That, in the opinion of the House, the government should establish a Pan-Canadian Palliative and End-of-life Care Strategy by working with provinces and territories on a flexible, integrated model of palliative care that: (a) takes into account the geographic, regional, and cultural diversity of urban and rural Canada; (b) respects the cultural, spiritual and familial needs of Canada’s First Nation, Inuit and Métis people; and (c) has the goal of (i) ensuring all Canadians have access to high quality home-based and hospice palliative end-of-life care, (ii) providing more support for caregivers, (iii) improving the quality and consistency of home and hospice palliative end-of-life care in Canada, (iv) encouraging Canadians to discuss and plan for end-of-life care.
He said: Mr. Speaker, it is always a great honour to rise in this House representing the people of Timmins—James Bay. Tonight I am particularly proud to represent the New Democratic Party as we bring forward a motion that we believe is essential for the development of long-term planning for health in this country, which is a pan-Canadian strategy for palliative care.
[Translation]
I am very proud to be here this evening to move this motion on behalf of the New Democratic Party. We are asking the federal government and Canada's Parliament to establish a pan-Canadian strategy, ensure access to palliative care, and work with the provinces and territories so that all levels of government can develop a standard of care that ensures access to quality palliative care.
[English]
To begin, I would like to make note of a few things for the people watching across Canada.
I would like to thank the medical leaders, medical organizations, front-line service providers who are serving people in need, and the social workers, pharmacists, nurses and doctors, for the support that we received. I would also like to thank members of the various spiritual communities of Canada who have supported the New Democrats in this motion.
On a personal note, I would like to mention that my late brother-in-law John King, who was a close friend and a brilliant young man, lost his life much too early to cancer. After the 2008 election, I came home and spent the last few nights with John at Perram House, in Toronto.
Perram House was an extraordinary palliative care centre. At the time, I thought it was the norm. I thought that when Canadians became sick, there were Perram Houses everywhere. It was after Perram House closed, in the city of Toronto where my brother-in-law was dying, that I realized there was a lack of good quality palliative care beds.
Certainly there is good quality palliative care in hospitals. However, with regard to community-centred, spiritually centred, communal-familiar centred care, it made me realize that across this country we do not have a standard forum for ensuring that families and individuals have the support they need.
I would also like to thank the incredible work of the all-party committee. The Parliament of Canada is known as a relatively toxic place at most times, but members of all parties came together on this vital issue and worked hard. I would like to recognize the members of the Conservative, Liberal, and New Democratic parties who worked on the study and wanted to bring forward to Parliament the need for us to establish this pan-Canadian strategy on palliative care. I believe that the motion I am bringing forward on behalf of the New Democratic Party is carrying forward the work of this all-party committee.
One of its key recommendations is that the committee strongly urges that the federal government re-establish a palliative care secretariat for the sake of developing and implementing a national palliative and end-of-life care strategy. In honour of the work that my colleagues in the other parties and New Democrats did on that committee, we are bringing forward that motion tonight.
There has been much discussion lately in the media. Many terms are being used on the issue of dying with dignity and what it means. People are grappling with very complex and emotional issues that touch all of us.
Tonight I would like to use the definition of palliative care that has been offered by the Canadian Medical Association.
The Canadian Medical Association tells us the following:
Palliative care is an approach that improves the quality of life of patients and their families facing the problems associated with a life-threatening illness. [It involves] the prevention and relief of suffering by means of early identification, assessment and treatment of pain and other physical, psychosocial, and spiritual symptoms.
We can see from the Canadian Medical Association's definition that palliative care is not just about dealing with someone in their final bleak hours. It is the notion of an integrated health strategy that is there for families in their homes. It is not just about the alleviation of suffering, but allowing the individual to have a higher quality of life than they might have otherwise had. It also assures support for the family, community members, and loved ones, who sometimes face an extremely traumatic time.
The fact that we are having this debate today at the end of the national health accord is very timely. The New Democrats believe, and have believed this since our founding and the days of Tommy Douglas, that the federal government has an important role to play, not in the delivery of service but in working with the provinces and territories to establish norms across this country.
If we look at the situation with an aging population and our increasingly frayed health care system, and with the end of the health accord and less and less money to be delivered to the regions, urban and rural, it becomes incredibly important to ensure that we have an integrated health care strategy.
