What Does National Family Caregivers Month Ask of You?

By: Jessica Cannon

What Does National Family Caregivers Month Ask of You?

National Family Caregivers Month asks nothing of you that you are not already giving: it is a November observance, led by Caregiver Action Network since 1997, that exists to recognize family caregivers and connect them to help, so the most useful way to spend it is on a short checklist that protects your money, your family’s roles and you. If you are a few years into caring for a parent with dementia, the month can land strangely. The posts thanking caregivers arrive in the same weeks as the care bills, and the tip lists about walks and deep breaths can read like one more thing you are failing to do. Doubting that an awareness month has much to offer someone who is already this aware is a sensible response.

The stakes are quieter than a crisis, and they do not pause for the calendar. AARP’s Valuing the Invaluable 2026 report counts 59 million Americans caring for an adult and values their care at an estimated $1.01 trillion a year, and it finds family caregivers averaging 27 hours of care a week. None of that recognition signs a power of attorney or gets a sibling to take a weekend, and November is also the month Medicare Open Enrollment closes, on December 7. A month spent only on gratitude can end with the same open documents, the same uneven load and a caregiver more tired than when it began.

Jessica Lizel Cannon of The Proactive Caregiver, a dementia caregiving strategist, works with families at exactly this point, alongside the attorneys, doctors, counselors and respite programs a family also needs. She is a CPA with 28 years of financial experience and a Certified Dementia Practitioner, and she cared for her own mother through frontotemporal dementia and four misdiagnoses over more than 15 years. From that history she now works with families nationwide through virtual coaching, with in-person roots in Austin and Central Texas.

Estimated reading time: 11 min read

Key Insights

National Family Caregivers Month is led by Caregiver Action Network, and its 2026 theme, Care Connects Us, is about linking caregivers to community support and trusted resources. For a dementia caregiver the month overlaps two practical windows: Medicare Open Enrollment, which ends December 7, and whatever time remains for a parent to sign legal documents while capacity holds. The second window is the one that cannot be reopened: once a parent can no longer sign, the family’s options narrow toward guardianship.

Table of Contents

What National Family Caregivers Month is, and what it leaves out

Caregiver Action Network has led the observance since 1997, the year a presidential proclamation named a National Family Caregivers Week in late November, and the network says the month is now marked through presidential proclamations, nonprofit campaigns and community events. The 2026 theme is Care Connects Us, which the network’s partner overview describes as an invitation for caregivers to see themselves in each other and to reach community support at every stage.

The Senate resolution recognizing November 2025 described family caregivers as often facing “financial strain, physical and emotional exhaustion, and social isolation,” and closed by encouraging Americans to learn more about caregiving and support the people doing it. What follows that accurate list is encouragement, and no plan. The month can name the load, and sorting it is still left to the family that carries it.

The same resolution calls the month an opportunity to advocate for policies that support family caregivers, and that is where Jessica spends part of this November: she plans to attend the Caregiver Nation conference and March on Capitol Hill in Washington, D.C., November 16 to 20.

The money and coverage items that fall inside November

Start with the items that carry a date, because those are the ones a busy month erases.

  • Medicare Open Enrollment runs October 15 to December 7, and changes take effect January 1. If your parent has a Medicare Advantage or drug plan, this is the window to compare next year’s coverage against their medications and doctors. Jessica is plain about why it matters: drug lists and plan networks change from year to year, and the change lands on the family that did not check. Your state’s SHIP offers free Medicare counseling to people with Medicare and their families.
  • A one-page picture of this month’s care costs and what pays for each, so the next family conversation starts from the same numbers.
  • The status of the five documents Jessica says every caregiver needs before a crisis, set out in her financial wellness framework for family caregivers: a durable power of attorney for finances, a medical power of attorney, a HIPAA authorization, a living will and a last will. The question for November is whether each one exists, names the right person and can be found when it is needed. Drafting or changing them is work for a licensed attorney.
  • Your own line in the budget: the wages, retirement contributions and out-of-pocket spending that caregiving is quietly taking from your household. Jessica treats that line as part of the care plan, and she sets out how to protect your own finances as a dementia caregiver in detail.

Why the document window matters more than the calendar

The Proactive Caregiver Method, Jessica’s named approach, treats the money, the disease, the family, the systems and the caregiver’s own health as five connected pillars, and as a CPA and a Certified Dementia Practitioner she reads the care costs and the diagnosis together. The documents depend on capacity, and capacity follows the course of the disease. Her rule of thumb, which she has stated publicly, is that after a cognitive diagnosis families typically have about a year to get powers of attorney, advance directives and banking forms signed while their parent can still sign them. When that window closes, the options narrow toward guardianship, accounts nobody can reach and care bought at full price.

If the diagnosis in your family is recent, that window outranks any awareness post this month. If it is years old, the documents may already be settled, and November’s money work is more likely to be the Open Enrollment comparison and your own household line. Either way, these deadlines are not announced to the person carrying the care. They sit in plan rules and in the progress of an illness, and the cost of finding them late falls on the family.

The family roles worth settling while attention is on caregivers

A month that publicly says caregivers deserve support is a reasonable moment to ask for specific support. Jessica starts from the fact that family members contribute differently, and her Sacred Assignment gives each one a role: the Daily Caregiver, the Financial Supporter, the Respite Provider, the Researcher, the Emotional Support and the Distant Witness.

  • One named owner for each recurring job: bills, medications, appointments and the weekly check-in call. Jessica walks families through how siblings get organized about who pays for care, because the money is where an unnamed role turns into resentment.
  • One specific request, in writing, to the family member who does the least.
  • A respite date on the calendar. Respite can happen at home or at an adult day center or care community, and a provider tried before an emergency is easier to call on during one. Respite is one of the services the federal National Family Caregiver Support Program funds through grants to states.
  • An agreement on who decides what when the next decision lands, made before it does.

