Looking for
something specific?

Hey 👋 So after not having success with ocrevus or achthar gel my neuro wants to switch me for now to IV steriods for five days bc of new symptoms. Then I’m also switching to Tysabri. What was your experience with IV steriods? I really didn’t like the steriod taper I was on it made me hyper and p...

For you're first relapse was you given steroids to recover not knowing it was ms?

I’m so sorry for the long post but the relief I feel that I’ve found this app is unreal!! ❤️ So I’m curious if anybody can give me some advice on ways to exercise my feet and leg to help build its strength. In September I had covid which brought on a relapse resulting in optic neuritis. I was given...

This is simply just a random rant, why do I get a nauseating metallic taste in my mouth after treatment?! 🤮😡

Hey there, just stumbling into this world. It all started two weeks ago when I started feeling a little lightheaded, this got more severe and then gained vertigo and double vision. The symptoms happened over the last couple of weeks and ended up bedridden with a car crashing headache when I sit or s...

Has anyone here been put on prednisone ? I was given IV steroids for three days and now have been put on 60 mg prednisone for 10 days and then slowly taper it down over 8 weeks. Just wondering what side effects others have faced ?

A high percentage of Shift.ms users are female, and most of the recommended exercises are yoga, which isn't very masculine. The diet consists of things my food usually eats! What infuriates me the most is the fact that it bloody works too. I hate that part the most. Why can’t the cure be 0.3 IU of ...

It’s been 32 days since my last flare up off my speech from the day it started and have now got the same problems again, I was fine in the morning but my voice changed at work today. I’m on my period and have had a lack of sleep and poorly. I’m so worried that I not going to get the right help becau...

After all the years of different MS therapy drugs, the pills, the shots, the infusions, the pulse steroids what not finally got a neurologist who strictly deals with multiple sclerosis. He did research on maven clad, and I was a test subject, and I got put on maven clad, and I am so glad that he pu...

I had my diagnosis of MS they are needing to do a MRI with contrast to see if it’s “active” or not. Depending on what the results show I’ll either be put on the medication or have treatment when need it for example steroids through a drip to help relieve the symptoms. It affects me every day in some...