What would the strategy look like? We know that Parliament played a role before. In 2007, the Conservative government cancelled the palliative care secretariat that had been established and was beginning to do work in terms of a national vision. We had an all-party committee that came back and said we needed a strategy.
However, what we are seeing across the country is a real patchwork of services. I believe there are only four provinces that even have a provincial strategy in place for palliative care. In some areas we see incredibly strong resources. For example, downtown Regina and Saskatoon have extraordinary services, but even in a city as big as the GTA or Montreal, we are dealing with a patchwork. In rural areas, sometimes it is almost non-existent.
There is a belief that somehow palliative care is done with volunteer money. That does not really understand its importance.
Let us look at the delivery of services in the rural regions. What I have seen in my own region is that when families do not have access to proper support, it causes immense stress to the patient. Many times I have dealt with this when people have come to my office. I have heard about an elderly woman trying to bathe her husband who is dying of cancer, but who has not been identified for palliative care. They are trying to get home support workers, who do extraordinary work.
The overall vision is that this is a palliative issue as opposed to just someone who needs home support. Too often the person ends up in the emergency room waiting for a bed. It is the locum or the emergency room doctor who has to tell them that they are actually suffering from an incurable illness, which can be very traumatic.
I have seen families almost torn apart because of the pressure. Someone has to stay home with the loved one. We know that in at least a quarter of the cases, Canadians have said that they have had to miss upwards of a month of work or have used personal savings to look after a loved one who has an incurable condition.
In areas where we have good palliative care, we can actually save about $8,000 to $10,000 per patient because they are not then being cared for in emergency wards and there is not the struggle to find beds, because there has been a whole approach.
In the rural northern Ontario region that I represent, the provincial allocation for palliative care for a region of more than 100 kilometres with three hospitals and about 20 communities is $70,000. What can $70,000 buy when one is delivering health care, when one has to do the audits and to ensure travel? That is not to say it is the only money.
The province, through its LHINS, has a pain management program, but it is not under the palliative program but through someone else, another organization that could be 200 kilometres or 400 kilometres away. They do good work as well, but it is not integrated. We have personal support workers, but they are not necessarily working under the palliative network.
To get that $70,000, the local organizations are supposed to raise $25,000. So they are already having to bring forward about a quarter of the money themselves. Meanwhile, there are numerous other agencies, all delivering fragments of the service, but if those fragments were put together into a cohesive whole there would be a better health outcome.
We can learn from each other in different parts of the country. This is a really important opportunity. We need to talk to the medical front line, the social workers and the people who are dealing with the sick and the aging. They understand that if we work together and worked on the models that work, we could learn from each other and deliver better outcomes.
[Translation]
There is clearly a need for this program across the country. Palliative care is excellent in some regions and virtually non-existent in others.
Quality palliative care means integrated care: home care, social services and medical care to help improve people's health, emotional and psychological support and support for families.
Currently, less than 30% of Canadians have access to quality palliative care. That is why New Democrats are asking the other parties to work with them to support this vision for a pan-Canadian strategy to help families and individuals facing this situation and to implement similar models in both rural and urban areas.
[English]
I believe this is a moment when all parliamentarians can come together in a positive way. We all have to face the death of a loved one. We have all faced it. We all have our own stories. These are moments in the life of a family that is at a crossroads, the closing of one chapter and the opening of another.
I remember when my grandfather died and the responsibilities that were transferred, the cultural roles, the leadership roles, and the spiritual roles that people play in a family when someone leaves and the next generation has to take those on. That is an extraordinary moment in the life of a family, but if it happens in a crisis unit, if it happens in an emergency ward, if it happens because some of the family members have to be out working in the oil patch and cannot get back to be there, the sense of guilt and anger can tear families apart or seriously damage the spiritual vitality of a family or community.
When there is a better model out there, one that saves money and that ensures better access for people, I think it is incumbent upon us to say, let us embrace this model and let us show what dying with dignity in 2014 should be about, to ensure that we have everything in place around the person, around the loved ones, around the families so that they can make that transition and so that we, as their family members and loved ones, will also be able to make that transition to the next level of our own communities.
