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For Jasmine Ritchie, every day is a challenge. She has a rare skin condition called Epidermolysis Bullosa, and lives in excruciating pain. The condition means the 'glue' that holds the layers of skin together is missing, causing it to blister at the most delicate touch.

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63,788 views • 9 months ago •via X (Twitter)

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Every day is an uphill battle for 13-year-old Jasmine Ritchie, who has a rare skin condition called Epidermolysis Bullosa, also known as butterfly skin, which causes her skin to blister and tear at the slightest touch. Jasmine's mum, Anna, and Grandad Robert took on their own challenge to raise money for those living with the skin disorder by climbing Mount Kilimanjaro. Anna recalls the experience as Graeme Souness explains why raising awareness and money is so important. Susanna Reid | Ed Balls | DEBRA UK

Every day is an uphill battle for 13-year-old Jasmine Ritchie, who has a rare skin condition called Epidermolysis Bullosa, also known as butterfly skin, which causes her skin to blister and tear at the slightest touch. Jasmine's mum, Anna, and Grandad Robert took on their own challenge to raise money for those living with the skin disorder by climbing Mount Kilimanjaro. Anna recalls the experience as Graeme Souness explains why raising awareness and money is so important. Susanna Reid | Ed Balls | DEBRA UK

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Dean was born with epidermolysis bullosa, a rare genetic condition that causes his skin to blister and tear at the slightest touch. Despite being given just two years to live when he was born, he has defied the odds and is now 46 years old.

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anyone looking for a good cause to raise £ for look no further than DEBRA UK and the work they do for sufferers of epidermolysis bullosa (EB) a rare and painful skin condition. People - alot of them kids - living in 24/7 pain. Heartbreaking stuff. Graeme Souness is president

anyone looking for a good cause to raise £ for look no further than DEBRA UK and the work they do for sufferers of epidermolysis bullosa (EB) a rare and painful skin condition. People - alot of them kids - living in 24/7 pain. Heartbreaking stuff. Graeme Souness is president

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