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The phone calls I take from family caregivers usually happen at odd hours: late in the evening after the parent has finally gone to sleep, early in the morning before the day starts, or in a quick call from the car after leaving the pharmacy. There’s a particular tone to those calls, and after a few years of hearing it, I can recognize it in the first sentence.
It’s the tone of someone who has been holding too much for too long, who is starting to sense that something inside them is giving way, and who doesn’t quite know who to tell.
If that’s you right now — if you’re caring for an aging parent (or a spouse, or another family member) and can feel yourself unraveling in ways you don’t have words for — I want to walk through this with you. I’m not going to lecture you about self-care. I’ve watched many families in Washtenaw County navigate exactly this, and what helps is more concrete than that.
Below is what caregiver burnout looks like, why it happens, and the specific local options that can meaningfully change your situation without requiring you to move mountains.
Burnout is a word we use so often that it has almost lost its meaning. In caregiving, though, it has a very specific shape.
Physical signs can include persistent tiredness. You’re tired in a way that sleep doesn’t fix. You get sick more often than you used to. You have headaches or back pain that never quite go away. Your appetite is off, one direction or the other. You’ve stopped exercising even though you know you shouldn’t have. You feel older than you are.
Emotional signs may be what families notice about you before you notice about yourself. You cry more easily than you used to. You feel angry at small things. You feel numb at things that used to move you. You feel resentment toward your parent, sometimes flashes, sometimes a steady undercurrent, and then guilt about the resentment. You feel disconnected from your spouse, your kids, your friends. You catch yourself dreading the next visit or the next phone call.
Changes in concentration can be easy to miss. You’re forgetting things. You’re making small mistakes at work. Your concentration is shot. Decisions that used to be easy feel impossible. You feel like you’re moving through water.
Changes in behavior can be another sign. You start canceling on people. You skip your own doctor appointments. You use alcohol or food or scrolling to numb out each evening, and then feel worse in the morning. You lose your temper with your parent in ways that shock you. You start fantasizing about not being able to do this anymore, and then you feel horrified with yourself for the fantasy.
If several of these describe where you are right now, you are not weak. You are carrying more than one person was designed to carry, and your body and mind are telling you.
Family caregiving is one of the most silently intense jobs in the world, and almost nobody prepares us for it.
Most of us go into it thinking of it as a natural extension of our relationship with our parent. What could be more normal than helping your mother? What kind of person wouldn’t step up? We start with a few tasks — driving her to appointments, picking up prescriptions, checking in more often. We add a few more. We take on the medication management. We take over the finances. We start staying overnight some weekends. We take on the coordination of everything, all the calls to doctors, all the paperwork, all the decisions.
None of it feels like a decision at any single moment. Each small step feels reasonable. But over months and years, the accumulation is enormous. And unlike a paid job, this one doesn’t come with vacation days, or a manager who notices when you’re overextended, or a clear end to the day.
Add to that the emotional layer. You are watching someone you love decline. You are anticipating grief. You are managing your own fear about aging, sometimes about your own future, while trying to hold together someone else’s. You are often coordinating with siblings who don’t fully see what you’re doing. You are, in many cases, doing all of this while also holding a job, raising your own kids, tending to a marriage, and managing your own health.
Of course you’re exhausted. The surprising thing is that anyone is not.
Every community has its own texture, and Ann Arbor and Washtenaw County have some patterns worth naming.
The academic and professional culture of Ann Arbor tends to produce family caregivers who are used to being competent at hard things. Many of the caregivers I talk to are professors, doctors, lawyers, professionals of one kind or another, or the adult children of professionals. There’s often an implicit assumption that if we’re smart enough and thorough enough, we can manage this without asking for help. That assumption doesn’t survive contact with reality, but it can take a long time to give up.
Michigan’s geography also plays a role. Many of the adult children I work with live in Ann Arbor while their parents live somewhere else in Michigan, or they live somewhere else while their parents live here. The long-distance caregiver has a specific version of burnout — the guilt of not being physically present, the exhaustion of frequent travel, the anxiety of managing everything from a distance.
The seasonality of Michigan matters too. Winter is hard on older adults and on the people caring for them. Ice and snow make every trip to the doctor or the pharmacy harder, and the cold and dark can make it harder for your parent to get out and stay in touch with people. If you’re doing this work through a Michigan winter, that alone can push a manageable situation into an unmanageable one.
