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‏إظهار الرسائل ذات التسميات Andy Scott. إظهار كافة الرسائل
‏إظهار الرسائل ذات التسميات Andy Scott. إظهار كافة الرسائل

Happy Canada Day, Eh!


Canada flag photo by Harold L Doherty, very happy to be a Canadian,  
living in Canada, despite the lack of progress on the national autism front  

Today is Canada Day and I am very happy to be a Canadian living here in Canada.   We can still enjoy living in one of the world's freest countries in the world.  I am happy and thankful that Canada is my home. I am thankful for our freedoms, our beautiful natural environment and our national health care system that generally takes  good care of all Canadians not just those who can afford the very best care. 

Not much positive though can be said on our national autism front, a point that was reinforced by the death this week of former Fredericton MP, national autism champion and all aground great guy Andy Scott.  Andy did succeed in getting autism on the national agenda with his private member's motion M-172 and tried to follow up to push the Harper government to action. Our Prime Minister and his submissive federal health bureaucracy though have done absolutely nothing to advance the cause of Canadians with autism, particularly those with severe autism disorders ... Canadians like my youngest son.   

Notwithstanding lack of autism progress nationally though events of the past year have brought home to me all too forcefully that I am very lucky to be living in this wonderful Canada. When I could not breathe while waiting in an after hours clinic I received immediate care, was sent by ambulance to the emergency clinic of the local hospital and received acute care attention for a week at minimal expense.  When Conor suffered grand mal seizures and an adverse drug reaction he received care for two weeks at the same hospital including 6 days in the intensive care unit where he received the medical attention that saved his life.

My family and I are fortunate to live in Canada even without national level autism effort. 

I will continue to fight on the national autism front with wonderful autism advocates like the members of Medicare for Autism Now! 

In the meantime I wish everyone a very happy Canada Day, eh!

Canada Loses an Autism Champion: Andy Scott Passed This Morning


Andy Scott With A Megaphone Supporting Autism Cause with Andrew Kavchak

Canada has lost an autism champion with the passing this morning of former Fredericton MP Andy Scott.  In a telephone conversation with a friend and fellow autism advocate elsewhere in Canada I once suggested the person contact their federal Member of Parliament.  I was informed that had already been done but there would be a wait before the MP could be seen.  There was some apparent disbelief when I mentioned that I could literally walk across the street to the office of our then MP Andy Scott and if he was in he  would probably see me or any other visitor.  

Andy met with representatives of the Autism Society NB on several occasions and actively pushed for a National Autism Strategy which he ultimately realized with the passage of Motion M-172.  The motion was essentially a commitment in principle with no obligations being undertaken by our federal government but it did help put autism on our national agenda and it was Andy Scott being Andy ... getting done what could get done ... with a view to moving forward further in future.  He continued to advocate for autism as demonstrated in his June 5, 2007 statement in House of Commons:

Autism 

[Table of Contents]

Hon. Andy Scott (Fredericton, Lib.):

Mr. Speaker, it is regrettable that we have seen little action by the government toward implementing a national autism strategy.

It has been more than a year since I introduced Motion No. 172. My private member's motion called for evidence based standards, innovative funding arrangements for diagnosis, treatment and research, and a national surveillance program.

The motion was adopted in good faith and supported by the government. However, it was very disappointing to see no reference to a national autism strategy in the recent budget or any discussion this spring.

Recently, I joined my colleagues from Charlottetown and Sackville—Eastern Shore and Senator Munson at a rally in Halifax that reinforced that there are families with autistic children across Canada who need the government's help.

The Conservatives should move off their default position of jurisdictional excuses, show creativity and compassion and start helping these Canadians.

On a previous blog commentary about Andy I had referenced the National Autism Strategy and quoted from Tali Folkins 2003 Telegraph Journal article:

"Fredericton MP Andy Scott said Saturday he has been lobbying prime- minister-to-be Paul Martin for a federal program to help young children with autism. "I desperately want a national autism strategy - and let me just assure you that Paul Martin knows it," Mr. Scott told supporters at a party celebrating his 10th anniversary as an MP in Fredericton Saturday evening.

Early work by therapists with young autistic children, Mr. Scott said, can make a big difference in their capacity to lead fulfilling lives as adults - and can save money in the long run. But the costs of starting such early intervention programs are high and should be borne directly by Ottawa rather than each individual province, he said. "We have responses and therapies and so on that I genuinely believe can work," he said. "You're going to save millions of dollars over the lifetime of an autistic adult. If you can get in at the front end, you can make enormous progress.

"But it's very expensive, and there's not a lot of stuff being added to Medicare, generally - that's why we have catastrophic drug problems and other things," he said. "In the province of New Brunswick, P.E.I., or even Quebec or Ontario it's very, very expensive. The feds are going to have to step up to the plate." "

Andy Scott fought on behalf of autistic persons in Canada.  He did not achieve all the goals he wanted by any means but he did what was possible in the time he had. Autistic Canadians have lost a champion today.  

Jaden Lake's Autism on the Hill Rally - Well Done Jaden!


Edmonton MP Mike Lake, whom I have met (at IMFAR 2012 in Toronto) and communicated with a few times about autism in Canada, have different perspectives on the proper role for Canada's national government in addressing Canada's autism crisis.  The government of Stephen Harper, of which Mike Lake is a member,  is not a strong supporter of Canada's national medicare system generally and has done nothing to advance in a meaningful way the National Autism Strategy advocated for by former and present opposition MP's Andy Scott,  Peter Stoffer, Shawn Murphy and Glenn Thibeault and by Senator Jim Munson.   I know though that Mike Lake is a dedicated father and a strong advocate for his 17 year old autistic son Jaden, who appears to have many similarities to my own son with autism of the same age.  I enjoy seeing Jaden in television and video appearances and was pleased to read the Ottawa Citizen article about the Autism on the Hill Rally and the pictures featuring Jaden Lake.

Thank you for advocating for autism awareness and services Jaden! Well Done!

Medicare's Orphans: Autism and Civil Rights Activist David Marley and The Fight For a National Autism Strategy



Medicare for Autism Now! has released episode 10 of our "Medicare's Orphans" web-series. This episode features Medicare for Autism Now, Civil Rights Now and co-producer of "Medicare's Orphans", David Marley. David is a former trial lawyer and long-time political activist. In this 25 minute interview, he discusses why it is crucial for Canadians, particularly parents and families of autistic children to become politically engaged.


As a parent I have advocated, together with other parents, for over a decade for a real National Autism  Strategy. Here in New Brunswick our advocacy involved working with former Fredericton MP Andy Scott over a decade ago for development of a National Autism Strategy which resulted in a strong commitment by Andy as reported by Tali Folkins in the Telegraph Journal on October 20, 2003:

"Fredericton MP Andy Scott said Saturday he has been lobbying prime- minister-to-be Paul Martin for a federal program to help young children with autism. "I desperately want a national autism strategy - and let me just assure you that Paul Martin knows it," Mr. Scott told supporters at a party celebrating his 10th anniversary as an MP in Fredericton Saturday evening.