I am hoping to get the full support of the members of Parliament. I am certainly counting on the members who did the extraordinary work on the palliative care committee. I think this is something on which we can all agree. I would ask my colleagues to work with us to support this motion and then begin to push for its full implementation.
From this Parliament, it is incumbent upon as well to begin this discussion in Canadian society. This is a common sense solution that is staring Canadians in the face. This is a discussion that we need as Canadians. It is a positive discussion. It is a discussion that brings people in to talk together, as opposed to leaving people on the outside.
I would like to think that out of this motion can begin a positive discussion across this country.
:
Mr. Speaker, I rise today to speak to Motion No. 456, sponsored by my colleague from . Palliative and end-of-life care are important topics, and I would like to recognize the member for for raising these concerns in his motion.
I would like to briefly share an experience from my riding of Okanagan—Coquihalla that I believe is relevant to the motion we are discussing here today. Back in the early 1990s, Andy Moog, a citizen from Penticton and a former elite NHL Stanley Cup winning goalie, started up a unique charity golf tournament known as Moog and Friends. Each summer, some of the NHL's finest players, coaches, general managers, and media personalities gathered to raise funds for a very important cause. That cause was the Moog and Friends Hospice House, which provides palliative and end-of-life care for loved ones in my community.
Today, Mr. Moog and many of his friends are enjoying retirement, but the legacy of the Moog and Friends Hospice House lives on to serve the community. This hospice house, and the unique care it provides, was a first at the time for our region. It has made what can be some of life's most challenging moments more bearable, so that those we love can pass on with dignity and greater understanding. That is why Motion No. 456 is an important one and will become even more important as our population ages.
Indeed, we know that by 2020, Statistics Canada projects that there will be 330,000 deaths in Canada each year. By 2041, that number will rise to more than 432,000. These statistics demonstrate the need for palliative care services right across the country. We also have to recognize that providing these services will require significant resources. In fact, since 2006, our government has invested more than $43 million to support palliative care research and has delivered $3 million to the Pallium Foundation of Canada to support training in palliative care for front-line health care providers. Our government understands the very difficult challenges faced by Canadian families when they are caring for aging loved ones who need palliative care.
We must also recognize that ultimately it is our partners in the provincial and territorial governments who have the lion's share of responsibility for managing and delivering health care, including palliative care. That does not mean that as a federal government we cannot provide support to the provinces and territories in these efforts.
The question that is most often raised, and at times debated, is how best we can provide that support. One way to improve end-of-life care is to integrate palliative care through the health care system, in all settings where people spend the end of their lives. Integrated care systems, for which our government delivered $3 million in economic action plan 2011 to support the development of this, has shown promise. This funding supports the development of community-integrated palliative care models, fostering collaboration among all jurisdictions and the health care community. The $3-million investment to the Pallium Foundation of Canada announced recently by the will also support training in palliative care to front-line health care providers.
The motion before the House today highlights the need for integrative models of palliative care and the need to encourage Canadians to discuss their wishes for end-of-life care. It also focuses on taking into account the geographic, regional, and cultural diversity of Canada, both urban and rural. The federal initiatives from our government to date, implemented through non-governmental organizations with expertise in palliative care, align with a number of the components that the member for raises in Motion No. 456.
We should also not overlook that to better support front-line health care providers and to improve the quality of life and consistency of palliative end-of-life care is to make available the best and most up-to-date evidence. Research provides that evidence.
[Translation]
Federal investments in research also help increase the depth and scope of our knowledge of issues related to end-of-life care and the best ways to address them.
Since 2006, the Canadian Institutes of Health Research has invested over $43 million in the area of palliative care, including $7.8 million in 2012-13 alone. The Canadian Institutes of Health Research, the Social Sciences and Humanities Research Council and the Natural Sciences and Engineering Research Council are supporting the Technology Evaluation in the Elderly Network project, which is part of the Networks Centre of Excellence program, with an investment of $23.9 million between 2012 and 2017.
[English]
This network aims at improving the care of seriously ill, elderly patients and their families through the development, rigorous evaluation, and ethical implementation of health care technologies.
While my comments earlier highlighted the responsibility of the provinces and territories, our government recognizes the federal role in providing health care services, including end-of-life care, to a number of groups including first nations and Inuit, members of the Canadian Forces, the Royal Canadian Mounted Police, and veterans. These services are provided directly by the federal government or managed in conjunction with the provinces and territories.
