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I have an odd few questions about starting treatment shortly as im just waiting on delivery notice for tecfidera. I have RRMS, im not sure if im over thinking everything but hopefully you guys could share some light lol So when you start treatment/on are you more proun to getting ill as i heard y...

Hey everyone 👋 I wanted to share some amazing interviews we did with Shift.ms members about their MS symptoms and how it affect their day-to-day lives. I found these mega useful when I first joined here so I thought I’d reshare them :) Check the videos out below👇 • Grace on sensory Issues - ht...

I just finished my second round of Lemtrada. I feel is working so far. I am having the usual problems that others have, fatigue and brain fog being the worst. please feel free to share about the subjects listed below. I am new to this posting so I haven’t figured out how to put the topics ...

Hi all I live in Northern Ireland am 40 years old and had a stroke 2 years ago. I have had many symptoms since which a close friend now believes to be MS. I'm worried about going to doctor. My symptoms on and off consist of chronic fatigue, spasms in my legs, tingling and weakness in both hands, bla...

I'm just watching this on Stephs packed lunch, as we all know MS is a disability, It struck a chord with me because we deserve affection and intimacy. Things are hard enough. Question is for single people but people in relatioships can answer (I don't discriminate) people would you use this service...

I hope I am not alone with this problem but need advice has anybody tried viagra for women my sister told me it's a thing I can try to get my mojo back my husband is so caring and understanding about my complete lack of lust but I actually really miss the intimacy I love my husband so much and he i...

I’m really struggling with touch, my tactile sensations drive me crazy . Does any one have this and also it affects my intimacy and my partner wants to see someone and as this is private I’ve had to ask as having Ms has always lowered my sex drive and now after my transplant (Hsct) I feel it’s worse...

Hi guys, I would be grateful for any advice about being in a relationship while having MS. I have been with my partner for 2 years now, and I was diagnosed 10 months into the relationship starting. He has (and still is) very supportive overall and will bend over backwards to take care for me, bu...

So nobody else to really tell if I'm honest. I've been taking Tecfidera240mg for the bestter part of a month, no real issues apart from stomach cramps and headaches... All very manageable. Spoke to my MS nurse who said I should eat more to improve my fatigue issues, took the advice and what's the fi...