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Latest News

aHSCT petition delivered to Parliament – watch the video

July 27, 2022 | Media

Such an exciting day yesterday when we were able to witness Joan Perry’s aHSCT petition, with over 10,000 signatures, being received by ACT deputy leader Brooke van Velden on the steps of Parliament. It was then presented to Parliament later […]


aHSCT in the news: We’re fed up waiting for it to be made available here

July 26, 2022 | Advocacy, Life with MS, Media, Treatments

A 10,000-strong petition asking Health New Zealand to extend “game-changing” stem cell treatment to multiple sclerosis (MS) patients is set to be delivered to Parliament. The petition started by Aucklander Joan Perry​, whose daughter Anne Besley​ has MS, calls for autologous haematopoietic […]


Media Release: Government urged to “get a move on” and approve cost-effective, proven, stem cell treatment for Multiple Sclerosis

July 26, 2022 | Advocacy, Life with MS, Media, Treatments

Tuesday 26th July 2022 A private petition is being delivered to the steps of parliament at lunchtime today – calling for the government to green-light a treatment, readily available overseas, which is delivering remarkable improvements to the health of many […]


Join us on the steps of Parliament to present the aHSCT petition!

July 11, 2022 | Life with MS, Media, My Story, Support

                                                    Download a copy of the poster here: aHSCT Petition Presentation Public Invitation – 26th July […]


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 […]