MS: Busting the Myths
February 27, 2025 | Advocacy, Carer, Carers, Event, Life with MS, MS Voice, News, Newsletter
Welcome to the February edition of MS Voice—your trusted source for the latest news, updates, and real-life stories from Multiple Sclerosis New Zealand and the MS community. This year promises to be a dynamic one as we continue our commitment to […]
February 25, 2025 | Advocacy, Carer, Carers, Event, Funding, Life with MS, News, Survey
Consultation is underway across the country to help shape future disability funding and service models. This is your opportunity to have your say and we encourage you to do so, now more than ever. Note: This consultation is for people […]
March 27, 2024 | Advocacy, Carer, Life with MS, Petition, Survey
In 2020-21 more than 1,600 family carers completed the first State of Caring survey. The Carers Alliance are repeating this survey every two years to understand how family carers are doing: their wellbeing, what help they get, what help they […]
January 31, 2024 | Aids, Carer, Carers, Life with MS, Support
Since the Covid-19 pandemic shifted the goalposts in the world of work, more people are realising the benefits of remote and hybrid setups. On top of the added flexibility that naturally comes with home working, many professionals have noted higher […]
December 5, 2023 | Carer, Carers, Event, Life with MS, MS Voice, Newsletter, Petition, Support, Treatments, Webinar
Welcome to our November 2023 edition of MS Voice. This month we introduce you to our new banger, invite you to our bladder and bowel health webinar and provide you with up-to-date research and development, amongst other exciting updates. View […]