Nick

Nick

Sunday, April 6, 2008

Autism Yesterday Premier - Press Release

FOR IMMEDIATE RELEASE

Biomedical Intervention Group of OKC/Edmond

Contact Information - Bigofokc@yahoo.com

405-488-7609, 405-306-9184, 405-204-1713

IS AUTISM TREATABLE AND EVEN REVERSIBLE?

Join the Biomedical Intervention Group of Oklahoma City/Edmond and Aaron’s Bridge (www.aaronsbridge.org) for the world wide premiere of the documentary, “Autism Yesterday”. Oklahoma City will premiere this documentary along with over 100 other venues across the world simultaneously on Thursday, April 17th, 2008 at 7:00 p.m. The Oklahoma premiere will be shown at the Oklahoma City Metropolitan Library Downtown Location, 300 Park Avenue, Oklahoma City, 73102 (on the corner of Hudson and Park Avenue). The event will be in 46th Star Auditorium located on the 4th floor of the library. Admission is free and garage parking is available South of library at the cost of $3.00 for 2 hour parking.

The documentary was created by Generation Rescue (www.generationrescue.org) and follows the lives of five families on their journey to heal their children from a disorder that had been previously deemed a life long condition. In the film you will see the progress and recovery of the children using biomedical treatment as only families living through it can tell. A parent/doctor panel discussion will follow the film. The featured doctor will be Neurodevelopmental Pediatrician, Dr. D.L. Gheen of Edmond. The parent panel will consist of experienced parents who are successfully treating their children with biomedical treatments.

David Kirby, best selling author of ‘Evidence of Harm” reviews the film and writes, “In each story, we see clear before-and-after evidence of a child’s heartbreaking descent into the silent, baffling world of autism, and then their steady, sometimes miraculous progress back towards health, happiness, communication and, yes, recovery. The film, in elegant detail, shows us exactly how far these kids have come. A trailer may be viewed at http://www.autismyesterday.com/trailer.html.

The primary goal of this event is to present hope. Many families are not given hope and are told that “autism is not treatable”. Biomedical Intervention Group of OKC/Edmond and Aaron’s Bridge were founded by local parents that have witnessed their children become healthier with consistent biomedical treatment supervised by well-trained physicians. Their belief is based on new research that autism is a medical condition and that over time “autistic” symptoms can be reduced and sometimes alleviated with consistent biomedical treatment. Currently, Oklahoma has a shortage of physicians specializing in the biomedical treatment of this neurobiological disorder. The hope is that additional Oklahoma medical professionals will become specialized to treat more Oklahoma children with autism spectrum disorders. Currently, more children are diagnosed with autism than all types of childhood cancer, diabetes, and AIDS combined (Centers for Disease Control, 2007).

Rubicon School 2008 Annual Conference on Autism & PDD

The Rubicon School and Learning Center

2008 Annual Conference

on

Autism and Pervasive Developmental Disabilities

The University of Central Oklahoma

Nigh University Center

Edmond, Oklahoma

April 21, 2008 8:30 a.m. – 4:30 p.m.


Click Here for more information

A Letter to the Citizens of Oklahoma

Over the course of the last several months, I have received a lot of emails from people of Oklahoma and across the nation about Nick’s Law. Most of them have been good and complimentary of the efforts of Nick’s Law.

I have also received many from ordinary people who have hate, ugliness, and selfishness in their heart and soul. They simply don’t get it. They say how dare you call your special interest bill after a child, that’s just a cheap trick for sympathy. You have no right to increase my insurance. You are going to bankrupt my business. You are a socialist, a special interest wacko. You are the reason for your child’s condition. Take care of your child, we do not want to. Those are some of the comments. Today was no exception.

Instead of answering to those persons specifically, I want to honor and say thank you to the parents, grandparents of children and their efforts at the capitol, in the schools, and in your homes for advocating for their children. I want to share an article that I submitted to a couple of national publications back in February. This clearly shares the ideals, the concerns, the hopes, and prayers that so many of you have for your children. The article highlights the struggles that many families deal with on a daily basis, whether your child is diagnosed with autism or other disorder. Hopefully, our legislature is listening and will help us.