Early work by therapists with young autistic children, Mr. Scott said, can make a big difference in their capacity to lead fulfilling lives as adults - and can save money in the long run. But the costs of starting such early intervention programs are high and should be borne directly by Ottawa rather than each individual province, he said. "We have responses and therapies and so on that I genuinely believe can work," he said. "You're going to save millions of dollars over the lifetime of an autistic adult. If you can get in at the front end, you can make enormous progress.

"But it's very expensive, and there's not a lot of stuff being added to Medicare, generally - that's why we have catastrophic drug problems and other things," he said. "In the province of New Brunswick, P.E.I., or even Quebec or Ontario it's very, very expensive. The feds are going to have to step up to the plate." "


As reported on Facing Autism several times Andy Scott, with NDP MP Peter Stoffer, and other MP's, was ultimately successful in getting a National Autism Strategy motion passed in the House of Commons. That effort was important in obtaining recognition of the need for a national autism strategy but it did not provide what parents of autistic children were fighting for from BC to Nova Scotia: a federal commitment to provide Medicare funding for ABA which to date remains the only evidence based effective intervention for autism.

The federal government has done nothing, absolutely nothing, to address the real needs of autistic children, school kids with autism or adults with autism needing assistance in the workplace or needing residential care. The federal government has done nothing to help those adults with severe autism who need 24/7 residential care and treatment. The federal government has stayed outside the battle content to hide behind constitutional jurisdiction line while ignoring the challenges faced by autistic Canadians and their families.

The fight for a real National Autism Strategy, one that includes medicare coverage for autism treatment has been long and difficult. I have met David Marley on several occasions, and very much appreciate having David with his his commitment and determination in our corner.  The fight for a real National Autism Strategy, a strategy built on inclusion of evidence based ABA treatment for children with autism disorders in our national Medicare has not been easy.  It is not easy now and will not be easy in the future.  We need everyone to pull together and fight.  

The current government, despite having within its ranks Alberta MP Mike Lake, father of an autistic son, is ideologically opposed to taking positive steps to ensuring that all children with autism, not just those living in Alberta, receive treatment under Medicare.

The Toronto Star reports that children in Ontario wait up to 4 years for therapy: The Autism Project: Children face up to four-year wait for therapy.  The significance of a 4 year wait is that children in Ontario are not receiving treatment during the critically important early years of 2-5.  In Ontario, early intervention for autism is largely non existent. The most effective treatment for autism is not generally available in Ontario.

Canada's 1 in 88 autistic children are, for the most part, doomed to move through the critical early years without the medical intervention they need.  The fight for medicare coverage for autism must continue and we need strong leadership, strong advocates.  David Marley has been answering the bell in this fight for many years.  Join David Marley and the Medicare for Autism Now! team, join the political fight to help Canadians with autism disorder receive the effective, evidence based autism treatment.  

Renewed Calls for a Real National Autism Strategy

Canada does not have a real national autism strategy but it is not for lack of trying by some dedicated federal politicians  including  Liberal  Senator Jim Munson and  NDP MPs Glenn Thibeault and Peter Stoffer who     have renewed calls for a real National Autism Strategy for Canada.

The struggle for a National Autism Strategy began many years ago including here in New Brunswick where Andy Scott issued a public call for a National Autism Strategy on October 18 2003:

""Fredericton MP Andy Scott said Saturday he has been lobbying prime- minister-to-be Paul Martin for a federal program to help young children with autism. "I desperately want a national autism strategy - and let me just assure you that Paul Martin knows it," Mr. Scott told supporters at a party celebrating his 10th anniversary as an MP in Fredericton Saturday evening.

Early work by therapists with young autistic children, Mr. Scott said, can make a big difference in their capacity to lead fulfilling lives as adults - and can save money in the long run. But the costs of starting such early intervention programs are high and should be borne directly by Ottawa rather than each individual province, he said. "We have responses and therapies and so on that I genuinely believe can work," he said. "You're going to save millions of dollars over the lifetime of an autistic adult. If you can get in at the front end, you can make enormous progress.

"But it's very expensive, and there's not a lot of stuff being added to Medicare, generally - that's why we have catastrophic drug problems and other things," he said. "In the province of New Brunswick, P.E.I., or even Quebec or Ontario it's very, very expensive. The feds are going to have to step up to the plate." "


Tali Folkins, Telegraph Journal, October 20, 2003

Mr. Scott was successful in getting a commitment by the federal government to a National Autism Strategy recognized in principle but the strategy at that time did not commit to the hard action necessary to provide assistance to all parts of Canada in providing early autism intervention programs.  Even the National Autism Symposium which came out of that commitment was a sham, pure and simple, a sham.  Public autism advocates, including me were excluded from the Symposium.  Those in attendance were all screened by federal health agency involved with organizing the event to ensure that they would go along with the government's do nothing to help autistic children agenda.

Senator Munson has been literally crossing the country for several years fighting for a real national autism strategy  and he has not given up on his efforts.  He organized and  spoke in Ottawa yesterday at an event to mark World Autism Awareness Day this Friday, April 2, 2010:

“There’s no reason why we cannot treat autism within our own communities equitably across the nation,” said event organizer Senator Jim Munson. “There is a crisis and I know that we can come up with a plan to deal with the issue that is so important to all of us.”



The event was also co-hosted by  NDP MP's Glenn Thibeault and Peter Stoffer who spoke at the event.  Mr. Thibeault also  introduced a private member's bill, seconded by tireless autism advocate Peter Stoffer,  to create a real national autism strategy, one that would actually help autistic children and their families by having the federal government work with the provinces:

"“Autism doesn’t discriminate based on geography.  It’s time for federal leadership to ensure that no matter where a child is born with autism, they receive equal treatment and services of the highest caliber.”


“I’m very pleased that my colleague has done this.  We’ve been asking for many years for the federal government to work with the provinces to develop a national autism strategy. I hope this will become a reality in the near future.”


Senator Munson and MP's Thibeault and Stoffer have been fighting for a National Autism Strategy for several years.  

As World Autism Awareness Day approaches this "autism dad" says thank you.

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A REAL National Autism Strategy Request for Mr Ignatieff and Mr Layton

Dear Honourable Leaders, MP's and Senator Munson

I am the father of a 13 year old boy with Autistic Disorder, assessed with profound developmental delays living in Fredericton, New Brunswick. I have addressed this email correspondence to Mr Ignatieff and Mr Layton as the leaders of the two parties, Liberal and NDP, that have recognized the need for a real National Autism Strategy. I have also copied some of the members of both parties in the House, and Senator Munson, who have made outstanding individual efforts on behalf of autistic children and adults in Canada and who have fought for a real National Autism Strategy.

The motion by Mr. Stoffer and our former Fredericton MP Andy Scott achieved recognition by the House of Commons of the need for a National Autism Strategy. Unfortunately the private members bill brought by Mr. Shawn Murphy from PEI which would have done so much to ensure that autistic children across Canada have real access to evidence based autism interventions was defeated notwithstanding the solid support demonstrated by both of your parties. I humbly ask that both the Liberal and NDP parties not give up on autistic children and adults and continue the fight for a real National Autism Strategy one that would see a federal government commitment to funding evidence based autism interventions and decent residential care for all Canadians with Autism Spectrum Disorders regardless of their province of residence.

