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Ugg! The summer heat has finally arrived here and my limbs are almost useless. Flopping around like a fish out of water. Wish it would rain... gasp, ugg, gnhhh (that last one is when I get up and do something).

Hey guys I’m in need of urgent help! I’ve had extreme bloating and abdominal discomfort for as long as I can remember ! The doctors have ran all the tests and don’t know what’s wrong :( I was wondering if anyone follows a certain diet that might help with this because I have a feeling it’s connected...

From MS Society With shielding set to be paused in all four nations of the UK in August, we want the UK Government to support people with MS who can’t safely go back to work. We’re campaigning with Age UK, the Trade Union Congress (TUC) and 9 other charities. Together, we’re calling for the furlou...

hi guys I've been diagnosed for many years thinking they were wrong , but over the last 2 years o.m.g I should of listened ive gone from rrms to spms since I lost my dad and anti social behaviour from my neighbours ive had to give in and think shit they was right ive 4 kids 3 under the age of 7 and ...

Hi there, I just finished my 1st cycle of Mavenclad treatment...free now for 4 weeks before the next lot No real side affects...just a little exhausted...more than the usual kind I could feel burning sensation while swallowing the medication..make sure anyone taking this medication has plenty of w...

Hi , I had my first Tysabri infusion on Wednesday . I felt fine after it & just felt a bit tired. I’m feeling a little off balance when I’m walking since yesterday. Just wondering if anyone experienced anything similar after infusion . Thanks

Hi all, I started on copaxone 4 weeks ago. The first two weeks went really well & I had no side effects. Since then every time I have injected I’ve come out in a hot red swollen rash, which has then turned into a hard lump, like a marble (sometimes bigger) in the injection site. Has anyone e...

My doctor told me that I have dormant multiple sclerosis meaning that I have the gray areas in my head and most of the symptoms but not the bands in my spine. My question is : is it normal to have symptoms for years before a real diagnosis? My dr told me that dormant ms isn’t a real diagnosis. So as...

Hi I have had a recent mri identifying inflammation on both spinal cord and brain. I’m seeing neurologist on Friday. Did anyone get a diagnosis with the same mri result? My symptoms are weak left leg, tingling in right hand and poor balance. I also tend to be very sensitive to alcohol.

Has anyone ever heard of lions mane mushrooms? They are suppose to help with brain repair? I've heard that it helps rebuild the myelin sheets. Has anyone else heard anything about it?