Cure EB Foundation

Cure EB Foundation Be a part of it... Funding research into a cure for the worst condition you’ve NEVER heard of. Help us ! Be a part of it. We need your help to

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.

Are you ready? The countdown is officially on to the Jayco Discovery Gala 2026! 🎉In just 10 days, we’ll come together at...
19/08/2026

Are you ready? The countdown is officially on to the Jayco Discovery Gala 2026! 🎉
In just 10 days, we’ll come together at The Forum Melbourne for an unforgettable night of celebration, connection and fundraising — all in support of Cure EB Foundation and our mission to fund vital research towards a cure for Epidermolysis Bullosa (EB).
🥂 An incredible night ahead
🎤 Inspiring stories
🪩 Entertainment
🏆 Live & silent auctions
💙 And, most importantly, helping create a future without EB
Every ticket, bid and donation helps fund research and brings us one step closer to a cure.
Are you ready for Gala night? We certainly are!
📅 Saturday 29 August 2026
📍 The Forum Melbourne
⏰ 6:30pm

One unforgettable night of discovery…Jayco together with CureEB Foundation invite you to a black-tie evening of live ent...
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

14/05/2026

✨ 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.

Join us for an inspiring afternoon of connection, conversation, and impact 💙The Cure EB Business Lunch, hosted by Matthe...
06/05/2026

Join us for an inspiring afternoon of connection, conversation, and impact 💙

The Cure EB Business Lunch, hosted by Matthew Campbell, is back—bringing together our community to help fund vital research towards a cure for Epidermolysis Bullosa (EB).

📅 Friday 12 June
🕧 12:30pm – 4:30pm
📍 The Glasshouse, Olympic Boulevard

Enjoy a three-course lunch with premium beverages, exciting live auctions and raffles, and hear from our special guest speaker Ian Robson (CEO, Kooyong Tennis Club).

🍸 Plus, keep the conversation going with post-event drinks from 4:30–6:30pm.

🎟 Tables of 10 and individual tickets available

Every ticket helps bring us closer to a cure.

Secure your tickets via the link in bio.

24/04/2026

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

Telephone

+61413636766

Website

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