Latest News

My aHSCT story – Lucy Kerly

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 […]


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  


My Steinlager 2 adventure – Duncan Grant

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 […]


Relationships and MS Webinar with MS Auckland – Recording available

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/