[FEAT BC Admin]

In this topic area, discussion is about the fight to secure Government funding for your A.B.A. treatment program. It is also the place to talk about your thoughts and ideas about how to establish new Government programs specifically designed for autism treatment.

This is the place to hear input from parents who have fought for funding and won, as well as those who have fought for funding and would like to share their horror stories. There is a tendency to not share success stories once funding is secured. Please fight that tendency. By sharing our experience, we all become stronger.

 

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—-By FEAT BC (Freeman) on Saturday, January 3, 1998 – 03:16 pm:

-Hi everyone!

These are some things to think about in your dealings with government to help you to obtain support for your child’s Autism Treatment Program. These are my personal opinions and do not represent those of FEAT of BC or any other organization.

Many of these observations are based on my personal experiences (and I believe it poetic justice to help every parent avoid being systematically abused by their social worker the way I was).

Good luck to everyone! (Let’s all pull back the curtain on the Wizard of OZ).

Sabrina

 

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How To Fight for Funding for Autism Treatment and Appropriate School Placement

1. Establish a Paper Trail

Always take notes, documenting major points of all conversations with government and school officials.

This includes casual, in person conversations with social workers as well as ALL telephone conversations. All key points of discussion must be written down in your notes including the date and time of the discussion. This includes what was agreed upon, as well as what was not agreed upon.

Then the notes should be used to write a letter recapping the substance and content of the conversation. This letter must then be mailed or faxed to the person with whom you had the conversation. In addition, a copy must be kept in your file (see section on the icci game).

Why?

It is important to formalize the interaction between you and Government officials. In addition, everyone is put on notice that they must closely adhere to their responsibilities, regulations and laws., Furthermore, they must then consider the paper trail you have created. This lets everyone know that the interaction can become public and that any abuses of power and authority can be formally appealed and/or publicized.

In other words, they canit use discretion unfairly under the cloak of secrecy.

2. Submit all Requests in Writing

All your requests for your child must be submitted formally in writing with a copy included in your file and a copy, if necessary, sent to their immediate superiors.

3. Set Deadlines for Action

All formal requests for action must have a reasonable deadline set for that action. If no action or response is received by the deadline you have set (two weeks for example), then you will interpret the lack of response as a formal declination (a formal NO) of your requests.

Why Set Deadlines?

When bureaucrats do not want to do something, they will stall by ignoring you and your request. (As an aside, in the study of the bureaucracy, this is known as ithe power to do nothingi). They can string you along for years. When you have determined that the person you are interacting with is not inclined to help you or is not dealing in good faith, then you must take the initiative and formally label his/her behavior as obstructionist and de facto as a declination (a NO to your requests). This allows you to move to the next level of authority on your timetable to present your case. This takes the power to do nothing away from the bureaucrat with whom you are dealing. Simple stated, a bureaucrat who stalls and does nothing becomes irrelevant (use your invisible spray) and you move on to the next level of authority.

How to icci?

A cc. is a copy of your letter sent to someone other than the person you are writing. You put the cc. at the bottom left-hand corner of your letter followed by 2 spaces and the name of the person or people to whom you want to send a copy of the letter.

Who to icci to?

Sometimes it is best not to icci at all, especially in the early stages of the relationship (for example, your first letter to a social worker requesting assistance). This gives them the opportunity to do the right thing and does not present you as an overly combative person. When you start to run into problems, it is a good idea to send the icci to the 2 immediate superiors of the person you are having problems with. We do not recommend icciing all the way up the chain of command, since you want to give them a chance to solve the problem at the local level.

Why send a icci copy?

The reason for playing the icci game is that you want your interactions with the official to be known to his superior and possibly to other organizations so that 1) their action or inaction becomes a matter of record and 2) the individual knows he is being monitored. This helps minimize abuses of power and authority and helps encourage the official to meet their obligations and do the right thing.

What is the sequence of letters?

Find out the chain of command of the particular bureaucracy you are battling.

TOP

Minister
Deputy Minister
Children’s Ministry’s local region chain of command, all the way down to the District Supervisor
and Social Worker
Contacts can be found at the government directory: http://www.dir.gov.bc.ca/

BOTTOM

Start at the bottom and climb. At the Regional Operating Officer (ROO) level (once you have been declined) you have to decide whether to jump up to the top, threaten and then go to the media, or both. A word of wisdom: DO NOT BLUFF. If you are not willing to go all the way, they will ‘smell’ this. You must be prepared to take it right up to the Minister and beyond.

Documentation from Experts:

In your arsenal to fight for your child, it is wise to get his/her pediatrician and/or psychiatrist to write a letter on your childis behalf. In addition, any other experts who know your child and are sympathetic to what you are trying to do should become involved.

When to hire a lawyer?

If money is not an issue, you can hire a lawyer when you get to the area manager level. Make sure that you have a paper trail so the lawyer has something to work with. Also, have the lawyer give F.E.A.T. of B.C. a call, and we will send him/her information that will help.

If money is an issue (as it is for most of us running autism treatment programs), you might want to hire a lawyer once you have been turned down by the Minister.

How to hire a lawyer?

The type of lawyer needed is a litigator, or trial lawyer. S/he does not need to be an expert in autism, or special needs; s/he needs to be experienced in suing governments, and enjoys being in court. Word of mouth is a good way to find a lawyer.

Topic

[Andrew Kavchak]

Hi Folks,

Looks like autism came up a couple of times in the House yesterday in the context of an Opposition motion on healthcare…Are they arguing over who did the least for autism? (The passage below is edited…full text available from http://www.parl.gc.ca)

___________________
HOUSE OF COMMONS
EDITED HANSARD
Tuesday, November 28, 2006

Business of Supply

Opposition Motion–Health Care

Ms. Ruby Dhalla (Brampton—Springdale, Lib.)
moved:

That, in the opinion of the House, the Conservative government has broken its promise to reduce medical wait times
…………

Mr. Blair Wilson (West Vancouver—Sunshine Coast—Sea to Sky Country, Lib.):

Mr. Speaker, I listened intently to the hon. member's speech. I have three points to bring up. One deals with the much talked about broken promises of the Conservative government, not only the broken promises on income trusts, but the broken promises on the patient wait time guarantees and the broken promises on dealing with a national strategy for autism.

Obviously health care is an important issue in Quebec, as it is in my riding of West Vancouver–Sunshine Coast–Sea to Sky Country and the province of British Columbia. Could the member tell me how Quebec is going to deal with this string of Conservative broken promises, the most important of which, I believe, is the broken promise to deal with health care on a national basis and to deal with health care and the wait time guarantees?

I have been in a number of meetings with the province of British Columbia and the premier of B.C. to deal with health care issues in B.C. We are having a conversation right now with British Columbians to get to the root of the problem. The question I have for the hon. member is this: what specifically is Quebec going to do to deal with this broken promise of the Conservatives on their wait time guarantee?
………………

Ms. Penny Priddy (Surrey North, NDP):

Mr. Speaker, the New Democratic Party has, since its inception, and the CCF before that, put health care first. It is not a partisan issue. It does not come up from time to time. It does not come up only during elections, before elections or as some crisis hits the health care system. It is a part of the founding of this political party. I believe I am speaking to this motion without attempting to make health or wait times a partisan issue.

…..

The government has not taken up its role on national strategies, although I see the national cancer strategy was announced. I am waiting for the national strategy on autism. If we can do it on cancer, we can do it on autism. As I said, the government has not taken up the national leadership role regarding accountability.

………..

Mr. Blair Wilson (West Vancouver—Sunshine Coast—Sea to Sky Country, Lib.):

Mr. Speaker, I listened intently to the hon. member's speech. I have three points to bring up. One deals with the much talked about broken promises of the Conservative government, not only the broken promises on income trusts, but the broken promises on the patient wait time guarantees and the broken promises on dealing with a national strategy for autism.

