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 | Advocacy, Research, Study, Treatments
New Zealand Neurologists are undertaking a survey of people who have travelled overseas to have a bone marrow (stem cell / aHSCT) transplant for multiple sclerosis. The study involves answering a questionnaire and giving consent for doctors to access your […]
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, […]