> Your SEO optimized title

How Dungeons & Dragons and Writing a Graphic Novel Helped One Man Fight A Chronic Health Condition



Over the last year, creative play and games like Dungeons & Dragons (D&D) have made a resurgence, helping players escape a real-life monster – the COVID-19 pandemic. One man decided to use the resurgence to help him fight his chronic health condition.



Not only has Jonathan Hill been using the role-playing game his entire life as an escape from the challenges of his chronic health condition, severe hemophilia A, but he has also channeled his creative energy into writing a new graphic novel.



“Blood of the Paladin” details his journey of accepting, managing and embracing his bleeding disorder. In the graphic novel, he draws support from his father, close friends, and the iconic fantasy role-playing game.  Jonathan is sharing his story through this graphic novel in the hopes of shedding light on the challenges that people living with hemophilia face.  



Jonathan shares more about his personal experience, the therapeutic process of writing and his work to help others facing similar trials. He’s joined by his dear friend and former President of the National Hemophilia Foundation Val Bias, who discusses the challenges that people living with the condition face.




About Our Guests 


Jonathan Hill was born with severe hemophilia A in 1971. In the 1980s, Jonathan learned that he had been infected with hepatitis C and HIV from contaminated blood products. Later, he developed severe liver disease, undergoing a liver transplant in 2017. For several years before his transplant, Jonathan sought a creative outlet, writing about his experiences on Facebook. The response was huge. Family and friends shared how his posts helped them better identify with the struggles of people with rare diseases. Over time, he compiled his writing into a memoir, “Blood Brothers: A Memoir from the Lost Generation of Hemophiliacs.”  After a meeting at the National Hemophilia Foundation (NHF) 2019 Bleeding Disorders Conference, Jonathan partnered with BioMarin and Believe Limited to create a graphic novel illustrating his journey. 




From 2008 through 2019, Val Bias, who also lives with hemophilia, led the National Hemophilia Foundation to the forefront of the healthcare reform debate on such issues as the elimination of lifetime caps and pre-existing conditions with insurers. In addition, he greatly expanded the NHF’s research agenda and created the Women’s Health and Bleeding Disorders Institute to address the growing needs for awareness and treatment for women with bleeding disorders. Before becoming CEO, Bias maintained a long history with the National Hemophilia Foundation from his service as NHF’s Board Chair in 1992 to his tenure as volunteer, consultant, and lobbyist/advocate for NHF – culminating with the passage of the Ricky Ray Hemophilia Relief Act of 1998. He has interfaced with key decision makers in executive and legislative branches of federal government and has long-standing working relationships with such federal agencies as the CDC, NIH and FDA.




Wife. Mom. Believer. Writer. Advocate.

Notify of

This site uses Akismet to reduce spam. Learn how your comment data is processed.

Inline Feedbacks
View all comments
error: Content is protected !!

Newsletter Signup

Sign up now and never miss a thing!

You're Signed Up!

Now that you are signed up, we will send you exclusive offers periodically.

Would love your thoughts, please comment.x