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https://www.youtube.com/watch?v=R1RpZtnUrsw&feature=youtu.be Inspired by conversations from right here in the Shift.ms community 💬 'AWAKE' is the latest film that explores the interplay between MS, sleep and mental health 🛌💤😪 THANK YOU so much to all those involved in the filming of AWAKE. A...

I know there is lots here about optic neuritis, but I wanted to ask if anyone has had their vision recovered but been left with discomfort ever since. I had ON a year ago and lost partial vision in the eye but it returned within 2 months. However now a year on I Continue to get intermittent but dail...

I am in the process of applying for PIP and have completed the online mock PIP tests on the Benefits And Work website. All the questions seem to be geared towards assessing mental illness and physical disability though. Non of them seem to assess fatigue, which is my main symptom (especially on bad ...

Kanavance CBD Pharmaceutical grade fish oil is oil that has been purified through a process called molecular distillation. It is the only grade fish oil approved for humans. The best fish sources of Omega 3 fatty acids include herring, mackerel, and salmon. Kanavance CBD The Hoki fish from New Zeala...

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...

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...

Hello! I was recently diagnosed with PPMS. Ever since I have had usually heartburn and swallowing issues. I visited gastroenterologist some months ago and according his review I had no visible problems when swallowing. The question is that can MS cause problems with swallowing? Whenever I try to sw...

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...

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...

Hi. I'm Piper. I have PPMS. I've never experienced a remission. This month has been extremely frightening because at 1st, it was just my right foot getting cold..(noticeably much colder to the touch)..(not the numb-like feeling as much). Now, by midday, the coldness has reached just up above my knee...