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Hi everyone, I hope you’re all well! I’m feeling a little lost at the moment. I gave birth to my beautiful baby boy 9 weeks ago - unfortunately my epidural was placed in the wrong spot and wasn’t picked up until I went completely numb from the waist down and needed to be moved with a sliding she...

hi all, I have MS on gilenya I have just found out a guy i am dating has herpes. Im concerned that if i do have it which is highly likely that being on my immune suppressant could be an issue for me. Has anyone been through this and can give me some advice. Can I keep taking my meds?

Hello MSers, I haven't posted in a while but I wanted to talk about COVID19. Is anyone else worried about not receiving their treatment? I'm on ocrevus and doctors have stopped my treatment as it can suppress my immune system, however, they have also confirmed that the ocrevus inside my body will ...

<p>I was diagnosed with MS in 2009. </p> <p>My complaint is my neurologist. She says I have no need for medication at this time and never calls or has me schedule an appointment. She doesn’t listen to my symptoms. I asked many questions and she didn’t answer any.</p> <p>What can I do?...</p>

does anyone ever feel really alone in their relationship??? I do it seems that my partner either doesn't listen or just doesn't want to acknowledge how things are. Having a tough time at the moment, don't feel great MS wise. I work full time- from at the moment, they have retired. Having a bad weeke...

Hi guys, i am right now taking treatment for MS in India (Ayush Prana) in a specialized center for Multiple Sclerosis. If I can talk from my own experience I personally must say that it is really very effective. Not only for me but other patients around me are improving also. We all suffer from dif...

Afternoon, Have had MS for 10 years and been having B12 injections for about the same time. Have injections every 8 weeks until Monday when the appt was cancelled. Have been told today that injections are no longer available and it’s pills now which I can get a prescription for in 2 weeks! Anybody...

I am one of those people who has all MS symptoms, but especially loss of eyesight. Anyhow I got a jpb. mostly home work, translation, etc. I told them I have MS but did not tell them I am registered blind. I have done this job for about 4 months. In face to face situations I can fake it, and mostly...

Hi all We are looking for people to participate in a research project aimed at understanding the impact of MS on pregnancy and having children. The results from this research would be used to help raise awareness and support for people with MS with children or who would like to start a family. If ...

Apologies, this is a UK-focused post, but all perspectives welcome. There is a well documented variance in MS services from one area of the UK to the next. The UK MS Society has referred to this as a postcode lottery. What are your experiences? Do you feel lucky to be under the care of your MS cent...