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What is your biggest fear when it comes to hep C?

Do you have any fears when it comes to living with hep C? This is a safe space to share how you feel.

  1. I don’t really think I had a fear about living with Hep C. Although my story is different from every one else, I willingly contracted Hep C from an organ donor. I knew what I was doing when I signed the paperwork to receive a high risk organ and at the time, I was running out of options, so my best case scenario was to receive a high risk organ or die. I chose to receive a Hep C donor’s heart and I’m abundantly grateful that I made the right decision for myself. I’m currently 3 years post heart transplant and I’m healthier than I’ve ever been in my life.

    Leslie (Community Moderator)

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