You may have seen in the news that Ascension hospitals have suffered a cyber attack. In order for you to be able to receive the best care for your sickle cell disease, we are asking that if time allows, please call IHTC prior to presenting to the emergency department...

Dear Patients, As you may be aware, a cyber-attack that has impacted Ascension facilities, including the 86th Street location and other associated sites across the region and state. We are not affected by this incident but are providing guidance as many of our...

We are excited to share an update about our organization. IHTC is now a part of our new parent organization Innovative Hematology, Inc. (IHI)

By: Nico Pennisi, WRTV GREENTOWN — March is Bleeding Disorders Awareness Month. The National Bleeding Disorders Foundation says it's a time to let patients and families with hemophilia, von Willebrand disease, rare factor disorders, and more, share their lives,...

By: Divine Triplett The Indiana Hemophilia & Thrombosis Center stands as the state’s sole federally recognized facility dedicated to addressing hemophilia and thrombosis. Operating as a nonprofit entity in Indianapolis, it extends its services to patients across...

By: Fox59 WATCH: Griffin was diagnosed with hemophilia shortly after his birth. Learn what Dr. Charles Nakar, IHTC pediatric hematologist, Griffin, and his father have to share about the diagnosis process and living with hemophilia.

By: Rachel Law TERRE HAUTE, Ind. (WTHI) - More than 300 million people worldwide are living with a rare disease, according to the National Rare Disease Day organization. To honor that statistic, National Rare Disease Day falls on February 29, a rare date. Allyson...

By: Shelby Reilly TERRE HAUTE, Ind. (WTWO/WAWV) – Rare Disease Day is February 29 and one local woman hopes to spread awareness about a disease she was born with, but didn’t know she had for most of her life. Allyson Newport was born with Hereditary Hemorrhagic...

By: Jade Jackson Hoosiers from across the state gathered at the Indiana State Capitol to encourage lawmakers to consider the needs of Hoosiers living with sickle cell disease. The rare inherited blood disorder occurs when red blood cells become hard, sticky and...

By: Ryan Trares The spikes of severe pain seemed neverending. Lena Harvey has lived with sickle cell disease throughout her entire life. The 39-year-old Indianapolis resident has suffered through the constant fatigue, the sores, and most frequently the pain that the...