“I’m Maria Shriver, and I’m a child of Alzheimer’s.”
That’s how I introduced myself last year when I testified before the Senate Special Committee on Aging. I was there to support the Alzheimer’s Study Group, a blue-ribbon panel Congress had charged, at the request of the Alzheimer’s Association, with designing an action plan to deal with Alzheimer’s disease.
Alzheimer’s is an epidemic. Every minute or so—in fact, before you get to the end of this page—someone in this country will develop Alzheimer’s. Millions of people already have been formally diagnosed. Millions more are undiagnosed—or diagnosed with some form of dementia that could actually be Alzheimer’s. And with the 78 million baby boomers now moving into their later years, the cost of Alzheimer’s to American society is expected to be $20 trillion between now and the year 2050.1 That’s right—$20 trillion.
There’s no doubt about it. We are in the midst of a national emergency, and we’re woefully unprepared.
So there I was in that packed hearing room, sitting with Alzheimer’s Study Group members—former House Speaker Newt Gingrich, former Sen. Bob Kerrey, former Supreme Court Justice Sandra Day O’Connor (who had left the High Court to care for her husband with Alzheimer’s) and Larry Butcher, chairman of Alzheimer’s Community Care in Florida (who would lose his wife months later to youngeronset Alzheimer’s). We were all there to ask this powerful congressional committee to listen up, pay attention, increase funding and take on Alzheimer’s.
I must admit it was something of a surreal experience for me, because the truth is, for so many years it was my father, Sargent Shriver, who would be sitting in that chair, pleading with senators to listen up, pay attention and increase funding. My dad was the one who would go up to the Hill to testify for his beloved Peace Corps and for all the War On Poverty programs he started and fought for, including Head Start, Vista, Job Corps and Legal Services for the Poor. My father was legendary for the way he worked the Capitol. He knew every senator and congressman by name. He knew their careers, their interests, their politics and their soft spots. He was a brilliant, idealistic and optimistic public servant. My dad was sharp and witty, a walking encyclopedia—his mind a beautifully-tuned instrument that left people in awe and inspired.
That was then. Today he doesn’t know I’m his daughter, and he doesn’t even know my name. To be honest, it’s still really difficult to wrap my own mind around that. But so goes the reality and the heartbreak of Alzheimer’s. It’s a mind-blowing disease—not just for the people who get it, but for everyone around them. That’s why I’m so passionate about defeating it.
“As one of my dad’s doctors told me, ‘Once you’ve seen one case of Alzheimer’s, you’ve seen…one case of Alzheimer’s.’ ”
When my dad was first diagnosed in 2003, my mother, four brothers and I all felt we were entering a world that was confusing, dark and depressing. People just didn’t talk about it when Alzheimer’s hit their families. They whispered about it, a diagnosis shrouded in shame. There was little information and even less hope.
We struggled to learn about medication and caregiving. We wrestled with handling our father’s diminishing independence. How would we explain to him he couldn’t drive anymore? How would we tell him he could no longer engage in one of his favorite pastimes, giving rousing speeches about the joys and rewards of public service? When the invitations came in, we’d just send his regrets.
I understand that when people look at Alzheimer families like ours from the outside, they often see dependent parents now cared for by their own offspring, and it seems like the parent-child roles are simply reversed. Not so. The truth is, you hardly feel like you’re the parent. You still feel like the helpless child. Even though your father or mother can’t work, can’t live alone and is as needy as a toddler, you don’t feel in control or in charge. No matter who you are, how old you are, what you’ve accomplished, what your financial situation is—when you’re dealing with a parent who has Alzheimer’s, you feel powerless. And as the disease unfolds, you feel ever more powerless, because you don’t know what to do or what to expect.
As one of my dad’s doctors told me, “Once you’ve seen one case of Alzheimer’s, you’ve seen…one case of Alzheimer’s.”
In fact, there was so little information back when my Dad was diagnosed that I wrote a book called What’s Happening to Grandpa? At the time, I said I did it to help my own and other children understand what was going on. In truth, I wrote it to explain Alzheimer’s to myself. After it came out, I noticed very few people came up to me to talk about it, because of the stigma still attached to the disease. And when I wanted to put on my broadcast journalist’s hat and shine a brighter light on it by turning the book into a TV special, no one was interested. I was told Alzheimer’s was a downer and would make for what they called “bad TV.” They said Alzheimer’s wasn’t big enough. It was just “an old person’s disease.”
