The Loss of Hope

The topic of todays sermon is “hope.”

The audience for said sermon is me.

You see I woke up this morning with good news. My white blood count had climbed from 0.1 to 0.3. This is the first concrete sign that my stem cell transplant is working. My sores should start to heal, my pains subside. Good news. My wife was ecstatic, my kids did a happy dance video. I, on other hand, got depressed.

You see my life for the past two years have been full of false starts and promising milestones. I am declared seizure free, and two weeks later I am in the hospital with dangerously low platelets. This, in turn, lead to a cancer diagnosis, so into chemotherapy I went -a chemo with a nearly 90% cure rate. As July rolled around we all celebrated the end of chemo, and a seemingly clean PET Scan. Three months later after another PET scan, another biopsy showing that the lymphoma had not gone.

And so I now sit here, in the bone marrow transplant wing of the hospital, at the end of 3 months of lethal chemotherapy and stem cell collection, after 16 days of the systematic destruction of my digestive system, and there is hope? How can I hope again? How can I convince myself one more time, that THIS time, THIS treatment, THIS procedure will be the one? When does optimism simply dissolve into deliberate ignorance?

Many have called me brave, or inspirational in my fight with cancer. There is nothing brave about battling cancer. The alternative to the battle takes the decision away. Chemo or death? Easy choice. Chance to live 5 to 40 more years…yes how brave of me to chose that.

Then I think about my new life, the one we celebrate the day the stem cell are injected into my chest, February 24th. What will this life be? Should I return to my former ways? Grants, speeches, projects, advisees? Should I recommit to changing the world? This work involves more than me. It involves commitments of others, others that I have, over the past two years, let down…a missed meeting, a failed project, dropping of commitments. Can I change the world and avoid that? Is it time to become the tenured full professor who teaches his class, writes his book, and disappears into the ivory tower?

Haven’t I earned that? Don’t I deserved to be selfish and live every day just for itself, with my only effort to change the world through my wife and kids? Isn’t that enough.

Then I think “WHO THE FUCK DO YOU THINK YOU ARE?”

Who among us is promised a full day on this earth? Who among us is free from the threats of disease, or violence, or stress or poverty? How many people do I know that every day fight to pay the bills, who may go hungry? How many of the “lucky people” I walk by without cancer are fighting their own demons of drugs, or discrimination? Retreat to the Ivory Tower?!? Talk about a privilege problem. How many people would be happy with any job? How many people would long for a roof over their head? It must have been tough going through this medical procedure….with health care!

I had cancer and it might come back, and you may lose your job, and he may have a heart attack, and she may lose her child. We cannot live life cataloging potential disasters and saying “at least that didn’t happen to me” ignoring that it happened to others. That is not living, that is hiding, and the only greater sin is believing that you have no part to play in the alleviation of other people’s pain.

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.

I have made a career of calling people to service. In the classroom, on the web, on stages around the world I have tried to equip an army of the hopeful to improve society. I never made a promise to that legion that our cause was guaranteed, or easy, or simple. But I did try and give hope. That hope continues with or without my cancer, or my very life. But while I have the ability to put towards to it, I will do so with hope.

Today my white blood count went from 0.1 to 0.3. The doctors and nurses are hopeful that my levels will continue to rise to the point I can go home next week. They can’t promise it, but they can hope for it. I hope they’re right, because I have a lot of work to do.

Free copies of Lankes book now available to ALA Members, Library Trustees and Friends of Libraries

Thanks to ALA for getting out the word and all of their support:

For Immediate Release
Tue, 02/18/2014

Contact:

Mary Ghikas
Senior Associate Executive Director
ALA
312-280-2518
[email protected]
CHICAGO — The American Library Association has consciously and vigorously embraced the position that libraries of all types are the locus of community engagement. As the facilitator of the first round of Midwinter Conversations, R. David Lankes, professor at Syracuse iSchool, knows first-hand ALA’s commitment to community engagement and to turning outward.

Through Lankes’ generosity, ALA members and United for Libraries members are being given the opportunity to access for free Lankes’ book “Expect More: Demanding Better Libraries for Today’s Complex World.” Download this book for free or read it through Medium by going to the following webpage: https://davidlankes.org/?page_id=4598. Also included are brief videos explaining specific concepts and providing practical examples.

