Remembering My Father

youngdadandkids_116 years ago today my father died. I think of him often, and miss his wit and guidance. It is also not lost on me that he was just about 10 years older than me now when he died. As I grow older, I remember him and our time together differently. There is a nuance where I am either understanding our time together differently, or I am simply projecting my own time as a father into his actions.

As a bit of a remembrance of dad, I’m posting another excerpt from my new book The Boring Patient. It is the first time that I have really written about my dad and his passing. I also think that my father, as the consummate salesmen, would appreciate me using his memory to drum up sales.


The Family

Once my medical team suspected cancer my wife called my mother to tell her the news. My mother, who lives in Ohio, was in a car in Tennessee on her way to Florida when she got the call. She found the closest airport and flew to Syracuse the next day to be with me and help out at home.

It took me a few days to truly understand the depth of my mother’s concern. Somehow in my 40s I had forgotten that I was still her son. If my son was diagnosed with cancer you better believe I would be in that hospital room. My mom was there for the first chemo, and she was there when we had to tell my two sons what was going on. In a way my father was there too, even though he had died over 15 years ago at just 55 years old.

I was at my father’s bedside when he died. He had gone to the hospital complaining of abdominal pain. He had a gallstone (thanks genetics). Normally, as I have said, this is painful, but not dangerous. Your liver makes bile, a soup to help you digest fats, and stores it in the gallbladder, which spits it into your small intestines via the bile duct when you eat. A gallstone is when some of this soup hardens sitting around in the gallbladder. If that “stone” finds its way to the bile duct and gets stuck? Ouch!

momdaddaveIn a small part of the population the bile duct joins up with something called the pancreatic duct before it joins the intestines. The pancreatic duct delivers digestive juices (technical term) into the small intestines. The problem is if a gallstone stops up a joint duct like this, particularly just after you have eaten: not only do you get the pain of a backed-up gallbladder, the pancreatic juices also back up into the pancreas, causing acute pancreatitis. There is no elegant way to put this: the pancreas begins to digest itself. If this can’t be controlled, these juices begin leaking out of the pancreas and this leads to organ failure. My father was part of that unlucky population.

I was 28 when this happened. I still think about my father every day. By the time I got home to be with him the doctors had put my father into an induced coma for the pain. He never woke up. He died surrounded by my mother and me and some friends. As we told stories and laughed celebrating his life his vital functions slowed. At the moment his heart stopped a doctor and nurse rushed into the room to revive him. However, he wanted no “heroic measures,” and his doctors had made it very clear that they had done everything that could be done and there was no chance for recovery. So my mother, with a strength I cannot fathom, stayed the hands of the doctor.

hatondavidI would note, however, that his heart, an organ that he had struggled with (a quadruple bypass, multiple stents, and endless battles over smoking and a bad diet) was the last thing to go. “Listen son, I could get hit by a bus tomorrow,” he would say as he downed a fried baloney sandwich. After his bypass he had me bring Kentucky Fried Chicken to his hospital room. I believe it was my father’s final “screw you” to the doctors that the heart went last. He was a man with a great sense of humor so I wouldn’t put it past him.

My father’s death made me (and still makes me) think a lot about my kids and being left fatherless. I have two sons that my dad never got to meet. Riley was 12 when I was diagnosed. Andrew was 9.

There was not much debate between my wife and me when it came to informing the kids. Be open and honest and ready to answer all their questions. I don’t think the idea of hiding my condition from my kids ever really occurred to us. Yet, I have had several folks tell me about having a parent die of cancer, and never being told what was going on. They told me they are still dealing with that as an adult. We didn’t want that.

For Andrew the talk was relatively easy. Daddy is sick. He has cancer. He will be tired and probably lose his hair. Andrew didn’t really have a grasp on death and such, so to him, it was just some more information. “Can I get ice cream now?”

Riley’s talk was tougher. There are way too many ways in which my eldest son is like me. One way that was evident during this conversation was using humor to mask our emotions and/or break the stress. With every bit of information he made a joke while clearly tearing up. Finally, at the end he said, “Yeah, but it’s not like you’re going to die.”

“Actually son, yes, I could die.” May you never have to say those words to your child.

The only thing that saved me from breaking down at that point was having my wife and mom in the room. “But grandma had cancer, and she’s fine. Uncle Joe had cancer, and he’s fine.” Never mind that he remembered Joanne who had died from cancer, and his good friend’s mother. Riley is smart. Riley knew the possibilities. Later, however, Riley would also be the first to make jokes about my lack of eyebrows and hair. All of Riley is smart, including his ass.


