Friday, August 31, 2012


I was doing a little research this morning, and while I was in the Yahoo! home page, I saw a link for "Health." Curious about what they had to day about cancer (I'm always curious about such things), I clicked some links until I found their page on Lymphoma.

It's horrible.

About a year ago, I wrote about a story that ABC News had done on NHL, in response to an actor dying. It made me very angry -- it was misleading, squished all 40 or so types of NHL together, gave some downright dangerous misinformation, and just generally did a horrible job or informing anyone about NHL.

The Yahoo! page is worse, in some ways (though not all).

They make the same mistake of conflating different types of NHL, but even worse, they squish Hodgkin's and Myeloma in there, too. They have links to the individual general types of lymphoma, but they're not much better: a list of symptoms.

The lymphoma page itself has just a weird mix of information. There is mention of the different types of NHL ("at least 10"), and their different classifications, but even here, there are problems:

"grouped (staged) by how aggressively they grow: slow growing (low grade), intermediate growing, and rapidly growing (high grade); and how far they spread."

 First, this is a misuse of the term "staged," which does have to do with "how far they spread," but not with how fast they grow. The "low grade/high grade" terminology is old; the preferred terms now are indolent and aggressive.

Under the "Diagnosis" section, the procedure that gets the most description is the Lymphangiogram, "an x-ray of the lymphatic system." True enough, but generally not done anymore. In fact, I've never heard of anyone getting one; they've been pretty well phased out, replaced by CT and PET scans.

The section on "Treatment" is devoted to acupuncture, hypnotherapy, and guided imagery. his comes after a paragraph saying that lymphoma is life-threatening, and you need chemotherapy and other traditional treatments. But then we get the alternative therapies for pain management. Eventually, we get the "allopathic treatments" -- that is, traditional Western medicine. Chemotherapy. Radiation. Bone Marrow Transplants.

Several problems here: First, radiation is used much less often in lymphoma -- at least in NHL -- than in other cancers. It's just too hard to hit a moving target, and that's what you have with a blood cancer.  Second -- no mention of Rituxan? When was this written, in 1997?

Guess what: I think it was. Because the last section lists the References for this article, and this is what we get:


Dollinger, Malin, et al. Everyone's Guide to Cancer Therapy. Kansas City: Andrews McKeel Publishing, 1997.
Fauci, Anthony, et al., eds. Harrison's Principles of Internal Medicine. New York: McGraw-Hill, 1998.
Murphy, Gerald P. Informed Decisions: The Complete Book of Cancer Diagnosis, Treatment, and Recovery. New York: American Cancer Society, 1997.


"Alternative Cancer Therapies Popular Today." Cancer. 77, no. 6 (March 1996).

Wow. The most recent thing you have on lymphoma was written in 1998?  Yahoo! was incorporated in 1995, so it's possible this article hasn't been updated since 1998. Is it seriously possible that this article hasn't been updated in 14 years? Yes, I think it is indeed possible.

My only consolation is that few people have probably read this, anyway.

At least I hope so. But what if there are more people who turn to Yahoo as their information source? Yes, unlikely; they'll more likely to go to WebMD or even Wikipedia. But what if they don't?

The internet is a wonderful thing. But for a page that purports to try to help people -- on a site that is trying to focus more on content -- this is inexcusable.

Please, please look to multiple sources for information. Go to Join a support group. And don't believe everything you read -- especially if it's 14 years old.

Wednesday, August 29, 2012

"Cancer is Funny..."

"...Cause People Die."

Wait -- what?

Yeah, that's the name of a Facebook page that popped up on my feed this morning: "Cancer is Funny Cause People Die."

It certainly had me curious. As long-time readers know, I'm a big fan of cancer humor. So I tried to do a little investigating, to see just what was going on with this page. Is it some kind of twisted-humor "cancer support" page? Maybe a way of making people see the positive in a bad situation? Kind of an odd way of doing it, but whatever...

The "About" link on the page, where I would expect to find such an explanation, was blank.

