Hello, I was diagnosed with RRMS in 2017 and have spent the last year ‘managing’ my condition. However, after my first big wobble in April, I’ve had a new MRI and lumbar puncture and my neurologist has suggested two treatment options: Mavenclad or Lemtrada. I’ve Googled and read and watched…

Hi again everyone! Upon doing research all I keep seeing is people controlling their MS via diet and holistic healing. I asked my Neuro about how much diet can contribute towards relapse and remission and he just said oh theres not enough research but just maintain a balanced lifestyle. I have se…

Hi everyone, Thank you for the lovely and useful comments you left on my post two months ago (“Newly diagnosed teacher”). I apologise for not responding – I wasn’t sure if there was a function for directly replying to comments – and I was also busy with many things, including mov…

Hi, I’m new to all this. Newly diagnosed with RRMS and awaiting medication. Taken them ages to get me to this point. I really didnt realise that so many people were in the same boat. It will be nice to chat with other people who understand.

Hi. I was diagnosed with RRMS in March of this year and informed the DVLA as instructed to do so. I have now received a letter from the DVLA saying that they have had information telling them that i may need my vehicle adapted with special controls. I then have two options – one to fill out a…

Hi all Hope you all are having a day. I’m Gemma (34) I began have sympsons in spring 2013 but the doctor never seemed to put them all together so my offical diagnois of relapsing/remitting didn’t come till 2016. Im December 2017 a MS consultant said I was that the diseases had progressed to se…