MS: Busting the Myths
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/
March 28, 2022 | Advocacy, Life with MS, MS Voice, My Story, Newsletter, Treatments
Our March edition of MS Voice gives you information on what happens to the immune system of people with MS after receiving aHSCT, plus Keryn’s aHSCT journey and we’re still working hard to achieve 10,000 signatures on the aHSCT petition, […]