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Hi all. First post as I await confirmation of my MS diagnosis, and apologies in advance for my long post!! However, my path that has led me here appears unusual based on usual early symptoms and what I have read here and elsewhere. I am currently 38 years old, and going as far back as 15 years ago...

I have had nerve pain in my neck back for about 16 years over the this has spread to all parts of body. I have also with brain fog alot over the last month I have now developed a tremor in my right hand and arm also my legs feel like they are jelly also my balance has been really bad to the point th...

Hello all, I was just looking for anyones advice who has had Lemtrada, I know I have a nurse and neurologist but wanted opinions from those who have had the treatment and what advice they were told regarding isolating after Lemtrada. I was told there was actually no need but everyone I follow on so...

I'm learning I'll have good days and bad days but today has been awful. Mainly my fatigue but also back pain, more unsteady than normal and at times very confused. There are no new symptoms as it were, just a mammoth increase of familiar ones. Do I need to be concerned? Do I need to tell anyone or d...

Hey all, I’ve been on Tysabri since March 2020 and have been fortunate to have no relapses but my MS team told me a couple of days ago that I need to change to Gilenya due to a change in my JC status. I had my last Tysabri infusion earlier today and the neuro nurses seemed very confused about wh...

I am currently taking steroid tablets over 5 days at home. Those were prescribed by GP (it wasn't easy to get prescription) for very serious relapse - I wasn't able to walk. What is concerning, that my MS nurse advised me not to take them, only wait and see, maybe it will improve by itself! And that...

I am such a lucky lady!!! If u read my last post you will see that PIP decided I don't need my car any more even though I walk with a stick, ankle braces and ankle straps. I was diagnosed with Primary Progressive Multiple Sclerosis in February this year. I wrote to PIP to disclose my Change of Ci...

Morning everyone, can anyone please help me? I was diagnosed 3 years ago, but has symptoms for the last 5-6 years. I am on Tysabri and have done wonders, my last MRI showed nothing, I had a very active MS, lesions seemed shrink, the remaining ones not active anymore. It is just in the last MRI resul...

I have had an underbite and it has always been my biggest insecurity. As a child, I remember people always staring at me very confused when I would eat. As I got older and became conscious, I became more aware of my underbite and chewed differently to mask it. My teeth bites only on the sides and a ...

https://www.instagram.com/p/Ch-Waz1tpl0/?igshid=YmMyMTA2M2Y= If you know this feeling yourself, please talk to me because I'm still very confused with it and would like to talk about it 😥