Ingargiola v. Kijakazi

CourtDistrict Court, E.D. Missouri
DecidedJune 27, 2022
Docket4:20-cv-01776
StatusUnknown

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

Bluebook
Ingargiola v. Kijakazi, (E.D. Mo. 2022).

Opinion

UNITED STATES DISTRICT COURT EASTERN DISTRICT OF MISSOURI EASTERN DIVISION

THERESA INGARGIOLA, ) ) Plaintiff, ) ) v. ) No. 4: 20 CV 1776 DDN ) KILOLO KIJAKAZI, ) Acting Commissioner of Social Security, ) ) Defendant. )

MEMORANDUM This action is before the Court for judicial review of the final decision of the defendant Commissioner of Social Security denying the applications of plaintiff Theresa Ingargiola for disability insurance benefits (DIB) under Title II of the Social Security Act (Act). The parties have consented to the exercise of plenary authority by a United States Magistrate Judge pursuant to 28 U.S.C. § 636(c). For the reasons set forth below, the final decision of the Commissioner is affirmed.

BACKGROUND Plaintiff was born on August 5, 1957. (Tr. 182.) She protectively filed her applications for DIB on December 28, 2018. (Tr. 182-83.) She alleged a disability onset date of June 1, 2016, and in her Disability Report, alleged disability due to multiple sclerosis (MS), attention deficit disorder (ADD), anxiety, depression, confusion, concentration, and pain. (Tr. 182, 220.) Her claims were denied, and she requested a hearing before an administrative law judge (ALJ). (Tr. 75, 83-89.) On April 23, 2020, following a hearing, the ALJ concluded that plaintiff was not disabled under the Act. (Tr. 26-36.) The Appeals Council denied review. Accordingly, the ALJ’s decision became the final decision of the Commissioner subject to judicial review by this Court under 42 U.S.C. § 405(g). (Tr. 1-6.)