Canadians have moved from province to province seeking appropriate help, particularly Applied Behavior Analysis (ABA), for their children. Gains have been made by provincial action across Canada but there are huge gaps in the services available. As a New Brunswicker I am proud of what our province has done with relatively limited resources to help autistic children but much more needs to be done here, particularly for autistic youths and adults in need of decent residential care. Even a family with two medical professionals left Nova Scotia to seek ABA help for their autistic child in Manitoba. In Ontario, where I visited in the spring of 2008 as part of a national autism advocacy tour organized by our good friends from FEAT BC, more autistic children are languishing on waiting lists than are actually receiving treatment.

I remind you of the well informed comments of Ms Dhalla when she spoke on behalf of the Liberal Party in the House of Commons, on October 27, 2006, in support of the Scott-Stoffer motion calling for a National Autism Strategy:

"We must make sure that regardless of where one lives in Canada, whether it is on the west coast, the east coast or in the Northwest Territories, all children who are affected by autism actually have the opportunity to receive the treatment they need throughout their lives until the age of 18.

I am sure this national strategy is going to ensure that we have the proper investment to do further research into whether there are other treatment options available and into how this type of condition can be prevented. We must invest in a comprehensive strategy to address this very complex disorder. (1420)

As I have mentioned, we know the cost is upwards of $70,000 per year, but we have to ensure we give the opportunity to these families so their children can obtain treatment and provide them with the quality of life they need. These families should be able to do this without having to mortgage their homes, or sell their cars, or go through those financial hardships. Many families that have been affected by autism simply cannot afford this treatment.?"

I ask that both the Liberal and NDP parties keep the need for a real National Autism Strategy in mind as you go forward and work toward a strategy which sees Canada invest in autistic children and adults regardless of their province or territory of residence. Canada is more than a place where one's health, one's quality of life depends entirely on jurisdictional boundaries. Our national health care scheme generally, which results in longer life expectancy and greater infant survival rates than that of our good neighbours to the south, is a testament to that fact.

Please do your best to ensure the enactment of a REAL National Autism Strategy for all autistic Canadians.

Respectfully,

Harold L Doherty
Fredericton, New Brunswick



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National Autism Strategy Fredericton Flashback October 18, 2003

The struggle for a REAL National Autism Strategy has been waged for many years across Canada.

In Fredericton, New Brunswick representatives of a group called FACE, the Family Autism Centre for Education, met shortly after being formed, with Fredericton area MP Andy Scott to begin discussions about autism and ask for his assistance in seeking a national approach to dealing with Canada's autism crisis. I had the honor of being one of those early representatives meeting with "Andy" as he has been known here in Fredericton.

On October 18, 2003, at a high profile event at the Fredericton Farmer's Market which included guest speaker and former Premier Frank McKenna, amongst others, Andy Scott dedicated himself to pushing then Prime Minister Martin to implement a federal autism program as set out in this excerpt from a Tali Folkins article in the NB Telegraph-Journal, October 20, 2003:

"Fredericton MP Andy Scott said Saturday he has been lobbying prime- minister-to-be Paul Martin for a federal program to help young children with autism. "I desperately want a national autism strategy - and let me just assure you that Paul Martin knows it," Mr. Scott told supporters at a party celebrating his 10th anniversary as an MP in Fredericton Saturday evening.


Early work by therapists with young autistic children, Mr. Scott said, can make a big difference in their capacity to lead fulfilling lives as adults - and can save money in the long run. But the costs of starting such early intervention programs are high and should be borne directly by Ottawa rather than each individual province, he said. "We have responses and therapies and so on that I genuinely believe can work," he said. "You're going to save millions of dollars over the lifetime of an autistic adult. If you can get in at the front end, you can make enormous progress.


"But it's very expensive, and there's not a lot of stuff being added to Medicare, generally - that's why we have catastrophic drug problems and other things," he said. "In the province of New Brunswick, P.E.I., or even Quebec or Ontario it's very, very expensive. The feds are going to have to step up to the plate." "


Andy was ultimately successful, with NDP MP Peter Stoffer, in getting a motion passed, during the current reign of Prime Minister Harper, which acknowledges the need for a national autism strategy but it does not begin to address the funding issues needed to ensure access to effective evidence based interventions such as ABA for autistic children regardless of where they live in Canada. Nor is anything in place to address the needs of Canada's rapidly growing autistic adult population, including the need for multi-level residential care facilities for the more severely affected by autism disorders.


The fight for a National Autism Strategy in Canada has been ongoing for several years. Here in New Brunswick it long pre-dates Andy Scott's 2003 announcement. At present we have a mediocre web site, a sham National Autism Symposium with parent activists excluded and national health bureaucrats that dole out research funding to researchers who do little or nothing to help advance our knowledge of environmental causes of autism or possible treatments. And there is not even mention of the need to flow funds to ensure that autistic persons across Canada who need decent residential care receive it regardless of which province they live in.

It has been, and will continue to be, a long struggle but we must not quit. We must keep fighting. We have to keep fighting for a REAL National Autism Strategy for autistic Canadians.




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Autism Society Canada Applauds Bill C-360 And Calls For A National Autism Strategy


Autism Society Canada hopes the introduction of Federal Autism legislation will pave the way for a National Autism Strategy in Canada


Ottawa - April 15th, 2009 – for immediate release - Autism Society Canada (ASC) applauds the introduction into the House of Commons of Bill C-360, An Act to amend the Canada Health Act (Autism Spectrum Disorder). In introducing the Bill, Sudbury M.P. Glenn Thibeault said: “Yesterday was World Autism Awareness Day. I still wear my awareness pin proudly. We as parliamentarians need to work together to provide individuals with ASD and their families with the right supports.”

Support for improving and augmenting services for persons with Autism is widespread. In separate letters acknowledging World Autism Awareness Day on April 2nd 2009, the Leaders of Canada’s federal Parties recognized the growing need to assist those affected by Autism Spectrum Disorder (ASD).

The summary of the Act states that: “The purpose of this enactment is to ensure that the cost of Applied Behavioural Analysis (ABA) and Intensive Behavioural Intervention (IBI) for autistic persons is covered by the health care insurance plan of every province.”

ASC encourages all within the Autism community to ask their Member of Parliament to support Bill C-360 which gives universal access to this scientifically validated and effective treatment. ASC also urges that work continue in order to provide other needed treatments and services in the best interests of all individuals with autism.

Christine Dade, President of Autism Society Canada, remarked: “Providing Applied Behaviourial Analysis and Intensive Behaviourial Intervention in a timely and effective way for all those who need it is definitely a step in the right direction. It isn’t everything that is needed, however, and ASC strongly urges Canadians and their leaders to work towards a National Autism Strategy as well.” A National Autism Strategy, as called for in former Fredericton M.P. Andy Scott’s Private Members Motion M-172 (passed in the House of Commons over two years ago), includes:
  • the development, in cooperation with provincial-territorial governments, of evidence based standards for the diagnosis and treatment of autism spectrum disorder;

  • the development, in cooperation with provincial governments, of innovative funding methods for the care of those with autism spectrum disorder;

  • consulting with provincial-territorial governments and other stakeholders on the requirements of implementing a national surveillance program for autism spectrum disorder;

  • the provision of additional federal funding for health research into autism spectrum disorder.

