Spotlight on Elaine Letourneau:

Honouring my mom, Lorraine

November 2022

Elaine Letourneau

My mom Lorraine was diagnosed in 2001 with smouldering myeloma (SMM) when she was 68 years old. Of course, we had never heard of multiple myeloma, much less this smouldering business.


The SMM stage lasted for about a year, maybe a year and a half, and then it turned into full blown myeloma. Sadly, my mom lost her fight six years later in 2006.


At the time my mother was going through her battle, Myeloma Canada didn’t exist. I did a lot of reading and as much research as I could. There was some information out there but not a lot, and there weren’t a lot of treatment options, which was the problem.

Thankfully, we did have some support through a local support group in Edmonton. We were about 15 – 20 members who got together to try and learn about myeloma and whatever limited treatments that were available at that time.


I believe my mother was on Velcade. She underwent a stem cell transplant which did bring her a bit more time. I know that since then myeloma treatments have improved substantially! Even though there still may not be a cure, so many people are living so much longer and are almost dealing with the disease as more of a chronic but relapsing condition. Sadly, this wasn’t the case for my mom.

A little bit about how my mother's smouldering multiple myeloma was found:

My mom was a seamstress. In 2001, she started to mention feeling very tired and having a lot of back pain. Her fatigue and pain kept getting worse and worse, to the point where she couldn’t even sit and sew anymore.


I believe it was her primary care physician who decided to do a blood work-up on her to see what was going on. It was actually the lab technician who noticed the M-protein in my mom’s test results and just knew what it meant.


I don’t really know how long my mother’s overall diagnosis actually took because at the very beginning, she didn’t tell anyone about how she was feeling or what she was going through. I guess she didn’t want us, her family, to worry or suffer.

My mother, Lorraine

We didn’t find out my mother had myeloma until she was referred to a specialist in Edmonton, Dr Belch. Unfortunately though, my mom’s myeloma progressed really quickly. Combined with the lack of treatment options available for her specific situation plus other health complications she experienced, my mom lost her battle far too early.


It's interesting that some people tend to hide their diagnosis. For one reason or another they don’t want to, or feel they just can’t, tell their families. I understand... it’s what my mom initially did it, and it’s unfortunate. Many people still feel like there’s a stigma with coming out and saying you have cancer. And, when you hear things like you’ve got a cancer that’s not really well known, that's not yet curable, and that’s more common in older people and you’re not part of that older demographic, you kind of think, 'how did I get this' (or my mom, my dad, my sister, my brother…)? I think for my mom, it was part of what made sharing her diagnosis more difficult.

When I read about other people’s experiences with the disease, it’s validating to learn we weren’t alone in not having known what myeloma was when my mother was diagnosed. I’m so thankful that there was at least a support group for us to join…it really was a great thing.


Knowing that today, there’s a national organization [Myeloma Canada], and a national network of support groups, is very comforting.


It must be so encouraging for someone who's living with myeloma now to reflect on how far things have progressed and be able to say, "Wow, because of all the investments and advancements that have been made in research and treatment, I'm still here, and I've got options ahead of me!!"

Me and my mom

My mother was also an accomplished artist

My mother was 68 when she was diagnosed. All of her ancestors lived well into their 80’s and 90’s so it was such a shock to learn she had cancer...to us, she was still young. You start analyzing and wondering if there was anything that she did in her life that could have caused or contributed to this. We couldn’t come to any conclusions.


My mom lived at home and sewed for people. She wasn’t exposed to chemicals. We ate wild meat and vegetables from our garden most of our lives. It’s one of those things that we’ll never understand.

That’s one of the reasons why I want to do what I can to help advance research for a cure and raise awareness to help others know about this disease.

I’m also hoping my story will help people open up and say, Hey, I want to fight this. I know there are other treatments out there and I’m going to do my research to find out more about them. I’m going to get more involved with the support group network or the organization itself and I’ll move forward from there with others instead of alone’.

After my dad passed and when his estate was finalized, I decided I wanted to donate to Myeloma Canada. You know, it still breaks my heart that I couldn't have done more for my mom when she was going through this horrible disease. 


That her story might help others, and maybe even help lead to a cure, is amazing.

I wanted my mother’s story to be a part of a campaign that helps further funding for research and improving quality of life for others living with this disease. 🙏 If my $50,000 donation can help raise $100,000 that would be unbelievable!

I feel like doing this in my mother’s name is another way to honour her memory and her battle with multiple myeloma.

Thank you,

Elaine

Editor's Note:


  • For more information on Elaine's generous matching program, click here.


  • To learn more about legacy giving, or how to bequeath a donation to Myeloma Canada in a will, click here.

We hope you enjoy meeting our 2022 Spotlight Stars and your fellow Myeloma Canada community members. The Spotlight section of Myeloma Matters features stories and reflections supplied by members of our community - those living with myeloma, caregivers, healthcare professional - in their words. The views expressed and shared are those of that individual. We recognize that everyone’s journey and experience with myeloma is different.

 

To all of you who have shared your stories in the past, and those of you who continue to do so today, we are indebted...you are an inspiration.  


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Myeloma Canada's mission: To improve the lives of Canadians impacted by myeloma through awareness-building, educational efforts, advocacy, fostering an empowered myeloma community and support of clinical research so that a cure may be found.