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The Long Goodbye


"The Alzheimer's Project" / Seth Freilich

TV Reviews | May 13, 2009 | Comments (39)


Jesus Christ. HBO’s four-part, five-hour documentary special on Alzheimer’s killed me. It fucking destroyed me, man. As I write this and think back to the five hours I watched over the past few days, I’m doing my best not to weep like a little girl, because I’ve just never had a documentary hit home the way this series does.

My body has never been a physical specimen of, uhm, excellence. I’ve always had full-fledged Jew-boy Syndrome, lacking all but the most basic of coordination. (But at least I’m also horribly unathletic!) And as I’ve gotten older, complete with two back surgeries under my belt, I’ve started to accept the physical failings of entropic life. If my body breaks down as I get older, I know that I can accept it and will, hopefully, be able to deal with it. However, I like to think I’m a pretty smart dude, and even though I already have an embarrassingly terrible memory, I remain absolutely terrified of the prospect of my mental facilities fading.

As a young lad, I saw glimpses of mid-stage Alzheimer’s through a few family dinners with a distant uncle. Later in life, I became much more familiar with it analogously — my grandfather had a devastating stroke which left his mind in a state of dementia pretty much identical to late-stage Alzheimers. He generally did not know who I was, where he was, or what was going on. For a while, there were still tiny windows when the Grandpa Danny I knew was there, although he was usually living in an amalgamated memory from years gone by. But by and large, the awesome man I knew growing up was gone. It was brutal. And presently, I’m watching a very good friend be continually crushed by the enormous undertaking of caring for his mother, whose Alzheimer’s has progressively gotten worse over the last few years.

Point being, Alzheimer’s is a devastatingly frightening disease, and it scares the living fuck out of me. One of the films in “The Alzheimer’s Project” states that Alzheimer’s is the second most feared disease in America, behind only cancer. Well, having seen first-hand the worst that cancer can throw at someone, and having also seen the singular vacuousness that comes with dementia, I’m infinitely more afraid of Alzheimer’s.

So the last thing I really wanted to do was watch HBO’s four-part documentary series, “The Alzheimer’s Project.” But I watched it anyway. And I’m glad I did. Because yes, it was sad, painful, depressing and frightening. But it was also touching and fascinating, wildly informative and, at times, hopeful and spirit-lifting.

The first part of the series is the hour-and-a-half “The Memory Loss Tapes,” which follows several patients afflicted with the disease, along with their family and loved ones. This documentary is astounding. The filmmakers manage to successfully dig deep into who these people were before the Alzheimer’s set in. Getting this real sense of understanding as to who they were, the tragedy of seeing where the disease is or has taken them just kicks you right in the balls. Through the film, we see folks in various stages of the disease including a moment that is so not for the faint of heart….

(*I’m loathe to mention the next two scenes I’m going to talk about, because they carry such an emotional punch that I hate to take away from that viewing experience. But if I’m going to recommend watching this, which I do, I feel like I have to warn you about the first scene. And in light of that, I think the second scene warrants mentioning for its counterpoint. If you want to go into watching this blind, skip the next three paragraphs.*)

Late in the film, we wind up literally watching a man die on film, hearing his last breath and seeing his awesome and doting wife break at his bedside. This scene is one of the saddest moments I have ever seen put to film, especially because in clips just minutes before, taken only a month prior, you see how amazingly bright, sweet and wonderful this man was, even though he was already in the fierce late-stages of the disease. Now your general inclination might be, as mine would be if I were reading this review without having seen the film, to just attribute the strength of this moment to emotional manipulation. Of course filming a death is going to be sad and depressing. But it’s very clear that emotional manipulation isn’t the intent here at all. The intent is simply to be open and honest (and the folks who allowed these filmmakers so intimately into their lives are so incredibly strong and courageous for doing so) and, unfortunately, the fact is that Alzheimer’s has no cure, and death is the inevitable outcome.

