Who We Are
The Lymphoedema Association of Queensland Inc. was founded in 1989 by people with the condition, health professionals and concerned others. It supports the establishment of local branches and support groups throughout the State.
The Association is a self help organisation and offers support, information and education to anyone affected by lymphoedema.
We are a registered charity, and funds are raised by membership fees, fundraising events, philanthropic trusts and donations which are tax deductible.
Download our brochure to learn more.
The Benefits Our Members Enjoy
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Invites to attend Support Group Meet Ups
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A subscription to our quarterly newsletter ‘Node News’
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Opportunity to submit editorial for our newsletter ‘Node News’
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Discounted rates when advertising in ‘Node News’
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A free listing in LAQ’s Treatment Directory
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Member discount for LAQ functions and events
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Opportunity to speak at educational events and seminars
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Opportunity to exchange information and experience
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Member discount for expo displays at LAQ events
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Entry to LAQ’s Facebook Group
Our Aims
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Offer support and services to Queenslanders with Lymphoedema.
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Provide information and education about the condition, treatment programs and self-help for patients and their families.
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Increase public and health professional awareness of the condition of lymphoedema.
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Liaise with health professionals interested in lymphoedema and the needs of Queenslanders with it.
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Work towards improving the availability of better resources for the treatment of lymphoedema in Queensland.
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Network with interstate lymphoedema organisations and participating in national activities.
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Lobby the State and Federal Government on issues relating to the health and wellbeing of LAQ Members.
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