ActivismAdvocacyDisabilityDisability RightsMS

Where do you live?

This is a long post. Stick with it. There’s some tough stuff in here.

As part of my volunteer work with the MS Society of Canada, I’m involved in a campaign to look for better housing solutions for people with MS who need a high level of care but are under the age of 65. Here’s why.

For a small proportion of people with MS, symptoms can come on really fast, and when you’re still young. When that happens, you’re in a wheelchair full time. You probably have limited movement in your limbs. Maybe swallowing, speech, eyesight issues. You’ve lost your independence. 

If you’re lucky, like me, and you have someone at home that can care for you, like me, you stay in your own home, like me. There is a program in BC called CSIL – Choice in Supports for Independent Living – where you get control of the funding for your care, and you employ carers to come into your home. I do that too, as it gives Ian and I a break from each other! (Or as ‘they’ put it, respite for the carer from me!). But that only funds you for up to 4 hours a day. What if you need more care than that and there’s no-one at home who is capable of doing that?

The answer is, you move to a care home. A residential facility. A senior’s home. All names for the same thing. But what if you’re in your 30s or 40s? Yep, that’s the only option for you. And, once you enter one of the facilities, that’s it. You live the rest of your life there.

In BC 60% of the people in residential facilities are aged over 85, and 15% are aged under 65. 

So the life of one of these homes is built around the elderly. The social life, the music, the pictures on the walls, the expectations of the staff. But you’re still young inside! You don’t want “old time music” and bingo – you want movies, and the Internet, and to live with people your own age.

This campaign is trying to do everything it can to bring this situation to the attention of those who have the power to make a difference. The politicians. Our MLAs. And for them to want to make a difference, they have to know these people, the ones who live this life.

In July I met with Steve Thomson and Norm Letnick, two of our local MLAs. They were interested in the topic and the statistics, and really got stuck into thinking about what the lives of these people are like. I explained to them that in many ways, without Ian, I’m close to being in one of those facilities – at which point they looked at me in horror and joked about the poor staff who would have to look after me! (It doesn’t sound funny, but it was. You had to be there…)

The key point of the meeting was for me to ask them to meet people in our community who are in that situation – young people who are living the life of an 85 year old in a care home. They both said yes, to their credit – “they’re our constituents! Of course we will see them!”

The next stage was to find someone in this situation and ask them if they’re willing to meet with the MLAs – because it appears that not everyone is keen to talk to politicians – go figure. At this point Sherry (our programs and services coordinator) stepped in, and found two women in the same facility that would be prepared to talk to us about this. And that’s where we got to, today.

I went to visit this care home firmly thinking about the campaign, the MLAs, the possibilities for change. When I got there, I realised this was all about me, partially. 

We entered the facility and it was lovely. None of that clinical smell. The hallways, the decorations. Birds in a cage. A hairdressers called Scissorhands. The first sign that this was a senior’s home was this beautiful mural of old photographs of Kelowna – not because we were in a museum, but because this was age appropriate for the people who lived there.

We turned a corner, and there was an open area, again beautifully laid out, leather sofas but no-one sat in them – because everyone was in wheelchairs, and very, very old. I could feel this tight grip around my throat, because I suddenly realised that this is where people my age and younger, who are not much ‘worse’ than me, live. It all became very, very real.

We got to the room of the young woman we were meeting. I’m going to keep this vague, for obvious reasons – her privacy. She’s in her early 40s. Had MS for a few years more than me, and been living in these homes for the last 5 or 6 years, so really needs a high level of care. We talked about what she would want to tell these MLAs. The first thing – the loneliness. She spends most of the day alone, in her room. She hasn’t left the facility since she arrived, 18 months ago. There’s no-one her age, nothing to do for her interests. People see her disabilities first, but forget that behind those is a young, vibrant woman, who not that many years ago lived a full, very active, outdoors life. She’s still there. She’s not ready to be 85.

We also asked her about a few things on her wish list. I’m not going to say what they are yet, just that Sherry and I are going to do the best we possibly can to make them happen. We have a mission and nothing is going to stop us!

I came away choked up with anger. Why is it like this? Why has no-one stopped this from happening? 

The next step is September 19th, when the MLAs come with us to meet this amazing woman. From there, the ball is in their hands to some extent, but I will be that squeaky wheel. There must be change for people like this young woman, and the 4500 people like her in BC. There are many creative solutions that could be tried. The three of us brainstormed just a few in our conversation – if we can do it, so can anyone else. There has to be that will to change. 

I have told people so many times how lucky I am, and they don’t really get it. I have great benefits, great LTD, I live at home with a husband who didn’t run for the hills when I got sick – and 50% of them do! I love my live, my dogs, everything we do together – and not to mention this summer and Winnie. Sure, my MS is not an easy thing to live with, but I have learnt that I am very fortunate, and there are too many whose lives have been made a living hell with MS. People ask me why I spend my time doing advocacy – and that’s why. It’s not because I want better HandyDart for myself, or better ‘age appropriate’ housing (to use the jargon) for myself, or whatever it is that I expect the City of Kelowna to wake up and do. It’s because I cannot live with myself having met these people and knowing that with a few emails and a little bit of my time, I could possibly make their lives a little more bearable. I would challenge any of you to meet these people and see if you could walk away and do nothing.
The photo is of the wall in her room – of paintings that she did herself a few years ago when she still had movement in her arms and hands. I asked if I could take a photo and share it on my blog, and she said yes.

4 comments on “Where do you live?

Thank you for posting this. May I share it with my students as we look at ways that they can be of service to others in our community?


Absolutely. And of course it’s not just people with MS in this situation. All kinds of diseases/accidents and so on.


Way to go! This is SUCH an important issue for all of us. I understand they do this differently in Ontario so that there are homes specifically for younger patients, or at least a dedicated wing of the home. BC needs that too.


That’s exactly the sort of thing we are hoping to achieve. They have group homes for people with development disabilities, where 4 or 5 people with similar needs live together. I think that would be great – but a first step would be to group people of similar ages in their own wings of current care homes, right now, they are scattered through the homes, and scattered through the city.


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