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Love that ms nurse says oh I respond to emails faster... Last time I got no response at all. This time well I'm 4days in not holding much luck. Guess I'll phone tomorrow and see. Legs been giving out multiple times a day for almost three weeks now. Plenty of bruises have been collected and pulled m...

I know I have sensitive ears, for example I don't like watching things too loud. Other people moan it's too quiet for them to hear at the level I watch stuff. I used to get it every now n then when the TV is too loud or people are rasing their voices. It feels like the thin part of your inner ear i...

Hi all, I am 22 and was diagnosed with rrms in July after an attack in May. I’ve just started a dmd. Still have some symptoms - fatigue, feeling faint and I overheat quickly. My managers know, but they just don’t get it. My job is so fast-paced and they still think I can do anything and everything...

I did it. I finished my 5 day 100 mile (160km) unsupported walk of the South Downs Way in 4 days. It was s big push and I as completely broken now. Yesterday was a 51km 13 hour day and I made Eastbourne by 2030h. I promptly demolished a massive fish supper. You may not be able to afford to donat...

Ik on more than 1 med for MS my legs and arms get very heavy. I have a baclofen pump inside of me don't think it helps much. Heat and cold sensitive. Hard time walking gaining weight do to gabapentin and lack of ability to exercise. Sound familiar? Any suggestions?? Any would be appreciated

Hi I am Sarah. Diagnosed with ms in 2012. Over the past few weeks I seem to have got really weak legs that has starting going heavy and giving way after about 5 minutes of walking. I was wondering if anyone had any advice on the best way to tackle this as I want to be able to live my normal life....

My name is Ana. I was diagnosed with MS relapsing remmiting type in 2015. The onset of my MS started in 2011 but I didn't know it. I was diagnosed first with severe Anxiety/Depressive disorder with Panic attacks. I am in constant nerve pain, numbness, spascisity and other symptoms. The evenings are...

Hello! I’ve been told today how amazingly positive this site is and I can already see from just having a little nose it’s just what I need! I was diagnosed 3 weeks ago, shock probably was an understatement. I haven’t googled anything really, just had conversations with the Neurologist and my nurse. ...

Hi all. So, I know, a couple of weeks ago, I had an MDT DMT meeting, discussing my medication and recent relapses and new lesions. Still not received a letter from them, but I know that it can take a couple of weeks. However, a nurse from my MS team called me today, telling me that they'll be booki...