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Hello, Has anybody here changed from teaching career to something else? I've recently gone back full time as I can't afford to be part time but I am *struggling*. I'm tempted to try starting an online tutoring business but I'm nervous about the fluctuations in income and not having the same sala...

Hey everyone! I'm kinda brand new here. Just seeing how this is. I haven't yet got an official MS diagnosis, but the MRI scans of my brain shows demyelinating disease.i do have a lot of the symptoms for MS. Im going back to neuro on the 9th.idk just scared of it all. Idk if my wife really quite unde...

Hope your all well.Does anyone live in the United Kigdom? I'm in the Midlands. Would love to meet other people with MS. I have such a big family and alot of friends, but as most of you must know it can be a lonely place when nobody truly understands. Would love to meet others on this path, Drop me ...

https://www.independent.co.uk/news/health/ms-tyruko-tysabri-drug-side-effects-nhs-b2754395.html How widespread is this and is it only Tysabri and (from what I read on another site) possibly Tecfidera affected at the moment? I would hate to be pulled away from Kesimpta and onto a "simillar" drug wh...

In their quest to get me on a DMT that doesn't want to keep me in bed, I've been asked to make a choice of the two above. Thoughts? Horror & Success stories please.

This generation of dating is so hopeless, ppl intentions aren’t pure, everyone lying, cheating, or the obvious using your medical diagnosis against you because they don’t have the courage to understand you as a person. Let me know your thoughts…

Hey all, I currently have some kind of awful bug right now. A cough, runny nose, migraine and fever. Any tips on how to manage this better? I have a compromised immune system due to my treatment and don’t fancy battling/coping with this for however many weeks haha

Does anyone use cold compression socks or cooling blankets for burning sensations in lower limbs? Wanting to know what’s best. I know lots of people take Gabapentin but I am really struggling to get a doctors appointment and the pain is keeping me up at night!

Are we now just shifting too calling it RMS rather than RRMS? As I keep see8ng an Ad for a new medicatuon that is for RMS. ??? Iwas just diagnosed in March This Year. Is the name already changing?

As if symptoms from MS weren’t enough before the actual diagnosis. Living with the diagnosis and knowing what’s wrong with your body can be draining some days.. I don’t want to constantly think about it, even though it’s my new reality. It sits on my mind that one day this sht might take another w...