Sort 3569 results by

@Malvina11 

Last reply

Malvina11

After living with MS for over 23 ye.I’m looking for PA. Any ideas?

Dearest All I would very much appreciate if could give me an advice of how to find a part time PA for myself. Thank you! With my kindest regards Elena
Worsley, United Kingdom

RV Living with MS

Does anyone here live in an RV full-time with MS? If so, where do you live? My husband and I looked at an RV the other day as an alternative home because the housing prices are so high but the salesman told us that it may not work for us because the AC only will get it down to 20° cooler than the am...

@Shaa8766 

EditedLast reply

Shaa8766

Newbie living with MS

Hey guys! I’m new here. So one day, I woke up with slurred speech, my tongue was going sideways, the left side of my face felt icy and numb, and I was so exhausted. I went through a couple of long steps but I found out last month that I have MS; after a brain MRI with contrast. I had multiple white ...

My Super Power while living with MS-Falling Asleep Quickly

I have the ability to fall asleep really quickly. I used to lie in bed dwelling on the day; the stresses; What I could of done differently; The consequences of my actions; and What the possible outcomes will be for the next day. After living with MS "officially" since 2001, I have established to ...
Castle Rock, United States

@Caitlinb22 

Last reply

Caitlinb22

How having living with MS affected you?

How has living with Multiple Sclerosis affected yourself and the people around you? My name is Caitlin Bird, and I am a final year BSc Psychology degree student at the University of East London. My brother was diagnosed with MS 3 years ago and seeing how it has affected him physically, psychological...
Scheduled

@Shiftms 

EditedScheduled for

Shiftms

Feelings of safety as a member of society living with MS

Happy Saturday Shift.ms community 👋 We want to hear from you about your feelings of safety as a member of society living with MS. Do you feel like you are treated with the same respect and understanding as those without the disease? Have you ever experienced discrimination or stigma because of you...

@Shiftms 

Edited

Shiftms

Which aspect of living with MS is misunderstood by others the most?

Hey Shift.ms community 👋 Is it the physical symptoms, the emotional impact, the treatment options, or something else entirely? How have you found yourself having to educate people about your experience with MS, and what do you wish more people knew about the disease? Your insights and experiences ...

@DominicS 

Edited

DominicS

Dr Dan has MS. Hear his 5 tips for living with MS.

This Sunday at 5pm GMT on theMSguide.com (a YouTube channel) Dr Matterson shares his strategies to live with MS. If you subscribe to the channel and ring the bell you'll always be notified every time a new video is released. Follow Dan on Instagram @the.ms.doctor https://youtu.be/Ol8oQ6sFF-8

Living with M.S

Hi All My name is David and I'm from Mid Wales. I have had M.S since 1999 first symptoms were double vision had my M.S confirmed by an MRI scan and lumbar puncture had a really bad relapse in 2003 just before I started on Rebif injections, the relapse affected my Right hand side of my body but stil...

@Graham1972 

Last reply

Graham1972

50 years old living with MS

Hello, this is my first post on this website so here goes, had symptoms in my late 20's, it was just heavy legs as if I was walking through treacle. Wasn't nice at all so went to doctors and was told it was just age. Being absolutely flabbergasted by such a ludicrous diagnoses I went to see a differ...