Kristy K. Schumacher Obituary

Kristy K. Schumacher


CHIPPEWA FALLS, Wis. — Kristy K. Schumacher, 48, of Chippewa Falls passed away Sunday, June 4, 2017, at Wissota Health and Vent Center in Chippewa Falls, after a long battle with myotonic dystrophy.

She was born in La Crosse to Edwin and Valeria Schumacher Jan. 3, 1969. She went to school at Onalaska High. She loved to play bingo, Yahtzee and enjoyed making arts and crafts. She was Tim McGraw’s and Shania Twain’s biggest fan. Kristy was also an avid dolphin collector. Those who knew her, knew that she was as sassy as they come, especially to those at Wissota Health & Vent Center. Kristy was known for saying “It is what it is.”

Kristy is preceded in death by her parents; her brother, James; her nephew, Michael; grandparents, Walter and Mae Volk, and Edward and Kathrine Schumacher.


She is survived by her daughter, Kayla of Madison, Wis.; her siblings, Jeff (Mary) of La Crosse, Peter (Maureen) of La Crosse, David (Patty) of La Crosse, Paula (Chris) Kettner of Mazomanie, Wis., Stevie (Carol) of Fond du Lac, Wis., Ronnie (Carmen) of Menomonie; special nieces and nephews, Cameron, Jordy, Syrus, Aubrey, Khloe and many more; her special friends, Kathy Greener, Scott and Lisa Neumister and Libby Scarpelli.


A celebration of life will be held at 1 p.m. Sunday, June 11, at Wissota Health & Vent Center, 2815 County Hwy. I, Chippewa Falls, WI, 54729, at the Chapel.

Chippewa Valley Cremation Services of Altoona, Wis., is assisting the family with arrangements. To sign the guestbook or share a memory online, please visit


In lieu of flowers, memorials may be sent to Paula Krause, 313 Scott St. Mazomanie, Wis., 53560.

Kristy’s family wishes to extend our sincere thanks to Wissota Health & Vent Center for the love and compassion you gave Kristy, and for their patience with Kristy’s sassiness. A special thank you to Janet, Amy, Lindsey, Kareen, Kris, Sheri, Lolly, Cythnia, Becky, and the rest of the wonderful staff.

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Sad Day for Myotonic Dystrophy Community

We were saddened to hear of the Death of Kayla who was brave and choose to be the face of this disease. She warmed everyones heart, now the hearts are a little colder.


