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Hey everyone, I’m wondering if anyone could pass on any advice or information for something like counselling surrounding living with MS? 😌 I’ve recently been diagnosed and I’m having a tough time coping with the bizarre symptoms that seem to just keep snowballing. I don’t feel like I’m strugglin...

Welcome to my life for the next 10 months. Follow theMSguide.com to see my training, the ups, the downs, the trip and for all the fundraising details to follow. “In May 2025, Dominic, who has been living with Multiple Sclerosis (MS) for 33 years and has taken five different Disease-Modifying Thera...

Hello, I’m new here😃 I’m Callan and Im from Scotland. I have suffered with health issues mainly chronic pain since I was 15/16 years old. I was told I had fibromyalgia even when my symptoms worsened and I got more new bizarre symptoms I was reassured it was fibromyalgia and told to ‘stop searching...

Hello all, I know that talking about long term prognosis with ms is like asking how long a piece of string is, but I'm going to try and pick your collective brains anyway! I was diagnosed at 16 years old (rrns) and my ms probably started when I was 14 or so. I am 39 next month and although my ms i...

Hi team, I hope everyone is well today! 🤞🏻 I'm so excited and just had to share; I've just finished the 4 week trial of Fampyra and had my assessed walk earlier. I HALVED the time it took me to walk 25ft in the initial assessment, and haven't stopped crying since! 😭🤣 I really needed this toda...

Hello again, So since its the back to school season, & I meet lots of parents & kids, Ive just got a viral respiratory infection, a rough cough with mucus, flu & some fever. The dr said that the Tysabri im taking suppresses my immunity, so whatever disease I get, I need to take extra medicine, & ex...

Is anyone else having a really hard time with trying to do better health wise. After my diagnosis of RRMS I got so depressed. It seems like I cannot find even an ounce of motivation to get me to eat better or exercise. I just don’t even understand. With everything else I have to deal with, kids, inj...

Sorry for another moan but I feel like absolute crap since my 2nd half dose infusion on Monday. I feel so flat, fatigued, fuzzy headed, my spatial awareness is none existent and I’ve fell over and almost fell off the steps to my house, my right arm is aching and can barely feel from it or do anythin...

I’m fortunate that we have space to build an extension for wheelchair accessible ground floor living. If anyone else has done this are there any tips or suggestions to make it work best?

Came down with cold/flu. Plus side not covid… however the fatigue is scary 🫣 is this normal. It feels like my body isn’t waking up and moving in slow motion.