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Hi All, I was diagnosed November 2019 with RRMS. I was put on Rebif which the only complaint i have is the red marks it leaves but would have happily gone on with it. Yesterday i met with a new neurologist after my previous one had left. I had an MRI in advance and there was one small new very sma...

Hi- with Covid really just passing through my area I have restarted my PT. I left off in December when they shut down. He left me with some good exercise options and I tried some of the other options so readily available on-line. The good news is that I think I have been able to maintain strength p...

Need some advice please guys. Has anyone else lost their ability to urinate following an excessive hospital stay due to a physical trauma. Recently I broke my femur so was hospitalised. Whilst in hospital, I was urinating via a long term catheter. My bladder had gone into retention caused by the tra...

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...

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....

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...

I don't feel good....My left leg has been having spasms all day, my right hand and arm is acking and I'm feeling depressed about all of it. I don't want to go to the hospital with all covic 19 going on....so what do I do...just be in pain? Signed I'm really just over the whole Multiple Sclerosis...S...

Does anyone else experience bruising easy or not remembering where bruises came from. I find bruises all the time and have no idea where they have came from. Could it be ms or my meds, I recently started tecfidera.