Then almost out of nowhere came what I call The Alzheimer’s Turning Point. That was March 21, 2007, when The New York Times reported new Alzheimer’s Association statistics showing the number of people with Alzheimer’s was ballooning—rising by 10 percent in just the previous five years.2 They reported that fully 13 percent of Americans had Alzheimer’s—which meant one in eight people over the age of 65—and unless a cure was found, there would be more than 13 million people with Alzheimer’s by 2050, the best guess back then.3
That was the wakeup call the baby boomers heard. After all, we were the generation that believed ourselves to be so smart and savvy, that we were very sure our brainspan would match our lifespan. But now, just as the oldest boomers were entering their 60s, these new numbers meant we were at the leading edge of a tsunami—and it was happening not to some nameless old “them” out there. The surge was headed for us, too. And that, I believe, scared a lot of people right out of denial.
It seemed to me that all of a sudden, Alzheimer’s became frontpage news and people really started paying attention. That’s when HBO came to me and said, “We want to take an indepth look into Alzheimer’s disease, and we want you to be involved.”
So, starting on Mother’s Day last year, HBO aired the most comprehensive television event about the disease ever, “The Alzheimer’s Project.” There were four broadcasts and a companion book covering in great depth the cuttingedge science, the issue of caregiving, what it’s like to have the disease and the impact on the children and grandchildren of Alzheimer’s. Along with HBO’s legendary Sheila Nevins, I co-executive produced this massive project. All of a sudden, everywhere I went people approached me to voice their fears, share their experience and ask for advice. “The Alzheimer’s Project” won several Emmys. It attracted 11 million viewers when it aired, and people are still watching all four parts of it at www.hbo.com/alzheimers/the-films.html.
About the same time last year, I was working on the very first The Shriver Report: A Woman’s Nation Changes Everything. It was a landmark study—published in collaboration with the Center for American Progress—exploring a transformational moment in the United States. It arose from my work as First Lady of California, where I’ve helmed The Women’s Conference, the biggest forum for women in the nation.
The transformational moment was this: For the first time in our nation’s history, women were becoming the majority of the workforce—and also primary or co-breadwinners in almost two-thirds of American families.4 We were now what I called A Woman’s Nation. I knew this shift would impact every institution in our country: the family, the workplace, the healthcare system, government services, even the relationship between men and women themselves.
“More than 40 percent of women said that they were the main caregivers
for elderly parents.”
What came out of that report—its studies, analyses, essays by cultural leaders and a huge, groundbreaking nationwide opinion survey—was the first comprehensive and accurate portrait of The Way Things Are Now in the American home and workplace. It was also the first accounting of exactly how out of step our institutions are with the needs of women today.
We learned that women aren’t just primary breadwinners. They’re still the primary caregivers in their families as well. Almost 70 percent of the women we surveyed for the first Shriver Report told us that despite working full-time, they’re still the ones most responsible for taking care of the children.5 More than 40 percent of them said that they were the main caregivers for elderly parents.6 And almost a third of them said they were primary caregivers of both their kids and their parents.7
We wondered whether their employers were adjusting, offering help like child care and ﬂexible hours. You’d think so, because studies show that when “employees have greater access to ﬂexible work arrangements, they are more committed and loyal to their employers and are willing to work harder than required to help their employers be successful.”8 Yet we found that so many companies and institutions were simply out of touch with workers’ needs today.
We held roundtables around the country, where women who knew I was dealing with four kids, my own sick mother and a father with Alzheimer’s would come up to me and say, “Me, too! I’m in the same boat, and I need help!”
Bingo! That’s when I realized that Alzheimer’s was emerging as another huge transformational force exerting a powerful pressure on women, families and our institutions. Alzheimer’s was in the process of changing A Woman’s Nation forever.
- Today, women are not only a dominant economic force in this country. They also make up 65 percent of the people with Alzheimer’s—and up to three-fifths of all Alzheimer caregivers are women as well.9
This perfect storm made me realize it was time for another Shriver Report, this time in partnership with the Alzheimer’s Association.
