In Beni Mellal, Saliha is appealing for urgent help to save her two daughters, aged 9 and 5, who suffer from Epidermolysis Bullosa, a rare genetic disease that makes their skin tear at the slightest touch. Alone, without income and still grieving a first child lost to the same illness, the mother says she can no longer afford treatment, food or the heart surgery her eldest daughter urgently needs.