Looking for
something specific?

Update it has now started to go hot and cold? Like a slight burning sensation but not painful, nurse said it sounds like a new symptom 🤔 but I start my Plegridy for the first time Monday 😊 Good afternoon everyone 😊 I don't know if what I'm experiencing is a ms hug? I woke up and the right s...

Just want to vent really as It’s all so new and I have no one to relate to! My story starts with Lhermitte’s sign out of the blue from the 1st September 2024, it was initially so intense and every time I looked down. I also noticed deteriorating vision at the same time which lead to a stronger gla...

This will be my 2nd relapse in 4 months and I didn’t expect another for a while as from as far as I know it’s on average twice a year but I had optic neuritis in July and I believe I also had one in March which caused unbelievably bad vertigo. Woke up this morning to my left leg unable to feel any t...

1 month since diagnosis after years of supposed migraines, 2 months since methylprednisolone....so much stress from universal credit basically calling me a liar and it all starts again.... Another 5 day course of methylprednisolone, still no contact returned from ms nurse or dmt information and this...

Hello, I have ms and under treatment with ocrevus. I’ve just got a question. I was abroad recently on summer holiday and caught a cold. I had a fever was doing really poorly for two days and then started becoming better. However my horrible cough has stayed and I’m constantly brining up phlegm. The ...

I was diagnosed in June with RRMS after starting symptoms in Sept 2022. I'm trying to come to terms with my new normal. I'm struggling to return to work after being off since April. Today I went on site and trying to be mindful to not push it I used a mobility scooter for an outdoors meeting (the si...

I’m not one to normally talk about this, and I’m not sure why I am typing this in here. But do any of you get so down you really can’t think of 10 reasons to carry on? Me feeling like this isn’t new, I’m in my mid 50s and have had these feeling on and off since childhood. Long before MS. Not sure...

Came down with cold/flu. Plus side not covid… however the fatigue is scary 🫣 is this normal. It feels like my body isn’t waking up and moving in slow motion.

I have the 7-Day pack of steroids what do you all take when you have MS flare-ups it's over 100° here in SoCal for a few days. Heat and recent stress kind of took me down

… this is just a rant! ‘Cause I’m so fed up with having MS. I just can’t believe that there is STILL no cure!! And I’m bored hearing that there’s so many good treatments now. Not that good, I say, since I’m in pain every second of the day. And I think lots of you are too. So that sucks!! I can’t run...