That being said, “The Memory Loss Tapes” also has one of the most amazing things I’ve ever seen put to film. One of the patients, before coming down with Alzheimer’s, used to sing with a group. He did so for years, well into his later life. Now, his mind is so ravaged by Alzheimer’s that when his wife and daughter are driving him to watch his old group perform, he repeatedly asks them where they’re going. Each time they tell him, and he says something along the lines of “oh, that’ll be so nice to see them” or “they’re such nice people.” And then moments later, he’s again asking why he’s in the car and where they’re going.

And yet, when the group invites him up on stage during their performance, this man, this man who doesn’t even remember his wife to the point that he essentially has another girlfriend at the nursing home, gets up on stage and sings one of his old songs with them. As the lead vocal. From memory. And for those few minutes, he’s living both in his memory and in the moment. And it’s astounding. But Alzheimer’s shows no mercy, and on the drive back to the home, he’s forgotten the performance entirely, again asking why he’s in the car.

HBO smartly aired this film on a night by itself, because you can’t watch another documentary after it. Especially part two, “Grandpa, Do You Know Who I Am?” Jesus Christ. I literally watched about two-thirds of this through perpetually glassy-eyes. This half-hour film focuses on children coping with grandparents afflicted with Alzheimer’s, and I’m simply at a loss for words to describe it. Most of the kids are amazing, in how they can deal with the situation and accept it so head-on and matter-of-factly. They get what’s going on, they get what’s going to inevitably happen as things get worse, and most of them just take it all in stride. One boy talks about how he knows that it will be sad when his grandfather no longer remembers him. But he’s just not going to be sad now. Another boy notes, “I have to help because I’m the biggest one and I can’t just go to mom for everything.” This kid is only seven-years-old for Christ’s sake.

And then there was this 15-year-old girl, who goes to the home with her mother and sister to see her late-stage grandmother: “I don’t like seeing grandma anymore. I used to enjoy it a lot when we were really young and before it all. But I don’t enjoy it much now because everytime I see her, it’s one more time I see her like this and one last time that I see her the way it was. And it’s more just replacing the memory of how she was.” These are pretty much the exact thoughts and feelings I had as time went on with my Grandpa Danny, and the empathy I have for this girl and her family knows no bounds.

The only problem with this short film was that the pieces were cut-up with narrative bits from Maria Shriver, who is a producer of the entire film series. I understand why, because this particularly film is based on a book she wrote about dealing with her father’s Alzheimer’s, and how her kids have dealt with it and how she’s learned from them. But the cuts were more jarring than anything else, and I found that her bits didn’t really add much substance to the film. That being said, they did at least offer moments of respite in what’s simply a brutal half-hour of television. This time, HBO did air another part of the series right after, but there was just no way I could delve into it. I was spent, I had no idea what the next film was going to do to me, and I just couldn’t take anymore.

When I did get around to part three, I realized that HBO was very wise, as this hour was the first part of “Momentum in Science,” an in-depth look at the science behind the disease. It’s generally a much colder and “just the facts” presentation, although it does have some personal stories threaded throughout. And it’s really a fascinating film, particularly as you see how much doctors and scientists have managed to learn about this disease in a relatively short amount of time. I imagine many folks have the general understanding that I once did of this disease, that it’s really just about the brain failing. Of course, it’s infinitely more complicated than that and, as the film points out, Alzheimer’s is really a disease of the whole body, not just the mind. The mental breakdown is just the ultimate symptom. In any event, it was really cool to see folks talk through what they’ve learned, and how they research the disease in the hopes of putting pieces together in a way to eventually deal with the currently incurable disease.

Part four of the series, “Caregivers,” was the weakest film of the bunch. This hour-long film focuses on the loved ones helping to take care of several patients in various stages of early-onset and late-onset Alzheimer’s. Don’t get me wrong, it’s sad, but it just didn’t carry the same punch as the first two films. I think this is, in part, because each of the caregivers are so strong and, by and large, have managed to come to grips with the stark reality of living with this disease. And, because of the spin the film takes, particularly with the last story, the ultimate feeling of the film as a whole is a bit more hopeful. But the real difference here is that, because the film focuses less on the patients and doesn’t delve into their lives and histories as much as “The Memory Tapes” did, there’s more emotional separation from what you’re watching. Which isn’t to say that “Caregivers” is bad, mind you. It just lacks the emotional punch of the first two films, and the intellectual punch of the third, and so it winds up coming off a bit thinner by comparison.

