Tag Archives: University of Glasgow

It’s day 23 and today’s letter is from Nina. Nina was diagnosed with MS 19 years ago and writes powerfully about her diagnosis. Please click on the link below to read her story. Nina’s letter

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

Today’s diagnosis letter is from Lorna. This positive letter shows the way a sense of humour can be a great help when you’re dealing with adversity. Please click on the link below to read her story. Lorna’s letter

Today’s MS diagnosis letter comes from Lorisa in North Dakota. In it, this courageous mum of three describes the way she’s replaced her initial fear with hope for the future. Please click on the link below to read her letter. Lorisa’s letter

Today is day eighteen of thirty-two and I’m delighted to post the letter I received from Liz. In it, she writes, “I don’t think I have much to add to the topic of MS; millions around the world live day to day with this illness and have probably experienced similar steps so my words andContinue reading “A Letter A Day… Liz”

Kirsty began experiencing symptoms of MS at 18. In today’s letter she writes, “MS is something I have had to embrace and take control of, and not let it control me.” Please click on the link below to read her inspiring letter. Kirsty’s letter

Today’s diagnosis letter is from Kevin. Please click on the link below to read his short, but very powerful, letter. Kevin’s letter

It’s week three and today I’m posting Karrie’s letter. In it, we share the moment she learned she had MS: “He introduced himself and shook my hand. His hands were cold, similar to his personality. He said, ‘You have Multiple Sclerosis and you will need to follow up with a neurologist.’  He handed me a brochureContinue reading “A Letter A Day… Karrie”

It’s day thirteen and today I’m posting a letter from mum of three, Joanne. She was diagnosed in February 2007 and writes, “I don’t know what the future holds for me, I only know that every day is a blessing and I don’t take anything for granted.” Please click on the link below to read Joanne’sContinue reading “A Letter A Day… Joanne”