<?xml version="1.0" encoding="utf-8" standalone="yes"?><rss version="2.0" xmlns:atom="http://www.w3.org/2005/Atom"><channel><title>bullosa on Birmingham Daily</title><link>https://birminghamdaily.co.uk/tags/bullosa/</link><description>Recent content in bullosa on Birmingham Daily</description><generator>Hugo -- gohugo.io</generator><language>en-us</language><lastBuildDate>Sat, 06 Jun 2026 06:24:00 +0000</lastBuildDate><atom:link href="https://birminghamdaily.co.uk/tags/bullosa/index.xml" rel="self" type="application/rss+xml"/><item><title>'Heartbroken' Mum Discovers Baby Has Inherited Rare 'Butterfly Skin' Condition</title><link>https://birminghamdaily.co.uk/heartbroken-mum-discovers-baby-has-inherited-rare-butterfly-skin-condition/</link><pubDate>Sat, 06 Jun 2026 06:24:00 +0000</pubDate><guid>https://birminghamdaily.co.uk/heartbroken-mum-discovers-baby-has-inherited-rare-butterfly-skin-condition/</guid><description>Jennifer Taylor, a 34-year-old mother from Prescot, Merseyside, has lived her life with dystrophic epidermolysis bullosa (DEB), a rare genetic condition often described as &amp;lsquo;butterfly skin&amp;rsquo; due to the extreme fragility of the skin, resembling a delicate butterfly’s wings. The disorder causes skin tears, blisters, and severe pain from everyday activities such as writing, walking, and eating.
Jennifer first showed symptoms as a baby when her thumb blistered and lost a fingernail.</description></item></channel></rss>