Liz was an NHS doctor for over 10 years, during which time she became acutely aware of multiple health inequalities both professionally and personally. After being diagnosed with mixed connective tissue disease (Lupus SLE related), recurrent miscarriages, Stage 4 Endometriosis requiring multiple surgeries, eventually Liz stepped away from a clinical facing role. Since the age of 18 Liz had worked as a freelance artist, and during the Covid-19 pandemic working frontline in Emergency Medicine Liz began to use her art to convey important messages regarding health which saw her recognition as an artist grow. When her son was born premature needing NICU after a traumatic delivery, Liz experienced PND. These experiences of realising the enormity of social stigmatisation of disease, gender related health inequalities and the need for better support planted the seed of an idea. Liz spent the next five years planning a way to use art on an enormous scale to shine a spotlight on the reality of what people are experiencing in an attempt to raise awareness, educate and provide support through sharing messages of hope and strength. Taking it one step further, Liz wanted to utilise the opportunity for creating such a large scale online and offline platform for health awareness to support other charities in a way never before done. Bringing together communities previously working in isolation (cancer, endometriosis, autoimmune) to increase the impact of education and awareness to change the stigma of disease and maximise the impact of the campaign.