
This is Chloe. She's 11-weeks old.
Husband and I took a road trip for Christmas. We began the trip late on an icy cold Friday night in Seattle. After icy and snow-covered roads, a break-down (ignition coil, which meant a two-day delay), big scary trucks on mountain passes, and too much fast food, we made it to our destination: Chula Vista CA.
It’s been ten years since we spent Christmas with my parents. Dad isn’t “right” anymore. The doctor’s said it was probably Alzheimer’s but after exhausting research, I’m convinced he has Lewy Body Dementia, which is like Alzheimer’s but with Parkinson-like symptoms, off and on memory problems, and horrible hallucinations.
Mom will take the information I printed to the doctor. She said she’ll shake the papers at him and ask him to read. LBD is very similar to Alzheimer’s except that some of the anti-psychotic medication the doctors might (and have tried to) prescribe for hallucinations can make the disease worse, much worse, and I don’t want that to happen.
My dad is convinced he has two wives and that his wife of over 50 years – my mother – is his “lesser” wife. She’s the mean woman who won’t help him get better.
“Why won’t she let me see a doctor?” he asks. He’s convinced she’s trying to ruin his life, that she’s not helping him when she clearly could, that for some reason, somehow, she’s making these things happen to him.
My brother tried to explain that Lewy Body Dementia isn’t curable. “Fix it,” dad said right before he broke down in tears. I don’t think he understands completely. Something in his spirit can’t accept what’s happening to him and I think the hope (even though it’s probably misplaced) helps.
I’ve never seen my father cry. I don’t belong to an emotional family (and my understatement makes me snort, but I don’t have the energy to explain).
Dad has been my north star forever and I’m not taking this slow loss well. I guess it’s fair to say that I’m taking it better than he is, though. I get to watch his decline but he lives within it, and he knows he’s losing his mind. He’s not that old – only seventy-three. I think that’s far too young, especially for him, my always upbeat, friendly, and hard-working dad.
Next Saturday I’m flying back home to spend a couple of days with Mom and Dad. That’s all I’ve got today. I suppose this little essay is my simple explanation (to you, all of my lovely friends) about why I’ve been so quiet.
And let me add that there’s a wonderful website written by a family who lost their mother to Lewy Body Dementia that I highly recommend. Knowledge helps us walk through difficult situations and this website is full of information. http://www.lewybodyjournal.org
So. Then. Art, art supplies, books on art and creativity, music, beautiful blue sky, sweet puppy, kind husband and wonderful friends. That’s the rest of my life. My kids are too busy living their own hectic lives and I’ll never get my fill of conversation with them, so I move on and build other things: coffee with friends and strangers, researching stuff on the Internet, cleaning up after the pup.
Did you see that pup? Look at those eyes. She’s a Shiloh Shepherd, one of the most magnificent kinds of dogs in all of the world. She’s so smart. She’s going to be as big as a small horse. I am doomed.