What is hereditary hemochromatosis?

Hereditary Hemochromatosis (HH) is a genetic disorder in which the human body accumulates excess… (more)

What’s the treatment for HH?

The condition that causes iron overload cannot be cured, but it can be controlled by… (more)

What can I do to stay healthy?

It is important to maintain your health while you are receiving therapeutic phlebotomies… (more)

How can I help others?

Help spread the word about the dangers of too much iron… (more)

How do I join HIS?

Join our Facebook cause!

How do I learn more about the dangers of iron?

Visit these other websites to learn more about… (more)

 

Mission Statement

The mission of the Hemochromatosis Information Society is to promote public awareness about the genetic disorder hereditary hemochromatosis. The organization strives to meet the needs of those individuals, their families and friends diagnosed with hereditary hemochromatosis. In order to prevent adverse health effects and premature death, the Hemochromatosis Information Society supports routine screening of patients for hereditary hemochromatosis.

Message from the President

The goal of the Hemochromatosis Information Society web site is to provide valuable information for people with hereditary hemochromatosis. We want to be THE online resource for hemochromatosis information.

We strive to provide accurate, timely information regarding hemochromatosis and its treatment.

Sincerely,

President

Featured News

- January 2010 –
New Website

In November 2008, we were lucky enough to participate in a wonderful program offered by the Art Institute of Dallas. AID sponsored a competition to design a new logo for our organization. Students worked very hard and came up with several excellent designs. Ultimately, the design of Adrianne Riehn was selected as the winner. We have incorporated Adrianne design into our new website.

Healthcare Reform

HIS is pleased to offer our support of the Affordable Health Care for America Act (H.R. 3962). The Affordable Health Care for America Act will end discrimination against people with hemochromatosis and other related conditions caused by iron overload by prohibiting insurance companies from denying coverage or charging higher premiums to people with pre-existing conditions.  It will eliminate annual and lifetime caps on benefits, limit out-of-pocket expenses, and provide subsidies to those who otherwise could not afford insurance.

Healthcare reform is an important step towards helping people with hemochromatosis to live long and healthy lives.

Need to find a location that will perform a therapeutic phlebotomy? Click on the map to locate a facility near you.

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