Watching Their Dance: Three Sisters, a Genetic Disease and Marrying into a Family At Risk for Huntington’s
My story is about the power of HOPE than the wages of Huntington’s. It may sound strange to most folks, but my marriage was actually fortified by its precariousness—I learned to love more deeply in the shadow of John’s mortality. Knowing that my world could change overnight taught me to live MINDFULLY each and every day and never take John, our life, our love for granted. Living with this huge uncertainty also taught me to FORGIVE, LOVE UNCONDITIONALLY and NOT SWEAT THE SMALL STUFF.
“A true story that is as uplifting as it is heartbreaking”. KirkusReviews
Through this experience I learned that, We Can Never Lose HOPE
For U.S. residents, please purchase a copy at Amazon, B&N, IndieBound and other book websites. Available in Kindle, Nook, Kobo format. Also, see the book on Huntington’s Disease Society of America website.
Since 2017, I’ve donated approximately $16,000.00 from book sales to the nonprofit, Huntington’s Disease Society of America.
If you live outside the U.S., please purchase the book on an Amazon website in your country.
Making changes in your life is not always easy and sometimes it’s hard to take those first steps. We have to step outside our comfort zone and that takes energy and bravery. But if that is what it takes to survive, or to achieve a goal, wouldn’t you do it? Through my experience of living in a family AT RISK for the cruelest disease on the planet, I chose to change in order to survive. And guess what? I did survive and you can too by being open to altering your way of thinking or the way you react or do things.