OMF Canada Triple Giving November logo

 TRIPLE YOUR IMPACT during Triple Giving November | All Donations to OMFCA are TRIPLED through December 2

Bring Hope to Nicky and Millions More

During Triple Giving November, every donation to Open Medicine Foundation Canada (OMFCA) will go three times as far to advance critical ME/CFS and Long COVID research. All gifts are tripled through December 2, 2025, up to $500,000.

TGN logo: #TRIPLEGIVINGNOVEMBEROMFCA. The phrase is written in bold, uppercase letters with a mix of dark blue and light blue colors. The "OMFCA" text is in light blue, and there is a stylized heart shape in reddish-orange next to it.

Meet Nicky: A Life Transformed by ME/CFS

Before ME/CFS, Nicky was always on the move — raising her children, volunteering, and giving back. She and her husband even opened their home to more than 20 foster children, creating a safe and loving space for each one.

“I loved holding many balls in the air and juggling it all,” Nicky recalls. “Seeing other people have fun and enjoy themselves always gave me much joy. We were basically living the Australian Dream.”

But everything changed for Nicky and her family when she became severely ill with ME/CFS.

This image is a side-by-side comparison, labeled “Before ME/CFS” and “After ME/CFS.” On the left, Nicky is sitting in a café in Paris, holding a cup of coffee with both hands.On the right, Nicky is lying in bed, living with severe ME/CFS.

“For years, I was bedbound for up to 24 hours a day. I couldn’t work, socialize or even shower independently. Often during work and school days, my food and drinks had to be placed next to me in bed, as I was too ill to get to the kitchen.” 

Today, Nicky is still predominantly bed and housebound, but she’s grateful for each small improvement. “I can now cook the occasional meal, have dinner with my family, and help facilitate an online support group for other ME/CFS patients. About 1,800 steps a day in total is my current average and I need to use a wheelchair for the rest. 

I am very grateful for the improvement, but still every time I do something fun or even a normal daily task, I often feel worse due to PEM. I constantly need to choose between my already limited options— for example, if I wash my hair, I can’t spend time with family or friends.

“Living with a disability, chronic or serious illness is hard. Living with an illness that robs you from almost every aspect of your life is extremely difficult. But doing so without the illness being recognized nor receiving the essential support that many other illnesses receive, is very cruel.”

ME/CFS is… Hear the Voices. Triple Your Impact.

Individuals around the world used their limited energy to complete the sentence “ME/CFS is…”

These voices reveal the harsh reality of living with this disease—the challenges, the losses, and the urgent need for change. Watch their stories.

Your support today helps bring hope to people like Nicky — and to hundreds of millions more around the world who are waiting for answers.

OMFCA also accepts gifts of stock, cryptocurrency, real estate and retirement assets.

Learn more today!