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Just wanted to say hello, I just joined today and thank you for the membership and nice to be part of a community that understands what it's like living with MS.

Hi I’m new here with my first recognisable symptom (docs thought I had vertigo) to MS diagnosis in just 6 months last year. Trying to come to terms with what is my ‘new to me’ future but need crutches to walk and can’t do anything for more than 20mins so struggling to get any motivation to do any e...

So I have accounts on mymsteam and bezzy and a few others…but i wanted to set up one here. Its been a lil over a year since i was diagnosed (relapse remitting) and im still forever learning about MS. Just wanna say im so grateful for the internet lol! Cuz without it i wouldnt know a quarter of what ...

Hi there. I am new here. I AM 49 years old and I was just diagnosed with PPMS this past Tuesday. I've been through so much testing over the past 6 months. Deep down, I new it was MS, but I didn't expect to be PPMS. I know I have a ton to learn and a challenging journey ahead of me. Because thi...

Hi guys new and haven't officially been diagnosed but tick everything that this is I also suffer from Ehlers-Danlos syndrome and fibromyalgia x

So I haven't officially been diagnosed by neurologist.. but for years I've experienced weird symptoms dizziness feet numb legs etc but they never last long this month I woke up thinking I fell asleep on my hand but it never woke up then the numbness and pain continued down my arm now m...

Hello, I’m new to the group and I hope to meet awesome friends and learn more about MS.

Hey there everyone! I’m PJ and this is my first post being a newbie to the world of MS and this wonderful group. I was diagnosed RRMS only in January, so I’m coming to terms with life ahead. You will all know how that feels.. but I’m positive and focused to live as normal life as I can. I love ...

Hi. I’m new here. Have no idea if I have MS but, until recently I have had my suspicions. Been unwell for the last 2 and a half with an ever growing list of symptoms. I don’t think I’ve ever really been physically unwell at all until this. Finally had my first ENT appointment in May (!!!) and an MRI...

Hi guys :) So, 2 months ago I had first symptoms, still have them but worse. They did CT and MRI first and found multiple demienilisation lesions on/in brain and on C1/C2 vertebra, all about 1cm size. My neurologist said its MS. They did lumbar puncture (it was horror) last week and now I am waiting...