Dear Supporters, You may have recently received a fundraising letter from us with an incorrect name […]
Read more →The 2019 Voice of Rare Disorders survey is now live! Please click this link to complete […]
Read more →Save the Date! The Annual General Meeting of MDANZ will be held on Friday 24th of […]
Read more →Coronavirus & Neuromuscular Conditions MDANZ is concerned that the new coronavirus (COVID-19) may have a disproportionate […]
Read more →Dear all Members, Given the current circumstances related to COVID-19, MDANZ is continuing to take further […]
Read more →Covid-19 and people with neuromuscular disorders: World Muscle Society position and advice The category of […]
Read more →Dear Supporter, I do hope that you are safe and well and have access to any […]
Read more →Skinny wants to support all New Zealanders to get affordable broadband. It is aimed to support […]
Read more →MSNZ have put together a wonderful resource that shows a list of ways people can experience […]
Read more →The membership organisation representing New Zealanders living with rare neuromuscular conditions, Muscular Dystrophy New Zealand (MDANZ), […]
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