Burgett v. Social Security Administration, Commissioner

CourtDistrict Court, N.D. Alabama
DecidedAugust 30, 2024
Docket2:23-cv-01256
StatusUnknown

This text of Burgett v. Social Security Administration, Commissioner (Burgett v. Social Security Administration, Commissioner) is published on Counsel Stack Legal Research, covering District Court, N.D. Alabama primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Burgett v. Social Security Administration, Commissioner, (N.D. Ala. 2024).

Opinion

UNITED STATES DISTRICT COURT FOR THE NORTHERN DISTRICT OF ALABAMA SOUTHERN DIVISION

DEBORAH CARPENTER BURGETT, } } Plaintiff, } } v. } Case No.: 2:23-cv-01256-RDP } MARTIN O’MALLEY, } COMMISSIONER, SOCIAL SECURITY } ADMINISTRATION, } } Defendant. }

MEMORANDUM OF DECISION

Plaintiff Deborah Carpenter Burgett brings this action pursuant to Section 205(g) of the Social Security Act (the “Act”), seeking review of the decision of the Commissioner of Social Security (“Commissioner”) denying her claims for a period of disability and disability insurance benefits (“DIB”). See also 42 U.S.C. § 405(g). After careful review of the record and the briefs submitted by the parties, the court concludes that the decision of the Commissioner is due to be reversed and this matter remanded. I. Proceedings Below Plaintiff filed her application for a period of disability and DIB on May 26, 2020. (Tr. 96). The application was denied initially on August 11, 2020, and upon reconsideration on December 2, 2020. (Tr. 147, 160). After a was hearing held on September 15, 2021 (Tr. 71-95), Administrative Law Judge Renee Blackmon Hagler (“ALJ”) issued a decision on October 4, 2021, finding Plaintiff was not disabled. (Tr. 124-34). On April 25, 2022, the Appeals Council remanded the case to the ALJ for further proceedings. (Tr. 142-43). The ALJ held a second hearing on October 3, 2022. (Tr. 45-70). In her second decision, dated December 22, 2022, the ALJ determined that Plaintiff had not been under a disability within the meanings of §§ 216(i) and 223(d) at any time from January 1, 2015 (the alleged onset date) through December 31, 2019 (the date last insured). (Tr. 24-36). After the Appeals Council denied Plaintiff’s request for review of the ALJ’s second decision (Tr. 1), that decision became the final decision of the Commissioner,

and therefore a proper subject of this court’s appellate review. At the October 3, 2022 hearing, Plaintiff testified that she was fifty-six years old and held a Bachelor’s Degree. (Tr. 52). Plaintiff last worked in December 2014 in the finance department of Blue Cross of Alabama as an enrollment services specialist. (Tr. 53, 337). Plaintiff alleges that she suffers from fibromyalgia, Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (hereinafter “chronic fatigue syndrome”), chronic migraines, anxiety, and depression. (Tr. 54). Plaintiff complains of debilitating migraines that currently occur around four days per week, but they previously occurred every day. (Tr. 59, 64). When she experiences these migraines, Plaintiff states that she is nauseous, dizzy, unable to function, and must lay in a dark room, cover

her eyes, and use an icepack to alleviate her pain. (Tr. 60). Additionally, she complains of severe fatigue that takes over her entire body and lasts for weeks at a time. (Tr. 59). On days where her fatigue is extremely bad, Plaintiff states that she needs her husband’s help to shower and get dressed. (Tr. 59). Plaintiff also struggles with anxiety and depression. (Tr. 60). Plaintiff takes a host of prescribed and over-the-counter medication to treat her symptoms. She takes the following medication on a daily basis: Cartia for mitral valve prolapse (180 milligrams 1x each day); Topamax for migraines (100 milligrams 2x each day); Zocor for cholesterol (40 milligrams 1x each day); Synthroid for thyroid issues (100 MCGs 1x each day); Wellbutrin XR for depression (150 milligrams 1x each day); Buspar for anxiety (15 milligrams 2x each day); Propranolol for anxiety (10 milligrams, 1-2x each day as needed); Vitamin D (50,000 IC 1x each week); Tramadol for pain (50 milligrams 1x each day); Flexeril (10 milligrams, 1-2x each day); and Adderall (10 milligrams as needed). (Tr. 56-58, 372-73). Each month, she receives an injection of Aimovig for her migraines. (Tr. 56). In addition, she regularly takes over-the- counter medicine such as Tylenol, Motrin, and Excedrin Migraine. (Tr. 55, 60). Although Plaintiff