The items that protect you, including the spiritual ones

Jessica treats self-care as strategy: in her Method, a caregiver’s own health collapsing is one of the marks of reactive caregiving. She counts five types of self-care, physical, mental, emotional, social and spiritual, and finds that most caregivers are probably tending only one; her guide to self-care for family caregivers takes each in turn. Spiritual self-care, in her telling, asks for no religion. It means staying connected to meaning and purpose through faith, nature, creativity or community, so that caregiving does not shrink your life down to survival.

That matters most for the caregiver who has stopped recognizing herself. Grieving a parent who is still alive, feeling faith or meaning shift, or finding a flatness where feeling used to be are, as she writes about protecting your soul while caregiving, among the most predictable experiences of long dementia care.

  • The one type of self-care you have dropped entirely, named honestly. In her view the abandoned one is where the crisis is building.
  • One thing each week that belongs only to you, protected the way you would protect a medical appointment.
  • A second look at the empty-cup advice. To Jessica the cup is cracked, so more sleep and the occasional break help only for a while, until the cracks themselves are addressed: the nervous system strain, the inherited scripts and the grief that has had nowhere to go.
  • A licensed therapist or counselor if depression, anxiety or grief will not lift. Many of the people she coaches also see a therapist, because the two do different jobs.

Choosing what November leads to: ongoing coaching or her course

By the end of the month, the checklist usually shows where the biggest gap sits, and the decision after that is how much support the next stretch needs.

If you need someone to build the plan with you and keep it moving, her ongoing monthly coaching is the fuller path. Tier One is built for caregivers who are new or overwhelmed and need to get grounded, and the higher tiers add a personalized plan updated quarterly and 30-minute one-to-one calls with her, all virtual. If you mostly need the frameworks and can work through them on your own, The Caregiver’s Trinity Toolbox is her self-paced course, with three pillars you can take one at a time. Its Spiritual Wellness pillar carries her line “Protect your soul” and covers a meditative mindset, reflection, connectivity and end of life, with journal prompts.

Jessica Cannon makes that choice with you on a discovery video call, and she approaches it the way her Method approaches everything else. You tell her what is happening with your family, and she tells you which pillar your biggest vulnerability sits in and which way of working together fits: coaching, the Toolbox, or neither. If coaching is not right for you, she says so and points you somewhere better, to an elder law attorney or another specialist when that is what the situation needs. Her own summary of her work is blunt: she does not do support groups, she does not do sympathy, and she does strategy.

You do not have to finish this whole list in November. Getting the dated items done and naming the one gap costing you most is a real use of a month meant for you, and you are allowed to want a plan rather than another thank-you.

Protect Your Family’s Financial Future

Jessica Cannon is a CPA with 28 years of financial experience and a Certified Dementia Practitioner. What she does is help families with the financial side of dementia care: reading a Medicare denial letter, a memory care contract and a dementia timeline together, so the money makes sense before decisions get made. If you would like help applying any of this to your own situation, you can book a discovery call.

15 minutes, to work out whether this is something she can help with.

Book a discovery call

Frequently Asked Questions

Q: When is National Family Caregivers Month, and what is the 2026 theme?

A: National Family Caregivers Month is every November in the United States. Caregiver Action Network has led it since 1997 and chooses a new theme each year. The 2026 theme is Care Connects Us, focused on connecting caregivers with each other, with community support and with trusted resources. The network counts November 2026 as its 29th anniversary.

Q: What should a dementia caregiver actually do during National Family Caregivers Month?

A: Start with the items that have dates. Medicare Open Enrollment ends December 7, so a parent’s Medicare Advantage or drug plan for next year can be compared before then, with free help from your state’s SHIP. If the diagnosis is recent, check whether the core legal documents exist while your parent can still sign, and take any drafting to a licensed attorney. Then book one respite date and name the one part of your own life you have stopped tending.

Q: Who can help a family caregiver who feels worn down or lost in the role?

A: Several people, each with a different job. A licensed therapist or counselor handles depression, anxiety or grief that will not lift. Your local aging network can connect you to counseling, caregiver training and respite funded by the National Family Caregiver Support Program. A SHIP counselor helps with Medicare choices, and an elder law attorney handles legal documents. Jessica Lizel Cannon, a dementia caregiving strategist, coaches the caregiver on the plan that ties the care, the money and the family together, and keeps it moving.

Q: Is a self-guided course or monthly coaching the better fit after November?

A: It depends on how much support the next year needs. Ongoing monthly coaching suits a caregiver who needs accountability, community and a plan built for their family. The Caregiver’s Trinity Toolbox suits someone who wants Jessica’s frameworks to work through alone, one pillar at a time. Her discovery video call is where that gets sorted out, and it can end with a referral elsewhere.

Citations

About this article. Jessica Cannon is a CPA with 28 years of financial experience and a Certified Dementia Practitioner. She provides financial coaching, not legal or medical services. This article is general information about how these systems work, not advice about your situation, and it is not a substitute for the advice of an attorney. It is not medical advice, and it is not individualized tax or financial advice.

For the legal instruments themselves, including wills, powers of attorney and guardianship, you will need a licensed attorney in your own state. Medicaid and long-term care rules also differ by state and change over time, so any Texas detail here is an example rather than a rule that will apply to you.


About the Author

A former corporate accountant turned caregiver advocate, Jessica Lizel Cannon is the founder of Proactive Caregiver. She combines her financial background with her experience as a Certified Dementia Practitioner to empower families navigating the "emotional storm" of caregiving. Through her book, podcast, and consulting, Jessica helps caregivers find balance, guilt-free living, and spiritual strength.