A google search provided a little history, as well as some reactions: the page seems to have been set up by a "troll" -- someone who is deliberately offensive or provocative, who "trolls" for reactions. The internet, with its anonymity, makes it easier to do that without consequences. Apparently, the same person also has Facebook pages that make it clear that AIDS and battered women also tickle his funny bone.

I don't recommend visiting the page, especially if you are easily offended. It's basically a series of people using bad language to let the person know that they find the page offensive, and then other people using similar language to respond to them. There are a few comments that don't include the offensive language, but convey similar feelings -- written by people with cancer, or who have lost someone to cancer, who don't find either the Facebook page or the disease to be all that funny.

So, as I said, I'm a big fan of cancer humor. But let's be clear -- while cancer is funny, death isn't. There's a difference between laughing at the disease and laughing at its ultimate effects. Jokes about hair loss, radioactive bodily fluids, and gastric distress from Barium beverages? Funny. Leaving behind a family? Not so much.

But really, this isn't even about cancer (or AIDS, or battered women). It's about the intersection of information, attention-getting, and free speech.

On the one hand, we are all entitled to some level of free speech. The page itself isn't really going to physically harm anyone, the way the classic shouting of "Fire!" in a theater might harm someone. Emotionally scarring? Most definitely, for some people. But probably half of what is online will be offensive (if not scarring) to most people. It's rough out there. And if you are easily offended, the internet is no place to be, anyway.

But having that free and open forum that the internet provides is a necessity. Who would otherwise be the one to decide what is offensive? And what would the consequences be? There was a time -- not too long ago -- when no one talked out loud about cancer, because it made people sad and potentially offended them. Who wants to hear about cancer of the breast, the colon, the testicles? What if we lived in a world where the internet existed, but we weren't allowed to search for information about those things, because people didn't talk about those things? Where would we be?

Back in 1930, that's where. (That's before modern chemotherapy, by the way.)

So, we need to take the bad with the good. The free flow of information will result in some wonderful things. But it will result in a lot of crap, too -- misinformation, superstition, and trolling. In a world of 900 million Facebook users, a few of them are going to want to do something to stand out from the rest. Some will start pages like "HOPE for Lymphoma." Others will start pages like "Cancer is Funny...."

If you're feeling active, then search for the pages that are trying to shut down the "Cancer is Funny..." page. Join them. Let your voice be heard. Maybe Facebook will shut it down. My guess is, though, that the owner of the page will start a new one.

The other option is, of course, to ignore it.

And for the record, I'm not offended by it. I've seen dozens more offensive things on the internet. (In fact, I've seen a few of them in the last 24 hours.) It doesn't inform me, and it doesn't make me laugh. So why bother?

Monday, August 27, 2012

Happy Birthday, P.W.

I have to acknowledge a birthday today: Paul Reubens, whose most famous character is Pee Wee Herman, turns 60 today. No cancer connection -- I just really, really love the movie Pee Wee's Big Adventure.

I saw it four times during the first two weeks it was in theaters. My mom bought me a talking Pee Wee doll for my 21st birthday (it's on a shelf in my office. Students regularly comment on it). I spent way too many Saturday mornings watching Pee Wee's Playhouse in college.

And now, my kids are fans. Pee Wee brings them as much joy as he brought me.

Happy birthday, P.W.

Sunday, August 26, 2012


Suleika Jaouad, the young leukemia patient who writes the column "Life, Interrupted" for the New York Times, has written a bunch of great pieces lately. The one from last Thursday especially struck me .

Jaouad is very wise, especially for someone in her early 20's. I don't know if adversity brings that kind of wisdom, or if she's just an old soul. Whatever the case, she has a very nice perspective on her disease and her life.

This column is fairly straightforward -- one of many out there (as she herself notes) that gives advice on dealing with cancer. It's called "Six Ways to Cope with Cancer." And, as promised, she offers six ways of coping.

