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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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.

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