|
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 |
| |
email: |
Secretary@hfact.org.au |
| |
|
| President |
Mr Fred Wensing
|
| |
telephone: |
(02) 6291 9720 or 0409 831844
|
| |
email: |
President@hfact.org.au |
| |
|
| Counsellor |
Mr Philip Öhman |
| |
telephone: |
0409 830472 |
| |
email: |
Counsellor@hfact.org.au |
|
