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MS I feel worse when it's wet weather

Hi. My name is Cara & I have had MS for 15 years. I started a company, The SwitchVR, 3 years ago. Our purpose is to develop holistic therapeutics (i.e. meditation, mindfulness, Qigong) using technology so that we can offer complementary practices for MS patients, like myself. Our first product i...

Hello, have you been able to check out the new shift ms site? it's pretty nice.

Hey Peeps. Spoke to the consultant yesterday, my yearly follow-up which went ok apart from mentioning about armpit, arm and neck and shoulder pain. I was referred to the breast clinic in March which they checked me over and just said lumps were normal and having no history in the family was a good...

I tried to draw some sketches to describe how my MS felt to me and people thought I was depressed. I'm really not. I just wanted to show how badly the sickness gets sometimes. Soon after, I stopped drawing about the negative impact of my MS and started making a fairytale out story out of it. 💪🔥

Hey guys, I've been diagnosed with Ms since I was 13 and had lots of scarring before then, had nearly 10 years of treatment. However, my Ms keeps becoming active. The next and only drug they are suggesting is cladribine /mavenclad. So taking it for the short amount of time over two years. I'd lik...

Hi All, I am new to this site and wanted to introduce myself. I was unofficially diagnosed with MS whilst living in the US but due to limited understanding and MRI facilities in the UK, not officially diagnosed until 2008. Currently medically retired and enjoying life. I have spent the lockdown peri...

A few years ago before leaving the country I wanted to create a "breakfast club" in London for people with ms to meet up for a cup of coffee and a chat. Now that I'm back I want to continue from where I left. Covid permitting. Raise your hand if you might be interested!

Well after a few weeks of rest at home I'm now back to work, and so thankfully to be. My son's would like to see me take off more time, but as I have told them I have always liked working and I will continue to for as many more years as I'm able. I'm a stubborn women, I guess but I will not give in...

Hello everyone! I was recently diagnosed with optic neuritis (and what apparently has been MS for several years now) and after long consideration I finally decided to opt for steroid pulse therapy (5 x 1000 mg methylprednisolone). The first few days were fine, I didn't experience any euphoria, slee...