National Strategy for Alzheimer's Disease and Other Dementias Act

An Act respecting a national strategy for Alzheimer’s disease and other dementias

This bill was last introduced in the 42nd Parliament, 1st Session, which ended in September 2019.


Rob Nicholson  Conservative

Introduced as a private member’s bill.


This bill has received Royal Assent and is now law.


This is from the published bill. The Library of Parliament often publishes better independent summaries.

This enactment provides for the development and implementation of a national strategy for the health care of persons afflicted with Alzheimer’s disease and other forms of dementia.


All sorts of information on this bill is available at LEGISinfo, provided by the Library of Parliament. You can also read the full text of the bill.

National Strategy for Alzheimer's Disease and Other Dementias ActPrivate Members' Business

February 3rd, 2017 / 1:30 p.m.
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Rob Nicholson Conservative Niagara Falls, ON

moved that the bill be read a third time and passed.

It is a great honour to rise in this chamber to address my bill, Bill C-233, an act respecting a national strategy for Alzheimer’s disease and other dementias, on the occasion of its third and final reading. I am most gratified that, to date, this proposed legislation has had the support of the majority of the members of the House.

Alzheimer's disease currently affects three-quarters of a million Canadians and their families, and that figure is expected to double within a generation. In addition, three out of four Canadians know someone who is affected by Alzheimer's or dementia. That is 75% of all Canadians.

It is imperative as we prepare to cross the finish line with this legislation that we complete this task together. Canadians are counting on it. It is most heartening to know that in matters of great concern to the citizens of our country and their families that we, as members of Parliament, can work together across party lines to unite and advocate for research, collaboration, and partnerships to find cures, provide timely diagnosis, and offer support for treatment. This co-operation will lead to positive health outcomes for Canadians who suffer from Alzheimer's and dementia, and will reassure their loved ones who provide care. Canadians expect that parliamentarians will work on their behalf to resolve these critical issues.

Members from across the aisle have demonstrated their willingness to work together to ensure that a national coordinated strategy is put in place to alleviate the suffering of Alzheimer's victims and their families. They have brought the very best of Canadian principles to the floor of the House of Commons to ensure that Bill C-233 will be passed for the greater good of Canadians.

I reiterate that no one should have to witness the slow and painful deterioration of a loved one or a family member suffering from this cruel illness. Far too many Canadians endure the long goodbye.

I know that I do not stand alone, as I am joined by many of my colleagues in this House who have dealt with, or are dealing with, a family member, a friend, or a loved one who is suffering from various forms of dementia.

Alzheimer's is no respecter of persons. From former President Ronald Regan to our next-door neighbour, this terrible disease knows no bounds. It takes a terrible toll among its victims and their families.

It is important for me to once again acknowledge and express my gratitude to the member for Don Valley West for seconding this legislation when it was introduced in Parliament. The member has shared heart-wrenching stories of parishioners he dealt with in his work as a United Church minister, and I know he shares my desire to see this bill become a reality. I thank him for his support. I want to acknowledge as well the work of former member Claude Gravelle on this important issue. It once again demonstrates that we can work together in a non-partisan manner. When we do that, we can accomplish much for Canadians.

It is in this vein that I once again ask my colleagues in the House to walk shoulder to shoulder with us to ensure that Bill C-233 is passed into law for the millions of Canadians who will depend on it. We have come too far to let them down now. By acting now, we are remembering those who cannot.

National Strategy for Alzheimer's Disease and Other Dementias ActPrivate Members' Business

February 3rd, 2017 / 1:35 p.m.
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Guy Caron NDP Rimouski-Neigette—Témiscouata—Les Basques, QC

Mr. Speaker, I thank the member for the work he has done on this extremely important file, which was also very dear to the heart of one of our former colleagues, Claude Gravelle.

Claude introduced a similar bill in 2012, Bill C-356, which sought to create a national strategy for dementia. Unfortunately, the bill was defeated by a single vote in 2015. Those who opposed it were mainly Conservative and Bloc Québécois members. In the end, because one Liberal member forgot to stand up and vote, the bill that Claude had been working on for a long time was defeated.

I would like the Liberal member to tell me why he wanted to introduce this bill. What is the difference between this bill and the bill that our colleague introduced a few years ago?

National Strategy for Alzheimer's Disease and Other Dementias ActPrivate Members' Business

February 3rd, 2017 / 1:35 p.m.
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Rob Nicholson Conservative Niagara Falls, ON

Mr. Speaker, there are a couple of changes in this. I was very careful to make sure that the bill did not require a royal recommendation, which in effect would kill the bill here in the House of Commons. As well, I wanted to ensure that it did not in any way restrict the jurisdiction that applies to health care issues. There are provincial jurisdiction issues here, and we wanted to be very careful.

That is why I sat down with my colleague across the aisle. I let him have a look at it and told him the reasons there were some challenges with the previous bill, which was well intentioned. He had a chance to look at that. He spent a couple of days with it. He agreed with me that with the new wording, we would not have the worry about a royal recommendation. We would also make sure that there was nothing too restrictive with respect to the health ministers across the country.

National Strategy for Alzheimer's Disease and Other Dementias ActPrivate Members' Business

February 3rd, 2017 / 1:35 p.m.
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Winnipeg North Manitoba


Kevin Lamoureux LiberalParliamentary Secretary to the Leader of the Government in the House of Commons

Mr. Speaker, it is great that we have wonderful support from the House, but I am sure the member would agree that it is also great to recognize that there are many organizations, non-profit groups, and individuals that have put an incredible effort into supporting this legislative initiative and providing advice on an important issue that affects so many Canadians.

As the member has pointed out, over a quarter of a million Canadians are affected, and that number is going to continue to grow. We know that in excess of $250 million has been invested in research on dementia over the last decade. These are all positive things. There are a lot of people we should be recognizing who poured their hearts and souls into such an important issue, which I believe all Canadians recognize. Would he not concur?

National Strategy for Alzheimer's Disease and Other Dementias ActPrivate Members' Business

February 3rd, 2017 / 1:40 p.m.
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Rob Nicholson Conservative Niagara Falls, ON

Mr. Speaker, that is actually a very good point. I will start off with the Alzheimer Society. It has been very supportive and encouraging. I recognize the effort it has made to get information out about this particular piece of legislation. It has acknowledged, as well, how important it is that we move forward on this. It is important for individuals and groups to make sure that these issues are not buried or lost here in Ottawa. I, for one, have been very appreciative of groups like the Alzheimer Society and others.

I am quite appreciative as well of the many people who have contacted me, or even stopped me on the street, to raise this issue with me. As I indicated in my opening remarks, three-quarters of Canadians know or have a family member, a neighbour, or someone they know who has suffered from Alzheimer's or other types of dementia. They know what a toll it can take.

