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How does the disease affect the caregiver?

Sunday, February 7, 2010 Leave a Comment


No two people experience Alzheimer’s disease in the same way. As a result, there's no one approach to caregiving. Your responsibilities can range from making financial decisions, managing changes in behavior, to helping a loved one get dressed in the morning.

Handling these duties is hard work. But by learning caregiving skills, you can make sure that your loved one feels supported and is living a full life. You can also ensure that you are taking steps to preserve your own well-being.


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I am a caregiver to my husband who has MS and with the MS there is a mild (sometimes I think moderate) form of dementia. It's the part of MS few people talk about. Fortunately, he's been in the same job long enough that he can still work but is not supposed to drive to work. I tend to take him around to med appts because they are stressful and I want to know everything that docs are telling him and meds he's on. The moodiness and irritability is hard to live with. I pretty much manage the finances although I give him direction on when to pay certain bills and let him know what we owe and when. This morning he left the stove on, the other day he left the fridge door open, and a few days ago he forgot to put the car in "Park" when he was trying to park it and get out. He "makes up" stories when he doesn't know the facts. Getting doctors to understand that and listen to me and take me seriously has been one of the harder tasks.

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