In addition to an indepth examination of the issues and trends by experts—and searingly honest personal essays by people from every walk of life affected by Alzheimer’s, including several women who have the disease—we have conducted an enormous nationwide survey of 3,118 adults, including more than 500 Alzheimer caregivers. Our findings show the huge impact of Alzheimer’s behind closed doors in this country:
- Almost 90 percent of Americans who know someone with the disease are concerned that they or someone close to them will get Alzheimer’s.
- Half of women caring for someone with Alzheimer’s are providing more than 40 hours a week of care. A third of women caregivers care for their loved one 24/7.
- Nearly 41 percent of the women caregivers said they had no choice in taking care of their loved one with Alzheimer’s.
- More than half of the family caregivers of people with Alzheimer’s we surveyed said it’s straining their family finances.
- Nearly 65 percent of working caregivers of people with Alzheimer’s told us they need to come to work late, leave early or take time off from their jobs as a result of their caregiving responsibilities.
- Nearly a third of women caregivers rate the physical stress level of caregiving a 5 out of 5.
- The greatest fears women voice about getting Alzheimer’s is that they will forget their loved ones, become a burden to their families and not be able to care for themselves.
My hope is that this Shriver Report triggers another Alzheimer’s Turning Point and gets the national conversation focused on this disease and its ramifications. It’s time. We must face up to some big questions: With Americans living longer and with the incidence of Alzheimer’s growing, what’s going to happen to our women, our families, our workplaces, our attitudes, our society, as the Alzheimer wave hits over the next few decades? We’re talking crisis.
Doctors and researchers at the National Institute on Aging and the Alzheimer’s Association are now looking into the possibility of revising how and when they diagnose Alzheimer’s. They’ve begun the long process of reviewing what they call “the diagnostic criteria” for the disease.10
Why the review? Well, until now, Alzheimer’s has been diagnosed only when clinical symptoms are apparent. This means significant damage is already done in the brain, such as the telltale plaques and tangles so long considered the definitive sign of Alzheimer’s. But now, better diagnostic tools like MRIs and brain scans and spinal taps looking for specific biomarkers could mean that doctors might one day be able to detect changes in the living brain much earlier—years before there are even any signs of dementia.
But any possible revision of the way Alzheimer’s is diagnosed is still a long way off. And until then, some researchers are warning about using these very expensive high-tech tests for screening the general population, for two reasons. One, the tests sometimes find plaques in the brains of people who never even develop Alzheimer’s. And two, there’s no effective treatment or cure for Alzheimer’s anyway.11
So how many people do we think actually have or will get Alzheimer’s disease? Well, until there are new standards for diagnosis, it’s unclear. The estimates are all over the map. The actual number of Americans with Alzheimer’s disease today may be far more than the official 5.3 million number we all use.12 And what about the projection that by 2050, there’ll be up to 16 million people with Alzheimer’s disease in this country?13 I bet it could turn out to be a bigger number than that.
But whatever the number of cases is, this much we know for sure: Most of them are expected to be women. And most of the people who will end up taking care of them will be women, too.
- The President’s Council of Economic Advisors reported this year that 43.5 million Americans—most of them women—are providing unpaid caregiving to relatives and friends over the age of 50.14
- More specifically, our poll showed that today, the average unpaid Alzheimer caregivers are working women over the age of 50 providing care most commonly to their mothers (31 percent) and spouses (15 percent).
And that unpaid caregiving—which so often comes on top of a paying job and childrearing—is tough physical and emotional work.
- The truth is it’s women who are the ones who generally do the hands-on grunt work of caregiving15—cleaning their parents or spouses and changing their diapers, feeding them, babysitting them, dispensing medication to them. While men do represent about a third of family caregivers16, they tend to arrange or supervise outside services.17
For decades, women have fought for respect for mothers and recognition that mothering is real work. Now we have to fight for respect for caregivers and recognition that caregiving is real work, too—billions of dollars worth of work.
