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when I was first diagnosed in 2006 a hell of a lot of drugs offered to me seemed to end in 'zumab'or 'mab'. Does anyone know what it stands for?

Three days ago I had the honour of being a member of a small team of counsellors who supported participants at a Kairos Blanket Exercise. This exercise is an emotional, eye-opening look at the relationship and history between Canada’s Indigenous People and Canadian immigrants for the last 300 years....

https://youtu.be/iZOrYcdkjoA Post yours and we’ll dilute the drepressing stuff until Monday

I have M.S. and Fibromyalgia... Pain is neva ending.. just have dif levels of pain.. You have the pain that's nagging always.. then the pain that BUSTS THE DOOR.. saying..OOH U THOUGHT I WAS GONE... knocked u off your feet and u want a cool.. quiet / silent spot wit no scent... NO MOVEMENT...

I had my first injection of Copaxone on Friday morning and I was unprepared for the stinging that followed which lasted over an hour. I had my second one today and again the stinging was unbearable. Has anyone been on Copaxone injections? Did you have this experience? If so, how did you combat it?...

Hi guys! I’m wondering where everyone’s thoughts are on continuing with your anti-CD20 meds given the world just kind of pretending like Covid no longer exists at this point. Do you plan to continue and just roll the dice with Covid? Switch to another medication? Lock yourself inside your house for ...

So had my appointment with my neurologist to discuss a few things especially how my journey so far on Ocrelizumab so far has been. He said it’s seems that the 3 lesions on my brain have shrunk and they are stable. He is also extremely happy with how the ocrelizumab (infusions) are working. There ...

I am hopeful to the rest of this year being very calm and easy going for everyone ! Whether you are new to this journey or years in !! Feel freee to message me let’s chat !

Rock bottom has called me once again and here I am. Mentally I feel done. Physically I feel done. I don’t know what else can help me right now. Suffering from so many more symptoms will of MS. It’s 1 year since my first ever relapse and official diagnosis. I had an MRI over 5 months ago…still no ...

To my American #EndMS #HelpFindACure family, yes I'm from Canada but unlike @Bernie sanders will have you believe that the healthcare system in Canada is really good. I barely eat anything literally one meal every 2-3 days a week. There are medications that I can't afford. My MS is almost at the sta...