You can read the column for yourself, but I want to comment on a couple of her suggestions:

"Find Your Community." A friend of mine who moved to another state told me she had a hard time "finding her tribe." I liked that phrase -- it signals a deep connection between yourself and the people you interact with. Important for all of us, but especially for cancer patients. I think it's vital to be able to talk with someone who knows exactly what you've been going through, and who can offer some advice for getting to the other side. I was lucky enough to find my own tribe pretty soon after I was diagnosed, an online support group that I still belong to, and that has been a source of information, support, and inspiration for almost five years. Jaouad says she has found a community online, too, through Facebook and other sources, but she still values face-to-face interaction most of all. So be it. For me, with my kids' busy lives (which I wouldn't give up for anything), the idea of driving downtown at night to get to a support group was just too stressful. Being online works. The point is, find your tribe. Don't do it alone.

"Be Kind to Yourself." She describes some of the physically difficult days she has, side effects of her treatment. So some days she sleeps into the afternoon. Some days she has "chemo brain," and is forgetful. She tends to beat herself up for these things, seeing them as signs of failure. We all need to give ourselves permission to be cancer patients, to have bad days, to remember that things aren't what they used to be (and to hold out hope that maybe someday they will be that way again). It's OK to have a bad day, physically and emotionally. (And it's also nice to have a community that can pick you up a little when it happens.)

Finally, "Set Goals Unrelated to Cancer." I think, for me, this was the most important, and the hardest to get to. Naturally, when cancer hits, it makes us focus on little else but the disease. For someone as young as Jaouad, that was probably especially devastating -- a whole lifetime of dreams planned out, and put on hold. But it's not just the 22-year-olds that have those feelings. They are there whether we're 40 or 70. And it's not just big life plans we hold off on, either. It can be day-to-day things. We can't even plan a week ahead, wondering if the way we feel that day will get in the way, or if a sudden need for a treatment will spoil everything. As I said, it took me a while to get past those feelings. Eventually, I thought, " If I say No to this little thing, and then to the next little thing, when will it end? I'll eventually talk myself into not getting out of bed in the morning. If I plan something, and I can't do it, the world isn't going to stop without me. The work will get done anyway. The movie or the festival or the baseball game -- they'll all happen whether I'm there or not. So why not move on with life -- until I can't?"

A wise young lady, that Jaouad. As she said, lots of people give advice to cancer patients. And the advice that she gives really isn't all that original. But it's nice to have a reminder every now and then.

Friday, August 24, 2012


Lance Armstrong has announced that he will not fight accusations that he cheated during the years in winning his Tour de France titles. The U.S. Anti-Doping Agency announced it was erasing 14 years of race results, including his Tour de France victories. Armstrong released a statement expressing his frustration with the process, which he sees as unfair, one-sided, and in violation of the organization's own rules.

It's been interesting to see the reaction of the cancer community (or, at least, my chunk of it). It has been very much pro-Lance. For the most part, people seem to not care about how he got to where he got, only that he has been such an outstanding advocate for cancer patients. I've read stories about his personal interactions with cancer patients -- personal visits, cards and letters, phone calls. He's been such a role model for cancer patients. It's best summed up in this clip from the comedy Dodgeball: A True Underdog Story. The hero, Peter, has quit on his dodgeball team, and as he runs away, he meets Lance at an airport bar:

Lance is certainly someone who has something to teach us about quitting.

On the other hand, some other people in the cancer community are frustrated by what they see as Lance's quitting -- not fighting the charges. But mostly they are in his corner.

So, did he do it? Who knows? Not the USADA, it seems, since they are going on testimony and not on the samples that have been tested during his career. Kind of hard to be definitive when the physical evidence isn't there, though criminal trials are certainly won and lost on witness testimony alone.

Interesting perspective from one cancer survivor, who tried to post a comment on the USADA Facebook page (which he says was erased 4 times): Lance, like many survivors, had so much poison pumped through him during his treatment that there's no way he'd put more into his body, knowing that some of them could give him cancer again. Interesting....

(It looks like the USADA has stopped erasing comments on their Facebook page. About 300 of them in the last hour -- all negative.)

