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Our Mission
"To improve the well-being
of the Haemophilia community
through mutual support,
networking, advocacy and striving
for optimal health care"
About Us
The Haemophilia Foundation ACT (HFACT) is an incorporated body representing people
and their families affected by Haemophilia, Von Willebrand's disease and other bleeding disorders in the
city of Canberra, and the surrounding region of the Australian
Capital Territory and southern New South Wales.
HFACT is a member organisation of the Haemophilia Foundation of
Australia (HFA).
Services
HFACT provides mutual support to its members through social
events, education programmes and one-to-one support between
members.
We offer the services of a counsellor / support worker who is
available to assist members, their families or other people
affected by bleeding disorders.
We also provide logistical and educational support for the
Haemophilia Treatment Centre at The Canberra
Hospital.
Strategic Plan
The five main areas in which HFACT operates are:
Advocacy
Awareness of Haemophilia issues through education and constructive representation.
Services
Ready access to optimal and attention to issues that may arise.
Networking
Ongoing interaction with related agencies.
Membership
A strong and enthusiastic membership body.
Governance
Open and effective management.
More details may be found in our Strategic Plan document.
Contact Details
| Postal address |
GPO Box 936,
Canberra City ACT 2601 |
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email: |
contact@hfact.org.au |
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| President |
Mr Fred Wensing |
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telephone: |
(02) 6291 7920 |
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email: |
President@hfact.org.au |
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| Counsellor |
Ms Clare Reeves |
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telephone: |
(02) 6255 6779 or 0409 830472 |
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email: |
Counsellor@hfact.org.au |
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