At first I just thought it was my ongoing MS symptoms but the pain and burning is now unbearable, might just contact my neurologist before my next appointment which is in a few weeks time.
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Just wondering ,has anyone travel while taking meds? I am taking Teriflunomide tablets and want to do some traveling . I have double checked if I can have the meds in the country I want to go to . But I more thinking like the touristy part. Like the all the walks or hiking.
Hi would like to chat with others who have secondary progressive 😊
Seem to be posting a lot recently but it’s on my brain.. has anyone got any positive stories of living with ms? Everything is so doom and gloom has anyone had the condition say for 20 years with little progression? I think everyone needs some positivity
hello! My name’s Jean I don’t follow western medicine I try to be the healthiest I can with my Molecular enhancer that I have had for 20 years I stick with wahls protocols the best I can and I’ve had MS for 40years. I have been paralyzed for the last 25 years. Not much gets in my …
Hi I’m Nora. I was diagnosed at the age of 19 was told I had it since I was 15 and now I’m 47. So that makes 28 years diagnosed. I have Relapsing Remitting MS. Started with Avonex then Rebif and ended with Copaxone. I am currently not on any MS meds. But I will be looking into getting o…
Hello everyone how are you all doing? I haven’t been on here for ages! So just catching up on the forum with a cheeky glass of wine. Why not it’s the weekend! So my last post was about me stopping treatment (tecfidera) which still remains. I haven’t had any flare ups (touch wood)…
I’m not sure anyone can answer. Lately I’ve been having a new symptom where it feels like cold water is running down the inside of my right ankle. I’m not worried, I know it’s just a part of MS, but I’ve always wondered, when symptoms happen like that, what is going on…
I am excited because my wife and I just started an MS support group for us with MS and their caregivers. We are just trying to help greate another safe place to share and communicate. Come che k it out. We are all here to support each other. https://www.facebook.com/groups/411184656403843/
Hello Everyone!👋, My name is Audrey, and through the years I’ve been on a few social support sites. I haven’t posted about my MS or been on a support site in many many years, though. I’ve been officially diagnosed with MS since Nov., 2009 (bout of O.N.). My mother was diagno…
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