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Hi everyone, I know that it just isn't possible to stay positive all the time in the face of MS, and we shouldn't be expected to, sometimes it's tough and we just need to let ourselves feel how we do in that moment. BUT I would really love it if from time to time we could all share something that w...

Here's somebody aiming to raise megabucks for MS through shift, the MS Society and the MS Trust. His efforts look really impressive (check out the link bit.ly/MS3SDW) I think he deserves all the support we can give him...

It touches home as I am a 45 years old female with very aggressive Multiple Sclerosis that does stand up comedy. Ms has negatively impacted my life in so many ways, but I gotta say that it has made me stronger and a better person in a lot of ways. I feel so happy and excited to see myself recover fr...

My doctor told me that I have dormant multiple sclerosis meaning that I have the gray areas in my head and most of the symptoms but not the bands in my spine. My question is : is it normal to have symptoms for years before a real diagnosis? My dr told me that dormant ms isn’t a real diagnosis. So as...

Hi friends. It's been a while since I posted so I'll give you a quick run down. I went off all ms meds in sept of last year due to having a 1 in 100 chance of contracting PML. Then in december I had a flair up that had me in bed until march. It was horrific to say the least. So in march I started my...

Just went to the dentist and saw the dental hygienist. She asked if anything had changed with my health so I mentioned being recently diagnosed with MS. She didn't say anything. AT ALL. For 30 minutes until the appointment was over at which point she launched into a talk on functional medicine and t...

Hello everyone, I've headache which last for a long time. Painkillers can not do anything with it. I really suffer much sometimes like now I do. Does anyone have the same problem and what do you do for coping with it?

Hi to my old friend! That is SHIFT MS! - Not you, well it could be? I guess a stranger is a friend you just haven't met just yet! I was speaking to my OT via video call at hospital during this crazy and unusual time. She suggested going on SHIFT MS and it is a website I joined several years ago and...

Hello I hope everyone is doing well ! I was just wondering if anyone else has experienced hard lumps under the skin !? I spoke to my GP and he told me it could be a cyst or my lymph nodes and I think it is my lymph nodes. Does anyone know how this correlates with Ms ?

Are there any others of the LGBT community who are members of ShiftMS interested in forming a separate support sub group away from the usual heteronormative? Me thinks MS affects our LGBT lifestyle in so many different ways so wold be good to share experiences