UNIQUE NEED
Cancer remains the #1 cause of death by disease for kids under the age of 19 in America, and at any given time approximately 40,000 children in the U.S. are on active treatment. Of those diagnosed in the U.S., one out of every five children will not survive. Every child we lose is one child too many.
Of those that do survive, two out of three will face at least one of the following long-term effects: secondary cancers, heart damage, lung damage, infertility, chronic hepatitis, alterations in growth and development, impaired cognitive abilities, or a psycho-social impact. One quarter of childhood cancer survivors face a late effect from treatment that is classified as severe or life-threatening.
Our mission was born out of this adversity, and it recognizes a twofold need:
- that children who are experiencing cancer need more psychosocial supports to help them through the treatment process; and
- that treatment itself needs to become safer, more effective, and ultimately provide a cure.
The Pablove Foundation is unique in that it approaches the issue of childhood cancer from both of these angles.
To date, the Pablove Shutterbugs program has served nearly 1,500 six- to 18-year-old children who have been diagnosed with cancer. Over half of our Shutterbugs are female, and the ethnic demographic breakdown is as follows: 51% Hispanic/Latino, 17% Caucasian, 13% Multi-Racial, 9% Black/African-American, 2% Other (the remaining 8% declined to state their race in our surveys).
Equally important, research into underfunded, cutting-edge pediatric cancer treatments benefits all children and families who are impacted by this disease. Globally, more than 400,000 children are diagnosed with cancer each year.