Obviously health care is an important issue in Quebec, as it is in my riding of West Vancouver–Sunshine Coast–Sea to Sky Country and the province of British Columbia. Could the member tell me how Quebec is going to deal with this string of Conservative broken promises, the most important of which, I believe, is the broken promise to deal with health care on a national basis and to deal with health care and the wait time guarantees?

I have been in a number of meetings with the province of British Columbia and the premier of B.C. to deal with health care issues in B.C. We are having a conversation right now with British Columbians to get to the root of the problem. The question I have for the hon. member is this: what specifically is Quebec going to do to deal with this broken promise of the Conservatives on their wait time guarantee?
…………………………….

Mr. Michael Savage (Dartmouth—Cole Harbour, Lib.):

Mr. Speaker, I welcome the opportunity to speak to the motion on the issue of the health care wait times and to the record of the government in this regard.

………

However, it is a privilege that not all Canadians can actually share. We had great nurses and respite workers, but in my own province of Nova Scotia I know of a family with two children with autism. The parents were getting two hours a week respite. That was cut off because their income had gone over the level that they were allowed, and that was only because they saved every penny they had for when those kids were there and they were not.

The system is not working. It brings up a system of two tier health care, not only public-private but among provinces, rich provinces and poor provinces. I believe the federal government has a responsibility to act in that area. We need to do more there as well.

I believe that federally we need to take responsibility. A lot of these are provincial areas of direct responsibility, but the federal government has a role to ensure, as much as possible, equal access across Canada.

I do want to commend the government for the commitment to the Canadian strategy for cancer control. This is our initiative that came out of the cancer community from people who were working in cancer, people in Nova Scotia like Dr. Andrew Padmos, who has now left Cancer Care Nova Scotia, Theresa Marie Underhill, and researchers like Gerry Johnson.

Many people have come together to say that we can actually make a difference in cancer. We need to take it a little bit out, at arm's length of government, and work with research agencies, do better surveillance and identify what research we need. I was proud last year in this House to vote for the implementation of the Canadian strategy for cancer control. I commend the government for following through on that last week.
………………….

Mr. Ed Fast (Abbotsford, CPC):

Mr. Speaker, I listened carefully to my friend's comments. Of course he was critical of the progress, or lack thereof, on wait times guarantees. However, I think the member will agree, given the fact that our government has only been in power for some 10 months, that it is somewhat ambitious for him to suggest that by now we should have solved all of Canada's health problems.

In fact, first I would remind him that we recently have implemented a pilot project to implement wait times for first nations. Then I want to remind him of his own party's record. In fact, over 13 years of Liberal government rule in this country, we saw $25 billion in cutbacks in transfers to provincial governments. Wait times doubled during those 13 years.
I have a question for the member. How is it that his government was unable to achieve wait times guarantees, unable to fund a national cancer strategy and unable to address autism in Canada during those 13 years, yet he expects our government to have solved all of the problems his government created in 13 years?

………………….
Mr. Steven Fletcher (Parliamentary Secretary to the Minister of Health, CPC):

Mr. Speaker, I realize the hon. member objects to national programs and initiatives such as our strategy to fight pandemics. That is known, even though most people agree that pandemics do not respect boundaries. I think the same logic goes to why the Bloc objects to the national cancer strategy, an autism strategy and other things that will benefit all Canadians, including Quebeckers.

Would the member agree that under the previous Liberal government, wait times doubled and $25 billion was cut from health care? Would she agree that the reason the Supreme Court said what it did in the Chaoulli decision was because of the lack of leadership and poor management of federal dollars by the previous government?
………………

[Andrew Kavchak]

Hi Folks,

It looks like December 5 is going to be a big autism day in the House of Commons. We expect a vote on M-172 and an intial first reading on Bill C-304 on the same day.

It will be absolutely critical for our community across the country to flood MPs with messages asking them to support and vote in favour of Bill C-304 because if passed, it will be LAW and BINDING! (See article below!)
____________________

MP says new autism initiatives don't meet families' expectations; Shawn Murphy introduces private member's bill calling for national strategy, funding for behavioural programs

The Guardian(Charlottetown)
Nov 29, 2006
Page: A8

New initiatives on autism announced recently in Ottawa don't meet the expectations of families of people with autism, says Charlottetown MP Shawn Murphy.

Murphy spoke at a Parliament Hill rally for the families of children with autism, organized by Families for Early Autism Treatment, an organization that is calling on the federal government to develop a National Autism Strategy.

The organization also seeks to increase the access autistic persons have to medically necessary services.

The rally and Murphy's comments came a day after Health Canada unveiled a number of new initiatives on autism.

"Aimed at limited research initiatives and early detection measures, the announcement fell short of providing increased services to those affected by autism, and I strongly believe this is what is needed," Murphy said.

Research shows that children with Autism Spectrum Disorder, which affects two in every 1,000 Canadian children, can grow up to function independently in society when they receive Applied Behavioural Analysis (ABA) and Intensive Behavioural Intervention (IBI) from an early age through to adulthood.

Provincial health insurance programs differ widely in the level of coverage they provide for ABA and IBI.

Murphy has introduced a private member's bill in the House of Commons that calls on the government to produce a National Autism Strategy by the end of next year and to amend that Canada Health Act to ensure that the cost of ABA and IBI is covered by the health-care insurance plan of every province or territory.

It is set to be debated at first reading stage on Dec. 5.

[Andrew Kavchak]

Hi Folks,
It appears that the wording of M-172 has changed as a result of a Tory amendment. From the first version below to the second…
Andrew Kavchak
Ottawa
_______________
Original motion table by Andy Scott:
Motion no. 172

M-172 That, in the opinion of the House, the government should create a national strategy for autism spectrum disorder that would include:

(a) the establishment, in cooperation with provincial governments, of national standards for the treatment of autism spectrum disorder and the delivery of related services;

(b) the study, in cooperation with provincial governments, of the funding arrangements for the care of those with autism spectrum disorder, including the possibility of transferring federal funds to assist provincial governments to provide no-cost treatment, education, professional training and other required supports for Canadians with autism spectrum disorder without unreasonable wait times;

(c) the creation of a national surveillance program for autism spectrum disorder to be managed by the Public Health Agency of Canada; and

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

Motion as amended November 27, 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.

[Andrew Kavchak]

There was more debate on Motion M-172 (to create a National Autism Strategy) in the House of Commons yesterday.
____________________________

HOUSE OF COMMONS
39th PARLIAMENT, 1st SESSION
EDITED HANSARD • NUMBER 087

Monday, November 27, 2006

PRIVATE MEMBERS' BUSINESS

Autism Spectrum Disorder

The House resumed from October 27 consideration of the motion.

Mr. Russ Hiebert (Parliamentary Secretary to the Minister of National Defence, CPC):

Mr. Speaker, I appreciate the opportunity to complete my thoughts on Motion No. 172 addressing a national autism strategy.

There is no doubt that autism spectrum disorders have an enormous impact on affected families. As the parents of individuals with autism spectrum disorders have attested, the impact is often discouraging, both financially and emotionally.

As the member from the Lower Mainland of British Columbia, I have been hearing from constituents on this issue for some time now. I have heard from many parents who are concerned for their children's future and who are concerned about accessing appropriate treatment and therapy.

The primary concern many parents in B.C. have is the level of funding they receive for treatment. Currently, the Province of British Columbia pays up to $20,000 annually for treatment for children up to age six. It pays $6,000 annually for treatment of children six years of age and older.

However, depending on the amount of treatment an autistic child needs, some parents find themselves paying much more than the $20,000 maximum the province currently covers. These parents look around and see some provinces, such as Alberta, covering the full cost of treatment. Other provinces address autism as a component of their public education systems, again, without imposing a financial burden on parents.

As such, many parents in my province have lobbied the B.C. government for additional funding. They have also gone to court to try to obtain more provincial funding.