R. David Lankes is a professor and Dean’s Scholar for the New Librarianship at Syracuse University’s School of Information Studies and director of the Information Institute of Syracuse. Lankes is a passionate advocate for libraries and their essential role in today’s society. He also seeks to understand how information approaches and technologies can be used to transform industries. In this capacity he has served on advisory boards and study teams in the fields of libraries, telecommunications, education, and transportation including at the National Academies. He has been a visiting fellow at the National Library of Canada, the Harvard School of Education, and the first fellow of ALA’s Office for Information Technology Policy. His book “The Atlas of New Librarianship,” co-published by the Association of College & Research Libraries, a division of the American Library Association, and MIT Press, won the 2012 ABC-CLIO/Greenwood Award for the Best Book in Library Literature.

For further information, contact Mary W. Ghikas, Senior Associate Executive Director, ALA, 312-280-2518 or [email protected].

Mundane Miracles

For the past three days I’ve lay in a bed as my blood flows from my chest into a machine that separates out my stem cells and then back into my chest. The stem cells are pumped throughout the day into a collection bag. This bag is literally my life as next week I will go into a hospital and voluntarily take a lethal dose of chemicals. Chemicals that will kill off any remaining cancer (hopefully). Chemicals so potent that they will wipe out my bone marrow. Chemicals so toxic they will also rip away at my entire digestive track leaving blisters and sores in their wake. Without that bag of stem cells to regrow my bone marrow I will die. No way to heal, no way to stop bleeding, no way to feed my body the oxygen it needs to live.

I was marveling at this sci-fi like procedure when I saw that bag of stem cells (i.e., my life) was put into a Ziploc bag and transported to a lab in an Igloo cooler. That’s right, the inventory of crucial pieces of equipment to keep me alive include the same equipment used to safe guard cheese sandwiches, and transport six-packs of beer to the beach.

Now I’ve been trying to write up some inspiring sermon-esque post on this transplant process. I’ve tried to figure out soaring rhetoric on faith, medicine, science, and such. After all, this is a big deal. An organ transplant…poisons…epic drama kind of stuff. But then I keep coming back to the Igloo cooler and the Ziploc bag. When you think about it, this whole thing is pretty absurd.

I mean I had to sign a consent form that said:

  1. I can pull out of this procedure at any time, and
  2. If I pull out of this procedure I will face “certain death.”

I actually signed a document that had the phrase certain death in it. I mean, seriously?! Who sits through a lethal dose of chemo and says “you know what? I’m good.”

“But sir, if you leave now you will face CERTAIN DEATH!”

“Yeah, I’m OK with that, I got Tylenol at home.”

And seriously, an Igloo cooler? Who will be the first lab tech to mistake that for their lunch. “Ah, man? Stem cells again?”

I mean when I get a PET scan they give me a shot from a syringe encased in friken titanium. When I get a chest X-Ray, they wheel an armature with a full color display into my room – an X-Ray that can only take black and white images mind you. I’ve had my brain scanned with magnetic beams, and my gut outlined with protons and gamma rays…but the fluid that will save me from CERTAIN DEATH? Igloo and Ziploc.

How insane is this? I’m sitting all day as my blood is processed by a set piece from the original Star Trek series watching the Olympics where the Curling team uses high tech granite pucks with embedded hand sensors. Meanwhile, my stem cells will be injected into an IV line over the course of about 15 minutes…that’s the transplant. No lasers. No high-tech imaging device. Just a doctor and the same medical instrument that Sherlock Holmes used to shoot up over a century ago. How do they prepare the stem cells for transplant? They thaw them out in a warm water bath. Water! I hope they at least play some dramatic music on a Zune (yes I went there Microsoft).

It gets more absurd still. A year after I have this transplant, I have to go back to the hospital to get my childhood vaccinations. In a year I will have to stare down the Jenny McCarthys of the world on the risks of diphtheria and MMR vaccination. After this miracle of science transplant my biggest fear is polio…POLIO!! The way this is going I’ll probably end up sitting in the well kid waiting room of my kid’s pediatrician working on a puzzle out of a 1973 issue of Highlights magazine.

So, is there some lesson in this; some larger take away? I suppose it would be this: when the extraordinary becomes the mundane, it is no less important. Those who deliver the essential, but expected, are doing something important. When my doctor delivers my stem cell in a routine infusion from an Igloo cooler, she will still be saving my life. When an optometrist fits you with optical technology (glasses) that has been around for centuries, you still can see. The world around is filled with the extraordinary that we have become so used to as to make it seem mundane…but it is spectacular.

I pray you don’t have to fight cancer to see the extraordinary. Sure, we see it in toys and gadgets every day. We have become enamored with iPhones and smart watches and marvel at how fast/small/stylish they are. But try and recognize how incredible the everyday is. Next time you wash your hands, remember that indoor plumbing has saved more lives than any miracle drug.

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.

