March 16, 2023

Tactics for Surviving Nervous Times


Today in a guest blog post on, I wrote about tactics for surviving nervous times:

“For starters I engage in the power of realistic thinking. March 18th is my six-month check up, at which I’ll learn the status of two tumors perched on my jugular vein. Of course I’m afraid that my tumors have grown. Who wouldn’t be? And, when I get real with myself about how truly hard this waiting game is, I feel surprisingly better. The same is true for the majority of patients interviewed in my book.

A meditation teacher once gave me this instruction: When a thought enters your mind don’t slam the door on it. Notice it. Gently say to yourself ‘Oh, I’m thinking,’ then come back to focusing on your breath. I do the same with worry too. ‘Oh, I’m worrying again. Right, tumors are scary business.’ Then I go back to folding laundry, writing a chapter, or walking my dog with much less stress than if I were sweeping my fears under the rug of denial.”

I was also sure to mention additional tactics like consuming copious amounts of raw cookie dough, crying on Shannon’s shoulder, and calling my mom at 3 AM.

Whether you have cancer or not, what are your tactics for slugging through nervous times - like worrying about a family member, or managing economic uncertainty? Is it true for you that acknowledging your fear sometimes makes it easier? Or does it do the opposite for you?

Post to Twitter Post to Facebook

March 13, 2023

Butthole Surfers

Some will fall in love with life
And drink it from a fountain
That is pouring like an avalanche
Coming down the mountain

I wanted to use this quote as the first page of my new book, but then I thought better of it. If you had never heard of this band, cracked open a book and saw the words “Butthole Surfers”, you might be slightly deterred.

The song has nothing to do with cancer and is a pretty harsh reality check about young people dying. So why do I love it so much? First, the music is an incredible receptacle for the of non-verbal, physical angst that piles up in my body, like right now as I’m only six days away from my check up. Blasting this song and dancing in my living room is an essential in my repertoire of fidgety distractions.

Secondly, I love the combined images of swallowing up life and having it cave out from underneath you. Avalanches are the most accurate depiction I have ever seen of what it feels like to be diagnosed with cancer as a young adult. You are sailing along, and it is not that you trip, or fall, it is that the entire face of the mountain you are on crumbles away beneath your feet and you go flying with it. Forget chanting or peaceful meditation; watching the intensity of avalanche videos just feels down right healing to me. Step away from the You Tube!

Do you have a cancer anthem song? What symbols, images, or metaphors do you relate to that describe your cancer experience or what it means to be a “survivor”?

Post to Twitter Post to Facebook

1 comment
March 10, 2023

What Would You Tell A Newly Diagnosed Patient?


Flirting in Bars

In today’s Huffington post I talk about 20 and 30-something cancer patients cramming for finals, flirting in bars, climbing the first rung on our career ladder, and changing stinky diapers.

In my interview with Christine Hassler she asks: If you had one thing to share with recently diagnosed 20 and 30 somethings that you wish you had been told, what would it be?

My Response

You do not have to become a glittery superhero in order to fight adversity. Cancer is hard stuff. Strength comes from being real. Allow yourself to sometimes feel vulnerable and to have meltdowns. They do not last forever and you may even feel invigorated afterwards.

Secondly, the definition of hope is fighting for your best care. Cancer is not only emotional and physical, it is administrative too and the burdens of paperwork can really impede our healing. Many hospitals have patient representative services or ombudsmen. If after your second try you are unsuccessful at getting records, obtaining procedural approval, or resolving a financial matter, have one of these professional advocates intervene on your behalf. Think, question, and shout when you need to.

What is one thing you would share with newly diagnosed cancer patients that you wish you had been told?

Post to Twitter Post to Facebook

1 comment
March 09, 2023

Should You Write A Cancer Book? #2
Writing Mentors


A Chronic Dose
Laurie Edwards wrote a great post today about mentors on her chronic illness blog A Chronic Dose. An excerpt reads: “Persistence is a huge component of success in any field, but having people who are willing to share their time and expertise is, I’d argue, just as valuable. For as long as you keep evolving personally and professionally, I think you never outgrow the value of a mentor.”

For the second post in my ‘Should You Write A Cancer Book?’ series I want to look at the issue Laurie raised of mentorship and writing.

Confessions of a Novice
Many authors of young adult cancer books were journalists, editors, or freelance writers prior to their diagnosis. But what if you are thinking about writing a cancer book and have no background in the field of writing or publishing? How do you learn to write? Who are your mentors?

I was a choreographer when I was diagnosed with cancer at age 27. As an undergrad, I had taken one semester of creative writing from a sweet but utterly unconstructive professor. To this day, that class is the extent of my formal writing training. Yet, a few weeks ago a large sized publishing house just released my first book Everything Changes: The Insider’s Guide To Cancer in Your 20s and 30s. Many mentors have gotten me to this stage in my new writing career, some more obvious than others.