Late in 2004, the Supreme Court of Canada addressed this issue in its unanimous ruling in the Auton decision. The chief justice, writing for the court, determined:

–the legislature is under no obligation to create a particular benefit. It is free to target the social programs it wishes to fund as a matter of public policy, provided the benefit itself is not conferred in a discriminatory manner.

The Supreme Court also found that funding for ABA or IBI treatment was not required under the provisions of the Canada Health Act. As such, the provinces are exclusively responsible for deciding on the level of funding they will provide for autism treatment.

Of course, parents with autistic children are not so much concerned with questions of legal obligation on the part of the provincial governments as they are with the question of whether their children are getting the held they need.

Motion No. 172 is important because it gives federal representatives an opportunity to consider and debate the contribution we can make to help families affected by autism. In doing so, our new Conservative government will continue to respect the jurisdiction of the provinces to make health care funding decisions. We will also continue to respect the judgment of the Supreme Court.

However, it is clear that even though the primary responsibility for funding treatment is an exclusive provincial responsibility, there are ways that our new Conservative government can, and already does, help.

First, our government provides general funding to the provinces and territories through the Canada health transfer for the provision of health services. This year we are providing nearly $20.1 billion exclusively for health care, $1.1 billion more than last year. Our budget commits to increasing that amount by 6% per year. Next year the provinces can count on $21.3 billion and, the year following, $22.6 billion.

Also, our new government gives families affected by autism direct financial support through the tax system. In budget 2006, our new government included a number of measures that either were proposed by the technical advisory committee on tax measures for persons with disabilities or that even go beyond its recommendations.

Among these measures were: increasing the maximum annual child disability benefit, effective July 2006; extending eligibility for the child disability benefit to middle and higher income families caring for a child who meets the disability criteria, effective July 2006; and, boosting the maximum amount of the refundable medical expense supplement.

While direct assistance for families is important, the federal government also plays a key role in medical research.

The search for a deeper knowledge into the causes of autism and for better treatments is an area where our new Conservative government believes it can make a meaningful contribution. For instance, the Public Health Agency of Canada funds Centres of Excellence for Children's Well-Being, two of which are doing important work on autism spectrum disorders.

We realize we can do more, which is why last Tuesday the Minister of Health announced some very important initiatives. These initiatives include: first, funding for a new research chair into the causes and treatment of autism; second, consultations leading to a national autism surveillance program; third, a stakeholder symposium to be held in 2007; fourth, a new Health Canada website focused on autism related information; and fifth, leadership by Health Canada in coordinating our government's response to autism related issues.

Families in my community and across Canada have been waiting a long time for a comprehensive federal response to the challenges posed by autism. I believe the leadership our government has shown in the past week will make a significant difference in the effort to better understand and treat autism.

Therefore, I would like to present an amendment to my hon. colleague's Motion No. 172. This amendment would further reinforce our government's commitment to build a strong, national strategy for autism spectrum disorders.

I move:

That, Motion No. 172 be amended by deleting all the words after the word “include”, and substituting the following:

(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;

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

The Deputy Speaker:
It is my duty to inform hon. members that pursuant to Standing Order 93(3) no amendment may be proposed to a private member's motion or to the motion for second reading of a private member's bill unless the sponsor of the item indicates his or her consent. Therefore, I ask the hon. member for Fredericton if he consents to this amendment being moved.

Hon. Andy Scott (Fredericton, Lib.):
I do, Mr. Speaker.

The Deputy Speaker:
There is consent.

Mr. Paul Szabo (Mississauga South, Lib.):
Mr. Speaker, what just happened in the House is extremely significant. It extends to the whole House an opportunity to embrace a subject matter that is substantively to adopt a national strategy to address autism.

The member for Fredericton has been a champion on this file for a long period of time. I have known him since 1993 and I and many of his peers and many Canadians have come to know that when he champions an issue we can be assured that he will give it due diligence and his full attention. I know he has worked very hard with Autism Canada as well as with other NGOs who have been working so hard to get recognition here.

I take what has happened as a sign that the House will strongly support this resolution in principle to adopt or develop a national strategy to address autism. The member should be very proud of having brought this to the attention of the House and to have earned the respect and the support of the House in terms of taking this one step further.

I was here to speak on behalf of the resolution but the resolution has changed somewhat. However, the spirit of the resolution is still there.

What I thought I might do in lieu of that is to remind all hon. members, and those who happen to be watching the proceedings or who may read them in Hansard later on, a little about autism. As public education is a very important part of resolving social problems, I will briefly outline the characteristics of autism spectrum disorder.

Autism spectrum disorder is a complex biomedical condition that can affect the normal function of the gastrointestinal, immune, hepatic, endocrine and nervous systems. It impacts normal brain development, leaving most individuals with communication problems, difficulty with typical social interactions, prone to repeat specific patterns of behaviour and a markedly restricted repertoire of activity and interests.

Individuals on the autism spectrum tend to have varying degrees or a combination of symptoms and therefore the treatments will be as varied as the individuals. It shows that there is a difference in terms of maybe some of the other challenges that we face in terms of childhood diseases and issues such as autism. In fact, the research is actually trying to deal with a multiplicity of targets and it is very difficult.

In the early signs of autism, which become prevalent between the ages of 12 months and 24 months, a child may demonstrate only a few of the following symptoms.The child starts to develop language and then loses it or does not acquire language at all. The child may appear to be deaf or may respond unevenly or not to all sounds. It is sometimes difficult consoling the child during transitions, resulting in tantrums, which are a big challenge for parents. The child has difficulty sleeping or frequently awakens at night. The child does not point or look. The child fails to bond, reacts to vaccines, is on a self-restricted or selected diet, has limited imaginative play, has no interest in playing with other children, has chronic gastrointestinal problems and has repeated infections.

When we look at the list of the possibilities that a child may experience, one or several at any one point in time, it shows the enormous challenge that this presents to parents who are trying to provide that loving care to a child in desperate need of some help.

Individuals with autism do exhibit some strengths. Although some areas of development in a child are delayed, children with ASD often exhibit skills beyond their years in other areas.

These intellectual strengths may overshadow the developmental problem experienced by the young child. These strengths may include one or more of the following. Their non-verbal reasoning skills may be better. Their reading skills may be very good. Their perceptual motor skills may also be positive, as may their drawing skills and computer interests and skills. They may have exceptional memory, visual and spatial abilities, and music skills. These are important. These children have various pockets of skill sets in areas in which they can perform, but like most children with childhood diseases, they have many challenges as well.

Although there are these exceptional skills, there also may be significant delays in other areas. I will give just a brief summary. There is going to be an impairment in social relationships. Children need to interact and they need to play. They need to learn from others' experience and to have interpersonal relationships, but these children often demonstrate a lack of awareness and a lack of normal seeking of comfort when they are stressed, as well as abnormal toy play and an inability to form friendships. These are some of the things that may be observed in terms of social relationships.

There are deficits in communication and language and a lack of perseverance on interests and activities. They are not able to keep up that interest. When I see some of these, I also see some of the evidence of the symptoms of other childhood diseases. For instance, fetal alcohol spectrum disorder also has some very similar symptoms. There also may be a dependence on routine as well as abnormal responses to sensory stimulation, behavioural problems, variability in intellectual functioning, uneven developmental profiles, difficulties with sleeping, toileting and eating, immune regularities, nutritional deficiencies, and, of course, gastrointestinal problems.

These are the kinds of things that people should keep in mind. Many of us have received many communications from constituents all across the country who have asked parliamentarians to take a special interest in this autism spectrum of disorder. It is one that tugs at the heartstrings, but we should do things not because they tug at our heartstrings, but because they are right to do.

I believe that the good faith shown by all hon. members in the House in terms of making a concerted effort to ask the government to pursue a national strategy to address autism is an enormous step that we are taking. I again want to thank the member for Fredericton for his initiative and the leadership role he took to make sure that this will become a reality in this Parliament.

Ms. Penny Priddy (Surrey North, NDP):
Mr. Speaker, I am pleased to rise today and support the motion put forward by the hon. member for Fredericton.

