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MS Voice Newsletter – May 2023

May 25, 2023 | Advocacy, Carer, Carers, MS Voice, Newsletter, Support, Training, Webinar

Welcome to the May edition of the MS Voice Newsletter! Your trusted source for the latest updates, inspiring stories, and valuable resources in the world of Multiple Sclerosis. We are excited to bring you another month of insightful content that […]


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 […]