Benjamin Rubenstein's Blog, page 9
October 11, 2015
From Awareness to Acceptance in Two Months: MFA Bound
I apologize to you, my awesome readers, for writing infrequently the past two months. This is why, with some added fiction because, well, it fits.
July 23: I tell JD I’m thinking about becoming a part-time barista so I can write more.
I am dedicated to my health and fitness and full-time job, the latter of which I care for less than writing. Dammit, integrity.
Over the last decade I authored two books. I have spent my time writing, marketing, taking marketing classes, speaking, receiving training in public speaking, starting a company, and creating a super-sweet spreadsheet to track my inventory and expenses. In exchange I have sacrificed or neglected undergraduate grades, video games, television and pop culture, dating, probably friends, and definitely the news besides staying updated on everything related to Miley Cyrus. Unless I experiment with polyphasic sleep, I have no more time for my true passion.
JD says, “I'd be happy to sit down and discuss your future plans. For what it's worth, I think it's something that would make you happy and help you to focus on what means the most.”
July 25: I meet with the Whiskeys over some whiskey to pick their brains on how to accelerate my writing skills. Mr. Whiskey is also a writer and even attended Viable Paradise, a prestigious writing workshop. Mrs. Whiskey is currently working towards her MBA. They know shit.
I take notes as we discuss and compare a master’s in literature, writing classes and workshops like those offered at the Writer’s Center in Bethesda, and a master’s of fine arts in creative writing. I tire of taking notes and Mrs. Whiskey continues for me. She also writes all the books I should read, and draws pictures.
Our brainstorming leads me to conclude that a two-year low residency MFA program is perfect for me. This would allow me to rapidly learn and improve my writing, work towards a goal (a master’s degree), and stay in the Washington, D.C., area, except during the two-week residency each semester which is either on the university campus or in Europe. And in D.C., there’s always a new Starbucks that is hiring part-time workers.
July 29: I spend hours at Starbucks to study baristas and low residency MFA programs. I create a new super-sweet spreadsheet to track programs and their rankings, costs, requirements and application deadlines. I filter out any program that requires applicants to submit GRE scores. I don’t have time or intelligence for that shit.
Mr. Whiskey connects me with his friend who graduated from the Stonecoast MFA at the University of Southern Maine. “I spent two years at Stonecoast's low residency program, got my MFA, and had an utterly delightful time,” she emailed me.
Stonecoast’s website, faculty, and nearby breweries are so welcoming. That is my number one choice with everywhere else a distant second. The application deadline is September 15. I have seven weeks to write a super-sweet 15+-page short story. Ready, set, go!
Sept. 1: I finish my first draft and send it to Mr. Whiskey who will review it for me. “Took me forever and taught me that I know nothing about writing,” I emailed Mr. Whiskey.
Have you ever begun doing something without having learned the proper way how, and you continued doing it and improving? That is how I became a writer. When I was 20 the idea to write a book flew into my head and like a bird stuck in a chimney, it wouldn’t leave.
I’ve been writing for 11 years and will continue writing forever but I can’t describe how; I don’t know the basic writing techniques that all graduate-level writing students probably learned when they were small children.
I don’t believe I will get into Stonecoast, a top four ranked low residency program in the country.
Sept. 14: I complete my short story after days of back and forth with Mr. Whiskey. I really owe him lots of whiskey. I also complete my two shorter essays and online application. Just before Rosh Hashanah dinner, at 6:01 p.m., I email my materials to Stonecoast’s admissions department. “Thank you for your consideration. I can't wait to be a student at the University of Southern Maine,” I write.
Sept. 25: I list other programs to apply to that all have an application deadline of September 30. My literary agent is leaving the country and won’t be able to submit her letter of recommendation through the schools’ online systems. Ahhh!
My phone beeps. I have an email which I open and read. “After reviewing your application, the Stonecoast faculty believes you have the talent and drive necessary to succeed as a writer. We feel strongly about your work and about your ability to take advantage of the unique opportunities offered by a Stonecoast education. We look forward to the possibility of welcoming you to our community of writers.”
I temporarily black out from excitement and shock and when I revive, I scream non-English sounds at my dad who is next to me driving.
I begin at the Stonecoast master’s of fine arts in creative writing program, in fiction, at the University of Southern Maine on January 8. Over two years that will include five residencies in Portland, Maine, and possibly Ireland, I will probably get kicked out of many coffeeshops for “camping,” especially if I camp on the job when I become a barista. I am MFA bound. Ready, set, go!
July 23: I tell JD I’m thinking about becoming a part-time barista so I can write more.
I am dedicated to my health and fitness and full-time job, the latter of which I care for less than writing. Dammit, integrity.
Over the last decade I authored two books. I have spent my time writing, marketing, taking marketing classes, speaking, receiving training in public speaking, starting a company, and creating a super-sweet spreadsheet to track my inventory and expenses. In exchange I have sacrificed or neglected undergraduate grades, video games, television and pop culture, dating, probably friends, and definitely the news besides staying updated on everything related to Miley Cyrus. Unless I experiment with polyphasic sleep, I have no more time for my true passion.
JD says, “I'd be happy to sit down and discuss your future plans. For what it's worth, I think it's something that would make you happy and help you to focus on what means the most.”
July 25: I meet with the Whiskeys over some whiskey to pick their brains on how to accelerate my writing skills. Mr. Whiskey is also a writer and even attended Viable Paradise, a prestigious writing workshop. Mrs. Whiskey is currently working towards her MBA. They know shit.
I take notes as we discuss and compare a master’s in literature, writing classes and workshops like those offered at the Writer’s Center in Bethesda, and a master’s of fine arts in creative writing. I tire of taking notes and Mrs. Whiskey continues for me. She also writes all the books I should read, and draws pictures.
Our brainstorming leads me to conclude that a two-year low residency MFA program is perfect for me. This would allow me to rapidly learn and improve my writing, work towards a goal (a master’s degree), and stay in the Washington, D.C., area, except during the two-week residency each semester which is either on the university campus or in Europe. And in D.C., there’s always a new Starbucks that is hiring part-time workers.
July 29: I spend hours at Starbucks to study baristas and low residency MFA programs. I create a new super-sweet spreadsheet to track programs and their rankings, costs, requirements and application deadlines. I filter out any program that requires applicants to submit GRE scores. I don’t have time or intelligence for that shit.