I want to tell you, Mr. Speaker, and the House how appreciative I have been that so many people have reached out and supported what we are doing here today. I particularly wanted to mention the Alzheimer Society and other groups for their support on this.

National Strategy for Alzheimer's Disease and Other Dementias ActPrivate Members' Business

February 3rd, 2017 / 1:40 p.m.
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Alaina Lockhart Liberal Fundy Royal, NB

Mr. Speaker, it is an honour to rise today to speak to Bill C-233 and to have the opportunity to speak about dementia.

I want to praise the hon. member for Niagara Falls and heartily agree with his sentiment that this issue does transcend partisanship.

Dementia is a syndrome caused by a variety of brain diseases, the most common of which is Alzheimer's, which is characterized by slow and progressive deterioration of cognitive function. It affects memory, thinking, language, and judgment, along with mood and personality. This is a most curious and mysterious disease.

As our population ages, dementia is of growing concern in Canada and internationally. From 2011 to 2030, the number of Canadians with dementia will double. Right now, more than 7% of Canadians over the age of 65 are affected by dementia. Over 35% to 40% will be affected by the time they reach 85.

My home province of New Brunswick is particularly sensitive to this issue. As it stands, New Brunswick has the highest proportion of population over the age of 65 compared with other provinces. Dementia is on the rise in New Brunswick with over 16,000 people diagnosed and another 3,000 diagnoses expected this year. The impact is compounded by the fact that many seniors are also dealing with additional chronic diseases.

Keeping seniors in their homes helps them to thrive. Knowing this, I am reassured that the provincial and federal governments have made home care a priority when addressing health care in New Brunswick. The Government of Canada has committed over $125.1 million over the next 10 years for home care in New Brunswick.

The fact that there is no current treatment to cure dementia can be devastating to people with dementia and their loved ones. However, we know that research can help find a cure or a way of altering the course of dementia.

I cannot emphasize enough that our government believes in the power of research evidence, which is what we have signalled strongly in the last months. The Government of Canada will undertake and use research evidence to make informed decisions concerning health care. Investing in health research is an investment in a healthier Canada and healthier Canadians.

Research drives the way we diagnose, treat, and care for those with dementia and their caregivers. It has not only helped improve our understanding of dementia and the neurodegenerative diseases causing it, but it created new possibilities for better diagnosis, treatment, and quality of life for patients and their families.

The Alzheimer's Society continues to promote the benefits of early diagnosis. As a 2011 study revealed, 50% of Canadians live for more than a year with their symptoms before seeking diagnosis. We need to do better.

Canadian research has highlighted a link between dementia and stroke. Dr. Sandra Black of the University of Toronto has been collecting brain scans of patients with dementia since 1995. These scans uncovered the prevalence of silent strokes, or strokes that leave small holes in the brain without any obvious symptoms. This research has opened the door to the possibility for earlier diagnosis for Canadians using brain scans. It suggests that reducing the risk of stroke may help prevent dementia. Continued research like this is vital. Our investments in this area are essential to changing the course of dementia and unlocking a cure.

The Canadian Institutes of Health Research, or CIHR, is the Government of Canada's primary vehicle through which we support research and move results into practice. In the last five years, CIHR has invested more than $193 million in dementia-related research. This funding supports the best, most intriguing research questions that Canada's brightest and most promising scientists have to offer. This is research that has the potential for big impacts for Canadians and the Canadian health care system.

For example, Halifax researcher Dr. Janice Keefe has spent 20 years focusing on at-home, family caregivers who she calls "the backbone of our current health system". As Canada's aging baby boomers increasingly care for a spouse or parent with dementia, these family caregivers need support to avoid becoming patients, and not necessarily for dementia. Dr. Keefe co-developed a ground-breaking, evidence-based questionnaire that captures the diverse and complex needs of family caregivers.

The C.A.R.E. tool is influencing policy development and support programs for this often overlooked but vital population. First piloted in Quebec and Nova Scotia, practitioners are now using C.A.R.E. in Ontario and Alberta and it has been culturally adapted for use in France and New Jersey. As the prevalence of dementia increases in Canada, so will the number of caregivers. A tool like this, which helps identify needs and therefore support programs for those who are dedicating themselves to others, is invaluable.

I am pleased to say that by leading its dementia research strategy, CIHR is acting strategically to focus research efforts not only in Canada but internationally. This approach brings together partners from different sectors to support the latest dementia research related to three specific themes: prevention, treatment, and quality of life for those affected by the disease and their caregivers.

The domestic component of the strategy, the Canadian Consortium on Neurodegeneration in Aging, is known as Canada's premier research hub on neurodegenerative diseases affecting cognition, including dementia. The number of funding partners CCNA has brought together is now up to 15.

With these funding partners from across Canada, CCNA helps accelerate the development of dementia treatments and care for Canadians. To do this, it involves over 350 researchers, who are examining issues important to all Canadians, including specific vulnerable groups, such as indigenous people and those living in rural communities. In this regard, dementia rates in Canada's indigenous communities have been steadily increasing for the last seven to 10 years. Alarmingly, the onset of dementia is now occurring an average of 10 years earlier than in non-indigenous communities.

Drs. Kristen Jacklin and Carrie Bourassa are leading research into how indigenous culture and community affect how people experience dementia. Their team is working with indigenous communities to develop culturally grounded approaches to dementia diagnosis, care, and health education. This research will produce a range of results to help clinicians. It will help them adapt their approach to ensure that indigenous people feel more comfortable and safe when meeting with health professionals. It will also help build appropriate community and cultural strengths into existing programming for people with dementia and their partners.

The dementia research strategy developed by CIHR also has an international component, which has enabled Canadian researchers to participate in key international partnerships across its three themes. Through this component, Canadian researchers have been able to collaborate with colleagues from across the globe.

Canada is recognized as a leader in this domain. For example, Canada was the first country outside of Europe to join the joint program on neurodegenerative disease, the largest global research initiative tackling the challenge of neurodegenerative diseases. Let me give members concrete examples of the research funded through the international collaboration.

This program funds the work of Drs. Jörg Gsponer and Paul Pavlidis from the University of British Columbia. They are working on an international team with researchers from Germany, Norway, and the Netherlands to shed light on the genetic risk factors of neurodegenerative diseases like Alzheimer's. This fundamental research will help us find new biomarkers as ways to measure deviations from healthy aging, along with novel treatments and diagnostic tools.

Together the scientific efforts through the strategy's domestic and international components have defined Canada as a leader in dementia research. We are proud to support world-class researchers as they participate in the global pursuit of finding a disease-modifying treatment for dementia by 2025.

