Ferguson v. Saul

District Court, District of Columbia·Decided November 14, 2022·No. Civil Action No. 2021-1201·Published

Opinion

UNITED STATES DISTRICT COURT FOR THE DISTRICT OF COLUMBIA

OKIA FERGUSON, Plaintiff,

v. No. 21-cv-1201 (DLF)

KILOLO KIJAKAZI, Defendant. 1

MEMORANDUM OPINION

Plaintiff Okia Ferguson, on behalf of her minor son K.J., challenges the Social Security Administration’s (SSA’s) denial of K.J.’s claims for Supplemental Security Income benefits. Before the Court are Ferguson’s Motion for Judgment of Reversal, Dkt. 13, and the Social Security Commissioner’s Motion for Judgment of Affirmance, Dkt. 16. For the reasons that follow, the Court will grant the Motion for Judgment of Reversal and deny the Motion for Judgment of Affirmance. I. BACKGROUND A. Statutory and Regulatory Background “To qualify for disability insurance benefits and supplemental security income under Titles II and XVI of the [Social Security] Act, [a claimant] must establish that []he is ‘disabled.’” Butler v. Barnhart, 353 F.3d 992, 997 (D.C. Cir. 2004). The Act considers a minor disabled if he “has a medically determinable physical or mental impairment resulting in marked and severe functional limitations” that is either fatal or will last for more than one year. 42 U.S.C. § 1382c(a)(3)(C)(i);

1 Pursuant to Rule 25(d) of the Federal Rules of Civil Procedure, Kililo Kijakazi, the acting director of the Social Security Administration, has been substituted for Andrew Saul as defendant.

accord 20 C.F.R. § 416.906. A minor cannot be considered disabled if he “engages in substantial gainful activity.” 42 U.S.C. § 1382c(a)(3)(C)(ii).

For child claimants, the Commissioner uses an “abbreviated version” of its normal five-

step process to determine whether the claimant is disabled. Sullivan v. Zebley, 493 U.S. 521, 526 (1990); see 20 C.F.R. § 416.924. First, the claimant must show that he is not “doing substantial gainful activity.” 20 C.F.R. § 416.924(a), (b). Second, he must demonstrate that his impairment is “severe,” as opposed to a “slight abnormality . . . that causes no more than minimal functional limitations.” Id. § 416.924(a), (c). Third, the claimant must show that his impairments “meets, medically equals, or functionally equals” one of the listings at 20 C.F.R. Part 404, Subpart P, Appendix 1. Id. § 416.924(a), (d). If he does, and the impairment “meets the duration requirement,” then the Commissioner will deem the child disabled. Id. § 416.924(d). But “[i]f a child cannot qualify under these listings,” or his impairment does not meet the duration requirement, then “he is denied benefits.” Zebley, 493 U.S. at 526. “There is no further inquiry corresponding to the fourth and fifth steps of the adult test.” Id.

The listing relevant here is Listing 112.10, which describes autism spectrum disorder for children aged three to eighteen. To meet or medically equal the severity of the impairment in the listing, the child must show “[m]edical documentation of both . . . (1) [q]ualitative deficits in verbal communication, nonverbal communication, and social interaction; and (2) [s]ignificantly restricted, repetitive patterns of behavior, interests, or activities.” 20 C.F.R. pt. 404, subpt. P, app. 1, § 112.10 (emphasis omitted). In addition, the child must also establish “[e]xtreme limitation of one, or marked limitation of two, of the following areas of mental functioning:

(1) Understand, remember, or apply information.

(2) Interact with others.

(3) Concentrate, persist, or maintain pace.

(4) Adapt or manage oneself.”

Id. (citations omitted). To functionally equal the listing, the child must similarly show “‘marked limitations’ in two . . . or an ‘extreme’ limitation in one” of the following domains:

(1) Acquiring and using information;

(2) Attending and completing tasks;

(3) Interacting and relating with others;

(4) Moving about and manipulating objects;

(5) Caring for [one]self; and (6) Health and physical well-being.

20 C.F.R. § 416.926a(a), (b)(1).

B. Factual Background In K.J.’s early childhood, his mother became concerned about his delayed “speech and language development.” A.R. 253. She brought him into Children’s National Health System for an evaluation on October 23, 2018 (at one year, six months old). Id. At that visit, an evaluator tested K.J.’s hearing, and his “[r]esults were consistent with normal hearing for at least part of the speech frequency range in at least the better ear, if one exists.” Id. (quotation marks omitted). An evaluator also administered the Receptive-Expressive Emergent Language Test (REEL-3) to test K.J.’s receptive language, expressive language, and language ability. Id. at 254. K.J. scored below the first percentile on all three. Id. K.J. would “not stop if someone call[ed] his name,” was “not consistently responding to commands,” “d[id] not appear to understand the mood of others,” reportedly understood only a handful of words, and could say only the word “mama.” Id. On several of the indicators, including articulation, voice, and fluency, the evaluator wrote that K.J. “could not be appropriately assessed . . . due to paucity of output.” Id. at 254–55.

Approximately one month later, on November 14, 2018 (at one year, seven months old), K.J. had ear tubes placed in his ears due to recurring ear infections. See id. at 295. An evaluation of K.J.’s hearing at a follow-up appointment showed “normal hearing in sound field testing,” and his mother reported that she felt K.J.’s “hearing ha[d] improved.” Id.

A few months after the surgery, on January 7, 2019 (at one year, eight months old), K.J.

was given another standardized assessment called the Battelle Development Inventory-2 (BDI-2). Id. at 272. K.J. again scored below the first percentile in both receptive communication and expressive communication. Id. His overall communication score was in the 0.1st percentile and indicated a sixty percent delay in communication skills. Id. at 272–73. At that point, while K.J. sometimes (but not always) “respond[ed] to his name by looking up,” he did “not yet respond to different tones [of] voices, pay attention to the conversations that go on around him, or follow routine directions.” Id. at 272. He still did not use any words other than “mama.” Id. K.J. was given an Individualized Family Service Plan that included weekly therapy with a speech and language pathologist and an occupational therapist. Id. at 284, 286.

On March 20, 2019 (at one year, eleven months old), K.J. had another developmental evaluation at Children’s National. Id. at 310. The doctors observed, among other things, that K.J.’s “[r]eceptive language skills [we]re broadly delayed and presently appear to be slightly below the [twelve]-month level,” and they described him as “nonverbal.” Id. at 312. The doctors diagnosed K.J. with autism spectrum disorder. Id. at 313. In addition, they recommended that K.J. continue to receive weekly speech and occupational therapy and add applied behavioral analysis therapy, which would “have a direct and positive impact on [his] current functional skills as well as his long-term prognosis.” Id.

On September 25, 2019 (at two years, five months old), K.J. was again evaluated at Children’s National. Id. at 483. At that time, the doctor observed that K.J. had “made some progress in the areas of language, socialization, and play skills.” Id. at 485. But the doctor noted that K.J. “continue[d] to demonstrate problematic behaviors, some of which are quite dangerous such as throwing himself down and running away from caregivers.” Id. K.J. was “consistently

using” only two words: “Mommy and blue,” and he was “not tuning into spoken language,” as he responded to his name only half of the time and could not follow instructions. Id. at 484. The doctor estimated that K.J.’s cognitive skills were now “at the [eighteen] to [twenty-one]-month level, which illustrates an improvement of approximately [six] months in as many months.” Id. at 485. She recommended an increase in weekly therapy. Id.

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