Thanks

Wayne Rohde

The Insurance Industry’s Folly of Autism Coverage.

For the last decade many parents and families have received the same message from their insurance companies when submitting for insurance coverage of autism related expenses and services. DENIED.

Why is that a business that is in business to insure for medical expenses, not provide coverage for a medical condition? Their excuse is that most treatments and therapies are “experimental or educational”. Yet, we have nearly 30 years worth of data, studies, and research (hardly experimental) that ABA behavioral therapy provides the necessary treatment to help reverse and recover many autistic children. We have living proof of what bio-medical interventions can do, just look at the pictures of many children before and after.

For many, we followed one government mandate (vaccinations), and we watched our children disappear right in front of us. Now as we are asking our government for a mandate to recover our children, we are being told DENIED.

The insurance lobby uses talking points like mandates will increase the cost of insurance and prevent people to obtain health care insurance. I would like to ask the insurance lobby one question about Nick’s Law, an autism insurance equity; PROVE IT! Show me the data or costs that would be associated with Nick’s Law and how it would prevent others from purchasing insurance. Remember, you have had 6 years to do this in Indiana and there is no data to show any accountable increase. Texas and South Carolina legislatures passed similar bills in 2007. Both had similar comments, “This is the most fiscally responsible thing to do for the taxpayers, and we are morally obligated to our future generations.”

The idea of trying to keep insurance policies affordable is a noble one. However, how we get there is a tale of two cities. The insurance lobby wants to stop or roll back existing mandates. The result in their eyes is that the costs will be lowered. Do you think if they roll back an existing covered disorder or condition, would they immediately lower our insurance? It’s an insult to the intelligence of the parents. What we know is that the policy holders will then have to depend on the state taxpayers for these services and treatments. Shifting health care costs from private insurance to taxpayers is what will happen.

The insurance lobby wants to provide a basic health care plan so more people will purchase policies. There are only two ways to lower the costs of insurance; lower the benefits or lower the reimbursements to the medical providers. We have all heard of the stories of families purchasing low cost insurance policies only to find out later, their child who was stricken with leukemia, the medical costs will not be covered.

Let’s explore an example of what the insurance companies and several legislators would consider a major accomplishment. A family of four, living in Oklahoma making $ 35,000.00 per year, struggles to make ends meet with rent, utilities, and food expenses. They can not afford to purchase health care insurance at an estimated cost of $ 600.00 per month. Legislators and the insurance lobby want us to think that if they can lower the cost of that insurance to $ 300.00 per month, then in their eyes, they have accomplished a very lofty goal. Not bad except for one over looked detail. The family of four still can not afford to purchase the insurance policy at $ 300.00. They will still be dependent on state run and paid for health care.

We hear a lot of rhetoric about the number of uninsured and mandates will lead to more uninsured. Today in Oklahoma, that number is around 708,000 people. Yet in our state, there has been no health care mandates passed since 1999. The uninsured number keeps increasing, but it is not from mandates. Our legislature and our Insurance Department should study the real reasons for this instead of talking about hypothetical’s that do not exist or spend time trying to determine what they want in an insurance policy.

In the Oklahoma Legislature, we hear a lot of talk about family values, defending the sanctity of marriage, and protecting the rights of children. To the legislators, you have no right to talk about family values when you support policies that destroy the family unit. You have no right to talk about marriage and preventing divorce when you unite with forces that are actually destroying marriage. You talk about protecting the rights of children, but yet you do not defend the right for the child to receive the medically necessary treatment to pursue and achieve the opportunity for a normal life. To many of the legislators at the capitol that will not provide us this remedy, then I ask you this: What is your solution for the devastation as a result of this epidemic. Please do not just tell us I am sorry, but I can not help you. We as voters and citizens demand to here your solution.

