@Hollys 

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Hollys

Diagnosis ...

Finally had my neuro appointment in a MS clinic ( my appointment letter for this clinic was what revealed I had MS earlier this year.) They said I have PPMS and it's neither progressing or active so no treatment. I have a load of old lesions in my brain and one on my spine - they said I could have had this for many years without any symptoms. I have a what I'd call minor symptoms - slightly unbalanced, a weak leg after I've been out walking for a while that's been the same for about 4 years plus a tingly foot (I only went to GP last year cos I thought i had a knee injury) I know it won't always be stable and it'll be with me forever - but I'm in some kind of get on with life, one day at a time daze ... I think
@Runningonempty

Chin up, arse out and keep waddling 😉 welcome to the club

@Si2020

I feel as if I just read my own story/journey back just now. PPMS diagnosis since May 2020 - nearly 2 years & still no treatment as MRIs show no change. I hear you loud and clear 😕