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Hey all, Hope everyone is well. Been not doing to bad here the last little while. Excluding today. But the last I don’t know 5 weeks or so now been feeling pretty good. Been getting stuff done outside that hasn’t been able to get done in the last 3 years. So was a lot of work. Also had to move ...

Can you imagine Jesus turning up at a nightclub? ‘I don't care who your dad is pal, you're not getting in with sandals on’."

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.

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 ...

Good morning folks, hope everyone is keeping well. I have just come across a support group for carers and thought that there may be some here who could benefit from the group. Copy and paste time 😊 https://www.mobiliseonline.co.uk/our-story About Us There are more than 7 million people in the ...

Please let me start off by saying I'm not whining or being ungrateful...my current neurologist has been very efficient in organising scans and treatment over the years. But...I am wondering if I can change my neurologist. When I saw him about a year ago he encouraged me to get back with my ex husban...

I was diagnosed in 2012/2013 , but have had symptoms for 15 years or so. I'm on Fampyra and Lyrica which seem to help. Magnesium and Lecithin very important too. I am in Germany at the moment where the treatment is amazing compared to Ireland where I am from. Anyone else out there with questions on...

Hi all! I was diagnosed very recently with MS, on Feb. 26th 2020. Feb. 12th, 13th, 14th '20 I had a Methylprednisolone cure for 3 days, which didn't help me out of my relapse. Complaints are getting worse and my neurologist says DMT is not an option right now because of the corona virus. He says "I...

Hey there... New to this... I’m wanting to hear feed back from folks who have opted out of DMT... I was diagnosed 7 months after my son was born in 2010. I am currently having my 3rd relapse, though this one has required a 3 day dose of solumedrol. I completely changed my lifestyle after diagnosis, ...

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...