Stonecoast’s website, faculty, and nearby breweries are so welcoming. That is my number one choice with everywhere else a distant second. The application deadline is September 15. I have seven weeks to write a super-sweet 15+-page short story. Ready, set, go!

Have you ever begun doing something without having learned the proper way how, and you continued doing it and improving? That is how I became a writer. When I was 20 the idea to write a book flew into my head and like a bird stuck in a chimney, it wouldn’t leave.
I’ve been writing for 11 years and will continue writing forever but I can’t describe how; I don’t know the basic writing techniques that all graduate-level writing students probably learned when they were small children.
I don’t believe I will get into Stonecoast, a top four ranked low residency program in the country.
Sept. 14: I complete my short story after days of back and forth with Mr. Whiskey. I really owe him lots of whiskey. I also complete my two shorter essays and online application. Just before Rosh Hashanah dinner, at 6:01 p.m., I email my materials to Stonecoast’s admissions department. “Thank you for your consideration. I can't wait to be a student at the University of Southern Maine,” I write.
Sept. 25: I list other programs to apply to that all have an application deadline of September 30. My literary agent is leaving the country and won’t be able to submit her letter of recommendation through the schools’ online systems. Ahhh!
My phone beeps. I have an email which I open and read. “After reviewing your application, the Stonecoast faculty believes you have the talent and drive necessary to succeed as a writer. We feel strongly about your work and about your ability to take advantage of the unique opportunities offered by a Stonecoast education. We look forward to the possibility of welcoming you to our community of writers.”
I temporarily black out from excitement and shock and when I revive, I scream non-English sounds at my dad who is next to me driving.
I begin at the Stonecoast master’s of fine arts in creative writing program, in fiction, at the University of Southern Maine on January 8. Over two years that will include five residencies in Portland, Maine, and possibly Ireland, I will probably get kicked out of many coffeeshops for “camping,” especially if I camp on the job when I become a barista. I am MFA bound. Ready, set, go!



Published on October 11, 2015 16:21
September 25, 2015
I’ve Been Arrogant for 15 Years and Now I Atone
As published on Gather the Jews
It is Yom Kippur, the Day of Atonement. In synagogue I recited one of the most important prayers Jews read each year called viddui, or the confession. Al chet she-cha-tanu l’fanecha. For the sin we have committed against you.
There are many sins. One stood out to me.
“. . .The sin we have committed against You by our arrogance. . .
For all these sins, O God of mercy, forgive us, pardon us, grant us atonement!”
* * * * *
I distributed stickers of my Instagram character named Cancerslayer to the sticker-hungry children who visited my table. “Cancerslayer fights illness by day and bad guys by night!”
I stood at my Cancerslayer table at CureFest on the National Mall and talked about my Cancer-Slaying Super Man books, which I displayed along with information on how to purchase them. “My memoirs are about how I survived childhood cancer twice by believing I was superhuman,” I said to interested visitors.
My table was wedged between two nonprofits that raise awareness and research money for childhood cancer. The two nonprofits’ founders were present to represent their organizations. The three of us talked to each other and also to cancer victims and their family members who attended CureFest and visited our tables. Each nonprofit founder sat and listened to me repeatedly share a concept that I have embraced since my first diagnosis almost exactly 15 years ago: Cancerslayer is the attitude that has helped me survive and thrive. Keep reading I’ve Been Arrogant for 15 Years and Now I Atone.
It is Yom Kippur, the Day of Atonement. In synagogue I recited one of the most important prayers Jews read each year called viddui, or the confession. Al chet she-cha-tanu l’fanecha. For the sin we have committed against you.
There are many sins. One stood out to me.
“. . .The sin we have committed against You by our arrogance. . .
For all these sins, O God of mercy, forgive us, pardon us, grant us atonement!”
* * * * *

I stood at my Cancerslayer table at CureFest on the National Mall and talked about my Cancer-Slaying Super Man books, which I displayed along with information on how to purchase them. “My memoirs are about how I survived childhood cancer twice by believing I was superhuman,” I said to interested visitors.
My table was wedged between two nonprofits that raise awareness and research money for childhood cancer. The two nonprofits’ founders were present to represent their organizations. The three of us talked to each other and also to cancer victims and their family members who attended CureFest and visited our tables. Each nonprofit founder sat and listened to me repeatedly share a concept that I have embraced since my first diagnosis almost exactly 15 years ago: Cancerslayer is the attitude that has helped me survive and thrive. Keep reading I’ve Been Arrogant for 15 Years and Now I Atone.



