I was diagnosed 20 years ago! My son was 9 years old and daughter was 4! I sat them down and told them the truth. Their grandma (my mother) had Multiple sclerosis at the time so they knew a little about it! Now I am 54 and on Tecfidera (it is just right).
Shift.ms is more than just an MS forum.
Whether you're looking for advice about living with multiple sclerosis, information about symptoms or just someone to talk to who gets it, you've come to the right place.
A short film following one woman's adjustment to the invisible side of multiple sclerosis.
Hi anybody can recommend something good for spasciticy? My legs go crazy at night. Gabapentin is useless…
Has anyone heard of ‘MS burn out’, ? My neurologist thought that this was where I was at, about 2 years ago. Whereby the patient doesn’t get worse NOR become any better, just remaining as you are. Here I’ve found although having to go private (cos going public is an absolute…
Hi I am new to this. Diagnosed with RRMS 2 years ago. One relapse so far. I guess I just don’t know what I feel. Petrified of the future, angry that it was me but almost free in a way. Does that sound weird? Life priorities completely changed so I don’t worry about the little things an…
Is there anything promising in researches? To get us cured.. https://msra.org.au/news/
And, you probably thought it was all bad news………… https://patient.info/health/dyspareunia-pain-having-sex/features/sex-toys-health-benefits-for-women-men
Hi all, I’m new on here. Just been diagnosed with relapsing remitting MS and have decided to go with Tecfidera medication which j will be starting in the next few weeks. Any advice you can give me that I need to know in the first few weeks/months. Thanks in advance
I have refused to even accept my ms after being diagnosed for 15 years , its now grabbed me and put me down and unable to do anything for myself , I can’t accept this and I’m struggling , please help xx
Am new here but just wanna get some stuff out there to fellow m.s.ers! I was diagnosed with The Beast in 2013, 6 weeks after taking voluntary redundancy from a great job rather than move my then family to Puerto Rico, a BIG hit of m.s! Spent 4 months in hospital with it, came out in a wheelchair, …
Hi, I have been advised to change meds as they are not working as well as they could. Please could people give me their experience of Ocrelizumad (Ocrevus), Cladribine (Mavenclad) and Alemtuzumab (Lemtrada). These are the ones ive been told to check out. Many thanks.
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