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Mission Statement
To help relieve the suffering and distress
- of children born with complex heart conditions, and
- their families, including those families that have lost
their children to Congenital Heart Disorders.
by providing non-medical support, information and other
assistance directly to families.
To raise community awareness of complex Congenital Heart
Disorders.
- Our goal is to create a broader understanding of the challenges faced by
families and their children who are affected by these conditions.
To support the Medical Community by:
- providing feedback and information about our activities to
hospitals, doctors and other medical professionals, and
- raising funds for the purchase of medical equipment and
for research programs.
To work co-operatively with other organisations that share
our goals.
To achieve our aims, we raise funds:
- to assist families living away from home for extended
periods while their children are hospitalised,
- for the purchase of goods/services to increase the comfort
of hospitalised children and their families,
- for events where the children and their families can enjoy
social activities,
- to disseminate information about Congenital Heart
Disorders and our activities.
- to support Paediatric Cardiac Research Programs in
Australia that lead to higher survival rates and a better quality of life for
children born with heart conditions, and
- for the purchase medical equipment to improve the
management of these disorders.
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BACKGROUND
Hearts of Hope (HoH) Australia is a non profit organisation
that is incorporated under the Corporations Act 2001.
The organisation was first setup in 2002 by a
group of families with HLHS children. For two years we operated as
the Australian HLHS Information Network. It was decided to formalise
our group so we could provide better support for families.
HoH incorporated in July 2004 and is
self-funded from donations, members subscriptions and fundraising. Our
programs are run by volunteers and co-ordinated by the HoH Executive
Committee.
We offer
non-medical support to all families with with a child born with a heart
condition that cannot be cured through medical intervention. This
includes, but is not limited to, disorders such as HLHS and other single
ventricle anomalies.
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