‼️ We are almost at 2,500 signatures!! ‼️

Two thousand five hundred voices demanding that British Columbia stop being the only province in Canada restricting access to essential Multiple Sclerosis medications.

That’s not small. That’s movement.

If every person reading this shares the petition just one more time..one post, one story, one message…we don’t just hit 2,500.

We double it.

We send a message that cannot be ignored.

When I started this fight, I was one patient facing the possibility of losing the treatment that protected my brain, my vision, my mobility, my independence. Since then, this has grown into something far bigger than me.

Here’s what’s happened behind the scenes:

• Ongoing back-and-forth with the Ministry 
• Continued follow-ups with the BC Ombudsperson investigation, including submitting further documentation 
• Direct outreach to government officials and other advocacy organizations 
• Media interviews to keep public attention on this issue 
• Constant social media campaigning to keep pressure where it belongs 
• Working alongside my medical team 
• Communication with the drug manufacturer 
• And now being invited as a Patient Panelist at the 2026 MedAccessBC Forum

This fight is being heard.
But we are not done.

Access in British Columbia still does not reflect the standard of care available across the rest of Canada. Treatments like Ocrevus and Kesimpta remain restricted here, despite being widely accessible elsewhere. That should never depend on a postal code.

This battle has been exhausting. It has been emotional. It has been overwhelming at times.

But I am not giving up.

And I can’t do this alone.

This isn’t just about me. It’s about current patients. Future patients. Families. Children. It’s about protecting brains before damage is irreversible. It’s about mobility. Vision. Independence. Dignity.

Please…one more share. One more push. Help get this where it needs to be.

Let’s blow this wide open. 🧡