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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...

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...

Does anyone else get this.... I am seeing double but only in my right eye pain under and to the back of my eye. Been of phone with the ms nurse she said it doesn’t sound optic neuritis or classic symptoms of. Please I Just want to know if I’m going mad or not

Hi . . . Would just like to know if this could be yet another symptom of m s . . . This mornin when I got up to make a cuppa I suddenly went all shaky and found it difficult to even pick up a spoon . . . I then proceeded to go all clammy and hot . . . Literally had to strip off and sit down . . . Di...

Can someone help me? I’ve searched the web and all the MS sites and can’t find the answer. I would like to hear from someone who has symptoms daily that come and go. Like everyday. For instance I permanently have numb feet but sometimes in the day it travels up to my knees then goes away back to jus...

Hello all, Well I don't know where to begin!? Guess I should start here. Joined this site nearly 4 years ago just after I was diagnosed. I have had this thing approximately 20 years. Not on any medication, not that there seems to be much, the same as help with this - not much. I suppose when I w...

Hi, hoping for some advice - I have emailed my neurologist but waiting a while to hear back so thought I'd see what people on here think. I work as a secondary school teacher. Have been teaching remotely but deciding about returning. This week there is a training day (staggered in small groups) the...

I'd like to hear first or at most second hand an account of what it's like for a PwMS to go through COVID. I'm surprised and a bit concerned that I've not seen one here yet. Either we're very good at shielding, or we tend to die of COVID, or both. Or it's just a quirk of stats, and the rate of inf...

What 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...

Sorry 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 been exiled from my home and banished to my nanna'...