Hi, New to this site so hopeful of a good response. I have Relapsing Remitting MS although I don’t see too much of the Remitting part. I am a positive person day to day so posting anything remotely negative is hard for me but I realise I need some perspective now any any comments will be gratef…
Shift.ms is more than just an MS forum.
Whether you're looking for advice about living with multiple sclerosis, information about symptoms or just someone to talk to who gets it, you've come to the right place.
A short film following one woman's adjustment to the invisible side of multiple sclerosis.
Just wondering if people get muscle twitching / pulsating after exercise or long walks? I’m presuming it’s an MS thing
Hi all just joined this forum hopeing for advice basically I received my first round of lemtrada in March 19 what I would like to know is if the pre-existing symthtoms get better mine are left leg weakness and balance problems. Thanks for reading 😀
Hey there… recently diagnosed with Primary Progressive MS… don’t really know what I was expecting support wise but so far… just kind of feel alone
I’m so sorry for such an angry post but I need to rant and there is no one at home (even the bloody dog has gone out for the day!) I contact DVLA in March when my diagnosis was confirmed. Filled the 5 page report in as much as I could, sent it off. I then received a letter saying they were contac…
Has anyone does an NHS fatigue management course? I’m starting one next week and wondered what people’s experiences of it have been like
I never thought that loneliness could have gotten worse but then i was diagnosed with MS in 2016. I have had 4 boyfriends breakup with me because of it. Stated tbey can not handle the changes. I have alsways been up front and honest with men when dating but dating in it self is hell. It’s har…
I’m really hesitant to post since every other MS forum I have been on I have felt ignored. Just like real life! I’m generally ok mentally about having MS, but I have trouble managing my symptoms. I have been dealing with depression and anxiety most of my life to begin with, and I get ve…
Well as you all know I wanted to see my neurologist on Friday and I told him the truth He kept me on 3mg Klonopin three times a day and he said stop drinking he left all the other medication the same except the Copaxone own he’s taking me off of and he wants to try me on tecfidera, I believe…
Ms took my vision last week im battling severe depression and suicidal thoughts im throwing in the towel this disease can take me away now im done fighting a battle i can’t win
End of content
No more pages to load