reports filed by Drs. Gersh and Hamiel reflected that they had reviewed the medical records underlying all of the POI cases. See Pet'r's Ex. 13, Tab 1 at 12-13, Culligan; Pet'r's Ex. 15, Tab 1 at 17, Culligan.
The undersigned convened a status conference on April 1, 2015, after having reviewed Petitioner's expert reports. See Scheduling Order (Apr. 2, 2015) at 1, Culligan, ECF No. 55. The undersigned noted that, "notwithstanding the fact that Petitioner's onset experts have now reviewed the medical records associated with every [POI] case, Respondent's onset expert(s) will review only the cases' factual summaries, the Culligan record, and Respondent's list of hypothetical questions." Id. Also, having expressed some concern about the extent to which Petitioner's expert reports reflected an understanding of the relevant question regarding timeliness, the undersigned reiterated the following:
Id. (full citation omitted).
Respondent then filed an expert report regarding timeliness, as well as relevant medical literature, on May 8, May 28, and June 1, 2015. Resp't's Ex. A to A.32, Culligan, ECF Nos. 57-1 to 59-6, 63-1 to 63-3, 66-1 to 67-4. Respondent's expert report was authored by Dr. David Frankfurter. Resp't's Ex. A at 6, Culligan.
At a status conference held on May 14, 2015, Respondent confirmed that, in preparing his expert report, Dr. Frankfurter had reviewed only the factual summaries submitted by Petitioner (and the medical record from Culligan). See Order (May 15, 2015) at 1, Culligan, ECF No. 61. Mr. Krueger agreed that, notwithstanding the fact that his experts had reviewed all of the medical records in all of the POI cases, "his experts would be referring to the factual summaries rather than to the medical records themselves" at the timeliness hearing. Id.
The parties filed their pre-hearing briefs simultaneously on June 1, 2015, see Pet'r's Prehearing Submissions, Culligan, ECF No. 65; Resp't's Prehearing Submissions, Culligan, ECF No. 69; and the hearing took place on June 16 and 17, 2015, see Minute Entry (June 18, 2015), Culligan. Petitioner's experts, Drs. Gersh and Hamiel, and Respondent's expert, Dr. Frankfurter, testified. Tr. at 4, 255.
On July 1, 2015, the undersigned issued an order identifying nine POI cases
On August 28, 2015, Respondent filed a status report in which she stated that she did not intend to contest the undersigned's preliminary findings in any of the presumptively timely cases filed by Mr. Krueger. Resp't's Status Report (Aug. 28, 2015) at 1, Culligan, ECF No. 84. In status reports filed on September 2 and 30, 2015, Petitioner argued that all of the preliminarily precluded cases were, in fact, timely. See Pet'r's Status Report (Sept. 2, 2015) at 2-7, Culligan, ECF No. 85 (addressing Culligan, Chenowith, Garner, Lee, Lydia McSherry, and Madelyne Meylor); Pet'r's Status Report (Sept. 30, 2015) at 1-2, Culligan, ECF No. 87 (addressing Fishkis, Meghan McSherry, Stone).
At a status conference held on October 13, 2015, the undersigned "informed the parties that, for purposes of an onset determination, the [POI] cases [would] be divided [into] two groups: petitioners who never menstruated . . . and the rest of the [POI] petitioners." See Scheduling Order (Oct. 14, 2015) at 1, Culligan, ECF No. 88.
Relevant post-hearing briefing
Section 300aa-16(a)(2) of the Vaccine Act provides that, regarding
42 U.S.C. § 300aa-16(a)(2).
This statute of limitations is not triggered by the administration of the vaccine, but "begins to run on the date of occurrence of the first symptom or manifestation of onset of the vaccine-related injury for which compensation is sought." Cloer, 654 F.3d at 1335. "[E]ither a `symptom' or a `manifestation of onset' can trigger the running of the statute [of limitations], whichever is first." Markovich v. Sec'y of HHS, 477 F.3d 1353, 1357 (Fed. Cir. 2007).