Exploring Digital Libraries

I was delighted to find a copy of Karen Calhoun’s Exploring Digital Libraries: Foundations, Practice, Prospects in my mail. While many may know of my more recent work around new librarianship, I spent a good amount of my time as a starting scholar in the world of digital libraries.

One thing that always bothered me about the digital library field was a sort of bipolar approach to the topic. On one side were the computer scientists, and on the other the librarians. To be sure there were plenty of folks who bridged this world, but the literature and meetings felt like a sort of parallel play.

This is why I love Karen’s new book. She has done an amazing job of capturing the digital library world from the 90’s to today. She does this not as some sort of annotated bibliography, but as a conceptual evolution. You can see the development of digital libraries from collections of stuff, to communities of interest.

She also merges the disparate worlds of computer science and library science together in a masterful way. She uses the history to create a robust platform for understanding digital libraries today…in essence making the field feel relevant and refreshed. If you have a chance I strongly recommend the book.

Here is some additional information:

Calhoun, Karen. 2014. Exploring Digital Libraries: Foundations, Practice, Prospects. Chicago: ALA Neal-Schuman.
(table of contents available at http://www.alastore.ala.org/detail.aspx?ID=4247)

Facet has prepared a chapter by chapter synopsis at http://www.slideshare.net/amarintha/exploring-digital-libraries-chapter-by-chapter-summary.

Beyond the Bullet Points: PET Scans and Water

I tell you the following story of what happened to me today to:

  1. To amuse the twisted and snarky
  2. As a cautionary tale for those who seek to serve
  3. To let those following my health know about the results of my PET scan

Normally when you get a medical test, you get a result. Often times, these are nice and definitive. For example, this morning I had blood taken and I found out that my platelets were 17. That’s good, because two days before they were 7. You see what I mean about definitive. “Hey Dave, how are those platelets coming?”

“17, thanks for asking.”

Well, PET Scans aren’t always so nice. They require professional interpretation. A radiologist looks at them and says things like “appears normal.” Or “some indication of abnormality in the mesentery region.” This can be very unnerving. “Hey Dave, how’s that mesentery region?”

“Ah, you know, showing signs of abnormality.”

It is with this background that I can start my story. This morning I went to see my oncologist. As is normal, the first doctor to see you is not your doctor, but one of a seeming endless mass of fellows. It turns out this fellow I had seen before. She is the one that a year ago (almost to the day) told me that I had lymphoma and then kicked my wife out to do a bone marrow biopsy before the pathology lab closed. This was remarkably like “Hi, your husband is probably dying of cancer, now please wait in the lounge as I drill his hipbone with a very large steel needle.”

Anywho, “Bringer of Doom,” as my wife and I now refer to her, came in today, asked how I was feeling, and then stated that the PET results showed uptake in the abdomen, meaning that the chemo wasn’t working. Worse still, as my wife pointed out, it seems to have spread since the last PET scan didn’t show anything in the gut.

I will pause here for my more excitable readers to point out that this story does, as far as it can, have a happy ending…just wait for it.

“Last PET scan? Was that in May” asked Bringer of Doom.

“No it would have been October.” I responded attempting not to notice my wife’s tears welling up and a low refrain of “oh shit oh shit oh shit.”

“Was it here?” asked Bringer of Doom.

“No, it was at Brittonfield.”

“Oh, I’ll have to look at that in the external record. I only went back to November and I didn’t see anything. In any case, your doctor will be in soon,” and Bringer of Doom felt for my lymph nodes, listened to my lungs and left.

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. I had to have a social worker do an assessment of me for my insurance. By the way, best question asked? How do you cope with stress…answer shrug. N case the social worker is reading this, I would like to change my answer – sarcastic social media postings.

So the social worker leaves, and in walks my doctor, a new nurse and, of course, Bringer of Doom.

“So I’ve looked at the PET scan results and actually they look pretty good to me” says my doctor.

“Glurp?!” is what I am guessing I said…just imagine Scooby confused at something profound Shaggy just said and you’ll get the picture.

“Well, reading from October’s PET scan it is clear that all of cancer in the neck and chest, where it was growing, is now gone.” Said the angel wearing a lab coat. “What’s more, I’ll have to talk to the radiologist this afternoon, but PET scans always find junk in the mesentery region.”

“What is the mesentery region” asked my wife who was clearly now paying very close attention.

“It is the tissue and such that interlace the bowels. The PET scan could be picking up bowel activity, or inflammation. I’ll know more when I talk to the radiologist. The point is that I see this as very positive. The chemo is working. The question is now whether to do one more round of chemo to be sure, or move into the harvest and transplant.”

