MS: Busting the Myths
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
May 3, 2022 | Grants, Life with MS
In July 2020 I was diagnosed with Multiple Sclerosis, after always being a fit, healthy and active person, with a senior management role in school sports. To say this was a shock is an understatement. Now nearly 24 months into […]
April 5, 2022 | Education, Event, Life with MS, Support, Training, Webinar
The recording of this webinar is available to watch: https://www.msakl.org.nz/our-resources/webinars/relationships-and-ms-webinar/