This government's contributions, which I have just described, complement services provided by provinces and territories. In addition, the funding we have delivered for research serves to inform palliative program delivery and quality improvements at the federal, provincial, and territorial levels. Taken together, these federal actions help address the needs identified by the motion put forward by the member for .
Indeed, this government agrees that palliative care is the best option for end-of-life care.
However, we would like to see this motion amended to instead seek the establishment of a federal framework instead of a pan-Canadian strategy as it is currently worded. This amendment would clarify the federal, provincial, and territorial roles in health care as I laid them out earlier. The development of this framework would engage provinces and territories, as well as key stakeholders, so that federal activities complement their emerging and ongoing activities; reducing the potential for duplication.
A federal framework could also provide opportunities to raise awareness, share information on federal palliative care activities, and support public awareness about advanced care planning, palliative care, and caregiving.
Without further ado, I would like to move that the motion be amended by first replacing all the words between the word “should” and paragraph (a) with the following: “develop a federal palliative and end-of-life care framework to guide the Government of Canada's efforts to improve palliative and end-of-life care. This framework will complement flexible, integrated approaches to palliative care developed by provinces and territories with relevant stakeholders; and,” and second, replacing paragraph (c) with the following: “aligns with the goals of improving access to high quality home-based and hospice palliative end-of-life care for all Canadians; supporting family caregivers, particularly those balancing paid work and caregiving responsibilities; improving the quality and consistency of home and hospice palliative end-of-life care in Canada; and encouraging Canadians to discuss and plan for end-of-life care”.
Again, I appreciate the opportunity to stand in this House to speak to the member's motion, show our support, and bring forward an amendment that we think could allow us all to rally behind this cause.
:
Mr. Speaker, I applaud the hon. member for bringing forward this very important motion. I want to suggest, however, that we add one amendment to the motion. I know that we are not allowed to do that, but I would like to include after the word “integrated” the word “comprehensive”. It is because it is not only about integrating a system of care we are talking about. It is about looking at all the elements of care that are necessary. The hon. member, in putting forward what is a broad-based recommendation, leaves it open for some of us to talk about areas that we feel are missing. The word “comprehensive” would encompass all of this.
The whole concept of palliative care is not a simple thing that happens when one's life is ending or when one is dying and wants to die a good death, as the word euthanatos means. What we are talking about here is the issue of palliative care as part of a continuum of care that should be divided, actually, into three parts. The three parts we want to look at have to be divided into the different levels of the end of life.
First, there are seniors ending their lives with chronic diseases who need to or can live in their homes. While those chronic diseases may eventually speed up their deaths, the point is that they are able to take care of themselves in their homes with a system that facilitates good home care.
The second part is a diagnosis of impending end-of-life, when the patient needs assisted care but is not yet dying.
The third piece we need to look at is the final piece, which is when the person is dying, which is when palliative care fits in.
Currently, palliative care and any of these levels of care are not considered to be core, mandated levels of care under the Canada Health Act. Therefore, they are spotty at best. We have some places where there is a wonderful integrated, comprehensive system in place and some places where there is practically nothing at all. That is why the motion is important.
The thing to remember is that 26,000 seniors die each day in Canada. Only a small percentage of them have the ability to get the kind of care they need as they lead up to and eventually end up needing palliative care.
The parliamentary committee, in 2011, had some excellent recommendations. As we develop a model to implement this, we can look at them, because some were quite comprehensive.
We need to talk about an integrated, comprehensive system, because we need to look at some areas that are not mentioned in the motion. One of them is support for caregivers. It is not only support for caregivers to take time off work so that they can look after the chronically ill and/or diagnosed patient. We need to have respite in place for caregivers. If caregivers are the only people on whom the care falls within the family, and they do not have an opportunity to take some time off to deal with some of the stress and emotional pain they have while they are looking after a loved one, we will not have fitted the system out properly. We would only consider burdening the actual family member with all the care and compensating them for it. Respite and time off is an important part of any support for caregivers.
