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ALLERGY & ASTHMA NETWORK/MOTHERS OF ASTHMATICS
(AANMA)
AANMA is dedicated to helping people affected by allergies and asthma through education, advocacy, community outreach and research. AANMA offers educational materials, monthly award-winning publications, a toll-free help line, Hispanic outreach, and a Website, www.breatherville.org. Visit or call 1-800-878-4403.2751 Prosperity Avenue, Suite 150
Fairfax, VA 22031
Phone: 800/878-4403
Fax: 703/573-7794
www.aanma.orgAMERICAN LATEX ALLERGY ASSOCIATION (A.L.E.R.T., Inc.)
The mission of the American Latex Allergy Association (A.L.E.R.T., Inc.) is to create awareness of latex allergy through education and to provide support to individuals who have been diagnosed with latex allergy.3791 Sherman Road
Slinger, WI 53086
Phone: (888) 972-5378
Fax: (262) 677-0324
E-mail: alert@execpc.com
Web site: www.latexallergyresources.orgAMERICAN PARTNERSHIP FOR EOSINOPHILIC DISORDERS (APFED)
APFED is a non-profit organization dedicated to patients and their families coping with eosinophilic gastrointestinal disorders. APFED strives to expand education, create awareness, and support research while promoting advocacy among its members.3419 Whispering Way Drive
Richmond, TX 77469
Phone: (713) 498-8216
E-mail: apfed@sbcglobal.net
Web site: www.apfed.orgASTHMA & ALLERGY FOUNDATION OF AMERICA (AAFA)
The Asthma and Allergy Foundation of America is a not-for-profit, voluntary health organization dedicated to improving the quality of life for people with asthma and allergies and their caregivers through education, research and advocacy.1233 20th Street, NW, Suite 402
Washington, DC 20036
Phone: (800) 7-ASTHMA (800) 727-8462 or (202) 466-7643
Fax: (202) 466-8940
www.aafa.orgAlaska Chapter: www.aafaalaska.com
California Chapter: www.aafa-ca.com
Greater Kansas City Chapter: www.aafakc.org
Maryland/Washington DC Chapter: www.aafa-md.org
Michigan Chapter: www.aafamich.org
New England Chapter: www.asthmaandallergies.org
Texas Chapter: www.aafatexas.org
St. Louis Chapter: www.aafastl.org
FOOD ALLERGY & ANAPHYLAXIS NETWORK (FAAN)
FAAN's mission is to raise public awareness, to provide advocacy and education, and to advance research on behalf of all those affected by food allergies and anaphylaxis.11781 Lee Jackson Highway, Suite 160
Fairfax, VA 22033
Phone: (800) 929-4040 or (703) 691-3179
Fax: (703) 691-2713
www.foodallergy.org
FOOD ALLERGY INITIATIVE (FAI)
FAI's mission is to raise public awareness about the seriousness of food allergies. Through effective educational programs and public information, FAI heightens awareness of food allergies and anaphylaxis among the media, healthcare workers, education and childcare professionals, while also working with the nation's policy makers to create a safer environment and improve care for the food allergic population.1414 Avenue of the Americas, Suite 1804
New York, NY 10019
Phone: 212/207-1974
www.foodallergyinitiative.org
info@foodallergyinitiative.org
IMMUNE DEFICIENCY FOUNDATION (IDF)
Devoted to research and education in primary immune deficiency diseases, IDF has established chapters across the country. On behalf of those with primary immune deficiency diseases, IDF promotes and supports scientific research in the causes, prevention, and treatments; promotes and supports training in medical research and clinical treatment; coordinates and disseminates information; and conducts educational campaigns to increase public awareness.25 West Chesapeake Avenue, Suite 206
Towson, MD 21204
Phone: (800) 296-4433 or (410) 321-6647
Fax: (410) 321-9165
www.primaryimmune.orgTHE MASTOCYTOSIS SOCIETY (TMS)
The Mastocytosis Society is a nonprofit organization dedicated to supporting patients affected by Mastocytosis/ Mast Cell Activation Disorders as well as their families, caregivers, and physicians/health care providers through research, education, and advocacy. TMS offers educational materials, a quarterly newsletter, a written resource guide for physicians/health care providers who need assistance in diagnosing a patient with a suspected mast cell disorder, an email list, and support groups. We hold an annual conference that starts off with a Walk-a-thon to raise funds for mast cell research and education, and is attended by patients and mast cell disease specialists. For more information, please visit our website at www.tmsforacure.org .The Mastocytosis Society
P.O. Box 511
Plainville, CT 06062
Phone: 508-842-3080 or 413-862-4556
Fax: 508-842-2051
vslee@tmsforacure.org
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