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@Teide_Barrett 

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Teide_Barrett

Ocrevus infusions

Hi I’m teide I’m 24 and I have RRMS. I was diagnosed in October 2018.. I spent 1 1/2 years on tecfidera but my ms just kept progressing. I started ocrevus last Tuesday and had my first 1/2 dose.. Tuesday I felt ok! I was surprised how well I felt on Wednesday but since then it’s been horrific! Sle...

@calNFFC 

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calNFFC

pneumonia vaccine?

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?

@pauley 

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pauley

Mavenclad 101

@msers Hi all Happy Friday...or whatever day it really is in this COVID19 black hole. Just looking for some info on Mavenclad as am over due starting...hopefully soon-ish... Any issues, tips,advice...affects Am kinda a virgin mser...only officially dx since april 1st this year...confirmed by neurolo...

Mavenclad 101

@msers Hi all Happy Friday...or whatever day it really is in this COVID19 black hole. Just looking for some info on Mavenclad as am over due starting...hopefully soon-ish... Any issues, tips,advice...affects Am kinda a virgin mser...only officially dx since april 1st this year...confirmed by neurolo...

LIVE mental health Q&A

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

Feeling alone

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...

@Massery 

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Massery

Alone!!

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)

@Sophietest 

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Sophietest

📢 US volunteer opportunity

📢 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.

@DominicS 

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DominicS

Remylenation: The Holy Grail

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...

Type 1 Diabetic & MS Warrior

Hello fellow Warriors! I’m one, like many others, who enjoy a variety of autoimmune afflictions; MS, Type 1 Diabetes, Fibromyalgia, Pernicious Anemia, Hypothyroidism and a bout of Autoimmune Gastritis. As a veteran diabetic (33 years) and an MS’r since 2010, I find that these two impact me the most ...