Our vision is a world where all genetic diseases
are cured and no patient or illness is neglected
Daybreak Children’s Rare Disease Fund is a 501(c)(3) not-for-profit organization whose mission is to support the best research aimed at the cure of rare genetic diseases. Daybreak choose as primary beneficiaries of its efforts Fondazione Telethon Italia and its two world-class research centers, TIGEM and SR-TIGET.
Daybreak Children’s Rare Disease Fund is committed to raise awareness on rare genetic diseases and to promote timely development and availability of safe and effective diagnostics and treatments for affected persons.
In pursuing its mission Daybreak Children’s Rare Disease Fund is inspired by the absolute value of each unique person.
Highest ethical standards and utmost respect for any individual involved or touched by our activities.
Absolute transparency over every aspect of our operations and grant-making.
Reward of merit, talent and competence. Continuous effort to improve the way we work and the quality of our outcomes.