Dr. Alex Mihailidis, from the University of Toronto, has developed a mobile robot to help people living with dementia. Sometimes people with Alzheimer's disease have a hard time remembering the sequence of steps required for everyday tasks. Dr. Mihailidis has created an automated prompting system, called the COACH, which helps them remember the steps required in basic tasks like handwashing. Already working well in long-term care facilities, his team is now adapting the COACH to help those living at home.

As members can see, the results of research provide hope that new tools, services, and treatments will soon be available to better prevent dementia and improve the outcomes for Canadians living with this terrible disease.

I am pleased to say that through CIHR, the Government of Canada has established a clear research strategy on dementia. This government will continue to invest in dementia research. We know that our investments in research will go a long way to improving the lives of Canadians living with dementia, their families, and caregivers.

It was an honour to participate in today's debate, which highlights the challenges and growing concerns surrounding dementia. My father, and by extension, my mother and my entire family, is currently struggling with the impact of this terrible disease. Knowing that such amazing research is happening right here in Canada is not only comforting but provides hope for all of us that we may someday find a cure that will allow more Canadians to live a longer, healthier, and happier life.

National Strategy for Alzheimer's Disease and Other Dementias ActPrivate Members' Business

February 3rd, 2017 / 1:50 p.m.
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Sheila Malcolmson NDP Nanaimo—Ladysmith, BC

Mr. Speaker, the Nanaimo Alzheimer's walk raised $18,000 last year to promote critical research to reduce the effects of Alzheimer's, to provide services for those living with or assisting those with Alzheimer's, and to ease the personal consequences that exist for people and their families every day. I hope people in my region will come to the fundraising walk in Nanaimo on May 7.

It is in that spirit that I speak today on Canada's responsibility to improve care for the hundreds and thousands of Canadians suffering from dementia and to better support their families and caregivers. I support Bill C-233, which calls for the development and implementation of a national and comprehensive strategy to improve health care delivered to persons suffering from Alzheimer's disease and other forms of dementia.

Here is a call from Susan Barr, who wrote to me from the riding of Nanaimo—Ladysmith. She wrote, “I am a senior with Alzheimer's on my father's and mother's line, and am now starting down that dark path of dementia myself.... Unless a dementia patient has sufficient means they have to share rooms with others who often are difficult to live with and/or are violent. I urge you to go and spend two or three hours in a government funded senior's care home with a closed dementia ward and ask yourself — do you want to be treated like this?”

She also describes her brother-in-law, who used to be the gentlest, kindest soul. He has been held in hospital with Alzheimer's for long periods of time because there is no space for him in a care unit elsewhere on Vancouver Island. He has been tied on stretchers and denied showers because of fears about his aggressive behaviour. This is bad for caregivers, for families, and, of course, for the patients.

The need is great. Three-quarters of a million Canadians lived with dementia in 2011, which is 15% of seniors, and this costs our economy $30 billion each year in medical bills and lost productivity. Left unchecked, that number could skyrocket to $300 billion within 25 years.

Canada has fallen behind countries such as the U.S., the U.K., Norway, France, the Netherlands, and Australia, all of which have coordinated national dementia plans in place. Canada is one of the few G8 countries without one. As our population ages, we must prepare our health care system and communities for the increasing number of Canadians suffering from dementia. It is expected to double by 2031. To paraphrase Tommy Douglas, the father of medicare and a New Democrat, “Only through the practice of preventive medicine will we keep the [health care] costs from becoming...excessive...”

In talking last night with the Canadian Association for Long Term Care, I was reminded that Canada has had 40 years to get ready for this wave of aging baby boomers and yet our country had no strategy and failed to plan. The Canadian Association for Long Term Care notes that the proportion of long-term care residents with Alzheimer's disease or other forms of dementia has grown steadily, with 87% of residents affected by the disease since 2010. It also notes that modern home designs and increased privacy are increasingly important for residents with dementia, who could become upset and aggressive when they are unable to get the personal space they need.

Canadians have lost precious time on this, something that is especially important to those suffering from a degenerative and progressive illness. This has had real human impact. I have heard countless heartbreaking stories about the impacts of Alzheimer's disease and dementia on my constituents.

Lynn Myette gave me permission to read this note. She said:

Our Grandfather suffered from Alzheimer' an now our Mom is in a secure unit with Alzheimer's, too. We know what it is like to watch a loved one decline and loose all of their dignity to the point that they are no longer their former being. To be tied into a wheelchair and left to fall asleep sitting there, to loose all their appetite and not eat, to wear diapers and lose control of bodily functions, to no longer recognize close family members, to develop anger, these things along with drugs to numb their being to the point of comatose, happen.

Many cannot afford quality home care for their parents. I talk to so many people in my riding who are trying their very best to look after their aging parents at home. They are not getting the support they need. The smallest amount of support would make a big difference to them. They know they are saving the health care system money, and yet it is shameful that the Liberal government abandoned its election promise to invest $3 billion in home care.

The Liberals promised $3 billion over the next four years during the 2015 campaign. They separated this from the health accord. That means the money should have flowed in 2016, but it has not been delivered almost two years into their mandate. Instead, the Liberals are using home care dollars to try to lever agreement around the health accord. Provinces representing 90% of Canadians still have not received a nickel of this promised home care support. The need is pressing. The burden of caring for patients with dementia and Alzheimer's falls heavily on family members.

In Canada, family caregivers give millions of unpaid hours each year, caring for dementia patients. That represents $11 billion in lost income, and one-quarter of a million lost full-time equivalent employees in the workplace. If nothing changes by 2040, it is estimated that family caregivers in Canada will spend 1.2 billion unpaid hours per year caring for their loved ones. A quarter of family caregivers are seniors themselves.

Long-standing under-investment in care homes means that the alternatives can be dire. Lori Amdam from my riding writes the following:

Why does Canada need a national dementia strategy? We need one because the baby boomers I know are scared to death of developing dementia—they believe that life in a Canadian nursing home would be a fate far worth than death.

When I teach dementia care to students, I often ask them to bring to mind the worst care facility they have seen. They describe an old, hospital-like unit with narrow corridors, paint chipping off the walls and no access to the outside. Then I ask “What if we exchanged the twenty people with dementia who live on this unit with twenty children dying of cancer? Would this place be an acceptable environment for them to live out their last months?” Of course the answer is a resounding no. Why, then, is it an acceptable place for persons with dementia, who have no voice and no power, to live their last years?

...I see more and more incidences of unsafe and unethical practices in acute care. Recently, I had to intervene on behalf of a 90 year old woman with dementia when the hospital tried to admit a young man into the other bed in her double room. She was terrified, yelling “Get that man out of my house! Get him out!”

Creating the framework which would mandate provision of dignified and respectful care for this population of vulnerable people is simply the right thing to do. It is no less than they deserve—they deserve to live in comfort and safety—they built this country.

