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This MS Awareness Week, Shift.ms have partnered with MS Society, MS Trust, Neurotherapy Network, Overcoming MS, MS Together and MS-UK to launch the #MSUnfiltered campaign. Together, we're dropping the filter and getting real, shining a light on those not-so-glam symptoms. Have you had any symptoms...

While it's difficult to think of anything other than all things COVID-19 right now, MS is never far from my mind. Every day, there are reminders that my current MS life is vastly unlike my pre-diagnosis life, from the twice-daily medication I take and my frequent MS migraines, to muscle spasms and f...

I just added a new design of one of my MS paintings to my online shop!!! Check out my shop directly https://www.redbubble.com/de/people/Adams-Lilith/shop?asc=u or watch my latest YT video to find out what this is all about :) https://youtu.be/1cRc9TxEZpQ

Makes me laugh every year, always miss it and socials tend to be late announcing it we all have a good excuse tho 😂

#MSmakesme determined to do everything I can to stay healthy, and grateful for all the little things I took for granted before MS. It’s MS Awareness Week in the UK. Is anyone doing anything special this week? Some MS charities are sharing this hashtag to raise awareness. ☺️

Today is the start of MS awareness week, my first one. I thought I'd share with you guys my awareness post I shared on Facebook; my first MS coming out post in a sense. as a disclamer (i wrote one on my post at the end) I had to over simplify some aspects so I didn't bore the life out of people, so...

Just read that next week is MS Awareness week in the UK. For the first time ever, 7 of the UK’s MS Charities have come together, including Shift MS to shine a light on this illness. They are posting a hashtag #MSMakesMe and thought maybe we could start a thread here? Have a safe weekend everyone.

I wanna be able to get the awareness of MS out more

What people don't understand is that I may look ok , but what we feel inside is not ok. My legs are extremely weak feeling and i have burning and tingling in my let's from time to time, i have chronic fatigue, zero energy, and nerve pain in my arms and legs just to name a few symptoms. So i may lo...

Do you think they make a difference? Is raising awareness another burden on top of MS symptoms? Can people without MS truly understand the ins and outs of living with it? What does MS awareness mean to you?