Now I put quotes around that last part like it is what the doctor said. Truth be told I know that was the gist of it, but a mix of relief and rage made the dictation a bit difficult. Relief that things were now looking up, and rage that we didn’t start at that point.

So I’m going to finish this story up in two ways:

  1. Where I am for my treatment and transplant, and
  2. Why this is a cautionary tale for those who seek to serve.

So, for my treatment, the doctor is consulting with the radiologist to look at the current and previous scan. If they are convinced that chemo has been effective, and the mesentery stuff is just ghosts, then we proceed to harvesting my stem cells and the actual transplant. It may be delayed by a week until my platelet count recovers over 50. If the docs are still undecided about the scan, or feel there is some cancer traces left in the gut, then another round of ICE, then the harvest.

So, good news? Yes. Clearest best possible news? No, but those are frankly pretty hard to come by in medicine of any complexity.

Also, be assured that we brought up Bringer of Doom’s delivery issues and were assured it was a problem that would be dealt with.

Which bring us to those who seek to serve: we (librarians, teachers, professors, doctors) often like to talk about “informing” as if it was a verb that means something. The assumption we make is that by providing more information faster, we can help people make better decisions. What’s more, there is an unstated assumption that information is like water. Bad information can simply be flushed away with good information. This is wrong.

It is wrong because no matter how much water you use to flush something it leaves a mark; it leaves an imprint that will color all the information to follow. I now have more doubts about PET scans, my treatment, even the current state of my health and prognosis because that was where I started.

But the view of informing and canceling out is wrong because it represents a detached, and clinical view of people. To inform sounds objective. It sounds like we present the facts, or some nuggets of data that is entirely up to those receiving it to interpret. Too often we hide behind this idea to somehow distance ourselves from the troubles of those we seek to serve. I am not saying this from one bad day with one doctor with bad people skills. Research shows us that how we get information and in what order matters.

Instead of informing users, we must see our job as helping a person to learn. Doctor, professor, teacher, librarian all can no longer believe that simply pushing information at someone and if necessary fixing it later is acceptable. When I learn, when I am “informed” it is more than my memory and reason you effect. It is my emotion, my needs, my image of self.

There is a responsibility for those in the professional services to see beyond a question, or a task, or an interaction, and into the person they seek to serve. This is why we do not have customers who can simply return an item they do not like. Nor consumers who vacuum up our output. Nor do we have users that might as well be reading off a glowing screen. We have students, and patients, and faculty, and members, and people who come to us with what seem like questions, but are really needs, aspirations, and dreams.

I can already see many of my librarian colleagues dismissing their importance. Cancer and PET scans are one thing, but all you have are hold requests, or finding books, or figuring out the right website for a class project. Look deeper. Is that book about changing their life, or their cancer, or escaping an abusive relationship? Does that web site represent the start of a new career, or is about a hobby an awkward teen sees as part of their self-worth?

I recall Betsy Kennedy, the director of the Cazenovia Public Library, talk about a program to give new books to poor kids. She talked about how one child upon receiving the book began to tear up. “It’s the first new thing that I’ve ever owned,” said the child. That was not just a book, but worth, meaning, hope to that child, and Betsy knew it and used it to create programs to help other needy families. When the families came for books for their kids, she and the other librarians and volunteers recognized the need for educational opportunities for the parents as well. She helped create GED programs located in food pantries for the needy of her region. She doesn’t serve readers, or patrons, she lifts up whole communities.

If all you do is stand behind the desk (real or metaphorical) and answer questions or inform – If all you do is lecture – If all you do is listen to a list of symptoms and prescribe drugs, then you are not doing your real job. Patients have better outcomes when they are part of treatment decisions. Students have better outcomes when they shape their learning. Members have better experiences when a librarian takes the time to get beyond the question to the real need. What we know may make us experts, but whom we serve makes us noble. It is not in your insight and expertise we find the true measure of worth for a librarian, lawyer, doctor, or teacher. It is in the success of the communities we serve.

If you know you can impact someone’s life, take care and take the time to know when and how to teach. And if you don’t think you can have that kind of impact? Then please understand that you may well be the Bringer of Doom and not even know it.

Follow Up: Had a talk with my oncologist and after consulting with the radiologist, she feels the PET scan is clean (if not clear) and we are going to proceed with harvest and transplantation…more on that on my Caring Bridge site soon.

Libraries as Community

“Libraries as Community” Information Resource Center Directors (branch libraries in US Embassies) from East and Central Africa, U.S. Embassy, Kigali (via pre-recorded video).

