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Leave a gift in your Will

A line drawing of an adult and child embracing appears next to the text: "Leave a Legacy with a gift in your Will" on a dark blue background with small butterflies.

 

We want a world free from the pain of EB. A gift in your Will could: 
  • Fund future EB drug repurposing trials to help relieve the pain of epidermolysis bullosa (EB).
  • Fund a moment of respite and family memories in a DEBRA holiday home.
  • Positively change the lives of people living with EB.
  • Expand specialist EB nursing and family support
Your legacy could mean cuddles bring comfort, not pain.
Find out why leaving a legacy matters, what kinds of gifts you can leave, and how to get started – it’s simpler than you think!
A woman in a floral dress sits on a wicker sofa in a garden, smiling and hugging a large German Shepherd dog.

How to make a Will

If you wish to leave a gift in your Will to DEBRA, it is incredibly easy to do, whether you are writing a new Will, or updating an existing Will.
Learn more
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Request your gifts in Wills guide

Creating a Will can feel overwhelming, which is why we’ve put together our gift in Wills guide to make the process as straightforward as possible.
Get your guide now
DEBRA member Scarlett and her mum smiling and holding hands.

Write your Will at no cost to you

We have two simple FREE Will writing options: you could write your Will online, over the phone or visit a local solicitor.
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A woman in a blue "debra" shirt sits at a table, smiling and listening to a young girl in a wheelchair holding a teddy bear—showing how your legacy will help EB patients find comfort and support.

How your legacy will help EB patients

A gift in your Will to DEBRA can help fund vital community support and research into life-changing treatments for all types of EB.
Learn more
A person in a blue shirt is writing on a piece of paper with a pen.

Wills FAQs

Find answers to frequent questions about leaving a gift in your Will to DEBRA and helping change the lives of people living with EB.
Read the FAQs

“There needs to be a day when no one knows what EB is, not because it is rare, but because it no longer exists”

Wendy Hilling, DEBRA member and supporter