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DEBRA Butterfly Children’s Charity is appealing to government agencies to cover the cost of the much needed, specialist, EB team of nurses that work tirelessly to support and care for children with Butterfly Skin
Read moreThese costs are currently met by the charity: DEBRA Spain is the only national support system available for families with Butterfly Skin: a rare and currently incurable disease that causes extreme fragility of the skin. The charity is also bidding for further investment into research and appealing for more commitment and greater financial support. Within […]
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Celebrate with us: join the 304 families with Butterfly Skin in Spain
Read more304 families: the most recent campaign launched by the Debra Butterfly Children’s Charity to raise awareness for children with Epidermolysis Bullosa. Known as the most painful condition you have never heard of. EB is a rare and extremely debilitating disease that gives no respite over the festive season for families who have to live with […]
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After the success of the Guadalmina event held earlier in the summer, the Butterfly Children’s Charity raised more than €17.000 at the Aloha Golf Club Tournament
Read moreThe funding will be used to improve the quality of life for families with Epidermolysis bullosa, a rare and currently incurable disease that affects 500 people in Spain. The charity was delighted to hold this tournament after 5 long months of cancelled events due to the Coronavirus crisis. After months of uncertainty the Butterfly Children’s […]
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Celebrating European Patients Rights Day
Read moreThis important day takes place on the 18th of April: it is a marked occasion for open discussion and serves to reinforce commitment to the 14 rights established for European citizens. These rights were established to encourage the cooperation between the different health care providers and to reinforce the degree of protection for patients affected […]