Cure EB Family Forum

overlaid black and white photos of children with EB overlaid with 'Epidermolysis Bullosa. Hard to Say. Hell to live with.'

As a charity set up by a family directly affected by Epidermolysis Bullosa, Cure EB understand the desperate need for, and the potentially life-changing impact of, research into this devastating condition.

The Family Forum has been created in order to keep those impacted by EB updated on current and potential EB research, as well as how to support our search for a cure. It is free to join.

If you or a family member have EB, sign up to the Family Forum to hear about:

  • Regular email updates on EB research and Cure EB news.
  • Annual Cure EB newsletter.
  • Access to research webinars.
  • Online get together for people living with EB and their families.
  • Entrance to Cure EB Family Day.
  • Information on Cure EB fundraising events.

How else can I get involved?

You don’t have to join the Family Forum to be a part of curing EB!

You could:

Your support will help us continue to fund research into effective treatments and ultimately a cure for EB.

Upcoming events

EB Family Day 2026

4 October 2026

Our EB Family Day is back on Sunday 4th October – if you or your family member has EB, we’d love you to join us at this free event. Find out more & register now.

Visit our calendar to see all of our upcoming events.