“We’re thrilled to know she has helped so many people,” shares Emilia’s dad, James. We recently had the pleasure of presenting Emilia with a special letter to celebrate how she has inspired over 2,400 people to register with DKMS, after hearing her powerful story. ✨ Emilia's story beautifully illustrates the life-changing potential of a stem cell transplant. Let's continue to spread awareness and encourage others to register at dkms.org.uk/register . Together, we can help more individuals like E
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🎥✨ Watch the heartwarming moment when 8-year-old Jacob meets his lifesaver, Lorna! ❤️ At just 19 months old, Jacob was diagnosed with a rare, life-threatening condition called haemophagocytic lymphohistiocytosis (HLH). His only hope was a stem cell donation, which he received in March 2019 from a woman he had never met. Five years later, Jacob finally got to meet his hero in person for the very first time. You have the power to save a life, just like Lorna. Register as a stem cell donor today a
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7-year-old Adeline and 5-year-old Josie are two sisters living with Shwachman-Diamond Syndrome (SDS), a rare genetic condition. Their mum, Steph, shares their story so far... In 2021, Adeline found her stem cell match and had a successful stem cell #transplant, giving her a new chance at life. But little Josie is still searching for her match. ✨ By registering as a stem cell #donor with DKMS UK, you could be the one to give someone like Josie the gift of hope. 📢 Help Steph and her family by sha
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This week, we're talking about #HerStory - a series of stories shared by the wonderful women of #DKMS and #DKMSBMST. First, we have the founding ladies of this flourishing organization. Due to Mechtild Harf's unfortunate passing, her husband Peter Harf and her daughter made it their life's mission to eliminate the struggle that patients suffering from blood cancer and blood disorders face on a daily basis. Join us in our fight against blood cancer by clicking the link below!🙂 dkms-bmst.org/regi
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This is the incredible story of Brandon and Brian #DKMS | DKMS US
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This #AplasticAnaemiaDay, we're celebrating Emilia's incredible journey! Diagnosed with aplastic anaemia at just 5 years old, she faced painful and life-threatening symptoms - but thanks to a stem cell transplant, Emilia is now a thriving 7-year-old. Not only has she overcome so much, but she’s also dedicated to helping others by raising awareness and fundraising for vital causes. Her story has also inspired thousands to join the stem cell register — potentially saving countless lives! 🙌 Emilia
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Kathleen Hogan describes the most challenging time in her life, searching for a bone marrow match for her son Owen, who was suffering from a life-threatening blood disorder. With the help of a bone marrow donor, Owen found his hero. Owen who was two years old at the time suffered from aplastic anemia, a life-threatening blood disorder, and needed a bone marrow transplant to survive. Without a matching bone marrow donor in the family or the donor pool, the family began hosting a series of bone ma
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