I can think of no better testimonial for the need for Canada to have a national strategy on Alzheimer's care. Canadians deserve no less. The New Democrats have a long and proud history of advocating for federal leadership on health care issues. We stood unanimously in the House supporting an NDP bill on a national dementia strategy in 2015.

We stood in the House in 2016 and will stand in 2017, despite the fact it was voted down by the previous Conservative government. We are very much encouraged that the member is bringing this bill forward today, even though he voted against our version of it.

We will stand in the House this year and we will vote in favour, and we will work so that every Canadian, every Canadian family, and every caregiver can have a world-class dementia strategy. All parliamentarians should continue to fight for this good cause.

National Strategy for Alzheimer's Disease and Other Dementias ActPrivate Members' Business

February 3rd, 2017 / 2 p.m.
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John Nater Conservative Perth—Wellington, ON

Mr. Speaker, it is indeed a great honour to rise in this House today to debate this important bill brought forward by my friend and colleague, the hon. member for Niagara Falls. I do want to thank the member for Niagara Falls not only for bringing forward this bill, but for his years of service in this place. I think his service to this august chamber is a testament to his hard work. Certainly as a new and younger MP, it is a great honour to receive guidance from people like the member for Niagara Falls. I thank him for his great service to this institution and for bringing forward the bill.

The bill, an act respecting a national strategy for Alzheimer's disease and other dementias, is an extremely important bill. I think all Canadians, no matter where they may live, will be in one way or another affected by Alzheimer's disease or other dementias. Certainly this is true for places like Perth—Wellington.

In Perth—Wellington we are lucky and quite privileged to have great organizations like the Alzheimer Society of Perth County and the Alzheimer Society of Waterloo Wellington. These organizations provide great opportunities and services to individuals suffering from Alzheimer's and other dementias, and also to their families and their loved ones.

Just last night, in fact, I was speaking with my sister who works at a long-term care home in the small town of Milverton in my riding. She told me about a program at that facility called iPods for Memories. It is a great program that provides an individual with Alzheimer's or dementia with an Ipod that has music and memories from the individual's younger days which the person can listen to and have a spark of memory. To see the smiles on their faces, to see the laughter of those individuals who all of a sudden have a happy recollection, a happy memory of their younger days is so important. My sister said that anything we can do as a federal Parliament to encourage programs like that, to encourage the ability of those suffering with this terrible disease to have that spark of memory, to have that opportunity to go back to some of those great memories from their younger days is so important.

Just last month I met with board members from the Alzheimer Society of Perth County. We talked about the importance of the bill and the importance of other opportunities that we as parliamentarians and as Canadians can do to help those who suffer from Alzheimer's and help those whose families are also suffering from the effects of having a loved one with this terrible disease.

One way I am hoping to help, and my office is helping, is by becoming a dementia friend. My office staff and I will be undertaking training to make us more aware of the challenges of dementia and how we can serve our constituents that much better by being aware of the challenges of individuals who may come to our office for service who may be suffering from dementia.

We think about the challenges of Canadians who are suffering from Alzheimer's, and also their loved ones. I think we are all impacted by it in one way or another, to see a loved one slowly slipping away, losing their memories, and almost losing a sense of themselves as well.

The unfortunate thing is that each and every year, as many as 25,000 more Canadians will be diagnosed with Alzheimer's or another form of dementia. While we as individuals often assume this is a disease that affects only seniors, unfortunately, we are seeing a growing trend of younger and younger Canadians being affected and being diagnosed with early onset dementia and Alzheimer's and the unique challenges that face younger Canadians, whether it be a loved one, whether it be a husband, a wife, or a parent, who is being robbed of those years of fellowship and comradeship and family that they are no longer able to experience because of the impacts of this terrible disease.

In fact, as many as 747,000 Canadians are currently suffering from Alzheimer's or some form of dementia. I think of Canadian seniors, those who built our country, those who are often referred to as the greatest generation, who have developed so much of our history and who, within themselves, have such great memories, such wisdom, but who, because of the tragedy of this disease, are having these memories, this wisdom stolen from them, taken away from them. When they lose those memories, when they lose that wisdom, we all lose something.

I am very proud to speak in favour of this important bill. I know the Alzheimer's Society of Canada has encouraged all members of Parliament to support the bill, and I am extremely heartened to hear members on all sides of this House speak in favour of the bill.

It is a testament to not only the work that the hon. member for Niagara Falls did on this bill, but to all Canadians and all members of this House who are impacted, and who listened to their constituents and loved ones who suffer from this disease.

Therefore, I am proud to speak and to vote in favour of this bill.

National Strategy for Alzheimer's Disease and Other Dementias ActPrivate Members' Business

February 3rd, 2017 / 2:05 p.m.
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Rob Nicholson Conservative Niagara Falls, ON

Mr. Speaker, I would like to thank all of my colleagues in the House of Commons for their support for this bill. The support is across the aisle and throughout the chamber, and one that I very much appreciate.

As a cabinet minister for about 10 years, I was not able to introduce private member's bills. Even though I have been here for close to 22 years, this is the first bill that I have had pass. Even when I was not in cabinet, back in the eighties, one had to have unanimous consent of the House of Commons to proceed with a private member's bill. My private member's bill was to have a national holiday for Sir John A. Macdonald at around this time of year, and I could not get unanimous consent on that. Nonetheless, I was proud to have the opportunity.

One of my colleagues around that time, the Hon. Pauline Browes, introduced a private member's bill for a statue of John Diefenbaker. She gave me the honour of seconding that bill. Much to our surprise, to a certain extent it was supported by all members of the chamber, and the statue of John Diefenbaker is outside here. I remember that Prime Minister Mulroney was so pleased and excited, he said, “Make sure you let everybody know and we'll put one up to Lester Pearson as well.” It is appropriate to have the statutes of those two prime ministers.

My colleague from Don Valley West, a member of the Liberal Party, was good enough to support this. He had a look at it and was in favour of it. I very much appreciate that. This is a great example that, on many occasions, this chamber can work together in the best interests of all Canadians.

National Strategy for Alzheimer's Disease and Other Dementias ActPrivate Members' Business

June 8th, 2016 / 5:55 p.m.
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Dianne Lynn Watts Conservative South Surrey—White Rock, BC

Mr. Speaker, I rise in the House in support of Bill C-233.

The bill calls for the development and implementation of a national strategy for Alzheimer's disease and other dementias. We need to develop and implement concrete plans and actions to address the needs of those suffering from these diseases. As well, we need strategies to support those who care for family members and friends who are living with and struggling with these diseases.

It is a staggering number, with almost 750,000 Canadians living with Alzheimer's or other forms of dementia. Of that, 72% are women. Equally concerning is that 70% of the caregivers are also women. My mother was one of the 72% and I was one of the 70%.

