100 crunches a day for FoxG1 Research Australia

Hi, my name is Denise, my son Adam was diagnosed with this Rare Genetic Syndrome, FoxG1 when he was 6yo.

Adam is now 19 and the impact of this syndrome is extremely devastating.

Some of the symptoms are severe epilepsy, extreme involuntary movements, non verbal, uses wheelchair and that’s just to name a few.

Please take the time to have a look at this link https://foxg1research.org/australia

also https://foxg1.org/ click on faces of FoxG1 and read Adam’s early years story.

November is FoxG1 Awareness month, please support us in raising as much as we can to help find a cure for this debilitating disease.

Any donation, no mater how small is greatly appreciated.

TOGETHER WE WILL FIND A CURE

Do you want to join me in making a difference? I'm raising money in aid of FOXG1 RESEARCH FOUNDATION (AUSTRALIA) LTD and every donation will help. Thank you in advance for your contribution to this cause that means so much to me.