I bring all the lovely questions to the table don’t I 🙈 am really struggling with going was given tablets and an orange powder to drink mixed with water non of it’s work eating quite healthy so having fibers and fruits
Hi,
I've not been here for ages because it wasn't good for my mental health. I just really needed a safe space to vent. I'm on the maximum dose of Sertraline at the moment but I don't feel that it's helping enough.
I was diagnosed with RRMS in December 2022 and my life has completey changed sin...
Hi
I thought I would introduce myself
Firstly, thank you for letting me in to your community
I have not yet been diagnosed but I have been referred to a MS specialist team by my neurologist due to having legions in both my spinal cord and brain, as well as fatigue, PEM,memory issues, spasticity in...
I felt numbness and pain in my hand, turns out it was ms. This was a few days ago. I have been told by my doctor that these days people can live relatively normal lives and that I don’t have to necessarily loose my mobility or cognitive functions. Still, I wanted to ask, what has been your experienc...
Has anyone had a change in career, or studied to do something different.
I am interested in going into mental health or funeral care . Not sure whether it would be MS friendly
I was diagnosed at 21, been 10 years now, I’ve been in remission for about 7 years now, and I’ve only ever had relapse while not on treatmen, so I am glad to say my treatment (Ocrevus) is working!
What is the longest you guys have been in remission?
I do occasionally have fears of relapses but ...
Hello, my name is Phillip and I’m new here at this site. A 63 yo male and have been suffering from MS symptoms serious since the 80’s. I blew them off for years, then in 2004 the symptoms started to increase. The would hit all of the sudden and then disappear for a while. First it was muscle cramps...
I was initially told I had a b12 deficiency and treated for that, no improvement of symptoms but I’m in a b12 deficiency group on Facebook and people in the group say I was never efficiently treated (every other day for two weeks and then moved to every 3 months, apparently injections should be ever...