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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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