Published on September 25, 2015 05:04
August 14, 2015
I Hope They Allow Crutches in Hell
As published on The Ulman Cancer Fund for Young Adults
Crutching is a great way to help injuries heal and bypass the lines at Disney World, and able-bodied individuals may treat crutchers with kindness. If you use crutches and think people are nice to you only because they consider you weak, and you must prove your strength until your death by always taking the challenging path through life, then follow these steps.
On the Washington, D.C., Metro, people will ask, “Do you want my seat?” Don’t let them snatch your completely irrational pride. You need to stand on one leg while holding crutches with one hand and the pole with the other as the train jerks and halts. There are several ways to respond to this offer:
The polite way: “No, thanks.”
The jerk way: “I’M NOT TAKING YOUR SEAT!”
The 16-year-old boy way: “I only sit for lap dances.”
When you reach the sidewalk you must speed-crutch so people think you’re crazy and intimidating instead of weak. Your loud crutch tips and long, quick, repetitive strides will make you sound like a galloping horse. You will quickly pass pedestrians walking in the same direction, though they will hear your approach for hundreds of steps. Here, you should politely say, “ON YOUR LEFT!” when you are 50 feet behind them, as a warning. For individuals who are hard of hearing, you should scream directly into their left ears when you are next to them. Since you won’t know who is and isn’t impaired, do both every time. Keep reading I Hope They Allow Crutches in Hell
* * * * *In the Media
Tom Coccagna interviewed me on his "Living With…" podcast. You can hear our awesome hour-long discussion (also available on iTunes, Soundcloud and Stitcher).
Crutching is a great way to help injuries heal and bypass the lines at Disney World, and able-bodied individuals may treat crutchers with kindness. If you use crutches and think people are nice to you only because they consider you weak, and you must prove your strength until your death by always taking the challenging path through life, then follow these steps.
On the Washington, D.C., Metro, people will ask, “Do you want my seat?” Don’t let them snatch your completely irrational pride. You need to stand on one leg while holding crutches with one hand and the pole with the other as the train jerks and halts. There are several ways to respond to this offer:
The polite way: “No, thanks.”
The jerk way: “I’M NOT TAKING YOUR SEAT!”
The 16-year-old boy way: “I only sit for lap dances.”
When you reach the sidewalk you must speed-crutch so people think you’re crazy and intimidating instead of weak. Your loud crutch tips and long, quick, repetitive strides will make you sound like a galloping horse. You will quickly pass pedestrians walking in the same direction, though they will hear your approach for hundreds of steps. Here, you should politely say, “ON YOUR LEFT!” when you are 50 feet behind them, as a warning. For individuals who are hard of hearing, you should scream directly into their left ears when you are next to them. Since you won’t know who is and isn’t impaired, do both every time. Keep reading I Hope They Allow Crutches in Hell
* * * * *In the Media
Tom Coccagna interviewed me on his "Living With…" podcast. You can hear our awesome hour-long discussion (also available on iTunes, Soundcloud and Stitcher).



Published on August 14, 2015 13:30
July 13, 2015
Hi Mom, I Got a Tattoo!
As published on Gather the Jews
Hi Mom,
Please sit so you don’t keel when you read this, and remember to inhale and then exhale, in that order: I got another tattoo.
I know you thought my final would be the survivor tumor tattoo I received three years ago, or even the tattoo dots I received before my radiation 14 years ago. I know that you, Dad, and ten percent of women like me exactly how I am. Please let me explain my tattoo and then you will love it like I do.
In Judaism, we use trees to celebrate holidays, weddings and births. I love
consuming food and booze on holidays, and Mom, your other son just got married and maybe he’ll have a child. (No pressure, JD.)
Rabbis debate the species of the Tree of the Knowledge of Good and Evil in the Garden of Eden. One opinion is that the Tree of Knowledge was a fig tree and that after the sin, Adam and Eve knew they were naked and sewed fig leaves to make girdles, meaning they used the very object that caused their downfall to correct the mistake. The very drug—Cytoxan—that killed my first cancer caused my second cancer, and then killed the second cancer, too.
We attain wisdom by learning intellectually or through life experience. I hate myself when I make a mistake: make the wrong decision, say the wrong thing, fail to approach a woman because I fear rejection, eat a single chocolate when I hadn’t planned to. The fig tree symbolizes that I can make a mistake and bounce back and grow from it. Very few mistakes cannot be reversed (besides getting a bad tattoo). Keep reading Hi Mom, I Got a Tattoo!
*****Updates
I built a new online store within this blog that makes it simple to buy all my products including my books and stickers of Cancerslayer. The stickers are two inches wide by three inches tall on a white background with gloss paper.
Hi Mom,
Please sit so you don’t keel when you read this, and remember to inhale and then exhale, in that order: I got another tattoo.

