“What will matter is the good WE did, not the good we expected others to do. May you listen to the voice within the beat of your heart even when you are tired. And if you can wait for me…like I waited for you…I will be there.”
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Excerpts from counseling chats, #1
The last few years culminated into feeling like a dream for the last several months – I have literally survived, I realize now, by living in a whole non-reality, on autopilot, and there are very few everyday experiences and mundane daily tasks that I do now without being in an almost confused state. Like, “what is this?” or, “how did I ever do that…I don’t remember…”
I am beginning to realize that I actually exist – and can exist – as a being separate from continuous worry and fear about/for my mother, and I have completely forgotten how to be that person. I still wake up some mornings, if I’m not already at my moms, with this programmed state of, “I have to go check on my mother,” being the first literal and conscious thought in my head. Even if I stay there, which I haven’t been able to peacefully do yet, I find myself in the mindset that I have to get up every few hours to check and feel guilty when I wake up and think I forgot to set alarms to wake up.
Everyone says, “it’s got to be such a relief, though, since she died…” It is, in some ways. But in others, it is the same, just different, level of stress to readjust to “normal,” which is difficult now anyway because WHAT IS NORMAL in a world of COVID? I focus myself on cleaning and doing what needs to be done before anything else (music, photography, etc.) when the things I used to do I was only able to do mindlessly, really – just as a distraction from insanity.
I don’t know if this will make sense to anyone who reads. It has to sound like the ravings of a lunatic mind – but as I’m remembering my intelligent, creative, indulgent, passionate, and subconscious mind I find myself feeling everything from confusion to guilt to elating freedom to even complete blankness and emptiness.
It’s not the grief. Well, it’s partially that but only about 3/4. I don’t know, in this moment, WHAT the word or feeling or experience is. I remember going to through it to some extent after Dorie died and I had been such an integral part of taking care of her, but it wasn’t the same as this, nor was the care.
24/7 worry and anxiety about someone for years, and then 24/7 for months – even to the point of every single daily task they needed to do and then to the point of helping them through every moment of their death…it’s a completely different experience to readjust to existing without that task attached to your back when it was there for so long.
So yeah, you’d think it’d be lighter, more peaceful existence…but it’s actually more like a feeling of chaos. I hope like hell it doesn’t last long. I have too much to do – and, too much I want to do. I assume it will last through and a bit beyond probate because that limits me on the speed at which I can chose to move forward and move on… If it were up to me, I’d snap my fingers and life and the “me” I was “pre-Alzheimer’s parent” would click right back into place.
We don’t get into any state of being in the blink of an eye and we become the next version of ourselves even less quickly, I suppose. That’s been my past experience. So trudge along and get it done, I guess… ((Yawn.))
🤷♀️
The End of the Road (Last Blog Before My Mother Died)
TW: the dying experience. Do not read further if you can’t deal with that kind of reality, or if you’ve had a recent loss that this will gnaw at…
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Seriously, I’m going to share this reality so don’t keep reading if you’re not comfortable with this type of thing. This is my coping mechanism. To write. To share with those who can handle and understand it. To feel like my support system is with me…
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This morning around 3:30am my mom’s oxygen started dropping. First it was 92. Then it was 90. Then it was 88. Then it was 85. She kept yanking the oxygen away. I stuck it in her mouth until the higher dose of morphine kicked in and she relaxed. Then, I put it back in her nose.
I called the after hours line. I was told I was doing everything I needed to be. I mean, it’s kind of common sense at this point, after the others, for me – but that doesn’t mean adrenaline and norepinephrine don’t fly and dopamine and seratonin don’t plummet…and you need that reassurance because you second guess. You feel responsible for more than comfort. You feel responsible for the pain, too. You can’t help it.
I cranked the oxygen up to 3. I started giving half doses of morphine every 30 minutes. Her chest would rise when she gasped, then cave in. Then the fluid rattle started again with her shallow breaths.
She would draw up in a fetal position, moaning and gasping, still with oxygen in her nose but oxygen levels still rising and falling at will because of the mouth breathing and the breath holding and the inability to get enough oxygen with the fluid.
She has not eaten in 12 days. She has not drank in 3 days. She is in the final phase of the dying process. I knew that. I know that. But nothing prepares you for that. I am grateful that she is home, and that I moved here. I am grateful that it is not the nursing home I fought for, or the hospital, where I likely couldn’t be with her…where she would be alone.
