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Histiocytosis Association of America Mission Statement

The Histiocytosis Association of America is dedicated to raising awareness about histiocytic disorders, providing educational and emotional support, and funding research leading to better treatments and a cure.


Histiocytosis Association of America Vision

A world free of histiocytic disorders.


Research Program

The objectives of the Research Program are to fund worthy scientific research projects, educate physicians and scientists, encourage and support symposia into histiocytic disorders, directly participate in research projects, and encourage publication of scientific information.


Member Services

These programs include educational brochures, networking directories, regional education meetings, newsletters, toll-free phone number, annual awareness campaign, online virtual community website, physician-linking network, and volunteer coalition.


Fundraising Program

The goal of the Histiocytosis Association's Fundraising Program is to provide resources for the Association's research program, member support programs, administrative and fundraising costs through a cooperative effort of the Board of Trustees and Association staff with assistance from patients, families, physicians and friends of the Association.

HAA Fundraising Statement

The Histiocytosis Association of America and its members host fundraising events and campaigns throughout the United States. The Association relies on the proceeds generated through these programs to raise awareness about histiocytic disorders, provide educational and emotional support, and fund research leading to better treatments and a cure.

Getting involved in fundraising for the HAA is a great way to affect others positively while having fun!


HAA Membership

The Histiocytosis Association of America, a non-profit organization registered with the Federal Government, is dedicated to helping those dealing with the effects of rare histiocytic disorders by providing a variety of educational programs and emotional support services. There is no cost to become a member of the Histiocytosis Association of America.  Membership is automatic at the time of initial contact and/or original request for information.  Members are entered into the Association's database and coded according to his/her relationship with a histiocytosis patient.  This coding system insures that members receive all pertinent and appropriate materials.

Why should you support the Histiocytosis Association of America?

The Histiocytosis Association of America was recently awarded the coveted Four-Star Charity Rating from Charity Navigator, the nation's leading evaluator of charitable organizations. This honor is only bestowed upon charities that have demonstrated outstanding financial practices, based upon a review of their annual financial statements and other organizational documents. With a small, dedicated staff and a number of highly skilled volunteers, the Association has worked since 1986 to provide vital services to individuals affected by the histiocytic disorders. The Association funds essential clinical trials and basic research projects, hosts national and regional conferences, and provides high-quality information to patients and their loved ones, as well as physicians.


 



 

Copyright 2007 Histiocytosis Association of America
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