Hi everyone,

I wanted to share a personal update and a heartfelt thank-you to each of you who has signed, shared, and stood beside me in this fight for fair MS care in British Columbia.

When I was diagnosed with Relapsing-Remitting Multiple Sclerosis (RRMS), my world changed overnight. Between fear, uncertainty, and physical decline, I didn’t know what my future would look like — until I started Ocrevus.

For eight years, Ocrevus gave me my life back. It restored my vision, stopped my relapses, and gave me hope that MS wouldn’t define my future. But now, because of changes to my husband’s insurance, I’ll lose access by spring — and with it, the medication that has kept me stable and strong.

What’s even harder is knowing I’m not alone. Across British Columbia, countless others are facing the same terrifying reality. Despite overwhelming medical support for modern treatments like Ocrevus and Kesimpta, our province still refuses to fully cover them for people with RRMS. Other provinces already do — why is B.C. still so far behind?

This isn’t just about medication. It’s about protecting our independence, our health, and our hope.Early, effective treatment prevents disability and long-term costs for the healthcare system — yet B.C.’s outdated coverage rules continue to hold us back.

Your voices matter. Every signature and every share brings us closer to change. Together, we can show the government that compassion and fairness must guide health policy.

Let’s make sure no one in B.C. has to lose their vision, mobility, or hope because of where they live. 💙

Thank you for being part of this journey — please keep sharing this petition and spreading the word.