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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...

Hello Just thought I would say hi and try to reach out to anyone who are successfully managing their MS and are fortunate to be their own boss. I feel that I need to start to work for myself as whenever I have been in employment I seem to get unlucky and hit problems. Mainly down to having MS and...

Hi I’m so sorry if this is inappropriate but I’m just upset and don’t have anyone I feel will understand to talk to. I have just come off a telephone consultation with my (very nice) GP. I had an MRI as I have been having symptoms that my GP agreed sound like MS for ages - even years. I’m 36yrs old....

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

Hi! I am hoping to get some feedback. I am dx RRMS. Doing pretty well, on Glatopa (copaxone) about three years. Anyway, I am having serious joint pain in both hands and mainly thumbs. Maybe carpal tunnel but I have much joint pain in other areas like knees and feet. But the hands are the worst. An...

Does anyone know if they have started ocrevus infusions at kings London again yet? I was due to start infusions in March but it was obviously cancelled. Told I was near the top of the list but haven’t heard anything. I have been waiting since September. 2019

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...