Hi again everyone 🙂 so I’ve just got the dreaded brown envolope declining me for PIP and scoring me 0 points on everything has anyone else had this problem? They’ve pretty much lied on my report saying I can see fine even though I’ve had optic neuritis in both eyes in the past 5 month and …

I have now had diagnosed MS for two years. At moments like these I like to look back at the journey and think about what has been good and bad. So here goes: The Good – Had two beautiful children who’s smiles light up my life – Quit a high stress job and joined a great organisati…

I have been quiet on this site for a while as I had to make a decision on what DMT to take and wanted to clear my head. I have highly active RRMS and this week I started on Cladribine I have not had any side effects or adverse feelings yet at all so I’m pleased about that I’m almost week one …

Hi Does anyone have any information about how graves adds or mimics and makes your rrms worse?

…if you are RRMS transition to SPMS? My tingling is getting worse I think and I’ve convinved myself it is very active and going on to SPMS even though no new activity at last MRI. I’ve tried to read up on it but don’t quite get the transition – I am sure it isn’t…

Hi everyone, It is both lovely and horrible to find so may people battling MS. Hope you are all having a good day. Quick background: I’m a newbie, diagnosed with RRMS in October following a double vision relapse a couple of years ago and a bout of vertigo in February (unclear if that was MS or BP…