I have laid with her – some would say a gift, and I agree…though in the moment it doesn’t feel like one. I suppose it will one day, just like with both my grandmothers, my Daddy, and Dorie, and pets… I held her hand. I cried silent tears, watching her face grimace and her eyes open with the moans only to reveal cloudy, lifeless eyes. I waited patiently for the nurse.
The nurse came at 8:30. Upon assessment, the things are happening. The limbs are cooling. The bp is dropping. The heart rate is rising. The temperature is rising as her core fights to hang on. All the things.
It could be today, it could be three days. It could be a week – probably not longer than that, because of the lack of food and fluid. I have chosen to make her comfort the priority, with oxygen, and liquid morphine and Ativan. Myself and the doctor have chosen to forego the feeding tube, and IV fluids. There is no point in drawing it out, and a DNR is a DNR – all those things are at this point are life support. She doesn’t want that. It’s documented. I will not allow myself to feel guilty for those choices. She made them long ago – not me.
But it’s not easy. It’s not a happy choice. It’s not a good choice, in many’s eyes, I’m sure – but for her it is the right choice. And I will live with having to make it for the rest of my life. But I will also live for the rest of my life, however long or short that may be, knowing I’ve done all I could and what we felt was best for her. She has fought me tooth and nail, even changing the locks to keep me out of the house and away from her business, and now she groans when I’m not there. My, how things change. How they heal. How they induce growth. How they make you a different person.
I have been many different people the past year and a half, through the worst of all of this – some not always graceful, some quite angry, some extremely depressed…and now, regardless of the amount of time left, I feel nothing but…strength. Courage. And love.
I will see you all on the flip side… Love one another. Be kind. And live with an open heart. 🙏❤️
Dementia, a Mother, and an Adopted Child
**Edit: my mother passed away 26 hours after I posted this.**
About five months ago, my mother was mentally bad and had wandered and broken her arm. Three and a half months ago I brought her home from the hospital. For years before this, from about six months after my dad died, I had struggled and fought for her and tried to care for her but she didn’t want to let me. I heard, “I am FINE,” at least 72,000,000 times. We had all made jokes about her condition – jokes about “NaNa” – jokes about how bad she was getting, “but there was nothing we could do…” Yet, I still fought…and I know those battles, and they’re why I’m here tonight.
I wish we hadn’t done that…made jokes, because it’s not funny. But I’m glad I never stopped fighting, even if we never had the mother/daughter relationship I always wished we’d had and even if I didn’t get her the help she needed WHEN she needed it because of a broken system that doesn’t correctly diagnose dementia/Alzheimer’s until it’s too late to really slow it down. It shouldn’t be this way – not with the research and the knowledge we have, medicine we have, and resources we have in this country.
I am at peace with the fact that I did my best – that I did everything I could. I don’t need to be externally validated for that…but it makes me feel and have almost a need to validate others who are or have been or will be in my shoes. All these years…they’ve culminated so quickly – in just a matter of weeks.
Three months ago, my mom looked like this (first photo) when I picked her up from the hospital. Tonight, she looks like this (second photo), grimacing and clenching in pain, almost choking on even oral liquid Ativan and Morphine, and her own phlegm and fluid, coughing like a weak squirrel, moaning and crying out in pain to the God that she believes in and still praying incessantly (again, quietly like a weak squirrel, but in pain all the same, barely able to verbalize it).
Dementia and Alzheimer’s are considered mental health issues and illnesses. Don’t tell me you can’t SEE IT because “it’s a mental disorder.” You CAN see it, right there on the MRI. Don’t tell me it’s not real or difficult or physically painful because it’s JUST a “mental disorder.” That’s what I was told for so many years – she’s just getting older. She’s just getting forgetful. She’s just having “mental problems” because of age. No – not just mental problems. A DISEASE – and a terminal one at that.
And you know what else? Especially if you’re a doctor? Don’t pretend to care when you don’t. When you belittle. When you get annoyed with children who are fighting for a better life and end for the parents. Don’t pretend to advocate because for the moment you feel sorry for someone. Don’t pretend like you’re Gucci just because you give to this or that charity or “buy your way” out of having to actually GIVE CARE.
