Dear Dan,

The Ehlers-Danlos Society is delighted to announce its first vascular Ehlers-Danlos syndrome (vEDS) family camp, taking place in Ohio, USA, on July 7-9!

This three-day camp experience is in collaboration with The VEDS Movement, and will be facilitated by Camp Joy. This camp is for families where at least one member has a genetically confirmed vEDS diagnosis, to meet, connect, and spend time with those who understand.

The camp is fully supported by generous donations, with registration fees, accommodation, camp activities, and meals covered at no cost to you. Families will be responsible for travel and travel-related expenses. Places will be granted to families on a first-come, first-served basis via scholarship application.

What is Camp Joy?
Camp Joy is an 86-year-old, year-round camp that combines discovery, adventure, and fun while celebrating the growth and success of children. It includes everything one would hope to have at camp: campfires, nature hikes, swimming, crafts, face painting, songs, dancing, fishing, superheroes, S’MORES, and so much more! They are devoted to creating supportive and enriching experiences that provide campers with opportunities to grow intellectually, personally, and socially as they develop healthy friendships and create long-lasting memories. Campers will participate in activities that foster development in relationships, self-esteem, purpose, and learning new skills. Camp Joy’s counselors teach and lead young people in a variety of activities utilizing safe, fun, intentional, and experienced-based approaches.

LEARN MORE & APPLY FOR A PLACE!

vEDS Support Groups

vEDS virtual Let's Chat support groups take place monthly! Click the buttons below for individuals living with vEDS, and parents of children with vEDS or who have vEDS.