Autism Society Canada looks forward to working with all stakeholders and the Government of Canada to develop a National Autism Strategy. Much more needs to be done to address the glaring gaps in services and supports across the lifespan of the individual with autism. The inherent Rights of all Canadians living with an ASD should be enhanced, protected and enforced by appropriate legislation in each province and territory.

Autism Society Canada / La Société canadienne de l’autisme Box/C.P. 22017, 1670 chemin Heron Rd, Ottawa, ON K1V 0C2 Phone/Tél: (613) 789-8943

E-Mail: info@autismsocietycanada.ca

Website: http://www.autismsocietycanada.ca

FB: http://www.facebook.com/home.php#/group.php?gid=49558557641

Charitable registration number: 13160 7657 RR 0001





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Autism Action NOW! Contact Your MP to Support Bill C-360 An Act to amend the Canada Health Act (Autism Spectrum Disorder)

Contact your MP - TODAY - and urge him or her to support Bill c-360

An Act to amend the Canada Health Act (Autism Spectrum Disorder)

Canada, like the US and the UK, is experiencing a national autism crisis. In the UK the latest figures report that 1 in 60 children have, or will have, an autism spectrum diagnosis. In the US the figure is reported at 1 in 150. Both of these figures are shockingly higher than the 1 in 1000 figure that existed prior to the change in diagnostic criteria in the 1993-4 DSM revision period. Even since those revisions which do account for a significant increase the numbers have risen dramatically. It is long past time to stop pretending that we are not experiencing an autism epidemic.

Here in Canada it is long past time that we stopped pretending that we are not experiencing a national autism crisis with families relocating from province to province in search of funded effective ABA treatment for their children and ABA based education when they reach school age. This is not a partisan political issue. Both Liberal and Conservative governments have ignored the autism crisis in Canada. NOW is the time to do something about it. Andy Scott, Peter Stoffer, Shawn Murphy and Senator Jim Munson have been valiant advocates begging their political colleagues to take autism action. Now Glenn Thibeault, Sudbury NDP MP, has moved to introduce Bill C-360, an Act to amend the Canad Health Act (Autism Spectrum Disorder).

Canada's National Autism Crisis is a matter which ""goes beyond local or provincial concern or interests and must from its inherent nature be the concern of the Dominion as a whole" as the Privy Council said in upholding the POGG, Peace Order and Good Government, constitutional authority of the federal government to act to address national issues beyond the scope of the province's ability to address. The National Autism Crisis begs for a national solution. The Government of Canada has to stop ignoring this crisis.

Ask your MP to deal with Canada's National Autism Crisis and support Bill C-360. Your MP can be contacted via the link provided at this site:

http://webinfo.parl.gc.ca/MembersOfParliament/MainMPsCompleteList.aspx?TimePeriod=Current&Language=E

.......................................................................................................................................................................

40th PARLIAMENT, 2nd SESSION
EDITED HANSARD • NUMBER 040
Friday, April 3, 2009

Canada Health Act

Mr. Glenn Thibeault (Sudbury, NDP) moved for leave to introduce Bill C-360, An Act to amend the Canada Health Act (Autism Spectrum Disorder).

He said: Mr. Speaker, I would like to thank the seconder of this bill, the hon. member for Nickel Belt.

I am pleased today to introduce this private member's bill, an act to amend the Canada Health Act, and to look at how we can include autism spectrum disorder in it.

Yesterday was World Autism Awareness Day. I still wear my awareness pin proudly. We as parliamentarians need to work together to provide individuals with ASD and their families with the right supports. IBI training is a step in the right direction, but we need a national strategy.
I look forward to the day when all parties can stand together and show our support for individuals and families dealing with autism.

(Motions deemed adopted, bill read the first time and printed)


SUMMARY

The purpose of this enactment is to ensure that the cost of Applied Behavioural Analysis (ABA) and Intensive Behavioural Intervention (IBI) for autistic persons is covered by the health care insurance plan of every province.


BILL C-360
An Act to amend the Canada Health Act
(Autism Spectrum Disorder)


Her Majesty, by and with the advice and consent of the Senate and House of Commons of Canada, enacts as follows:

1. Section 2 of the Canada Health Act is renumbered as subsection 2(1) and is amended by adding the following:

(2) For the purposes of this Act, services that are medically necessary or required under this Act include Applied Behavioural Analysis (ABA) and Intensive Behavioural Intervention (IBI) for persons suffering from Autism Spectrum Disorder.


"Peace, Order and Good Government" (POGG)

In particular, the "national dimensions" (originally called "national concerns") doctrine was an alternate means of applying the POGG powers that found use in the mid 20th century. It allowed Parliament to legislate on matters that would normally fall to the provincial government when the issue became of such importance that it concerned the entire country.

The doctrine originated from a statement by Lord Watson in the Local Prohibition case, wherein he stated:

"Their Lordships do not doubt that some matters, in their origin local and provincial, might attain such dimensions as to affect the body politic of the Dominion, and to justify the Canadian Parliament in passing laws for their regulation or abolition in the interest of the Dominion".

After this case the doctrine was completely ignored until 1946 when Viscount Simons brought it back in the case of Ontario v. Canada Temperance Foundation, [1946] A.C. 193 (P.C.). The test as stated in Temperance Foundation was whether the matter "goes beyond local or provincial concern or interests and must from its inherent nature be the concern of the Dominion as a whole".

Find your M.P. at:

http://webinfo.parl.gc.ca/MembersOfParliament/MainMPsCompleteList.aspx?TimePeriod=Current&Language=E





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An Open Autism Challenge To MP Mike Lake, Canada's Official Autism Dad


Mike Lake
Conservative Member of Parliament
Edmonton-Mill Woods-Beaumont


March 3, 2009

Mike Lake
Conservative Member of Parliament
Edmonton-Mill Woods-Beaumont

Dear Mr. Lake

I am the father of a 13 year old boy diagnosed with Autistic Disorder, assessed with profound developmental delays. I have in all candor been disappointed, very disappointed, with the positions you have taken in support of your party's refusal as Canada's governing party to take serious steps to address Canada's national autism crisis. I have read your statements in particular on treatment and funding of autism treatment for autism in Canada. I know that you do not need to be convinced of the benefits of ABA (Applied Behavioral Analysis) for the treatment of autism disorders. There have been several serious, credible reviews of the hundreds of studies which have examined the evidence basis in support of the effectiveness in treating autism. Apart from the ideological positions of a very small minority of professionals and autism advocates there has for some time been an overwhelming consensus endorsing ABA as an autism intervention. Yet you, as an autism father, and Member of Parliament, a member of the governing party in Canada, have taken no steps to ensure that funding mechanisms are put in place in conjunction with the federal and provincial governments to ensure provision of ABA for autistic children regardless of where their parents happen to live in Canada. I challenge you, as a fellow autism dad, one that has actually fought with some success to ensure the provision of autism services, to take steps while your party forms the government to ensure that all Canadian children with autism in need of ABA services are able to obtain them regardless of what province their parents live in.

