Loving a Spicy, Fiercely Independent Human (Without Completely Losing Your Mind)

Loving a Spicy, Fiercely Independent Human (Without Completely Losing Your Mind)

Caring for someone fiercely independent is nothing like the usual idea of caregiving. It’s not peaceful music, color‑coded pill boxes, or constant thank‑yous. It looks more like this:

Early alarms.

Lukewarm coffee.

Being told, “I don’t need your help” … while they’re holding onto the wall to walk.

And emotional landmines before 9 a.m.

If your loved one has always been stubborn, strong‑willed, or hates being told what to do, that doesn’t just go away with dementia or Alzheimer’s. Often, it gets stronger. This guide is here to help you get through caregiving — and maybe even find some laughs — when you’re caring for someone who would rather fight the world with a butter knife than give up.

Part 1: When “I’ve Got It” Means “I Really, Really Don’t”

You know that moment: they’re struggling with the zipper, the stove, the shower, or the stairs, and you step in … only to get the look.

“I can do it myself.”

You hear:

“Back the fuck off.”

But what they might really be saying is:

“I’m scared of losing who I am.”
“I don’t recognize this version of me either.”
“Let me feel capable for one more minute.”

How to help without becoming the enemy

Offer choices, not orders.

Instead of:

“You need to take a shower now.”

Try:

“Do you want to shower before breakfast or after?”

You’re setting the boundary (the shower’s happening) but giving them a say.

Blame the schedule, not yourself.

Let the invisible “doctor” or “schedule” be the bad guy:

“The doctor wants us to do meds with breakfast.”
“We have to leave by 10, so let’s team up and get dressed now.”

In our journey, I’ll throw in a “Sassy ass, let’s shake it,” or “Come on, sassy pants, we have a Starbucks barista to torture.”

Follow the “assist, don’t replace” rule.

Help only with what they really can’t do, and let them handle the rest, even if it takes longer and tries your patience. Every bit of independence you protect helps keep their dignity.

“Hey, doing dishes without a sink stopper is old school. I know you can teach me a thing or two.”

So: no to finding the sink stopper, but yes to clean fucking dishes.

Remember that being efficient and being respectful don’t always go together.

You could do things faster, but your relationship matters more than speed. Most days, taking it slow is the real win.

If you’re short on time, change what you can in your schedule. Your peace of mind matters too.

Part 2: Small Changes, Big Emotional Cost (For Both of You)

It’s never just about a missing sink stopper, a removed lock, or a new label on a cabinet. For you, it’s a safety fix. For them, it’s another sign they’re losing control or are not trusted.

Or maybe it’s the stove that suddenly won’t turn on anymore.

The safety shift you don’t see on Instagram

You quietly:

  • Remove the bathroom door lock.

  • Hide the car keys.

  • Add alarms, auto door locks, grab bars, and pill organizers.

  • Label drawers, rooms, and light switches.

  • Swap real candles for battery‑powered ones.

Every small change brings a bit of sadness, and sometimes a lot of anger:

  • Grief for the version of them who didn’t need any of this.

  • Grief for the version of you who wasn’t constantly calculating risk vs. respect.

How to cope with the emotional whiplash

Acknowledge what’s really happening. You’re not overreacting. You’re grieving slowly, day by day. It’s grief, loss, and love all mixed in with daily tasks.

Let yourself feel annoyed. It’s okay to think, “I hate that I have to do this,” and still do it because you care. Both feelings can coexist.

Document the changes. Take photos or jot notes as things shift: the locked cabinet, the new whiteboard, the labeled drawers. It helps you see:

  • Why are you so exhausted?

  • How much you’ve actually done.

If possible, keep one area the same. Maybe a chair, a corner, or a shelf, just the way they like it. Having one spot that doesn’t change can help both of you feel more grounded.

Part 3: The Exhaustion No One Sees (Yes, Including the Anger)

To others, your loved one might seem calm, patient, and loving as always. Meanwhile, you might feel like you’re losing your mind, always in the middle of chaos. Even if you follow the expert advice, things can still go wrong, depending on the people around you.

From the inside, you:

  • Snap at commercials that show peaceful caregiving scenes.

  • Have cried in the bathroom, hallway, car, or laundry room.

  • Have thought, at least once, “I can’t do this anymore,” and then, “I’m a terrible person for thinking that.”

You’re not a bad person. You’re just human, and you’re tired in ways most people can’t imagine.

