Some of what is covered by insurance companies is
mandated by law while other aspects of an insurance policy is the option of the
employer if they want it made available to their employees. There are some companies out there, not many,
that do offer insurance coverage to their employees and family members for
autism related services. Recently, a few
state governments have passed laws mandating that coverage for autism related
treatment and services be offered to all employees who receive health insurance
benefits, and other states are starting to consider similar laws.
Call your insurance company and ask why they do not
cover treatment for autism related symptoms, and you will receive various
reasons for the exclusion of coverage. Since, there is no known cure for autism
any treatment provided is an effort in futility, right? There are no approved medications that can
help reduce the symptoms and behaviors of those living with this incurable
disorder either. The speech and
occupational therapy a person with autism needs is deemed as developmental or
educational, and can be obtained through a child’s school district by way of
Individual Education Plan (IEP).
Call them a “can response” or just plain bullsh*t,
the line you receive from the insurance companies could be easily applied to
other health conditions that are covered. Last I checked there was no cure for
depression, but there is approved medications and clinical therapy to treat
this mental disorder. Insurance
companies do cover the cost for some prescription medications proven to reduce
the symptoms of depression and also provide funding to assist with paying for
clinical therapy. Similarly, autism may have no cure, but it is treatable and
there are many treatments and therapies shown to reduce the symptoms of autism.
Like many issues we face during the course of our
life, money becomes a factor in the decision making process and insurance
coverage for the treatment of autism is no exception to this rule. It can cost thousands of dollars per year to
provide some of the treatments necessary to help a person with autism. On the
flip side, by not providing services to give these individuals on the autism
spectrum an opportunity to improve their abilities will potentially be more
expensive when you factor in the government assistance they will need to
receive over a lifetime. The goal is to
get individuals on the autism spectrum as best prepared as possible for the
opportunity to live independently or semi-independently in order that they are
not a constant fixture on the government assistance payroll.
Personally, I hope that one day our son will be
capable of living independently with someone checking on him from time to time
to make sure he is getting everything he needs.
Our goal has always been to give him the greatest opportunities for
potential success, but there is no telling what his capabilities will be when
he becomes an adult. He may be capable
of holding a job, paying his own bills and having his own place to live, with
limited assistance from third-parties (social services and government
entities). We need to stop with the
attitude that no cure equals no hope for change and improvement, because we as
parents have hope for improvement and a better life for our children.
Stay tuned for “Show me the Funding” Part 2.
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