Together we will find a cure for Histiocytosis.
Providing research, education, and support to patients and their families.
Friends of the Artemis Association is the U.S. affiliate of The Artemis Histiocytosis Association, an international non-profit that provides advice and comfort to those affected by Histiocytic Disorders. For more than 30 years we have worked to find a cure for this rare set of diseases.
We are proud to offer our community of parents, patients, friends, and doctors a place to come together and share their experiences. Through public advocacy and fundraising initiatives, we continue to raise awareness and contribute to medical research around the world.
$1.3M +
Funds raised and donated globally to investigate histiocytosis epidemiology, diagnosis, treatment, and clinical care for children and adults with these disorders.
315 partners
Scientists, clinicians, and researchers have joined our symposium to share discoveries, meet with parents and patients, and work towards a cure.
30 years
Supporting research projects at Memorial Sloan Kettering, Institute of Child Health at University College, London, University of Lausanne, Switzerland and others.
The Nikolas Symposium
Held each year in Greece, our symposium is the leading scientific think-tank focused on Histiocytic disorders. We bring together scientists, researchers, and medical professionals from all over the world to examine, deliberate and debate the pathogenesis and structure of these diseases.
We are here to help!
Navigating the emotional, physical, and financial effects of Histiocytic Disorders can be overwhelming. It’s important to remember that you are not alone. Find out what resources and support organizations can support you and your family.
Make a Donation
Our work is made possible thanks to donations. Your support makes a vital difference to our research goals and to the lives of patients around the world.
