pixiedragon 26/05/20Hi this is the first time I’ve posted on anything but I’ve just got that angry and upset I need to do something. I was diagnosed with rrms in 2018 having symptoms for 3 years. I applied for pip after my last relapse, late last year that got me diagnosed with ataxia that has robed me of my balan…
Natale_J_Berube 31/05/20I am getting a new med for my ms and I am wondering what would be a good one to change from copaxone?
Christopher_Paul_Gill 30/05/20What is it like to have Multiple Sclerosis? MS is a strange disease. It attacks you, from every angle, but some you cannot imagine. If you walked around in a space suit that gave you general MS symptoms you would miss a lot. Basically if you have MS you really should be living on a space station. T…
DominicS 30/05/20https://multiple-sclerosis-research.org/2020/05/happy-world-ms-day/
supermum1983 30/05/20I used to get a massage every month as I have chronic pain in my back, with covid Ive not had one for ages but Im concerned because I cant never have a massage ever again. But I’m concerned, you obviously cant social distance when having a treatment unless they are wearing ppe?? Anyone else …
jade770 30/05/20Sorry in advance … I just need to vent a little and I thought this would be the right place. It’s nice to have a group of people that know what you’re going through. I’m seriously on the struggle bus. I’ve been deemed “high risk” for covid so I’ve bee…
Sarah_Thornton 27/05/20Hi even though I have multiple leisons on brain and spine the neurologist still will not diagnose, but she has suggested the GP prescribing Gabapentin for chronic pain. Was just wondering whether anyone else takes this and if so how effective is it?
TinaM 30/05/20How does one overlook a main family member thinking I faked the diagnosis of MS..?
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