This foundation was established following the death of our beloved Max Clayton Robinson.

Max was diagnosed with Leukaemia when he was 1 and a half and battled the disease until he passed away just after his 5^th birthday.

During his treatment, we weren’t satisfied with just following conventional protocol and researched away where we came across many alternative therapies that could complement his treatment protocol or atleast reduce the harsh side effects from the toxic treatments.

Unfortunately, these weren’t commonly discussed/brought up as literature was not accessible (or in a digestible format). Then, even if they were known they were unaffordable to most (no govt or private healthcare funding available and families usually struggling financially with the burden of illness) and even harder to access for children.

After so much research and understanding, we felt compelled to share this information.

This is where the vision of MAXX Living was born.