Abstract: As professional services (medicine, higher education) move to a more participatory approach, so too should libraries. This presentation discusses how the mission of librarians pushes libraries past documents and spaces to conversations.
Slides: https://davidlankes.org/rdlankes/Presentations/2014/Embassy.pdf
Audio: https://davidlankes.org/rdlankes/pod/2014/Embassy.mp3

Screencast:

Library a Community from R. David Lankes on Vimeo.

The Bad, The Good, and The Great

“The Bad, The Good, and The Great” 2nd Annual Wild Wisconsin Winter Web Conference (via pre-recorded video).

Abstract: It is not the collection or array of services that makes a library great, it is the difference it makes in the community.
Slides: https://davidlankes.org/rdlankes/Presentations/2014/Wisc-Lankes.pdf
Audio: https://davidlankes.org/rdlankes/pod/2014/WiscScreen.mp3

Screencast:

The Bad, The Good, and The Great from R. David Lankes on Vimeo.

Beyond the Bullet Points: When will the Mission Die?

I asked my doctor how I would die. Her answer was that If this treatment didn’t work we had more treatments after that and another treatment after that and still more tries after that. And if all that doesn’t work no one dies in pain. None of this, of course, answered my question which is how does one actually die from lymphoma. It was, however, the answer I expected. No one wants to accept failure. No one wants to be part of a loss of hope.

To be sure, my path with cancer has had its times of lost hope when, as my wife and I refer to it, “I go there.” However, this is not why I asked the question. I wasn’t giving up. I didn’t ask out of despair. I wanted to know. I needed to know. I needed to understand because, for me, I need to know what I am fighting against.

I tell you this story because I have been talking with a few people I really admire who are asking tough questions that could also be easily mistaken for despair. They are questioning professional choices. They are, in their words, becoming cynical. They are “going there” and beating themselves up for it. They seem to feel that people who fight for progress, who are pioneers, aren’t allowed to ask those questions. For some reason questioning a mission is a sin and an admission of defeat. It is not.

I wrote before about using cancer. Using it to re-prioritize, to take a break. While I had hoped that my using cancer days were done, I find myself again facing that re-prioritization. This chemo is tougher than the last. I find it harder to concentrate. I have less stamina. Where the last chemo regime resulted in keynotes and a MOOC, this one is focused on treatment and teaching. This is not a defeat. This is a chance for a professional break and a useful distance. Rather than pumping out the next keynote, I can listen. Rather than pushing out a paper I can read beyond libraries. This is a necessary pause. I have had them before after the closing of AskERIC and after virtual reference went from hot topic to standard service. But that time lead to participatory librarianship and the Atlas. It allowed me to look deeper.

A pioneer and a professional should have a mission and seek to change the world. They will also encounter resistance. They will question the mission and they will question themselves. They will go there. Do not despair. Do not punish yourself for doubt. Do not be afraid to ask how that mission or how that passion will die. Because here is the secret. A good mission and a solid passion will not die easily.

Do you want to know the answer to how this cancer will kill me? It will kill me if I do nothing. It will kill me if I ignore it or if I feel the price of the fight is greater than the price of death. It is not. Changing the world is hard. The cost of the mission is high. It is only reasonable to ask how high and you can only know that answer if you honestly assess the cost of failure. If that cost becomes too dear, then perhaps you were meant to change the world another way.

Illinois Librarians Join NOW

Excuse the location based post, but ILEAD U is the best continuing education programs going. I encourage Illinois librarians to join up:

2014 ILEAD U Applications: Deadline Extended! Due Friday, February 14, 2014

The State Library will host ILEAD U: Illinois Libraries Explore, Apply and Discover, The 21st Century Technology Tools Institute for Illinois Library Staff at the University of Illinois Springfield on March 24-27, June 23-26 and October 27-30, 2014.

The ILEAD U Steering Committee is looking for participants, mentors and instructors to implement web technologies that foster community participation as well as develop leadership, innovation and positive change. Project ILEAD U will encourage both the experimentation with and building of participatory Web services and programs.

Do you have a technology skill or knowledge of technology tools? Be an instructor! Want to learn? Be a participant! Want to facilitate in a team environment? Be a mentor!

Applications are now available for PARTICIPANTS, INSTRUCTORS, and MENTORS until February 14, 2014, at http://www.webjunction.org/documents/illinois/ileadu/ileadu-applications.html.

Interested but single and looking for a team? Please visit https://www.surveymonkey.com/s/join-ILEADU to send your information and we will generate a list of potential team members.

An archive recording of the Statewide Day of Application webinar that was held December 4 is available online.

Teams that applied by the original due date will be notified about your applications by January 31, 2014.

For questions, please contact Project Director Gwen Harrison at [email protected], 217-785-7334 or Assistant Project Director Sandra Fritz at [email protected], 217-558-2064.