These are the resources I would want every Washtenaw County family caregiver to know are out there, not generic suggestions but actual named options.
Respite is time off from caregiving. It’s not a luxury. It’s a specific service designed to give family caregivers a break, whether for a few hours, a full day, a weekend, or longer. Options in the area include:
Michigan’s MI Choice Waiver includes respite services for eligible adults who need nursing-facility-level care and meet the program’s income and asset rules. Some long-term care insurance policies cover respite care as well, so check your parent’s actual policy.
If dementia is part of your picture, the Alzheimer’s Association offers:
Check their pages for current group times and locations. If your parent’s needs aren’t dementia-related, JFS CARES or AgeWays (below) can point you toward caregiver support that fits. And if dementia is part of your picture, our companion piece on dementia care at home walks through what to know.
AgeWays serves Washtenaw County. They can help with:
Their resource and referral line is 800-852-7795 (see their contact page). They are a good first call if you don’t know where to start.
Jewish Family Services of Washtenaw County runs WISE, which supports older adults and their families regardless of religious background. Its CARES caregiver program includes respite for families caring for someone age 60 or older in Washtenaw County. Check eligibility and current availability with JFS directly.
The Alzheimer’s Association runs support groups for dementia caregivers, and JFS CARES or AgeWays can refer other caregivers to a group that fits. Talking with other people who understand what you’re carrying, without having to explain, is something the internet cannot replace.
This one is easy to skip and shouldn’t be. If you’re seeing several of the burnout signs above, tell your own primary care doctor what’s happening. They can help with the physical piece (sleep issues, mood, blood pressure), and they can also make referrals for the mental health piece. Depression and anxiety are extremely common in family caregivers, and both are treatable.
Ask your own doctor for a referral to a therapist who has experience with family caregivers. A therapist who understands anticipatory grief, ambiguous loss (a term that includes the grief of watching someone with dementia become a different person while still alive), and family systems around aging can make a real difference.
If you’d like to think through what kind of help would fit your situation, you can schedule a free in-home assessment and we can talk it through together. It doesn’t have to end with you hiring us. Sometimes the useful thing is just having a real conversation with someone who can help you name what would help. There’s no cost and no pressure to decide that day.
It helps to be clear about what bringing in a caregiver can and can’t do, because families often expect either too much or too little from it.
What it can do: give you back real hours. If a caregiver is with your mom eight hours a day, you have eight hours a day to sleep, work, be present with your kids, exercise, see your friends, or just sit in silence. That is not a small thing. Compounded over months, it’s the difference between sustaining this and collapsing under it.
What it can do: create a professional partner in the coordination of care. Someone who notices things you’d miss because you’re too close, who may notice a medication issue before it becomes an ER trip, who tells you gently when something is changing.
What it can do: give your parent someone who isn’t you. Older adults often relate differently to a professional caregiver than to their own children. There’s less baggage. The caregiver can sometimes get your parent to eat or bathe or take medication when you cannot, not because they’re better than you but because they aren’t you.
What it can’t do: make the emotional weight go away. You are still watching your parent change. You are still doing anticipatory grief. You still have the deep, mostly wordless work of loving someone as they decline. A caregiver can share the physical load, but the heart of the caregiving stays yours.
What it can’t do: eliminate the need to make hard decisions. There will still be doctor’s appointments, care conferences, decisions about the next level of care, financial decisions, family conversations. In-home care shares the load — it doesn’t remove it.
For most families, what in-home care does is make the situation sustainable when it had stopped being sustainable. That is the most important thing it can do, and it is often the difference between the family caregiver crashing and continuing.
One of the hardest parts of caregiver burnout is admitting it to the people who might expect you to keep going.
A few things I’ve watched help.
Talking to siblings first, and being honest about specifically what you’re carrying. Not “I’m tired” but “I have slept less than five hours a night for three months, I’ve gained fifteen pounds, my marriage is under strain, and I don’t think I can keep doing this at this level.”
Being specific about what you need. Not “help” as an abstraction, but “I need someone to take Wednesdays” or “I need money to hire ten hours of professional care a week” or “I need a break, one full weekend a month, and I need us to figure out together how to make that happen.”
