Autism spectrum disorders affect Florida families in unprecedented, epidemic proportion. For this growing segment of the population, there is a disproportionate and inverse relationship as it relates to the amount of health insurance coverage the parents, family members and caregivers have to effectively treat these children for sickness and medical impairments in the following areas: neurological (including seizures and motor impairments), behavioral, immunological, social skill deficits, sensory and gastrointestinal disorders, dental and eye care, occupational. speech/language and physical therapies.
Early diagnosis and intervention in these areas is critical to effectively treat this disease. In many cases, families have no insurance coverage to treat any of these conditions and are in a state of financial devastation as a result of out of pocket expenses paid to treat their child who will have medical illness and disease in 1 or more of the costly medical conditions noted above.
It is imperative that the appropriate interventions needed by each Florida child who has an autism spectrum disorder be accessible, in the areas noted above, through mandatory health insurance coverage in the state of Florida. This is PARAMOUNT, so that long term outcomes will be improved. Our current private insurance accessibility/coverage make these crucial interventions impossible to receive. As a result, these sick children are either not receiving these services due to high costs, or; families are having to forego helpful but costly treatments for their child to try and avoid being cast into a state of financial ruin. Many times, families do end up in a state of bankruptcy due to their desperate attempts to try and pay for treatment for their child, in spite of the lack of insurance coverage.
Autism spectrum disorders affect Florida families in unprecedented, epidemic proportion. For this growing segment of the population, there is a disproportionate and inverse relationship as it relates to the amount of health insurance coverage the parents, family members and caregivers have to effectively treat these children for sickness and medical impairments in the following areas: neurological (including seizures and motor impairments), behavioral, immunological, social skill deficits, sensory and gastrointestinal disorders, dental and eye care, occupational. speech/language and physical therapies.
Early diagnosis and intervention in these areas is critical to effectively treat this disease. In many cases, families have no insurance coverage to treat any of these conditions and are in a state of financial devastation as a result of out of pocket expenses paid to treat their child who will have medical illness and disease in 1 or more of the costly medical conditions noted above.
It is imperative that the appropriate interventions needed by each Florida child who has an autism spectrum disorder be accessible, in the areas noted above, through mandatory health insurance coverage in the state of Florida. This is PARAMOUNT, so that long term outcomes will be improved. Our current private insurance accessibility/coverage make these crucial interventions impossible to receive. As a result, these sick children are either not receiving these services due to high costs, or; families are having to forego helpful but costly treatments for their child to try and avoid being cast into a state of financial ruin. Many times, families do end up in a state of bankruptcy due to their desperate attempts to try and pay for treatment for their child, in spite of the lack of insurance coverage.
We, the undersigned, are asking you to please support HB 1291 and/or SB 2654 to stop health insurance companies from discriminating against those who have been diagnosed with autism. This bill is a public-private solution that ends discrimination based on diagnosis. We also ask that you would support additional funding for covering these costs when small businesses have employees, the self-employed or those who have no insurance have family members who are autistic.
Autism spectrum disorders affect Florida families in unprecedented, epidemic proportion. For this growing segment of the population, there is a disproportionate and inverse relationship as it relates to the amount of health insurance coverage the parents, family members and caregivers have to effectively treat these children for sickness and medical impairments in the following areas: neurological (including seizures and motor impairments), behavioral, immunological, social skill deficits, sensory and gastrointestinal disorders, dental and eye care, occupational, speech/language and physical therapies.
Early diagnosis and intervention in these areas is critical to effectively treat the various medical aspects of autism. In many cases, families have no insurance coverage to treat any of these conditions and are in a state of financial devastation as a result of out of pocket expenses paid to treat their child who will have medical illness and disease in 1 or more of the costly medical conditions noted above.
It is imperative that the appropriate interventions needed by each Florida child who has an autism spectrum disorder be accessible, in the areas noted above, through health insurance coverage in the state of Florida. This is PARAMOUNT, so that long term outcomes will be improved. Our current private insurance accessibility/coverage makes these crucial interventions impossible to receive. As a result, these sick children are either not receiving these services due to high costs, or; families have to forego helpful but costly treatments for their child to try and avoid being cast into a state of financial ruin. Many times, families do end up in a state of bankruptcy due to their desperate attempts to try and pay for treatment for their child, in spite of the lack of insurance coverage.
Here are some key points to consider:
Thank you for taking the time to consider this very important issue that impacts thousands of families across the state of Florida.
My son Brian really needs your help with passing these bills through the House and the Senate. He has been receiving sporatic treatment and would benefit greately by getting consistent treatment. He has had Speech off and on, and could use Occupational Therapy and Physical Therapy and more speech therapy.
I have known many families, including friends and parents of students of mine, that have taken out excessive loans, refinanced their homes or have gone deeply into debt to pay for critical services that have the potential to be life changing for their child. I have also seen familie go without services for their child because they couldn't affort them. How heartbreaking for parents to be unable to meet their child's most basic and necessary needs at a critical time in their development and to always wonder "What if we could have done more, what if we had been able to pay for those services...".
My sister has to work two full time job leaving her very little time with her son.So we all have to pull some weight.
How has lack of funding or inaccessibility to insurance coverage of needed services for your autistic family member affected your family and loved one
A single mom. No child support or alimony. Credit cards maxed from Dr. bills and medicines and supplements not paid for by insurance. Injured my back while struggling to get my autistic son out of the van one morning to try to get him to go to school. Unable to work short term, no health insurance. Lost my home, my car, had to claim bankruptcy. Five years later, I have saved enough money to see the autism specialist we had been seeing five years ago that was making an impact on my son's digestive and behavioral issues. We were on the waiting list to make an appointment for 8 months, and had to wait two more until the appointment. It is next month. My son has been complaining daily of "stomach hurt, belly x-ray, need belly medicine" and two GI specialists on his current insurance have not been able to help him. "He is autistic, he will have a nervous stomach" or "try Mylanta" is not an answer to a child that is in pain and can't express how he feels. I will keep searching for help for him, in every dollar I save to be able to pay for it.
OT treatments are expensive! The school provides this service several times each week at their facility, but home treatments provide the comfort of knowing that my son is getting consistent, professional treatment for his disability.
My insurance only pays 15% of my son's therapist bill. All intellectual testing was not covered - we had to pay over $3,000 for all his testing.
IT HAS PUT MY SISTERS FAMILY IN FINANCIAL STRESS AND ALONG WITH THE STRESS OF HAVING AN AUTISTIC SON IT IS JUST OVERWHELMING. iT IS A DOUBLE PUNISHMENT FOR THESE FAMILIES.
We have spent thousands of dollars that insurance will not cover trying to help our Autistic child. Add this to the fact that one of us must stay home to care for our child. We just want our child better so that he too can function in life and reach his full potential, which we now know is possible with treatment. We are not alone. In our small town’s support group alone, there are 70 other children like ours- all with families struggling with the immense financial burden. Please help.
My sister has had to quit her job to stay home to take care of my niece. Fortunately she has health insurance, but unfortunately many therapies are not covered by insurance including ABA. Medical bills from diagnostic testing and lab work to multiple doctors including neurologists and developemental pediatricans, and the different therapies including speech, OT, physical, and now ABA are continuing to add up and will continue indefinately until we get our Amelia back.