I can personally say that my journey with my mother was an extremely difficult one, especially because she lived in Alberta and I lived in British Columbia. Initially, she refused to believe that she had Alzheimer's, but knew that something was wrong.

She like many others are often afraid to confront the disease. She found ways to mask the daily symptoms, wanting to give the impression to her loved ones that everything was okay. It became very problematic because my mother was a diabetic and she could not remember how much insulin she was giving herself or if she had taken any at all.

As the caregiver, trying to navigate the medical system in another province was simply a nightmare. I tried to get her transferred from Alberta to B.C., but I had no other choice, no other alternative, than to take her from her home and into the emergency department where I knew the hospital system would keep her safe. That was in the month of September. By November, she was placed in a facility, and by April she had died.

During that time, I flew to Alberta every few weeks to see her for a few days. However, during those times, I came to realize that there was no standardized care, nor a full understanding of Alzheimer's or dementia at staff levels.

When she fell and broke her collarbone, they waited two days to get her to the hospital for X-rays. The nurses and caregivers would ask her if she was in pain, and she would say no because she did not remember falling. She did not remember breaking her collarbone, so they gave her nothing. A broken collarbone and no pain medication.

I can list hundreds of times when they asked questions about her well-being and they took the answers to be the truth. The only problem was that she had Alzheimer's and did not know who these people were nor why they were asking her those questions. When I came to visit, she always wanted me to stay with her because she knew me and I was her sense of security and comfort.

I tell this story because of the many others across this country where loved ones are suffering with this terrible disease. We need a strong national strategy because of the 750,000 Canadians who are currently suffering, but also for those yet to come.

Early detection, research, collaboration, and partnerships remain key to early diagnosis and treatment, and to ultimately finding a cure.

Research is currently underway in my community between the Simon Fraser University and an incredible partnership with the Sagol Neuroscience Center at Sheba Medical Center in Israel to identify the correlation between diabetes and Alzheimer's. As this begins to be proven out, one can only imagine the impact of Alzheimer's and dementia on those suffering from diabetes.

We need to be ahead of the curve. We need to put measures in place to assist those who are potentially at risk. There is excellent research being done currently right across the country, but a national strategy will bring all of those pieces together to ensure a solid plan is in place.

I have walked down this road with my mother. I have seen and experienced significant gaps within the system. I have lost my mother to a terrible disease that many do not fully understand.

This is the first step of many more to follow, and I am proud to give my support to Bill C-233 today.

National Strategy for Alzheimer's Disease and Other Dementias ActPrivate Members' Business

June 8th, 2016 / 6 p.m.
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Joe Peschisolido Liberal Steveston—Richmond East, BC

Mr. Speaker, I too am pleased to rise today to speak in support of Bill C-233, an act respecting a national strategy for Alzheimer’s disease and other dementias.

Just like the member of Parliament for South Surrey—White Rock, I was in a similar situation. I was not the caregiver, but my parents were the caregivers to my beloved grandma, my beloved nonna. As was eloquently, passionately, and poignantly pointed out by the member for South Surrey—White Rock, there are 750,000 people suffering from all types of dementia. As the proposed act properly states, it is Alzheimer's and other forms of dementia. Our family's situation was a bit different from that of the member for South Surrey—White Rock. My parents were able to give everything up and basically they became the caregivers. I would try to get home as much as I could to see a bittersweet situation. I always referred to my grandmother as Nonna Me, because as a little boy I was unable to say her name, Domenica. I saw first-hand where my grandma became a child. My mother and father had the resources and the time to stay home. My aunts and uncles also had the time to take care of my nonna.

However, a lot of folks are not blessed. We have many situations throughout Canada of different family dynamics and situations from coast to coast to coast, and that is why I am very pleased to rise today in full support of Bill C-233.

I am also very pleased to note that this bill has bipartisan support. I listened to the eloquent and passionate presentation by my colleague from South Surrey—White Rock and also to the member of Parliament for Niagara Falls who put forth this piece of legislation; as well as to my colleague, the member of Parliament for Richmond Centre. The Parliamentary Secretary to the Minister of Health also spoke eloquently as did the co-sponsor, the member of Parliament for Don Valley West and the member of Parliament for Vancouver Kingsway.

As well, I believe the member of Parliament for Abitibi—Témiscamingue spoke eloquently about not the exact bill but a similar bill put forth by the former NDP member of Parliament, Claude Gravelle, back in 2012. While not exactly the same approach, it was a similar bill to deal with a national strategy on dementia. We need a national strategy on dementia because Canada is big.

As others have done, I will talk about the elements of the bill. After 180 days, the Minister of Health would put forth a conference, bringing experts from all the provinces and territories, from all the stakeholders and people. There would be an advisory board of no more than 15 folks from different sectors of Canadian society who would advise. As well, every two years the minister would report to Parliament on the approach and the success of the national strategy.

There are big buzz phrases such best practices and evidence-based. Ultimately, what this means is that the Parliament of Canada would work with the provinces and also with the levels of government closer to the people: the municipalities, health boards, and universities.

Kwantlen College in my riding of Steveston—Richmond East is also doing research. Yes, we need a national strategy to deal with the folks who are suffering from a horrific disease. I saw that with my nonna, my grandmother. We also have to figure it out. Dementia or Alzheimer's should not be part of the natural process of aging. It does not have to be that way. It will be tough. It will require the investment and the research. I am not a scientist but it requires research with respect to how the brain works and how everything is connected.

This strategy would do that. It is the first step, but it is a very important step. I urge all members of the House to fully support the bill.

National Strategy for Alzheimer's Disease and Other Dementias ActPrivate Members' Business

June 8th, 2016 / 6:05 p.m.
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Sheila Malcolmson NDP Nanaimo—Ladysmith, BC

Mr. Speaker, last month, I joined my community in Nanaimo on the walk for Alzheimer's where our community walked in support of Alzheimer's patients and their families.

The honoree this year was the late Dale Horn. She was born in 1933 in Australia and she came to Canada at the age of 24. She was such a strong part of Nanaimo's community boards and the life of its community spirit.

At this Alzheimer's walk a month ago, her son, John Horn, honoured her at the walk for all the hundreds of participants ready to get started, saying: “Dale was a fantastic companion, fully engaged, witty and keenly observant. She drew you in and made you feel lucky to be included in her world.” With “a steely resolve and genuine grit,” Dale was unfazed by her disease, said John. “When affected by Alzheimer's, she insisted on helping others with the disease. She retained a wicked sense of humour and immense grace, right up to the end of her life.”