Being honest with your spouse. Marriages under caregiving strain can deteriorate, and the drift can be reversed with real conversation, but only if the conversation happens.
Being honest with your own kids, if they’re old enough. Adult children of family caregivers often see more than the caregiver realizes and worry more than the caregiver imagines.
And in some cases, being honest with your parent. This is harder, and it depends on your parent’s specific situation and cognitive status. But saying to your parent, gently and directly, “I love you and I want to keep helping you, and I need to bring in some help so I can be at my best for you” — that framing is often received better than families expect.
Several paths. In-home respite through a home care agency (including ours) may be one-time, weekly, or ongoing. Ask about caregiver availability and shift minimums for the daytime, overnight, or weekend help you need. Adult day programs in Washtenaw County offer daytime respite. The Alzheimer’s Association can tell you about any current respite assistance for families dealing with dementia, including eligibility and funding. JFS CARES offers respite for eligible families caring for someone 60 or older in Washtenaw County, and AgeWays can help identify state-funded respite options for families who qualify. And some assisted living and memory care facilities offer short-term stays for respite purposes.
Original Medicare does not cover in-home respite care as a standalone service. For someone on hospice, Medicare’s hospice benefit covers short inpatient respite stays arranged by the hospice team, and a copayment may apply. Some long-term care insurance policies include respite coverage, so check the actual policy. Michigan’s MI Choice Waiver includes respite for eligible adults who need nursing-facility-level care and meet its income and asset rules. And VA respite care is available to enrolled Veterans who meet clinical criteria, depending on local availability. The Veteran’s VA social worker can tell you what applies.
The right number depends on your specific situation, caregiver availability, and shift minimums. It helps to name what you need time for, whether that’s work, appointments, or a reliable break, and build the schedule around those needs.
There are more options than most families know about. VA Aid and Attendance adds monthly support to a VA pension for Veterans and surviving spouses who qualify for the pension and meet specific care criteria; veteran status alone doesn’t establish eligibility. MI Choice Waiver, for families who qualify medically and financially, can cover in-home care through Michigan Medicaid. Long-term care insurance, if your parent has a policy, may help pay for care, so check what the actual policy covers. The Alzheimer’s Association can tell you whether any respite assistance is currently available and who qualifies. Our companion piece on home care costs and payment options walks through the full picture. And even if paid care isn’t yet in reach, some of the support group and mental health resources above are free or low-cost.
If a full night of sleep and a real day off would improve things, you might just be tired. If sleep and rest don’t touch what you’re feeling — if you’re having persistent low mood, difficulty concentrating, changes in appetite, thoughts of hopelessness, or a sense that you’re not yourself — a conversation with a therapist or your primary care doctor is worth having. Family caregivers are at elevated risk for clinical depression and anxiety, and both are very treatable.
If you are a family caregiver in Washtenaw County right now and you have read this far, I want to say one thing to you directly.
What you are doing is real work. It is undervalued by everyone around you, including sometimes yourself. It is heroic in ways that will probably never get named at a funeral. And it is not sustainable without support.
Asking for help is not evidence that you are failing at love. It is evidence that you understand the difference between short-term willpower and long-term capacity.
If you’d like to talk through your specific situation with someone who has watched a lot of families in exactly this spot, you can schedule a free in-home assessment. It doesn’t have to end with you hiring us. Sometimes the useful outcome is just a real conversation, an honest read on where things are, and a specific recommendation for what might help. There’s no cost and no pressure to decide that day.
Whatever the next step for you is, please do not keep going at your current pace and pretending you can sustain it. The people who love you (including your parent) need you to still be here in a year.
About the author
Elizabeth Snyder Corman is the owner of Home Helpers Home Care of Ann Arbor, serving families in Ann Arbor, Saline, Dexter, Chelsea, Pinckney, and Whitmore Lake. Before opening the agency, she served as a hospital chaplain through the COVID-19 pandemic and as a hospice chaplain, walking with families through some of the hardest transitions of their lives. She holds an M.Div. and delivers community presentations on grief, aging, and cultivating joy in the last chapter of life.
If you’d like to understand more about what tips a family from managing to overwhelmed, our piece on the 8 signs your parent may need in-home care includes the family caregiver’s own exhaustion as one of the signs. Or schedule a free in-home assessment to talk through your specific situation.