My Big Three
1. My public high school English teacher Mrs. Kogut was an old fashioned type who wore a wool skirt suit and heels to work everyday. She docked one percentage point off of our papers for each grammatical or usage error. Everyone hated her. I ate her class up. She taught me the value of rules in writing.

2. My Dad and Strunk and White go hand in hand. My dad gave to me as a Chanukah present one year Strunk and White’s book The Elements of Style (glamorous huh?) My dad is a mechanical engineer. He is interested in efficient and sound construction, and latched on to a Strunk and White dictum: omit needless words. This is my top writing mantra.

3. Michael Denneny is a 35-year veteran senior editor from St. Martin Press, whose real life experience backed up the mentoring advice he gave me. The rejections my agent received from the first few publishing houses on my manuscript for Everything Changes could have been used as endorsement quotes on the book jacket: “Gripping stories.” “Excellent writing.” “Could not put it down.” Always followed by, “I’m sorry our publishing house cannot take your book. Our sales department feels that cancer does not sell.” Michael Denneny is responsible for getting published the first books ever written on HIV and AIDS. Following his lead, I never gave up on my mission to get one of the big publishers to believe in the need for, and the salability of, a guidebook for twenty and thirty somethings facing cancer. Michael and I were right. Many Barnes and Noble and Borders are selling my book faster than they can stock the shelves.

Writing Chops
Formal training is something missing from my resume– MFAs in Creative Writing or Masters in Journalism were not in my schedule or my budget after my cancer diagnosis.  Working in the vacuum of self-education often feels freeing because I don’t know what or who I’m up against: ignorance is bliss.  At other times, I’ve needed to grab a mentor because I’ve felt lost without a map.  In upcoming posts in my ‘Should You Write A Cancer Book Series’, I’ll investigate other ways to brush up our writing chops. Until then:

Have you ever formally studied writing? Who are your writing mentors or inspirations? If you do not have any writing mentors, where would you look for them and who would you ask? Are there any bloggers or authors of books on writing who you consider your mentors?

Post to Twitter Post to Facebook

March 09, 2023

Young Adult Clinical Trials 101 on the Stupid Cancer Show


The Flat Line
Most of us were either not born, sporting pampers, or wearing size 6X bell bottoms and Holly Hobby dresses when Nixon declared war on cancer. Since then, five-year cancer survival rates for peds and older cancer patients have risen steadily. However, survival rates for young adult cancer patients have seen zero improvement.

One of the culprits is our lack of access to health insurance (see my young invincibles schpeil!) But, another huge factor is our lack of access to clinical trials. Clinical trials study new and promising cancer treatments, providing access to cutting edge medication well before they are released on the market. Ready for another shocking statistic? Sixty-percent of pediatric patients participate in clinical trials. Yes, 60%. Only 1-2% of twenty and thirty-something patients participate in clinical trials.

Only now is the first ever large-scale clinical trial being designed to study a particular cancer type in young adult patients. This means that all of the cancer drugs that are infused or beamed up into our 20 and 30-something cancer ridden bodies have only been studied on folks the age of our parents and grandparents. Why is this a big deal? Their bodies are drying up, they have no periods, different hormone levels, and are experiencing middle and end of life health changes.

Life Saving Juice
While researching my book Everything Changes, I ate up Dr. Archie Bleyer’s study on barriers to clinical trial participation for young adult cancer patients. It may sound dry and boring, but this is actually the juicy information that can help extend our lives.

Listen tonight to the Stupid Cancer Show, at 9 PM EST when co-host Matthew Zachary and I will be talking about Young Adult Clinical Trials 101 with clinical trial experts Deborah Vollmer Dahlke and Ellen Coleman.

Have you ever participated in a clinical trial? What was that like? Have you wanted to participate in a clinical trial but it didn’t pan out for you? If so, what were the obstacles? What questions about clinical trials would you like me to ask our guests on the show tonight?

Post to Twitter Post to Facebook

March 04, 2023

Naked Cancer


In The Buff
I’ve been blogging and thinking about cancer and moms this week since my Monday night Stupid Cancer Show interview with Pat Taylor, filmmaker and the mother of a young adult cancer patient.

Today I dug up an outtake from my book, an excerpt from a conversation I had with young adult cancer survivor Chrissy Coughlin about moms. It opened up a different avenue of thought about nudity and cancer care. Here’s Chrissy:

“It was definitely strange when my mom was taking care of me and seeing me unclothed. But then I just got to the point where I felt very comforted by the care. It was like a job for her too. She had to do a lot of work and we had a little system down and you just kind of get over it. At first you’re like, “I don’t want you to see my boobies!” and then you just get over it. You just realize the most important thing is you have a mother there who cares about you that much to be able to help you in that way.”

