Help us raise vital funds for Mind Body EDS through Abbie's Wonderland
This charity is incredibly close to our hearts. As many of you know, Loretta lives with Hypermobile Ehlers-Danlos Syndrome (hEDS), a genetic connective tissue condition. Due to severe complications, she is unable to eat or drink and relies entirely on Total Parenteral Nutrition (TPN), alongside managing multiple associated conditions.
Abbie was also diagnosed with hEDS. She experienced gastrointestinal issues, joint instability and similar comorbidities, making this cause especially meaningful to our family.
Mind Body EDS is a small, volunteer-led charity dedicated to raising awareness, improving education within the medical community and supporting patients. Funds raised help with diagnosis pathways and provide grants so individuals can access vital treatment and healthcare support.
Our first event is BBQ, Bar & Bakes on June 13th. Please head to the Abbie’s Wonderland Facebook page for full details.
Funding method
Keep what you raise – this project will receive all pledges made