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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...

As the title suggests, whats everyones gut feeling on the future advancements of MS? Are you optimistic or unsure? The world of MS recently discussed. Fasting, along with 2 known diabetes drugs. Some proteins that can aid recover and maybe half progression. I think, a cashew molecule was looking ...

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!

hello everyone, a couple of days ago i found out this new way of breathing which was introduced by Wim Hof. In further examination i discovered that it is also helpful for people with MS. Did someone or does someone use this breathing method? if yes, how does it affect your condition?

I would appreciate if someone could discuss with me privately about MS and share own thoughts. If you have been diagnosed recently it is abaolutely fine.

Hi I have recently been diagnosed with Ms and am reluctant to take medication and therefore have been looking into alternative treatments. I feel hopeful about Dr Coimbra's vitamin d protocol which has been backed up by many other doctors such as Dr Berg. I have started taking high doses of vitam...

Hello everyone. I just wanted to say hello and maybe get any useful info from anyone who may have had similar experiences. Firstly I want to point out that I am not suffering badly and am well aware that I am more fortunate than many so really don't want any sympathy, just thought my story might be ...

https://www.youtube.com/watch?v=mzaidLfVgSY&feature=youtu.be The world 🌍 of health is adapting to an entirely new way of operating, including switching to digital delivery of care and telemedicine. But what does this mean practically for people with MS? 🤔💭 In episode 1 of this miniseries, we’re ...

Hello all, I'd like some thoughts from you knowledgable folk plz. I was diagnosed rrms in September 2017 and have been on tec since March 2019. I have remained stable, however my most recent MRI last month (delayed from March) has shown 4 new areas of inflammation. I have not had a noticable relap...