03/04/2026
“‘There’s always pain… there’s always an itch… there’s always a hospital appointment.’
Jennifer and her son William both live with dystrophic epidermolysis bullosa (DEB).
Their strength, love and determination shine through every single day.
Jennifer has shared her family’s story in a new blog, offering an honest look at life with EB and the support from DEBRA & their family that helps them through. 💜
🔗 Read the full blog: https://bit.ly/4bKtFXJ