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Just received result of annual MRI of brain and CSP. Quick recap is diagnosed w MS 1998. No DMT or identifiable symptoms until 2017, been on copaxone for 3 years. Most recent MRI says new lesion r fr lobe, and a Highlighting peri ventricular lesion which is also new. I’m feeling a bit alarmed! I ...

Hi im new to all this, i got diagnosed with MS last year and have just tried my best to carry on. I have had many of the symptoms for years and a rather big relapse but didn't seem understood back then lots of different tests. In the end just carried on dealing with it all, then i got optic neuritis...

Hi all, hope everyone is doing ok Slightly confusing situation here: i got diagnosed with RRMS in 2018. I had a brain and neck/spine MRI and my brain looked normal but i had 3 lesions on my C spine which accounted for my symptoms. Fast forward to a few a weeks ago and my neuro sent me for another MR...

Hi was just diagnosed with MS, but going back on the last few years it has affected much longer than just finding out now. My brother has lived with MS for over 40 years. So MS is nothing new to me except learning to live with it myself now, one day at a time. Thanks and take care folks

Just saying Hi... just joined. Was diagnoised with RRMS last year... live in the Uk hope to have some good chats nad get some help and advise 🙂

Hi all, I'm new to this site. I feel a slight veteran as I was diagnosed in 1992 aged 20 ( 1st episode aged 15) so have lived with it all my adult life, I'm now 48! so if I can help with anything please ask!

Hi all New to the site. Been given 3 options for treatment and I am siding with Rebif as we are thinking of starting a family soon. What’s people’s thoughts on it? So much information to take it. I’m feeling very confused and overwhelmed. Got diagnosed about 3 weeks ago. Thanks in advance Lucy

At this point I have to just laugh. I was in hospital last week, was diagnosed with MS. Discharged last Friday, put on steroids while in hospital, symptoms cleared up by Tuesday and I woke up this morning with a very, heavy arm with horrible cramps and pins and needles. Tried to contact enable but n...

Hi folks. I was diagnosed with MS 2018. I've recently retired on health grounds and have just been granted PIP which is a great help. I'm very reluctant to visit anywhere where I dont know where the nearest loo is. Nightmare in the current climate !!! (covid19) Mobility is a problem re walking and b...

Hi, first post. I was diagnosed almost 7 years ago, in 2013. Initially, I was diagnosed with PPMS, this was changed to RRMS a year later after a big relapse that made it difficult to speak and walk. Almost straight away, I was put on Baclofen and began 2 years of Tysabri. Eventually, I was able to w...