I’m fundraising in support of my cousin, Ethan.
Here is Ethan’s story:
Ethan was a healthy, active child, until one day out of the blue, he wasn’t quite right, frequent ear and throat infections and joint stiffness. His parents knew something was very wrong.
Doctors found something wrong. Many DNA tests to determined Ethan’s diagnosis- Hunter Syndrome, mucopolysaccharidosis type II (MPS II). They are lucky that his treatment is covered, but it means Ethan and his family attend weekly treatments that help slow the progression of his disease.
Medical research is so important to get any answers for any genetic condition. Research needs to continue so the next child diagnosed with a genetic disease —it can help them.
I care about the 1 in 20 Aussie kids who face a birth defect or genetic disease, like cancer. Most people don’t know that cancer is caused by changes in genes—but almost everyone will be touched by it. So, the research you and I support today may one day help someone we know, someone in our family or community.
There’s lots of work to do, but there is also lots of hope.
Join me. Share this message. Donate. Thank You!
Raised so far
With your help, I have raised...
$475
You’re helping fund research to find cures for kids with genetic diseases. Every dollar counts!
Biggest Donor
Jen Ming
$238
Thank you so much to my biggest supporter, Jen Ming, for donating an incredible $238 to help fund vital research into curing children’s genetic diseases.
My Impact
So far this year, I've helped fund...
10
Hours of research
Every $50 raised funds an hour of vital research.
Thank you to our donors
$238
Matched Donation
$238
