This year for my birthday I am raising funds for a cause that is now so important to our family. Little Willah was diagnosed with Juvenile Arthritis almost three months ago. Willah now has daily oral medication, weekly injections and sometimes trips to the Royal childrens for treatment. Willah experiences pain daily in her joints and now sees different specialist regularly to support her condition. JAFA are a cause now so important to our family. JAFA aims to - Raise awareness of juvenile arthritis among politicians and government, the education sector, the broader community and potential funders. -Lobby governments to provide optimal and accessible health care and support for children and adolescents with juvenile arthritis. -Influence and partner with funders to invest in research into the causes, treatment, care and possible cure for juvenile arthritis. Every bit counts to raise more awareness for Juvenile arthritis and help little people like little Willah