2.3K reactions · 158 shares | Join us as we go #BehindTheMystery of Epidermolysis Bullosa (EB) where we meet 5-year-old Brady who has #epidermolysisbullosa. See how his family is determined to give Brady a full life, despite his #raredisease. ELONGATE's generous donation to EB Research Partnership established them as the founding member of the #CryptoForCures Fund with the goal to raise $1 million in cryptocurrency donations by the end of 2021. | The Balancing Act | Facebook

1.1M views · 38K reactions | His lungs could barely hold on. But he couldn’t contain himself when he saw his mom. - Guilherme Granda Moura had been struggling for his life for 15 days. One day, his eyes opened and he only had one wish: To see his mom. Life has not been easy for little “Gui”. His strange illness has taken a toll on his body, harmed his skin and wreaked havoc on his body. This is what the mysterious Epidermolysis bullosa causes. | Vitamin | Facebook

4.1M views · 63K reactions | Isla Grist shares her experiences living with epidermolysis bullosa and discusses her friendship with Liverpool legend Graeme Souness. | Good Morning Britain | Facebook