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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 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 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

I was just diagnosed in July. My first symptoms and lesions were in 2019 but I was in limbo until a lumbar puncture recently for diagnosis. Partly because symptoms overlap chronic migraine and FM which I have. So my neurologist was looking for something strictly MS. I did get drop foot but that wa...

Last month i was told that i could be started on the Ocrevus treatment because i was in the category for it with all my symptoms ! since been diagnosed last month was the first time i was given any information or saw a MS nurse to talk about my condition it been hard trying to cope with all this in ...

Hi Everyone 👋 I'm brand new to the world of MS having been diagnosed a month ago. It's been a whirlwind of emotions as you can probably relate to. I've been proactive and mostly positive since the diagnosis but every now and then feel quite overwhelmed. My symptoms are mainly numbing in my feet...