Hyper Eosinophilia Syndrome (HES) Idiopathic Eosinophilia This site has been established in order to be a specific meeting place for people with this condition. This is a very rare condition - even more rare when the cause is unknown or unidentified. The medical profession has not yet developed a means of tracking or counting folks with this condition - whether the cause is identified or not. Therefore, we also have no way of knowing how many people in the world are affected by (HES) or any way to track the different treatments that are being applied to the patients and their success. The doctors are just now beginning to organize a committee for this purpose, which will not be fully functional and able to officially track information for a few years. Our goal is to find as many people affected by (HES) as possible and to accumulate and organize as much information as we can. This information may be provided to the medical community to assist them in their desire to know more about (HES), develop important statistics and treatment options.

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CHECK Out Our Support Group ALSO The American Partnership for Eosinophilic Disorders is a non-profit advocacy organization for those living with eosinophilic esophagitis, eosinophilic gastroenteritis, eosinophilic colitis, hypereosinophilic syndrome, and other eosinophilic disorders.

©Copyright 2000 (Barb Shiely) All Rights Reserved The content provided by on this site is for information purposes only and is in no way intended to be a substitute for medical consultation with a qualified professional. We encourage Internet users to be careful when using medical information. If you are unsure about your medical condition, consult a physician. Although we carefully review our content, we cannot guarantee nor take responsibility for the medical accuracy of documents we publish, nor can we assume any liability for the content of Web sites linked to our site.