There are a few points that I would like to make. Sometimes people do not think of these points unless they know families involved in this issue.

One of the things that was just said concerned the failure to bond. Any parent knows the great joy of coming into a room, having their child smile at them and put up his or her arms, wanting to be picked up and hugged. Parents recognize the fact that the child has bonded with them. I am thrilled and pleased to say that my 11 year old grandson still does that. It is very difficult and hurtful for a family if a child is not able to do that easily. Sometimes these children can do so with their parents, but often not with other people in their lives.

We need a national autism strategy. We are in the process of getting a national strategy for cancer, although one could say it is a health issue so therefore it is a provincial issue. We now have leadership on a national cancer strategy and we could have a national autism strategy, and part of this debate has been about whose responsibility this really is.

We know about early intervention leading to success no matter what challenge a child may have. The earlier we can identify that a child needs support and the earlier that appropriate support can be provided, at the right time and in the right way for that particular child, it is a thousandfold more likely that the child will be far more successful than he or she otherwise would have been. Because they have had early intervention, we see children who are now in the regular school system and we see children graduating from high school.

As with any other challenge a child faces, autism has a variety of effects. Some children, with early intervention, will do very well. In particular, children with Asperger's will go to school and participate with their classmates. They may have a challenge when it is a bit unstructured, but they will do very well.

Some children will always need ongoing support in a significant way. If we do not do that, if we do not pay for the cost of a national strategy, the costs that we will pay down the road in health care, in the education system, in foster care and in group home support are going to grow at a rate that I cannot even imagine. This is why I am a bit worried about the amendment. It does not talk about those nice parts, about what the strategy should do.

We do pay for treatment for people in Canada, and while I will admit that the numbers are not large, these people are on drugs that cost the taxpayer $90,000 to $100,000 a year. Without those drugs, those people would not be able to function. We spend that much money on these other people to enable them to be the best they can be during their growth. Therefore, I think the economic argument fails. If people have no moral support for this, then the economic argument should move them. I hope both would.

We are seeing increased numbers in regard to autism now. I am not sure that we know all the reasons for the increase. They are increasing dramatically, more in some places than in others. Sometimes we see more than one child in a family being affected. We have not figured out all of the pieces, which is certainly why research is so important, but the research may not be available to us for five or ten years. I do not know. I have no idea how long it will take.

However, I do know that today there are parents at home who cannot leave their home because they cannot find someone to care for their child. If someone says to them that there is a great movie on and they should go to see it, they cannot, because they cannot get a babysitter who is able to meet the needs of their child. Their world becomes quite insular, although they do amazing things. They were on the steps of the legislature and they were out advocating to every MP, MLA and municipal councillor, every place they could, and they have been doing so for some time.

They manage to do that, but they do it against such odds that I do not know if all of us would be able to do it. If we can support the needs of children with autism, not just with our good feelings or a strategy, but also with financial resources, then we help not only the child with autism, although that is the first and most important thing, we also help their brothers and sisters, because their brothers and sisters may then have a little more time with mom and dad.

Moms and dads have to spend a lot of time with their children who have autism, particularly if they are children who may not yet be able to go to the bathroom independently or feed themselves independently or even tolerate the feeling of most foods in their mouth because of their tactile defensiveness. So this support is not just for the child; it is for their moms, their dads, their grandparents and their siblings. They will all benefit from our ability to support families not just with a national strategy, which I do support, but also with financing.

There is another thing I would say about a national strategy. When we talk about children with autism, because we have been talking about it for 10 years, 12 years or 15 years at the most, we talk about children, and that is where we focus, but we need a national strategy that looks beyond when they are 12 months old, 2 years or 5 years of age, or in elementary school or high school. How do we get past that early age and successfully into the teenage years, which are even more difficult for any child with a challenge, and then into adulthood? These are children who will be adults in our communities and they need support. We need to look at that strategy about the kind of support or kinds of resources that will be needed, not just for them as children but lifelong.

As somebody who has worked with people with disabilities for 40 years now, I can say that if we do not do this for children with autism, if we do not do something now and those children and adults are not in our community, we lose too, because they bring something to us. It is not just about us giving. They bring their special gifts and talents into our community, so we lose if we do not provide support.

There are many families looking at us to see what will happen with this motion. I hope that every member of the House will be able to support this strategy but I hope too that members understand when they support it that it is not only a strategy; it is a strategy with the pieces that were in the original motion, which I have to say I liked better.

If the member who proposed it agrees, then so be it, but the fact is that it will take funding for related services. It will be in cooperation with provincial governments that will have a surveillance program and that right now are probably desperate because we are seeing such increasing numbers of children with autism. The numbers are increasing in ways that I cannot imagine with any other kind of health or disability issue. Without proper surveillance and research, we will have no idea of how to stop this increase in numbers or about what it is in our environment that is causing this and then causing us to see it in a second child in the family.

I would hope that supporting the national autism strategy will also mean that people understand that what goes with that support is the costing for treatment, education, professional training and support for the parents.

Mr. Mike Lake (Edmonton—Mill Woods—Beaumont, CPC):
Mr. Speaker, I dedicate this speech to someone who has more impact on people than most of us could ever dream. As amazing as it may sound, he is an individual who does not have a mean bone in his body. He is incapable of hate. He is incredibly intelligent and never says anything he later regrets. He has taught me more about myself than I ever imagined there was to know, and he is only 11 years old. He is my son, Jaden, and he has autism.

Today I am not going to give the definition of autism. Members can look that up along with enough stats to make their heads spin. Instead, I want to share the story of our family's initial experiences and in my last few minutes relate them to the motion before us.

Before I do that, however, I want to commend the member for Fredericton for introducing a motion that goes beyond the political games we often see when we talk about autism in the House. His motion is actually designed to accomplish something for families and individuals affected by autism. I am thankful that we have been able to work together to come up with amended wording that we can all support.

To that end, I also want to thank the health minister and the parliamentary secretary for health for putting aside partisanship and finding common ground on which we can agree. I was particularly pleased to see the health minister begin to take action in the spirit behind this motion with his announcements last week.

Eleven years ago today I was 26 years old. I had been married for two and a half years and had a three week old baby boy. We named him Jaden, which means God has heard, something we did not know at the time, but which has tremendous meaning to us now. Jaden is almost completely non-verbal. He uses a special computer and sometimes a pen and paper to communicate.

However, going back to my three and a half week old son, like many new Canadian dads I had a clear vision for his future. It was certain that Jaden was destined for the NHL. I had it all planned out. I would not be a pushy father like Walter Gretzky. I would build a rink in my backyard upon which I would invent the most ingenious and fun drills that Jaden would enjoy for hours upon hours every day. When Jaden was not playing hockey, he would be studying hard to maintain his A-plus average.

As time went on during Jaden's first year or so, my wife Debi and I saw nothing to indicate that my carefully crafted plans were anything but on track. He was a very good baby and around the time he was one he seemed to be developing some typical first words, “dada, momma, bye-bye”.

Between 18 months and 2 years old Jaden started doing some pretty amazing things. Like just about every kid his age, he had one of those foam alphabets that fit inside a foam frame. One day on a whim Debi took the frame away and left him with just a jumbled pile of letters. Jaden proceeded to put the letters in order just as fast as we would do it the very first time.

Then to our amazement, a friend of ours mixed up the letters in a pile and put out the letter Z. Jaden, without missing a beat, put the letters in reverse order Z, Y, X, W, V and so on just as fast as he had done forward.

As amazing as things like this were, during his second year we started to notice some other things that caused us some concern regarding Jaden's development. He was extremely content playing on his own with little or no interest in playing with other kids or interacting with adults. His speech was not really developing beyond the first initial few sounds and he was very focused on patterns, often spending an inordinate amount of time lining up his videos or stacking cups in perfect order. He paid little attention when we tried to talk to him or play with him. We would have thought he had a hearing impairment except for the fact that if he heard a video he liked start up in another room at very low volume, he would instantly stop what he was doing and go to watch it.

