Respite care helpful but difficult option

24/4/2009 ·

My sincere thanks once again to those of you sharing your stories. There are probably hundreds who are reading and relating to what you have to say.

Obviously, there are no easy answers to the epidemic of Alzheimer's disease that brings with it nearly 10 million Americans providing 8.4 billion hours of unpaid care (mostly family). As stated in our previous dialogue, some of you find relief by attending support groups if they are available, others mentioned that writing and venting provides benefit at some level, others have suggested the importance of respite.

Once again, I realize obtaining respite care is easier said than done, there can be numerous obstacles, including our own reluctance (feelings of guilt or abandonment are common). However, none of us are equipped physically or emotionally for 24/7 caregiving. I would appreciate hearing some of your stories and experiences around respite care.

Here is a small list of the types of services (both paid and volunteer) that may be available in your communities, as well as some excellent resources and Web sites to check out.

Bottom line: Getting or accepting respite care often means that you can keep your loved one at home longer, which for most of the families I have met, is the ultimate goal.

Remember, that getting a break yourself gives you the opportunity to rejuvenate, pay attention to who you are outside of your caregiving role. This period of respite often helps you to be a better caregiver. Think of respite as a gift not only to yourself by also to the person you are caring for.

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