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Hi I was sent email about having MS buddy today which I would love to happen as recently been diagnosed and waiting to see neurologist. I’m have 404 error. Can someone help x Thanks K x

Neuropsychologist Jo Johnson & is LIVE right now with MSer Gemma, who are speaking about mental health & MS. Watch & ask your questions here ➡️ https://www.facebook.com/shift.ms/videos/1564035427092929/?v=1564035427092929&notif_id=1590158895499563&notif_t=live_video

Over the past 15 years or so I have taken a host of drugs (ending with ‘in’) without success. Even the last course of lidocaine infusions failed to have the same affect that they originally did. The pain management consultant informed me that the only other way to go was Morphine patches. My GP was...

Hi all, Got a text message from my local doctors to see if I want a pneumonia vaccine, just wondered if any other msers have had this?

I've had symptoms for the past 8 years but was only officially diagnosed in February. I thought I was handling it ok - wasn't looking to change anything I'd been doing just maybe not push myself as hard - then Covid-19 hit. Again was ok at the start but now my fatigue is hitting me earlier and earli...

Hi. I was asked yesterday to document my idea of 'My Perfect Day'. I started to write...my perfect day certainly didn't include MS but my reality is that everyday includes something about MS. I'm tired, I'm sore and I don't want to play MS anymore. So back to my narrative. For every few sentences I...

Finding a way to get the human nervous system to grow back the myelin, the nerve covering that MS attacks and causes the symptoms, be they minor or major, we all experience is the next huge hurdle. - I link to a total science paper here: https://www.cell.com/cell-reports/pdf/S2211-1247(20)30611-2.pd...

📢 Calling all US-based MSers 📢 Do you live in the US? Fancy helping Shift.ms with something? We have a new volunteer role available that is based around the US MS community. If you're interested please email sophie@shift.ms today 📨 Thank you.

I am one of those people who has all MS symptoms, but especially loss of eyesight. Anyhow I got a jpb. mostly home work, translation, etc. I told them I have MS but did not tell them I am registered blind. I have done this job for about 4 months. In face to face situations I can fake it, and mostly...

I am look for something that I can do that will help me to not feel so worthless. ( I am67 years old and my ms Has me confined to a wheelchair. I was dx in 1981)