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About Author, Fundraising

3rd Leg of Therese’s Book Tour

John and I are entering the last month of my book tour.  The time on the road, two months, has gone so fast; I don’t want it to end! Here’s what we have planned.

August 1-Akron Ohio. Attend a local HDSA Support Group to share the purpose of my book. A HDSA social worker facilities a support group for folks with HD and those living at risk.

August 5-Dayton Ohio. Participate in HDSA Team HOPE Walk and promote my book Watching Their Dance: Three Sisters, a Genetic Disease and Marrying into a Family At Risk for Huntington’s. https://hdsa.donordrive.com/index.cfm?fuseaction=donorDrive.event&eventID=1221  

August 8-Sterling City Michigan.  Attend the HDSA Support Group meeting and share my book with attendees.    

August 12-Traverse City Michigan. Attend HDSA Team HOPE Walk and ask folks to use Watching Their Dance as a tool to heighten HD awareness.  https://hdsa.donordrive.com/index.cfm?fuseaction=donorDrive.event&eventID=1151 

August 19-Madison Wisconsin. HDSA Team Hope Walk to promote Watching Their Dance.      https://hdsa.donordrive.com/index.cfm?fuseaction=donorDrive.event&eventID=1152

August 27-Omaha Nebraska.   HDSA Team HOPE Walk.   https://hdsa.donordrive.com/index.cfm?fuseaction=donorDrive.event&eventID=1098

 

 

Enjoy our trip back home.   WooWoo!!!!!!

To purchase Therese’s book, please visit her Author Website:  http://www.theresecrutchermarin.com  100% of the proceeds from the book is being donated to Huntington’s disease organizations around the world.

We can never lose HOPE…………………Therese

Watching the Dance Huntingtons Disease
Fundraising

A Personal Fundraising Project Close to my Heart

I published the nonfiction book, Watching Their Dance: Three Sisters, a Genetic Disease and Marrying into a Family At Risk for Huntingtons on April 1, 2017, which is a personal fundraising project. It’s the driving force behind the promotion of my book.  

If you are interested in supporting a worthwhile cause, funding research to find a therapy or cure for the genetic Huntington’s disease, and is a good read, please purchase my book.  Kirkus Review said, “This is a story more about the power of hope than the wages of Huntington’s”.  If you are reader who enjoys a love story with passion, you’ll find it here.

I’m donating 100% of the proceeds to the non-profit, Huntington’s Disease Society of America http://www.hdsa.org  in the U.S., because this is how John, my husband, and I can help in the fight against the cruelest disease on the planet, Huntington’s disease (HD).  In the U.S., 30,000 people live with HD and 250,000 live at risk, like John and his three sisters.

Watching Their Dance can be found on many sites on the internet.  To purchase it, please go to  http://www.theresecrutchermarin.com 

or  https://www.amazon.com/Mrs.-Therese-Marie-Crutcher-Marin/e/B06ZY85776   

Huntington’s disease is a fatal, genetic disease that progressive destroys the nerve cells in the brain. It’s like having Alzheimers, ALS and Parkison’s disease at the same time.  http://www.mayoclinic.org/diseases-conditions/huntingtons-disease/home/ovc-20321431 

We can never lose HOPE………………………Therese