I know you thought my final would be the survivor tumor tattoo I received three years ago, or even the tattoo dots I received before my radiation 14 years ago. I know that you, Dad, and ten percent of women like me exactly how I am. Please let me explain my tattoo and then you will love it like I do.
In Judaism, we use trees to celebrate holidays, weddings and births. I love
consuming food and booze on holidays, and Mom, your other son just got married and maybe he’ll have a child. (No pressure, JD.)

We attain wisdom by learning intellectually or through life experience. I hate myself when I make a mistake: make the wrong decision, say the wrong thing, fail to approach a woman because I fear rejection, eat a single chocolate when I hadn’t planned to. The fig tree symbolizes that I can make a mistake and bounce back and grow from it. Very few mistakes cannot be reversed (besides getting a bad tattoo). Keep reading Hi Mom, I Got a Tattoo!
*****Updates
I built a new online store within this blog that makes it simple to buy all my products including my books and stickers of Cancerslayer. The stickers are two inches wide by three inches tall on a white background with gloss paper.



Published on July 13, 2015 20:48
June 22, 2015
I Remember Rachel for Her Ferocity for Life, Not Cancer
I first wrote about my amazing friend Rachel "Lings" Yingling three years ago, and today likely won't be the last time. She was among the best and my favorite people I have met. Besides her inexplicably odd-shaped feet which she didn't mind showing off, we could all benefit from acquiring her characteristics: passionate, positive, resilient, adventurous, alive. Fiercely alive.
This is for Rachel.
As published on The Huffington Post
The skeet whooshed towards the heavens. My right eye stared ahead with the barrel flush. I had developed a rhythm with the saucer: After it launched I waited until it reached a precise point in my field of vision and then I pulled the trigger. Without patience, my aim would be low and the saucer would continue its original trajectory until it fell to the ground. So I waited and then, click, the target erupted, its orange pieces blending with the sky like a perfect match on the color wheel.
I hit 11 of 25 skeets. My friend Rachel, who I'm sure shot guns growing up based on my generalization of people from Arkansas and who say things like, "My drinking water had tadpoles," only shot two. She hit her first, missed the next 23, and ended with a bang. Rachel sat against a rock and watched others in our group shoot. She smiled and now said things like, "I have not spent time outside in days. It is beautiful."
There was not a cloud above us and Rachel, a Fulbright scholar, began telling me a story about the sky. If people had never been told the sky was blue then they may see it as white, another color, or simply a void. Those people may have as much trouble wrapping their heads around the blue sky as I have around not seeing it as blue.
I can't see Rachel in a different light, either. When I met her 2.5 years ago I saw a radiant and beautiful 27-year-old whose attitude matched her use of exclamation points. She told me stories back then, too, like the meaning of interrobang, which is a combination of an exclamation point and a question mark, and how she was diagnosed at 26 with stage 3 colon cancer that would later spread to her ovaries and omentum, "upgrading" the cancer to stage 4. Rachel would stay on treatment forever, in a concept that is new to me and the way I had "finished" cancer treatment when I was a teen: Rachel was living with cancer. Keep reading I Remember Rachel for Her Ferocity for Life, Not Cancer.
This is for Rachel.
As published on The Huffington Post

I hit 11 of 25 skeets. My friend Rachel, who I'm sure shot guns growing up based on my generalization of people from Arkansas and who say things like, "My drinking water had tadpoles," only shot two. She hit her first, missed the next 23, and ended with a bang. Rachel sat against a rock and watched others in our group shoot. She smiled and now said things like, "I have not spent time outside in days. It is beautiful."
There was not a cloud above us and Rachel, a Fulbright scholar, began telling me a story about the sky. If people had never been told the sky was blue then they may see it as white, another color, or simply a void. Those people may have as much trouble wrapping their heads around the blue sky as I have around not seeing it as blue.
I can't see Rachel in a different light, either. When I met her 2.5 years ago I saw a radiant and beautiful 27-year-old whose attitude matched her use of exclamation points. She told me stories back then, too, like the meaning of interrobang, which is a combination of an exclamation point and a question mark, and how she was diagnosed at 26 with stage 3 colon cancer that would later spread to her ovaries and omentum, "upgrading" the cancer to stage 4. Rachel would stay on treatment forever, in a concept that is new to me and the way I had "finished" cancer treatment when I was a teen: Rachel was living with cancer. Keep reading I Remember Rachel for Her Ferocity for Life, Not Cancer.