Finally, HBO wound the project down with the second part of “Momentum in Science.” While it’s just a continuation of the first-half, and continues to be an in-depth look at the past and ongoing scientific efforts to fight the disease, this one also packs a bit more punch. That’s in large part because it focuses more on patients and their ability to help scientists conduct the research necessary to hopefully tackle the disease. Most touching of these is an early segment that looks at a family who’s been pivotal in one arm of Alzheimer’s research, due to the tragic fact that five-of-six siblings inherited the dominant gene responsible for early-onset familial Alzheimer’s. (And that sixth sibling is yet another inspiring figure in these films, as she shows remarkable strength in talking about doing everything she can to care for her brothers and sisters as they inevitably are taken down by the disease.) The second part of “Momentum in Science” is also rather hopeful, as scientists appear to be getting ever closer to being able to detect the disease at earlier stages, perhaps even before the symptoms strike and, hopefully, are on the path to developing successful treatments, if not a full-blown cure.

While I think everyone should see the whole series, it’s a decision you have to make for yourself, particularly as to the first two films, because they’re hard, man. “Momentum in Science” is a bit easier to recommend to the masses, because it’s a more straightforward scientific documentary about a tragic disease. If you have HBO, you can set your DVR to record any of these films at various times throughout the month. But even if you don’t have HBO, you can still watch one or all of the documentaries, as HBO is streaming all of them on its website. One piece of advice though — don’t watch “The Memory Tapes” or “Grandpa, Do You Know Who I Am?” in the office. Because your office-mates will want to know why you’re getting misty-eyed over some bullshit TPS Report you’re supposed to be preparing.

Here’s HBO’s trailer, which is a little deceptive of the Project as a whole, as it primarily focuses on “Momentum in Science.”

Seth Freilich just made a contribution to The Alzheimer’s Association and plans to add the group to his list of yearly donations.


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Comments

Man, I think this is one of those things I'd have to record and then brace myself to watch on a night when I felt strong enough to take it. Even though I've never had any connection to anyone with Alzheimer's, I've always feared it. When I saw the description for it in TV Guide or wherever, I immediately dismissed it as something I'd not watch. But somehow, you make it sound like something I perhaps should.

Posted by: Cindy at May 13, 2009 2:12 PM

I saw the segment that you are talking about with that girl. It was on GMA. I remember being that little girl and talking about my great grandmother. She was brutally smart, funny, and could be condescending at a moment's notice in that special way that only school teacher's can. As much as want to see this, I don't think I can sit through it. The mere possibility that it runs in my family terrifies the hell out of me. I don't want to live if my mind isn't intact.

Cancer's a bitch, Alzheimer's is the dirty $5 hooker on the street corner.

Posted by: Melody at May 13, 2009 2:13 PM

I'm living with and taking care of my grandmother who is in the mid-stages of Alzheimer's. And it is absolutely the hardest thing I have ever had to deal with. Its come to the point where I have to struggle to remember the smart and wickedly funny woman I remember from my childhood. I couldn't bring myself to watch The Alzheimer's Project seeing as how I stare it in the face everyday while it slowly steals my grandmother.

Posted by: Sarah C at May 13, 2009 2:22 PM

Jesus. I've got enough problems with a grandmother who doesn't know any of her children or grandchildren. My hat's off to you, Frylocke, for having the fortitude to make it through.

Posted by: TK at May 13, 2009 2:22 PM

This sounds wonderful, but I'd really have to be in the right frame of mind to handle something like this. Alzheimer's is such a despairing disease, I can't imagine watching this without sobbing myself into hyperventilating. (Like I did recently with Band of Brothers. HBO is evil.)

