A Day in the Life of Bev, Her Story, Part 17!
Greetings Friends and Family: The 2020 event is our 11th annual celebration and much has changed since our last update. Thank you for being such...
A Video on Huntington’s Disease: “Team Bev” for a Cure!
Learn more about Huntington's Disease and how our organization has helped in funding research to find a cure. https://youtu.be/IRXGJh5Xqh0
Virtual/Facebook Live: Bev’s Bootlegger Ball 2020
Amid the pandemic, we held a virtual ball! Thank you to everyone who participated live with us and watched the replay following the event. Bev and...
Interview with IndyStar
10th Annual – A Musical Celebration of Giving 2019
A Day in the Life of Bev, Her Story, Part 16!
This is the insert update in the invitation to the Year 10, 2019 annual fundraiser! Greetings Friends and Family: This year’s celebration is our...
Bev and HD are featured in the “At Geist” and “At Fishers” Towne Post Publications
Did you read the story? Bev and the annual event are highlighted in a wonderful write-up about HD and the 10th annual celebration! Visit the link...
Interview for GlycoScience Research
A Day in the Life of Bev, Her Story, Part 15
January 2019 –By Mindy Irish After we last wrote in April, the rest of 2018 was noted as “The Summer of Bev”! She turned 50 in July and several...
Learn More
What is Huntington’s Disease?
Huntington’s Disease is a degenerative brain disease
that strikes in mid-life, usually between the ages of
30-40. People lose their ability to walk, talk, and even
feed themselves. Even though people may live for
10-20 years with this disease, their quality of life is
taken from them.
Who Was Bev Hartig?
In 1998, about one year after getting married, Bev
received a paralyzing phone call that her birth father
had been diagnosed with HD. This meant every
sibling had a 50% chance of inheriting this disease.
She found out that she also carried the gene and
would suffer the same tragic fate.