"[I]t is the first symptom or manifestation of an alleged vaccine injury, not first date when diagnosis would be possible, that triggers the statute of limitations." Carson ex rel. Carson v. Sec'y of HHS, 727 F.3d 1365, 1369 (Fed. Cir. 2013), reh'g & reh'g en banc denied, 2013 WL 4528833 at *1. "A symptom may be indicative of a variety of conditions or ailments, and it may be difficult for lay persons to appreciate the medical significance of a symptom with regard to a particular injury." Markovich, 477 F.3d at 1357. While the symptom of an injury must be recognized as such "by the medical profession at large," Cloer, 654 F.3d at 1335, even subtle symptoms that a petitioner would recognize "`only with the benefit of hindsight, after a doctor makes a definitive diagnosis of injury,'" trigger the running of the statute of limitations, whether or not the petitioner or even multiple medical providers understood their significance at the time. Carson, 727 F.3d at 1369-70 (quoting Markovich, 477 F.3d at 1358).
There is no explicit or implied discovery rule under the Vaccine Act. Cloer, 654 F.3d at 1337. The date of the occurrence of the first symptom or manifestation of onset of the alleged vaccine-related injury "does not depend on when a petitioner knew or reasonably should have known anything adverse about her condition." Id. at 1339. Nor does it depend on when a petitioner knew or should have known of a potential connection between an injury and a vaccine. Id. at 1338 ("Congress made the deliberate choice to trigger the Vaccine Act statute of limitations from the date of occurrence of the first symptom or manifestation of the injury for which relief is sought, an event that does not depend on the knowledge of a petitioner as to the cause of an injury."); see Markovich, 477 F.3d at 1358 ("Congress intended the limitation period to commence to run prior to the time a petitioner has actual knowledge that the vaccine recipient suffered from an injury that could result in a viable cause of action under the Vaccine Act." (internal quotation marks omitted)).
Primary ovarian insufficiency can begin abruptly, see Tr. at 69; see also Nelson at 2-3; but it may also develop over several years, see Tr. at 70, 198-99, 398; Meylor Tr. at 447; see also Nelson at 2-3; Pet'r's Ex. 17, Tab 50 at 2 (Paolo Beck-Peccaz & Luca Persam, Premature Ovarian Failure, 1 Orphanet J. Rare Diseases, at 2 (Apr. 2006)) (hereinafter "Beck-Peccaz"). Thus, a woman could have symptoms of POI for several years before actually ceasing menstruation or being diagnosed with POI. See Tr. at 70, 198-99, 398; see also Tr. at 319; Nelson at 2-3; Beck-Peccaz at 2. The experts agreed that the symptoms of primary ovarian insufficiency include menstrual irregularities, including primary and secondary amenorrhea, cycle and frequency irregularity, and excessive or prolonged bleeding; delayed menarche; lack of breast development and poor growth velocity; night sweats; hot flashes; sleep disturbances; mood changes; joint pain; recurring ovarian cysts; arrested puberty; and marked hirsutism. Tr. at 38, 57, 68, 319, 366; Meylor Tr. at 59-60, 68-70, 77, 410. Most of these symptoms are not "normal" for a woman under the age of 40. Petitioner therefore does not dispute that they can constitute the "first symptom or manifestation of onset" of POI for purposes of the Act's statute of limitations.
In fact, both Petitioner's experts and the medical literature emphasize the degree to which symptoms other than menstrual irregularity signify POI. In her expert report, Dr. Hamiel called hot flashes and night sweats the "hallmarks of the menopausal transition." Pet'r's Ex. 15 at 5, Culligan. At the Meylor hearing, both Dr. Hamiel and Dr. Shoenfeld testified, on multiple occasions, that sleep disturbances constituted a symptom of POI, Meylor Tr. at 47, 53, 60, 68, 77, 126, 130, 233, as are joint pains and emotional problems such as anxiety and depression, Meylor Tr. at 68-70. Of particular note, Dr. Shoenfeld attested that sleep disturbances are a "major criteria" for diagnosing the autoimmune disorder, POI, and explicitly clarified that sleep disturbances are "symptoms, . . . not signs." Id. at 233. Furthermore, Dr. Bercu, Respondent's expert, testified that sleep disturbance and night sweats were "more typical of premature menopause" than they were of normal pubertal development. Id. at 381-82. And the medical literature supports the attestations of Drs. Hamiel and Shoenfeld. See Nelson at 4; Pet'r's Ex. 15, Tab 6 at 2, ECF No. 53-7 (Vincent T. Martin, Migraine and the menopausal transition, 35 Neurological Scis. S65, S66 (2014)); Resp't's Ex. A.1 at 6, ECF No. 57-3 (Corrine K. Welt, Primary ovarian insufficiency: a more accurate term for premature ovarian failure, 68 Clinical Endocrinology 499, 504 (2008)). Given this (and Petitioner's failure to argue otherwise), the undersigned now concludes that the aforementioned symptoms (beyond menstrual irregularities and delayed menarche), constitute symptoms of POI.