I luckily enough have no experience with Alzheimer's. It was hard enough when my grandfather died last year from cancer, and his depleted mental state was more pain med induced than anything. To watch someone you love slowly pass on, and to not have them with you mentally...it's the worst thing I can imagine.

Posted by: Julie at May 13, 2009 2:24 PM

I care for my mother, who has alzheimers. The beautiful, kind, funny woman I knew my whole life has changed into a child-like, scared person. That's the worst part of this disease, how scared the person who has it gets. She knows something is up, she doesn't know why she is where she is, and she doesn't have any understanding of time anymore. And the sad thing is, she lives with several women with the disease, and many of these people are totally alone, with no one to visit or talk to them. Try to give a hour a week, or even a month to volunteer at one of these homes if you can.....these people are shunned and ignored because of how scared others are of this disease. And even if they don't remember the visit, you will. And for that time, you will have made someone very happy.

Posted by: jennifer at May 13, 2009 2:26 PM

lovely review. really really want to see this now. especially as someone whos been in a cycle of the grandchild aspect of this documentary for all most of my life.

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Posted by: gate green at May 13, 2009 2:28 PM

I lost both of my grandmothers to Alzheimers. One had early onset and died at 69. Her symptoms began about seven years earlier. The other one deteriorated pretty rapidly and died at 80. Her symptoms began about 2-3 years before, but were complicated by another condition she had that was related to Parkinsons Disease. I feel like I have a huge target on my back. It was hardest seeing my younger grandmother progress through the disease, mostly because of the bad family circumstances surrounding it, but I only saw her once during the last two years of her life when I had grown up seeing her weekly. It still kills me. My dad, her son, is only 3 years younger than she was when she started forgetting things, but I think he's going to be ok. I'm not so sure about his four siblings though. My uncle is already showing some marked memory issues, but my aunt refuses to acknowledge it and get him any sort of treatment. It's a huge mess. I wish I could add some positive outlook to this whole thing, but there's nothing positive to report with Alzheimers at this point. I just feel fortunate that there's another 25-30 years of research to go before I get to the danger ages.

Posted by: katy at May 13, 2009 2:35 PM

My grandpa always said that it wouldn't so bad for the mind to go, if your body was going with it. He died at 95 and lamented that his brain was still sharp but his body couldn't keep up with it. He figured that one good thing about losing your mind was that you wouldn't know it.

I think what makes Alzheimer's so scary is how it affects everyone else. I wouldn't wish that experience on anyone, and my heart goes out to all of you struggling to take care of a loved one with Alzheimer's.

We all like to think we're more than the sum of our parts, and there's life beyond the physical, so it's terrifying to see that your mind, your memories, everything that makes you you, can be stripped away by a disease, by a physical process taking place within your cells.

I don't think I'd be able to watch this.

Posted by: DeadBessie at May 13, 2009 2:40 PM

I'm kind of glad I don't have HBO. This sounds amazing, and like something I could absolutely not sit through. Alzheimer's terrifies me. Nobody in my family has had it, though my father's mother had an aneurysm that caused dementia (or a dementia-adjacent condition) and my father died of a brain tumor. However, I already have a crap memory, which is definitely worsening as time goes on. So, I have multiple brain-paranoias.

Anyway, I think it would kill me, and not in the good way.

Posted by: Anna von Beaverplatz at May 13, 2009 2:51 PM

Damn - I watched "Caregivers" and was crying like a child. There's sadder segments? Mercy! I thought it was really well-done and important.

Posted by: samantha t at May 13, 2009 2:56 PM

I can't believe I missed this. I'm going to have to DVR it.

