This is a guest post by Shelley Hendrix, the Director of State Based Advocacy at Autism Speaks.
If you were planning to call Governor Brewer again today to ask her to veto SB 1593 – HOLD ON! THINGS ARE DIFFERENT TODAY! WE HAVE A NEW MESSAGE BECAUSE YOU DID IT AUTISM COMMUNITY! SHE GAVE SB 1593 A BIG VETO STAMP!
We are thrilled to report that late yesterday afternoon Governor Jan Brewer of Arizona officially vetoed SB 1593, a bill which if enacted would have effectively reversed the accomplishments achieved under Steven’s Law – Arizona’s autism insurance reform. The autism community in Arizona, and all across the country, laser focused their efforts contacting Governor Brewer – speaking with ONE loud united voice.
You can read a copy of her veto message here:
“My mother always taught me that when someone does something nice for you, you thank them. For something as important to our community as this, I hope that each and every one who participated in this campaign – whether you made a call or sent an email or whatever — will take the time now to thank her profusely. Thank her profusely and publicly – through your favorite social media outlet – and get your friends and family to thank her, too!
So, speaking of social media outlets, we are collecting messages for her on this blog below and on our Facebook pages for Autism Votes, Autism Speaks-Arizona and Autism Speaks-National. We want her to see, in public, how grateful we are that she listened to all of you. Please thank her by leaving a message for her below, then write a quick thank you note on one of our Facebook pages. If you would like to send her a more personal email thanking her and telling her how much this means to you and your family, you can visit our Arizona page on the Autism Votes website and take action there.
Her veto also sends a strong message to our community. For one thing, look what we can do when we focus our efforts. We are not weak and helpless. We can move mountains. We can change things. But we have to be diligent and persevere.
Winston Churchill once said, “Sure I am this day we are masters of our fate, that the task which has been set before us is not above our strength; that its pangs and toils are not beyond our endurance. As long as we have faith in our own cause and an unconquerable will to win, victory will not be denied us.”
What a smart man.
Sometimes in our community with all the battles we have to fight on a daily basis we just feel so incredibly helpless but no truer words were ever spoken. We are, in fact, masters of our own fate. The important word to me in this statement is “we,” not “I,” “we.”
WE are a team. WE are all in this community together. WE cannot sit here wringing our hands and whining. WE have to ACT! And when WE do, things change.
Look what changed as a result of your action everyone! Governor Brewer heard you loud and clear over the noise of our opposition. And believe me, they were giving it everything they had to get her to sign it.
The defeat of SB 1593 in Arizona is no small thing. So thank Governor Brewer, then pat yourselves on the back for a job well done.
It’s on the other side of a country three time zones away from you. You have never been there. You don’t know anyone who lives there. You have enough on your plate with your own family and your child’s needs.
Why should you care about what is happening in the state of Arizona?
Arizona became the fourth state to enact autism insurance reform legislation in the spring of 2008. In 2011, their legislature became the first state to pass a bill that would effectively reverse the progress made three years ago. That legislation now sits on Governor Brewer’s desk awaiting its fate – to become law or to get her veto stamp.
On its face, this new legislation appears harmless and expansive of our free enterprise, capitalist society. Let the interstate commerce trading of insurance policies begin under the premise of increased competition in the market to allow for reduced health care costs! But at what price? If SB 1593 is signed into law by Governor Jan Brewer, it will allow companies to shop outside the great state of Arizona – perhaps in states where autism insurance reform has not passed – potentially leaving families alone holding the bag once again for their exorbitant children’s health care costs which can quickly and easily be upwards of $75,000 each year.
Just watch the evening news any given week and you can see that Arizona politics these days are writhe with state’s rights and state pride. “Don’t tell us what to do. We are Arizona.” That said, how is it possible that Arizona legislators would then choose to hand over regulatory authority of healthcare coverage for their constituency to say…Rhode Island? If SB 1593 is signed into law, policies will be purchased across state lines, or even across the country. Citizens will have no recourse – subject to the whims of the other state’s legislature, regulation committees and judicial system. They will have no representation at all.
