Fla. Admin. Code Ann. R. 65G-4.014 - Eligibility for Agency Services - Definitions
(1) Autism means a condition which meets the
requirements of section
393.063, F.S., that the
condition is:
(a) Pervasive, meaning always
present and without interruption;
(b) Neurologically based, meaning that the
condition is not the result of physical impairment;
(c) A developmental disability with age of
onset during infancy or childhood;
(d) With extended duration, meaning that the
condition reasonably can be expected to continue indefinitely into the
future;
(e) Causes severe learning
disorders resulting in both severe communication disorders affecting both
verbal and nonverbal skills, and severe behavior disorders. Autism is
characterized by an individual evidencing at least six of the following twelve
features from the following subparts 1 and 2, with at least one feature from
subpart 2:
1. Severe communication disorders,
which may include:
a. A delay in, or total
lack of, the development of spoken language (not accompanied by an attempt to
compensate through alternative modes of communication such as gesture or mime),
b. Stereotyped and repetitive use
of language or idiosyncratic language,
c. For those applicants with speech, marked
impairment in the use of multiple nonverbal behaviors such as eye-to-eye gaze,
facial expression, body postures, and gestures to regulate social interaction,
d. Failure to develop peer
relationships appropriate to developmental level,
e. A lack of spontaneous seeking to share
enjoyment, interests, or achievements with other people (e.g., by a lack of
showing, bringing, pointing out objects of interest, or achievements to
others),
f. Lack of social or
emotional reciprocity,
g. Marked
impairment in the ability to initiate or sustain a conversation with others in
individuals with adequate speech, or
h. Impaired imaginative ability evidenced by
a lack of varied, spontaneous make-believe play or social imitative play
appropriate to developmental level.
2. Severe behavior disorders, which are
restricted, repetitive and stereotyped patterns of behavior, interests, and
activities which may include:
a. Encompassing
preoccupation with one or more stereotyped and restricted patterns of interest
that is abnormal either in intensity or focus,
b. Apparently inflexible adherence to
specific, nonfunctional routines or rituals,
c. Stereotyped and repetitive motor
mannerisms (e.g., hand or finger flapping or twisting, or complex whole-body
movements), or
d. Persistent
preoccupation with parts of objects.
(2) Cerebral Palsy - means a group of
disabling symptoms of extended duration that result from damage to the
developing brain during the prenatal period and characterized by paralysis,
spasticity, or abnormal control of movement or posture, such as poor
coordination or lack of balance, which is manifest prior to three years of age.
For purposes of the rule, cerebral palsy also means the presence of other
significant motor dysfunction appearing prior to age 18 due to perinatal or
external events such as anoxia, oxygen deprivation, or traumatic brain injury.
Excluded from this definition is motor dysfunction caused by medical events,
including stroke or progressive diseases such as muscular dystrophy. The
impairment from cerebral palsy must constitute a substantial handicap which is
reasonably expected to continue indefinitely.
(3) Mental Retardation or Intellectual
Disability - is evidenced by the concurrent existence of:
(a) Significantly subaverage general
intellectual functioning evidenced by an Intelligence Quotient (IQ) two or more
standard deviations below the mean on an individually administered standardized
intelligence test; and,
(b)
Significant deficits in adaptive functioning in one or more of the following
areas:
1. Communication skills,
2. Self-care, home living,
3. Social and interpersonal skills,
4. Use of community resources and
self-direction,
5. Functional
academic skills,
6. Work, leisure,
health and safety awareness and skills,
(c) Which are manifested prior to age 18;
and,
(d) Constitute a substantial
handicap which is reasonably expected to continue
indefinitely.
(4)
Prader-Willi Syndrome - means a genetic disorder which is most often associated
with a random deletion of chromosome 15. Commonly associated characteristics
include insatiable appetite, chronic overeating, hypotonia, short stature,
obesity, and behavioral issues. Individuals diagnosed with Prader-Willi
syndrome generally have mental retardation; however, an individual with
Prader-Willi syndrome can be determined as eligible for services without an
accompanying diagnosis of mental retardation.
(5) Spina Bifida - For the purposes of agency
eligibility, spina bifida refers to a confirmed diagnosis of spina bifida
cystica or myelomeningocele.
(6)
Down Syndrome - means a condition caused by the presence of extra chromosomal
material on chromosome 21. This disorder is often associated with impairment in
cognitive ability, characteristic physical growth and features, and congenital
medical conditions.
(7) Eligibility
Rules - rules 65G-4.014 through
65G-4.017, F.A.C., inclusive,
which apply to eligibility determinations for services provided through the
Agency for Persons with Disabilities for individuals with developmental
disabilities.
(8) DD Waiver - Home
and Community-Based Services (HCBS) waiver authorized by
42 U.S.C.
1396n(c)(1) of the federal
Social Security Act and section
409.906, F.S., that provides a
package of Medicaid-funded home and community-based supports and services to
eligible persons with developmental disabilities who live at home or in a
home-like setting.
(9) Agency
Services - home and community based supports and services to eligible persons
funded through general revenue allocations or sources other than the DD
Waiver.
Notes
Rulemaking Authority 393.065(10), 393.066(8), 393.501 FS. Law Implemented 393.065, 393.066 FS.
New 5-16-12.
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