Debi brought up our concerns to Jaden's pediatrician at his 18 month check-up, a very well regarded pediatrician. She did not see overly concerned and suggested that some children, especially boys, simply developed their speech later than others. Debi filled out speech assessment forms with public health and she and I started attending classes to learn how to help him work on his speech.

During the summer of 1997, when Jaden was about 21 months old, we were at a family wedding when one of my cousins mentioned autism as a possibility. Debi and I had both heard the term autism, but we knew very little as to what it meant. We assumed that if this was what he had, surely his doctor would have recognized it.

Three months later at Jaden's two year old check-up, his pediatrician finally brought up autism as a possibility and put us on a six month waiting list to see a specialist in Edmonton. Shortly afterwards, we came across a book that changed our lives forever. Let Me Hear Your Voice by Catherine Maurice. My mom received it from a friend. After reading just a few chapters, she called us to tell us we had to read it.

It is the story of a mother whose two children have autism and undergo a form of therapy that helped them to overcome it. We now know the therapy as applied behavioural analysis or ABA. Sometimes it is referred to as intense behavioural intervention, IBI, but they are the same thing. As we read her description of her own son as a toddler she could have been describing Jaden word for word.

By the end of one evening with that book, we knew, with absolute certainty, that our son had autism. We had a pretty good idea what we needed to do about it. We just did not know yet how complicated and frustrating the steps were in between.

Beginning the next day, Debi started making phone calls throughout North America to find out more about ABA and what we needed to do to get started. We learned that the therapy was going to be expensive. Even then, we were looking at between $50,000 and $60,000 a year. At that time, I was making probably between $35,000 and $40,000, so the numbers did not add up.

We learned we needed to start as soon as possible, as the research showed the treatment had more effect the earlier it was started. We also learned there was a significant battle going on between parents of children with autism and provincial governments across the country over the funding of ABA therapy.

In 1997-98, in Alberta, the financial picture was not as rosy as it is today. As in other provinces, a dedicated group of parents had recently taken the Government of Alberta to court and won the right to have ABA funded. However, unlike other provinces, the Alberta government made a choice not to appeal the court decision, I believe, due to the conviction and leadership of a few key ministers. This must have been a difficult decision, given the dollars involved at the time, the questions surrounding ABA and the mystery of autism in general.

Despite these considerations, the province decided that autism and the families affected by it were a priority, and it has shown leadership in this area ever since.

Returning to Jaden, from November to April 1998 was a very frustrating time for us. We knew Jaden had autism, but we had to wait six months for an appointment to get the diagnosis, which we needed to access funding.

As for the funding, the practice of the government in those early months was to automatically reject everyone and then make them go through a rather stressful appeal process. Since we were not certain we would receive funding, we did what many parents across the country still do in the same situation today. We had no choice. We started making arrangements for the program and then lined up a loan to cover the costs.

Fortunately, at the same time that we were getting organized, the group of parents that had taken the government to court in the first place kept the pressure on. Shortly before our ABA program was set to start, we got word from Handicapped Children’s Services, in Alberta, that we would not have to go through our appeal and that we would be funded 95% of the cost of our approximately $60,000 program for the first year.

Time does not allow me to go into all the intricacies of Jaden's program. It has evolved over the years as the government in Alberta has fine-tuned the process. Parents no longer have to pay for a percentage of the program. Jaden's situation is now monitored by a multidisciplinary team on an annual basis to determine what his needs are and this helps to determine what the budget for his specific program will be. Since he is in school full time, his ABA time has been cut down significantly, to 10 hours to week from the 40 in the beginning. However, he receives some additional funding for things like occupational therapy and speech because of the multidisciplinary team approach.

Most important, there is no question in our minds that Jaden's life is better now because the province of Alberta made some courageous decisions almost a decade ago. The fact remains that where Alberta showed leadership and made autism treatment a priority, other provinces have not. That is why this motion is so important.

In my view, the preamble to the amended motion, which talks about a national strategy for ASD, is the most important part. It is obvious, for whatever reason, that the provinces are not taking appropriate action on this issue. To understand this, in part, one only needs to look at what has happened in Alberta over recent years. Because we have the programs in place, families have been moving there in droves to avoid taking out massive lines of credit or remortgaging their homes.

If, for example, P.E.I. were to decide to properly fund ABA without other maritime provinces doing the same, it would probably overwhelmed by the influx of families moving there from surrounding provinces to get the treatment. The same rationale could be applied across the country.

For this, and many other reasons, we need to approach the issue at the national level, with the federal government playing a key role in coordination and facilitation. Everything else that follows in the amended motion is placed in the context of that national strategy. The wording throughout the motion rightly refers to cooperation and consultation with the provincial and territorial governments, which is where the responsibility for the delivery of treatment, the main area of contention in recent years, lies.

The first clause refers to the development of evidence based standards for diagnosis and treatment. The diagnosis part of this hits home with me. In retrospect, I think Jaden could have been diagnosed as early as 18 months of age, almost 14 months before his program started.

As for evidence based treatment standards, I believe we are beyond the point where there is any debate that ABA works for most kids with ASD. However, we need to learn more about the long term effectiveness of the treatment, how and when to withdraw it when a child has reached the stage where he is “indistinguishable from his peers”, and whether there are better alternatives for some individuals, for example, adults with ASD.

In regard to the development of innovative funding methods for care, we have talked a lot about children and ABA. I want to point out that thousands of adults in Canada require some form of treatment as well. Any discussion of care and treatment must not forget them.

In terms of surveillance, there is some question as to whether autism is becoming more prevalent. We need to find out if this is the case or if we have become better at recognizing it. We also need to look at the question of whether autism is more prevalent in certain areas of the country and if so, why.

Finally, on the research end, Canada is doing some amazing things with genetic research in connection with autism. While parents rightfully demand more than just research, this area is crucial to a national strategy as we try to ensure that both levels of government get maximum value for money on an ongoing basis.

I wish to reiterate my obvious support for this motion, as amended, and to give my thanks to all members who will be supporting it. What happened here today and what will happen when we vote on this is extremely important for my family and for all Canadian families who deal with autism every day of their lives.

I look forward to working with our health minister and members from all parties in the House to make Canada's national autism strategy a reality.

Mr. Steven Fletcher (Parliamentary Secretary to the Minister of Health, CPC):
Mr. Speaker, I speak today in support of Motion No. 172 as the House has accepted the amendments just moved by the member for South Surrey—White Rock—Cloverdale.

I would like to say how moving the words were from my colleague who just spoke. Talking about his son, and the joy and happiness his son has given him, his family and the people who know Jaden speaks to why we have all worked together in the House to bring forward this amended motion.

Motion No. 172 will pave a path to a better understanding of autism spectrum disorder or ASD. I want to begin by saying to all Canadians with ASD, their families and so many tireless activists, that this motion is far from marking an end point. I say this because initiatives in this motion call for a will to bolster Canadian research capabilities and, therefore, our overall knowledge of ASD.

For far too long Canadians with ASD and their families have been trapped in the dark. Today there is still so much we do not know. With knowledge, however, comes light. With greater knowledge, the more informed and effective future actions will be from the government, provinces, territories and stakeholders. In turn, more help will be provided to Canadians with ASD and their families.

I have worked in cooperation with the members for Fredericton and Sackville—Eastern Shore. We have taken action that crosses party lines for the good of thousands of Canadians and I am asking my fellow members to support this motion for the same reason.

Above all, this amended motion, if accepted, calls on the federal government to do what it can within its jurisdiction to lay the foundation of hope for all Canadians affected by ASD. It commits the federal government to launch a consultation on implementing a national surveillance program and calls on the government to provide additional support for research and to develop evidence based standards for diagnosing ASD. Finally, it recommends that the government work with the provinces to develop innovative funding methods to help Canadians care for their loved ones who have ASD.

