Trinad 23/04/19Hi all , I am new to this, but just wondering your experiences accessing DMDs. I have had MS for two and a half years, finally diagnosed a year ago , I was originally diagnosed with Clinically isolated Syndrome. I was told last year that I have an 80% chance of getting it full blown within the next…
rayrayjean 19/04/19I know that MS is super complicated to diagnose, but I am just struggling to accept the diagnosis. My first relapse was two years ago with optic neuritis. A few weeks ago was the first notice of two small brain lesions. I got the diagnosis of MS. I met with a specialist and he started doing tests a…
Blackiris_Reed_Lindsey 23/04/19Hello everyone! My name is Mandy. I am new to this site. I will share my story. I was Diagnosed In November 2018, with severe Chronic MS. I have never had any symptoms prior to the day I was hospitalized and diagnosed. I have legions covering my entire brain. Since then I have numbness in my right …
Finn15 28/02/19Hi All On 30th March (Saturday) a Leeds City Centre Meet-up is due to take place at 1pm Venue TBC (Dependant on numbers) Would be good to meet as many people as possible. if you are interested then drop me a message and I can give you more details Cheers
fiona_payne 21/04/19Dear everyone, just needed someone to talk to this evening. I was diagnosed in January with MS. sort of knew about it for 14 years ago when I had an mri and steroids for numbness in my body. The words were mentioned then as a possibility but all this time I have been healthy and active with just a …
jennlmt1 23/04/19Hello! Iv been posting every now and then on here, I’m still not diagnosed and I have done everything I possibly could do, in January I was sent to a specialist and we did 3T imagining on my spine and brain, my brain has lesions but no change in the last 6 months and they are non specific and my …
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