Last week, Autism Speaks launched an aggressive campaign asking Governor Brewer to veto the bill. Members of our Government Relations team met with her office. We purchased television air time for commercials. We sent eblasts to rally the Arizona community.
This week we are asking people all across America to pitch in with the heavy lifting. We need it.
There is a company generating robocalls to call for Governor Brewer’s signature into law. And their ever efficient robodialer is delivering calls to Governor Brewer’s office at a higher rate than our community – a community exhausted from fighting our fight at every turn.
Help us prove that our grassroots advocates are better than robots.
This is simply a domino that we cannot afford to let fall. A victory for the opposition would bolster resolve to introduce similar legislation in every state where reform initiatives have passed.
Who cares about Arizona politics? You should. Your insurance coverage, or your hope of obtaining it, is now in great jeopardy. As a community we must stand strong. We must come to Arizona’s aid. We must politely ask Governor Brewer to do the right thing – to veto SB 1593 and preserve the accomplishments of Steven’s Law.
Regardless of what state you live in, please call Governor Brewer’s office at 602.542.4331. Press #4 for a live person. Say “I am calling to ask Governor Brewer to veto SB 1593.” Tell your friends. Post it on your Facebook. Send it out through Twitter. Ask for accountability from your friends and family. Ask them to demonstrate publically that they have completed the mission by writing “DONE” below your post.
Nothing in life is ever easy. To preserve progress, we must be ever vigilant.
To learn more about what is happening in Arizona or to learn how you can become more involved in federal and state initiatives, please visit www.autismvotes.org and sign up today!
This is a guest post by Lorri Unumb, the Senior Policy Advisor and Counsel with Autism Speaks. She teaches a class called “Autism and the Law” at George Washington University Law School and, along with her husband Dan, is the author of a newly-published book by the same name.
Today, as I sit at my kitchen table reading news accounts of the 25th state autism insurance bill being signed into law by the governor of West Virginia, I get emotional. Six years ago this summer, I sat down at this same kitchen table to write my own bill. The mother of a then-4-year-old son with autism, I was frustrated that health insurance wouldn’t pay for the treatments my son’s doctor recommended. I was tired of reading EOBs that deemed my son’s treatment “experimental.” Or “educational.” Or “non-restorative.” And mostly, I was tired of sitting in support groups with parents who, without coverage from their insurance, could not provide treatment to their children at all.
I wrote a very simple bill – one page of common sense — that said not much more than “health insurance must cover what a doctor prescribes to treat autism.” As a lawyer and law professor at the time, I could not think of any reason why health insurance should not cover our children’s health condition.
I sent my one-page bill to a couple of legislators in South Carolina and asked them to file it in the fall of 2005. The insurers came out swinging against it, as did the Chamber of Commerce and the National Federation of Independent Businesses. But I had assembled a strong group of committed South Carolina families – the “Ryan’s Law Grassroots Gang” – who had compelling stories to tell and were willing to share them.
For two years we fought and negotiated and persevered. We contacted legislators one by one and asked for 15 minutes to explain our situation. We had no lobbyist, no money, and no organizational backing. Our opponents had multiple lobbyists, deep pockets, and their own parking spaces at the state capitol.
In the end, the legislators in South Carolina did the right thing. They passed our little autism insurance bill – twice. They passed it first in the usual course of proceedings and a second time – unanimously – on the last day of the session – June 7, 2007 — after the governor of South Carolina vetoed it.
The law became known as Ryan’s Law, after my son.
In the minutes after Ryan’s Law passed, I stood in the lobby of the state house exchanging hugs, kisses, and tears with families, legislators, and staffers who had become friends in this journey. When the hugging was done, my two best autism pals and I went to a Mexican restaurant, toasted each other with margaritas, and drove home. The celebration was over, and we went back to our real lives.