My great-grandmother had dementia (I'm not sure if it was Alzheimer's, though). She was an incredibly strong, independent, fun-loving smart ass. She was sharp as a tack and full of spunk. In the late 90s she started forgetting things here and there, she'd forget to take a medication or to draw both eyebrows on (we laughed hysterically when that happened). Then she started forgetting to eat, then she set her kitchen on fire. Eventually we had to move her to a place where she could get 24-hour care, and it was the most difficult decision for our family. It's devastating to tell someone who was always so strong that she couldn't make her own decisions any more. That was the worst part - seeing her like that. As her memory continued to fade away, her recollection of us started to erode as well. Sometimes she'd jump back to the 30s or 40s. She'd call me Lisa, or Donna, or Cookie, but rarely by my own name (because in her mind I hadn't been born yet). When she passed away, we were there, and while it was terribly sad, I felt relieved that her life would no longer be defined by the state she was in at that time - instead we could begin again to see her the way she had been before, the way she would have wanted to be remembered. Sorry. My Nonnie was a great woman and didn't deserve to lose everything like that.

Anyway, I plan to watch this show.

Posted by: Kolby at May 13, 2009 3:06 PM

This just makes me want to go out and lobby for assisted suicide. If I ever get diagnosed with Alzheimer's, I'm killing myself while I still remember how to, and recommending that anyone else I know who gets it do the same.

Seriously. Long, painful decline into dementia and oblivion? Or quiet death by one's own choice? Is there really a contest?

As for the documentary, it sounds excellent, but I doubt I'll watch it--too much pain, really. Maybe someday.

Posted by: Fi at May 13, 2009 3:17 PM

Mi abuelita has Alzheimer's. She's had it for the past five years. My mom and I have been her legal guardians ever since she passed out at a bank. That was when the doctors told us she was in the late stages and would never be able to live alone again.
We considered homes at first, but between the cost and the crushing guilt, we decided to take care of her at home. It's the Hispanic way.
It is mentally and physically exhausting. She has absolutely no idea who I am and constantly fights me whenever I try to get her dressed or to do anything at all.
She used to be this crazy, vivacious woman who cursed loudly and made no apologies. Now she's in diapers and reduced to being shuttled to Alzheimer's Day Care. In between, she takes so many medications that I damn near have to bring a U-Haul to pick them up every month.
I don't think I'll watch this. It sounds too morbidly close to my own life to shed any sort of light.

Posted by: Trouble at May 13, 2009 3:20 PM

Seth - thanks for the recommendation. Not sure I could make it though this documentary, but it's good to know that it's so powerful and well done.

Posted by: tamatha at May 13, 2009 3:20 PM

Trouble - I'm so sorry to hear about your abuela. My heart goes out to you and your mom.

Posted by: tamatha at May 13, 2009 3:23 PM

All I could think the whole time was a. what the hell did people do before they even knew what Alzheimer's was? and b. what the holy hell do poor people who are alone do when they have Alzheimer's? Ditto the caretakers who are struggling to make their own bill payments.

Posted by: samantha t at May 13, 2009 3:25 PM

I lost my dad to AZ several years ago. He had been my best friend in the world, an absolute rock of a guy who was a Kenpo blackbelt and the most well-read guy I've ever met. Watching him turn into, in effect, a helpless child was the hardest experience I can ever imagine. Much as I'd like to, I don't think I'd be able to make it through this documentary. My sister gave it a go, and she said she watched it pretty much blinded by tears and ended up lying awake in bed until three a.m.

As an aside, though, the disease will shock you at times by allowing little glimpses of the person you once knew to surface. As a surprise Mother's Day gift, my sister and I escorted my dad back home from his nursing home so he and my mom could enjoy lunch together. My dad was rummaging through a drawer of knick knacks, pulled out his old harmonica, and began playing a long and complex song like he was suddenly disease-free. We all sat around in utter amazement.

The other time was the day of my wedding. Before heading out to the ceremony, I stopped at the nursing home and poured dad and I each a shot of smuggled-in Johnny Walker (his favorite) and shared a wedding toast with him. At that point he hadn't spoken in over a year, but he downed his drink, looked me in the eye and said, "Ahh, that's good." By far my best wedding gift.

