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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 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...

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 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 was diagnosed with RRMS mid May 2020 at the age of 28. All rather shocking because the only symptom I've experienced is optic neuritis. It has been said that I need to start on Tecfidera next week. I'm feeling pretty anxious about this. More so because all my neurologist seems to say is 'No-one ha...

Dear All, Hope you are all safe and remaining healthy in this lock down, I have a very strait forward question. Is there a period of time for a relapse to form or strike in other words, how long does it take for a relapse to occur? Three years later after having my first relapse, I started having...

Hey there... New to this... I’m wanting to hear feed back from folks who have opted out of DMT... I was diagnosed 7 months after my son was born in 2010. I am currently having my 3rd relapse, though this one has required a 3 day dose of solumedrol. I completely changed my lifestyle after diagnosis, ...

Never meet a group of people that are not updated on new discoveries and cures.I posted a message here to help but it was removed because admin claimed i broke house rules..How am i suppose to help other patients in the community when i can not direct them where to get a cure???If you are still with...

I was diagnosed last year, i thought I was lucky with relatively light physical symptoms. Balance, some pain but cognitive problems are really starting again.............. Does anyone have issues of trying to make simple calculations work in your head? I find it difficult at the moment. I'm trying t...