There are few aspects of parenthood that are as visceral as the need to protect our children. So it’s no surprise that when there’s a scraped knee, bully, or fire-breathing dragon threatening our children, we are on the front lines with artillery ready to comfort, then fire.What IS a surprise is that insurance companies all across the country continue to discriminate against individuals with autism by denying medically necessary, evidence based treatment that is prescribed by a doctor. Now, we as parents are forced to deal with the biggest bully of them all. It’s unfortunate, but true, that this large, powerful industry and lobbying group can withhold something so vital to our children’s health and future. And it’s up to us to change public policy for our country’s children and for future generations.
I'll never forget the wave of sick that swept over me when I realized appropriate life-saving treatment for our son could cost up to $50,000 per year. We risked bankruptcy, became deeply in debt, and suffered immeasurable stress so we could implement treatment prescribed by our son's physician. 72 children are diagnosed with autism each day. Families are placed in this agonizing situation, most of whom will never be able to afford a proper diagnosis let alone treatment no matter what they sacrifice. So what results? Divorce. Bankruptcy. Job loss. And a child who never has the opportunity to progress or even recover from autism.
Justice.
Please join me by calling and emailing Speaker Pelosi (202) 225-0100 and Majority Leader Reid (202) 224-3542. All you need to say is this, "Health reform that does not stop autism insurance discrimination is unacceptable." It only takes a couple clicks to make an impact. Take action HERE!
Together, we can save the futures of countless children with autism all across the country.
For those of you who followed me through Clay's Law, this is federal legislation (vs state) that will be much more comprehensive, helping families all across the nation.
