Wednesday, August 29, 2012

The Communication Challenge


Communication with an Alzheimer’s patient is challenging at best and nonexistent at worst. Communication with an Alzheimer’s nursing home is also challenging but should never be nonexistent.

Dad’s nursing home is constantly communicating with me about Dad’s condition and situation in the nursing home. A few weeks ago the nursing home advised me that Dad would be temporarily moved to a room next door so that his room could be renovated. A couple of days later the nursing home advised me that Dad had fallen and cut his forehead (2 centimeters) in his old room. Alzheimer’s patients do not do well with change; their life patterns must remain as constant as possible so as not to distress the patient and to keep the patient as safe as possible. Dad’s cut has healed and is doing fine.

Another method the nursing home uses to communicate with me and family members is to hold quarterly “care” meetings. At these meetings we (family members) are updated by the unit nurse, social services director, activities director, and other staff members about Dad’s condition. We are able to ask questions, make recommendations, brainstorm ideas, etc. in our joint efforts to maintain Dad’s quality of life at the highest level possible.

Our last care meeting was held on August 22nd. Following are some of the updates we received:
  • Dad had an x-ray done due to the fall the previous week. There were no fractures, only mild abrasions and contusions. He is under observation to make sure there is no evidence of a concussion.
  • Dad still thinks he can get up on his own and walk around the facility whenever he wants. He never developed a pattern of using a walker so the idea never presents itself to use one. He must be assisted by a CNA or other person or be reminded to use a wheelchair or walker for support. (This is an on-going communication challenge.)
  • He is weighted once a month and has shown a gain from 123 lbs. to 126 lbs. He eats well for someone his age and he takes protein supplements with each meal. If he looses a drastic amount of weight they will weight him more often, otherwise he is stable for now.
  • Dad has been moved to room 3B from room 1A while renovations are taking place. We may just keep him in 3B if he seems to get used to being there however if he continues to go back to room 1A then we will put him back there once renovations are completed.

After the care meeting, Shelley and I went to visit with Dad but all he wanted to do was sleep. He said he was tired and just wanted to go back to sleep. So we said goodbye, gave him kisses and let him sleep.

Within 48 hours of the care meeting I receive a call from the Social Services Director to advise me that Dad had been moved again! This time he had been moved to room 27 on the other side of the facility. The reason given for the move was his roommate was being hostile with Dad so was moved for safety concerns.

I went to see Dad the next day and I could clearly see that Dad was not doing well at all with the latest move. His behavior and speech was erratic and seemed very agitated (see the video below; he even took my camera from me, something he has never done previously). I spoke with his nurse and she agreed Dad should not have been moved for a third time.

The next day, Sunday, I called the nursing home for an explanation for the third move and I demanded that he be placed back in his previous room for his safety’s sake and if his roommate was causing problems to then move the roommate and not Dad. After nearly an hour of conversations with three different persons, I was told someone would get back to me. I received a call back and was promised Dad would be moved back to his room that afternoon.

Even though the staff was able to accommodate my demand, I now had some concerns about the nursing home’s ability to handle Alzheimer’s patients and requested a meeting with the nursing home’s administrator on Monday morning.

On Monday morning, Shelley, Bruce and I met with the nursing home administrator and the nurse I had spoken with on Sunday. We expressed our concerns and a half hour later we were reassured that Dad’s best interests are first priority. The administrator even gave us his cell number so we could contact him on a 24/7 basis if needed, which is reassuring. At the end of the meeting we agreed to strive to communicate more effectively with one another despite the challenges.


Wednesday, August 8, 2012

Tuesday Evening with Dad


When we arrived at Dad’s nursing home for our regular Tuesday evening visit, the nurse advised us that Dad would probably be sleeping. An hour before we arrived, Dad had been given medication to help him regulate his sleep for nighttime versus being up all night and sleeping during the day.

However, upon entering his room, we found Dad eating. His dinner tray was still at his table and it looked like he had barely touched his food, looking closer we noticed he was eating a cookie. He had cookie crumbs all over his shirt, which you might be able to see in the first photo. You can see from his smile that he really enjoys the cookie.

When he finished the cookie I suggested he might like the spaghetti with meat sauce and he agreed to try some. I gave him a few bites and seemed to enjoy it. Shelley took over feeding him and he eventually ate all of his dinner.

While Dad was eating, I called my sister so she could talk with Dad for a few minutes. Dad seemed to recognize Joyce but he was more interested in eating.

After finishing eating and about 40 minutes since we had arrived for our visit, Dad could not seem to keep his eyes open. The medication was working. We said our good-byes and left him to sleep.

Following is a short video of Dad eating his dinner and some photos.  

Eating his cookie and enjoying it too!

Getting help with eating his dinner.

Almost done.

Done and going to sleep!