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Hi all, I'm new to Shift MS, nice to meet you all. I got diagnosed over a year ago, but haven't talked to anyone else with MS before, so just looking to say hi and catch up with someone who might be having a similar experience. How do people deal with day to day stuff? My most annoying thing is work...

Hi! I<code>m not usually the one to write and ask, but there come moments like this when it</code>s just a natural action. So to the point...I understand your questions, life challenges, your ups, and down days. I`m an MS mom and have the disease for 17 years now. So the first time I met MS as a dia...

Hello Lovely People.... I have RRMS, late diagnosis at 55, after 20 years of misdiagnosis. I’m on Tecfidera. I am experiencing more and disabling issues. I have to use walking sticks and by the end of the day, a mobility scooter. I have extreme pain in both feet, some evening spasms and string elect...

Hello to everyone, I have just joined you. I was initially diagnosed in 2009 with ADEM &amp; thought it was benign MS. I have had ongoing symptoms over recent years which led to a recent MRI showing multiple lesions. The Consultant has diagnosed MS and referred me to Queens Square in London. I ...

I was diagnosed with MS Nov 97 so nearly 23 years. I have been on various treatments . I am now on Ocrevus 6 monthly infusion. But because of COVID-19 my treatment has been delayed my last dose was the 26th September 2019 I was supposed to have my next dose In March . I just wanted to know if anyo...

I have read that rrms always eventually becomes spms. Is this so? I have a neuro who says that usually by my age (53 and diagnosed at 29), ms has established the pattern it is going to be. One sounds promising and one not so much. What would clue me in that it’s becoming spms? I have more difficu...

Hi guys, I have always wanted to be a paramedic (am currently an RN) but have recently been tentatively diagnosed with MS. I am wondering if anyone has successfully gained employment as a paramedic with a known diagnosis of MS or whether I need to put this dream to bed. Thank you :)

Hi all, I wondered if anyone could help answer some questions/give their experience.... I was diagnosed in May this year with rapid RRMS following loss of sensation/power in right leg/Side in December 19 and then optic neuritis in April 20. First MRI was in March 20. I was originally told I would r...

Anyone who lives in the city of Chicago in Bangladesh, called Henderson, who might have PPMS but was diagnosed in 2006, is definitely dodgy. ⚡Accept a Friend Request at your peril!!!!⚡

Today is a good day. Going to write some words to see how they're classified. Like Lemtrada...... It actually needs more text than this and we're going to make it content that talks about medical diagnosis of multiple sclerosis.