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About us OUR PEOPLE The Muscular Dystrophy Association of New Zealand Inc., commonly known as MDANZ, began in the late 1950s. Since then MDANZ has broadened its scope to support many other neuromuscular conditions. Our unique governance structure ensures leadership of the organisation by individuals and family members with lived experience of a neuromuscular condition. We have three regional branches that are supported by the National Support Office based in Auckland. MDANZ supports individuals, families and whānau by MDANZ is a trusted source of specialist information and provides a range of free services and practical support for individuals, families and whānau with lived experience of rare neuromuscular conditions. providing specialist information, practical resources, personalised support services, social networks, campaigns for public awareness and advocacy. And through our research trust, we work to improve care standards and facilitate access to potential treatments for neuromuscular conditions. Our organisation is a registered charity, and we rely almost entirely on voluntary donations from the general public, trusts and other businesses/organisations to continue our work. See more about us at www.mda.org.nz National Support Office Team Kristin Cross Fundraising and Partnerships Advisor Brian Hadley Accountant and Business Manager Natalie Foote Executive Assistant Denise Ganley Member Services Manager Trevor Jenkin National Executive Chairperson Shelley Butler Accounts Assistant Melanie Glenn Clinical Services Advisor Central Region Talitha Vial Fieldworker Our Branches Northern Region Lynn Williams Fieldworker Ph: 09 415 5682 or 0800 800 337 support@mdn.org.nz Mike Schneider Fieldworker Denise Ganley Office Manager South Island Region Jane Hazlett Fieldworker Ph: 0800 800 337 southern@mda.org.nz Vivienne Fitzgerald Branch Manager Lisa Mora Fieldworker Debbie Hoskins Community Co-ordinator Ph: 0800 886 626 members.central@mda.nz Ph: 0800 800 337 info@mda.org.nz