MS Matters

2 months ago | mssociety.org.uk | Yolanda Barker

Yolanda is Group Coordinator of our South East Kent Group and a national campaigner for the MS community. She tells us how supporting others has given her purpose and confidence during the challenges of living with MS. My name’s Yolanda Barker. I’m 53, and a proud mum to two grown-up boys and nanna to four lovely grandchildren. My life’s been shaped by many experiences. But a significant part of my story began in 1993 when I was diagnosed with MS.

Oct 7, 2024 | mssociety.org.uk | Matt Ward

My journey with MS began in 2006. It was a year of uncertainty and confusion. One day, I noticed something off with my eyesight. The optician immediately referred me to the hospital, where an MRI scan ruled out a brain tumour. I was then referred to a neurologist who informed me that I had some lesions on my brain, but not enough to conclusively diagnose MS. He reassured me, telling me not to worry, and that the sight problems might never happen again.

Sep 27, 2024 | mssociety.org.uk | Clara Stein

Imagine that to follow a conversation, your brain uses a complex network. Think of this network as similar to the streets of a busy city. You may be used to driving home from school or work using street A. But today, the street is blocked. Fortunately, you know that there are other ways to get home. It might take a bit longer, but you’ll get there safely. By engaging in enriching everyday activities, we may be able to help our brains be more flexible.

Jul 25, 2024 | mssociety.org.uk | Annie Jones

My MS symptomsIn 2006, at the age of 55, I was diagnosed with primary progressive MS (PPMS). My main symptoms now include a painful numbness or tingling in my hands and feet – which can (and has!) led to accidents over the years. My limbs often feel as if they’re turning to wood or stone. My mobility’s decreased, and I walk slowly with a stick, for short distances only.

Jun 12, 2024 | mssociety.org.uk | Fiona Blades

I was first diagnosed with relapsing remitting MS when I was 33, I'm now 59. Sadly, I wasn't told in the usual way. I didn't find out until I applied for life insurance and was advised to refer back to my doctor. I made an appointment and my GP said, very matter of fact, “I told them about your MS.” It was a totally devastating discussion as no one had ever mentioned it to me. After a long-winded battle and a second opinion I got the same diagnosis.