Self-Care for Caregivers: A 101 Guide

The Crucial Importance of Self-Care When You’re a Caregiver

The Crucial Importance of Self-Care When You’re a Caregiver

For caregivers, practicing self-care is vital for protecting your health. But supporting your loved one can take a significant amount of time and energy, hindering your ability to take care of your own health and well-being. Nonetheless, it’s crucial to prioritize self-care, even though finding the time can feel impossible.

If this sounds familiar, know you’re not alone. According to a report published in July 2025 by AARP and the National Alliance for Caregiving (NAC), 63 million Americans are family caregivers supporting an adult or child with special needs. That’s nearly a quarter of the adults in the United States. For new and seasoned caregivers alike, the stress can become too much when it outweighs your capacity to care for yourself and your loved one.

If you’re feeling stretched beyond your limits, know there are ways to help you find your center again. As you do, you may find your relationship with the person you care for improves, too. A July 2021 article published in Supportive Care in Cancer states that the key to caregiving success is not to put more work on your plate, it’s to offload some of it, even if temporarily.

Sharpening your self-care routine and caregiving strategies is important for building strength and fortitude.

Here’s everything you need to know about the unique challenges of caregiving and how to cope with and recover from caregiver burnout.

The Caregiver’s Mental Load

Caregiving brings a variety of challenges that are unique to each person. One of the most common and significant challenges is the tax on your time and ability to manage stress. Juggling your care recipient’s everyday needs, medical care, financial and legal considerations, and more may affect your ability to think clearly and sustain your own energy level. As your loved one’s needs grow, managing the emotional burden and finding time for self-care can become more difficult.

Sometimes caregivers may be aware that self-care is important, yet they aren’t able to find the time or space to prioritize it. In this case, the caregiver may feel guilt around their perceived failure to practice self-care, says Simran Malhotra, MD, a triple board-certified physician in palliative care, hospice, and internal medicine and medical reviewer for Everyday Health. “Struggling to prioritize self-care is often a reflection of caregiving intensity and not personal failure,” she says.

According to the AARP-NAC report, 1 in 5 family caregivers rate their own health as fair or poor, and nearly 25 percent indicate their caregiving role has compromised their ability to care for themselves. Scientists who authored an article published in 2021 call the cumulative burden of this day-to-day stress on your body allostatic load.

 The heavier the load, the higher the risk of illness and disability.

The Challenges of Family Caregiving

While every situation is different, research finds many family caregivers face similar struggles. Among others, such factors include the following, according to the AARP-NAC report:

  • Lack of Time for Self-Care On average, caregivers provide care for 27 hours a week. But nearly 1 in 4 put in 41 or more hours per week — the equivalent of a full-time job. This time is often spent supporting activities of daily living like getting in and out of bed, getting dressed, going to and from the toilet, showering, feeding, and dealing with incontinence. There’s also the need to communicate with healthcare professionals, advocate for your loved one, and manage medical, nursing, financial, and legal tasks. All of this work takes away time to care for yourself.
  • Complex Medical Needs Many caregivers take on significant medical and nursing tasks, such as injections, tube feedings, and catheter and colostomy care. Most say they have no choice but to do it, despite having` little to no training.
  • Inadequate Support The AARP-NAC report found that about 7 in 10 caregivers have no paid help, and many struggle to find affordable services. Navigating a fragmented and confusing healthcare system — often without acknowledgment of your role — can be frustrating and expensive.
  • Employment Issues Most working caregivers say they have to take time off from their jobs to meet their loved one’s needs, sometimes resulting in a loss of benefits, depletion of savings, and need to delay retirement.
  • Financial and Economic Strain About 3 in 10 caregivers have stopped saving, and nearly 1 in 4 have taken on more debt — effects that could have even more significant repercussions over years of providing care. Most say an income tax credit or program to pay caregivers would help.
  • Loneliness Caregiving can be isolating, especially if you are living with your care recipient, they have high needs, or you’re in a rural area. Many people say caregiving can be a rewarding and meaningful experience, but 1 in 4 family caregivers also say they feel alone.
  • Loss of Identity Caregiving can also eat up time and mental space once devoted to your own needs, interests, and social life. Research suggests that a result of caregiving for some is the loss of sense of self beyond the identity as a caregiver.