Posted by: boscobarbell at May 13, 2009 3:27 PM

"what the holy hell do poor people who are alone do when they have Alzheimer's?"

Based on my professional experience, I can, unfortunately, answer that. Nine out of ten times, they end up homeless. Chances are, the majority of the tragically crazy homeless folks you see are either elders with Alzheimer's or dementia, or schizophrenics. Either way, they're people without a support system, and likely little or no access to health care that can actually help them.

So instead, they wander the streets, secretly terrified and confused, talking to people who aren't there and futilely trying to find homes that they don't remember. Think about that, the next time you find yourself making fun of those people.

Posted by: TK at May 13, 2009 3:35 PM

Thanks, tamatha.

Posted by: Trouble at May 13, 2009 4:18 PM

I can't watch this, can't even read the review.
Just so sad.

Posted by: Jules at May 13, 2009 5:04 PM

TK: You confirmed my worst suspicions. "There but for the grace of God go I" is my reaction to those people.

Aren't we all so proud of how we treat our elders in this fabulous country?

Posted by: samantha t at May 13, 2009 5:06 PM

Yeahhhhhh, no. Alzheimer's is my #2 most feared disease behind Ebola. And that is only because Alzheimer's doesn't liquify your internal organs. You may not know who you are but at least you are not bleeding from every available orifice.

My grandmother had dementia but she was also a functioning alcoholic and it did not seem related to Alzheimers. She is the only member of the family to have had it so fingers crossed it's not a genetic thing.

But this is too damn scary and anything to do with watching people die of a disease tends to put me in a bad place.

But it sounds interesting, maybe I'll read the Cliff notes.

Posted by: TylerDFC at May 13, 2009 5:48 PM

Jesus. I have never known a single person who was diagnosed with this disease, but just reading Seth's review and everyone's stories has me near tears. What a cruel, cruel disease. My heart goes out to all of you.

Posted by: Dingles at May 13, 2009 7:33 PM

I was already on the fence about watching this, as I've been dealing with Alzheimer's since my Nan was diagnosed ten years ago. Now I'll have to say that I'm definitely going to pass, but I'm glad that it was given a thoughtful and honest treatment, and your review was excellent, Seth.

Posted by: Nicole at May 13, 2009 7:49 PM

I've seen my grandmothers go through this, and now this is where my MiL is headed. I might add that these folks also sometimes get mean, and meaner the more you try to help them. MiL now swears and throws things and took a swing at my wife, who estimates MiL is about 50-50 here and not here now.

The worst thing, Mrs. , points out, the real nightmare is that MiL is otherwise in perfect health. She could live another 20 years.

Posted by: , (the commenter formerly known as bucdaddy) at May 13, 2009 9:45 PM

Oh man. I consider myself fortunate to not know anyone affected by this after reading all of your comments.

This disease scares the fucking shit out of me. All I have in this world, when you strip all the material goods and all the physical attributes away, is my mind. I'm terrified of the thought of losing that, of not knowing who I am, or who the people I love are. Terrified. I don't know if I could watch this, even knowing it got a great review.

Posted by: Melissa at May 13, 2009 11:07 PM

You know, this is the one that makes you question your faith. My one grandmother went to church ... um, religiously, prayed and sang hymns around the house, endured years of marriage to a drunk, was about as good a granny as anyone could want, and her earthly reward for this in her last years was to be a jibbering nobody who got passed around among the daughters often enough that thankfully none of them went stark fucking mad.

This one, and 4-year-olds with terminal cancer.

Posted by: , (the commenter formerly known as bucdaddy) at May 13, 2009 11:28 PM

A friend of the family's mother passed away of Alzheimers a few years ago.... and then my Nan was diagnosed. It is so heartbreaking seeing her now. She is now at the stage where all she knows is my Poppa. I want to sit down with the family and watch this but I live in Australia so I have no idea if I can get my hands on the doco.