We all know that in today's world, no insurance means no care, and insurance companies should not be allowed to red line autistic children out of treatment. Nick’s Law aims to stop that.

Nick’s Law will provide greater access for all to health care. Many medical practitioners in the state have quit accepting Medicaid patients. There is such an acute shortage of providers. Yet in other states that have passed autism insurance coverage, there is a resurgence of practitioners that will provide the necessary services and will start to accept Medicaid once again.

State services are max’ed out. The waiting lists for state services are many years long. These children can not wait. Parents are literally racing against the clock to help recover their children that were taken away from them at such an early age.

To the citizens of Oklahoma and across this great nation who do not understand what the financial devastation of autism does to the family and ultimately to the children, you argue that our cause will only increase insurance costs, I have a question for you. Right now we are talking about insurance coverage for autism. Who will step up and defend you when in the future, you or one of your family members is diagnosed with disease or disability that is no longer covered? What happens when breast cancer is no longer covered? What happens when your son/daughter is diagnosed with leukemia only to find out that your insurance will only cover the first $50,000 of the $500,000 total bill?

In a recent story, HealthNet, a California insurance company lost an arbitrated decision and appeal for $ 9 million dollars to a lady who had her insurance policy canceled because she was diagnosed with breast cancer. In a prepared statement, the insurance company stated that they were trying to hold down costs in order to provide an affordable insurance. Now, HealthNet’s appeal has been answered. DENIED!

The insurance companies are leading us down a path of ignoring the people who can not speak for themselves, ignoring who provide care for the people who cannot, ignoring whose parents and families have exerted all of their energy and hope without any recourse or chance to recover, and whose lives that have been taken away.

Every so often, our legislature has the opportunity to do something, which is right and just to its very core. Now is the time and place to do so.

Wayne Rohde

Edmond, Oklahoma

Friday, April 4, 2008

California Democrats push bills to fight spread of autism

"West Wing" series actor Gary Cole speaks Wednesday at the Capitol about his daughter's autism. Cole said he was "thrilled" with the legislative package by Democratic lawmakers to deal with the nation's fastest growing developmental disability.

To read more, click here.

Update on Nick's Law in House Committee

Way to Go Parents!!!!

Rep Ron Peterson (Tulsa) Chair of the House Economic Development Committee deleted the language of Nick’s Law off SB 1895 prior to committee, yet he was forced to deal with the HUGE number of parents in attendance. His first item of business was to announce that Nick’s Law would not be heard in the committee hearing and ask that we were free to go. Many of the legislators and other guests expected us to leave. WE STAYED AND IT WAS NOTICED BY ALL!!!

One outside observer asked during the committee hearings why so many of the legislators where asking questions of the parents or just speaking to the parents in between breaks in the committee hearing. AND WE WERE NOT ON THE AGENDA!

We need to do three things by Monday .

STEP 1

Please contact the Republican House Leadership and ask that SB 2157 be heard next week (by April 10th) in House Economic Development Committee. Rep Peterson met with nearly twenty of us after the committee meeting and we got our chance to discuss with him why Nick’s Law and OUR CHILDREN need to be heard!! So very proud of all of you!! We now need to make sure that the House leadership knows that we are very serious. SB 2157 to be heard next week (by the 10th of April).

There will be a list of the contact information on the bottom of this email. It is time to get your friends and neighbors involved.

STEP 2.

Be careful what we wish for. We need to make sure that we have the votes in the committee. SB 2157 is not a compelling bill for members to vote on. It is about DHS attaching child support payments to Fire Fighter Pensions. The members will need to support Nick’s Law straight out. Rep Charlie Joyner will be the presenter during the hearing.

There are 10 republican members and 7 democrat members. We have been told by the dems in the committee and I have been told by the Dem Leader in the House that we have their vote. We need 9 votes minimum to pass. We should work to get 10. Please contact the republican members of the committee and ask for their support of Nick’s Law in the committee. Some have said that they will vote for Nick’s Law on the floor. That is a BIG DIFFERENCE. We need their support in a committee vote.

