Loving Your Partner with Parkinson's

When Caregiving Means Losing Yourself—How to Survive Burnout, Guilt, and Loneliness Without Abandoning Them

De: June M. Reed

Narrado por: Virtual Voice

If you've ever asked yourself "Where am I, where my life is?" you're living what the Parkinson's community calls "living bereavement."

You're loving your partner deeply while grieving "the person I knew is gone." The disease is changing him—not erasing him.

There's a phrase: "If one partner has Parkinson's you both have Parkinson's."

But only one of you receives the sympathy, the medical attention, the concerned phone calls.

You receive the exhaustion. "I am always tired." The fractured sleep. The physical strain. The years of watching "him lose his strength, self-reliance, vibrance, & independence" while trying not to lose your own.

You've become what one wife described as "a skivvy. Worthless. Exhausted. Stuck." And then you feel guilty for even noticing.

Loving someone with Parkinson's is a unique and profoundly difficult challenge.

It's not role reversal like adult children caring for aging parents.

You're navigating what researchers call "role confusion." The impossible paradox of trying to be "his caregiver as well as his wife or lover" when these roles cannot coexist in the same moment.

You haven't just taken on extra responsibilities. You've lost "an equal partner, as well as my romantic and 'relational' partner." Every decision you once shared, every dream you built together—now you shoulder alone.

Standard caregiver resources don't address what actually destroys you. Not the medication schedules or mobility equipment—those are manageable. The deeper losses:

• When "I've lived in a sexless marriage for two years" and nobody permits you to grieve this death of intimacy.
• When "he does not appreciate. He does not love me as much as I love him" and you wonder if your sacrifice has meaning.
• When "his personality has changed 180 degrees. He ONLY takes his anger out on me" while putting up a front for everyone else.
• When "family members deserted us" and "the neighbors won't come around" because "unless you are in this situation no-one else understands."
• When you think "I have lost myself" and don't know if you'll ever find your way back.

This is where most resources fail you—and where this book begins.

Inside, you'll find honest guidance for spousal caregivers—practical strategies for the decades ahead and tools for surviving the conflict of loving while wanting to escape.

I spent fifteen years living with Parkinson's alongside my husband—learning what works, what doesn't, and what no one tells you until you're already drowning.

You'll understand:

• What to expect as Parkinson's progresses through each stage—and how to prepare yourself emotionally and practically for what's coming in the next 5, 10, 15 years
• How to recognize when personality changes, apathy, or anger are the disease (not him)—so you can respond without taking it personally or letting it destroy you
• Why you can love him deeply AND fantasize about escape at the same time—and why both feelings can be true without making you a terrible person
• How to reclaim pieces of yourself while finding moments of connection that still matter—without abandoning him or losing yourself

Somewhere between nurse and wife, you forgot which one you are.

You can emerge from this experience still recognizable. Not because you're more patient or more loving than you are now. But because you'll learn what nobody teaches: how to stay without disappearing.

"In sickness and in health" never meant erasing yourself.

Let me show you how to love the extraordinary person your husband is—and care for him—without disappearing.