Looking for
something specific?

Years ago I needed to change my life completely! Why? That was not my choice but my health conditions. I was diagnosed with MS and it felt heavy to carry with me. After 17 years living with MS I feel that there is something more I can do. I`m thinking of creating MS mom needs serving, supportive, a...

Years ago I needed to change my life completely. Why? That was not my choice but my health conditions. I was diagnosed with MS and it felt heavy to carry with me. I was afraid to dream about the future or even live a day with love, care, and understanding to myself. I felt guilty when I wanted to ...

Hi community, Does anyone have experience of neutropenia after Lemtrada? Horrid to have to deal with extra things on top of the MS. If anyone has I would love to hear if it’s reoccurred/needed treatment or went away naturally. Thanks, Sal

Hi everyone! I'm just coming back to check in as I realise I've not been around for a while. I had NEDA (No Evidence of Disease Activity) on my last MRI and have been feeling fine since then *touch wood* I became friends with an amazing woman who also has MS and hosts a podcast about living with a...

Hey, I have been in lockdown with my family since 17th March and as of recent (the past week or so), I have really struggled with my mental health. I suffer from depression which is believed to be due to MS, so I take 50mg Sertraline a day. As I have been extremely down the past few days my partne...

Hi everyone. Apologies that my question is not MS related but as Psoriasis is also an autoimmune condition I'm hoping someone will have some advice. For the least 5 years, my friend has been struggling to get treatment or even get an appointment at the local NHS Trust because her "condition is not ...

Need to get something off my chest....... so fed up, diagnosed 24th March 2020. Still no communication, phone calls or anything else from any health care professional. I keep reading about asking your ms nurse for advice - think I’m losing it cos I’m still waiting.

recently got diagnosed with RRMS. its hard to digest. i m really keen to make every effort for healthy life. i was wandering if anyone has benefitted from OMS recovery ?

Hi all MS trust are in the running for a 5k health lottery grant. Please click here to vote for them (only takes 30 seconds) https://www.easypolls.net/poll.html?p=5ee377f6e4b017b74559f713 Thanks

Never meet a group of people that are not updated on new discoveries and cures.I posted a message here to help but it was removed because admin claimed i broke house rules..How am i suppose to help other patients in the community when i can not direct them where to get a cure???If you are still with...