This site is a research tool for past or current childhood cancer survivors diagnosed between ages 0-20 and their immediate family members. Note: This is not a registered organization and does not accept donations.
Our mission is to identify survivors and/or their families globally. We aim to have at least four survivors in each country to establish a local network, which will connect and partner with existing local cancer organizations.
Our vision is to create a support network for survivors and their families. This network will enable survivors to share their experiences and effective aftercare practices across different regions, considering the varying resources available in the Middle East, Asia, Africa, Europe, Oceania, and The Americas.
This initiative is being led by a childhood survivor with the support of many kind-hearted individuals and qualified psychologists as volunteers. The objective here is to create a safe space for survivors to find support and a community.
My journey was full of hardships and difficult lessons. In 1990, at age 7, I was diagnosed with a rare cancer in Riyadh, Saudi Arabia, at a time when medical advancements were limited. My parents were devastated when doctors told them, “There’s nothing more we can do for your son.
Cancer changes a person, fundamentally altering their very being. Despite undergoing chemotherapy and radiation, my tumor wouldn’t shrink, setting a new benchmark for fear and bad news. Unable to fend for myself, my parents took me to the Mayo Clinic in Minnesota, USA. My father, being in the pharmaceutical business, had connections in the global medical community. After 1.5 years of battling cancer, I finally went into remission. However, the psychological toll on my family was immense—survivor guilt, parental torment, and the constant fear of recurrence created an unhealthy ripple effect that needed bridging with understanding and support. Over the years, I learned much about myself. I’ve lost and gained friends, partners, and family members.
I’ve closed off parts of myself and opened others, experiencing both pain and liberation. My faith as a Muslim provided hope, and I found common values with people of different beliefs. I’ve faced setbacks and made progress, but through it all, I learned that thoughts are fuel. Good thoughts propel you forward, while bad ones stall you. I was blessed with supportive people who uplifted me during tough times and helped me succeed in my industry. Unfortunately, not everyone has such support, and that is what I aim to change. To quote Walt Disney "It's Kinda of fun to do the impossible."
Hiba Salem is a compassionate psychologist dedicated to providing comprehensive mental health services to individuals, couples, and families on their journey towards improved well-being.
Specializing in palliative psychology and psycho-oncology, she offers evidence-based support to those navigating the challenges of cancer. With a bachelor’s degree in psychology from the American University of Beirut,
Hiba continued her education in the United States, earning a master’s in Clinical Mental Health Counseling from Lesley University and a master’s in psychology from Boston University. Her robust academic background, complemented by ongoing professional development, serves as the cornerstone of her clinical practice. During her tenure at the American University of Beirut Medical Center, Hiba made significant contributions to the fields of clinical psychology, palliative care, and psycho-oncology.
Through her compassionate and evidence-based approach, she has had the privilege of supporting patients and their families through various psychological and medical challenges.