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Things
are really picking up on Parliament Hill,
with significant developments on the autism front in both the House of
Commons and the Senate!
Take
ACTION!
Call
to Contact MPs to Support Bill C-304 - National
Strategy for the Treatment of Autism Act
Find your
MP's contact info at this link:
www.parl.gc.ca/information/about/people/house/mpscur.asp?Language=E
Please consider sending
a message to thank MP Andy Scott (Liberal MP, Fredericton, NB)
for his motion in the House May 15th, 2006. (Mr. Scott
attended the Autism Rally held April 24th in Ottawa)
Parliamentary Address:
House of Commons
Ottawa, Ontario K1A 0A6
Telephone: (613) 992-1067
Fax: (613) 996-9955
Email: Scott.A@parl.gc.ca
Bill
C-304
First Session,
Thirty-ninth 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
first reading,
May 17, 2006
Mr. Murphy (Charlottetown)
SUMMARY
This enactment requires the Minister of Health to convene a conference
of all provincial and territorial ministers of health for the purpose
of working together to develop a national strategy for the treatment of
autism. It also requires the Minister to table a report in both Houses
of Parliament specifying a plan of action to implement this strategy.
The enactment also
amends the Canada Health Act 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
or territory.
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.
_____________________________________________
Shawn Murphy's
email: Murphy.S@parl.gc.ca
______________________________________________
HANSARD * HOUSE
OF COMMONS
Wednesday, May 17, 2006
Routine Proceedings
National Strategy
for the Treatment of Autism Act
Hon.
Shawn Murphy (Charlottetown, Lib.) moved for leave to introduce 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.
He said: Mr.
Speaker, I rise to introduce a bill that would provide much needed support
for many Canadians and their families who are affected by autism spectrum
disorder. This bill would see that two forms of very effective treatments,
applied behavioural analysis and intensive behavioural intervention, be
covered under the Canada Health
Act.
It would also compel
the federal Minister of Health to work with his provincial counterparts
in developing a national strategy for the treatment of autism. The bill
would require that a first ministers conference would be held this year
before December 31, 2006, and that a national strategic plan be developed
and tabled in the House before December 31, 2007.
I hope my colleagues
in the House will join me in supporting this very important issue.
(Motions deemed adopted,
bill read the first time and printed)
______________________________________________
Senator Ione Christensen's
email is: chrisi@sen.parl.gc.ca
______________________________________________
Debates of the
Senate (Hansard)
1st Session, 39th Parliament,
Volume 143, Issue 15
Wednesday, May 17, 2006
Funding for Treatment of Autism
Inquiry-Debate Continued
On the Order:
Resuming debate
on the inquiry of the Honourable Senator Munson calling the attention
of the Senate to the issue of funding for the treatment of autism.-(Honourable
Senator Di Nino)
Hon. Ione Christensen:
Honourable senators, I wish to thank Senator Munson for raising
the inquiry on autism. Incidence of ASD [Autism Spectrum Disorder],
in all its many forms, is now prevalent in one out of every 106 children.
In the 1970s it was rarely diagnosed. It is now 10 times what was experienced
just 20 years ago.
Certainly, the challenges
are many. Be it autism, FASD [Fetal Alcohol Syndrome Disorder], schizophrenia,
MPS [Maroteaux-Lamy syndrome] or Down's syndrome, just to name a few,
the children with these damaged brains and bodies are often referred
to as "the angels among us." In the past, they were often
not long with us, but their short lives always left a bright, shining
light and they were never forgotten. Their intellect, their loving nature
through adversity, their insight into what life is all about and their
happiness with small things were gifts that helped others to grow. However,
all of this came at a huge cost to the child, to the parent and to society.
With research and
medical advances, these angels are living longer. As a result, the financial
needs to help them to be productive members of society are much more
than any family can realistically cope with, and the limited coverage
under provincial health care programs is nowhere near enough.
In the United States,
the federal funding has more than tripled in the past 10 years for autism;
it is now over $100 million. However, by comparison, $500 million was
spent on childhood cancer, which affects even fewer children.
There are programs
that do work, but they require one-on-one therapy, which is hugely expensive
and offers no ongoing medical coverage. Parents must literally mortgage
their lives to provide for these needs.
With Maroteaux-Lamy
syndrome, or MPS, the cost of replacement enzyme treatment is $200,000
a year, and that is not covered by any of our health care systems. MPS
is an enzyme deficiency that is very rare; there are only 10 cases in
Canada, but I personally know of two of them - one in the Yukon and
one in Ontario.
The cost of FASD
to Canadians is upwards of $344 million a year. The cost for each person
affected with FASD is $1 million over their lifetime. There are 4,000
new cases of FASD every year in Canada. Can we really put off taking
action?
I believe that Senator
Munson will be asking the Standing Senate Committee on Social Affairs,
Science and Technology to undertake to study the financial needs and
how they can best be addressed. What better than a Senate committee?
However, we should be looking at all afflictions that fall outside of
our health care guidelines. There is a great need.
There should be
a special health care fund established to deal with these very special,
difficult and extremely expensive requirements. It could be of national
scope, and available for provinces and territories to draw from.
Over and above the
treatment expenses, research chairs should be established to deal with
the prevention - as in the case of FASD - and the causes and the cures
in the cases of ASD and MPS. With modern medicine, these children are
becoming adults. With care and nurturing, they, for the most part, can
be functional and productive in society.
It will be very
costly, but without such assistance they will become non-functional
adults and will be dealt with through institutions, both criminal and
otherwise, that is also very costly, I would argue even more costly
than helping in the first instance.
Governments of all
stripes are not good at committing to long-term programs, but this is
one area where funding must be ongoing to be of any help or assistance.
We must find ways to accommodate the need. The burden on a parent to
help such children is enormous. The responsibility to help these angels
rests with all of society and the governments that society puts in place
to represent them.
Hon. Madeleine
Plamondon: Would the senator accept a question?
Senator Christensen:
Yes.
Senator Plamondon:
What does the honourable senator mean by "being productive in society"?
I have the feeling that if we are to obtain funding, we must always
include the buzzwords "productive in society."
Not every Canadian
will be able to be productive and they will still need care. Could the
honourable senator elaborate more on what she means by "productive"?
Senator Christensen:
I thank the honourable senator for the question.
Without any assistance
in providing for treatment and therapy, all of those children will grow
up as a burden on society. With assistance and care, some of those children
will be able to function well in society. For example, Fetal Alcohol
Syndrome Disorder is preventable but, once afflicted, a child will be
a burden on society and will need ongoing assistance for life. If the
inquiry is referred to committee for further study, the area of funding
for ongoing assistance will certainly be a focus. The honourable senator
is right when she says that being a productive member of society is
not the be-all and end-all. However, many people need continuing assistance
and that must be built into the program as well.
On motion of Senator
Di Nino, debate adjourned.
The
newly-tabled motion in the House of Commons
House of Commons
Private
Members' Notices of Motions
M-172
- May 15, 2006
Mr.
Scott (Fredericton):
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."
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