- AARP estimated that 34 million caregivers over the age of 18 in the United States provided $375 billion worth of unpaid services a year—more than the yearly state plus federal Medicaid spending—and that was three years ago!18 By the way, add this to the mix: Nearly 1.4 million kids aged 8 to 18 are helping take care of an adult relative —250,000 of them caring for loved ones with Alzheimer’s or other dementias.20
This Woman’s Nation has truly become a Caregiver Nation as well, and Alzheimer’s is putting the pedal to the metal. To be specific:
- This year it’s estimated there are 11.2 million Alzheimer and other dementia caregivers, and 6.7 million of them are—you guessed it—women.21
So with women shouldering the biggest brunt of the burden of all this caregiving, I find it ironic that we’re still seeing articles like, “Why Aren’t Women Happy?” They wonder why women aren’t satisfied with their advanced degrees and new corner offices. They ask, “What’s Happened to Her Sex Drive?” and “What’s Wrong With American Women?” Excuse me?
What’s right with American women is that they’re rearing and providing for the next generation of Americans, while at the same time caring and providing for the last generation of Americans. What’s right with American women is that they’re doing it, even though studies show that caregivers pay a steep price in terms of their own health—increased stress, depression, lost sleep, chronic anxiety, immunesystem deficiency.22 They’re paying a financial price as well, because full-time workers who are also caregiving at home have lower earning power.23
American women are stressedout and maxedout. There’s nothing wrong with them! They just need support. What has to get right is our institutions. They need to respond to the changing dynamic in the American home. People with Alzheimer’s cannot live alone, and the family members who live with them and take care of them need help.
Health and Human Services Secretary Kathleen Sebelius lays out for us in this report many provisions in the 2010 healthcare reform legislation, The Affordable Care Act, that provide relief for Alzheimer’s caregivers.
It’s a start. But we also need to have a national conversation about what else the growing millions of Alzheimer families need:
- We have a Dependent Care Tax Credit for employment-related child care expenses. But what about a meaningful Elder Care Tax Credit?
- How about incentivizing ﬂextime programs, so employers are really encouraged to offer ﬂexible work hours to their caregiving employees?
- The federal government and some states provide for Maternity Leave and Family Leave. How about Elder Care Leave, including coverage for emergencies at home? Maybe more men would step up and help out at home if they knew taking time off was OK with their employers.
- How about more access to high-quality Alzheimer training for both family members and paid home healthcare aides? How about actually teaching family members how to really stay on top of all the medications they have to dispense?
- How about more elder daycare programs staffed with people actually accredited for Alzheimer care? Believe it or not, less than 1 percent of practicing nurses nationwide are credentialed in gerontology.24
- And what about more government quality control of seniors’ programs, nursing homes and end-of-life facilities, before we have an epidemic of elder abuse accompanying the rise in Alzheimer’s?
- How about more intergenerational daycare centers, like the one I visited in San Diego, where toddlers and people with Alzheimer’s spend the day together? They eat together, they dance together, go to storytime together. It’s quite moving to behold. And what about more intergenerational playgrounds? We built the first one in California, so Sandwich Generation people like me—taking care of both kids and parents—can go to one place with all of them.
- And how about more governmental support for adult daycare and respite care programs in general, so we can give family caregivers a break now and then?
I know, I know. Let me say it before you do: “Who’s gonna pay for all these programs? We’re in a recession!” Many states, including my own, are struggling with staggering budget deficits. And many political leaders, including my own husband, are wrestling with cutting many of the same types of programs I’m advocating.
But that’s exactly why we need a new kind of national conversation about Alzheimer’s and growing old in America—just like the conversations heard around kitchen tables all over the country. Families are sitting down to figure out how to pay for their portion of the billions of dollars of unpaid care elders are receiving at home. American families are asking and answering the same questions we need to ask and answer on a state and national level:
- “How can we afford this care? How can we pay for it?”
- “Whose job is it—whose turn is it—to do the caregiving?”
We need more of us at that kitchen table. Not just the Alzheimer’s Association fighting the disease and providing support, but a partnership of families, businesses, faith-based institutions, unions, government leaders, insurance companies, healthcare institutions—everybody on the front lines, all of us accountable. And since personal and family responsibility will always be a huge piece of the Alzheimer’s care picture:
- How about Elder Care Savings Plans like the 401K retirement savings plans and 529 college savings plans? Since our parents are living longer, many families could start socking away at least some money now.