You know what means even more than your charity checks and your “honest opinions” to families struggling with ANY illness or disease or end of life process when you follow up your explanations with the words, “we care?” When you SHOW THE FUCK UP for them.
I am showing up, mama, and even when you don’t want me here, here is where I will be. Too little too late to heal all the old wounds, but not too late to SEE that bygones can be bygones, and despite all of our bad times, all of the good you’ve done for me.
I’m so sorry for the hell, all the chaos I brought to you. I’m sorry for all the hurtful words and for all the times I fought you. I’m sorry I’m not the daughter you’d always hoped I’d be, playing the philharmonic or writing novels or preaching the gospel…but so many of the good things I am are things that you taught me.
“I didn’t carry you in my belly for nine months, but I carried you in my heart for a lifetime,” is what you’d often say to me…and that “to do your best and leave the rest,” was sometimes the only way to be. These words I’ve never forgotten and these words I’ll never forget.
I will soon, again, be an orphan, a fate you once saved me from…and with these fleeting last moments I am sorry. I know I was wrong. I’ll always be a daddy’s girl, and this always broke your heart…but the reality I thought you lived in was creating jealousy into art. But I always had a mom…
I understand your love tonight and what made you who you are…and that even though we aren’t the same we aren’t that far apart. I want to say, “it’s ok, let go,” though it truly breaks my heart…because I understand after all these years who you really are.
Rest now, precious woman, I know you did your best…and your best was really always enough, though I often put you to the test. I thought you didn’t love me, but you just loved me in your way…and, “rest now, precious woman,” is all I can seem to say…
You’re Gonna Miss This.
One day, you will sit alone and look through old photos that seem like they were taken just yesterday but really, those moments are so far away. They’ve become memories, and a life that you once lived… Treasure good and happy, joy and thrill filled moments…indulge in those moments – whether experienced with those you care for or experienced alone – while you’re taking the photos and living the experience. Make them count. When they become just a memory, never look back at them with regret, because in those moments you were alive. You were living – not just existing. And being alive and not just existing is what life is really all about about. It is always “the good old days,” in one way or another… Never forget that.
“You’re gonna miss this
You’re gonna want this back
You’re gonna wish these days hadn’t gone by so fast
These are some good times
So take a good look around
You may not know it now
But you’re gonna miss this
You’re gonna’ miss this
Yeah
You’re gonna’ miss this…”
To those of you who have commented on different posts, dm’d, texted, or even called and I haven’t been able to speak to you with everything going on, I’m sorry and I truly appreciate your kindness and your concern for my mom, for my son, for my family, and for me. It means so much – even if I can’t respond right away I see you and feel you there. Love y’all…so very much. It breaks my heart open to be able to receive, and thus continue to give, love…and have hope. ❤️
#memories #summer #goodtimes #wine #water #warmth #sunset #goodolddays #love #hope #gratitude #keepgoing #changeisinevitable #growthisnotlinear #growthisnecessary
What the “Bad Apple” Analogy REALLY Taught Me
It might be one thirty in the morning but it is still Sunday, so Reverend Sister Christy is going to preach. We having church.
Today’s topic is: Don’t give up a good apple in your life just because you see a blemish and mistake it for a worm.
Misery may love company. But you know what miserable people really want? To be heard even in their silence. To be cared about even when they’re misunderstood. To be thought of even though they may not want to be seen. Even if they can’t or don’t want to express themselves or respond…they need to know they still matter, not tossed to the side because they or their struggles make you uncomfortable.
Why? Because disconnection is not humanly reasonable even if a human being doesn’t have the ability to express themselves – and all people are not going to express themselves in ways you can understand when they DO express themselves. We are meant to be a collective, supporting each other, even if it’s just with a comforting smile and soft eyes, or a simple, “Hey there, I was thinking about you and I’m here if you need me.”
People don’t necessarily always want or know how to express themselves. They may not necessarily want that. But what everyone wants and needs, whether they express it or not, is to have the option.
So get down off your high horse, Herod Agrippas of the world, and sit down and LET PEOPLE BE EXPRESSIVE in whatever ways they can be even if you can’t understand those expressions – and as long as they’re not abusing you in any way, if you don’t have anything nice to say or don’t know what to say? Just say so.
Stop punishing people just because you have your own issues and double standards, Herod Agrippas of the world. Get rid of those double standards, and if you have your own issues? Work on them rather than personifying them.