As an autism advocate I have advocated with other parents for many years to obtain ABA interventions here in New Brunswick yet my name, although put forth, was twice rejected as a participant in the national autism symposium, along with many other serious parent autism advocates for ABA services for autistic children in Canada. You participated as a keynote speaker at that staged symposium. Although the symposium was obviously designed to cast doubt on the consensus of professional and parent support for ABA as an autism intervention the effort was undermined by the release just days prior to that event of the American Academy of Pediatrics Report, November 1, 2007, Management of Children with Autism Spectrum Disorders which reviewed the professional literature and concluded much as the US Surgeon General, the New York State Department of Health, the MADSEC (Maine) Autism Task Force and the Association for Science in Autism Treatment that:

The effectiveness of ABA-based intervention in ASDs has been well documented through 5 decades of research by using single-subject methodology21,25,27,28 and in controlled studies of comprehensive early intensive behavioral intervention programs in university and community settings.29–40 Children who receive early intensive behavioral treatment have been shown to make substantial, sustained gains in IQ, language, academic performance, and adaptive behavior as well as some measures of social behavior, and their outcomes have been significantly better than those of children in control groups.31–4

American Academy of Pediatrics, Management of Children with Autism Spectrum Disorders

Your party has used you, as an autism father, to help quiet the voices of those who were seeking to amend the Canada Health Act to ensure that all autistic children would be able to receive ABA intervention in Canada. You faithfully quoted the party line that this could not be done for legal and constitutional reasons. Fine. Leave that argument aside.

You also voted on December 5, 2006, along with your party, in support of Andy Scott's private members' motion M-172, seconded by Peter Stoffer which called for the development of a National Autism Strategy on the following terms:

“(a) the development, in cooperation with provincial/territorial governments, of evidence based standards for the diagnosis and treatment of autism spectrum disorder; (b) the development, in cooperation with provincial governments, of innovative funding methods for the care of those with autism spectrum disorder; (c) consulting with provincial/territorial governments and other stakeholders on the requirements of implementing a national surveillance program for autism spectrum disorder; and (d) the provision of additional federal funding for health research into autism spectrum disorder.”

Your name was clearly recorded on the yea side right between MP's Kramp and Lapierre:

YEAS -- POUR
...

Khan
Komarnicki
Kramp (Prince Edward—Hastings)
Lake
Lapierre
Lauzon

While some money has been spent on research, with unknown objectives, no steps have been taken in 2 1/2 years to to develop, in cooperation with provincial and territorial governments, innovative funding methods for the care of those with autism spectrum disorder. In other words no steps have been taken to actually help autistic children and adults now living in Canada. Perhaps in 30 years the additional research dollars offered to Canadian researchers might play some role in offering some help to autistic persons not yet born. But here and now, in Canada nothing has been done by your government to help living autistic Canadians.

I know that you, as a Conservative MP from an Edmonton, Alberta riding have little to worry about politically. You could spend your time advocating for the protection of Bigfoot and other mythological creatures and still win landslide re-election for years to come. But I challenge you as an autism father who has actually advocated with some success for autism services for my son and other autistic children in New Brunswick, as one autism dad to another, to actually do something on behalf of Canada's autistic children and adults. You are a member of the governing Conservative Party. You have allowed your status as an autism parent to be used to support your government's refusal to act to include autism treatment in the Canada Health Act.

I ask simply that you use your standing in the party on autism issues to ensure that Prime Minister Harper and Health Minister Aglukkaq call a meeting of provincial health ministers to discuss funding of autism treatment and services for autistic children and adults living in Canada. This much you have already promised. This much you can do.

I challenge you as one "autism dad" to another, as one that has gotten some things done here in New Brunswick, to use your position in the governing party to actually do something for autistic Canadian children and adults.

Respectfully,


Harold L Doherty
Fredericton NB

cc. Facing Autism in New Brunswick





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Canada Still Awaits A National Autism Strategy

The following comment by Brian Rimpilainen, a friend and autism dad from Fredericton New Brunswick, was published in autism group networks and in the Telegraph-Journal. Brian is a dedicated autism advocate who has worked as a member of the Autism Society New Brunswick Board of Directors, the ASNB representative on the Autism Society Canada board and the Medicare for Autism organization. He has also been actively involved in direct citizen advocacy through local print media and internet media tools such as Facebook where Brian is the founder and administrator of the National Autism Strategy / ABA in Medicare NOW! group:


As 2008 comes to a close, I am reminded of former Fredericton MP Andy Scott's statement of June 5, 2007: "Mr. Speaker, it is regrettable that we have seen little action by the government toward implementing a national autism strategy ;


A year earlier Mr. Scott's private member's motion called for "evidence-based standards, innovative funding arrangements for diagnosis, treatment and research, and a national surveillance program."

I am the father of a son with Autism Spectrum Disorder (ASD). I watched hopefully as Liberal MP Shawn Murphy introduced a private member's bill, which would called for amendment of the Canada Health Act to provide coverage for autism treatments. The bill was defeated. The Liberals and the New Democrats both voted, by and large, in support of Bill C-304.

Autism is a serious neurological disorder that affects 1 in 150 Canadians. Persons with an ASD can display a wide range of intellectual, communication, behavioural and/or social deficits. While no known cure exists, a treatment that has been demonstrated in hundreds of studies to decrease the negative autism deficits, and in some cases virtually eliminate these deficits exists. Applied Behaviour Analysis (ABA) has been demonstrated to improve the abilities in all these areas and improve the quality of life of persons with autism.


Despite this, governments in Canada have an atrocious record in dealing with the autism crisis and in helping these vulnerable people.


I hope all MPs will carry the torch Mr. Scott has lit as we move into 2009.





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Harold Doherty's Autism Advocacy Awards


#1 Autism Advocacy Award - Conor's Smile, Joy and Happiness






















#2 Autism Advocacy Award - An ASNB Mug

Given To Me By Fellow Parents, Friends and Officers of the Autism Society of New Brunswick. The Mug was given to me a couple of years back and, like me, shows the wear and tear of time. The Hulk was a nickname given by former ASNB President Lila Barry, who has been a force for autism in New Brunswick. The picture is my "mug" superimposed on a target background.






#3 Loyal Order of the Flying Swine Award

I was one of the recipients of the Flying Swine Award handed out by Jean Lewis and David Marley. This award has been handed to few people but includes some very distinguished autism advocates including Jim Munson, Shawn Murphy, Andy Scott and peter Stoffer.

With these three awards I have been truly honored and will continue my autism advocacy efforts.




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October Is Autism Inaction Month In Canada

October is Autism Awareness Month in Canada. On the federal level though it would be more accurate to refer to October as Autism Inaction Month. Neither the Liberals, when they governed, nor the current Harper Conservative regime have taken any serious action to address Canada's Autism Crisis. With one in 150 Canadians and their family members affected by an autism spectrum disorder our federal government, despite its constitutional spending authority, does nothing of substance to provide evidence based treatment for autistic children.

