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Latest News

My aHSCT Journey – Matthew Price

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 […]


People with Multiple Sclerosis unable to access ‘life-changing treatment’ in NZ

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  


MS Voice Newsletter – March 2022

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, […]


My aHSCT story – Keryn Ashworth

March 16, 2022 | My Story, Treatments

People often asked me ‘what research I did’ before deciding on a stem cell transplant in Russia…. Short answer ……’nothing’. I learnt that over the years of having this disease and my steady decline, that MS does not allow you […]