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Awareness - definitely me some days (including today) I coped with work as long as I did by having notes in text files and documentation in Excel to pull up.

Research shows rise in number of people estimated to be living with MS - Research published today has shown more than 130,000 people are living with MS in the UK. This is over 20 per cent more than previously thought. mssociety.org.uk/what-we-do/ne

COVID-19 coronavirus and MS - The UK MS Society’s medical advisers, a group that includes some of the leading neurologists in the UK, have agreed on the following joint statement on the COVID-19 coronavirus and MS mssociety.org.uk/about-ms/trea

'Nothing can prepare you for a diagnosis of MS' shr.gs/UQlePqF

From experience I can tell you that it blows your mind and means that life is never boring.

Yes one is for MS but I am not on it - for now I take a mixture of 3 drugs (one of which is an opioid) for my leg spasms -
BBC News - Cannabis-based medicines: Two drugs approved for NHS bbc.co.uk/news/health-50351868

My physio was a bit different today - I got put into this piece of equipment. litegait.com/products/overview For someone who uses a wheelchair or holds something when walking it is scary to stand and exercise while not holding anything. 😨

Good health news for me - my August MRI result is in - there are no new inter-cranial lesions and there is no sign of PML, so no change from the previous one in March. Proof that my monthly trips to London for my drug treatment is working as I am not getting worse.

BBC News - Multiple sclerosis: Dad walks daughter down aisle after standing frame study bbc.co.uk/news/uk-england-devo

Please note I go in one of these in my physio and so arm exercises, I just don't do it every week.

Interesting MS research but I can also see it could be used for other illnesses too- MS breath test breakthrough that could have changed Kevin’s life edinburghnews.scotsman.com/hea

I'in a wheelchair now but I wasn't for years. I know folks with MS who are and others who are not. I think less that 1/3 are.

A myth about MS for you - I worked for 11 years after my diagnosis, never told my employer for 8 of them, and it wasn't obvious until the last 2 or 3. In my heart I would love to work even now if I could do so from home, in my head I'm not completely sure (self doubt is there now).

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Mandy 🇬🇧

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