Michelson, who runs a Los Angeles-based company that helps patients research their medical options and has written a book about how to avoid bad care, offers advice on how to navigate the health care system.
Researchers looked at women’s health services around the country and found stark disparities between cities but also within health care markets.
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 your online resource for hemochromatosis information.
We strive to provide accurate, timely information regarding hemochromatosis and its treatment.