Kayla Michele Vittek’s Obituary

July 28, 2005 – April 9, 2019 Resident of Santa Cruz, CA 

Kayla Michele Vittek, a beautiful, bright and deeply cherished 13 year-old girl, died peacefully in her sleep in the early morning hours of Tuesday, April 9, 2019. Kayla lived with her mother, Lisa Michele Harvey-Duren, her step-dad Paul Duren and her ten year-old sister in Santa Cruz.
Kayla embraced those that she trusted with her whole heart. For those special people that she let in, she showed a side of herself that not everyone got to see. She had a great sense of humor, she was gentle, kind, empathetic and she genuinely loved life. Kayla loved showing her affection by planting gentle kisses on her loved ones faces. She also gave the most amazing hugs. She loved to dance and adored music from an early age. She especially loved the music of Eric Hutchinson and wouldn’t go to sleep at night until we played his songs. Kayla has blessed our lives and her spirit will live on forever in our hearts.
Kayla was born at Sutter Memorial Hospital in Sacramento, California in 2005. She began her early intervention and education in Rocklin, CA, and transferred to the Soquel Union School District in Santa Cruz County in Kindergarten in 2011. She attended Soquel Elementary School, followed by almost three years at New Brighton Middle School, where she excelled academically thanks to the devoted care of her academic aides and teachers. Despite physical challenges, speaking problems due to the disease and hypersensitivity to sounds, she made the honor roll at New Brighton every semester and was just two month away from graduation and advancement into high school. Kayla loved to read and especially loved science and humanities. Her unexpected success in all facets of her life was miraculous considering the severity of her disease. She was not expected to survive her first year, nor to ever walk or talk. During her final year at New Brighton, she was invited to participate in the student council.
Despite her difficulties with mobility, Kayla loved sports, beginning at age three with horseback riding (hippotherapy) at Ride-To-Walk, and continuing with baseball and soccer from age 7. Kayla played baseball in the challenger league with the Angels, a team made up of individuals living with disabilities. Kayla’s father Jeff loved playing baseball with Kayla on their visits together. In their first game of this season, the weekend after Kayla passed, the Angels had a moment of silence in memory of Kayla and then played her walk-up music, Brave by Sara Bareilles. Kayla participated in Ride-A-Wave and Day at the Beach over the past 6 years. She participated in Day of Discovery snorkeling program at Monterey Bay Aquarium for the past few years. She was a recipient of Make-a-Wish Foundation gift to travel to Hawaii with her family in 2016. Kayla’s favorite event every year was by far MDA camp for kids living with muscular dystrophy. Kayla attended this camp since the age of 6 and with her very special friend Kali for many years and then this past year with Kali, Zoe and Cambry who all live with DM1.
Kayla faced a life-long struggle with congenital myotonic dystrophy (DM1), the most prevalent form of muscular dystrophy. Under the care of her mother and her medical team at Lucile Packard Children’s Hospital at Stanford, led by the chair of the Neuromuscular Department, Dr. John W. Day, MD, PhD., Kayla flourished. She became known throughout the global community of DM patients and caregivers through her blog, as many newly diagnosed patients would find Kayla’s story of hope and would reach out to us. Because of Kayla’s struggle, her mother Lisa helped to found and became the founding executive director of the Myotonic Dystrophy Foundation (MDF), which funds research into this genetic disorder and provides support to families living with this disease.
Kayla appeared regularly in news stories and on television over the past 13 years and she and her mother were spokespeople and strong advocates for DM. Kayla was named the Youth Ambassador for Easterseals Superior California in 2006 and her story was aired on the Sacramento news. Kayla’s story was updated every year on the Sacramento Muscular Dystrophy Association (MDA) Jerry Lewis Telethon from 2006 to 2008 and she was the 2009 face of myotonic dystrophy on the National MDA Jerry Lewis Telethon where she appeared with her father Jeff and her mother Lisa. In 2014 Kayla and Lisa testified in Washington D.C. in a Congressional hearing in support of the reauthorization of the MD-CARE Act which was eventually granted. Kayla participated in a longitudinal research study of congenital myotonic dystrophy patients every year for the last five consecutive years at the University of Utah. Kayla also participated in research at Stanford University. Kayla was about to begin a clinical trial at Stanford for a new drug that improves executive functioning. These are just a few of her accomplishments in her short life.
Kayla was predeceased by Robert and Patricia Vittek, paternal grandparents; June Hull Ferguson, great aunt; and Stephen Harvey, maternal uncle. She is survived by her other family members, who mourn her loss and cherish her memory: Lisa Harvey-Duren, mother; Jeff Vittek, father; Paul Duren, step-father, and her sister; Jane Hull Harvey and Rev. Pharis Harvey, maternal grandparents, Dr. Kathryn Harvey, maternal aunt, Christopher Harvey and Roxanne Ward Zaghab, maternal uncle and aunt; Mitch Vittek, paternal uncle; Rich and Sue Vittek, paternal uncle and aunt; Daniel Harvey, Noelle Pruett, Maya Pruett, Kathryn Harvey, Brenan Batten, Logan Batten, Andie Lee Batten, maternal cousins; Shelby Vittek, Lindsay Vittek and Sarah Hollenback, paternal cousins.
There will be a Celebration of Life of Kayla Michele Vittek at Aptos United Methodist Church on Saturday, April 27, 2019 at 11:00 a.m.. Please RSVP for the event or the live stream.
In lieu of flowers, please consider making a donation to either the Muscular Dystrophy Association or the Myotonic Dystrophy Foundationand note in the memo: Kayla Vittek memorial fund. 
Please leave messages for Kayla’s family in the comments below.

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