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Hi I’m so sorry if this is inappropriate but I’m just upset and don’t have anyone I feel will understand to talk to. I have just come off a telephone consultation with my (very nice) GP. I had an MRI as I have been having symptoms that my GP agreed sound like MS for ages - even years. I’m 36yrs old....

Need to get something off my chest....... so fed up, diagnosed 24th March 2020. Still no communication, phone calls or anything else from any health care professional. I keep reading about asking your ms nurse for advice - think I’m losing it cos I’m still waiting.

Hi all, I am seriously new to all of this, My RRMS journey has been a whirlwind. I had the MRI and got diagnosed literally overnight. Multiple MS occurences all at once. After a huge course of steriods Methylprednisolone 1000mg 5 days. My flares have calmed down. Not gone away, I my hands are numb a...

Hi everyone! I'm just coming back to check in as I realise I've not been around for a while. I had NEDA (No Evidence of Disease Activity) on my last MRI and have been feeling fine since then *touch wood* I became friends with an amazing woman who also has MS and hosts a podcast about living with a...

Is anyone worried about the whole coronavirus I’m starting to worry I already have a weak Immune system due to my MS treatment... would that make me variable to the virus because of that or am I just overthinking this?!? Get back to me in the comments what’s your opinion

Hey guys. I hope you are all well. My ms nurse phoned me today to tell me some good news....... I can start ocrevus in 4 weeks time. Whoop whoop. My question is I have a 3 year old daughter and a 2 year old dog (who eats everything he is not supposed to) what advice can you give for me to protect...

Hi everyone. Apologies that my question is not MS related but as Psoriasis is also an autoimmune condition I'm hoping someone will have some advice. For the least 5 years, my friend has been struggling to get treatment or even get an appointment at the local NHS Trust because her "condition is not ...

Hi there, so lots of recent reports around the EB virus and MS floating around. One of the doctors at the recent Berlin conference (Shift video clip) was specific about linking MS to contracting viruses in the teenage years. So, I had glandular fever really badly when I was fifteen, off school for a...

Hi all MS trust are in the running for a 5k health lottery grant. Please click here to vote for them (only takes 30 seconds) https://www.easypolls.net/poll.html?p=5ee377f6e4b017b74559f713 Thanks

I am looking for feedback to my MS experiences the last few weeks. I am 71, secondary progressive now. I have been able to walk and even do some dancing in my living room. Until about two weeks ago. My legs started giving out, I took a big fall on my walk (just bruised and scraped). I am super ...