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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...

I'm not doing good today. I've been crying all night & day. I'm tired of suffering. Now what I'm about to ask is a VERY VERY SERIOUS QUESTION. Once an animal is sick & would need medication for the rest of their lives more often than not it's better to put said animal down because it's a matter of q...

When I get depressed bc of the #EndMS. I like to listen to well most of the time it's speed medal & if not that the complete opposite of that & it's Pink Floyd. I love Pink Floyd because I was lucky enough to see them live.

I've been struggling with my MS, I've been stuck in bed worrying about how I'm going to go to the hospital and have my ankle checked bc I lost the use of my ankle completely & if I'm forced to move the only person I have to help me with everything is my 22yr old daughter who lives with me & pays ren...

When I get depressed bc of the #EndMS. I like to listen to well most of the time it's speed medal & if not that the complete opposite of that & it's Pink Floyd. I love Pink Floyd because I was lucky enough to see them live.

Welcome to this platform for people living with #EndMS #HelpFindACure #MultipleSclerosis & those who have a family member who has #EndMS. I've been on here for a few days & I feel welcome & it's nice to be able to reach out to people who understand. Hello friend. 👋👋👋

Hi Everyone! First of all, if you wish to read in Spanish please scroll down! Now we can begin... I really thought what my first post should be about. I start writing about having MS in Latin America, about my journey with MS this past 10 years or even what my diagnosis was like. Finally, I be...

Hi everyone! The MS society here in Canada has recently launched a new campaign and website (www.endms.ca) that a good friend of mine is a part of. I just wanted to share one of the ad's with everyone here because I think it's a pretty great one! While it is centred around Canada, I thought some o...

When you know you have been burning the candle at both ends and it’s come back to bite you and now your out of action an no legs and keeps falling everywhere An can’t get up..... thank you ms!!!

In case it's of interest to anyone, here's my diary of a first Ocrevus infusion. The day before, I was advised to drink a lot of water. Being hydrated helps the nurses find a vein. Got there at 8:20 for an 8:30 appointment, and was ushered straight through to a comfy chair. My blood pressure, hear...

I have been self employed for 13 years but I am currently down from working with dozens of clients to only two and one of those contracts ends on 1st April. I feel so sad about the thought of giving up, but I work alone and when I am unable to work then there is no one else there to do the work. I ...

Hello all, just wondering if anyone has had anything like this. I've had pretty severe symptoms since my diagnosis which made doing my job as a QC Lab manager for a chemical manufacturer pretty hard. The company offered me a different full time permanent job, more office based, less time critical wo...

Hello all, I’m recently diagnosed with MS, it’s a bit of a relief to get a diagnosis if I’m honest. It ties up a few strange loose ends and means I don’t have prostate cancer or a brain tumour! I have had several MRIs, second one was brain and spine with dye and it was after that that I got my f...

So, I was in the hospital for 5 days due to terrible stomach pains and digestive issues back in August 2022 after my first episode ever on April 27th, 2022, which was after I slowly developed diplopia aka double vision through December of 2021 which have worsened throughout this past year. Am I losi...

For the last couple of weeks I've felt like I have spiders crawling all over my face and head :( its driving me bonkers!!!!!!! I can't scratch it though as it feels like my skin is really badly sunburned, even the ends on my fingers are sore....has anyone else had this?!

Hi all. I'm new to the platform so firstly, it's nice to 'meet' you all. I was diagnosed in October 2016 with RRMS and I started Lemtrada in December of the same year. After recovering from the second round, I hit the gym hard, and I was at my lifetime peak of fitness before a major crash in marc...

My wife has ms. I am worried about the future. We have no one to rely on. I have mobility issues my self. I bought a stair chair for our basement we’re the washer and dryer are but now it’s not working . My wife is tired and sleeps a lot I work 10 hours a day 5 days a week to make ends meet best as ...

My wife has ms. I am worried about the future. We have no one to rely on. I have mobility issues my self. I bought a stair chair for our basement we’re the washer and dryer are but now it’s not working . My wife is tired and sleeps a lot I work 10 hours a day 5 days a week to make ends meet best as ...

Diagnosed April 2022 Everyday a different challenge. Fatigue though is the worst. Day ends around 130pm. I struggle cognitively and no knows I have it. Need a nap in the afternoon/early evening. Keeping up a front constantly.

I’ve always had itchy skin but the last couple of weeks I’ve had a constant itchy stomach like none stop. Today has been the very worst for it. Feel at my ends due to the discomfort. Does anyone have any advice on what I can try and do to ease it?!