Jade lives with GAMT (Guanidinoacetate Methyltransferase Deficiency), a rare creatine deficiency. Without the researchers and the Association for Creatine Deficiencies (ACD), she wouldn't have her diagnosis or treatment.

This 26th July, we're joining the WALK FOR STRENGTH to raise funds for research, treatment and awareness for GAMT, CTD, AGAT- all CCDS.

Because GAMT is ultra-rare, it is not easily recognised in the medical field at ground level, and we receive no government funding- every donation counts and is tax-deductible in Australia.

SHARE TO SPREAD THE WORD

By joining us in stepping out and raising money, it will mean so much to us, as crowd funding is not just about collecting funds, it's about people making a difference.