GI Motility Disorders Unit

The Inside Story: Gastroparesis Support Group was created to provide a platform for patients and supports to connect and share their experiences. Our partners, Gastroparesis Australia, offers resources and information for new patients. Some of our gastroparesis advocates have written their experiences and would like to share their stories with the world:

• Ashley (Sydney) was diagnosed with idiopathic gastroparesis at 25 years old after recovering from the flue. She is one of our most devoted advocates for gastroparesis awareness. Despite the difficult journey ahead Ashley remains optimistic and hopeful. You can read her story here.
• Anneliese (Sydney) suffers from diabetic gastroparesis. She endured a series of diagnostic tests and unsuccessful treatments before having a nasojejunal feeding tube implanted. The disease is putting an enormous mental strain on herself and her family. Anneliese founded Gastroparesis Australia and strives to increase awareness and provide information for suffers and carers. You can read her story here.
• Emily (Devonport) first experienced symptoms at 13 but due to the difficulties of identifying gastroparesis, she was not diagnosed until three years later. Although Emily lives a healthy and active lifestyle the symptoms of gastroparesis can completely immobilise her on some days. Emily is an acting gastroparesis advocate at Devonport Rotary Club and is helping raise much needed funds for gastroparesis research. You can read her story here.
• Dennis (Devonport) is the father to Jacinda, who was diagnosed with gastroparesis in 2015. It has been difficult for Dennis to watch his daughter suffer with the disease but he has made it his family's mission to one day find a cure. Dennis organises local fundraisers and does everything he can to help Devonport Rotary Club and Western Sydney University raise funds for gastroparesis awarenss and research. You can read his story here.