If we wait until the crest of the Age Wave hits—and it’s coming—it will be too late. It’s just like Katrina. If the levees were built strong enough the first time, they would have held.
Of course, our biggest hope for Alzheimer’s lies in medical research. As you’ll read in this report, we’re getting closer, but our scientists are still chipping away at critical questions like these:
- What causes Alzheimer’s? Is it inherited? What causes youngeronset Alzheimer’s? Is there any treatment that can delay the onset or slow down the course of the disease?
- What about new tests that may be able to tell you if you’re going to get Alzheimer’s? Are the tests ready for use? Are they accurate? Who would be a candidate to take them? If there are no foolproof treatments yet, what’s the good of knowing?
- What can we do to prevent Alzheimer’s? Do lifestyle changes really help? Should we all be hitting the treadmill, drinking tea, doing crossword puzzles, taking Omega-3 and Vitamin D?
- Why do more women get Alzheimer’s than men? Is it just because women live longer? Does estrogen play a part in prevention? If so, how much and when?
- What exactly is the natural course of the disease? Why does it play out in a few years for some patients, in a decade or more for others? Why do different people have different symptoms: some explosively angry, others hypersexual, still others mumbling or even silent? In other words, why is it that, “Once you’ve seen one case of Alzheimer’s, you’ve seen…one case of Alzheimer’s”?
- And for God’s sake, when will there be a cure?
For HBO’s “The Alzheimer’s Project,” I visited labs where our brilliant scientists work around the clock, deeply immersed in research they hope will lead to a cure. But while the federal government will spend about $6 billion on cancer research and about $4 billion for research on cardiovascular diseases this coming year, we’re investing a fraction of that, less than $500 million a year, on Alzheimer research.25 The 2010 healthcare reform act could boost that effort some, but it won’t be enough.
I’ve come to believe that brain research is one of the most important investments our country can make, period. I believe the brain is for America today what the moon was for America in the 1960s: The Next Frontier. I’m convinced if we make a national commitment and launch more of our best doctors and scientists at the brain, they’ll one day produce treatments and prevention strategies and even cures—not just for Alzheimer’s but for a whole host of brain diseases, like Parkinson’s disease, Huntington’s disease, stroke, dementia, mental illness, Down syndrome, autism, addiction, depression. Unlocking the secrets of the brain will teach us more about who we are, how we work, how we learn, what makes us tick and what makes us sick and how to fix it—so that fewer families will have to go through what my family has gone through because of a devastating brain disease.
Which brings me back to my father.
Several months after my mother’s death last year, my four brothers and I wondered what to do with our dad. The house my parents had shared was way too big for him: too lonely, too isolated, too much. We wondered if we should we leave him in Washington or move him to Florida or California to live with one or another of his children?
“We need a new kind of national conversation about Alzheimer’s and growing old in America.”
After much discussion and debate and advice from doctors, we concluded the best thing for our dad would be to keep him in his neighborhood, down the street from two of my brothers, in a facility with lots of people and activities and full-time medical care. It was an excruciatingly painful decision, as it is for any Alzheimer family who makes it. We called it a “temporary decision,” and we’d see how it went.
We sold my parents’ home, packed everything up, moved it all out and put my dad into a beautiful assisted living home right down the street. When I went to check it out for the first time, I sat on the ﬂoor and burst into tears, unsure whether we were making the right decision. We made his room look exactly like his room at home. I don’t think he noticed, but it made us feel better.
I remember the first time I went there to visit him. It was seven years after his diagnosis, mind you, but it felt like I was dealing with his disease headon for the first time. Why? I realize now that while my mother was alive, I was more focused on her—talking to her every day, dealing her declining health, her strokes, her many emergency hospitalizations. Focusing on her distracted me from really feeling the impact of my dad’s disease. Call it what it was: denial. But since she’s gone, my dad’s Alzheimer’s has hit me in the face, and it’s cracked my denial wide open.
When I went to visit my father recently in Washington, I took him outside. There we were, three people sitting quietly on a park bench—his caregiver and me, with my dad in the middle. After a while, my father put his head down on the caregiver’s shoulder and nuzzled him, just like a little kid. It was a sweet moment, looking as he did like a child seeking and getting comfort. But not from me. It was as if I, his only daughter, weren’t there at all. I could have been a bystander. Actually, I was a bystander. That blew my mind and broke my heart.
