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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 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...

Still in the throes of diagnosis. I was prescribed Baclofen for my left leg but reacted badly including losing all balance and having double vision. Then moved to Gabapentin. My left leg has now swollen and I cannot wear my trousers let alone shoes... What next? Your experience please…

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. ...

Hey all, I have just been diagnosed with very early RRMS. It hasn't really affected me physically as of yet but I keep getting adverts on my social media about thinking about life insurance. It is also all targeted at MS. My question to all of you is do you think it is something I should look int...

mentioning @will_berard tagging #diagnosis

I have had MS for years -diagnosed 1999. My husband has Parkinsons Disease. It’s so hard to cope - I try to be positive - he is always negative! Any advice?

I've had depression since I was a teenager. Now, finally diagnosed with MS, last year, I will get to look forward to when I can no longer fend for myself. Hasn't happened yet. Fortunately, I have worked since I was in highschool. I know that after 35+ years of taxes paid, I am now an elder. I deserv...