Hello, my name is Mary Adams-Powers, Founder of the Michigan Hepatitis C Foundation (MHCF).
MHCF began in 1996, five years after my mother was diagnosed with the hepatitis C virus (HCV). If you are newly diagnosed or the friend or family member of someone with HCV, let me reassure you that you are about to experience the assistance of a truly caring group of people. Why do I care? Five years after my mother’s diagnosis with HCV, I too tested positive for the hepatitis C virus. I suppose you could say I come from “both sides of the fence”.
On behalf of our Board of Directors, supporters and sponsors, I’d like to welcome you to the official MHCF website. The purpose of our website and our entire foundation is to provide public awareness, current information and emotional support for those living with or affected by hepatitis C.
Whether you are newly diagnosed or have known you are HCV positive for sometime you are welcome to join us. If someone you know or love is HCV positive, or if you simply want to learn more about the disease, I invite you to spend some time browsing our site.
Click on Facts about HCV to learn who is at risk, what the rate of infection is, and other valuable information to expand your knowledge. Click on Support Groups to see where you can find emotional support and help from others affected with and by this disease in your area of Michigan. If you are newly diagnosed, our F.A.Q. page will give you the information you are looking for. Our event calendar, photo gallery and news page will give you some insight as to what is going on in the world of hepatitis C, including the latest medical news and information.
We also have links to other websites we know you’ll find helpful.
Undoubtedly, the most important feature of the MHCF website is our forum. This is where you can share your experience, strength and hope with others in a sort of on-line support group. We also encourage your ideas and suggestions for MHCF as we embark on our 11th year of providing you with the best support available.
And finally, if you would like to support MHCF, please visit our donation page and give generously. If you would like to give your time and talents please let us know.
We must not turn our backs on suffering. The Michigan Hepatitis C Foundation was created 3 years before my mother passed away in 1998 from liver failure, due to hepatitis C. She lived through a 39-year battle with a disease we didn’t even know existed. MHCF is now dedicated in her memory.
Thank you for visiting the MHCF website.
Faithfully,
Mary Adams-Powers
“Sometimes the wounded are the best healers”
URGENT NEWS!
Please see our news page for information on how you can increase government funding for Hepatitis C research, awareness and treatment.
June 5, 2008 support group meeting we will have Donald Busta a Social Security Lawyer speak and answer our questions on filing for disability.
Other Important Info:
Hepatitis C Motivation & Well Being Study
Be sure to visit our news page and click on the Hepatitis C Motivation and well being study icon for patients and caregivers. Results will help you better manage your disease and the care you give to loved ones.