My only personal connection with Lance is through his book, It's Not About the Bike, which I read a couple of months after I was diagnosed, on the recommendation of my brother the long-distance bike rider. It was indeed an inspiration. I remember especially one scene in which a doctor tells him how extensive his cancer is, and how it will require an aggressive approach. The doctor tells him something like, "I'm going to kill you every day and put you back together every night." I think Lance ended up finding a different doctor, but I was struck by his reaction, which was to keep a level head even in the face of such a horrific-sounding approach to treatment. He made good decisions, and kept his eye on his goal -- much like he rode his bike.

I guess I like to think he continued to make good decisions, even as he strove to meet his goals.

Not sure where this is going to end up. Will other agencies strip him of titles? (Does the USADA even have the authority to strip him of titles?) Will the USADA's credibility take a hit? Will that an effect on other sports that it is involved with? Questions about Lance seem, to me, to be less uncertain: Will he continue to raise money and otherwise support cancer patients? Absolutely. Will he be able to be as effective? I think he will. Is his credibility lessened within the cancer community? Sure as heck seems not to be.

Despite Lance saying he's done talking about, and is moving on, I have a feeling that this isn't over. I'm not saying he's going to be vindicated, necessarily, but I'm guessing Lance isn't the only one who has his credibility called into question when all is said and done.

Wednesday, August 22, 2012


Call me old (my kids do all the time, the little punks), but I still love the show Survivor, which hasn't been culturally relevant since about 2003. I've always been intrigued by its "social game" -- people figuring out how to present themselves to others, how to align themselves with others for their best advantage, and how to keep from pissing other people off. It's fascinating. I've never missed a season.

And the upcoming season looks like it will be a good one. It will feature 18 contestants, fifteen newbies, plus 3 alumni who couldn't finish their previous games for medical reasons. There will be, naturally, the young beauties, both male and female, and the surprisingly competent older folks. There will no doubt be a wild card, who might snap at any moment, or who might insult everyone, but who will last long because it's always good to have someone crazy and hated going up against you at the end.

But there are some intriguing types, too, in the form of two celebrities. One is Lisa Whelchel, who played Blair on Facts of Life so many years ago. ("When the boys you use to hate, you date, I guess you best investigate the facts of life.") It will be interesting to see how she uses her celebrity, or doesn't, and how the older folks distinguish between her TV persona and her real self.

The other celebrity is Jeff Kent, former major league second baseman. He won the National League MVP in 2000, narrowly beating out teammate Barry Bonds, who, in turn, barely beat Kent at being the biggest jerk on the team. So it will be interesting to see how he deals with others. Again, the older contestants will be key here, because the youngsters will likely have no idea who the hell he is.

But the contestant I will be pushing for is a guy named Artis. As his intro video explains, Artis is a longtime fan of Survivor, but more importantly, is an actual cancer survivor. If he can keep that quiet for a while, he'll do great, because he seems like he understand Survivor history, and he knows he needs to present a particular persona. (Why hide the fact that he had cancer? Because other contestants will be afraid that it will win him sympathy in the end. That kills most people early on.)

As far as I can remember, this is the first time a cancer survivor has been a contestant (though a winner, Ethan Zohn, was diagnosed with Hodgkin's Lymphoma after he played).

Can't wait for the premiere in a few weeks. Go Artis!

Monday, August 20, 2012

Dr. Sharman -- Part 2

A few weeks ago, I posted a link to a blog by Dr. Jeff Sharman; I was very impressed with the entry, which focused on how he treats lower-risk Follicular Lymphoma. It was clearly written, provided lots of context and lots of links, and generally did a great job of explaining his approach.

I've finally caught up with part 2, where he discusses his approach to patients with higher risk fNHL.