At the time, I had no idea that our effort in South Carolina would attract national attention and would lead to hundreds of emails from families who wanted to pass the same law in their states. In spite of the standing ovation from our House of Representatives at the moment of final passage, notwithstanding the legislators who shook my hand and thanked me for giving them the opportunity to support the “most important bill we’ve ever passed” – I had no appreciation for the significance of the occasion.
Ryan is now 10. In the years since Ryan’s Law passed, I have had the good fortune to help families across the country advocate for similar autism insurance bills. In 2008, I was invited to join Autism Speaks and, because of their tremendous support, have been able, along with the other dedicated members of the Government Relations team, to develop the expertise needed to take on opponents of autism insurance reform in almost every state across America.
Last year I flew approximately 150,000 miles as part of Autism Speaks’ effort to assist local autism advocates in their efforts. As I reflect on my travels and the 50+ times I have testified in support of autism insurance legislation, what stands out most are the phenomenal families who have stepped out of their comfort zones and engaged in the political process. What stands out are their stories:
- The mom who compared the journeys of her two young children – one who had cancer and could get the treatment his doctor recommended, and the other who had autism and could not.
- The dad who was forced into bankruptcy and lost his home because he wanted to provide his son needed therapy.
- The teenager with autism who had overcome his deficits enough to testify beautifully before a legislative committee and thank his parents for the sacrifices they made so that he could receive therapy.
- The parents who had two children with autism but had to choose which one would get therapy because, paying out-of-pocket, they could afford only one.
I cherish memories of the families who never believed their voice could make a difference but now have seen the law change because of their efforts. And I applaud the legislators who have championed our cause only because they knew it was the right thing to do.
At a time when many criticize our government and political system, I am encouraged by the success of our grassroots activism. To me, the autism insurance reform movement is a shining example of democracy at its finest.
Although we have now reached the halfway point, we have a long way to go. Indeed, we have more than “halfway” remaining, because, even in the 25 states that have passed autism insurance laws, many families are still not able to access coverage. Insurers put up roadblocks – roadblocks that will require significant enforcement efforts and legal action to overcome. Many families are insured by self-funded companies that are not subject to their state’s autism insurance laws. (We were one of those families by the way, and, as a result, Ryan was not covered by Ryan’s Law when it passed!)
Nevertheless, today I pause for a moment to celebrate with the many families I’ve been privileged to meet and with my Autism Speaks colleagues – both my 6 Government Relations colleagues and the many others who raise funds to make our work possible and raise awareness to make our work easier. As I reflect on 25 journeys in 25 states that now require insurance to cover diagnosis and treatment of autism, I am reminded of the line I wrote to the Ryan’s Law Grassroots Gang on the day the South Carolina bill became law: “Although I obviously wish my son Ryan were not struggling with autism, I am today very grateful and honored to be part of this autism community.”
TV AD Blitz Calling on Governor Brewer to Veto Misguided Arizona Legislation to Repeal Autism Insurance Law
Autism Speaks has announced a major, intensive two-day TV ad campaign, running April 19-20, that will call on Governor Jan Brewer to veto a misguided bill that would repeal enacted autism insurance reform legislation and force hundreds of Arizona families to once again pay tens of thousands of dollars a year out-of-pocket for critical autism diagnoses and treatments –– even though they already have health insurance coverage.
Vodpod videos no longer available.
“Neighbors,” will run nearly 200 times over two days on Phoenix’s network TV affiliate stations – KNXV-TV (ABC), KPHO-TV (CBS), KSAZ-TV (FOX) and KPNX-TV (NBC). The ads juxtapose two families who have a child with autism – one of whom is getting the treatments he needs because his parents’ insurance company covers his therapies, and another who isn’t because his insurer is not required to provide coverage. The ad calls on viewers to call Governor Brewer and urge her to veto the bill.
For more information, please visit Autism Votes