Shearer v. Saul

CourtDistrict Court, M.D. Pennsylvania
DecidedNovember 16, 2022
Docket1:21-cv-00398
StatusUnknown

This text of Shearer v. Saul (Shearer v. Saul) is published on Counsel Stack Legal Research, covering District Court, M.D. Pennsylvania primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Shearer v. Saul, (M.D. Pa. 2022).

Opinion

IN THE UNITED STATES DISTRICT COURT FOR THE MIDDLE DISTRICT OF PENNSYLVANIA

APRIL R. MURRAY SHEARER, : Civil No. 1:21-CV-398 O/B/O J.K.M. : : Plaintiff : : (Magistrate Judge Carlson) v. : : KILOLO KIJAKAZI, : Acting Commissioner of Social Security, : : Defendant :

MEMORANDUM OPINION

I. Introduction The Supreme Court has underscored for us the limited scope of our substantive review when considering Social Security appeals, noting that: The phrase “substantial evidence” is a “term of art” used throughout administrative law to describe how courts are to review agency factfinding. T-Mobile South, LLC v. Roswell, 574 U.S. ––––, ––––, 135 S. Ct. 808, 815, 190 L.Ed.2d 679 (2015). Under the substantial- evidence standard, a court looks to an existing administrative record and asks whether it contains “sufficien[t] evidence” to support the agency’s factual determinations. Consolidated Edison Co. v. NLRB, 305 U.S. 197, 229, 59 S. Ct. 206, 83 L.Ed. 126 (1938) (emphasis deleted). And whatever the meaning of “substantial” in other contexts, the threshold for such evidentiary sufficiency is not high. Substantial evidence, this Court has said, is “more than a mere scintilla.” Ibid.; see, e.g., Perales, 402 U.S. at 401, 91 S. Ct. 1420 (internal quotation marks omitted). It means—and means only—“such relevant evidence as a reasonable mind might accept as adequate to support a conclusion.” Consolidated Edison, 305 U.S. at 229, 59 S. Ct. 206. See Dickinson v. 1 Zurko, 527 U.S. 150, 153, 119 S. Ct. 1816, 144 L.Ed.2d 143 (1999) (comparing the substantial-evidence standard to the deferential clearly- erroneous standard). Biestek v. Berryhill, 139 S. Ct. 1148, 1154 (2019). April Shearer applied for supplemental security income under Title XVI of the Social Security Act on behalf of her minor son, J.K.M., on May 19, 2017, alleging an onset date of disability of May 3, 2005. J.K.M. had previously been

awarded benefits, but in 2014, on reconsideration, an Administrative Law Judge (“ALJ”) determined that J.K.M. was no longer disabled as of January 31, 2014. Thus, a hearing was held before an ALJ regarding this new application for benefits.

On this occasion the ALJ found that J.K.M. was not disabled and denied the application for benefits. Shearer now appeals this decision, arguing that the ALJ’s decision is not supported by substantial evidence. However, after a review of the record, and mindful of the fact that substantial

evidence “means only—‘such relevant evidence as a reasonable mind might accept as adequate to support a conclusion,’” Biestek, 139 S. Ct. at 1154, we find that substantial evidence supported the ALJ’s findings in this case. Therefore, for the

reasons set forth below, we will affirm the decision of the Commissioner.

2 II. Statement of Facts and of the Case

April Shearer filed for SSI on behalf of her minor son, J.K.M., on May 19, 2017, alleging that J.K.M. was disabled due to panhypopituitarism, ectopic pituitarism, hypoglycemia, hypothyroidism, life threatening cortisol deficiency, and high functioning autism. (Tr. 121). She alleged that her son was disabled since May