If we get the hearing, we better have the votes. If we do not have the votes, we will go another route. Bottom line in the committee, if the vote count goes against us, it is checkmate. “Final Action Rule”

STEP 3.

Contact the Democrats on the committee and thank them for their support of Nick’s Law. We were not on the agenda but they made us the main focus of the hearing by asking the question to the chair “ In my version of the bill, I see Nick’s Law as part of the bill. What happened?” They knew that Rep Peterson issued a committee substitute on the bill and deleted the language. Yet they wanted to make the point to the committee.

The name of the game is to survive and advance. Please contact the list below and make sure that the republican members are committed one way or another. It is a vote count. Please let us know when you heard from them. Anne Roberts and the steering committee will be visiting with Rep Joyner next week on the vote count prior to any committee action.

A few talking points for your discussion.

· Similar legislation was passed in Indiana in 2001. The Indiana Insurance Commission’s office has yet to report any increase in health insurance premiums due to this legislation. That is over 6 years worth of research and study.

· Arizona past similar legislation to Nick’s Law last week, joining a list of over 17 states. Louisiana, Mississippi, and Connecticut have introduced similar legislation in March.

· The Insurance Industry’s own policy group CAHI.org reports that autism insurance coverage will cost less than 1%.

· Nick’s Law is about autism insurance coverage. There is some discussion that covering additional mandates (60+) will increase costs. We are only talking about Nick’s Law.

· Oklahoma is one of the least mandated states in the nation.

Republican Leadership

Speaker of the House - Chris Benge chrisbenge@okhouse.gov (405) 557-7444

Speaker Pro Tem - Gus Blackwell gusblackwell@okhouse.gov (405) 557-7384

Chair of Economic Development Committee - Rep Ron Peterson ronpeterson@okhouse.gov (405) 557-7338

Republican Floor Leader - Rep Greg Piatt gregpiatt@okhouse.gov (405) 557-7326

Majority Whip - Rep Rob Johnson robjohnson@okhouse.gov (405) 557-7407

Co-Majority Whip - Rep Mike Jackson mikejackson@okhouse.gov (405) 557-7317

Committee Members

Rep. Ron Peterson - Chairman R ronpeterson@okhouse.gov (405) 557-7338 406

Rep. George Faught – Vice Chair R george.faught@okhouse.gov (405) 557-7310 338

Rep. John Auffett D johnauffet@okhouse.gov (405) 557-7394 325

Rep. Mike Brown D mikebrown@okhouse.gov (405) 557-7408 539-B

Rep. Ed Cannaday D ed.cannaday@okhouse.gov (405) 557-7375 322

Rep. Wallace Collins D wallace.collins@okhouse.gov (405) 557-7386 500-A

Rep. David Derby R david.derby@okhouse.gov (405) 557-7377 337

Rep. Jeff Hickman R jwhickman@okhouse.gov (405) 557-7339 440

Rep. Chuck Hoskin D chuck.hoskin@okhouse.gov (405) 557-7319 510-B

Rep. Fred Jordan R fred.jordan@okhouse.gov (405) 557-7331 300-B

Rep. Jerry McPeak D jerrymcpeak@okhouse.gov (405) 557-7302 501

Rep. Ron Peters R ronpeters@okhouse.gov (405) 557-7359 328

Rep. Greg Piatt R gregpiatt@okhouse.gov (405) 557-7326 442

Rep. Earl Sears R earl.sears@okhouse.gov (405) 557-7358 300-C

Rep. Mike Shelton D mikeshelton@okhouse.gov (405) 557-7367 539-B

Rep. Paul Wesslehoft R paulwesselhoft@okhouse.gov (405) 557-7343 329

Rep. Susan Winchester R susanwinchester@okhouse.gov (405) 557-7333 305-A

www.okhouse.gov/Members/MemberListing.aspx.

Last thing; You have walked with us this far, are you willing to go a little further?

Thank You