This year's Nanaimo Alzheimer's walk raised $18,000. This is to promote critical research to reduce the effects of Alzheimer's, but also to provide services for those living with, or assisting with Alzheimer's. This is really to ease the personal circumstances that exist for the people suffering and for their families every day.

It is in that spirit that I am pleased to stand and speak today in favour of the bill at hand and to speak about Canada's responsibility to improve care for the hundreds of thousands of Canadians suffering from dementia, and to give better support to their families and caregivers.

Bill C-233, which calls for the development and implementation of a national and comprehensive strategy to improve health care delivered to persons suffering from Alzheimer's and other forms of dementia is something we can and should all support. Canada has fallen behind other countries such as the United States, the U.K., Norway, France, the Netherlands, and Australia. All of these countries have coordinated national dementia plans in place already.

Past president of the Canadian Medical Association, Dr. Chris Simpson, spoke to this when he said:

We have the dubious distinction of being one of the few G8 countries without a national dementia strategy. Meanwhile, our acute care hospitals are overflowing with patients awaiting long term care placement and our long-term care facilities are understaffed, underspaced and underequipped to care for our most vulnerable seniors. This leaves patients and their families in limbo, struggling to fill these gaps in our system.

He also said:

The reason your father has to wait nine months for a hip replacement is that the beds are being used by dementia patients.... That is the single biggest reason why elective surgery wait times are so long.

Now, it was the NDP that first introduced a proposal to the House to create a national strategy for dementia. In 2012, former NDP MP Claude Gravelle introduced Bill C-356 in Parliament, prescribing a national dementia strategy. Unfortunately, that bill was defeated at second reading a year ago by a single vote. The bill was opposed by a majority of Conservative MPs, Bloc MPs, and, critically as it turned out, a single Liberal MP who failed to stand for the vote. I was watching it on CPAC. It was heartbreaking because it would have made a big difference in our communities.

Inexplicably, the member for Niagara Falls, the sponsor of the bill before the House today, voted against the national dementia strategy just a year ago. If the House had followed New Democrat leadership in the last Parliament, Canadians would have a national dementia strategy in place right now. Canadians would not have lost precious time, and that is something that is so precious to people suffering from a degenerative illness.

This has had real human impact. I have heard countless stories in my riding about the impacts of Alzheimer's disease and dementia on my constituents. Many cannot afford quality home care for their parents and it is especially shameful that the Liberals abandoned their election promise to invest $3 billion in home care.

I have heard stories from personal care workers, nurses, and physicians who report emergency wards overwhelmed with patients, long-term facilities that are understaffed, and long gruelling hours for caregivers. These are very often offering low-pay work in the homes of dementia patients.

These stories underscore the need for real leadership in this chamber. So many are affected. Three-quarters of a million Canadians were living with dementia in 2011. That is 15% of Canadian seniors. That might double by 2031. This costs our country $30 billion a year in medical bills and lost productivity. Left unchecked, that number could skyrocket to $300 billion within 25 years.

As Canada's population ages, we must prepare our health care system and our communities for the inevitable rise in the number of Canadians suffering from dementia.

To paraphrase Tommy Douglas, the father of medicare and a New Democrat, only through the practise of preventative medicine will we keep health care costs from becoming excessive.

The need is pressing. The burden for caring for patients with dementia and Alzheimer's falls primarily on family members. In Canada, family caregivers give millions of unpaid hours each year caring for their parents and family. That is $11 billion in lost income and a quarter million lost full-time equivalent employees from the workforce.

If nothing changes by 2040, it is estimated that family caregivers in Canada will be spending 1.2 billion unpaid hours per year providing care, and a quarter of family caregivers are seniors themselves.

Dementia also has a disproportionate impact on women. Women are two and a half times more likely to be providing care. Women themselves represent 62% of dementia cases and 70% of new Alzheimer's cases. That puts them at the epicentre of a growing health care crisis. Also, women are nearly twice as likely to succumb to dementia.

Another group of vulnerable patients are affected by another bill in the House, and that is the government's physician-assisted dying bill. We keep hearing arguments again and again that people with a dementia diagnosis should have a real choice over how their lives end. The federal government's legislation for assisted dying would not allow Canadians with a dementia diagnosis, while they were still of sound mind, to make an advance request for physician-assisted dying. This puts up an enormous barrier for thousands of Canadians with dementia or other degenerative illness.

Without the right to make advance requests for assisted dying, Canadians with a dementia diagnosis are faced with what the courts call a cruel choice between ending their lives prematurely or, potentially, suffering immeasurably and unbearably. This is completely unacceptable. To us it looks as if those who most need physician-assisted dying may inexplicably be excluded from it. We remain optimistic that amendments will be made to ameliorate that very serious flaw.

Let us go back to the national Alzheimer's strategy.

The New Democrats believe that the bill must be crafted correctly to ensure the best outcome for patients, their families, and their caregivers. While we support Bill C-233, it is less ambitious in its scope and implementation provisions than last year's New Democrat bill.

We will work constructively at committee stage to bring about meaningful and substantive amendments to strengthen the final version of the bill. Canadians deserve no less than the best national Alzheimer's strategy possible. The New Democrats have a long and proud history of advocating for federal leadership on health care issues.

In fact, as my colleague, the member forVancouver Kingsway likes to remind me, we invented it. The New Democrats stood alone in the House unanimously for a national dementia strategy in 2015. We stand in the House in 2016 and work so every Canadian, every Canadian family, every caregiver, can have a world-class dementia strategy, as the New Democrats have fought for in the last five years.

National Strategy for Alzheimer's Disease and Other Dementias ActPrivate Members' Business

June 8th, 2016 / 6:15 p.m.
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Mark Warawa Conservative Langley—Aldergrove, BC

Mr. Speaker, it is a real honour to be here as official opposition critic for seniors and to speak to Bill C-233, the national strategy on Alzheimer's disease and other dementias.

I would like to begin by thanking, particularly, the member for Niagara Falls for introducing this important bill. The secret to the success of the bill moving forward is his non-partisan approach. This is not an NDP, Liberal government, nor an official opposition Conservative Party issue, it is a Canadian issue on which we need to work together as parliamentarians. It is moving forward because of his non-partisan approach and I congratulate the member for Niagara Falls. He is a well-respected member in this House.

Bill C-233 provides for the development and implementation of a national strategy for the health care of persons affected with Alzheimer's disease and other forms of dementia.

Just to divert for a moment, my understanding of what my NDP colleague said was that people with dementia, with Alzheimer's disease, deserve to have assisted suicide. I hope that is not what she meant because people with dementia already feel bad and they may feel stigmatized.

They realize that their brain is getting a little fuzzy and they are forgetting. It is frustrating for them and maybe even a little bit embarrassing. We would not want them to think people expect them to take the obvious choice, and we heard that from Dying With Dignity, saying that it would be sensible for persons with dementia, lying in bed in the last years of their life with an adult diaper, to ask for assisted suicide.

