In order to stay up to date on latest treatments, drug discovery, clinical studies and how to manage Hepatitis C everyday HepatitisC.net brings you frequent articles, points of view and advice from leading patient advocates and experts.
Abhinav Humar, MD
Dr. Humar is the Clinical Director of the Thomas E. Starzl Transplantation Institute (STI), and Chief, Division of Transplantation in the Department of Surgery at University of Pittsburgh Medical Center (UPMC). Dr. Humar oversees all clinical and clinical research activities at one of the worlds most active and prestigious transplant programs. Read More.
Barry is a novelist, musician, hepatitis C advocate, blogger, and medical journalist. His novel, Final Arrangements, a comedy about a southern funeral home, debuted in 2002, to critical acclaim. He was a finalist in Barnes & Noble’s Discover Great New Writers program. According to Barry, “After my novel, I wanted to do more with my writing than entertain.” So he dedicated himself to writing for the hepatitis C community. Read More.
Bill is a native Marylander but has lived in Vermont and California for most of his adult life. Having a passion for motorcycles, boats, and cars, Bill married his English degree and mechanical skills into a career as an automotive driving event planner/designer. He got paid to play with cars. Read More.
James and Carleen Mcguffey married 26 years ago. Together the Mcguffeys have 5 boys and 1 girl. Several years ago they learned Carleen was carrying the Hepatitis-C virus. Carleen went in for a Liver Biopsy when her son, Kyle, was just 8 weeks old, complications almost took her life. During that time James became frustrated with the lack of good information and resources for Carleen and other Hepatitis-C patients. Read more.
My name is Corinne Miga, I am a Licensed Master’s Social Worker born and raised in Buffalo, New York. I earned my Master’s degree from the University of Buffalo in the spring of 2012. For the past two years, I have been employed as a Medical Social Worker in the Immunodeficiency clinic at Erie County Medical Center (ECMC). In my role, I have the privilege of working in the HIV/HCV Co- infection clinic, offering support to patients coping with these chronic illnesses. Read more.
As a person who has lived with hepatitis c, it is my hope that through my efforts I can educate and inform. As a hidden illness -until the disease is more advanced, people are far too often isolated. This impacts quality of life in tragic ways for some. People are frequently marginalized by their hepatitis c diagnosis, and this is something I have experienced first-hand. Read More.
Debra is a writer, a scientist, a doctor of pharmacy, and has spent the last twenty five years in field research for pharmaceutical companies. Her areas of expertise include Gastroenterology, Hepatology, Hemostasis (blood clotting), and Cardiovascular/Stroke. Read More.
Jeanne Hecht, MPA, PMP
Jeanne Hecht is Senior Vice President and Global Head of Site and Patient Networks at Quintiles, a position she was appointed to in October 2014. In this role, Jeanne is responsible for leading, implementing, and driving a site and patient network-centric global strategy that leverages leading-edge technology. Read more.
Jenelle Marie Davis
Jenelle Marie Davis is the Founder & Executive Director of TheSTDProject.com – a multi-award-winning independent website and progressive movement, the STD Expert for Answers.com, an adjunct professor, and a professional speaker. Read More.
Joseph is not only a survivor of the horrors during the dark days of the pharmaceutical industry, but a living miracle by medical standards. Born with severe Hemophilia Type A (less than 1% clotting factor in the bloodstream), the very product used to treat the blood disease (Anti-Hemophiliac Factor VIII) to many became a death sentence in the late 80’s and early 90’s. Read More.
A Hepatitis C survivor who beat the virus, liver cancer, and is still living with end stage cirrhosis. She is an incurable optimist who refuses to quit. She is also a teacher who has learned a lot on her journey and gets a big kick out of sharing tips and tricks with others. Read More.
Kimberly Morgan Bossley
Kimberly Morgan Bossley President of The Bonnie Morgan Foundation for HCV, is a strong advocate for Hep C. Kim is very active within the liver community participating in numbers liver life walks, community fairs, and various city festivals across the United States putting a face to hep C. Through her own personal battle with the disease she shares her journey and experience in speaking engagements across the U.S. along with managing several blogs, posting personal victories, and struggles she has encountered through fighting hepatitis. Read More.
Mariah Zebrowski Leach
Mariah is a writer and patient advocate who lives in Colorado with her husband and two young sons. Diagnosed with rheumatoid arthritis in the middle of law school, Mariah now uses her law degree to help people with chronic health issues. Read more.
Matthew has extensive experience providing harm reduction, hepatitis C education and resources to persons who inject drugs. In May of 2016, he created Umbrella Way to provide specialized training and education to community members, organizations and providers. Matthew is a frequent guest speaker at universities and support groups. He has also presented at the Institute on Alcohol and Drug Studies (IADS) conference on three occasions. Read More.
I was diagnosed in March of 2001 almost by accident. At the time I was experiencing issues with my PCP over the way I was feeling physically. I couldn’t get him to listen to me. During this time I decided to get a second opinion. I was continuously so tired by mid-afternoon and needed naps after work. I was given a name of a new doctor and she was very pro-active; after listening to my past history and other information I provided she decided to get to the root of things. Together we couldn’t understand why at my age, at the time, I was worn-out, she gave me comfort while waiting for lab’s and other test results to return. Read More.
Hi, I’m Randy and I was diagnosed with hepatitis C in 1999. I was always known as the “energizer bunny”, healthy and tireless, teaching brain injured children and adults, constantly advocating on their behalf. I was able to take on one or two extra jobs on any given day. This was my life until I was no longer tireless in 1990. Read More.
Diagnosed at 12, He is a vertical transfer receiving Hep C (HCV) from his mother who successful cleared the virus in 2010. Rick was not so lucky, having failed five treatments including Sovaldi/Olysio and Harvoni, he has become an active HCV and invisible disability advocate. Read more.
Soon after her diagnosis she began to work in the hepatitis community as an advocate and an educator. In 1999 she started the Hepatitis C Association and with a mission is to educate patients and providers about this insidious disease and give patients a place to talk about their fears, their hopes and their dreams for a healthy life. Meeting and getting to know other patients inspired her and took away some of her fear. She learned that helping others helped her, as well. Read More.
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