I also want to talk about a piece that is not fully mentioned but that is really important. That is the issue of housing. I think we have forgotten that housing is a determinant of health and that housing is a core part of any kind of comprehensive and integrated system. As we get to the home care part, for instance, when people may be able to stay at home when they reach a particular point in their chronic disease and can still take care of themselves with help, we need to ask if we can retrofit homes. Do we have a program that would retrofit and renovate homes so that it would be possible for the person to live that period of their time at home?
Are we looking at new housing strategies through which people, once they get to the assisted living part, can move into an assisted living centre with all of the higher-level care that they may need, and eventually move on to palliative care in a facility particularly dedicated to palliative care?
The important piece that I would like to add is the comprehensive piece. We must talk about housing if we are to achieve that full system, and we must talk about respite if we are going to achieve proper support.
Pieces are missing. I support the intent, but there are pieces missing. For instance, we know that only 10 out of 17 medical schools in the country have any teaching program at all to train physicians in palliative care. Most physicians get something like a 10-hour course in those 10 universities, so most physicians are not really equipped to deal with palliative care.
The important thing is to look at how we educate and train caregivers, whether they are nurses, physicians, or others, to deliver appropriate care and to understand all of the pieces involved in end-of-life care, including the spiritual pieces, the cultural pieces, the emotional pieces, and all of that. We do not yet have that kind of training in place. That is one of the pieces that would be needed as we look at a comprehensive, integrated model of care.
The idea of helping people to develop a plan is very important. I think of the Canadian Medical Association meeting last summer. The doctors all talked about the fact that they did not do this very well, that they needed to start reaching out to their patients to talk about some sort of plan, and that patients need to understand that they can reach out to their physicians, or, if they are in a community care setting, to the nurse practitioners, the home care nurses, or whoever is looking after them to be able to discuss this matter openly.
The ideas here are excellent. I just wanted to add some elements to it that I think would strengthen it. That is why I wanted the word “comprehensive” in it. The mover of the motion may not agree with me, but after the word “integrated”, I would add “comprehensive” so that we deal not only with the health care system but also with other systems that would support it with palliative care.
That is what I had to say. I support the motion.
:
Mr. Speaker, I am very pleased to rise in the House today to support my colleague, the member for , and this great motion he has brought before the House.
It is a simple and straightforward motion, but it is incredibly important. As the member outlined, it is about establishing a pan-Canadian palliative care, end-of-life care strategy. It is about providing more support for caregivers, improving the quality and consistency of home and hospice, palliative, end-of-life care, and actually encouraging Canadians to discuss this issue.
When we look at our health care system, sometimes we think that things do not affect us. However, I think it is very true to say that we have all had experiences where a family member, a close friend, or maybe a neighbour, has been in the situation where they are approaching the end of their life, and it becomes a real struggle in terms of where they might be and what kind of care they might receive.
Palliative care and end-of-life care, whether in a hospice or at home, is something that is really very deep. It is very meaningful. For many years, we did not talk about these issues. We do not like to talk about death or think about what happens to us at the end.
However, we should talk about it. More than that, we need to have public policy around it. That is why this motion is so important. It shows us that across the country there are incredible examples of palliative care.
However, it is very patchy. For example, in my community in East Vancouver, the St. James Cottage Hospice, located in an historic building in Burrard View Park, is an amazing place. It is like a home. It is a place where people feel comfortable. It is where they have dignity. They do tremendous work there.
Every year in our community in East Vancouver, there is a festival of lights. The houses are dressed up with Christmas lights, and people vote and give donations in the street adjacent to the palliative care home. The money goes to palliative care. The whole community comes together to express itself. It is a wonderful initiative undertaken.
We need to state in this debate that, unfortunately, there are big gaps in the system. I was very proud last Monday when the NDP unveiled a very important document based on 18 months of consultation across the country about health care in Canada.
We went out and talked to Canadians. We did our homework about what needs to be done to improve and sustain our public health care system. It is a wonderful document, and I would certainly urge people to go check it out on the NDP website.
In the public forums and consultations we held across the country, one of the key issues people put forward, based on their own experience, their own need about what they know needs to happen, was that we need better home, long-term, and palliative care. That came through to us again and again.
I would like to quote from that document we put out a week ago.
Canadians want to see home care, long term care, and palliative care recognized as essential medical services just like treatment in the hospital. These services are not luxuries, and they need to be fully accessible, whatever a patient’s income, and provided at the same high quality and standards wherever they live.