The Harper government has established an autism web page. It also held a sham national "Autism Symposium" from which the voices of advocates for autism treatment for ALL autistic Canadians , regardless of province of residence, were excluded.

No real action is being taken. A federal election is now taking place. The NDP party leader Jack Layton reminds us all of the hard work for the autism cause of NDP MP Peter Stoffer, whose efforts are very much appreciated. But he makes no commitment to take action to address the autism crisis.

The Liberals have also had some strong autism advocates, Senator Jim Munson, and MP's Shawn Murphy and Andy Scott. Their efforts too are appreciated. But it is difficult to understand the Liberal party position on autism enunciated by Stephane Dion, He seems to be saying that, if elected, he might listen to the concerns of stakeholders and provinces. Whoop de doo.

In Canada, October is the month we should remind ourselves of all that our federal government is NOT doing to help persons with autism. And continue fighting on every level of government, including the federal level, to address Canada's autism crisis.

Ottawa's Unfinished Autism Business

Autism should not be a partisan issue.

Here in New Brunswick progress has been made under the former Conservative government of Bernard Lord and the current Liberal government of Shawn Graham. It is more difficult to say the same of the situation in Ottawa where the separatist Bloc Québécois and the Conservative government of Stephen Harper combined to defeat Charlottetown Liberal MP Shawn Murphy's Private Members Bill C-304 which would have provided a real National Autism Treatment Strategy to ensure adequate financing and ABA/IEBI treatment for Canada's autistic children whether they had the good fortune to reside in a province sitting on large oil reserves or not.

The rationale for defeating Bill C-304 offered by the Harper Conservative party - that health care is a matter within provincial legislative jurisdiction - ignores the reality that we already have federal health care legislation - the very Canada Health Act that Bill C-304 would have amended. If the Canada Health Act itself can exist, whether by some constitutional basis for federal health care competency; or by the cooperation, compassion and common sense of Canadians then so too can an amendment to that Act.

Even weaker is the argument, often advanced by the Harper government's offical autism dad, Mike Lake, that:

If this Bill were to pass, autism would be the one and only disorder or disease named in the Canada Health Act. Cancer is not named. Neither is diabetes or cardiovascular disease. Why autism and not these? Why not Down Syndrome? Why not Schizophrenia?

Under the Canada Health Act, the provinces are clearly responsible for decisions on which medical treatments they will fund. If we are to maintain the integrity of the Act, only the provinces can make those decisions.

To answer the first question the fact that autism would be the first to be named should be irrelevant. The need for a national effort to address Canada's autism crisis is clear. The Conservative government acknowledged that fact when it adopted Fredericton MP Andy Scott' s motion calling for a National Autism Strategy. While recognizing the need for such a strategy the Harper government has steadfastly refused to put any teeth in it. If the need for a National Strategy exists to address other disorders and diseases they can be looked at on case by case basis. There is no reason not to name autism now because other disorders and diseases may also have to be considered. Each can be examined on a case by case basis as required.

Provinces across Canada have begun financing, to the extent they are capable, the ABA that has been acknowledged, most recently (October 29, 2007) by the American Academy of Pediatrics, as the most evidence based effective treatment for autism:

The effectiveness of ABA-based intervention in ASDs has been well documented through 5 decades of research by using single-subject methodology21,25,27,28 and in controlled studies of comprehensive early intensive behavioral intervention programs in university and community settings.29–40 Children who receive early intensive behavioral treatment have been shown to make substantial, sustained gains in IQ, language, academic performance, and adaptive behavior as well as some measures of social behavior, and their outcomes have been significantly better than those of children in control groups.31–40

Even Mr Lake has acknowledged the effectiveness of ABA in treating autism; he just doesn't seem to understand that not all provinces have the finances to properly fund ABA for all autistic children:

In my opinion, it is completely unacceptable for any province not to fund Applied Behavioural Analysis (ABA) for those who need it. If voters feel as strongly as I do about this, they must let their provincial governments know and then hold them accountable at election time.

As for the integrity of the Act what is that? An Act is established to give effect to the will of the people through their elected representatives on a given matter. They can change the scheme, structure, or "integrity" of the Act if that reflects the will of the people at that time. If Canadians want to provide financing for ABA treatment for autism, and judging by the number of provinces that provide some level of ABA treatment funding they do, then the only challenge for those provinces not as well off, is to find the money to adequately fund the treatment.

The last I checked the federal government has no qualms about taking money, in the form of taxes, from the pockets of Canadian families wherever they live. They should have no qualms about spending some of that money to help provide effective ABA treatment for persons with autism.

Mike Lake's autistic son deserves the opportunity to access the ABA treatment funded by oil rich Alberta. So too does Joe Smith's son in PEI, Jacques LeBlanc's son in Quebec and Joe Kowalchuck's son in Saskatchewan. It is long past time that the Harper government ceased making a mockery of its commitment to a National Autism Strategy and amended the Canada Health Act as set out in Shawn Murphy's Bill C-304. There is no good reason not to.


C-304


First Session, Thirty-ninth Parliament,
55 Elizabeth II, 2006

HOUSE OF COMMONS OF CANADA

BILL C-304

_____________________________________________

FIRST READING, MAY 17, 2006
_____________________________________________

MR. MURPHY (Charlottetown)

1st Session, 39th Parliament,
55 Elizabeth II, 2006

HOUSE OF COMMONS OF CANADA

BILL C-304

An Act to provide for the development of a
national strategy for the treatment of
autism and to amend the Canada Health
Act

Her Majesty, by and with the advice and
consent of the Senate and House of Commons
of Canada, enacts as follows:

SHORT TITLE

1. This Act may be cited as the National
Strategy for the Treatment of Autism Act.


NATIONAL CONFERENCE

2. The Minister of Health shall, before
December 31, 2006, convene a conference of
all provincial and territorial ministers responsible
for health for the purpose of working
together to develop a national strategy for the
treatment of autism. The Minister shall, before
December 31, 2007, table a report in both
Houses of Parliament specifying a plan of action
developed in collaboration with the provincial
and territorial ministers for the purpose of
implementing that strategy.

AMENDMENTS TO THE CANADA
HEALTH ACT

3. Section 2 of the Canada Health Act is
renumbered as subsection 2(1) and is
amended by adding the following:

(2) For the purposes of this Act, services
that are medically necessary or required under
this Act include Applied Behavioural Analysis
(ABA) and Intensive Behavioural Intervention
(IBI) for persons suffering from Autism Spectrum
Disorder.

Another Autism Year Over and What Have We Done?

So this is Christmas
And what have you done?
Another year over
And a new one just begun


John Lennon, Happy Xmas (War Is Over)

A year can mean a lot in the lives of children with autism and other pervasive developmental disorders. On December 5 2006 the Canadian House of Commons passed a private members' motion, M-172, put forward by MP's Andy Scott and Peter Stoffer. Since then the government has done precious little to achieve the goals set out in the motion:
Motion M-172, as passed by the House of Commons on Tuesday, December 5, 2006.