This motion is consistent with the action and leadership that the health minister announced just last week. It includes a research chair that will focus on effective treatment and intervention for autism, a national symposium on autism that will be held in the spring of 2007, and a program on ASD that will be conducted by the appropriate branch of government.

A web page on autism has now been added to the Health Canada website. This web page will facilitate access to public information related to ASD. Finally, the minister also indicated that the health policy branch of Health Canada will be responsible in the future for the coordination of policy and program activities at the health portfolio level.

It is safe to say that I am not alone in hearing about the challenges posed by ASD from individuals and their families in my riding. The challenges range all the way from financial to emotional and the collective toll is enormous.

Canadians with ASD and their families deserve action. The motion before the House gives members the chance to take action. In supporting this motion, members can raise their voices in favour of laying the foundation we need for informed, effective future action. By supporting this motion members can further fuel our research down a path which may lead to finding the causes of ASD.

In conclusion, I want to add that this motion derives directly from parliamentarians successfully setting aside partisanship to help those in greatest need.

It is issues like this which attracted me to politics in the first place. I never planned to be a politician. I wanted to be an engineer like my father, grandfather and great-grandfather, and I actually became one. I worked in gold mines, but after my accident, a collision with a moose, I realized that my career as an engineer would be impossible. I had to make different choices.

It was after my accident that I realized that in our society we have a contradiction. We can and do invest enormously in treating illnesses, injuries and conditions like ASD, but then we do not invest enough in pursuing the actual causes or trying to ensure that these same individuals can live meaningful and dignified lives.

Canadians expect that everyone should have the opportunity to live the Canadian dream. This is a point related to public health and public policy that I have raised whenever I can, and in fact, it is this contradiction that has brought me to public life in the first place.

On a day like today, when this House has an opportunity to increase support for research to learn more about the causes of ASD, where we can all put up our hands to lay the foundation for helping individuals and families in need, and when partisan politics are bowed to spur public policy with principle and purpose, it makes me proud to be a parliamentarian, and I think we are all proud today to be here.

This is the right decision. I would like to urge my fellow colleagues to support this motion before the House.

I understand there is an objection from one party because of the word “national” in the motion. This House should always put Canadians first, regardless of the province they may come from because we are here together. As Canadians, it is our role to work together for the common good. This motion is an example of how Canada works well, and I am proud to be a Canadian.

Mr. Fabian Manning (Avalon, CPC):
Mr. Speaker, I am pleased today to join colleagues on all sides of the House and speak in support of Motion No. 172.

The issue of autism spectrum disorder is indeed an urgent problem that we all have to face. In the past six years the number of children with ASD has grown by more than 150%. While I stand here today in Ottawa in the House of Commons my mind goes back to my home province of Newfoundland and Labrador and indeed my own riding, where a few years ago I had the opportunity to meet a young boy by the name of Craig Walsh in a community called North Harbour in St. Mary's Bay in my riding.

Craig suffers from autism and he certainly opened my eyes to the challenges that he faces as a young person in society. He also opened my eyes to the challenges that his parents face and the community as a whole.

The reason we are here today and have the motion before us encompasses all those aspects of autism. Motion No. 172 addresses the concerns of the children themselves and hopefully the health care that is needed will be provided. It raises the concerns of the parents. As speakers before me have touched on here this morning, it raises how important it is that we as parliamentarians support the efforts of the parents of autistic children.

We stand here shoulder to shoulder giving the parents the tools and the research that they will need and indeed anything that we can do to make their life somewhat easier. We must also realize that their children too are an important part of our society. Their children need whatever we as parliamentarians can put forward. That is what we look forward to doing here today.

The fact that we are discussing this important topic in the House also gives us an opportunity to put autism on the front burner in the minds of Canadians from coast to coast. We have to address the concerns that Canadians have and also let the communities understand the importance of providing the proper assistance, funding and mechanisms that these children need and that these families need to address this very important concern.

It is estimated that anywhere from one out of 165 to one out of 200 children are now affected by autism and the numbers are growing. Autism spectrum disorders affect people in different ways and cause serious developmental disabilities in affected individuals and can affect all aspects of development. Each person with ASD will have different abilities, with symptoms ranging from mild to severe. Severe symptoms, such as compulsive behaviour and speech disorders can lead to isolation from friends, family and the community.

I congratulate the member for Fredericton for putting this motion forward. I have followed his work over the past couple of years. As previous members have said, this is not about politics. This is about children and their families. I congratulate the member for putting forward this motion and for giving us an opportunity to stand shoulder to shoulder in support of this very important aspect of life in Canada today.

I mentioned the isolation from friends, family and community. As we go through our daily lives, healthy and secure, we are always concerned about isolation ourselves from time to time. When I arrived in Ottawa less than a year ago to a much larger political atmosphere than I was used to in Newfoundland and Labrador, I was concerned about isolation. We have all the ingredients here to learn from each other and become educated.

Then we look at the children who are afflicted with autism and we wonder about the isolation they suffer. We wonder about the isolation that their parents experience. We can assist today and begin down the road to making sure that these children and their families become inclusive in our communities, our schools and indeed, society as a whole.

Canadian families with children diagnosed with autism spectrum disorders face serious challenges. They face the challenges of their child's development, behavioural issues and getting a clear diagnosis. I mentioned the young boy from Newfoundland, Craig Walsh. I have talked to his mom, Sherry, on several occasions about the diagnosis of children and the access to professional assistance. I certainly heard from that mother about her concern not only for her own child, but indeed, all children with autism. Professional assistance is what they ask for. I hope through Motion No. 172 that professional assistance will be on the way.

The cost of therapy and other services is an important issue, especially to parents of children with autism. I have heard the concern raised by parents back home about the fairness of making sure that these professional services, therapy and any other services are available to each and every child and that each and every child has the opportunity to avail himself or herself of those services.

The amended motion recognizes the challenges that many families face and suggests a comprehensive approach to addressing their needs. Once again, I am delighted that the member for Fredericton has accepted the amendments to the motion.

On November 21 the hon. Minister of Health announced a package of initiatives to improve knowledge and research on ASDs and to help children and families. In addition to the measures already undertaken, the federal government intends to sponsor an ASD stakeholders' symposium in 2007 to further the development of ASD knowledge and dissemination of information among health care professionals, researchers, community groups, teachers, individuals and family members.

The federal government intends to begin exploring the establishment of a research chair focusing on effective treatment and intervention for ASD. The federal government intends to launch a consultation process on the feasibility of studying and developing an ASD surveillance program through the Public Health Agency of Canada to help shape appropriate ASD programming and research.

We also intend to create a dedicated page on the Health Canada website to guide the public to ASD information. We also plan, with the help of the policy branch of Health Canada, to coordinate all actions related to ASD taken by the health portfolio in the future.

It is important that Canadians be educated about autism. It is important that we understand the concerns of parents, caregivers and health care professionals themselves. Just a few moments ago teachers were mentioned. I realize the challenges in the schools system. Hopefully, by our actions here today through Motion No. 172 we can begin to address some of these concerns.

There is no doubt that we all feel concerns for–

The Deputy Speaker:
Order. I am sorry to interrupt the hon. member, but the time has come for the hon. member for Fredericton to provide his five minute summation of the debate.

Hon. Andy Scott (Fredericton, Lib.):
Mr. Speaker, let me first thank the government for moving the amendment which allows the government to support the motion. I would like to thank the member for South Surrey—White Rock—Cloverdale for moving the amendment. I would like to thank the Minister of Health, the Parliamentary Secretary to the Minister of Health, and the House leader as well.

I want to particularly mention the member for Edmonton—Mill Woods—Beaumont and say hi to Jaden who I am sure is watching. The intervention by the member as a parent was a very appropriate way to focus on this issue and it is much appreciated.