That would not work in Canada. It is not dignified to expect people to leave this world because they are in a state of dementia. We need to show them dignity, show them love and support, and only in the most extreme cases should assisted suicide be considered.

When someone's pain is intolerable, irremediable, that is what the court said, and in extreme cases, but assisted suicide and euthanasia should not be considered the norm because it is a horrible loss when someone finds themselves in that situation. We should never put this on to people who are suffering with dementia through Alzheimer's disease or any other dementia disease.

As the seniors critic, I have met with the Alzheimer's Society and many other seniors organizations which are very supportive of this bill. Mimi Lowi-Young, the CEO of the Alzheimer Society of Canada had this to say about Bill C-233:

We’re thrilled that parties are working together so soon after the election to address the urgency of dementia. We all need to get behind this bill. We strongly believe that a national dementia strategy that focuses on research, prevention and improved care is the only solution to tackling the devastating impact of this disease. We’re ready to collaborate with our federal, provincial and territorial partners to make this a reality.

I am really thankful to her and the Alzheimer Society of Canada for supporting Bill C-233. According to the research done by the society, 83% of Canadians have said that they want a national dementia strategy.

I would like to give a brief summary on the issue of dementia. Alzheimer's disease and other forms of dementia are progressive, degenerative, and eventually fatal. They impair memory, judgment, and the ability to reason, think, and process information. Changes in personality and behaviour also result from dementia.

Currently, 747,000 Canadians have some form of dementia. This number is expected to nearly double to 1.4 million in my lifetime. Three out of four Canadians, 74%, know someone who is living with dementia. As Canada's population ages, the number of Canadians diagnosed with dementia is expected to double.

Research, collaboration, and partnership remain the key to finding a cure. Early diagnosis and support for treatment can lead to positive health outcomes for people with any form of dementia. Early diagnosis also has a positive impact on the family and friends providing care for their loved ones.

The Government of Canada, in consultation with the ministers responsible for the delivery of health care services in each province and territory, should encourage the development of a national strategy for the care of people living with Alzheimer's disease or other forms of dementia.

What is dementia? Dementia is a difficult disease, but it does not define the person who has it. People with dementia are people first. They can lead happy and vital lives for a long time, especially when the right care and support and understanding is in place. Timely diagnosis is very important. It opens the door to treatment and connects people with the disease and their families with helpful resources like the Alzheimer's Society.

While there is no guarantee, Canadians can reduce their risk of dementia by eating a healthy diet, doing more physical activity, learning and trying new things, staying socially active, quitting smoking, and watching their vitals.

While dementia is not a part of growing old, age is still the biggest risk factor. After age 65, the risk doubles every five years. Seniors represent the fastest growing segment of the Canadian population. Today, one in six Canadians is a senior. In thirteen very quick years, it will be one in four. That is a major demographic shift. Dementia also occurs in people in their forties and fifties, in their most productive years.

A good question that needs to be asked, and is asked, is this. What is the impact of dementia on families and the Canadian economy? For every person with dementia, two or more family members will be providing direct care. The progression of dementia varies from person to person. In some cases it can last up to 20 years. Because of its progression, caregivers will eventually provide 24/7 care.

In 2011, family caregivers spent 444 million hours providing care, representing $11 billion of lost income and about 230,000 full-time jobs. By 2040, caregivers will be providing 1.2 billion hours of care per year.

Dementia is a costly disease, draining approximately $33 billion per year from our economy. By 2040, it will be very close to $295 billion every year.

There is a need for a strategy that includes awareness and research.

It is commonly believed that dementia is a normal part of aging, but it is not. This kind of attitude means too many Canadians are diagnosed too late, and their caregivers seek help when they are in crisis mode. The causes of dementia are still not fully understood. Nor do we have a cure for dementia. Effective treatments are lacking and there is no proven prevention. Dementia can lie dormant in the brain for up to 25 years before the symptoms appear.

Alzheimer's disease is the most common form of dementia and accounts for over two-thirds of dementia cases in Canada.

What would Bill C-233 achieve? It would achieve a national strategy. The minister or delegated officials would work with representatives of the provinces and territories to develop and implement a comprehensive national strategy to address all aspects of Alzheimer's disease and other forms of dementia. Within two years of passing the legislation, every year after that the minister must prepare a report on the effectiveness of the national strategy, setting out his or her conclusions. The national objectives need to be given priority. A report will be tabled in the House during the first days of the sitting after the report is complete.

A number of western countries have a national dementia strategy: the United States, Mexico, Argentina, Belgium, Denmark, the United Kingdom, Finland, France, Luxembourg, the Netherlands, Norway, Switzerland, Japan, Israel, South Korea, New Zealand, and Australia. It is Canada's time to have a national strategy.

I again want to thank the member for Niagara Falls for bringing this forward. Together, if we work as a Parliament, we can pass the legislation quickly. It is needed in Canada.

National Strategy for Alzheimer's Disease and Other Dementias ActPrivate Members' Business

June 8th, 2016 / 6:25 p.m.
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Cheryl Hardcastle NDP Windsor—Tecumseh, ON

Mr. Speaker, I am pleased to speak today to Bill C-233, an act respecting a national strategy for Alzheimer’s disease and other dementias.

The New Democrats believe that a national strategy for dementia is long overdue. In fact, one should already be in place, and would be, had the current sponsor of this bill, the member for Niagara Falls, and his party not voted down a similar yet more comprehensive NDP bill that was tabled in the previous Parliament.

Dementia disease is a progressive degenerative disorder that attacks nerve cells in the brain, resulting in loss of memory, thinking, language skills, and behavioural changes. The disease forms lesions in the brain cells of patients, causing nerve connections to sever and nerve cells to die.

Alzheimer's is the most common form of dementia, which is a general term used to describe a group of systems, such as loss of memory, language, motor skills, and other brain functions. Alzheimer's is not part of the normal process of aging, and currently has no cure.

The New Democrats ardently support the need for national leadership to develop and implement a comprehensive strategy across Canada to address Alzheimer's and other dementias. Our caucus unanimously supported former NDP MP Claude Gravelle's bill in May 2015 to create a national dementia strategy. Further, in election 2015, the NDP committed $40 million toward the implementation of a national Alzheimer's and dementia strategy.

Our party recognizes the crisis facing Canadian health care as our country's population ages, including the growing prevalence of dementia among the elderly. We believe immediate action must be taken to tackle these serious challenges on a comprehensive basis. Accordingly the New Democrats are concerned by the decision of the Liberal government to abandon its home care promise in budget 2016. By abandoning the necessary investments now, the Liberal government will only further exacerbate the costs and suffering down the line .