That, in the opinion of the House, the government should create a national strategy for autism spectrum disorder that would include:

a) the development, in cooperation with provincial/territorial governments, of evidence based standards for the diagnosis and
treatment of autism spectrum disorder;

b) development, in cooperation with provincial governments, of innovative funding methods for the care of those with autism spectrum
disorder;

(c) consulting with provincial/territorial governments and other stakeholders on the requirements of implementing a national
surveillance program for autism spectrum disorders; and

(d) the provision of additional federal funding for health research
into autism spectrum disorder.

Since December 5 2006 little has been done to achieve the goals set out in M-172. Time was squandered on a secretive autism symposium that was NOT an exercise in community building.

The items requiring consultation and cooperation with provincial government, in particular the development of innovative funding methods for the care of those with autism spectrum disorder did not happen. Or at least it did not happen with any public participation or awareness.

Canada, under the government of Stephen Harper, another autism year over and not much has been done.

Canada's Autism Disgrace


What is Canada's National Autism Strategy? The answer is simple; we don't have one. And as long as Stephen Harper's Reform-Alliance-Conservative government rules Canada with an iron fist we will not have a National Autism Strategy. My friends of Conservative background in Canada may not like it but that is the hard brutal truth. Canada will not have a real National Autism Strategy as long as Stephen Harper is Prime Minister of Canada.

We certainly had the beginnings of a National Autism Strategy with the passing of the Andy Scott-Peter Stoffer motion in the House of Commons. And MP Shawn Murphy fought the good fight with his private member's initiative; defeated in the House of Commons by the alliance between the Harper Conservatives and the separatist Bloc Quebecois. Senator Jim Munson has continued his valiant efforts to keep the need to address Canada's national autism crisis alive in the media but even those efforts are becoming more challenging as the Harper-Clement team simply ignores these initiatives, ignores the needs of autistic children and adults in Canada, and proves day in and day out that they don't give a damn about the fate of autistic Canadians.

The National Autism Strategy of Prime Minister Harper really amounted to nothing but a mediocre web site and a promise of a National Autism Symposium. The National Autism Symposium was postponed when it became clear that real autism advocates, parents fighting for their autistic children, wanted to attend the symposium. A second symposium was scheduled for November 8 and 9 in Toronto. The invitation process was itself secretive, parents were largely unrepresented and any outspoken advocates were intentionally excluded from the Symposium.

The lists of speakers and symposium themes were never made public. The list of Harper government, hand picked delegates, to the symposium was never made public although it is a good bet that anti-ABA activists like Michelle Dawson and Laurent Mottron would have been invited. The Quirks and Quarks duo rarely miss an opportunity to promote their fringe anti-ABA views, contrary to hundreds of studies over 5 decades and numerous reviews of those studies by organizations such as the US Office of the Surgeon General and the American Academy of Pediatrics, that ABA is a scientifically supported, evidence based, effective treatment for autism. Their long held, closed minded views, so at odds with mainstream professional opinion, come in handy when needed by a government seeking excuses to camouflage their do nothing approach to addressing Canada's National Crisis. Just a guess, but I am betting that the Harper team was quite happy to invite Mottron and Dawson to the invisible, forgotten, National Autism Symposium.

The Autism Symposium went ahead on November 8 and 9 in Toronto and Canadians STILL don't know a thing about what was said; or what conclusions, if any, were reached. It is likely though that the Harper spin doctors will ultimately issue a summary indicating that there is lack of agreement on issues on the effectiveness of any one intervention in treating autism. The results of hundreds of studies over five decades of research, the reviews by the American Academy of Pediatrics, the Office of the US Surgeon General, the MADSEC Administrators, the New York and California state agencies, the Association for Science in Autism Treatment; all will be ignored.

The views of a few fringe anti-ABA activists will be used to prop up a cynical do nothing Harper autism policy. And Canada's National Autism Strategy will remain as nothing more than what it now is - Canada's Autism Disgrace.

Autism Dad Kavchak Asks Canadian Health Minister For REAL Autism Action

For several years Andrew Kavchak, parent of an autistic child/child with autism, has campaigned relentlessly for a National Autism Strategy. As the father of an autistic child Mr. Kavchak understands the need for a National effort to address Canada's autism crisis.

While movement appeared headed in that direction last year with the passage of the Andy Scott/Peter Stoffer private member's motion and the debate on Shawn Murphy's initiative, the momentum toward a National Autism Strategy has been stopped cold, as intended, by the neo-conservative ideology of the Harper government and Health Minister Tony Clement.

In his polite letter to Health Minister Clement Andrew Kavchak draws on the example of our American neighbors to try and kick start the Harper government's feeble National Autism Strategy.

Good luck Andrew. You will need it, or a change of government, to revive any prospect of a real National Autism Strategy in Canada.

......................................................

Hello Minister Clement,

Please see the information below from the US government about its latest initiative in dealing with the autism crisis.

Is there any chance that the Canadian federal government might take any similar action in recognizing the need for some federal leadership in developing a national autism strategy?

You may recall that exactly a year ago the House of Commons voted in favour of a motion that called for the creation of a National Autism Strategy. The proposed strategy had four components...three of which involved consultation and cooperation with the provinces. Under your watch, no consultation or cooperation has happened so far...at least, none that is known to the community. Perhaps the creation of such a "new interagency autism coordinating committee" could prove useful in turning the empty words of the motion into meaningful reality and provide some hope for the community?

Andrew Kavchak
Ottawa, ON
__

HHS Secretary Leavitt Announces Members of the New Interagency Autism Coordinating Committee

WASHINGTON, Nov. 27 /PRNewswire-USNewswire/ -- HHS Secretary Mike
Leavitt announced today the members appointed to the Department of Health
and Human Services' new Interagency Autism Coordinating Committee. This
committee coordinates efforts within the department to combat autism
spectrum disorder through research, screening, intervention, and education.
The committee will facilitate the efficient and effective exchange of
information on autism activities among member agencies, and coordinate
autism-related programs and initiatives.

"This important committee will play a key role in coordinating autism
research, services, and education related to autism spectrum disorder,"
Secretary Leavitt said. "I'm pleased that its members bring to the
committee a wide range and great depth of expertise, including research and
program administration, advocacy and personal experience with the
condition."

Authorized under the Combating Autism Act of 2006, the Interagency
Autism Coordinating Committee advises the HHS Secretary and the Director of
the National Institutes of Health (NIH). Secretary Leavitt delegated the
authority to establish the committee to the NIH, which designated its
National Institute of Mental Health (NIMH) to lead this activity.

The committee chair is Thomas R. Insel, M.D., director of NIMH.

"The committee's first priority will be to develop a strategic plan for
autism research that can guide public and private investments to make the
greatest difference for families struggling with autism," Dr. Insel said.

HHS is active in fostering research and making the results available to
aid people with autism.

Among the activities:

NIH funding and expertise support the Autism Centers of Excellence
program, which the agency launched after the Combating Autism Act was
passed, to seek the causes of autism and new treatments for the disorder.