I want to reassure the member for Surrey North that the amendment in fact captures the spirit of the original motion, specifically that there be a national strategy and that the strategy involve evidence based standards, funding, surveillance and research. All of those elements are there. They are not nearly as prescriptive as they were in the original motion and that was what was necessary to give the government the latitude to do it in a way that it sees fit. All of the elements of the original motion are there. We will hold the government's feet to the fire to make sure it is done in the spirit in which it was intended.

The ultimate objective is that Canadian families with autism have access to the appropriate intervention regardless of their means and it means something covered under a public health insurance program and is usually referred to as covered under medicare. We understand that the jurisdictional issue is difficult, but we cannot allow the difficulty of that jurisdictional issue to stop us from doing what we know is right. It is appropriate for the federal government to show leadership, but it cannot be for the federal government to do alone.

I want to thank the families, parents, kids and adults who have written, called and emailed their support and the organizations across the country which have done the same. I want to thank a teacher at Leo Hayes High School in Fredericton, Greg Peters. He suggested to me last spring when I advised them that we were doing this that he wanted his class to participate in this exercise. It was remarkable to see students in a grade 12 class in a Fredericton high school give their spring to this issue. They were involved in workshopping it, bringing in people who work for the province of New Brunswick as drafters, parents, scientists and so on.

At Leo Hayes High School, Greg Peters and his two classes worked all last spring on this motion. After they graduated, in September when the kids returned to school the previous class instructed the new class on how to carry the ball. I am sure all members of Parliament have heard from Leo Hayes. As a Frederictonian I am very proud of them.

I also want to make another point. Some of the interventions we have all received speak to the challenge of finding a balance between identifying the value in the family members so that when we talk about intervention it takes nothing away from the human beings that we love just as they are, special, remarkable people. It has nothing to do with that. It has everything to do with people having the most options possible in their lives. It is a collective responsibility to provide that.

I would like to thank all colleagues who have worked diligently on this issue. The member of Parliament for Sackville—Eastern Shore participated in the negotiations with the Parliamentary Secretary to the Minister of Health, with the member for Edmonton—Mill Woods—Beaumont, with the member for West Vancouver—Sunshine Coast—Sea to Sky Country and the member for South Surrey—White Rock—Cloverdale in this exercise. This has been a non-partisan, parliamentary initiative to do the right thing by a large number of Canadians.

It is a challenging file. There are jurisdictional issues which perhaps would get in the way of anybody taking responsibility to do the right thing. I do not think it would become us as parliamentarians to let those jurisdictional challenges stop us from doing what we know is right. We cannot let those difficulties get in our way. By doing what is right, Canada will be better for it, our consciences will be better for it, and a lot of Canadians will be better for it.

The Deputy Speaker:
It being 12:03 p.m., the time provided for this debate has now expired.

The question is on the amendment. Is it the pleasure of the House to adopt the amendment?

Some hon. members: Agreed.

Some hon. members: No.

The Deputy Speaker: All those in favour of the amendment will please say yea.

Some hon. members: Yea.

The Deputy Speaker: All those opposed will please say nay.

Some hon. members: Nay.

The Deputy Speaker: In my opinion the yeas have it.

And five or more members having risen:

The Deputy Speaker: Pursuant to an order made on Friday, November 24 the vote stands deferred until Tuesday, December 5 at the expiry of the time provided for oral questions.

[Super Dad]

Would someone please remind Mr. Clement that health care is a PROVINCIAL issue? Otherwise we'll end up with a NATIONAL aboriginal health care strategy. Why can't we just offer to set up a web site and a symposium?

Tony

———-

Premier Gordon Campbell announces plan to improve health of B.C. aboriginals

Nov. 27, 2006

Provided by: Canadian Press
Written by: CAMILLE BAINS

VANCOUVER (CP) – Ottawa has joined forces with the B.C. government and a First Nations group to improve the health of aboriginals in the province in the first such agreement in Canada.

Federal Health Minister Tony Clement said Monday the Conservatives have made some advances in aboriginal health issues in Ontario and Manitoba but haven't participated in any provincewide programs until now. "We're hoping that this will be a template for other agreements that we can reach with other provinces," Clement said from Ottawa.

"I really think it's the wave of the future to get this sort of comprehensive and systematic approach," he said about the plan designed to close the gap in health-care outcomes for aboriginals compared to other British Columbians.

[Mike & Jean]

Hello Everyone,

We are back from Ottawa. It was a very busy and productive four days.

We had two main objectives for our trip: 1.) To deliver the message, "Medicare for Autism Now!", and delivered before the next federal election, or we will actively campaign to elect candidates, (regardless of political affilliation) who will publicly commit to supporting legislation which will amend the Canada Health Act to include ABA/IBI under Medicare. We will do so in targeted ridings in B.C. and Ontario. We delivered this message to MPs, "the back room boys", Senators, many members of the press, and to parents. This objective was definitely met.

2.) Recruiting parent/activists in Ontario. We need more "F.E.A.T. soldiers" in B.C., but particularly in Ontario. This objective was also met.

Following is the transcript of my speech to the national press gallery. It was given during our news conference on Nov. 22nd. just prior to the rally on Parliament Hill.

"Hell hath no fury like a woman scorned."…so wrote William Congreve in the 1600's….Obviously, he had not met Canadian mothers of children who are being denied medically necessary treatment because of the failings of myopic politicians and blinkered, obdurate bureaucrats…

Speaking of which…I want to begin by commenting upon Health Minister Clement's announcement yesterday concerning this federal government's approach to autism…It is the worst of the worst that Ottawa produces…It's the Romanow Commission cojoined with the gun registry…It's also cheap politics…Mr. Clement is trying to upstage the Liberals and NDP who have been working co-operatively on a parliamentary motion proposing a national strategy on autism…Mr Clement is playing politics with the lives of autistic children and their fragile families….He should be ashamed of himself….

Today there is an epidemic of staggering proportions attacking children across North America…it's called autism…and it's being diagnosed in one out of every 166 children….Their parents, siblings, other relatives, school-mates and communities are all being affected….

It is not acceptable that children with autism remain orphans of the Medicare system….compassionate, fair-minded Canadians agree….According to an Ipsos-Reid poll taken following the Auton decision, 89% of respondents want Medicare coverage for autism treatment….it is only the political class and the health technocrats in Canada who continue to oppose doing what's morally right and economically sensible….

The U.S. Senate recently passed, unanimously, a Combating Autism Bill that will pour literally hundreds of millions of dollars into the fight against autism. Our national government remains in denial and sits on its hands….

It is beyond debate that science-based ABA/IBI treatment is the effective treatment for autism. This question has been tested repeatedly in the crucible of litigation and the courts have so found that this treatment is medically necessary…the B.C. Court of Appeal in Auton found as a fact that autism is a socially constructed handicap…it can be overcome…with the necessary political will…

Some people ask what will effective treatment for autism cost? True, it is expensive…but infinitely less expensive than a failure to provide such treatment…$60,000 per child each year versus $1.5 million per child over a life-time of institutionalization…not to mention the social cost of broken marriages (75% when an autistic child goes untreated)…the emotional and financial haardship on families…the loss to our society of the contribution that autistic children, with proper treatment, can make…like all children, they deseve the chance to be the best they can be…

In its Auton decision, the Supreme Court of Canada told parents of autistic children to "get political"…That's why we're here today…

In the last federal election, F.E.A.T. of B.C. took part in five local Vancouver constituenceis…in at least one, my home of West Vancouver – Sunshine Coast, it is fair to claim that we may have med the difference between the Conservative loss and the Liberal victory.

In the next election, we're going to expand our reach to include constituencies in B.C. and Ontario that were each won by narrow margins…these are located mostly in suburban Toronto and Vancouver…We're going to participate in as many constituencies as our financial resources and number of volunteers (F.E.A.T. soldiers) permit…We have and will use the Internet to great effect…

The glacial pace of bureaucratic time that afflicts the Canadian government in its approach to this urgent medical emergency is not acceptable…F.E.A.T. of B.C. is going after the politicains and our governing motto is attributable to the late U.S. Senator Everitt Dirksen, who once said, "When I feel the heat, I see the light."