acknowledges that the medicine helps, she states that nothing takes her pain completely away. (Tr. 59). In 2008, Plaintiff began seeing Dr. John Riser at Alabama Neurology Associates for her migraines. (Tr. 687). Dr. Riser diagnosed Plaintiff with migraine headaches and cervical degenerative disk disease and prescribed her Darvocet, Topamax, and Flexeril. (Tr. 687). At later appointments, Dr. Riser noted that Plaintiff had intact motor skills and no limitations with her gait. (Tr. 650, 655, 660, 665, 673, 675, 677). However, at most of these appointments, Plaintiff continued to complain of headaches. (Tr. 642, 661, 675). In 2010 and 2011, Dr. Riser opined that Plaintiff’s headaches were associated with stress and allergy problems, but were overall stable.

(Tr. 647, 667, 673, 675). In February 2011, Dr. Riser noted that Plaintiff had relatively infrequent headaches while taking Topamax, Ultram, and Flexeril and seemed to be doing “very well.” (Tr. 670). During multiple visits in 2012 and 2013, Plaintiff informed Dr. Riser that her headaches were stable and under control. (Tr. 647, 652, 657, 662). Plaintiff attributed her headaches to stress but was still able to work full-time. (Tr. 647, 652, 1087). In May 2014, Plaintiff returned to Dr. Riser with complaints of extreme fatigue, weakness, and exhaustion over the previous six months. (Tr. 642). Dr. Riser prescribed Plaintiff a trial dose of Cymbalta, which initially helped Plaintiff’s pain. (Tr. 456, 645). However, at follow up appointments, Plaintiff continued to complain of pain and emotional issues, and she requested Dr. Riser fill out an FMLA form related to her work. (Tr. 632, 637). Although Dr. Riser initially increased Plaintiff’s Cymbalta dosage in an effort to reduce her symptoms (Tr. 641), he ultimately decreased the dosage after her symptoms worsened. (Tr. 636). During this period, Dr. Riser opined that Plaintiff’s headaches and musculoskeletal pain seemed to have intensified. (Tr. 632, 637, 642). In November 2014, Plaintiff continued to complain of migraines, anxiety, and memory

loss, and informed Dr. Riser that she was no longer able to work. (Tr. 631). Dr. Riser opined that, although Plaintiff’s issues were most likely related to her medication and nothing in her evaluation suggested any type of dementia, she needed additional lab work and an evaluation by a psychologist or psychiatrist. (Tr. 627, 631). An MRI of Plaintiff’s head revealed ventricular asymmetry in the brain, with what appeared to be a right porencephalic cyst involving the lateral ventricle. (Tr. 680). In December 2014, Plaintiff was referred to see Dr. Jack Denver for her fibromyalgia. (Tr. 699). At her first appointment, Plaintiff complained of an inability to function for over six months due to pain, which she rated a 6/10. (Tr. 699-700). Plaintiff complained of feeling like her hands

and feet were constantly swollen and about pain in her neck, shoulders, left hip, and left knee. (Tr. 699). Dr. Denver’s examination revealed that Plaintiff’s gait and station was within normal limits, but that the range of her extension was limited by 50% and her fibromyalgia tender points at 10 and 18 were significantly painful. (Tr. 701). At a follow-up appointment a month later, Plaintiff rated her pain a 7/10 on average, with her best pain level of the previous month being a 3/10 and her worst being a 9/10. (Tr. 703). Dr. Denver recommended discontinuing her use of Flexeril and reducing her use of Topamax. (Tr. 704). Plaintiff reported an increase in her migraines when the Topamax was decreased and rated her average pain level at 6-7/10. (Tr. 706). In August 2015, Plaintiff informed Dr. Riser that she had stopped taking Cymbalta, and that her overall pain level was about the same, or slightly worse, since doing so. (Tr. 619). Dr.

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Burgett v. Social Security Administration, Commissioner, Counsel Stack Legal Research, https://law.counselstack.com/opinion/burgett-v-social-security-administration-commissioner-alnd-2024.