Histiocytosis-X

Histiocytosis-X

Self Help Clearinghouse

This information is provided as a resource and does not constitute an endorsement for any group. It is the responsibility of the reader to decide whether a group is appropriate for his/her needs. For evidence-based information on diseases, conditions, symptoms, treatment and wellness issues, continue searching this site.

Histiocytosis Association

(BILINGUAL) International network. Founded 1985. Mutual support and information for parents and patients with this group of rare disorders. Includes Erdheim-Chester disease, sinus histiocytosis Rosai Dorfman, xanthogranuloma, hemophagocytic lymphohistiocytosis, pulmonary eosinophilic granuloma, langerhans cell histiocytosis and familial erythrophagocytic lymphohistiocytosis. Website offers the opportunity for patients and families to network. Funds research. Literature and pamphlets (some available in Spanish) and newsletter.

Write:

Histiocytosis Assoc. of America

332 N. Broadway

Pitman, NJ 08071

Fax: 856-589-6614 / Jeff Toughill, President

Website: http://www.histio.org

E-mail: info@histio.org

Verified: 1/10/2013

This information does not replace the advice of a doctor. Healthwise, Incorporated disclaims any warranty or liability for your use of this information. Your use of this information means that you agree to the Terms of Use . How this information was developed to help you make better health decisions.

Healthwise, Healthwise for every health decision, and the Healthwise logo are trademarks of Healthwise, Incorporated.