The anger you don’t talk about

You might feel angry at:

  • The disease.

  • Your loved one.

  • Siblings who “would totally help if they lived closer” (but still have opinions).

  • Siblings who live closer but villainize you so they can feel justified not being responsible, available, or present—while still judging like the Supreme Court.

  • Doctors who rush you through appointments and only see the 10 minutes, not the entirety.

  • Friends who say, “Let me know if you need anything,” and never follow up.

  • People who vanish because it looks too difficult or their feelings were bent.

Feeling angry doesn’t mean something is wrong with you. It’s a way to release pressure.

Bite‑sized ways to take care of yourself (that don’t require a retreat in Bali)

Micro‑breaks instead of mythical free time:

  • Ninety seconds of deep breathing in the bathroom.

  • Drinking a glass of water while looking out the window instead of at your phone.

  • Sitting in your car in silence for two extra minutes before going back inside.

Lower the bar aggressively.

  • Dinner can be cereal.

  • “Clean” can mean “no obvious trip hazards.”

  • “Good enough” is not failure. It’s a survival strategy.

Practice one tiny “ask for help” per week. Not a whole care plan. One thing:

“Can you pick up milk when you’re out?”
“Can you sit with Mom for an hour on Sunday so I can go for a walk?”

Give your feelings a parking lot. Keep a notebook, notes app, or scrap of paper where you can dump:

“I’m furious.”
“I’m scared.”
“I miss who they were.”

The feelings aren’t gone, but at least they’re not banging around inside your chest.

Part 4: When Independence, Money, and Power of Attorney Collide

A few things bring out family drama, like:

  • Money.

  • Medical decisions.

  • Power of Attorney.

  • That one relative who suddenly cares deeply about everything—from three states away or three miles away.

If you’re the one handling the POA, the bills, the medical decisions, the daily care—or all of the above—you may have heard some version of:

“You got what you wanted.”

As if what you “wanted” was:

  • Sleepless nights.

  • Exhausting appointments.

  • Being the default complaint department for everyone.

  • Being cast as the villain so others can feel like the victim.

Why planning early matters (even if everyone rolls their eyes at first)

POA and wills are not about greed; they’re about clarity. They protect your loved one’s wishes so future‑you isn’t stuck:

  • Guessing what they would have wanted.

  • Fighting with siblings in parking lots.

Boundaries are not betrayal. Saying:

“I can’t do three overnights a week.”
“I need a day off.”
“No, you can’t just ‘drop by’ and criticize care without helping.”

Does not make you the villain. It makes you sustainable.

Document conversations when things get messy.

  • Keep notes after big talks with doctors, lawyers, or relatives.

  • Follow up important verbal conversations with a short text or email summary.

This isn’t paranoia—it’s protection.

Use outside professionals as a neutral ground. Sometimes it’s easier for a doctor, social worker, or elder law attorney to say:

“This is the safest choice.”
“This is what your parent chose in their documents.”

Having it come from a third party can calm (some) drama.

Part 5: You’re Doing Better Than You Think

You will never get a trophy for the number of times you:

  • Helped them find the bathroom at 3 a.m.

  • Answered the same question 14 times in an hour.

  • Re‑explained where the car keys went.

  • Swallowed hurt feelings after they snapped at you.

There is no Caregiving Olympics. No one is timing you. No one is judging your form. There are no style points.

There is just you, doing the best you can, with what you have, on a day that is probably already harder than you’re admitting.

Read this part twice:

You are not failing because you feel tired, angry, guilty, or resentful. You are not failing because you can’t do it all alone. You are not failing because you sometimes wish things were different.

You are a human caring for another human in an inhumanely hard situation.

If your loved one is spicy, stubborn, and fiercely independent, it means you are loving someone who has always fought to live life on their own terms.

Your job now is impossibly delicate: keep them safe without extinguishing that fire.

You will not get it perfect.

You will get it done—with dark humor, deep love, and a thousand imperfect decisions that add up to something beautiful: they are still home, still loved, and still themselves, in all their messy, complicated glory.

And for the record? You’re doing far, far better than you think.

Dazey's Diary

The person who shows up does the work: the dedicated individual who creates a happy, healthy, and palliative long-term in-home care environment for Alzheimer's memory care.

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Memory Care Survival Guide, Part 2: Adjusting Routines, Simplifying the Day, and Saving Your Energy