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MS I feel worse when it's wet weather

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. 💪🔥

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...

Is any one here from an African country? I'd like to not be the only one i know

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...

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...

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...