Kim-
While I appreciate this forum and the opportunity to learn and share with others like you, it is also heart wrenching to know that others are having to go through this. However, the strength I hear in you and others is the best source of encouragement I have found. I am so sorry that you, your husband and family are suffering. I am also sorry that you have a raging mother-in-law to contend with.

About two months ago I was ready to send my MIL on a slow boat to China, …but it has gotten better. I don’t think anybody can
understand care giving like another caregiver.
Like you, I stay busy and worn out. I feel like a shadow of myself and really don’t have time for anything recreational (except for at night). The teens help some, but they have part time jobs and school. We all miss Patsy being able to cook, but I ‘m coming along okay (made a decent chicken parmesan over the weekend). What I’d really like to do is play a round of golf or take the kids camping on the beach, but it is so difficult to find slots of time for stuff like that. This Friday some of Patsy’s girlfriends are coming over for a slumber party (her birthday is next week), so I’m gonna take the little ones and probably go to my mother’s in Myrtle Beach for a night.
Patsy isn’t having a good day. I hate this disease because it robs us of so much. We were planning on going to Orlando thanksgiving week to get away from all this, but I had to cancel the reservation fearing Patsy might not be up for it. The best I can hope for now is my MIL will go out of town since my plans have failed.

With that, I’ll rest from my venting and belly-aching for the night.
Since you have me talking, let me ask for your advice. As you know, this disease turns your life upside down. As soon as my feet hit the floor, I get in the mind-set of managing and fighting the problems associated with this wretched disease. Patsy on the other hand does not want to discuss anything critical, so naturally I shoulder pretty much everything. However there are some legal issues that we should address while things are fair, but when I bring it up she gets upset. I just want to take care of these things so they are behind us and I won’t have to think much about it. Do you have any suggestions how I might approach her in the future?
Anyway, thanks for sharing and being a friend. I hope Stan's appoint is encouraging. I do find it comforting to talk and share with others fighting this disease. I hope you have as great week.
conan