I am not, officially, in the category of "higher risk," at least not according to the FLIPI scale (as Dr. Sharman explains in part 1), at least not now. But, as he also points out, there is always the risk of transformation to a more aggressive version of NHL, and so it's worth thinking about. (I take issue, though, with Dr. Sharman's understatement: "Occasionally follicular lymphoma takes on a bad attitude and "transforms" into Diffuse Large B Cell Lymphoma (DLBCL)." The "occasionally" seems a bit off, given that, depending on the study, transformation occurs between 15 and 50% of patients. Transformation is too big a fear in fNHL patients to brush it off with that sentence). In addition, more aggressive treatments are worth thinking about because eventually they may become needed, even if things stay relatively low risk. Rituxan stope working at some point.

I liked what Dr. Sharman had to say about the state of chemo for fNHL. Essentially, R-CVP is out. I know it still gets used -- I just saw a post from someone in the support group who is in the middle of treatment -- but it seems like Bendamustine has replaced it as the alternative to CHOP with fewer side effects. According to Dr. Sharman, it seems like Bendamustine is going to be the first choice now, with CHOP reserved for transformation. This sounds very much in line with what I've heard elsewhere.

So, overall, I liked this post a lot. Once again, a very clear summary of the state of the field. Dr. Sharman's specialty is CLL, another version of NHL, but I'll keep an eye on what else he has to say about Follicular.

Friday, August 17, 2012

Vaccine Update

Biovest, the company that makes the (as yet unapproved) BiovaxID vaccine for Follicular NHL, announced on Wednesday that they are essentially getting a second shot at approval for the vaccine. In a deal with the FDA, Biovest is going to design and conduct a second phase III trial for the vaccine. If Biovest follws the FDA guidelines for the trial (which it intends to do), and the trial confirms the results from the first phase III trial, then BiovaxID will likely be approved.

I've always been excited about the idea of a vaccine. A few days after I was diagnosed, I saw a lymphoma specialist at Yale, who told me that there were many options for treating Follicular Lymphoma, and more in the pipeline. And he seemed especially excited about the idea of a vaccine. Such vaccines have been developed for other cancers, but NHL vaccines have been less successful. So far, anyway.

Cancer vaccines are not like vaccines for, say, measles. They aren't intended to prevent a disease. Rather, they are meant to train the body's immune system to recognize and attack cancer cells that already exist.

BiovaxID works by targeting cancerous B cells. (Something like Rituxan targets healthy B cells, too, since both cancerous and healthy cells have the CD20 protein).  BiovaxID is individualized for each patient -- it is made with each patient's cancer cells, so it is guaranteed to target those cells, rather than assuming all follicular lymphoma cancers are the same. The vaccine is developed so that the immune system is trained to recognize the unique idiotype (a protein on the surface of the cell -- this is what the "ID" in the name stands for) on the cancer cells. When the immune system encounters cells with this idiotype, it destroys them, the way it would destroy a flu cell, for example, or some other invader.

 Trial results have been pretty positive; patients who have received the vaccine after chemotherapy went disease-free for about 44 months (median). Those in the control arm went 30 months. Careful study of the results, though, showed something interesting: patienst who received the vaccine who had a specific kind of ideotype (IgM) did much better than those with a different type (IgG). This difference is going to be taken into consideration as they design the new phase III trial. We'll have to wait a few more months to see what happens, and how exactly they factor in the IgM idiotype.

So, overall, this is good news. The bottom line is, this is a vaccine that will likely work as a consolidation therapy -- kind of like Rituxan Maintenance, given to prolong the remission from chemo. But the differences between, say, Rituxan (or even Zevalin) are significant enough to give another option should those treatments not work after chemo.

More hope.

Wednesday, August 15, 2012


I'm back from a few days in the Adirondacks. I was told I'd have internet access in my cottage in the woods, but alas, I didn't. That meant no blog posts, and I'm way behind on all the cancer and lymphoma research and news that's out there.

But I have to post something. So I'll honor one of my favorite ladies of all time, Julia Child, who would have been 100 years old today. I have fond memories of watching her on PBS with my father, marveling at her process for making French onion soup -- starting with roasting beef bones for hours to make stock,  continuing on to cook down what seemed like gallons of sliced onions to get about a half cup's worth. I'm sure it was delicious, and it was fun to watch, but it seemed like a lot of work for a bowl of soup.