ADMINISTRATIVE RECORD The following is a summary of plaintiff’s medical and other history relevant to her appeal. On September 2, 2016, plaintiff saw ophthalmologist Mark Spurrier, M.D. for possible cataracts. Plaintiff reported difficulty with her near and distance vision, as well as difficulty focusing. She reported a decline in her vision over the past three months. Her visual acuity was 20/30 in her right eye and 20/30+ in the left. Examination showed weakness of adduction in the right eye and nystagmus, or involuntary eye movement, of the right eye on attempted left gaze, as well as early-stage cataracts that were asymptomatic or only mildly symptomatic. Dr. Spurrier diagnosed (1) internuclear ophthalmoplegia (INO), a disorder of conjugate lateral gaze in which the affected eye shows impairment of adduction, and (2) age-related, early-stage incipient cataracts bilaterally, and referred her to a neurologist. He recommended that plaintiff have her glasses remade. (Tr. 306-10.) On September 7, 2016, plaintiff saw internist and primary care provider Adam Michael Ralko, M.D., for diplopia or double vision, depression with anxiety, and attention- deficit disorder. She told Dr. Ralko that she “did not think much of” the double vision but that her eye doctor recommended further evaluation. Plaintiff reported that while she was worried about the diplopia, she was “not limited by [it] at all” and reported having no other symptoms. She denied blurry vision, floaters, or flashers. Examination showed plaintiff was pleasant, well-appearing, and in no acute distress. Neurological examination showed plaintiff to be alert and appropriate with full muscle strength throughout all extremities, intact sensation and reflexes, normal finger-nose-finger coordination, and a steady, normal- based gait. Dr. Ralko diagnosed monocular diplopia in plaintiff’s right eye and ordered an MRI of her brain for further evaluation. Adderall, for ADD, and Wellbutrin, an anti- depressant, were continued. (Tr. 265-67.) - 2 - On September 14, 2016, an MRI of her brain showed a pattern of extensive disease suggestive of a chronic demyelinating disease. (Tr. 292.) On October 18, 2016, plaintiff saw neurologist Amy Rauchway, D.O. at an initial visit for complaints of double vision. Plaintiff told Dr. Rauchway that Dr. Spurrier added a prism to her eyeglasses, and since then she felt much better. no longer had blurry vision, and was able to work at a computer. She reported no difficulty managing activities of daily living. On examination, she was alert and oriented, with normal strength and tone, no sensory deficit, and a normal gait. Coordination testing showed mild ataxia with heel-to- shin, but no dysmetria or inability to execute complex movement, on finger-to-nose. She had mild ataxia, positive Romberg’s (balance) testing, and a flicker of nystagmus, or involuntary, rapid, and repetitive movement, in her left eye, but other neurological testing was negative. Eye examination revealed full visual fields, and visual acuity of 20/25 in both eyes. Dr. Rauchway informed her that her MRI results were suggestive of multiple sclerosis. (Tr. 390-93.) On November 7, 2016, plaintiff saw Dr. Ralko for a routine physical. He noted that her recent MRI was suggestive of demyelinating disease, but that she was not limited at all by the diplopia and had no other symptoms. Examination showed plaintiff to be pleasant, well-appearing, and in no acute distress. Neurologically, she was alert and appropriate, her cranial nerves were intact, she had full muscle strength throughout all extremities, intact sensation and reflexes, normal finger-nose-finger coordination, and a normal gait. (Tr. 387-90.) A December 2, 2016 MRI of plaintiff’s cervical spine showed disc degeneration predominantly at C5-C6 with very subtle areas of T2 hyperintensity in the upper cervical cord at C2 and C3. (Tr. 423-25.) Plaintiff followed up with Dr. Rauchway on December 9, 2016, to discuss her MRI results. Her examination showed her speech to be mildly dysarthric (weakened or slurred) but fluent. (Tr. 383-86.) - 3 - On January 3, 2017, plaintiff saw Dr. Spurrier for difficulty with her long distance vision in the right lens of her glasses. (Tr. 310.) A January 27, 2017 CT scan of her chest showed small bilateral pulmonary nodules, measuring up to 5mm, questionable mild or early paraseptal emphysema in the right apex, sub centimeter low density hepatic lesions with a low-density rim calcified splenic mass and non-obstructing left renal calculus. (Tr. 419-20.) On February 6, 2017, plaintiff saw Dr. Rauchway for continued complaints of double vision. Examination revealed slight dysmetria with placing her finger to nose, with mildly dysarthric speech. Romberg testing was positive. Dr. Rauchway prescribed Copaxone, an immunomodulator used to treat MS, and vitamin D, and referred her to a neurologist for evaluation of multiple sclerosis. (Tr. 373-76.) Plaintiff saw Dr. Rauchway on May 8, 2017, for continued double vision. She reported having received three Copaxone injections in the past week, resulting in injection site redness, itching, and a crawling sensation in her leg. She reported fatigue and knocking objects over when trying to reach. On exam, plaintiff had slight dysmetria with her right finger-to-nose and positive Romberg testing. She reported plans to do volunteer work at a therapeutic horseback riding facility. (Tr. 368-70.) A June 9, 2017 MRI of plaintiff’s brain revealed “relatively stable disease without clear cut new lesions and no enhancing disease.” (Tr. 415-16.) On June 28, 2017, plaintiff saw ophthalmologist Michael P. Donahoe, M.D. for follow-up for her cataracts. She reported blurred visual acuity. On exam, plaintiff was positive for Duane’s syndrome Type 1, an eye movement disorder present at birth (congenital) characterized by horizontal eye movement limitation, in her left eye. Dr. Donahoe noted that plaintiff had been diagnosed with MS but had no symptoms. She was instructed to return in one year for a comprehensive eye examination. (Tr. 721-25.) On August 8, 2017, plaintiff saw Barry Singer, M.D., a neurologist, reporting mild fatigue due to her multiple sclerosis.

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