Today, I visit him and call him, because I know I should. It’s the right thing to do. It’s the respectful thing to do. It’s what a good daughter does. I would want it done for me. But I still struggle. I struggle to find my place in his life and his care, and I struggle for a connection. I say, “Hello, Daddy.” He says, “God bless you!” I say, “How are you, Daddy?” He says, “You’re fantastic!” Sometimes he just mumbles. Sometimes I don’t get even that.
I watch my dad in the facility’s day room, playing with the same puzzles and alphabet blocks my kids had when they were 5 years old. Doing the same things we used to do in Mommy ‘n’ Me classes. I can’t even describe what I feel when I see that. If I want to remember Sargent Shriver, the smartest person I ever knew, the World War II naval hero, the editor of the Yale newspaper, the devoted husband and father, the brilliant and successful public servant with the dazzling intellect—that Sargent Shriver, my dad, is in the pictures on the wall in his room.
I’m so grateful to my brothers and their wives who have homes in Washington down the street from the facility, who step up in such a substantial way to take care of our dad. They have him over for dinner every night and take him to their kids’ basketball games and recitals and to church. They are fully present with him. They know how to deal with him and talk to him. When he refuses to get out of the car, my brothers say, “Fine!” When he growls at them, they growl back. When he mumbles, they mumble.
We talk about how women are doing the lion’s share of Alzheimer caregiving in this country. But all four of my brothers and men whose stories you’ll read in this report show us that men have been stepping up to the plate to care for ailing parents as well. And more men will have to, as more and more women, including their own wives, get the disease. As we investigate in this report, men are having to change their attitudes about what helping out at home means, about asking for ﬂexible work schedules, about how to run their own businesses, how to juggle doctors’ appointments, how to manage medications, how to take care of their aging inlaws when their wives can’t—how to sit and look into the face of a spouse or parent who doesn’t know who on earth they are and deal with it.
It’s a tough change for so many of them. We women inhabit caretaking roles easily, and men have said for so long, “I just don’t know how to do what you do, and I’m just not as good at it as you are.” Now women are asking the men in our lives to help us—and they are.
I watch my four brothers give their kids a new kind of role model to emulate: the strong, nurturing man. My brothers treat my father with such love—fixing his jacket, smoothing his hair, telling him, “Lookin’ sharp, Daddy!” One more time, he says, “That’s fantastic!” They take him to Orioles and Red Sox games and to Special Olympics and Best Buddies events, where former Peace Corps volunteers come up to see him. They know he has Alzheimer’s, but still they take his hand and tell him stories from the old days. It doesn’t matter that he doesn’t know who they are or that he doesn’t even remember the Peace Corps. What matters is that he’s comforted by the warmth of the human connection. These are the gifts my brothers bring to him.
And I’ve learned from my own children and my nieces and nephews. I watch how they talk and laugh with their grandpa, funny and free and easy. They love him, they laugh with him, they play with him, they’re fascinated by him. They don’t get bogged down in the sadness. My kids and my nieces and nephews all accept my father for who he is today—and that’s been a lesson in acceptance for me.
For the summer, we moved our dad out of the facility in Washington to our family home in Hyannisport. We all took turns living there with him. It felt good and right to be in the same house with him, being next to him at dinner, playing ball with him or just sitting in silence with him, staring out at the sea. I talked to him about my mother, and we looked at old pictures together. When I had to leave to go home to California, I felt guilty and conﬂicted.
I know that all in all, my family is so lucky. We’re truly blessed we have been able to keep our father at home for a long time. We are blessed to have the choices we have today. We’re especially blessed to have the resources to pay patient and loving caregivers who help us take care of our dad and make him feel loved.
But I know millions of others aren’t as lucky. Many are forced to quit jobs to stay home— or go through the wrenching process of sending a parent away to a facility, feeling judged and mortified and ashamed that they can’t care for their loved one themselves. That’s the double stigma of Alzheimer’s—ashamed that you have it in your family, ashamed that you can’t cope. For so many, the financial, emotional and spiritual costs are just way too much to bear.
