MS: Busting the Myths
June 27, 2022 | Life with MS, My Story
Fifty-six is reasonably old to be diagnosed with multiple sclerosis given that the average age of onset is around thirty-four years and I will always be grateful that, even in the unlikely event that I live to be 100, I […]
June 8, 2022 | Life with MS, My Story
Hello, my name is Luis and I’m from Portugal. I am a 51 year old, drummer and I have MS. I’ve been active all my life on bikes, racing, gym, etc. On February 1, 2016, I woke up with a […]
May 23, 2022 | Advocacy, Life with MS, My Story, Treatments
Lucy Kerly had aHSCT on the NHS at Hammersmith Hospital in London at the beginning of 2022. Both she and her husband live with MS – Steve was diagnosed with relapsing MS in 2003 when he was 29 and travelled […]
May 9, 2022 | Advocacy, Life with MS, Media, My Story
Matthew was living in Florida in 2004, a very stressful time with numerous hurricanes battering the area. He had also just been diagnosed with Multiple Sclerosis by a Neurologist. At 37 years old he was learning how to inject himself […]
May 9, 2022 | Advocacy, Life with MS, Media, My Story, Treatments
Published in Stuff on 5th May 2022 https://www.stuff.co.nz/national/health/128482766/people-with-multiple-sclerosis-unable-to-access-lifechanging-treatment-in-nz