This year marks 3 decades since I became ill with ME/CFS (Myalgic Encephalomyelitis/ Chronic Fatigue Syndrome)
Every May 12 on Awareness Day we celebrate the #MillionsMissing – the millions around the world missing from day to day life due to ME/CFS.
My dear friend Karyn Crimmin is also severely affected by ME/CFS and has been housebound/bedbound for decades. I drew this portrait of her adorable granddaughter Immy, who advocates for the #MillionsMissing asking for more research. To me, this adorable picture is a celebration of love, loss and hope.