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Caregivers of dementia patients should understand that incontinence may be an inevitable part of the overall cognitive decline. As a person loses awareness of their surroundings, lifestyle, and loved ones, it is not surprising that loss of bodily functioning will also occur. It may be a tremendous source of frustration for both the caregiver and the patient. Communicating the incontinence issues early with the patient’s healthcare team can help reduce some of the frustration that the household may have with the issue. Even though it can be an uncomfortable subject, it is important that the full needs of the patient be addressed. The sooner incontinence is addressed, the quicker the patient and the caregiver can begin to work with options that may reduce the frustration or embarrassment that is involved.
As to what to do from this point--Can you contact a physician or neurologist for a professional opinion--as there is both pro and con on the subject, and I was just a caregiver for my Mom. You also might keep in mind, and is important, all cases are different and treated different-so what works for one, may not work for another...this my reason to contact a professional or the Alzheimer's Associaion, who deals with many types of dementia. A 24 Hr helpline # is (800)-272-3900.
Best~
Hap
Use BED PADS (two of them) and learn the proper way to 'roll' a person if need be. Have a 'bedside pottie' handy, so no long trips are necessary. Use aloe wipes for cleaning up, and WARM the wipe up before using, so there is no 'cold shock' to their sensitive skin.
Just imagine how you would feel if a stranger came into your bedroom inthe middle of the night, and decided to undress you!! Even if you think they know you they may NOT in the middle of the night. The best intentions can blow up in your face if not properly executed!
I'm sure there are others here that will share their experiences too!