Published on June 22, 2015 19:51
June 15, 2015
Biggest, Baddest, Raddest Wedding: My Bro Got Married
I didn’t dance with that pretty girl nearly enough. I missed seeing the bouquet toss, cake-cutting, mother-son and father-daughter dances, and my dad hopping on the drums to “Sweet Caroline.”
I accept all these failings because NoCommonSense and I crushed our best men speech that included Hulk Hogan’s theme song.
I have spoken many times to audiences as large as a few hundred about cancer stealing my physical abilities and chunks of my adolescence. Unlike those speeches, the attempted humor-to-realness ratio for our best men speech was a whopping 95 to 5 percent. And unlike all those others, this best men speech weighed on me for days because I had thought I might cry, a terrifying and previously unfathomable possibility.
Thankfully adrenaline ensured I didn’t. I was so relieved when we finished our speech. I said, “Shots!” and a few of us left the banquet room for the bar in the lobby. The bartender said she wasn’t allowed to serve shots.
“But we’re the best men!” I said.
I dont give a fuuuck, I saw her thinking.
We settled with drinks on the rocks.
My relief that we gave a good speech and that I didn’t mewl led to me mostly staying in the lobby for the next three hours of the biggest, baddest and raddest wedding I’ve ever attended. That’s why I missed seeing most of the traditional wedding activities.
JD and I grew up playing the same sports, listening to the same music, and enjoying the same tv shows and movies. Almost everything he enjoyed, I did, too, in part because I envied everything about my big brother and followed his lead.
There is some nature on top of all that nurture, though. Different people consider different types of foods their kryptonite, but for both of us it is candy and only candy. We are both organized and hyper-productive, often speeding through life in order to accomplish what we desire in our short waking hours. Lolo, my new sister-in-law, once noticed that we each stood holding our drinks in identical positions and had wet spots on our shirts in identical places from where our glasses touched.
We are different in ways, too. He has always been more outgoing, quick on his feet and magnetic. I always had a sense that he was my big brother, no matter that as time goes on our three-year difference in age becomes a smaller percentage of the total. I look back to six years ago when we visited NoCommonSense in Hawaii. I am three years older than JD was then, yet it feels like the opposite. I look back further to after my bone marrow transplant when JD was 22, and I still see him then as older than I am now.
We also differed in our ability to retain autobiographical memories. Until a few years ago, my memory was among my best assets. I could recall most every event and detail. I miss that ability, and blame its disappearance on the accumulation of memories, alcohol, restricting my calories (and energy for my brain), and especially cancer treatment.
Now I use tricks to recall and retain memories, which involve all the senses and not just sight and hearing. When I write about cancer treatment, I first think about how the big blue chemo chair felt. On my road trip last month I listened to the new Mumford & Sons album on repeat, and now when I hear “Believe,” visions of the Million Dollar Highway enter my mind.
I forgot to connect my brother's wedding to feeling or song, but I know I’ll never forget how happy JD was. I’m one proud younger brother as my family is now greater. Lolo is also a Redskins fan. That doesn’t add to the greatness; rather, it was a requirement to begin with.
Mazel tov!
I accept all these failings because NoCommonSense and I crushed our best men speech that included Hulk Hogan’s theme song.
I have spoken many times to audiences as large as a few hundred about cancer stealing my physical abilities and chunks of my adolescence. Unlike those speeches, the attempted humor-to-realness ratio for our best men speech was a whopping 95 to 5 percent. And unlike all those others, this best men speech weighed on me for days because I had thought I might cry, a terrifying and previously unfathomable possibility.
Thankfully adrenaline ensured I didn’t. I was so relieved when we finished our speech. I said, “Shots!” and a few of us left the banquet room for the bar in the lobby. The bartender said she wasn’t allowed to serve shots.
“But we’re the best men!” I said.
I dont give a fuuuck, I saw her thinking.
We settled with drinks on the rocks.
My relief that we gave a good speech and that I didn’t mewl led to me mostly staying in the lobby for the next three hours of the biggest, baddest and raddest wedding I’ve ever attended. That’s why I missed seeing most of the traditional wedding activities.
JD and I grew up playing the same sports, listening to the same music, and enjoying the same tv shows and movies. Almost everything he enjoyed, I did, too, in part because I envied everything about my big brother and followed his lead.
There is some nature on top of all that nurture, though. Different people consider different types of foods their kryptonite, but for both of us it is candy and only candy. We are both organized and hyper-productive, often speeding through life in order to accomplish what we desire in our short waking hours. Lolo, my new sister-in-law, once noticed that we each stood holding our drinks in identical positions and had wet spots on our shirts in identical places from where our glasses touched.
We are different in ways, too. He has always been more outgoing, quick on his feet and magnetic. I always had a sense that he was my big brother, no matter that as time goes on our three-year difference in age becomes a smaller percentage of the total. I look back to six years ago when we visited NoCommonSense in Hawaii. I am three years older than JD was then, yet it feels like the opposite. I look back further to after my bone marrow transplant when JD was 22, and I still see him then as older than I am now.
We also differed in our ability to retain autobiographical memories. Until a few years ago, my memory was among my best assets. I could recall most every event and detail. I miss that ability, and blame its disappearance on the accumulation of memories, alcohol, restricting my calories (and energy for my brain), and especially cancer treatment.
Now I use tricks to recall and retain memories, which involve all the senses and not just sight and hearing. When I write about cancer treatment, I first think about how the big blue chemo chair felt. On my road trip last month I listened to the new Mumford & Sons album on repeat, and now when I hear “Believe,” visions of the Million Dollar Highway enter my mind.
I forgot to connect my brother's wedding to feeling or song, but I know I’ll never forget how happy JD was. I’m one proud younger brother as my family is now greater. Lolo is also a Redskins fan. That doesn’t add to the greatness; rather, it was a requirement to begin with.
Mazel tov!




