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Getting married in November. Feel like the stress of this won't help the ms... If anyone has any tips or owt on how to deal with it that'd be great, also ways on making it cheaper would be handy too 😂

We all seem to be struggling a bit at the moment. Can you all give me one positive thing It could be anything just one glimmer of light? Mine is the local bakery had two bakewell croissants left this morning one for me and my daughter! Small victories every day.

As World MS day approaches (30th May) we ask ourselves why have a World MS Day? The answer is simple it’s there to raise funds and awareness, for and of MS. Raising funds Raising funds is important as without funds, research can’t happen. Without research a cure will never be found and a cure is w...

My next appt. with our M.S. Clinic is mid August. I do this twice a year. Tomorrrow is my birthday and will be going out to my favorite restaurant for dinner with my hubby. There may be other family coming also. Our son Darren & his wife and son may be there & also my brother-in-law. Our oldes...

Hey, so my partner and I are trying to move because where we live right now there are no services for people with autism or MS. Does anyone know where might be better? Even a community MS nurse would be amazing, there are none in our current borough.

A drunken man staggers into a Catholic Church and sits down in a confession booth & says nothing. The priest coughs to get his attention but he stays silent. He taps 3 times on the wall but the man still stays silent. After a while he says there’s no point knocking mate there’s no paper in here eith...

At times at random I will get a rush of flashbacks where I’ll remember things that happened in the hospital that I had forgotten and start to cry out of frustration. I will also recall the judgment and all the drama I just don’t want to deal with anymore between family members. I’m becoming more bit...

Hi and thanks for letting me join I was diagnosed with MS in 2012 after a a collapse, no symptoms before that. I was born in Dunstable England and moved to Ireland in the 70's when I found the green eyed redheaded beautiful girl who became my wife. After my diagnosis there was nothing, no help, n...

Hi, After having Lemtrada in 2016/2017 & being relapse free since, I've had two back to back relapses and will be switching treatments. The neuro is keen on Tysabri, but has also talked about Ocrelizumab, Kesimpta and Cladribine. I feel overwhelmed 😕 Does anyone have personal experience of these dr...

Hi everyone. I was finally diagnosed in November with RRMS after my lumbar puncture. I had a huge flare up January 2023 and that set ball rolling. I had 5 spots and 2 are not very small. I had a huge flare up in November and just over it now. I lost about half my sight and balance and motor skills....