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Hi, I live in Northern Ireland and have recently been diagnosed with RRMS and my consultant has given me 4 DMTs to choose from. I am just looking for advice with peoples experiences taking them and with the side effects. Beta interferons Copaxone and Brabio Aubagio Tecfidera Thank you

Hi All I'm just recently had a MS diagnosis 😢. I was with my MS nurse today and considering DMTs. My head is fried! I have been very anti all things medication my whole life and when I read the possible side effects of these meds... my anxiety is through the roof! I have stomach and Gastro issues s...

This is my first time posting on here and I'm feeling quite depressed and scared about talking about it. I am 25, have been diagnosed with MS as of the 25th of March. I know its been less than a month since my diagnosis but I still can't come to terms with it. I can hardly say out loud that I have...

Hi all 👋 I've recently these last two weeks been having stabbing pains in the left side of my head. They last between 30 secs and a couple of minutes but I've noticed I'm having them more frequently like 10-15 a day. Not sure if its ms related or not? My hubby thinks its because im so tired all the...

Hi All, I have recently been diagnosed and the neurologist has told me that they’ve referred me to the Ms clinic, but the wait time is 6 months ….. I feel like I’ve very little information about MS (never heard of the disease until I was diagnosed), I don’t know what type of MS I have, how many les...

Hi All, Diagnosed after around 2 months of private testing, all started after what was supposed labyrinthitis [I was unable to move without vertigo, double vision, fatigue and completely hearing loss in left ear] I then developed a hemifacial spasm in my left face which varies in severity, asked ...

I am 62 years old and had in July this diagnosis. I t seems that every case/person is different but I would like to share with someone who also has primary progressive.I have no complaints about my doctors physios etc but just feel a bit isolated and also because I am older it does not seem to ma...

Hi everyone! This is more of an introductory post I guess. My names Hannah and I am newly diagnosed. I was first diagnosed with Fibromyalgia in 2017. They started to suspect MS in 2020 after I developed Optic Neuritis. I have not started treatment yet, but I am due to give my decision to my MS nurs...

Hi I’m a 31 year old woman from Kent,UK diagnosed in July and awaiting neurology appointment to get more information. It was daunting at first but I’m coming to terms with it. All feeling back in my legs again just get VERY tired!! X