3rd Annual Walk & Roll for EDS Awareness: Central Valley
2870 Alamos Ave.
Sat, May 2, 2026 at 09:00:00
About this event
Hosted by the Clovis/Fresno EDS Support Group 📅 Date: May 2, 2026⏰ Time: 9:00 – 11:30 AM📍 Location: Thorburn Park | 2870 Alamos Ave, Clovis, CA💵 Registration: $10 per person | $30 per family (up to 6) | OPTIONAL to Waive Entry Fee: Fundraise, Volunteer, Donate, or Share your Art! Select "General Participant" to Fundraise as: An Individual: Create a personal fundraiser when you register—raising $20 will waive your $10 registration fee! A Team: Create or Join a team when you register. The suggested team goal of $200! Select "Volunteer" to: Donate to the Silent Auction: Donate a themed basket, product or service of $20 or greater value to waive your entry fee! Participate in the Art Exhibit: Share your art (as an EDS Artist or EDS-themed art) to waive your entry fee! 🎉 Event Highlights & Activities1️⃣ Walk & Roll – One Mile (or Less!)Join our 1-mile loop at your own pace—walk, roll, or wheel! Be part of the EDS Society’s International Walk & Roll Challenge and show your dedication to raising EDS Awareness. Every step counts! 2️⃣ Silent AuctionCruise the aisles and discover treasures donated by our generous supporters. From quirky finds to one-of-a-kind items, there’s something for everyone! 3️⃣ EDS Artists’ ExhibitMarvel at art created by local EDS community members. This is your chance to see creativity, resilience, and inspiration come to life. 🎨 4️⃣ Resource & Activity BoothsExplore arts & crafts, info from local providers, giveaways, hydration stations, and interactive activities—something for every member of the family! 💡 What is EDS?The Ehlers-Danlos syndromes (EDS) are a group of 13 rare connective tissue disorders caused by genetic changes affecting connective tissue. Features vary by type, but common traits include: Joint hypermobilityStretchy, fragile skinTissue fragility[Click here to learn more!] 🦓 How Rare is EDS? Hypermobile EDS (hEDS): Most common, ~1 in 3,100–5,000 peopleClassical EDS (cEDS): ~1 in 20,000–40,000 peopleVascular EDS (vEDS): ~1 in 100,000–200,000 peopleUltra-rare types: Affect <1 in 1 million; some reported in only a few families Even though some types are rare, the impact on individuals and families is huge, and raising awareness is key! 💛 Why You Should JoinWalk, roll, explore, and connect! This is more than an event—it’s a community celebration of strength, creativity, and support for those living with EDS. Every step you take and every connection you make helps raise awareness and resources for this often-misunderstood condition. Register today and be part of the movement!