MS: Busting the Myths
November 27, 2020 | Advocacy, Life with MS, Treatments
Media Release No More Dreaded 500 Metre ‘Walk of Shame’ For Kiwis With MS? A six year battle to allow multiple sclerosis patients continued access to vital funded drug treatments may soon be over, with news that Pharmac is finally […]
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 […]
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 […]
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 […]
April 9, 2020 | Advocacy, Life with MS, Research, Support, Treatments
NOTE: This post was updated on the 9/04/2020, to reflect the requirements of Alert Level 4 and emerging data. Key updates: Updated information based on very early emerging data Updated information about your upcoming appointments Latest travel advice Information for […]