AUTHOR

Amanda Rose

POSTS

Announcement: PHARMAC consultation: proposal to widen access and transition the process for funded access to multiple sclerosis treatments

November 27, 2020 | Advocacy, Life with MS, Treatments

Pharmac have released public consultation on a proposal to widen access to funded multiple sclerosis treatments and transition access from the Multiple Sclerosis Treatment Assessment Committee (MSTAC) Panel to a standard Special Authority. Please follow this link to read the […]


NZ MS Research Trust Webinar 3: Exploring how lifestyle modifications can improve MS outcomes

October 5, 2020 | Education, Life with MS, Research

NZ MS Research Trust Webinar Series 3: Exploring the relationship between brain insulation and cognition & how lifestyle modifications can improve MS outcomes Saturday 10th October  10am – 11.30am Our closest neighbours, Australia, are world renowned for investing in and spearheading life changing research […]


2020 MS Research Webinar Series

August 20, 2020 | Education, Research

We’re really excited to hear the latest in MS Research via the NZ MS Research Trust’s new webinar series. Replacing their Research Day in Auckland, this series of online webinars means we can hear the latest, from the experts, from […]


Survey – Barriers to Employment for People with Multiple Sclerosis

June 17, 2020 | Advocacy, Grants, Life with MS, Support

Have you ever experienced barriers to employment as a direct result of your Multiple Sclerosis diagnosis? Or do you know someone who has? Multiple Sclerosis New Zealand is interested to know what barriers to employment people with MS across the […]


Carers…How are you?

May 15, 2020 | Advocacy, Life with MS, Research, Support

The Carers Alliance wants to know how you, family carers, have been during Covid-19. Feedback received so far has shown that carers generally have come through the weeks of lockdown well, but it has been tiring. No respite, early reductions in […]