At this point, the undersigned notes that the parties engaged in a lengthy dispute in this case and the related cases regarding whether and when menstrual irregularity and delayed menarche constitute symptoms of POI. Although an extensive discussion of the parties' positions and the undersigned's conclusion was warranted in the related cases, it is ultimately not dispositive of this case. Therefore, the undersigned merely reiterates her conclusion that menstrual irregularity constitutes a symptom when it meets the criteria specified in the ACOG Opinion. See Resp't's Ex. A.2, Culligan, ECF No. 57-4 (Comm. on Adolescent Health Care, Am. Coll. of Obstetricians & Gynecologists, Menstruation in Girls and Adolescents: Using the Menstrual Cycle as a Vital Sign, Comm. Op. No. 349 (Nov. 2006)) (hereinafter "ACOG Opinion" or "ACOG Op."). The ACOG Opinion provides the following specific conditions under which menstrual irregularity is sufficiently abnormal so as to constitute a symptom of POI
Menstrual periods that:
Id. at 5. But again, the undersigned repeats that the ACOG Opinion is only reproduced herein to provide context; unlike many of the related cases, it does not play a dispositive role in Petitioner's case.
Petitioner filed her petition on November 8, 2010, see Pet.; her petition is therefore time-barred if "the first symptom or manifestation of onset" of her alleged vaccine-related injury, POI, occurred before November 8, 2007. See 42 U.S.C. § 300aa-16(a)(2). All of the parties agree that Petitioner had not manifested any symptoms of POI before her first HPV vaccination on July 6, 2007. See, e.g., Meylor Tr. at 59, 410; Resp't's Ex. C at 7. The undersigned agrees: Petitioner was at Tanner Stages I and I at age 12, Pet'r's Ex. 4b at 92, then III and III at age 13, Pet'r's Ex. 4a at 73, 78, which appears to be normal pubertal development (according to the ACOG Opinion).
However, the testimony of Petitioner's mother and of Drs. Hamiel and Schoenfeld all place the first symptom of POI long before the actual diagnosis. Dr. Hamiel testified that "[t]he decrease in estrogen [from POI] is gradual. It takes as long as a female in menopause. It may take years." Meylor Tr. at 71. Dr. Hamiel also testified that the fact that Petitioner was depressed, tearful, unmotivated, and suffered from sleep disturbances "could be signs [of POI] even before somebody has the first menses," Meylor Tr. at 60; "fatigue, sleeplessness, mood changes . . . were already signs that she's developing some sort of decreased estrogen level," continued Dr. Hamiel, Meylor Tr. at 77. Finally, Dr. Hamiel testified of Petitioner, "[t]he fact that she got [menarche] in the edge of the normal age of onset of the first menses could suggest that she already had the signs [of POI] even before that." Id. at 60.
In his article in the American Journal of Reproductive Immunology documenting the POI cases of Petitioner (Case 2) and her sister (Case 1), Dr. Shoenfeld wrote that Petitioner "complained, 10 days after the first injection, of general symptoms such as depression and sleep disturbances. She also experienced episodes of lightheadedness and tremulousness, anxiety, panic attacks, and difficulties in focusing/concentrating in her school work." Pet'r's Ex. 31 at 2. Dr. Shoenfeld confirmed at hearing that he had obtained this medical history from Petitioner's mother. Id. at 235. Petitioner did not testify at either hearing, and the majority of the factual testimony at both focused on the more complicated and somewhat confused medical history of Petitioner's sister.
Based on this testimony, along with the testimony of all of the experts cited above, providing that depression, mood changes, sleeplessness, and joint pain are symptoms of POI, the undersigned finds that the first symptom of POI experienced by Petitioner occurred approximately ten days after she received the first Gardasil injection on July 6, 2007.
Based on the foregoing analysis, the undersigned finds that the first symptom of Petitioner's injury occurred in July 2007. Because that date precedes the statute of limitations deadline by four months, the undersigned concludes that Petitioner's claim is time-barred. Her petition therefore must be, and is hereby,
In the absence of a motion for review filed pursuant to RCFC Appendix B, the Clerk of the Court is directed to enter judgment herewith.
