Cure EB Foundation
We're a part of it, raising awareness & much needed funds to cure EB. Epidermolysis Bullosa (EB) is a debilitating rare genetic condition that results in painful blistering and peeling of the skin at the slightest touch. EB children are often called 'butterfly children' or ‘cotton wool kids’ because of the fragility of their skin. EB is often referred to as "the worst disease you've ever heard of" and we must find a cure.
17/07/2026
One unforgettable night of discovery…
Jayco together with CureEB Foundation invite you to a black-tie evening of live entertainment, fine dining and premium wines, live and silent auctions, and a room full of glamour — all in support of life-changing EB research.
Tickets live now, link in bio.
Saturday 29 August
Forum Melbourne
✨ Flashback to last year’s Cure EB Foundation Business Lunch ✨
An incredible afternoon filled with great conversations, amazing supporters, and a shared commitment to making a difference for families living with Epidermolysis Bullosa 💙
We can’t wait to do it all again this year!
📅 Friday 12th June
🎟️ Tickets available via the link in our bio
Will you be joining us? We’d love to see you there.
Click here to claim your Sponsored Listing.
Contact the organization
Telephone
Address
L 4 114 William Street
Melbourne, VIC
3000
Opening Hours
| Monday | 9am - 5pm |
| Tuesday | 9am - 5pm |
| Wednesday | 9am - 5pm |
| Thursday | 9am - 5pm |
| Friday | 9am - 5pm |