You can read more about my family and our trip through cancer in The Boring Patient, now on sale.

Burn the Libraries and Free the Librarians

“Burn the Libraries and Free the Librarians” University of Maryland iSchool Talk. College Park, MD.

Abstract: The days when there was a single model for a library, if they ever existed, are gone. The idea that the library is a storehouse of books and materials is gone. The notion that a library can serve off to the side of the mission of a community is gone. What’s left: the centrality of librarians in meeting the needs and aspirations of the community. This presentation presents a librarianship unencumbered by buildings or a fealty to traditions. It talks about librarians as facilitators of knowledge creation in libraries, and offices, and schools, and classrooms, and the wide reaches of the Internet.
Slides: https://davidlankes.org/rdlankes/Presentations/2014/UMD.pdf
Audio: https://davidlankes.org/rdlankes/pod/2014/UMD.mp3

Screencast:

Burn the Libraries and Free the Librarians from R. David Lankes on Vimeo.

Re-Envisioning the MLS: Burn the Libraries and Free the Librarians

Join us as the iSchool and the Information Policy & Access Center Re-Envision the MLS with our thought leader speakers series. We are pleased to present Dr. R. David (Dave) Lankes as our first speaker on November 6, 2014. Please join us in-person or online! Details are below.

Burn the Libraries and Free the Librarians
Dr. R. David Lankes discusses: The days when there was a single model for a library, if they ever existed, are gone. The idea that the library is a storehouse of books and materials is gone. The notion that a library can serve off to the side of the mission of a community is gone. What’s left: the centrality of librarians in meeting the needs and aspirations of the community. This presentation presents a librarianship unencumbered by buildings or a fealty to traditions. It talks about librarians as facilitators of knowledge creation in libraries, and offices, and schools, and classrooms, and the wide reaches of the Internet.

When: Thursday, November 6, 4:30-5:30pm (EST; reception to follow)
Where: McKeldin Special Events Room, 6137 or online via Adobe Connect at http://umdischool.adobeconnect.com/lankes/
RSVP: Please RSVP at http://ter.ps/rsvpNov6

Publisher of the Community: We’re All Doomed

“Publisher of the Community: We’re All Doomed” Closing keynote for the NISO Workshop on “Using the Web as an E-Content Distribution Platform: Challenges and Opportunities.”

Abstract: We need to build platforms for scholarship and knowledge development, not information and content delivery. These platforms are not about APIs and eContent, but about people and content. We need to strive not for discovery, but epiphanies.

A special thank you to SAGE for supporting this keynote and the workshop.
Slides: https://davidlankes.org/rdlankes/Presentations/2014/NISO-Lankes.pdf
Audio: https://davidlankes.org/rdlankes/pod/2014/NISO.mp3

Screencast:

Publisher of the Community: We’re All Doomed from R. David Lankes on Vimeo.

Mapping the Community

“Mapping the Community” South Central Regional Library Council Annual Meeting. Cortland, NY.

Abstract: Libraries are changing. From a focus on collections to a focus on communities; from spaces of librarians to spaces of students, parents, faculty, and teachers. Of course all of this is just rhetoric. Real change requires tools to define the spate of services (new and old) that are needed to meet the needs of towns, college, and schools.

This session will explore the rhetoric of the new librarianship through a hands on exercise that maps the community you serve. The focus is on demonstrating real skills in the light of a new relationship between librarians and those they serve.
Slides: https://davidlankes.org/rdlankes/Presentations/2014/SCRLC.pdf
Audio: https://davidlankes.org/rdlankes/pod/2014/SCRLC.mp3

Screencast:

Mapping Conversations from R. David Lankes on Vimeo.

I’m Better…Now What?

[TL;DR version: I’m fine, but we all need to be better]

I'm a SurvivorMy good friend and colleague Jill Hurst-Wahl asked me to write a bit about my current state of health. I think she is tired of letting folks know I’m fine now, have been doing some travel, and not stuck in a bubble. I feel like I have said this, but have probably not put it in one succinct post. So…

I’m fine. I had a cancer free PET scan in June, and then another clean one in September. In three months I’ll have another scan, and then more after that as my oncologist follows-up. While there is no guarantee that the next scan will be clean, or that the one after that will be and so on; no one is promised a day on this earth, so I will take the bliss of cancer free for whatever period I’m given before a scan. For those keeping track 50% of transplant patients remain cancer free for 5 years.

