Annual Report 2017-18 | Monash Health
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A journey starts<br />
with one small step<br />
Seven years ago, three mums decided to make a difference and<br />
raise funds to support vital research into cystic fibrosis (CF).<br />
After significant planning and<br />
organisation, Susan Biggar, Julie<br />
Noorman and Kathy Ryan, (all CF<br />
Mums) launched ‘65km for Cystic<br />
Fibrosis’ (www.65kmforcf.com.au),<br />
a 65km endurance walk to raise funds<br />
for research. The event exceeded their<br />
own expectations both in terms of<br />
participation and fundraising.<br />
As parents of children living with CF,<br />
these extraordinary mums know the<br />
value of research to improve the quality<br />
It is truly<br />
inspirational<br />
to witness and<br />
support such<br />
dedicated<br />
fundraisers.<br />
Matthew Hannan,<br />
<strong>Monash</strong> <strong>Health</strong> Foundation<br />
of life for their children. This was the<br />
driving factor and the motivation<br />
to work tirelessly to raise money to<br />
support research into CF.<br />
Cystic fibrosis is a complicated disease,<br />
it primarily effects the lungs and<br />
digestive system and there is currently<br />
no cure.<br />
<strong>Monash</strong> <strong>Health</strong> provides lifetime care<br />
for over 200 adults and children with<br />
cystic fibrosis. Every year, an average<br />
of eight newly diagnosed babies are<br />
referred to <strong>Monash</strong> <strong>Health</strong>’s Cystic<br />
Fibrosis clinic.<br />
Funds raised from the <strong>2017</strong> event have<br />
funded three research projects we<br />
hope will have a lasting impact on the<br />
lives of these consumers.<br />
• Studying the impact of DNase<br />
with early stage lung disease<br />
to decrease inflammation and<br />
infection. This project has the<br />
potential to improve the long-term<br />
outcome in children with CF<br />
• Investigating the effect of an<br />
innovative treatment to improve<br />
sinus symptoms, quality of life,<br />
and the amount of infections<br />
for people living with CF and<br />
sinus disease<br />
• Develop the optimal, patient-centred<br />
model of care for people with cystic<br />
fibrosis Related Diabetes.<br />
The small but amazing team continue<br />
their unwavering commitment to the<br />
cause, raising over $600k since 2013<br />
and funding more than 10 research<br />
projects.<br />
The team has now been joined by Sue<br />
Emery and Phil Ryan which has seen<br />
the event grow in its participation rates<br />
and success, remarkably raising over<br />
$147,000 in 20<strong>18</strong>. The Committee will<br />
work with health care professionals,<br />
researchers, and the CF community<br />
to determine priority projects for<br />
consideration with funding from this<br />
year’s event.<br />
In 2016, the team was awarded the<br />
Premier’s Volunteer of the Year, Dame<br />
Elisabeth Murdoch Award for Teamwork,<br />
for their inspiring contribution.<br />
‘65km for Cystic Fibrosis’ Committee<br />
members, from left, Julie Noorman,<br />
Susan Biggar, Kathy Ryan and Sue Emery.<br />
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