While I had planned on writing today, a kick off for our 13th year of Yes, Virginia efforts, a call with my mother has clouded my merriest of thoughts and jolliest of intentions.
I have written about my father having been diagnosed with Parkinson's. I remember every single detail of the birthday trip to Vegas three years ago when they arrived and sat my sister and I and our husbands down in the suite we had arranged for them, and tried to wrap their mouths around the words. We tried to wrap our minds around the words.
At that point, the only visual evidence was the tremor - slight - in one of his hands. We all held each other, comforted him, reassured my mom - and vowed that we were all in this together. I count that day as one of the very few in which I have ever seen tears in my dad's eyes.
Parkinson's, like so many diseases that compromise neurological function, is cruel. There is no cure, only medications to help mitigate symptoms. And it progresses. There is no getting better. Like Alzheimer's it affects memory, lucidity, cognitive function. And like Alzheimer's it is especially callous in that it can ebb and flow in those areas. Good days, bad days, completely coherent, lose the plot, totally there, adrift somewhere else. I have watched all of these things happening to him. And physically he is diminishing.
It is heartbreaking. Because when he is "there" he is all there. And no one is more aware of his decline and descent as is he. From the outside, I can only watch and try to support him and my Mom - a woman who is shouldering it all for this man as they have entered the "for better or for worse" portion of their vows.
A proud Irishman, he has always been larger than life, the life of the party, a man who could light up a room, who could tell a thousand jokes. He has also always been a man who could be relied on by those in his professional life and personal life. That's not to say he has been Mike Brady - he hasn't. He and I have fought battles galore - some borne of generational gaps, some because we are too much alike, some simply because we are father and daughter. At this point in my life, however, they serve to have brought us closer, afforded me the privilege of being able to say things to him others cannot, and I know he trusts me in this awful, terrible, dark place where he is trapped.
Getting them moved into a CCRC - Continuing Care Retirement Community - was huge. It took months of effort with them, their house, the facility, etc, but they are there - they have a built in safety net. Their community goes from independent living (where they are now) all the way up to hospice.
Today I spoke with my mom who finally came clean on some of what has been transpiring of late. He is slipping. Hallucinations. Rambling, agitated. His doctor has upped some of his meds and added an additional one to combat the newest symptom - 50% of Parkinson's patients will experience hallucinations. The nursing staff has spoken to her about her feelings on him needing to be transferred to Memory Care. That is crushing for her. I know that. And we talked through her feelings about it, and mine. We both agree that he is not quite at that point yet, but we both know it is coming. And that when the decision is made, he sadly, cannot be a part of it.
After our call, I texted her, "People like to say “when push comes to shove” about difficult decisions. In Dad’s case it will be “when push comes to love” It is not a lack of love. It is an abundance of it and the burden of having to make a very hard, intensely personal decision. And it all sucks completely and is heartbreaking. But we cannot change it. We just have to manage it as it comes."
So, as I said at the beginning, I am sad.
But as I have sat here thinking about him, about what I had planned to write, the two formed a beautiful Venn diagram in my head - they do overlap.
My parents, like so many their ages, are not the most tech savvy or internet fluent. They do, however, know all about Yes, Virginia, donate each year, and love to hear the stories about the people we help. My Dad, James, has always loved Christmas. He loved putting up his train platform, showering his kids with gifts, opening his home to friends and co-workers for parties. And now, my father, biased as he is, looks at what his daughter does each year and is beamingly proud. I always stress that his daughter could not do any of this without the open hearts of so very many people who come to this blog.
I am honest with myself and I know that even if he is still physically here a year from now, so much of what makes him him, will not be. My hope is that I am able to share our stories with him one last season. To make him smile. To make him proud. To remind him that the good people still outnumber the bad in this world.
So through these tears falling on my keyboard, here is my first ask of season 13 - one I refuse to label as unlucky, and in my heart will be calling Yes, VirJIMia: Please donate to our efforts. Please send those my way who can use our help. And please help me give my father one last round of holiday magic.
The link on the left side of the page is always open. Paypal.com >Send Money>[email protected] (Note: Please choose the simple Send money person to person option, not the purchase -Send Payment - option that deducts fees from your donation.)
Yes, VirJIMia, there is a DGMS. And when push comes to love, they are able to move mountains.
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