I am not, in fact, living in a bubble. Yes, I am immune compromised and will be so for a few years. This is in part because I have a brand new immune system and partly because I have yet to get re-vaccinated for things like polio, and whooping cough (that re-vaccination happens in an accelerated fashion after 1 year). However, I have a working immune system that apparently does well with viral infections, but is more vulnerable to pneumonias (imagine how pleased I am to follow the recent news with Ebola and the Enterovirus).

I also have to be very careful with food born illnesses. Anyone would have problems with things like Salmonella and Listeria, but I would have a VERY hard time with them. So food needs to be served well done and hot. I also have to avoid buffets and food that has been sitting under heat lamps. Really folks, we should all avoid those…have you seen what people do at salad bars?

I also have, in fact, done a bit of traveling. I’ve done a few trips to Albany, to Fairfield Connecticut, and later this month I’m actually flying to Springfield Illinois to join my tribe at ILEAD USA. My doctors have given me the go ahead to get on planes as long as I wear a mask and douse myself in hand sanitizer. I think this is to freak out my fellow passengers so they give me more space.

I’ve been limiting my travel to mostly places I can drive to. This is really out of an avoidance of getting back in planes (those damn things shake in the air) than health issues. However, I am thrilled to announce that I have accepted speaking gigs in Liverpool (UK), Australia, and New Zealand. I’m also working on putting together a speaking tour through Italy in the summer (hey…want to host an academic in Italy this summer? Let me know). I’m also working on an idea to get me to ALA Midwinter in January.

Which brings me to a very weird spot. It would be very easy to fall back into a life of the traveling professor. I am teaching an amazing class of LIS students. I have offers to speak. I have a lot more to say on the future of librarianship. In essence, I have the incredible good fortune of being able to pick up my life where I left it before cancer.

So should I? As I have been recovering these past months I have seen a community I love, librarians, both profess noble principles (diversity, respect, concern for the well being of their communities, a call for greater service) and engage in the worst kind of pettiness, to the point of lawsuits and character assassinations. Do I really want to give more keynotes when the speaking contract seems to come with a target for my back?

When I had cancer I became part of an unfortunate club – cancer patients. It is an amazing club because it is amazingly diverse. Mothers get cancer, celebrities get cancer, children get cancers, black, white, yellow, old, tall, male, female all get cancer. Some of us blog, some us write books, some of us speak, and some of us become YouTube sensations. And no one-no one-talks about shiny cancer patients, or rock star victims. Because in that community, we are all rock stars, we are all shiny, and we are all deserving.

I have read your posts and your Tweets, and there are some great ideals expressed. Those with more attention, or more opportunities have a responsibility to bring along those around them. Yes. Those who live with cancer, who survive, teach. They teach their parents, and their kids, and their friends, and their co-workers. They teach because every cancer survivor knows they are alive because of the work and suffering of those who came before. My bone marrow transplant was a success because of literally thousands of people who died before me, hundreds who were willing to be a lab rat for new treatments, and doctors, researchers and nurses, who refused to stand by and allow more death. We teach, we write, we appear hairless on magazine covers because we have learned that every day without nausea or pain is a gift, and one that we must share for those who will come after us and need hope.

In the cancer club a 9 year old becomes famous…he or she inspires blood drives, and scholarship funds, and the building of new cancer centers. They are famous not because they “did cancer the best,” but because they can inspire others to action. Every rock star with cancer is reminded every day they are there, they are worthy, they are important not by autographs requested, but by platelets donated. Every cancer patient knows that in their veins course the immune system of others, their cells breathe due to red blood cells from across the nation.

