Alzheimers :: Mom Holding Her Urine And Not Eating


Jun 24, 2013

My mom is eating less and less everyday. I have been trying all kinds of food to eat, and only polish sausage and potato chips seem to work. When all else fails I give her a scoop of Ice cream in some glaucoma. Last night she had a ice cream cone and mashed potatoes for dinner. The Doctor told me to give her whatever she will eat.

She will go to the bathroom to make a bowel movement, and I help her when she is finish, but she holds her urine all day and she goes in her diaper while she is sleep. She wears depends during the day. She doesn't seem to be in any pain, and she is not agitated.

She underlines the words in her Dr. seuss books and plays with her doll. Her toes and foot have spasms as well as her hands, and its hard for her to snap her night gown. Its takes her a while to recognize me or other family members. She doesn't have many words left and i have to show her what to do. She went to bed without her meds because she kept trying to suck and chew the pill and she spit it out in the toilet and rinsed her mouth with the water in the cup. (LOL) This happened twice. Medicare only gives me 30 days worth of medicine.

My problem is I want to stop sending my mom to the adult center, because she will not let them feed her and she will not eat. She just sleeps, and doesn't participate and any activities. Shes stays 4 hours enough time for me to do whatever I want. I am retired and 53 yrs old, I can do this.
My family helps on weekends, but they seem to think she needs to socialize. They do not see her slump in a chair staring and looking weak with dried lips, and seeming depressed thinking she is going to stay there. I can't stand it anymore. I kept her home for two days and it takes two hours, but I got food, water and meds in her.

I let her sleep as long as she needs too, and every hour or so I offer her something to eat and encourage her to sip a drink from her cup. I walk her around the house and we look at the flowers. I have a nice wheel chair that medicare provided and my friends come along to help me run errands.
I don't need to send her away to be with other dementia people, cause I have support, and don't work. Today I called the social worker to request in home care for three days a week and 4 hours each day. Because I think at this stage she needs one on one stimulation and quiet. She sits in her chair at the window and sleep. The doctor told me her dementia is very severe and she needs 24 hour care and requested to see her in 4 months.
She is 71 years old. This all started in 2002 when dad died. She became very depressed, and in 2007 she started getting lost and not paying her bills, and doctor also says there were signs of mini strokes, and she is type 2 diabetes.I know my mother is not going to get better, but I want her to feel safe and secure. My sibling are all younger than me, and have jobs and children in school. I retired and moved back here to take care of things and my three little sisters are scared of whats happening. I don't know what's next but I and here for them and her.

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