Published on June 15, 2015 21:36
June 2, 2015
Road Trippin' from Denver to Las Vegas in a Chrysler 200: A Picture Story
Read this first: Remembering That One Memorable Trip
I miss the 11 a.m. tour of Balcony House at Mesa Verde National Park by six minutes, resulting in possible catastrophe: after the noon tour, Garmin estimates I will reach the South Rim of the Grand Canyon at sunset instead of with a time cushion. I roar down the two-lane US-160 West with its broken yellow center line, passing all the cars.
I stop for my afternoon coffee, a requirement for this addict. Garmin says I just lost five minutes. Now I pass cars that any other time I would consider too risky. My accelerator pedal lives on or near the floor. This rental Chrysler 200 was built to get me to one of the seven natural wonders of the world while it is still bright enough outside to see.
Then I cross into Arizona and the time changes because the state doesn't observe daylight savings time. Garmin can go ahead and steal a minute here and there because I just gained a virtual hour.
Grand Canyon: too spectacular for adjectives. In this moment I am certain that seeing this is life's purpose and this is why humans have sight and there is nothing else that matters.
*****Months ago my friend Scooter invited me to rock climb with him in Durango, Colorado. Before booking my flights on Frontier, my next-door cubemate at work, Sharknel!, invited me over to see her Google Maps webpage. "Look at all these cool places near Durango! You could take a road trip!"
Sharknel! was and is always right. I listened.
I couldn't drive 1,400 miles and not take tons of photos and video from the car. It was only weird when I angled the camera diagonally—when I looked at the screen it appeared like Garmin and I were driving off the side of cliffs. So here are some of the best moments of my road trip, with me, a Chrysler 200, and many new albums for which I won't share how I acquired though Verizon sent me a letter if that helps you figure it out.
I got through a short tunnel on my way from Fort Collins to Vail and a snow-capped mountain greeted me. My heart just about sank down to my penis.
I couldn't drive the Million Dollar Highway from Telluride to Durango, with its breathtaking views and sheer cliffs, without stopping at one of the overlooks for the most scenic pee of my life.
One of so many vehicles that Garmin and I would pass on US-160 West.
I sat at the Canyon for an hour with my quadsteppers and the rat that I saw scurry by. The rat declined to race me to the bottom.
Instead of paying $38 to sleep near Zion National Park, I paid $200 to stay overnight in Page, Arizona, to first see Antelope Canyon. Warning to potential travelers: Antelope is just a 1.5-hour photo shoot and if you're not into photography, don't visit. Instead, just ask me for the photos of the super cool rock formation.
Do not skip Zion National Park in Utah. It is one of my favorite places: vast and gorgeous like the Grand Canyon, user friendly and simple like a Nicolas Cage film. I completed the second most challenging hike which requires you to hold onto chains to prevent death, though next time I'll do the Angel's Landing trail that several have actually died trying to hike.
I joined fellow hikers at Red Rock Canyon in Las Vegas, though I did not follow them up this currently dry waterfall. He who goes up must eventually come down.
If you research and know ahead of time the few cities with high hotel costs and how to avoid them, and if you have a smartphone to book cheap accommodations on the fly, then road tripping out west can be less expensive than just about any other vacation. That part of our country is special and I had an amazing time exploring. I even recorded my first video on YouTube: The Road Trip Song: Denver to Las Vegas in a Chrysler 200. Hopefully Verizon doesn't send me another letter. Enjoy this video and stay tuned next year for The Road Trip Song: San Diego to Seattle in a Batmobile.
*****Appearances
I'll be speaking at the Gala for Action on Saturday benefiting The Leukemia & Lymphoma Society for the Man & Woman of the Year fundraising campaign.
Saturday, June 6, at 6 p.m.
Asia DC, 1720 I Street NW, Washington, DC
Tickets
I miss the 11 a.m. tour of Balcony House at Mesa Verde National Park by six minutes, resulting in possible catastrophe: after the noon tour, Garmin estimates I will reach the South Rim of the Grand Canyon at sunset instead of with a time cushion. I roar down the two-lane US-160 West with its broken yellow center line, passing all the cars.
I stop for my afternoon coffee, a requirement for this addict. Garmin says I just lost five minutes. Now I pass cars that any other time I would consider too risky. My accelerator pedal lives on or near the floor. This rental Chrysler 200 was built to get me to one of the seven natural wonders of the world while it is still bright enough outside to see.
Then I cross into Arizona and the time changes because the state doesn't observe daylight savings time. Garmin can go ahead and steal a minute here and there because I just gained a virtual hour.
Grand Canyon: too spectacular for adjectives. In this moment I am certain that seeing this is life's purpose and this is why humans have sight and there is nothing else that matters.

*****Months ago my friend Scooter invited me to rock climb with him in Durango, Colorado. Before booking my flights on Frontier, my next-door cubemate at work, Sharknel!, invited me over to see her Google Maps webpage. "Look at all these cool places near Durango! You could take a road trip!"
Sharknel! was and is always right. I listened.
I couldn't drive 1,400 miles and not take tons of photos and video from the car. It was only weird when I angled the camera diagonally—when I looked at the screen it appeared like Garmin and I were driving off the side of cliffs. So here are some of the best moments of my road trip, with me, a Chrysler 200, and many new albums for which I won't share how I acquired though Verizon sent me a letter if that helps you figure it out.
I got through a short tunnel on my way from Fort Collins to Vail and a snow-capped mountain greeted me. My heart just about sank down to my penis.