My hope is that as the veil is lifted, as information and funds and support programs are made available, families will see that they’re not alone. As more people, like the ones you’ll meet in The Shriver Report, step out and speak out, sharing their personal journeys with Alzheimer’s, more families will see that there’s nothing to be ashamed of—that there’s hope out there because, together, we are finally making Alzheimer’s a national issue.
The truth is that we simply must put Alzheimer’s on the front burner because if we don’t, Alzheimer’s will not just devour our memories. It will also break our women, cripple our families, devastate our healthcare system and decimate the legacy of our generation.
But if we do, I’m convinced that this Woman’s Nation will be able to say that, believe it or not, there once was a time when there was no cure for Alzheimer’s.
1 ”Changing the Trajectory of Alzheimer’s Disease: A National Imperative”, Alzheimer’s Association 2010.
2 “Prevalence of Alzheimer’s Rises 10% in 5 Years”, Jane Gross, New York Times, March 21, 2007, quoting data from 2007 Alzheimer’s Disease Facts and Figures, Alzheimer’s Association, p. 6.
4 The Shriver Report: A Woman’s Nation Changes Everything: A Study by Maria Shriver and the Center for American Progress, p. 17.
7 Ruy Teixeira, Center for American Progress, analysis of data from The Shriver Report: A Woman’s Nation Changes Everything, personal communication.
8 Ibid, p. 219.
9The 3.3 million figure was provided to the Alzheimer’s Association by Denis Evans, M.D., on July 21, 2010. The figure is derived from data published in Hebert LE; et al., “Alzheimer’s disease in the U.S. population: Prevalence estimates using the 2000 census,” Archives of Neurology 2003;60:1119-1122. Based on the data, Dr. Evans’ research team calculated the number of women age 65 and older with Alzheimer’s disease in 2010.
10 Proposed Revisions to Diagnostic Criteria for Alzheimer’s Disease, National Institute on Aging and the Alzheimer’s Association, July 2010.
11 “Alzheimer’s Isn’t Up To The Tests,” Dr. Sanjay W. Pimplikar, New York Times Op-Ed, July 19, 2010.
12 2010 Alzheimer’s Disease Facts and Figures, Alzheimer’s Association, p. 10.
13 Ibid, p. 14.
14 President’s Council of Economic Advisers, “Work-life Balance and the Economics of Workplace Flexibility,” March 2010, p. 2, quoting National Alliance for Caregiving, “Caregiving in the U.S.:A Focused Look At Those Caring for Someone Age 50 or Older,” November 2009.
15 “Caregiving in the U.S. 2009,” op cit, p. 6.
16 Ibid, p. 14.
17 Ibid p. 25.
18 Valuing the Invaluable: The Economic Caregiving, 2008 Update, AARP Public Policy Institute, p. 1.
19 Young Caregivers in the U.S., National Alliance for Caregiving and the United Hospital Fund, 2005.
20 2010 Alzheimer’s Disease Facts and Figures 2010, p. 26, Alzheimer’s Association.
21The 11.2 million figure is based on the estimated number of unpaid caregivers of people with Alzheimer’s disease and other dementias in 2009, as shown in 2010 Alzheimer’s Disease Facts and Figures (10.9 million), updated to 2010 by multiplying the 10.9 million figure by the percent increase in the U.S. population age 18 and older from July 2009 to June 2010 (the latest available figure from the U.S. Census), 2.8 percent, and adding that total, 300,000, to 10.9 million.
22 R. Schulz, L.M. Martire, “Family caregiving of persons with dementia: Prevalence, health effects, and support strategies,” American Journal of Geriatric Psychiatry, 2004, pp 240–249.
23 The MetLife Juggling Act Study: Balancing Caregiving with Work and the Costs Involved—Findings from a National Study by the National Alliance for Caregiving and the National Center on Women and Aging at Brandeis University, November 1999, p. 5.
24 Claudia Beverly, Ph.D., RN, “Aging Issues: Nursing Imperatives for Healthcare Reform,” Nursing
Adminstration Quarterly, April/June 2010, p. 99.
25 National Institutes of Health, Estimates of Funding for Various Research, Condition, and Disease Categories, Feb. 1, 2010, http://report.nih.gov/rcdc/categories/PFSummaryTable.aspx.