shift.ms

I started having visual and auditory problems in May of 2015 progressed to having memory problems extreme fatigue problems following commands it was like I was have to tell myself over and over how to do things that should just be able to do with out thought. Things significantly increased in in Ju…

i have just been told i have ms , although i am waiting for blood tests and lumber puncture to confirm 100 % ,neurologist is very positive this is the diagnosis . i am not certain what to expect , but now have muscle pain in righthand side ,under ribs and across stomach, pain in lower back ,left th…

Hi all, whenever I see my consultant or nurse I can never recall the specifics of my symptoms (when, how long etc.). I know I should probably pay more attention, but I prefer to focus on the more fun parts of my life! I thought a symptom tracker might be a good idea, but can’t find one that w…

Hi all! This is my second post and it’s update plus a big thanks to everyone who responded. I have completed my first week back at work, haven’t been doing my full time hours but I can’t imagine it will be long before I am. When I first posted after being diagnosed I had been deal…

Had 8 mini cups ._. Now I’ll sleep I hope my heart survives. 😕

I am wondering if anyone takes amitriptyline and cbd oil?

Hi all Just had the brown envelope arrive, such fun!!! I’ve filled out the official secrets act no end of times, plus I hold way above the clearance to be capable of accessing certain areas. To get this they asked very personal questions about me and my family which is kind of understandable.…

I am ineligible for the NHS shingles vaccination a) because I’m outside the age group it’s offered to and b) because it’s a live vaccine. I take fingolimod which means that all live vaccines are contraindicated. (I’m told that the jury’s out with regard to live vaccine…

Hi! This is my first post. I’ve had MS for almost 15 years. I was in my early 20’s when I was diagnosed. I’m a drama practitioner and writer. I’m in the process of writing a funding bid to create a piece of theatre exploring life with MS. I’ve never found a portrayal …

Well that’s the email off to my MSP. Will it make a difference? Probably not as I am not in the target group of his party.