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Hi All; I am new to the forum and i will be honest in that i have a problem speaking to my GPs due to neglect in the past which lost me my first born.. I have strong symptoms of MS and dared to mention it to 2 diferent GPs but was fobbed of,especially when i mentioned the heat intollerance; all i go...

Hi i am new to this site i am 53 and was diagnosed with RR ms when i was 19 only got told about this site recently nice to find people in the same situation and now what its like hope everyone is fine and safe at this unsure time. I am at the moment ok just sat waiting like some of you to start new ...

Hello everyone, hope you are all well.......... It looks like I am/ have been starting to relapse. For a few weeks now my legs are heavy and numb and I am waking up in the morning needing almost 30 minutes to get my legs moving before I can get out of bed. My vision is going hazy throughout the day...

Hello everyone, as the title suggests I'm new here. Although, I've been lurking for some time. I got diagnosed with MS last week after a lot of barking up the wrong tree. I'm a Police Officer and in 2016 I decided to apply to transfer to firearms. The fitness test is a bit harder for this but didn't...

Daniel & Kevin are live on the Shift.ms Facebook page talking about diagnosis, MS and relationships. Tune in and ask them your questions here: https://www.facebook.com/shift.ms/videos/969374456852750/?v=969374456852750&notif_id=1590677836563640&notif_t=live_video

Can anyone tell me if Tysabri infusions are free I have been recently been diagnosed with RR MS and will be starting this infusion soon. Are they free if you only have private health insurance 😊

Good short post and a film featuring several Shift.ms ers. https://multiple-sclerosis-research.org/2020/06/the-human-side-of-ms-and-research-a-short-film/ @longboat

He says, "I am interested to know if any of you who have COVID-19 are suffering from a persistent loss of smell and taste and how has it affected your life? Please let us know if smell training makes a difference." - Here is the full post: https://multiple-sclerosis-research.org/2020/06/mscovid19-lo...

Anyone any experience of this? https://www.taopatch.co/ms

gf.me/u/x7wuvv I have Ms / nmo and it is very severe with repeated attacks of optic neuritis and leg weakness At this point I am desperate to try anything Please can people donate Thank you