3, 2005, shortly after he was born. (Id.) At the time of the most recent disability determination, J.K.M. was fourteen years old and was in ninth grade. As we have noted, in 2009, J.K.M. was found to be disabled due to his panhypopituitarism. (Tr. 91). At that time, an ALJ found that J.K.M. had an extreme

limitation in the domain of health and physical well-being. (Tr. 92). However, on reconsideration in a decision dated April 20, 2017, an ALJ found that as of January 31, 2014, J.K.M was no longer disabled, reasoning that J.K.M. had less than marked

limitations in five of the six domains of functioning, and no limitation in the domain of moving about and manipulating objects. (Tr. 104-06). J.K.M. suffered from panhypopituitarism1 since he was an infant, for which he was prescribed a daily growth hormone. (Tr. 790). In January of 2015, treatment

notes from Penn State Health at the Hershey Medical Center indicated that J.K.M.

1 Panhypopituitarism is a rare condition in which the production and secretion of all hormones by the pituitary gland is reduced. See https://www.chop.edu/conditions- diseases/panhypopituitarism-children (last visited November 10, 2022). 3 would be treated for this condition for the rest of his life. (Tr. 881). It was also noted that J.K.M. had a history of high functioning autism and was on several medications

which had been stable for the past two years. (Id.) These treatment notes also indicated that J.K.M. used Benadryl to help him sleep, which he tolerated well. (Id.) At a visit in December of 2015, it was noted that J.K.M. had grown 3.4 centimeters

and had gained 9 kilograms in weight, and that he experienced no adverse side effects from his medications. (Tr. 845). At a follow up appoint in July of 2016, it was noted that while J.K.M. had sixty hospitalizations since birth, he had not had any hospitalizations in two years.

(Tr. 826). J.K.M.’s diagnoses were listed as autism spectrum disorder, childhood obesity, combined hyperlipidemia, and panhypopituitarism. (Tr. 829-30). At this time, he also had an x-ray of his spine, which revealed no significant scoliotic

curvature of his spine. (Tr. 823). At a follow up with endocrinology in July, it was noted that J.K.M. had been doing well since his last visit. (Tr. 815). A physical examination revealed largely normal findings. (Tr. 817). At a visit to Hershey Medical Center in January of 2017, it was noted that

J.K.M.’s mother was happy with his growth. (Tr. 801). At this time, treatment records stated that his “endocrine conditions [were] well managed” and his medications remained the same. (Tr. 804). A bone study was performed, which

4 indicated normal bone age with discordant delay in maturation of the carpal bones. (Tr. 799). It was noted that J.K.M.’s bone age “correspond[ed] to the standard of an

11-year 6-month-old male,” and this represented normal bone age. (Id.) At a follow up endocrinology visit in June of 2017, it was noted that J.K.M. was doing well, and there were no changes made to his medications. (Tr. 1095, 1098).

J.K.M. had his yearly examination in July of 2017, during which it was noted that he had started testosterone replacement therapy. (Tr. 1070). It was also noted that he had not done well in sixth grade, but that his school was attempting to provide him with additional support. (Id.) Treatment notes indicate a problem with

insomnia, but noted that J.K.M. took Benadryl, Melatonin, and Clonidine which worked well. (Id.) In June of 2018, J.K.M. presented to the emergency department at Hershey

Medical with complaints of respiratory problems. (Tr. 1294). His mother stated that he had nosebleeds everyday for 4-5 days, and that he had 3 nosebleeds the day he presented to the emergency room. (Id.) These episodes were preceded by an incident in March in which J.K.M. fell out of his bed and struck the left side of his face. (Tr.

1319). An ENT was consulted in the emergency department, and J.K.M. was discharged as stable. (Tr. 1300). J.K.M. saw an ENT again at an endocrinology visit in June of 2018, during which time it was noted that J.K.M. was growing 12.6

5 centimeters per year, which was deemed “an excellent rate of growth.” (Tr. 1287). A bone scan revealed normal bone age. (Tr. 1266). Regarding his nosebleeds, it was

determined that moisture care was needed in order for J.K.M.’s nose to be healthy. (Tr. 1274).

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