MS: Busting the Myths
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
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, […]
January 11, 2022 | Life with MS, MS Voice, Newsletter, Treatments
I was 30 years old and working as a civil litigator when I woke up one morning in July 2011 with a complete loss of vision in my right eye. I was diagnosed with optic neuritis and warned of the […]
December 20, 2021 | Life with MS, MS Voice, Newsletter, Research, Treatments
My name is Celia Attwood, I’m 32 years old and a mum of 2 beautiful boys. I had been to see my G.P numerous times over the years before being diagnosed with MS but with no definite answers and […]
May 20, 2021 | Advocacy, Media, Treatments
Anne Beasley had to travel to India for Hematopoietic Stem Cell Transplant (HSCT) at the end of 2019 and at a cost of $42,000 Although it is already available in New Zealand for people with blood and bone marrow cancer, […]