Walking the valley of Alzheimer's Disease closely with a parent reaffirms how much those words mean, especially today after seeing Dad and hearing him say this. I'm thankful for my brother who truly understands this "need" and "longing" for Dad to still affirm us as his kids.
Yes, we are all grown up.
Yes, I've taken that word "daughter" for granted in the past. These past few years I don't. Alzheimer's won't let me. So many times I feel like I'm in the background in his life, doing all of these things he has no idea about for his benefit, well being and quality of life. He has no idea what we do for him behind the scenes. He doesn't remember our times together after the fact too well at all. That is ok. Those thoughts of needing to be recognized for what I do, don't come to my mind. He is the one who is Dad. He is the one that needs our love the most because he is the one battling this disease. He'd never in a million years want me to do all that I am doing. He'd worry about me. He'd say, "That's too much Darlin'." So would Mom. They were the parents always looking out for everyone else's well being, never wanting to intrude on anyone else's life. They sacrificed and did wonderful things for me all my life.
So what do I do when the reality of dementia hits hard? Besides pray (a LOT) and shed a few tears (if I need to), and pour out my heart on this blog, I listen to a phone message left to me by Dad about 3 years ago on our answering machine. He and Mom were still living independently. I have it recorded on my phone so I can listen to it any time I want to. It is a message where he thanks me for being his daughter. It sounds like "Dad" before we truly started losing him. It is a reminder that what I see today is the disease, not my dad in his true form. Take away the beastly disease and there is my daddy, like I've known him all my life.
That is a huge comfort to me to hear his voice of yesterday.
So I go back to...."That's my daughter!"
How special those words are to me this afternoon as he looked at his caregivers with a smile on his face and gleam in his eye.
Those words are like food for my soul on this journey.
I am waiting for the day when I walk into his building and walk up to him and he won't know who in the world I am. That day may be coming faster than we realize. Not remembering loved ones is something heavy on my heart sometimes. I have selfishly begged, quietly whispered, and humbly asked God to spare us these moments.
Starting with Mom...... I prayed and prayed she would never have to go through the heartbreak of Daddy forgetting her after almost 60 years of marriage. She would have completely understood, but it would have been painful.
God answered that prayer. Daddy has forgotten after she has passed away, but never while she was living in his day to day life.
Selfish me asks the Lord to spare me too. "Please Lord, let me not experience this." Oh he knows this heart so very well! He knows that will be a heart crushing day for me. I do not dwell on it. I take each day as it comes. If it does happen I am not alone. So many experience this loss with a loved one with dementia. No, I do not want Daddy to forget I'm his daughter. I do not want him to forget Tom is his son.
I've already seen God's amazing miracles with my dad's dementia. I've mentioned before, this disease is sparing him the grief of his bride. The staff in Memory Care even recognizes it as a gift and blessing of God. They all smile when we talk about it, even today 2 months after Mom's passing! They all say the same thing about what an incredible blessing it is.
Sometimes I ask the Lord again, "Is this what 'working everything out for the good of those who love you?' looks like?" I just pinch myself seeing the goodness of God as we move forward. I should not doubt God's abilities to work in our lives or his goodness, or how BIG he his! "You are blessing my dad, just because you can Lord." This is just such a huge blessing! Perhaps Alzheimer's has enough pain of its own. "God, You are a loving God. You care for your children even when a disease of the mind does not allow us to petition you in prayer. You are caring so greatly for Dad right now."
And then I wonder if the Lord is saving Mom for Dad in heaven. She has brought him so much joy these past 61 years.....
"No Joe, no sadness for you, with Ethel. There will be only joy. You'll have to wait for heaven for that."
Sounds crazy, and God's ways are not my ways, but what if that was part of the plan? No matter what, Daddy's disease and joy are bringing God glory!
"That's my daughter!"
I'm still thinking of Mom. I hear her say it when he says it. She used to do the same thing with the staff in her building. For both of my parents all of our lives, (not just in a nursing home), it is not just an introduction for either my brother or I. It's an endearing, happy proclamation with emphasis on "son" or "daughter". It is a loving affirmation of us, adopted kids.....even over 40 years later.
I miss my daddy. I miss who he used to be. Yet, there are little pieces of him that God allows to remain for now. The pieces are becoming smaller as we move along. His joy is still vital to the well being of this heart of mine. When I see that face light up at the sight of our family it just makes my day! To see him so happy, makes my day! I don't say this to puff ourselves up or to say, "Hey, look at us! We're something wonderful!" I say it because Dad is wonderful to US. He is loved. He is cherished. And when we feel loved and cherished back in the middle of this crazy, unpredictable, depressing disease, we are not just happy. We are affirmed deeply.
It is what I'm hanging on to at this point.
"That's my daughter!"
He does not know my last name anymore.
He does not remember his grandsons' names.
Sometimes he may not remember my name specifically to other people.
But.... he knows ME. He knows my brother, when he sees our faces.
To be his daughter..... there is so much wrapped up in that word. I wish I could describe right now what it's meant to me for the past three years since I started investing so much of my life into my parents' lives for their health and well being. One day I will have to take the time and write down what it means to be just that..... a daughter. Not just any daughter. Their daughter.
God has brought me to a place as "daughter" like no other place. He's required more of me in this role than I ever dreamed He would. And I wouldn't change a thing..... and I'll still cherish those words of Dad when he tells other people (who yes, know exactly who I am) that I am his daughter.
I want him to "feel" loved and appreciated..... because he is.
In the darkness of Alzheimer's Disease you especially need to feel loved when you are in those places that do not make sense. When your world is turned upside down, and you truly have lost control of your life, it is essential to feel loved.
I am just so grateful Dad is still with me. If Mom cannot be, he still is.
God's grace through Dad's love carries me at times as we continue strolling along this long journey of this disease together. Dad still wants to walk me to where I'm going, when we say "I'll see you soon." Right now it is to the elevator in his building. He's still the gentleman. He wants to be wherever Tom and I are. I think that is because our heart strings are attached and he knows that.
"That's my son!"
"That's my daughter!"
Most importantly..... "That's my daddy!"