But my favorite memory of Julia came years later, very near the end of her life. She was a guest on Emeril Lagasse's show. Emeril was the king of the Food Network at the time, with his live show on at 8pm every night. Emeril knew damn well that he owed all of his TV success to Julia -- all of those TV chefs know it. And here was Emeril, on top of the world, cooking one of Julia's recipes as she sat off to the side, saying very little. She almost seemed like more of a prop than anything. It was a little sad.

Emeril was sauteing onions, talking to the audience, when Julia finally spoke, interrupted him, saying, "I'd add a little more butter." And Emeril about tripped over himself to get to the butter. "Yes, yes," he said, scooping up a couple of tablespoons and adding it to the pan, "it definitely needs more butter." Emeril Lagasse, king of cooking shows, and he's kissing Julia's ass. It was awesome.

So to celebrate her birthday, here's another of PBS's awesome remix videos:

(I have to say, though, I like the "Sweet Child of Mine" tribute almost as much....)

Happy birthday, Julia. Thanks for the memories.

(Back to that cancer stuff soon.)

Saturday, August 11, 2012

Tig Notaro

Earlier this week, the comedian Tig Notaro revealed that she had been diagnosed with cancer in both breasts. She did it during her standup act. After being introduced, she came on stage, and said, to the welcoming applause, "Thank you, thank you, I have cancer, thank you, I have cancer, really, thank you."

And the she said, "Tragedy + time = comedy. But I don't have the benefit of time. So I'm just going to tell you the tragedy and know that everything is going to be okay."

And then she told her story. According to another comedian who was at the show, she talked about how she was on both a professional high (a new album, a job writing for television) and personal low (her horrible illness, then her mom suddenly died), and then she was hit with the cancer diagnosis. And when it looked like the silent audience didn't want to hear anymore, she asked if she should go back to her prepared set, and they didn't want her to. So she went on.

Tig Notaro is pretty funny. She tells a story about meeting the singer Taylor Dayne, which I happened to hear on the radio, that had me in stitches. Her storytelling style mirrors her standup style -- understated, sly, ironic -- so it must have been pretty interesting to be in the audience when she broke the news.

I've been kind of turning the story over in my head for a few days, trying to come to some lesson from it. There's certainly something in there about courage -- it must have taken a lot to go onstage and talk about her diagnosis in front of a room full of strangers, especially when it was so new and raw. But I think comedians do that, and find a way to turn their pain into someone else's laughter. Certainly, it's something Notaro has been doing for a while. Still, she's facing her cancer head-on, which is courageous, no matter who does it, or how.

I think there's a lot to be said about laughter, too. If you've read Lympho Bob for a while, you know I'm a huge fan of laughing in cancer's face. Not at cancer -- this is serious business. But near it. With it. In spite of it. She did that, too.

But I think the ultimate lesson, for me, is about sharing. We all handle our cancer in our own way, and whether that means broadcasting it to the world or inviting just a few loved ones to help deal with it, I think the worst thing to do is hold it inside. Someone needs to be told. And while the telling is fraught with potential dangers (people reacting in ways you didn't expect, for example), I'm convinced that holding it in just makes it worse. It did for me.

So I admire Notaro's sharing her story. Especially because it's about breast cancer. For all of the pink ribbons (see my last post), breast cancer still has a spotty history of acceptance. For all the awareness that an "I love boobies" bracelet might bring to prevention, it's just as likely to be worn by a teenage boy. Talking about real experience, real pain, might not be much fun, and it might be fraught with danger, but it brings the real issue out in the open. If some laughs can come with it and make it easier to accept, that's great. Better it be covered in laughter than giggles, or ribbon, or rubber.

Good luck, Tig. And thanks for sharing.

Thursday, August 9, 2012


The Susan G. Komen for the Cure Foundation announced yesterday that its president was resigning and its founder/Chief Executive was stepping down to take on a different role.

It's too bad that things had to go this way, but maybe it's also for the best. Maybe some new leadership will give them a chance to rethink the way they do things.

