LDNZ believes that good networks among families leads to improved information and better support.
supporting families in all areas of health, disability and social supports, including holding family gatherings and assisting with travel to meetings on Lysosomal diseases. Empowering families with knowledge and confidence to better access their communities.
13 years of support and advocacy
on 24 Nov 2018
In memory of MMN.
on 10 May 2017
Thank you so much for the important work that you continue to do and the wonderful support you continue sharing with our families.
on 28 Feb 2017
Much aroha for everything you do.
Wishing they find a cure for this Jo & Ben. You never know, it might be in time for Cody??
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Lysosomal Diseases New Zealand (Charity)
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