Our Story
Forest Hayah is the first non-profit organization in Egypt dedicated to providing assistance and support for children with rare diseases. Our organization was founded by Ghada Mounib, who was deeply moved by a Facebook post from a desperate mother. The post highlighted the astronomical cost of her son’s medication, a staggering 2 million USD. Inspired by this mother’s struggle and determined to make a difference, Forest Hayah was established to ensure that no child is denied life saving treatments due to financial constraints.
Through our crowdfunding efforts, we aim to provide the necessary funding to cover the exorbitant costs associated with rare disease treatments. Join us in our mission as we strive to provide hope, support, and a brighter future for these courageous children and their families. Together, we can bring healing and transform lives, one child at a time.
Our Vision
A future where rare diseases in Egypt are no longer a barrier to health and wellbeing. We envision a world where patients receive timely and accurate diagnoses, have access to effective treatments and therapies, and are supported by a network of knowledgeable and compassionate healthcare professionals, policymakers, and the general public…
We aim to create a society where individuals with the rare diseases are valued, respected, and empowered to live their best lives.
Mission
Improve the lives of children and families affected by the rare diseases in Egypt.
We strive to provide education, support, and resources to empower patients and their families, while advocating for greater awareness and understanding of these conditions.