When Isaac was six years old, a tiny cut on his foot nearly cost him his life.
Several years ago, Isaac’s mom shared his story with Lupus Canada donors.
Today, Isaac is telling that story himself.
Diagnosed with lupus as a young boy, Isaac grew up navigating an unpredictable and often invisible disease. The fatigue, muscle pain and impact of the sun were difficult enough. But one of the hardest parts was feeling like no one else could see what he was going through.
Today, Isaac is a Lupus Canada Youth Ambassador and advocate, pursuing his future while helping make sure other young people living with lupus know they are not alone.
Your support helps make that possible.
“That Boy Was Me.”
Isaac’s road to diagnosis was overwhelming, mostly because it took so long.
Lupus is rare in young boys and typically affects women, so doctors tested Isaac for almost every disease except the one he had.
By the time the pieces fell into place, his immune system was so depressed that a small infection had ravaged his whole body, and his family was gently told to prepare themselves.
Isaac survived.
But receiving a diagnosis was only the beginning.
“The tests weren’t the hardest part. The hospitals weren’t even the hardest part. It’s the invisibility.”
Lupus does not come with one specific set of symptoms. It affects everyone differently, and for young people especially, that can be incredibly isolating.
From the outside, Isaac looked fine.
Inside, he was exhausted in a way he could not explain to anyone his age. Muscle pain made even a bedsheet on his skin feel unbearable. The sun, something his friends loved, drained him. He pushed through school days knowing his body was paying a price no one could see.
Some days, he simply wanted to be a normal kid.
Lupus did not always let him.
Finding Community Through Lupus Canada
Isaac learned to keep many of the difficult parts of living with lupus inside because he did not want to burden the people around him.
But sometimes, simply having someone ask how he was doing brought relief.
“That’s what Lupus Canada gave me. Relief. Community. People who truly get it.”
Becoming a Lupus Canada Youth Ambassador changed things for Isaac.
It connected him to the wider lupus community. Even without knowing everyone personally, knowing he was not alone in the battle was sometimes enough to keep going.
It also gave him a voice he could use for people who may not yet have found theirs.
And perhaps most importantly, it reminded him that his path may have changed, but there was still a path forward.
Your support helps Lupus Canada create opportunities for people living with lupus to feel seen, understood and connected.
Making an Invisible Illness Visible
A few years ago, Isaac decided he wanted to do something.
Not just talk about lupus, but act.
So he set out to swim 1,000 laps in 10 days.
It became the Lupus 1000 Challenge.
For Isaac, the challenge helped turn an invisible illness into something people could finally see.
What he did not expect was what happened next.
People across the country picked it up.
Today, Canadians complete 1,000 of anything, from laps and kilometres to other activities meaningful to them, to raise awareness and support for lupus.
“Watching it take on a life of its own taught me that when we refuse to stay invisible, people show up. They always show up.”
One young person’s decision to act became an opportunity for an entire community to act with him.
Helping Young People Living with Lupus Build Their Futures
Isaac’s path has not always looked the way he imagined it would.
But lupus does not get to decide what he becomes.
The Lupus Canada Scholarship Program has helped Isaac pursue his dream of becoming an aerospace engineer, and today, he is apprenticing in the field.
Now, he wants other young people living with lupus to have that same opportunity.
“I want every young person living with lupus to have that same chance: to follow a dream, build a future, and prove that this disease doesn’t get to decide what we become.”
Your generosity helps Lupus Canada support people living with lupus not only through the challenges they face today, but as they look toward what comes next.
Creating the Connection Isaac Once Needed
Finding people who truly understood lupus took time for Isaac.
The Lupus Peer Network, launching soon, will help create opportunities for people living with lupus to connect with others walking a similar path.
For newly diagnosed young people, that means access to something Isaac had to wait years to find: real connection with people who understand.
Because lupus can be isolating.
Symptoms can be invisible. Fatigue may not be understood. Schools and workplaces may only recognize the seriousness of lupus when a flare becomes extreme.
But it is often the daily challenges that wear people down.
No one should have to carry those challenges alone.
How Your Gift Helps Support Canadians Living with Lupus
Isaac’s experience is his own.
Every person living with lupus has a different story, different symptoms and different challenges.
Your gift helps Lupus Canada continue working to:
- Build connection and community for people living with lupus
- Increase awareness and understanding of an often invisible disease
- Support young people living with lupus as they pursue their futures
- Strengthen advocacy and amplify the voices of people with lived experience
- Advance research and improve the future of lupus care in Canada
Your gift does more than support one young person with lupus.
It helps make sure the next person diagnosed, and the person after that, knows they are seen, supported and never alone.
It Is Still Your Path
Isaac has a message for anyone who has just been diagnosed:
“Your path looks different now. Harder, maybe. But it is still your path. Walk it. Keep fighting. And remember, we will walk beside you.”
With your help, Lupus Canada can keep showing up for Canadians living with lupus.
Please give what you can today and help ensure people living with lupus have the support, connection and opportunities they need.
Be a steady force in an uncertain world.
Your support protects progress, strengthens advocacy, and ensures that Canadians living with lupus are not left behind.
Other Ways to Give:
Donate by mail
Please make your cheque payable to Lupus Canada and mail it to:
Lupus Canada
PO Box 8 LCD 1
Newmarket, Ontario
L3Y 4W3
Kindly also provide your email address so that we can expedite the delivery of your tax receipt.
Donate by telephone
Become a monthly donor
Monthly giving provides reliable, ongoing support that helps Lupus Canada continue its work throughout the year.
Questions about any of the many ways to give? Reach out to us!
Drop us a message: contact us
