βI Love Them, But Iβm Exhaustedβ: The Guilt No One Talks About in Caregiving
You love them. You would do anything for them.
And you're exhausted.
Maybe you've caught yourself thinking:
βI just need one day where nobody needs anything from me.β
βI feel terrible saying this, but I don't want to do this today.β
βEveryone asks how they're doing. Nobody asks how I'm doing.β
βI can't get sick. I can't fall apart. Everyone depends on me.β
Or maybe the thought that feels hardest to admit:
βI miss the person I used to be.β
If you're caring for a child or adult with a disability, a partner with a chronic illness, an aging parent, or another loved one with complex needs, these thoughts don't mean you don't love them.
They may mean that you've been carrying a lot for a very long time.
When Love and Exhaustion Exist at the Same Time
Caregiving is often talked about in terms of love, strength, and sacrifice. And it can absolutely include all three.
But there's another side we don't talk about enough.
Appointments. Phone calls. Medications. School meetings. Insurance. Advocating. Researching. Planning. Watching for symptoms. Making decisions. Worrying about what happens next.
And then there's everything you were already responsible for before caregiving entered the picture.
The emotional impact is real. In the United States, approximately 63 million adults are currently family caregivers. Research has found that caregiving can affect caregivers' emotional, physical, social, and financial well-being (AARP & National Alliance for Caregiving [NAC], 2025).
Parents caring for children with disabilities can experience particularly high levels of worry, stress, anxiety, isolation, and concern about the future (Ciciurkaite et al., 2024).
So if you're struggling, you aren't failing at caregiving. You may be responding to an incredibly demanding role.
βBut I Chose This. Why Am I Complaining?β
This is where guilt often enters the room.
You finally get a few hours to yourself...and spend them worrying.
Someone offers to help...and you think, βIt's easier if I just do it myself.β
You become frustrated...and immediately feel ashamed because βthey can't help being sick.β
You think about something you want for yourself...and another voice asks, βHow can I think about me right now?β
Parents whose children develop chronic illnesses commonly experience emotions including guilt, sadness, anger, and stress (American Psychological Association [APA], 2013). Research with parents caring for children with significant needs also describes a difficult paradox: caregivers may recognize that they need care themselves while continually prioritizing their child's needs over their own.
Needing something for yourself does not cancel out the love you have for someone else.
Both realities can exist at the same time.
When βThe Strong Oneβ Starts Losing Herself
Sometimes caregiver exhaustion isn't only about being tired.
It's realizing that almost every conversation is about your loved one.
That your friendships have changed.
That your career or plans have shifted.
That you're always anticipating the next problem.
That you can't remember the last time you made a decision based solely on what you wanted.
Research examining parents caring for children with intellectual disabilities has described exhaustion, social isolation, and even a sense of losing one's identity within the caregiving role. That can leave you asking: βWho am I when I'm not taking care of someone?β
That's an important questionβnot a selfish one.
Support Doesn't Have to Mean βJust Practice Self-Careβ
When your responsibilities are real, being told to take a bubble bath, go for a walk, or make more time for yourself can feel almost insulting.
Sometimes there simply isn't enough time.
Meaningful support may instead involve figuring out where you actually have choices, learning to recognize when you're reaching your limit, asking for help without automatically feeling guilty, setting realistic boundaries, managing anxiety about things you cannot control, and reconnecting with parts of yourself that caregiving has pushed into the background.
Research is encouraging here. A recent systematic review found that psychological interventions delivered online can improve stress, mental health, and well-being among parents of children with additional needs (Leo et al., 2025).
Therapy won't eliminate the realities of caregiving.
But it can give you somewhere to put what you've been carrying.
You Deserve a Place Where You Don't Have to Be the Strong One
You can be grateful and exhausted.
You can love someone and need a break.
You can be deeply committed to the person you care for and still have needs of your own.
You don't have to wait until you're completely burned out to seek support.
Therapy can offer a space that is yoursβa place to talk openly about the worry, guilt, frustration, grief, or exhaustion you may be carrying without feeling like you have to protect anyone else from how you really feel.
It can also help you find realistic ways to manage stress, strengthen boundaries, ask for support, and reconnect with parts of yourself that may have been pushed aside. The goal isn't to change how much you care for the person you love. It's to make sure there is room to care for you, too.
If you're a parent or caregiver in New Jersey and are wondering whether therapy might be helpful, we invite you to reach out to Vida Wellness & Counseling Services to learn more about our therapy services for caregivers.
You take care of so much. You deserve support, too.
References
AARP & National Alliance for Caregiving. (2025). Caregiving in the U.S. 2025. AARP.
American Psychological Association. (2013, August 1). When your child is diagnosed with chronic illness.
Ciciurkaite, G., et al. (2024). Health challenges faced by parents of children with disabilities: A scoping review. BMC Pediatrics.
Leo, M., et al. (2025). Online interventions for the mental health and well-being of parents of children with additional needs: Systematic review and meta-analysis. Australian Occupational Therapy Journal.