I couldn't drive the Million Dollar Highway from Telluride to Durango, with its breathtaking views and sheer cliffs, without stopping at one of the overlooks for the most scenic pee of my life.

One of so many vehicles that Garmin and I would pass on US-160 West.

I sat at the Canyon for an hour with my quadsteppers and the rat that I saw scurry by. The rat declined to race me to the bottom.

Instead of paying $38 to sleep near Zion National Park, I paid $200 to stay overnight in Page, Arizona, to first see Antelope Canyon. Warning to potential travelers: Antelope is just a 1.5-hour photo shoot and if you're not into photography, don't visit. Instead, just ask me for the photos of the super cool rock formation.

Do not skip Zion National Park in Utah. It is one of my favorite places: vast and gorgeous like the Grand Canyon, user friendly and simple like a Nicolas Cage film. I completed the second most challenging hike which requires you to hold onto chains to prevent death, though next time I'll do the Angel's Landing trail that several have actually died trying to hike.

I joined fellow hikers at Red Rock Canyon in Las Vegas, though I did not follow them up this currently dry waterfall. He who goes up must eventually come down.

If you research and know ahead of time the few cities with high hotel costs and how to avoid them, and if you have a smartphone to book cheap accommodations on the fly, then road tripping out west can be less expensive than just about any other vacation. That part of our country is special and I had an amazing time exploring. I even recorded my first video on YouTube: The Road Trip Song: Denver to Las Vegas in a Chrysler 200. Hopefully Verizon doesn't send me another letter. Enjoy this video and stay tuned next year for The Road Trip Song: San Diego to Seattle in a Batmobile.
*****Appearances
I'll be speaking at the Gala for Action on Saturday benefiting The Leukemia & Lymphoma Society for the Man & Woman of the Year fundraising campaign.
Saturday, June 6, at 6 p.m.
Asia DC, 1720 I Street NW, Washington, DC
Tickets



Published on June 02, 2015 21:51
May 15, 2015
Remembering That One Memorable Trip
Whenever I fly I recall my first trip to Minneapolis with my parents in March 2003 when I was 19 years old. My life was stalled, I had dropped out of college and cancer was rapidly invading my bone marrow. Though, physically I felt fine. I felt great. I loved that trip and I had life-or-death purpose, or maybe I loved it because I had life-or-death purpose.
We traveled across the country to spend a day at the University of Minnesota Medical Center and speak with Dr. Andre Million. It was one of the top children’s transplant centers and he was one of its rock star transplant oncologists. Minneapolis symbolized hope.
My mom and I teased my dad for his fear of flying. He stared out the window wondering why the wing was slightly bouncing. “That wing is flapping because it’s going to fall off!” he said. Mom and I introduced him to Benadryl after that. I smile thinking of his quizzical expression.
Right now I’m sitting in the airport to begin a ten-day vacation. I’m flying to Denver, renting a car and driving to Vegas, stopping all along the way. My smile has faded as I realize how much time has passed since that 2003 trip. Did I accomplish what my 19-year-old self envisioned?
Road trippin' from Denver to Las Vegas in a Chrysler 200Let’s say one of my books became a bestseller, I accumulated enough wealth to never need to work, and I gave the University of Virginia commencement speech instead of Peyton Manning. Those pretend accomplishments may actually be in descending order of likelihood: lots of books become bestsellers, far fewer earn their authors enormous wealth, and you have to be a sorcerer to overtop Manning for anything.
But none of those would have been as meaningful as searching for the transplant center we hoped would save me. It did. Minneapolis now symbolizes a clean slate, my cleanser, and my ultimate achievement.
I remind myself every day how fortunate I am. I must never forget: the Holocaust, what it is like to suffer with cancer, and what it is like to live with the clarity of life-or-death purpose. I ache for that purpose which is a losing battle. I never want to experience significant illness again, but without it I cannot experience that same purpose.
This vacation has a less meaningful purpose, of course. I just want to see the world and connect with people—some new people, and some old friends. Snooki and I will debate kale versus holy water in Vail. Colossus and I will catch up on the last decade while getting rich on Vegas blackjack tables. And Scooter and I will climb rocks in Durango.
It would take a lot more than Bendaryl to convince my dad to climb mountains with us. Mom and Dad can sit this one out.
We traveled across the country to spend a day at the University of Minnesota Medical Center and speak with Dr. Andre Million. It was one of the top children’s transplant centers and he was one of its rock star transplant oncologists. Minneapolis symbolized hope.
My mom and I teased my dad for his fear of flying. He stared out the window wondering why the wing was slightly bouncing. “That wing is flapping because it’s going to fall off!” he said. Mom and I introduced him to Benadryl after that. I smile thinking of his quizzical expression.
Right now I’m sitting in the airport to begin a ten-day vacation. I’m flying to Denver, renting a car and driving to Vegas, stopping all along the way. My smile has faded as I realize how much time has passed since that 2003 trip. Did I accomplish what my 19-year-old self envisioned?