  • Heavy Emotions Caregivers may experience complicated feelings about their relationship with their care recipient, such as resentment over the burden of caregiving, guilt over feeling that way toward a loved one, and worry and grief over their worsening health status. On top of this, they also have to help their care recipient manage their emotions and extend grace when anger and conflict arise.

How Caregiving Can Lead to Burnout

Caregiver burnout — or total physical, emotional, and mental exhaustion — can strike when you regularly give more than you have and are not getting the help or support you need. It’s a result of cumulative stress. As Cleveland Clinic notes, caregiver burnout often sneaks up on you because it’s hard to see you’re pushing yourself beyond your limits until you’ve completely run out of fuel.

Caregiver burnout can hurt your ability to care for yourself and your loved one. Many caregivers neglect their health while caring for someone else. When health problems are left untreated, you and your care recipient can experience a dip in your quality of life. In rare cases, caregivers could even face their own health crises due to the stress of caregiving.

Signs of Caregiver Burnout

Symptoms of caregiver burnout include:

  • Feeling overwhelmed
  • Feeling alone or left behind by others
  • Frequently feeling tired, worried, or sad
  • Sleeping too much or too little
  • Gaining or losing a lot of weight
  • No longer being interested in activities you used to enjoy
  • Easily getting irritated or angry
  • Frequent headaches or body aches
  • Coping with unhealthy behaviors like smoking or drinking too much alcohol

It’s important to remember that you deserve to be taken care of just as much as your care recipient does.

Self-Care

Dr. Patrice Harris and Dr. Corey Yeager, a therapist who works with athletes, discuss the importance of mental wellness in sports and in life.
Self-Care

Self-Care for Caregivers

Getting the support you need and practicing self-care can help you recover from burnout, boost your well-being, and become a better caregiver. The Supportive Care in Cancer article from July 2021 emphasizes the importance of addressing the imbalance between how much you are giving and how much you are receiving. That means opening yourself up to outside support and resources, including the following strategies.

Strengthen Your Personal Network

While a helpful and important strategy to implement, self-care alone won’t solve the issues of stress and burnout for caregivers. Letting your personal support system and community take care of you is essential.

Here’s how to build a stronger support system:

  • Find a caregiver advocate. Use the Eldercare Locator search tool or call 800-677-1116 to connect with an advocate at your closest Area Agency on Aging.

    With their help you can learn about support groups, adult day care centers, transportation services, and referrals for financial and legal support to lighten your load.
  • Offload some of the work. The belief that you can do everything by yourself is a risk factor for caregiver burnout. If you could use more support from other family members, use this guide from the National Institute on Aging to consider your strengths and limits and learn how to pass on responsibilities to others.

    The Family Caregiver Alliance (FCA) also has helpful tips for how to hold a family meeting to discuss common issues like feeling overwhelmed or managing finances.

  • Join a support group. Find people who understand what you’re going through to exchange personalized advice. A caregiver advocate, healthcare provider, or nonprofit organization could help refer you to a group.
  • Get workplace support. Contact HR to learn about what support your employer can offer. According to the FCA, some companies have employee assistance programs for counseling, could help you find eldercare or childcare, or offer paid or unpaid time off.

As you move forward, remember the importance of allowing yourself to ask others for help. Research published in December 2022 in the journal Psychoneuroendocrinology shows getting support from loved ones and advocates not only lightens the caregiving burden, but it can also help you become more resilient.

Practice Healthy Coping Skills

Beyond building a stronger support system, improving your approach to self-care can also help foster resilience. The following coping tips may help keep burnout at bay:

  • Eat plenty of healthy meals and snacks. Stock up on fruits and vegetables, whole grains, lean protein, and healthy fats. To save time, opt for precut or frozen fruits and veggies.
  • Prioritize sleep. If caring for your loved one means disrupted sleep, avoid using caffeinated beverages to stay awake. Instead, take naps when you can.
  • Weave in movement. In addition to supporting your overall health, exercise can help to boost your mood and energy levels. The physical activity guidelines from the U.S. Department of Health and Human Services recommends moderate-intensity exercise for 150 minutes per week or vigorous-intensity exercise for 75 minutes a week, in addition to strength training twice per week. If that amount of movement isn’t feasible for you right now, start smaller. Research supports that walking 7,000 steps per day can reduce the risk of heart disease and all-cause mortality. Even better, those benefits begin at 4,000 steps.

