Mark Redner - Waukesha, Wisconsin
The phrase “in sickness and in health” particularly resonates with Stephani and Mark Redner. Doctors diagnosed Mark Redner Lou Gehrig’s Disease in August 2008, three decades after he met Stephani and two years after he wed her. ALS typically limits a person’s life span two to five years following a diagnosis. In spite of these statistics, the Redners dedication to each other has strengthened, and they work together to inform and educate their community about ALS.
The Redners Surrounded By Their Family
The ALS Association’s Wisconsin Chapter is honoring the Redners during ALS Awareness Month for the annual “ALS Across America” campaign.
“Stephani and Mark have given so much strength and support to other members of the chapter through their own journey, and we feel so lucky to have these special people in our lives,” said chapter Care Services Director Lori Banker-Horner. “Their strong commitment to each other is evident immediately upon meeting them.”
The couple continues to keep active by working with the chapter’s patient and caregiver support groups that meet monthly in Milwaukee. “Stephani has been a regular member of the caregiver group where she immediately embraces new caregivers and makes them feel at home and welcome,” Banker-Horner said. “Mark is the humor in the support group, while at the same time he offers his support, experiences and valuable tips to others battling the disease. Neither of them is afraid to reveal their fears as well as their struggles so other participants feel open to sharing in these support group meetings.”
Redner, Stephani and their children also attend other chapter happenings such as the annual Walk to Defeat ALSŪ in Milwaukee and the Evening of Hope Dinner Dance. Both events raise funds for research and care services programs that aid families living with Lou Gehrig’s Disease. Redner additionally supports the chapter’s public policy efforts, especially those that benefit veterans. He served in the U.S. Air Force from 1963 1967.
Since his diagnosis nearly four years ago, Redner, 67, uses a motorized wheelchair for mobility and a hoyer lift to transfer him. His and Stephani’s upbeat attitudes, despite the challenges and progression of the disease, continually inspires Banker-Horner and her chapter colleagues.
“Stephani and Mark have truly lived since Mark’s ALS diagnosis,” said Banker-Horner. “They are a beautiful team—and their support of one another motivates us to continue to fight this disease.”
Due to the progression of Redner’s illness, neither he nor Stephani will travel to the National ALS Advocacy Day and Public Policy Conference in our nation’s capital in May. However, they
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