But none of those would have been as meaningful as searching for the transplant center we hoped would save me. It did. Minneapolis now symbolizes a clean slate, my cleanser, and my ultimate achievement.
I remind myself every day how fortunate I am. I must never forget: the Holocaust, what it is like to suffer with cancer, and what it is like to live with the clarity of life-or-death purpose. I ache for that purpose which is a losing battle. I never want to experience significant illness again, but without it I cannot experience that same purpose.
This vacation has a less meaningful purpose, of course. I just want to see the world and connect with people—some new people, and some old friends. Snooki and I will debate kale versus holy water in Vail. Colossus and I will catch up on the last decade while getting rich on Vegas blackjack tables. And Scooter and I will climb rocks in Durango.
It would take a lot more than Bendaryl to convince my dad to climb mountains with us. Mom and Dad can sit this one out.



Published on May 15, 2015 13:23
May 10, 2015
Join Me Again in Lighting Blood Cancer on Fire
Read the short story below, or skip it and immediately donate to LLS through my Circle of Hope page here.
“I read about this cancer-slayer . . .” the emcee said at last year’s Man & Woman of the Year Grand Finale Gala before announcing that I won an award for having dedicated myself to fighting blood cancers. I was a Man & Woman of the Year candidate and my CancerSlayer fundraising team raised over $50,000 for the Leukemia & Lymphoma Society.
Campaigning was exhilarating, rewarding and, I thought, my one chance to give back. It also required a time commitment akin to a second job, which is why I’ll likely never do it again.
Just like Kristen Stewart after cheating on that dude from Twilight, I have a second chance.
I love LLS and its mission and passionate supporters, so I joined its leadership team. I mentor a wonderful and upbeat fellow survivor as she campaigns for this year’s Man & Woman of the Year. I also raise money for the Leadership Team Circle of Hope.
As a whole leadership team we are trying to raise $100,000. I will not sit at a diner table until my computer battery dies like last year and text, Facebook-message, and email friends asking for donations. I will not put $6,000 on the line, determined to reach my fundraising target no matter what.
I am asking if you’ll help me fight blood cancers. I’m not asking out of desire for personal recognition or a title. I just want to fight fire with fire and you can help us build one gigantic match. Watch this four-minute video with LLS-funded researcher Carl June to see what that match can do.
Together let’s light cancer’s ass up by donating to the Leadership Team Circle of Hope.
Thank you.
-The Cancerslayer

Campaigning was exhilarating, rewarding and, I thought, my one chance to give back. It also required a time commitment akin to a second job, which is why I’ll likely never do it again.
Just like Kristen Stewart after cheating on that dude from Twilight, I have a second chance.
I love LLS and its mission and passionate supporters, so I joined its leadership team. I mentor a wonderful and upbeat fellow survivor as she campaigns for this year’s Man & Woman of the Year. I also raise money for the Leadership Team Circle of Hope.
As a whole leadership team we are trying to raise $100,000. I will not sit at a diner table until my computer battery dies like last year and text, Facebook-message, and email friends asking for donations. I will not put $6,000 on the line, determined to reach my fundraising target no matter what.
I am asking if you’ll help me fight blood cancers. I’m not asking out of desire for personal recognition or a title. I just want to fight fire with fire and you can help us build one gigantic match. Watch this four-minute video with LLS-funded researcher Carl June to see what that match can do.
Together let’s light cancer’s ass up by donating to the Leadership Team Circle of Hope.
Thank you.
-The Cancerslayer



Published on May 10, 2015 20:59
April 22, 2015
How Not to Raise Your Tween Daughter
As published on The Huffington Post
I am the "father" to my nearly-12-year-old bone marrow "daughter." Twelve years ago, I received a bone marrow transplant to treat myelodysplastic syndrome. My bone marrow donor was an anonymous baby girl, whose umbilical cord stem cells had been collected and stored and were then transplanted into me because they closely matched my cells. That baby girl's cells repopulated in my body and I now have her healthy, disease-free and totally female blood. I think of these new cells of mine collectively as my daughter, and I named her Bone Marrow.
Bone Marrow is a young woman now. I knew this day would come. I even tried slowing her white breast cell and other physical developments by taking tamoxifen, so that the boy bone marrows wouldn't get frisky. I stopped that after they caused my erotic dreams with Glenn Beck. Keep reading How Not to Raise Your Tween Daughter.
I am the "father" to my nearly-12-year-old bone marrow "daughter." Twelve years ago, I received a bone marrow transplant to treat myelodysplastic syndrome. My bone marrow donor was an anonymous baby girl, whose umbilical cord stem cells had been collected and stored and were then transplanted into me because they closely matched my cells. That baby girl's cells repopulated in my body and I now have her healthy, disease-free and totally female blood. I think of these new cells of mine collectively as my daughter, and I named her Bone Marrow.
Bone Marrow is a young woman now. I knew this day would come. I even tried slowing her white breast cell and other physical developments by taking tamoxifen, so that the boy bone marrows wouldn't get frisky. I stopped that after they caused my erotic dreams with Glenn Beck. Keep reading How Not to Raise Your Tween Daughter.



Published on April 22, 2015 21:11