A Letter A Day… Sue

Since her diagnosis with MS sixteen years ago, Sue has become actively involved with the MS Society’s Research Network, working with the media and representing patients’ views on progress in MS research. Please click on the link below to read her powerful diagnosis story. Sue’s letter

A Letter A Day… Ruth

Today I’m posting a letter from Ruth. In it, she writes, ‘I had my first episode aged 21, during my third year at University – a period of double vision which was terrifying and for a long time no one could tell me what had caused it.’ Please click on the link below to readContinue reading “A Letter A Day… Ruth”

A Letter A Day… Rebecca

Today I have the privilege of posting Rebecca’s letter. Her powerful letter ends with the following thought: ‘It isn’t a life I would have chosen for myself or for anyone else, but now I’m on this journey, I’ll do all I can to embrace it.’ Please click on the link below to read her story.Continue reading “A Letter A Day… Rebecca”

A Letter A Day… Nicky

It’s week four and today I have the privilege of posting Nicky’s letter. It begins, “Here’s the thing: in September 2010 I decided I had a brain tumour” and ends, “Cheers and let’s kick this disease in the butt, yeah?” Click on the link below to read Nicky’s powerful story of her MS diagnosis. Nicky’s letter

A Letter A Day… L

A few of the folks who wrote to me asked to remain anonymous. I am very grateful that despite their desire for privacy, they were willing to take part in the project. Today’s letter is from L. It eloquently describes a difficult journey to a diagnosis of MS. Please click on the link below to read thisContinue reading “A Letter A Day… L”