That quote has come to us in our document because of what people told us. We are very cognizant that palliative care is part of a bigger issue that needs to be critically addressed in this country, which is the issue of continuing care of which palliative care is a part.
We do need to have home care. We do need to have long-term care. Again, it is very spotty across the country. Some provinces do well, others do not. People who live in smaller and remote communities have very little access.
The reliance we have on acute care facilities, the over-reliance because there is nowhere else to go, people end up in hospital, as the member for pointed out. For people to die with dignity, they need to be in an appropriate place where there is support, resources, the right kind of medication to relieve pain, and the right kind of guidance, whether spiritual or emotional, from their family.
These are probably the most important times in anyone's life, yet these services really do not exist across the country in the way they should.
I really want to make the point today that in debating this motion, let us recognize that it is linked to a bigger issue around our health care system and that we have to make sure that the federal government shows leadership on this issue.
There are many reforms needed in our health care system. This is one of them. Today, I met with a group, the Parkinson's Association. I have met with many other groups. They all say the same thing, which is that the burdens financially and sometimes emotionally of caregiving create enormous stress for the family where people have to leave work, quit their jobs, and take out loans.
This is not what should be happening. There are incredible groups out there who have been calling for this kind of pan-Canadian end-of-life care strategy for so long. I think it is fantastic that we had an all-party parliamentary committee working on this issue.
Now that we are actually having this debate, we have our own power here to vote, one by one. We have the power to say that this motion has merit, that it is legitimate and has all of this groundwork, all of this homework, behind it. It is non-partisan. It crosses all political lines. We have this opportunity in the House to vote for this motion and to say to the government that this is the will of Parliament.
It is based on what we hear from our constituents. It might be based on our own experience. I certainly have my own experience. My partner of 24 years died of cancer just before I was elected. We were very fortunate that we had palliative care at home under the B.C. health care system.
I cannot imagine what that experience, as hard as it was, would have been like if my partner had been in a hospital, just in a ward or maybe in the hallway. Being at home and having people around him who loved him and cared for him on a daily basis and having the professional help and support that we needed was critical to how we went through our own process of grieving and losing someone that we loved so much.
That is just my experience, and this is manifest in hundreds of thousands of people across the country every day, so I want to say, let us pay attention to the motion. Let us look at how it is putting something forward that is real and legitimate. Let us put aside partisanship. Let us recognize the good work that has been done on this issue by an all-party committee. Let us unite, come together, and say to the government that we want to pass this motion so that the Government of Canada will establish a pan-Canadian palliative care strategy.
I would also like to move an amendment.
I move that the motion be amended by replacing the words “Canada; (b) respects the cultural, spiritual and familial needs of Canada's first nation, Inuit and Métis people” with the words “Canada, as well as Canada's first nation, Inuit and Métis people; (b) respects the cultural, spiritual and familial needs of all Canadians”.
:
Mr. Speaker, it is my pleasure and honour to stand and speak tonight to Motion No. 456, and to draw attention to the palliative care needs and the end-of-life care needs of many Canadians.
I want to say to the mover of this motion that I appreciate that it is a motion and not a bill. I personally believe we can accomplish more in private members' time with motions than we do with small changes to legislation. This one is a bigger picture issue and it is very important that it has been brought forward.
As we know, the senior population in Canada is growing. In 2012, there were more than five million seniors in Canada, which is about 15% of the population. Based on what I have read, I believe that number may even double within the next 15 to 20 years. That is because of advancements in medicine and other factors that allow Canadians to live longer.
It is important for us to be ready for that aging population, even though many seniors today are very active in their older years, and that is very important. A few weeks ago I presented a bill on obesity, diabetes, and staying active, not just for youth but also for seniors.
Today's motion before the House draws some attention to the role of family caregivers. A Statistics Canada study revealed that family and friends provide 80% to 90% of the care for ill or disabled persons in our community. It is important to note that one-quarter of these caregivers are seniors themselves and are helping other seniors, whether their own spouses or family members. It can be expected that this will only increase with the increase in baby boomers.