The resignations were, of course, prompted by the backlash from Komen's decision last January to stop any funding for Planned Parenthood. The funding (which was ultimately restored) had helped Planned Parenthood provide mammograms, especially in rural areas, to many women. The negative reaction was very large, and very public. Several Komen executives resigned soon after, and yesterday's announcement seems like the closing chapter of this controversy.

It's not the only controversy that Komen has been involved in. The organization has been very aggressive in its breast cancer awareness campaign, partnering with some corporations that make products that do not promote the healthy lifestyles that medical experts encourage. Many people do not like their corporatization of breast cancer, where pennies are donated from increased sales of products adorned with a pink ribbon. (The documentary Pink Ribbons, Inc. tackles some of these issues.)

It's hard to deny the good that Komen has done; they've raised over $2 billion for breast cancer research and awareness. I'm as sick of the pink bread wrappers every fall as the next non-breast-cancer patient is, and a little jealous that lymphoma doesn't have the same PR, but $2 billion is a lot of money.

But I think what ultimately bothers me about the Komen controversy is their lack of honesty. In the end, it really did seem to be a political decision, targeting Planed Parenthood by changing its rules specifically to provide an excuse to cut off funding.

The issue, for me, isn't which specific organization Komen targeted. It could have been the Dick Cheney Breast  Cancer Center. It doesn't matter. What does matter is that they hid that agenda.

People need to know what they are donating money to, so they can make an informed decision. If a donation has political implications, or has strings attached, so be it -- a fundraising organization is free to focus on whatever cause(s) they want to. And if I don't like it, I can donate somewhere else, to an organization that meets my political requirements (or, even better, stays neutral, and focuses only on cancer research). But saying you're neutral, and then getting caught having an agenda? Not cool.

So my hope is that Komen ends up with new leadership, and finds a way to focus on their core mission. My guess is that these resignations come eight months after the controversy because fundraising is way, way down. Maybe they'll emerge from this a leaner, more focused organization, like a business that has shed some under-performing subsidiaries.

I hope so. We, the cancer community, need the research. But not the negative PR.

Tuesday, August 7, 2012

Lighthouse Day

Happy National Lighthouse Day!

Established in 1989 to celebrate the 200th anniversary of the law that established lighthouses in the U.S., this day now recognizes and supports lighthouses and their preservation.

Two of my favorite lighthouses:
At Lighthouse Point in New Haven...

The Gay Head Lighthouse on Martha's Vineyard.

The Gay Head Light House

OK, honestly, I really don't have a whole lot of interest in lighthouses. I think they're cool and all, but I'm no fanatic.

What I like is the cancer connection. There are a bunch of groups, support organizations, etc. for cancer patients and their families that have "lighthouse" in their name.

Fascinatingly, I recently saw a blog post from a cancer patient that asked why the pamphlet she received on radiation therapy had a lighthouse on the cover. She was stumped as to why there would be one there, and asked for commenters to explain. I'm not going to link to the post, because her commenters didn't do a great job of explaining the connection. (They seem like an angry group. I'm not judging. Cancer does suck, after all.)

I suppose the light beam on a book about beams of radiation is a little ironic, and possibly upsetting.

But I choose to see them for what they are to many cancer patients -- a symbol of hope. A beacon of light in the darkness. A guide through rocky waters.

And finding a seemingly random bit about a kind of random "holiday" when I was searching for something completely unrelated, I'm going to ere on the side of serendipity and just take it as a reminder that on a tough day, when there are lots of things to worry about, it's nice to have a little ray of hope.

Monday, August 6, 2012

Pan Mass Challenge

The first day of The Pan Mass Challenge took place Saturday. My brother rode, and we met him at the Lakeville stop to cheer him on. It was a very warm, humid day, which made his ride even more impressive.

The PMC, of course, is a series of one- and two-day bike rides across Massachusetts. Riders raise money for cancer research at Dana-Farber  in Boston. Over the years, PMC riders have raised well over $350 million. I'm a beneficiary -- Rituxan is among the treatments that have gone through trials at Dana Farber.