I won’t even say “as long as they’re not hurting you,” because you know what? SOMETIMES THE TRUTH HURTS. Abuse is different. But just because someone’s behavior or choices bothers you, or you don’t agree with them, doesn’t make them invalid or constitute a behaviors they should be punished for by someone with their own flaws and faults. NONE of us are perfect – and for all who would argue that the biblical God was, he himself was not perfect and he KNEW that after he screwed up “man” (see https://lifehopeandtruth.com/god/who-is-god/genesis-6/).
Here’s the thing: You aren’t living someone else’s experience. THEY ARE. So be kind in the ways you can be, even if it is to explain to them that you can’t be of help to them. Be thoughtful. Add some good to the world by shutting up and just offering to listen, even if they don’t want to talk. TRUST ME – that matters. It counts. It’s worth the effort in the long term, even if it angers them or seemingly stresses them, if you truly care for them.
No. Don’t give up a good apple in your life just because you see a blemish and mistake it for a worm.
I can’t – and that’s OK.
I can’t, and that’s ok to know and to accept and to feel and to express. That’s what this post is about. I know I haven’t really updated here and none of you will know what is going on in full but basically my mom has been living with me and… Well…
There comes a point where you have to accept what you can not do and stop letting people keep trying to convince you that you can do in their “motivational” ways. Sure, they’re trying to help.
But when I say I CAN NOT DO THIS BY MYSELF I need people to understand something: i am doing this BY MYSELF and it’s not working – and it’s not about not wanting to. It’s not about not believing in myself. It’s not about the inconvenience. It’s not even about my own mental health (though it should be). It’s about LITERALLY not being able to care for someone with these needs BY MYSELF, and raise my son and care properly for him. I’m not sorry that that will always come first. I AM legally responsible for him, he’s a minor. And he can’t help me with this. And…she’s not really even my mother. Never has been, by blood or otherwise.
It’s about debilitating migraines. It’s about health issues I had long before this ever started.
It’s about I PHYSICALLY am not strong enough to help someone who refuses to help me help them – lifting dead weight every five minutes to go to the bathroom? Nope. Can’t handle it. Especially with a migraine. Getting her in the tub? Impossible. So we improvise with bowls of water and a tub chair OUTSIDE the tub. Getting her to eat? Also impossible. Which doesn’t help with her strength issues. Getting her to get out of the bed and sit up without arguing and telling me how disappointed and ashamed of me my dad would be that I am trying to make her do something she doesn’t want to do – on his birthday yesterday, when she knew how upset I was – because she KNOWS what she’s doing and she just wants to hurt me.
This is not the dementia. This is just her being hateful and stubborn, naturally. Does she even have dementia? No. Not according to the doctors. She checks out fine. So this is just an angry, bitter, mean, frail and weak old woman who needs help with physical things 24/7 and is being verbally and emotionally abusive to the only person who can keep her out of the one place she doesn’t want to go – the nursing home.
Can I even get her in a nursing home? I don’t know. But I’ll tell you this much – I’m going forward with trying because the few people who have even dealt with her for a half hour at her home or dealt with her at church or even the beauty shop over the past few years have straight up told me that she is faking a lot of this and how she acts when I’m not around.
When my helping you hurts me to a point where I am literally sick all the time? I can’t help you anymore. And I will no longer try. This is my honest, heartbreaking statement: if she wants to do it her way, I will take her to the hospital and leave her there and refuse to care for her. They can’t put her on the street. I don’t know what they’ll do with her but it’s not my concern – I have NO binding, legal obligation to be responsible for her. Why? Because she won’t LET me – and maybe that’s been a blessing in disguise.
She’s already getting bedsores because she won’t move and wants to lay in piss diapers and fights me to change her. It absolutely ridiculous.
I don’t care about how it looks if I do take care of her or if I don’t. It’s not about that. I don’t want accolades for doing it, and I don’t give a damn if people think I’m horrible for not being able to do it. But I can’t do it. I can’t care for someone with these needs BY MYSELF, and raise my son and care properly for him. I’m not sorry that that will always come first. I AM legally responsible for him, he’s a minor. And he can’t help me with this.
It’s always going to be a never ending battle I’m never ever going to win. I have finally accepted that.
Now. To take more meds and pray my head quits and I can fucking breathe for five minutes without feeling nauseous and debilitated.