The Centers for Disease Control and Prevention (CDC) supports a
multi-state collaborative study to help identify factors that put children
at risk for autism spectrum disorders (ASDs) and other developmental
disabilities. The five-year study, called SEED (Study to Explore Early
Development), is currently enrolling participants.

CDC has reported findings from the first and largest summary of autism
prevalence data from multiple U.S. communities. These findings, which found
autism spectrum disorders in approximately one in 150 children in these
communities, was reported by the Autism and Development Disabilities
Monitoring Network, which was designed to provide more consistent and
reliable estimates.

Federal members of the new panel:

Duane Alexander, M.D., is director of the National Institute of Child
Health and Human Development at NIH. The Institute supports research on all
stages of human development, from preconception to adulthood, to better
understand the health of children, adults, families, and communities.

James Battey, M.D., Ph.D., is director of the National Institute on
Deafness and Other Communications Disorders at NIH. The Institute supports
biomedical and behavioral research and research training in the normal and
disordered processes of hearing, balance, smell, taste, voice, speech, and
language.

Ellen Blackwell, M.S.W., is a health insurance specialist of the
Division of Community and Institutional Services, Disabled and Elderly
Health Programs Group, Center for Medicaid and State Operations, Centers
for Medicare and Medicaid Services where she serves as an expert on
policies that affect individuals with autism spectrum disorders.

Margaret Giannini, M.D., F.A.A.P., is director of the HHS Office on
Disability. Dr. Giannini serves as advisor to the Secretary on HHS
activities relating to disabilities. She is also a member of the Institute
of Medicine of the National Academy of Sciences and fellow of the American
Academy of Pediatrics.

Gail Houle, Ph.D., is associate division director of the
Research-to-Practice Division, Early Childhood Programs, Office of Special
Education Programs, Department of Education where she oversees programs for
children with disabilities and their families funded through the Individual
with Disabilities Education Act. Her expertise focuses on services for
children with autism spectrum disorders.

Larke Huang, Ph.D., is senior advisor on children and a licensed
clinical-community psychologist who provides leadership on federal national
policy pertaining to mental health and substance use issues for children,
adolescents and families for the Substance Abuse and Mental Health Services
Administration.

Thomas Insel, M.D., is director of the National Institute of Mental
Health at NIH. The Institute's mission is to reduce the burden of mental
illness and behavioral disorders through research on mind, brain, and
behavior.

Story Landis, Ph.D., is director of the National Institute of
Neurological Disorders and Stroke at NIH. The Institute's focus is directed
toward reducing the burden of neurological disease through research on the
normal and diseased nervous system.

Cindy Lawler, Ph.D., is scientific program director of the Cellular,
Organs, and Systems Pathobiology Branch, Division of Extramural Research
and Training, National Institute of Environmental Health Sciences at NIH.
The Branch plans, directs, and evaluates the Institute's grant program that
supports research and research training in environmental health.

Patricia Morrissey, Ph.D., is commissioner of the Administration on
Developmental Disabilities at the Administration for Children and Families,
which seeks to improve services to and assure that individuals with
developmental disabilities have opportunities to make their own choices,
contribute to society, have supports to live independently, and are free of
abuse, neglect, financial and sexual exploitation, and violations of their
legal and human rights.

Edwin Trevathan, M.D., M.P.H., is director of the National Center on
Birth Defects and Developmental Disabilities (NCBDDD) at CDC. NCBDDD is
focused on identifying the causes of and preventing birth defects and
developmental disabilities, helping children to develop and reach their
full potential, and promoting health and well-being among people of all
ages with disabilities. Dr. Trevathan is representing Julie Gerberding,
M.D., M.P.H., director of the CDC, on the committee.

Peter van Dyck, M.D., M.P.H., is associate administrator of Maternal
and Child Health at the Health Resources and Services Administration
(HRSA). Dr. van Dyck oversees HRSA's Maternal and Child Health Bureau,
which seeks to improve the health of mothers, children, and families,
particularly those who are poor or lack access to care.

Elias Zerhouni, M.D., is director of the National Institutes of Health.
A world renowned leader in the field of radiology and medicine, Dr.
Zerhouni has spent his career providing clinical, scientific, and
administrative leadership. He leads the nation's medical research agency
and oversees the NIH's 27 Institutes and Centers with more than 18,000
employees.

Non-federal members:

Lee Grossman is president and CEO of Autism Society of America (ASA)
and the parent of a young adult son with autism. Mr. Grossman is also the
chair of the ASA Foundation and a member of the ASA Environmental Health
Advisory Board.

Yvette Janvier, M.D., is the medical director for Children's
Specialized Hospital in New Jersey. Dr. Janvier is also a clinical
assistant professor in the Department of Pediatrics, Robert Wood Johnson
Medical School. Her specialties are autism and developmental and behavioral
pediatrics. Dr. Janvier is a fellow of the American Academy of Pediatrics.

Christine McKee, J.D., has developed and manages an in-home therapy for
her autistic child, creating and/or assembling all of the therapy related
materials. Ms. McKee participates in monthly consultations with a Board
Certified Behavior Analyst/Speech Pathologist. She applies the therapeutic
measures in her daily parenting and childcare routines.

Lyn Redwood, RN, MSN, is co-founder and president of the Coalition for
Safe Minds. Ms. Redwood is also on the board of the National Autism
Association. She became involved in autism research when her son was
diagnosed with pervasive development disorder in 1999. She is a nurse
practitioner with 25 years of experience.

Stephen Shore, Ed.D., is executive director of Autism Spectrum Disorder
Consulting. Drawing on his experiences as an individual with an autism
spectrum disorders diagnosis, Dr. Shore presents and consults
internationally on adult issues pertinent to education, relationships,
employment, advocacy, and disclosure. He also serves on the board of the
Autism Society of America, as board president of the Asperger's Association
of New England, and is on the board of directors for Unlocking Autism, the
Autism Services Association of Massachusetts, MAAP Services, The College
Internship Program, and the KEEN Foundation.

Alison Tepper Singer, MBA, is executive vice president of Autism Speaks
and is a member of the board of directors. Prior to joining Autism Speaks,
Ms. Singer spent 14 years at CNBC and NBC where she served in several
positions. She has both a daughter and an older brother with autism, giving
her long-term, personal experience with the disorder.

The following Web page provides links to additional information on the
Interagency Autism Coordinating Committee, including information about
upcoming meetings and highlights from meetings of the prior committee:
http://www.nimh.nih.gov/research-funding/scientific-meetings/recurring-meet
ings/iacc/index.shtml

NIMH's mission is to reduce the burden of mental and behavioral
disorders through research on mind, brain, and behavior. More information
is available at the NIMH Web site, http://www.nimh.nih.gov.

NIH -- The Nation's Medical Research Agency -- includes 27 Institutes
and Centers and is a component of the U.S. Department of Health and Human
Services. It is the primary federal agency for conducting and supporting
basic, clinical and translational medical research, and it investigates the
causes, treatments, and cures for both common and rare diseases. For more
information about NIH and its programs, visit http://www.nih.gov.

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