I could totally relate to Chrissy. I felt the exact same way as I got used to my mom bathing me after surgery and when I was exhausted during treatment. But what about friends seeing me naked?

During treatments my sweat became radioactive. I was in isolation for five days and had to scrub myself down in the shower like the scene from Silkwood. It was exhausting. The day my isolation ended, I was too tired to shower. My friend Loren filled a pot and helped sponge bathe me while I sat on a towel on my living room floor. There was also a time when I was so feeble, my friend Anthony helped me to walk to the bathroom and get on and off the toilet. He stood a few feet away with his back turned while I peed.

In my work as a modern dancer and choreographer, I was used to quick costume changes in make shift dressing rooms crowded with men and women. I also lived in crunchy Boulder” for a while, where it ain’t no thang to strip down naked and hop in a hot tub at a party. I think this made it a bit easier for me to be naked in front of some of my friends during cancer.

Have you ever had to be naked in front of friends and family so they could care for you? What was it like? Did it flip you out? Comfort you? Are you any more or less modest since cancer?

Post to Twitter Post to Facebook

March 02, 2023

Vicodin Earrings

Surfing online, I came across this great work by 20-something Becky Stern. It is an embroidery from an MRI of her kneecap. On her website I found earrings she made out of Vicodin, a plush stuffed animal-like version of her femur, and a copper band aid. I was captivated and interviewed her a bit more about her art.

Q: What medium do you like to work in the most?
A: I don’t have a favorite medium. I tend to prefer craft processes, but
also dabble in electronics.

Q: What subject matter fascinates you?
A: I’m really interested in our relationships with technology. A lot of
my work draws this. I also think it’s really neat how low tech things
like knitting can relate to digital images (stitches and pixels,

Q: So what was up with your leg? Why did you have surgery?
A: I have bad genetic knee anatomy. My shallow femur grooves mean that my
kneecaps dislocate a lot. This time it took out a piece of cartilage
with it. It felt like there were shards of glass inside my knee before
the surgery.

Q: Some people would be grossed out by pics of their surgery. Seems like you are not. Have you always had a strong stomach?
A: My first knee surgery was when I was 8. I had another when I was 14.
So I guess you could say it grew on me. I’ve never liked it when
doctors could see parts of my body that I couldn’t, so I just ask them
for a copy of my MRIs, x-rays, surgery pictures, etc. I even have my
wisdom teeth and knee screws (that had to be removes) in an envelope.
The pictures from this last one do gross me out a little bit, but I
like to play on the grossness factor a bit in my work. The plush femur
is cute and at the same time gross.

Q: Do you plan to make other medically related pieces?

A: I’ve been working on a series of embroideries from my MRI images, and
I’ve made some band-aid earrings as well as some earrings made from my
leftover Vicodin tablets (I can’t take the stuff, it turns out it
makes me sick).

What about you guys reading this post? Do you ever have daydreams, real schemes, or actual artwork, plays, films, sculptures that you’ve made about your illness? Have you seen other illness related artwork that has stayed in your mind? Any work by young adult cancer patients?

Post to Twitter Post to Facebook

March 02, 2023

Parental Low Down and Stupid Cancer Show


Wake Up Call

I call my mom in the middle of the night when I cannot sleep. She is always there to answer no matter how groggy she is or how early she needs to drag herself out of bed the next morning. We’ve always loved each other but were not always close like this, especially when I was younger and got caught stealing make-up from G.C. Murphey’s drug store on the day of my Sunday school confirmation. Or when I dropped out of Columbia University to study with modern dance choreographers around the country.

So what has changed? Is it that I’m less bratty now that I’ve gotten my teenage and early twenties angst out of my system? Is it that she is more laid back now that I’ve matured? Or did my young adult cancer diagnosis bring us closer together? During surgery and treatment, she spent weeks in my shabby (not so chic) studio apartment, crashed out on a futon on the floor. And while we are closer now than ever before, there are still parts of my cancer experience that we have a hard time talking about. Only recently did she confess to me some of her challenges in taking care of me during that time.

Chime In

I’ll be blogging more about cancer and our parents in the next couple of weeks. But for starters listen and call in tonight to the Stupid Cancer Show, (347) 215-6845, at 9 PM EST when Matthew Zachary and I will be talking with Pat Taylor, digging up the inside scoop on being the mom of a young adult with cancer. Pat made a documentary film about young adult cancer, called Chasing Rainbows. Check it out here.

Has cancer changed your relationship to your mom, dad, or other close family member? What issues/questions would you like to see discussed about this in upcoming blogs? Maybe I’ll bring my mom on as a guest expert!

Post to Twitter Post to Facebook

1 comment