  • Schedule checkups. Don’t neglect preventative care appointments. Your health and well-being matter, too.
  • Practice asking for help. It can be difficult to ask for help when you play the role of helper so frequently. Reflect on your needs at least once a week and find ways to ask for support.
  • Make respite a habit. Look at your calendar and mark down times to take a regular break every week, month, and year. Regular breaks can lower stress and boost positive experiences, protecting against chronic stress. Respite could involve recruiting a driver to help transport your loved one to appointments a few days a week, using adult daycare once a week, swapping duties with another family member, or scheduling a vacation. Use the ARCH National Respite Locator Service to find local services.

As a caregiver, you have the right to take care of yourself, ask for help, know your limits, and express difficult emotions. “The goal of self-care during caregiving is to maintain strength, emotional well-being, and the capacity to continue caring for your loved one — not necessarily achieving optimal peak health for yourself,” says Dr. Malhotra. “So even a little bit goes a long way.”

If you’re feeling mistreated or taken for granted by your care recipient, read through the caregiver rights provided by the American Heart Association (AHA) for a reminder of your value.

If necessary, share the list with the person for whom you’re caring.

Schedule Mental Health Care

Sometimes you need support to cope with the toll of caregiving. If you’re feeling anxious, depressed, or burned out, schedule a mental health appointment for yourself just as you would for your loved one. You can contact a primary care physician or mental health care professional for support.

If caregiving responsibilities make it difficult to carve out time, online therapy may present a more convenient and accessible option. Use our guide to find the best online therapy provider for you.

Resources for Caregivers

  • AARP Caregiving Forum Chat with fellow caregivers for older adults.

  • Alzheimer’s Association Join a support group and get advice on caring for a loved one with Alzheimer’s disease on community message boards.

  • Family Caregiver Alliance Support Groups Join online support groups for caregivers, young adult caregivers, or caregivers in the LGBTQ+ community.

  • Caregiver Action Network Community Ask about how to deal with medical professionals and care for loved ones with mental health issues, Alzheimer’s disease, Huntington’s disease, Parkinson’s disease, or COPD.

  • Veterans Affairs Caregiver Support Program Learn how to support veterans and their loved ones, or call its Caregiver Support Line at 855-260-3274.

  • FCA Family Care Navigator Find caregiving support services in your state, such as government health and disability programs and disease-specific organizations.

  • Medicare.gov Access resources for caregivers who are supporting someone on Medicare.

  • Well Spouse Association Join a support group and get resources for caregivers caring for chronically ill or disabled partners.

