あなたはちょうどHFE遺伝性血色素症と診断された人にどのアドバイスをしますか?

HFE遺伝性血色素症で診断されたばかりの人々に対するHFE遺伝性血色素症の経験を持つ人々からのアドバイスを参照してください

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Look at websites such as ironitout.org, irondisorders.com and the Canadian Hemochromatosis Society websites for info and downloads about how to inform relatives. They need to know they have the gene mutation. Urge them to get tested, too. There are many Facebook support groups for HH, as well.

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