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How are all the ms warriors today hope ye all had a good week

I’ve had numbness in the soles of my feet for a while now. Any tips for helping with this? My neuro physio has also identified something called hyperreflexia (a bit wobbly when going from sitting to standing and vice versa) Any help would be much appreciated and sending all the positivity to all yo...

Hello all, I’ve had numb feet since a relapse last year. Any tips for helping with this? It’s affecting my balance alongside hyperreflexia (wobbly when going from sitting to standing) Any help much appreciated and sending all the positive vibes to all you MS warriors

How are all ye strongl ms warriors doing today I have say it's a bad day not bad life even do it has its complaints

If you’re struggling, just remember we are at civil war with our ms, so don’t let your ms win!! #mswarriors

After diagnosis last January and my neurologist not perpepared to identify my sub type although he says it more than likely PPMS. I've decided to take the bull by horns and go for HSCT in Mexico in November. EDSS currently 3.5. I know Dr Burt and NHS health experts do not recommend HSCT for PPMS a...

I am a MS Sufferer of whom been diagnosed for over 10 years as some of my fellow warriors of whom gave me some sound advice advice bless you all . I have been noticing some alarming patterns with my MS team firstly I don't think I have a MS team the reason I feel that is because the do not respond w...

Hey everyone! 🌟 Just wanted to share a little bit about my journey with MS. Despite the challenges, I've come to see it as my very own superpower. It's a reminder that staying positive and resilient can truly make a difference. Let's keep pushing forward, supporting each other, and spreading hope. ...

looking for a good connection with people who understands this condition