The Takeaway

  • Nearly 1 in 4 Americans are caregivers, and of them, a quarter indicate caregiving has compromised their ability to care for themselves.
  • Caregiving can be a meaningful and challenging experience. Because taking care of someone else can take up so much time and energy, it’s common for caregivers to experience chronic stress and burnout.
  • With rest, support, and self-care, you can recover from burnout and build resilience to protect your health for the long haul.
EDITORIAL SOURCES
Everyday Health follows strict sourcing guidelines to ensure the accuracy of its content, outlined in our editorial policy. We use only trustworthy sources, including peer-reviewed studies, board-certified medical experts, patients with lived experience, and information from top institutions.
Resources
  1. Caregiving in the US, 2025. National Alliance for Caregiving and AARP. July 2025.
  2. Van Roij J et al. Self-Care, Resilience, and Caregiver Burden in Relatives of Patients With Advanced Cancer: Results From the eQuiPe Study. Supportive Care in Cancer. December 2021.
  3. Gallagher S et al. Caregiving and Allostatic Load Predict Future Illness and Disability: A Population-Based Study. Brain, Behavior, & Immunity - Health. October 2021.
  4. Sa E. Decoding the Mechanism of the Loss of Self in Spouse Caregivers of Alzheimer’s Patients: A Sociocultural and Communication Perspective. Alzheimer’s & Dementia. January 9, 2025.
  5. Caregiver Burnout. Cleveland Clinic. August 16, 2023.
  6. Caregiver Health. MedlinePlus. May 26, 2020.
  7. Eldercare Locator. HHS Administration for Community Living. July 7, 2025.
  8. Area Agencies on Aging. HHS Administration for Community Living.
  9. Sharing Caregiving Responsibilities. National Institute on Aging. October 12, 2023.
  10. Holding a Family Meeting. Family Caregiver Alliance. 2003.
  11. Caregiving at Home: A Guide to Community Resources. Family Caregiver Alliance. 2017.
  12. Løseth GE et al. Stress Recovery With Social Support: A Dyadic Stress and Support Task. Psychoneuroendocrinology. December 2022.
  13. Ding D et al. Daily Steps and Health Outcomes in Adults: A Systematic Review and Dose-Response Meta-Analysis. The Lancet Public Health. August 2025.
  14. Find a Respite Provider. ARCH National Respite Network.
  15. Caregiver Support. American Heart Association.
  16. Caregiving. AARP.
  17. Support Groups. Alzheimer’s Association.
  18. Support Groups. Family Caregiver Alliance.
  19. Caregiver Action Network Community. Facebook.
  20. VA Caregiver Support Program. U.S. Department of Veterans Affairs.
  21. Family Caregiver Services by State. Family Caregiver Alliance.
  22. Resources and Information. Medicare.gov.
  23. Our Organization. Well Spouse Association.
Simran-Malhotra-bio

Simran Malhotra, MD

Medical Reviewer
Simran Malhotra, MD, DipABLM, CHWC, is a triple board-certified physician in internal medicine, hospice and palliative care, and lifestyle medicine, as well as a certified health and wellness coach. She is currently practicing part time as an inpatient palliative care physician at Medstar Health after serving as the palliative care medical director at Franklin Square Medical Center in Baltimore for a little over four years.

Dr. Malhotra completed her internal medicine residency at Medstar Franklin Square Medical Center, where she also served as chief resident in 2015. She completed her fellowship in hospice and palliative medicine at Johns Hopkins Hospital in 2016. She was named Top Doc in Palliative Medicine in 2019 and 2020 by Baltimore Magazine.

On a personal note, she is a BRCA1 previvor with a strong family history of breast and female reproductive cancers, and underwent a risk-reducing bilateral mastectomy and total hysterectomy in 2020 at 32 years old. After learning about her own genetic risk of cancer, and grounded in her professional experiences in palliative care, she founded Wellness By LifestyleMD, a platform where she works with and educates women at high risk for cancer with or without genetic mutations on the powerful impact that positive lifestyle changes can have on their quality of life and even longevity.

In addition to being a diplomate of the American College of Lifestyle Medicine, she completed the T. Colin Campbell plant-based nutrition certification in 2019, the CHEF culinary coaching certification in 2020, and the WellCoaches health and wellness coaching certification in 2022. She is a member of the ACLM women’s health member interest group and serves as the co-chair of the breast cancer subcommittee.

Malhotra has been featured on several blogs and podcasts, where she has shared her unique perspectives and experiences from palliative care as well as from being a genetic mutation carrier who is passionate about using lifestyle as medicine.
Lauren-Krouse-bio

Lauren Krouse

Author
Lauren Krouse is a writer and advocate who covers health, domestic violence, trauma recovery, and LGBTQ+ issues. She is currently writing a book about sibling abuse, drawing from survivor stories, original reporting, and her own lived experience to break the silence around this hidden form of family violence. Her work has been published in outlets including Health, Women's Health, Men's Health, the Washington Post, Parents, USA Today, SELF Magazine, and HuffPost, among others. She also writes for nonprofit organizations like The Jed Foundation, which is dedicated to preventing suicide and protecting mental health in teens and young adults.

Lauren is passionate about meeting readers where they are and brings an intersectional lens to her work. She's committed to spotlighting inequity, researching solutions to address systemic barriers that prevent many from leading healthy and safe lives, and building a more compassionate and supportive community for all. When she's not writing or reading, you can find her climbing, trying out new recipes, or walking in the woods with her partner and friends.