Once again I went on a little break from blogging....seems to be a little routine I go through. It definitely ties in with coping with the disease. Some days its easy to write about it and others not so much. Sometimes I think about what I am comfortable sharing and what maybe I shouldn't. And yes, there are some days I just want to cry and write very explicit things about how much I hate this disease but I try and take deep breaths to work through it (so, maybe the deep breaths can lasts for days, weeks, months...).
It was so much easier coping in the first years because the progression was so much slower and the changes weren't so dramatic. Now, it feels as if each day brings a new saddening decreased function/ability. The speed of the disease is becoming more and more rapid or it at least feels that way. The good moments still exist in their own little ways. Yesterday I was sitting in the car and Mother kept trying to go into Kendra's car even though she was supposed to come into my car. I called for her and started to get up when she finally started walking toward me. Moments later Mother was trying to sit on top of me in the driver's seat. It was actually quite comical because I could see her thinking like ahhh, wait, this isn't right. I gently reminded her that she had to go on the other side and everything seemed to easily click for her. There are those times where it doesn't click for her and she gets agitated. They can be quite interesting. In case you were wondering what Mother has been upto here's a picture.
I vividly remember the days my dad would have "car issues", too! He would try to open the door when it was already standing open. Sometimes he would try to open in from the hinge side--and get really angry about it all, too. And trying to get him to actually SIT down in the passengers seat...oy! I have since learned that with losing depth perception, he had no idea if he was going to fall out into space, or actually sit his bottom down on the seat....
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