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Hi- with Covid really just passing through my area I have restarted my PT. I left off in December when they shut down. He left me with some good exercise options and I tried some of the other options so readily available on-line. The good news is that I think I have been able to maintain strength p...

Hi there, I'm testing the new swanky site on the hottest day ever in the UK. Fans are blowing to no avail. I think i fancy trying out the old hashtagging.. #toohot and @ting ... @maxllar

Love that ms nurse says oh I respond to emails faster... Last time I got no response at all. This time well I'm 4days in not holding much luck. Guess I'll phone tomorrow and see. Legs been giving out multiple times a day for almost three weeks now. Plenty of bruises have been collected and pulled m...

I did it. I finished my 5 day 100 mile (160km) unsupported walk of the South Downs Way in 4 days. It was s big push and I as completely broken now. Yesterday was a 51km 13 hour day and I made Eastbourne by 2030h. I promptly demolished a massive fish supper. You may not be able to afford to donat...

Hi I am Sarah. Diagnosed with ms in 2012. Over the past few weeks I seem to have got really weak legs that has starting going heavy and giving way after about 5 minutes of walking. I was wondering if anyone had any advice on the best way to tackle this as I want to be able to live my normal life....

I just had a mri and they said I have a tethered cord,can anyone explain what this is? I have an app tomorrow morning with a neurologist and I'm a nervous wreck!

Hey all, Hope everyone is doing we. I am hanging in there here. a bit run down today. Has been a busy few months and more recently in the last few weeks has gotten insane. Mostly all good things though so there is that at least. Firstly an up date on things with my son. Things are going so am...

#test

This is my first test post. I hope it's not going to the live site. Hi Miller!

2001 Optic neuritis. Go blind suddenly - and fortunately temporarily - in one eye. Ophthalmologist sends me to neurologist. The neurologist tells me in a jovial tone to say that I have had optic neuropathy to insurers - if I say optic neuritis they’d put me down as having MS. MRI done. No follow up...