A national strategy for Alzheimer's and other forms of dementia must include mechanisms to ensure that staff have the necessary knowledge about the disease and the skills to deal with it. This means that people have to share information. The purpose of a national strategy is to share that information. People should not be working in isolation.

We have to find a way to ensure that everything we learn, everything that might be useful, such as best practices, is communicated to people struggling with the same problems. It is essential for people to have ways to talk to each other. The goal is not to step in for the provinces, but to ensure that communication channels remain open and people work together. Real collaboration needs to happen so people can share best practices. We have to ensure that nursing staff, doctors and other professionals, such as police and emergency responders, know and understand how to deal with dementia. They need to have the right skills and knowledge to work with people with dementia and provide them with quality care that is appropriate for their situation.

They are often forgotten, but the volunteers who work in this field need to be able to understand the reality of a person living with dementia. It is not always an easy thing to do. There are certain situations that are very difficult to go through on a daily basis, and it is hard to know how to intervene. The volunteers who work at these centres must have access to the knowledge and skills they need to properly understand the reality of the field they have chosen to work in.

As far as research is concerned, we have extraordinary Canadian researchers. However, we could also form international partnerships to further our knowledge. In my opinion, the quality of daily life for people with dementia is an essential area of research. Lately, a lot of research has been done on daily life, and we have learned how significant and deeply impactful this research can be.

In many places there has been a shift from a very medically-based approach to one focusing on the daily experience of dementia sufferers. The goal is for the transfer to long-term care to go as smoothly as possible. For that to happen, the person with dementia needs to be able to create reference points.

A lot of advances have been made because of these various approaches that focus on quality of life and ways of providing care and intervention. Not only is this helping those living with dementia to live much more happily, it is enabling families to be an integral part of the care process.

There is a lot to do. With the challenges this will present in the coming years, it is essential to share information in order for us to adopt an effective national strategy for dementia. According to the Alzheimer Society of Canada, as we heard earlier tonight, the disease and other dementias now directly affect 747,000 Canadian patients, and this number is expected to double to 1.4 million by 2031. Current dementia-related costs, both medical and indirect lost earnings, of $33 billion per year are expected to soar to $293 billion by 2040.

Sadly, the burden of caring for patients with dementia and Alzheimer's falls primarily on family members. In Canada, family caregivers spend 444 million unpaid hours per year caring for dementia patients, representing $11 billion in lost income and 227,760 lost full-time equivalent employees in the workforce. Providing millions of hours of unpaid caregiving has forced people to cut back or leave work altogether, which harms them and our economy. I want to talk about that this afternoon.

I learned from the Canadian Medical Association that 15% of scarce acute care beds are occupied by people who could be placed elsewhere, and half of them are dementia patients. Beyond those statistics, I have learned the real face of the problem. The real face of dementia is not just older people. I learned that 15% of dementia patients are under 60 years of age. I learned that we have a health care crisis and a social and economic crisis that we must address.

This is therefore an issue that cries out for leadership from Ottawa, working with the provinces and territories, which of course, have primary jurisdiction duties for health care delivery. I want the leadership from Ottawa to tackle five main elements: early diagnosis and prevention; research; a continuum of care for people and families in the home, the community, and institutions; real help for caregivers; and training for the dementia workforce.

Alzheimer's disease puts enormous emotional stress on millions of families in Canada and costs our health care system billions of dollars every year. Delaying the onset of Alzheimer's by two years could save our health care system $219 billion over a 30-year period. A national strategy for dementia may be able to make an astounding difference in advancing research to work toward achieving this goal, which would diminish this enormous economic hardship and subsequently, and most importantly, improve the lives of those affected Canadians.

The challenge caregivers face needs to be discussed. Over the years, I have known people who have been forced to take a leave of absence without pay to take care of a loved one suffering from dementia, sometimes for several years. In such situations, money gets tighter as families try to keep their loved ones in their homes for as long as possible. They often have to draw on savings that were meant for their own later years.

Canada needs a national strategy for dementia that comes from Ottawa but one that respects provincial and territorial jurisdiction over health. One strategy tailored to the needs of each province or territory would be far better than 13 separate strategies implemented in isolation. We want a national strategy that goes beyond research to also help those now living with the disease, their caregivers, and the dementia workforce.

National Strategy for Alzheimer's Disease and Other Dementias ActPrivate Members' Business

June 8th, 2016 / 6:35 p.m.
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Rob Nicholson Conservative Niagara Falls, ON

Mr. Speaker, I would like to thank all members of the House who have contributed to this debate. I appreciate, in particular, my colleague from Don Valley West for supporting and seconding this piece of legislation. He has a great career, among other things, as a United Church minister. As a pastor, he was constantly challenged by the personal and social consequences of Alzheimer's and dementia.

One of the stories that he passed on to me was about one particular woman, Mae MacMillan, who was a vibrant, intelligent, committed, and compassionate woman. She was trained as a nurse and was ahead of her time in promoting women's rights. She loved strong and powerful women and she was one herself. However, dementia slowly crept up on Mae.

At first, she thought it was just part of the normal aging process, which I have heard before. She was slightly forgetful and misplacing objects, but as she moved on in age, she moved from being the object of affection to being the object of attention. Family, friends, and professional caregivers helped her to live with some independence for as long as possible. Sadly, this is a case of where the mind cannot remember, the heart never forgets. So many of us can relate to that sentiment.

When I introduced the bill, I told of my own family experience with this and one thing that has moved me over the last couple of months since introducing the bill is all the stories and experiences that people have shared with me. The members for Steveston—Richmond East and South Surrey—White Rock shared their encounters with this terrible disease, and all of us were moved by it.

In one sense, I was surprised, after introducing the bill, that so many people either contacted my office or sent emails and letters. People stopped me on the street, even when I was not in my hometown, to tell me about their experiences with these diseases.

The bill before us was very carefully drafted. When I showed it to my colleague, we were very concerned about ensuring that there was no restriction on provincial autonomy and that it was not framed in a way that would require a royal recommendation, which, as we know, would stop the legislation.

Again, I am pleased that so many colleagues have moved forward on this. I believe this is the right thing to do. I believe that we can make progress on these things. In all of our lives, we have seen the terrible consequences of diseases. There are cases where we know that changes can be made. I always remember, as a small child, what a terror polio was in this country. Then I remember hearing the news—I do not think I was any more than five—that a cure had been found for it. Every child in Niagara Falls went to the arena to get the vaccine.

I can appreciate that some diseases are very complex and it is not just a question of coming up with a special potion, but as my colleagues have said, there are so many different parts of this in terms of care, diagnosis, support, and working together. I firmly believe that supporting the legislation is the right thing to do, and again, I am deeply appreciative of all those who have indicated that they support it.