At this point, I know other speakers have made this motion a bit of a personal piece, and I would like to take this time to do that on two fronts. One is that we are talking about hospice care. When I was on the council in the City of Burlington in 1999, it came to our attention that there was a need for palliative care and hospice care. Through the leadership of the mayor at the time, Mayor MacIsaac, and the Rotary Clubs of Burlington, they came up with a plan. By 2002, we had a 10-bed hospice, or maybe 12-bed, which was also able to exist because of the generosity of a number of Burlingtonians including the Carpenter family, which was the lead donor on the Carpenter Hospice, as we know it today. That was in 2002. As of last check, it has served over 1,600 individuals who lived there in palliative care since its inception. I have been very proud to be part of the council that developed that.
The other area that is very important to me and my family is that I am very fortunate to have relatively long life in my family. In fact, my grandmother Wallace will be celebrating her 97th birthday in a week and a half, or so. We are very proud of grandmother Wallace. Her mother, Granny Lasalle, lived to 100 years old; so I might be here for a while. In fact my Granny Lasalle worked on Parliament Hill. She was a housekeeping employee and, in a picture I have seen, she is cleaning the Prime Minister's offices.
We have been very fortunate. I want to wish my grandmother a very happy birthday. What is important is that she lives with my uncle and aunt. She has lived with a number of my dad's brothers over the years, and they are providing the care and support for her. We are very fortunate that Grandma Wallace is in really good health, but that is not the same for every family.
I lost another grandmother in the fall who was age 96. She was living with my parents for about five years. Therefore, I completely understand, from a personal perspective, the need for family members and the responsibility that goes along with end-of-life care and palliative care and care for seniors. The role that my Uncle Jack and Aunt Marilyn are playing for Grandma Wallace and that my Uncle Miles and his wife Cathy played for my grandmother Wallace in past years and that my own parents, Len and Cassie Wallace, played for my Grandma Gray make a big difference in the quality of life for them as the end of years come closer.
I am hoping, based on the 10% rule, that my Grandma Wallace will outlive her mother by about 10%. That will make her about 110 by the time she needs palliative care, and I am looking forward to that. That also means I will be the member of Parliament for Burlington until I am 120. Hopefully, I will have moved on before then.
Our government recognizes the critical role that many Canadians play in caring for family and friends with health conditions or disabilities, in addition to balancing their own work lives and family responsibilities. In 2012, over eight million individuals, or about 28% of Canadian adults, provided unpaid care to family members or friends with a long-term or terminal health condition, disability, or aging needs. Of these caregivers, about 67% provided care to a senior. Most often, family caregivers providing end-of-life care were caring for their own parents, as was happening in my own family. About one out of every 13 caregivers has provided this type of care in the last year alone.
Our government recognizes that while family caregiving is both beneficial and rewarding, it can also be very difficult. Take, for instance, the negative health impacts experienced by caregivers, particularly among seniors caring for other seniors, and those caring for individuals suffering from very difficult diseases like Alzheimer's and other related dementia. As these individuals become less capable of taking care of themselves, caregivers assume the responsibilities for their personal care. This gradual loss of independence often creates additional levels of stress and anxiety for the person with the disease, the caregiver, and the caregiver's family.
We have also supported research that is helping inform decisions as to how best to help the families and caregivers of people with chronic and progressive conditions. Indeed, since 2006, we have invested more than $650 million in research in areas related to aging, including more than $100 million in 2012 alone. Ongoing research, supported by our government, is also filling gaps in knowledge about rates of neurological conditions in Canada, including Alzheimer's disease. It is also looking at the efforts of individuals with these conditions, their families, and other caregivers.
Supporting Canada's caregivers presents an increasingly complex challenge, in part because of the very needs of each recipient and because of the unique situation of each caregiver. Responding to such needs typically involves the engagement of several partners at all levels of government, with the support of community-based organizations and employers. In addition to the above-mentioned research, the Canadian government has provided a variety of supports for unpaid family caregivers. For instance, economic action plan 2014 announced our intention to launch the Canadian employers for caregivers plan. This plan would engage employers to identify and implement cost-effective and promising workplace practices that better support employed caregivers.
I appreciate the motion from the member opposite to highlight and bring attention to the issue of palliative and end-of-life care, the important role of family members and family care for those in need, for the other opportunities that need to be addressed in working with other partners, including the provinces, and making sure that we have these services for the growing senior population we will have over the next number of years.