Getting an Alzheimer’s diagnosis is the first step in a long journey, both for the person diagnosed and for his or her family members. For those caring for someone with Alzheimer’s disease, the challenges of caregiving can have a big impact on their own health and well being. Meet Dale Bruhn. Like so many people, Bruhn never contemplated becoming a caregiver until his wife Norma was diagnosed with Alzheimer’s disease in 1986. Since then, the Madison resident has become an advocate for the programs and services that assist the families of those with the disease, and knows first hand the special challenges facing those caring for someone with Alzheimer’s disease. “The caregiver’s role with Alzheimer’s is somewhat different because the disease is a long, drawn-out process and a lot of it is supervision in the beginning,” says Bruhn. “The stress comes from having to deal with a progressively worsening situation – things get tougher week by week, and it’s hard watching the person you love change into someone you don’t recognize and who doesn’t recognize you.” Bruhn was Norma’s caregiver for over 15 years until her death in 2002 – seven of those years he cared for her at home. He says that while it was difficult, he wanted to be the one taking care of his wife. Having information, support and assistance made that possible. “I just wanted to do my best for her, and I found that meant taking care of myself too,” said Bruhn. Caregivers in [YOUR COUNTY OR TRIBE] can find the Family Caregiver Support Program by calling [YOUR AGENCY NAME AND PHONE NUMBER]. Those caring for or concerned about someone in another county or tribe can find their local Family Caregiver Support Program by calling toll-free -- (866) 843-9810 -- or going to the website (www.wisconsincaregiver.org).
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