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🎵 “Tears in Heaven” – EOA When They Lose Someone… Differently (Eric Clapton)

Apr 21
3 min read

Updated: Aug 23


2019 March
2019 March

What’s the worst thing that can happen on top of Alzheimer’s?


👉 Real life keeps happening.


Illness.,

Hospitals.

Loss.





And you’re expected to manage all of it…


👉 While managing a brain that can’t process it the same way anymore


💔 When It Happened

I was coming home from a week-long convention.

Rob had caregivers all week and was already:

  • Anxious

  • Overstimulated

  • Ready for his routine back


And as I got off the plane…

👉 I got the call

His dad had a major stroke.

He was in a coma.


⚠️ What Goes Through Your Mind (All at Once)

You don’t just react as a wife.

👉 You react as a caregiver


My checklist started immediately:

  1. Make sure he eats


    → I knew this was going to be a long night

  2. Prepare for the drive (1 hour)


    → Time + stress + unknown reaction

  3. Prepare for HIS reaction


    → Anxiety?


    → Anger?


    → Confusion?

  4. Prepare the hospital


    → I mentally walked through:

    • What if he escalates?

    • What if he doesn’t understand?

    • What if he panics?

👉 You’re managing two crises at once

I called ahead and explained the patient and that I was bringing in his son with EOA, be ready to de-escalate, be ready to sedate, the intial reaction was BAD.


💥 The Moment You Have to Tell Them

This is the part no one prepares you for.

I said, gently:

“Hey… Pop’s is in the hospital. We need to drive down there.”

And…

👉 The world exploded emotionally, I won't get into Dirty Deets, but it was ugly and it was bad.


🧠 Why It Hits So Hard

With Alzheimer’s, especially at this stage:


👉 They still FEEL deeply

👉 But they can’t PROCESS normally

So what you get is:

  • Big emotion

  • Little regulation

  • Confusion layered on top


💡 What I Was Told (And It Helped)

One of his caregivers (an Alzheimer’s LPN) told me:

👉 “Tell it like it is… but keep it simple”


Not:

  • Long explanations

  • Not overwhelming details


Just:


👉 Clear

👉 Calm

👉 Direct


🧠 How Someone with Alzheimer’s Processes Loss

It’s different.

💭 1. Immediate Emotional Reaction

  • Intense sadness

  • Anger

  • Fear


🔁 2. Repeated Grieving

This is the hardest part.

They may:

👉 Forget

👉 Ask again( 2 months later, still says "My Dad's dead?"

👉 Learn it again

👉 Grieve again

Over and over.


❓ The Question Everyone Asks

👉 “Do I tell them again?”


There is no perfect answer.


✔️ Some Choose:

  • Gentle reminders

  • Re-explaining each time


✔️ Others Choose:

  • Redirecting

  • Protecting them from repeated trauma

👉 Both are valid


It depends on:

  • Their emotional response

  • Their level of distress

  • Your ability to handle it


🪦 Funeral Decisions (Also Not Simple)

Do they go?

Ask yourself:

  • Will it comfort them?

  • Will it overwhelm them?

  • Will they understand what’s happening?


Sometimes:

👉 Being there helps


Other times:

👉 It creates more confusion and distress


⚖️ Your Grief vs. Their Grief

This is the part that breaks you.

👉 You are fully aware

👉 They are not fully processing


You are:

  • Grieving the loss

  • Managing logistics

  • Managing THEM

At the same time


💛 What I Learned

  • You cannot predict the reaction

  • You cannot control the moment

  • You can only prepare as best you can


And then…


👉 Ride it out


💡 Practical Tips (From Someone Who Lived It)

  • Keep explanations short

  • Stay calm (even when they’re not)

  • Have a plan before you speak

  • Feed them first (seriously—it matters)

  • Give yourself grace if it doesn’t go perfectly


🎵 Final Thought

“Would you know my name… if I saw you in heaven…”

They may not process loss the same way anymore.

But they still feel love.

And that still matters


💬 Disclaimer

Keep in mind, I am writing this blog over years, not in one day- I repeat some things, but because it became more applicable today.   I’m not a doctor, lawyer, therapist, or expert—just a wife trying to figure this out one day at a time. Everything shared here is based on our experience and things that have helped us along the way. Take what helps, leave what doesn’t, and always check with professionals when needed. I also use AI to help clean up my writing, organize thoughts, and pull together resources because honestly… caregiver brains are tired too. If something here helps another family feel less alone, then it’s worth sharing.




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