The trade paperback of All Good Things is now available on Amazon worldwide.

Here is what people are saying about the book so far:

A raw and honest account of Erin’s journey with testing for the genetic condition Huntington’s disease and wanting to have children.
Huntington’s Disease Youth Organization (HDYO)

“There’s no way you can imagine!” That’s true. As familiar as I am with Huntington’s, I can’t imagine living at-risk, testing, living with a gene positive result, and depression. My wife and I have healthy adult children and grandkids; there’s no way I can imagine infertility, PGD, and adoption. But Erin tells her story in such candid detail, with her heart opened so widely, that I can get pretty close to imagining.
In the HD community and beyond, we often use the term “warrior” and say, “It takes courage to tell your story.” The reasons are self-evident as Erin compellingly shares her years of lows, highs, and surprises. Now when others share their stories, concerns, and worries with me, I can easily imagine how many, many times I’ll ask, “Have you read Erin Paterson’s All Good Things yet?” It’s her gift to the HD community and others far beyond.
Jimmy Pollard, activist and bestselling author of Hurry Up & Wait!

Erin’s memoir, All Good Things, provides an inside look at what it’s like living with a rare genetic disease. As someone living with Huntington’s disease, I found it very relatable, especially when it came to learning about a new diagnosis and how to adjust to a new normal. Whether you live with Huntington’s disease or another health condition, I highly recommend this book to remind yourself you are not alone while living with your health condition.
Seth Rotberg, patient advocate and TEDx speaker