I am shiny, I am a rockstar librarian, and people invite me to give keynotes…and when they do, I am keenly aware that I am there because of the work of mentors like Mike Eisenberg and Chuck McClure. I am there with the support of people like Liz Liddy, Corinne Hill and the wisdom I have drawn from Meg Backus. I am speaking because Lane Wilkinson took the time to argue epistemology with me; because Jill Hurst-Wahl lets me snark over lunch. I am there because of Mike Nilan, and Andy Dillon, and Kathryn Deiss, Scott Nicholson, Megan Oakleaf, Kim Silk, Wendy Newman, Nicolette Sosulski, Joe Janes, Barb Stripling, Ruth Small, Jeff Katzer, Todd Marshall, Anne Craig, Gwen Harrison, Joe Natale, Mick Jacobsen, Andy Bullen, Steve Thomas, Buffy Hamilton, Joyce Valenza, Joe Ryan, Bill Moen, Joanne Silverstein and an entire nation of genius. I am there because of Melvil Dewey, Ranganathan, Wilson, Buckland, Pask, and Taylor. I am there because my wife took the effort over two decades to beat out of me the misogyny that the Jesuits in high school used to push me forward. I am there because every year I get a sea of fresh faces of LIS students who push me further. I am there because of Mia, and Lauren, and Carl, and Bob. I am there because the librarians of Ferguson and Alexandria did their jobs in the face of uprisings, and the librarians of Fayetteville took a risk of 3D printers. And when I am at a conference, at work, on the Internet, or frankly anywhere, I behave with respect for myself and others because of those I represent.

I don’t think we need to get rid of Movers & Shakers. I don’t think we should get rid of Think Tanks, or Emerging Leaders or any awards that give librarians an opportunity to showcase how great librarianship is to the world around us. Do you think those awards are for librarians? Do you think these awards should be about self-congratulations or creation of a class system, or pushing one above the many? Do you think we place folks on pedestals for us to admire them? If that is the case, then tear them down. We must use all of these pouts of distinction as ways to scream to those that we serve that we are here, we are important, and we only succeed in the success of those we serve.

So be shiny and a rockstar and a leader. 3,000 years of librarianship are here to push you forward. But shine to your members, rock the worlds of your communities, lead the world to better days. That’s what I’m going to do with my gift of life…what about you?

Cancer Posts and the Boring Patient

Writing was part of my coping mechanism when going through treatment for Hodgkin’s Lymphoma and my stem cell (bone marrow) transplant. That writing was mainly in the form of blog posts. While The Boring Patient is much more than just a compilation of blog posts, these writings give you a good feel for the style of the book:

The Loss of Hope

You see, that’s the thing about hope – it is not a guarantee or a promise. It is a prayer, and desire, and it lies at the core of making this world a better place. We fight inequity, poverty, corruption because we hope for a better day. We teach because we hope we can impart some idea that will blossom into a better world for all. We raise children in hopes of a better future. We marry because we hope we can live up to the promise of our spouses. We work either out of the hope that our efforts will improve the world, or at least the wages of our labor can provide a better world for us.

Mundane Miracles

See the spectacular every day in the love of friends and family. When you wish your son would just be quiet, remember the wonder and thrill of his first word. Make the next peck on your wife’s cheek rekindle the passion of your first kiss. And laugh – every day – laugh. The world we live in is a wondrous mundane miracle. Rejoice in it.

Beyond the Bullet Points: PET Scans and Water

Now I would like to describe to you the immense awkward feeling you have when in a small examine room with your wife when you are told that your “salvage treatment” (actual medical terminology) is not working. You can’t lose it, or your wife will, and you have to be brave and not wanting to wail like a little girl amongst nurses you have come to know and like. I would like to describe that for you, but before I could figure it out there was a knock on the door.

Personal: Victory through Surrender

Then there is a final thought, a crucial insight that must accompany the surrender. If you accept the treatment, and the limitations, and the proxy battle, you can then focus on the other things in your life. You can focus on your son’s graduation. You can focus on your wife’s affection, and the love of friends. You can focus on your work, and your mission, and all the things that will be waiting for you after the poisons and the drugs, and the pain, and the limitations.

Percoset and Puppies

Cancer does not make me noble. It makes me afraid and sick. It makes me every day make promises of redemption to my family, friends, and co-workers. “Next year, we’ll do our anniversary in Hawaii,” “next birthday we’ll have a big party,” “next time I teach I’ll pay more attention.” My life has increasingly become a promissory note; one conditioned upon survival.

Click here for more of my cancer posts and Read a sample chapter and learn more about the boring patient here.

Cancer Videos

As part of the roll out of my new book, The Boring Patient, here are two videos I produced through the stem cell cancer treatment:

The actual stem cell transplant. The whole procedure took over an hour, so here is a much more watchable version. If you look carefully you can see a priest do a drive-by blessing at 1:37.

[vimeo 87505187 w=500 h=281]

“Face Journal” from biopsy to day 100 of the stem cell transplant.
[vimeo 97336093 w=500 h=667]