We need your support to raise funds & awareness.Help us find a cure for Cystic Fibrosis.

What's On!

Read about Jessie and her family, her battle with CF, fundraising events, people in her life and more.

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Jessie's Story Let's Cure CF

Our Mission

To increase Cystic Fibrosis awareness.
By sharing Jessie's personal story we aim to raise more awareness about Cystic Fibrosis.
To raise much needed funds for Cystic Fibrosis research.
There is little to no Government support given towards research.

Without your help recent advancements in treatments, medication, care and getting closer to a cure would be near impossible.
To make a contribution to the Cystic Fibrosis community.
The Team Jessie Lets Cure CF website will hopefully help continue to raise awareness, educate people about Cystic Fibrosis and serve as another resource hub for other parents walking the same path.
To help educate more people about Cystic Fibrosis.
Cystic Fibrosis [CF] is the most common, genetically acquired, life-shortening chronic illness affecting young Australians today.

Many people still don't know what Cystic Fibrosis is, even though on average one in 25 people carry the CF gene. 
To make CF stand for
Too many people are dying from Cystic Fibrosis.
Lung failure is the major cause of death for someone with Cystic Fibrosis.

While research has led to people living longer, lives are still cut way too short.

Ultimately our goal is to find a cure!
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Give From the Heart!

Help us find a cure by making a donation.

Your donation goes directly to the The Royal Children's Cystic Fibrosis Research Trust.

Research projects are based at the Melbourne's Royal Children's Hospital (RCH), one of the worlds leading paediatric teaching hospitals, The RCH currently has more than 300 CF patients under its care.

Every dollar raised goes directly to research