The infantile form tends to respond well to topical
Support and advocacy groups can help you connect with other patients and families, and they can provide valuable services. Many develop patient-centered information and are the driving force behind research for better treatments and possible cures. They can direct you to research, resources, and services. Many organizations also have experts who serve as medical advisors or provide lists of doctors/clinics. Visit the group’s website or contact them to learn about the services they offer. Inclusion on this list is not an endorsement by GARD.
These resources provide more information about this condition or associated symptoms. The in-depth resources contain medical and scientific language that may be hard to understand. You may want to review these resources with a medical professional.
8th International Eosinophil Society’s Biennial Symposium
Saturday, July 13, 2013 -
Wednesday, July 17, 2013
Location: Oxford, England
Description: IES Symposium organizers’ central goal is to provide a highly interactive, interdisciplinary forum for scientific exchange and collaboration amongst junior and senior scientists in the fields of allergy, immunology, hematology, and cancer in relation to the role of the eosinophil in health and disease.
Contact: Michael Minnicozzi, Ph.D., (301) email@example.com
Co-funding Institute(s): National Institute of Allergy and Infectious Diseases, Office of Rare Diseases Research
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I am trying to find out information about how this may be treated, if it is an autoimmune disorder (I have been told that it is autoimmune by one provider, and a second provider told me that is in not autoimmune, but an allergy disorder), and how it will affect my son during his life. Will this weaken his immune system? See answer