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This frase breaks my heart a little bit everytime someone I know that I know they love me, says it to me. I can see they are trying their best to adapt and change their life to help me but when they say it they do it because they want to see me healthy... Feels like a lot of pressure I'm so luck...

it’s been rough since the diagnosis. My relationship ended because of it, even if it wasn’t the only reason. A lot of little things stacked up, but when things got tough, she left. Just moved out over the weekend let her keep the apartment. I’ve been trying to reach out to the MS community, see if I...

I’ve got my first appt tomorrow with the MS nurse, I’ve read up on DMTs and pretty much made my decision. I’m happy to hear what my neurologist recommends based on his meeting with the MS MDT I’ve got a list of questions and a list of symptoms but my main question is - when can I start treatment! ...

Has anyone else found it very difficult to get help from the Ocrevus Patient Support Program? Here in Canada it is called Compass (not sure if it is the same elsewhere). My provincial health approved me for Ocrevus months ago. At first there was a delay to getting my blood work done but I got the d...

I've been diagnosed now for a couple of years but I keep going into these random feelings off been down want to cry, feel angry, worry feel like I'm stuck in a hole but it comes and goes...but my life is as good as it can be beautiful children lovely supportive partner but I keep having these moment...

They didn’t catch a virus. They caught MS. It started with a tingle. Then came the mysterious fatigue no one took seriously. By 28 days in, society hadn’t collapsed but a concerning number of people were falling over for no reason, losing feeling in random limbs, and quietly Googling “why does my e...

Dom AKA ‘The MS Guide’ has taken on the challenge of a lifetime, cycling 8,000km across Canada to raise $1m for global brain health. He’s even donating a portion of the money to Shift.ms, to enable us to further our support services. Why is Dom doing this? Having lived for 33 years with MS, Dom e...

I had a CT scan today and when I had to get on top of the bed it was very hard and I even couldn’t push myself up. I just felt so weak. I My support worker had to just push me slightly up. Just reminds me how weak I’ve become. Just wanted to share.

Living with Multiple Sclerosis (MS) felt like carrying an invisible weight every single day. The fatigue, the brain fog, the flare ups I had tried countless treatments over the years, but nothing brought lasting relief. I was exhausted, emotionally drained, and losing hope.Then I discovered NaturePa...

I’m still learning lol even how to properly post on here 🙃