The message is clear: "Medicare for Autism Now!" and before the next election or F.E.A.T. of B.C. will mobilize in B.C. and Ontario.

I would like to take this opportunity to thank all those contributed financially to our trip. It was a great help! I would also like to recognize the great help and assistance of Roxanne Black, Jennifer Ralph, and in Ottawa, Andrew Kavchak and Sam Yassine. Thankyou all for the work and dedication you've undertaken on behalf of all our children.

Stay tuned….

Jean

[Andrew Kavchak]

Hi Folks,

Jean Lewis of FEAT BC and I were on the Ottawa "all news" radio station on Tuesday, November 21, 2006 speaking on the Mike Harris show. His presentation and assessment of the situation was superb, as were Jean's points. You can hear the interview by going to the CFRA website, going to interviews, and scrolling down to November 21.
Andrew Kavchak
Ottawa

http://www.cfra.com/interviews/index.asp

580 CFRA Interviews

Tuesday, November 21, 2006
Michael Harris LIVE
Michael speaks with Jean Lewis and Andrew Kavchak regarding Families rally for a National Autism Strategy and in support of Motion M-172 and Bills C-211 & C-304 on Wednesday, November 22, 2006.

Families of children with autism will gather on Parliament Hill to mark the second anniversary of the profoundly mis-guided and eye-opening Supreme Court of Canada ruling in the Auton case. They will call upon the federal government to develop a National Autism Strategy. At 12:30pm there will be a press conference in the Charles Lynch Press Room, to be followed by a rally in front of the Centre Block beginning at 1:00pm.

Part 1 of 4
mp3 (click here to download)

[Andrew Kavchak]

Debates of the Senate (Hansard)
1st Session, 39th Parliament,
Volume 143, Issue 53
Thursday, November 23, 2006
The Honourable Noël A. Kinsella, Speaker

SENATORS' STATEMENTS

Autism Spectrum Disorders
Hon. Gerry St. Germain: Honourable senators, I rise to speak about a social issue that has caused, and continues to cause, a growing number of Canadians and their families a great deal of hardship. That issue is autism or autism spectrum disorders, ASD.

Perhaps some honourable senators have also met with individuals and families who deal with the challenges of ASD. Every day is a challenge for these people and their families. Every day is exhausting and every day presents yet another demand on their financial situation.

These stresses can become so great that many families find they can no longer carry the burden, and the effect on their marriages is unfortunate. Figures for divorce rates vary between 75 and 80 per cent.

Two days ago, the federal government announced it will continue to provide funding and work with its provincial counterparts. As well, the government intends to sponsor symposiums, fund additional research focusing on effective treatment and intervention and fund additional information-sharing mechanisms.

My concern is that our government's intentions and efforts to date have left those afflicted and their families with insufficient treatment and coping mechanisms. I speak in a non-partisan vein when I say that. Autism is a complex disorder and the needs of individuals and their families vary greatly. I have witnessed autism personally in my own family.

Governments need to reassess their positions as to how we support these needs. Canada needs to develop a national autism strategy, funded to provide the resources, treatment and supports necessary so that all autistic Canadians have the support that they require throughout their lives.

Hon. Senators: Hear, hear!

……

Budget and Authorization to Engage Services—Study on Funding for Treatment of Autism—Report of Committee Presented
Hon. Art Eggleton, Chair of the Standing Senate Committee on Social Affairs, Science and Technology, presented the following report:

Thursday, November 23, 2006

The Standing Senate Committee on Social Affairs, Science and Technology has the honour to present its

SEVENTH REPORT

Your Committee, which was authorized by the Senate on Thursday, June 22, 2006 to examine and report on the issue of funding for the treatment of autism, respectfully requests that it be empowered to engage the services of such counsel, technical, clerical and other personnel as may be necessary for the purpose of such study.

Pursuant to Chapter 3:06, section 2(1)(c) of the Senate Administrative Rules, the budget submitted to the Standing Committee on Internal Economy, Budgets and Administration and the report thereon of that Committee are appended to this report.

Respectfully submitted,

ART EGGLETON
Chair

(For text of budget, see today's Journals of the Senate, Appendix D, p. 820.)

The Hon. the Speaker: Honourable senators, when shall this report be taken into consideration?

On motion of Senator Eggleton, report placed on the Orders of the Day for consideration at the next sitting of the Senate.

_____________________________________

[Sam Yassine]

Hi Folks

An interesting article on Tony Clement Announcment in Kamloops This Week.

Cheers
Sam Yassine
Ottawa

By DALE BASS
Nov 24 2006

Why bother? Could someone tell me why federal Health Minister Tony
Clement even bothered to inject his government into the reality of
autism in Canada when it's definitely too little and probably too
late?

He wants to sponsor an autism symposium next year.

Maybe he should just come to Kamloops, where the Chris Rose Centre
for Autism Therapy – and its amazing director, Wanda Carisse –
spearhead just such an event every couple of years.

We've seen some of the most vital people involved in research about
and coping with autism come to town to share their vast knowledge.

Some have been controversial – one year, the British doctor who has
linked autism's prevalence with the mercury in basic childhood
immunizations spoke.

Some have been downright inspirational, like Temple Grandin, a
brilliant woman in the field of animal husbandry, with a PhD in the
field, but who must also deal with the reality of the disability
every moment of her life.

Just this year, the May conference included workshops on
socialization – one of the major dysfunctions in the autistic brain –
music therapy, sexuality and autism and tools for teaching these
children successfully.

Heck, there was even a workshop on toilet-training – and believe me,
if you think toilet-training a child with a normally functioning
brain is hard, try it with a child on the autism spectrum.

Yup, the work's already been done for our esteemed health minister.
Maybe our own MP might even mention the Kamloops conferences to
Clement and invite him to take in the next one.

If he did come, he'd discover that the other part of his strategy –
laying the foundation "to improve our understanding of autism and its
prevalence – has also already been done.

That foundation is all the families who are coping with the
disability that experts say now affects one in every 400 births.
There's prevalence covered off.

There's not much need for a research chair to look at effective
treatment and intervention for the disability. Once again, that vast
foundation – the parents and caregivers – already have that
information. For some parents, the most effective treatment is
applied behavioural analysis (ABA), an intensive, exhausting,
repetitive method of teaching that has been shown to make a vast
improvement in the lives of many children on the autism spectrum.

The only problem there is that ABA is prohibitively expensive for
most families, although they find the way to pay the tens of
thousands of dollars every year to ensure their child gets it.

You have to go to Alberta to get the government to pay for it – and
trust me, there are families who have made the jump to the east just
for that reason.

ABA funding isn't considered essential, and the governments won't pay
for it.

In fact, the Supreme Court of Canada has ruled that our provincial
government's are guilty of discrimination if they refuse to pay for
autism treatment through their health programs.

Clement's concern about autism apparently doesn't extend to the point
of insisting provincial governments provide the treatment. Nor did he
kick in any money to even make it a bit easier for the parents who
are mortgaging their children's futures in many cases to help their
youngsters deal with the present.

He's going to ensure a website is created to help the public
understand the spectrum.

Now that's a bright move.

How many of you out there who know nothing about autism are going to
wake up one day and decide you're going to go to the government of
Canada website to learn about it? Isn't typing the word "autism" into
your search engine just as easy, and more likely to give you a host
of references?

Maybe Clement should have done that himself, before making his
announcement.

And if he really does care, maybe he could use that research to come
up with a true national strategy that has nationally applied
standards, that provides funding for the provinces to pay for
treatment – and heck, with a surplus in the billions, the
Conservatives can probably handle it.

Then, I'll believe Clement and his government really does care.

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© Copyright 2006 Kamloops This Week

[Sam Yassine]

Hi Folks

An excellent interview on MPTV with Peter Stoffer and Jen Ralf. Please
distribute far and wide

http://www.garth.ca/mptv/

Sam Yassine

[Author]

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