Posted by: Seraf at May 13, 2009 11:28 PM

Terrific review. I never leave comments on sites but I'm doing that this time because I think it's extremely important for people to be aware of this terrible, terrible disease and do something to help cure it. My grandparents are both afflicted with Alzheimer's and it's a real struggle for me to watch them become less of who they used to be day after day and not being able to do anything to stop the process.

Also, most people may have some idea of how devastating the Alzheimer's can be to the someone who has it, but almost no one recognizes the psychological pressure the disease places on the family members who take care of their loved ones with Alzheimer's.

Posted by: jcklin at May 13, 2009 11:38 PM

This is what we have reaped from a century of medical "advancements." The profession has now succeeded in keeping millions of us alive to no fucking point.

"First, do no harm"?

Kiss my ass.

Posted by: , (the commenter formerly known as bucdaddy) at May 14, 2009 1:00 AM

I'm so sorry. All of you dealing with it. I had in mind to zip downthread to post how awful it is that Terry Pratchett (Discworld and Good Omens with Neil Gaiman) has Alzheimers's and how evil that information is to me - what a mind to lose!

...and then I stopped and read through and realized that everyone's mom, dad and abuelas are just as tragic.

Posted by: replica at May 14, 2009 1:04 AM

My hat is off to you Seth for having the strength to watch this and my heart goes out to those dealing with this disease in any form.

I have been lucky and have never had to endure the hardship of this disease, but I will definately watch this if only to expand my own understanding.

Posted by: admin at May 14, 2009 2:13 AM

When I was a teenager I volunteered in a care home. I was a cousin, a sister, a granddaughter, a niece . . . the people there would come up with so many reasons why I was there, to try to make sense of me. God, some of my saddest and happiest memories are in that care home. I don't think I have the heart to watch that documentary.

My mother has made it clear to me that if she is ever diagnosed with Alzheimer's she'd like an assisted suicide. Hopefully as an RN she'll have that option available to her somehow, or hopefully by that time, as a country Canada will have reached the point that we will be able to grant that mercy to our citizens.

I wouldn't wish that disease on my worst enemy.

Posted by: teacupnosaucer at May 14, 2009 2:19 AM

If you're scared of AZ, you should absolutely watch the Momentum in Science part of this series. It gives very concrete advice on how to slow the progression of this disease. I spent 10 years helping my grandmother die from AZ, and I have also spent that time trying to do anything I can to slow my inevitable onset. Genetically, I'm a sitting duck, but you can prepare your body and your mind.

Watch these wonderful documentaries. Get involved. Send some money to an organization to find a cure. It won't diminish your fear entirely, but at least you'll have the knowledge to begin helping yourself and your family.

Posted by: SketchyRecipe at May 14, 2009 10:55 AM

You are dead on about the "Memory Tapes". To watch these families whose loved one is so unaware talk about how they want more time with them was amazing and heart wrenching. The scene when the gentleman passes had me sobbing and still brings tears to my eyes now. I've got absolutely nothing to bitch about when I look at that.

Posted by: amylou at May 14, 2009 6:17 PM

I just lost my adopted grandmother to a combination of stomach cancer and Alzheimer's. The cancer took her before she was too far gone, but she had started to show signs of impairment - the memory lapses, the unexplainable rages, the vagueness. It was horrible to see the sweet, genteel Southern lady she was turn into someone you didn't know before your eyes, and know that it was only a matter of time before she didn't know you.

For the last two years, I've been active with the "Match it for Pratchett" grass-roots movement. Author Sir Terry Pratchett was diagnosed with Alzheimer's in late 2007. When he donated 1 million US to the Alzheimer's Research Trust UK, his fans decided that we could match his donation. And we've tried. It's too late to save my adopted grandma from the ravages of the disease, but the hope is the money we raise will help someone else in time.

Posted by: AG at May 15, 2009 12:03 AM

Just to let everyone know (and sorry if I am repeating this) HBO is streaming all parts of the documentary on their website for free. So if you have any interest in seeing it but don't have the channel you can still watch!

Posted by: LadyMissO at May 15, 2009 5:42 AM