My husband has MCI and he went through the testing. I was wondering what your loved ones experience has been
Thanks
Judy, my post today is as applicable to you beginning your journey as those of us farther down the road. On the internet, Teepa Snow (i think i remember it correctly) is one of invaluable resources. Get books on MCI, dementia &/or Alzheimers. Call or Go to your Alzheimers association & take advantage of any classes they have. They have book recommendations & information they will send you (i guess they still send copies in the mail . . .) that is so important to incorporate early.
And, to me, the most important thing for you (and your husband if there is one) is to get in a support group. Start early to learn to care of yourself. It may sound unimportant now, but it isn’t. Early on I got a wrist band from a class given by www.caregiveroc.org
(Orange County, California) that says, “Caregiving includes caring for me!” It’s years past then & I still wear it.
So:
1 books
2 internet support
2 Alz Assn for
classes & info to send
3 physical support group
4 self care
Sorry this is so wordy. Remember we eat an elephant just one bite at a time!!
Take care, breathe deep & just love him.
Mia
You found a good one right here
Mia, you are so helpful. I have been resistant to a support group and I don’t know why But I think I may be ready now.