Having Conquered Cancer, He Now Makes It Rock

Jim Ebert spent his whole career producing musicians like Madonna and Ice Cube. Now he produces his fellow survivors.

When he was a young man, Virginia native Jim Ebert played gigs around the Washington DC area as a guitarist, keyboardist, and vocalist. However, he soon discovered that producing and mixing music was his true niche. He proceeded to enjoy a career as a multi-platinum record producer, working with a number of famous musicians, including Madonna, Ice Cube, Toni Braxton, and Meredith Brooks.

But Ebert’s career and, indeed, his very life entered a dire situation in 2001, when he was diagnosed with terminal brain cancer. At that time, he received four different medical estimates. The most favorable estimate gave him 7 years to live. The least favorable estimate gave him just 1 year. Such news put him “in a state of mania,” he admits. “I had a two-year-old son, and he was all I could think about.”

Surgery was out of the question, as Ebert’s tumor was considered inoperable. So he embarked on a course of treatment that involved chemotherapy and brain radiation. He never spent any significant period of time as a hospital in-patient, though he was compelled to take short periods of time off from work at the end of each chemotherapy cycle.

By the time his chemo treatment was halfway through, he had already outlasted the one-year survival estimate. Then he proceeded to outlast the other three estimates. And then came the day when a brain scan compelled doctors to give him remarkable news – he had beaten the cancer and its supposed terminal virulence.

At that point Ebert was in a truly grateful mood. He wanted to give back in some way. So, merging his professional skill set with a desire to help people in his former embattled predicament, he established Cancer Can Rock, an organization that provides world-class recording services to musicians with cancer. Ebert credits the assistance of co-founder Bruce Parker, a musician who has fine organizational skills and “good positive energy,” with helping the foundation take off since its inception in 2013.

Jim Ebert formed Cancer Can Rock after beating terminal cancer.

Cancer Can Rock isn’t about seeking a cure. There are already plenty of organizations dedicated to that worthy cause. Rather, this Virginia-based charity organization is about “getting these musicians into a studio with professionals and producing a tangible result for them and their families during what is otherwise an unsettling time for them.” The songs Ebert has recorded for this charity “have provided both pride for those who have survived and solace for those who have survived them.”

Cancer Can Rock isn’t about seeking a cure… [it’s] about “getting these musicians into a studio and producing a tangible result.”

At this point, some 20 musicians have recorded with Cancer Can Rock. Ebert adds that two more musicians are slated for recordings in August. The recording sessions tend to last from 8-10 hours. And since these musicians are battling serious health problems, Ebert says he definitely keeps an eye on them to “make sure they’re holding up.”

Most of the Cancer Can Rock musicians are non-professionals, whose careers have involved something other than making music. They have ranged in age from 21 to 65. The majority come from the Washington DC metropolitan area, but some have come from other regions of the country. Ebert adds, “We also will travel to them when needed.”

Most musicians tend to record original compositions (as opposed to cover songs of famous bands). True to the “Cancer Can Rock” name, the majority of musicians record songs in the rock’n’roll genre, though some record songs that belong to the Americana genre, and several others have played music belonging to different genres.

Ebert relates that, regardless of genre, most of the songs have a positive message. On that note, he says that he aims to create a “positive vibe” and “easygoing atmosphere” in his studio. While the musicians are focused on recording their music, “hopefully they can forget they have cancer.”

Indeed, music has been touted for its ability to provide an escape from psychological distress. Ebert says “it’s an awesome experience” to watch these musicians escape their burdens while busy with their music in the studio. “I’ve learned and grown” through observing them, he adds.

“I try to stay in touch as best as possible with the musicians and their families,” says Ebert. Sometimes, however, the musicians or their family members are the ones who reach out to him. He relates how one musician’s wife approached him right after her husband had died and told him that Cancer Can Rock “had provided him with one of the greatest days of his life.”

Such feedback encourages Ebert to grow the foundation. He currently seeks to add to his volunteer staff and “eventually grow to full-time positions.” He hopes to reach the point where he can record about 50 musicians with cancer per year.

Cancer Can Rock has its own compilation CD, which features the songs of its first twelve musicians. Ebert adds that the musicians can put their songs on any sales platform they wish, and that the foundation splits any proceeds with the musicians.

He now has almost 30 years of experience recording and producing music. “It is my profession and what I love to do.” He now works with indie, major-label, and developing artists. He also provides recording and mixing instruction to small groups and individual students.

Ebert, who lives in his home state of Virginia, has spent significant time in the music epicenter of Los Angeles and still returns to the West Coast a few times a year, sometimes on behalf of Cancer Can Rock.

“You’re told you have a year to live as a matter of fact, when it’s actually an opinion,” he says. “Every couple of years, I let that doctor know I’m still here.”

He used to ride motorcycles for a hobby, but he says “that ship has sailed” due to his diminished vision. He still enjoys getting out and socializing, as well as spending time with his son. This son, now 20 years old, was just a toddler when his father was first diagnosed and told essentially that his condition was a death-sentence. As it turned out, Jim Ebert had a lot of life ahead of him.

As grateful as he remains, some part of him takes issue with his “terminal” diagnosis, particularly with the doctor who gave him the bleakest prognosis. “You’re told you have a year to live as a matter of fact, when it’s actually an opinion,” he says. “Every couple of years, I let that doctor know I’m still here.”

Musicians with cancer who are interested in the Cancer Can Rock experience can apply here.


When Your Doctors Become Your Family

For eight years, I was regularly in the hospital. I never thought I'd miss the people I met there when I finally got better.

When my affable, ginger-haired urologist said: “You are going to need a ureteral stent exchange at least every three months.” I thought to myself, I’m never going to have my life back.

I was first diagnosed with a rare abdominal cancer when I was a 38-year-old, freckle-faced nurse in NYC. Now suddenly a patient, the operation that saved my life made me cancer-free, but it also injured my ureter, causing my right kidney to slowly start to die.

After the operation, I made several attempts to get back to work as a nurse. Sometimes I would make it through the twelve hours shifts. But, more often than not, I would leave the hospital I worked at in midtown Manhattan and take a taxi uptown to be admitted to the one that cared for me.

I felt like my ureter and kidney issues ruled my social life.

I felt like my ureter and kidney issues ruled my social life. A much-needed girls’ beach trip to the Hamptons might be cut short by a sudden emergency room visit (sorry again, ladies). My holidays became shot: I spent seven Christmases in a row in the hospital. Some friends eventually stopped asking me to do things. I didn’t blame them. Even when I wasn’t sick, I was always on the verge of checking myself in for another procedure. Family and close friends assured me I was not a burden, but I knew I was. I became depressed and lonely. I thought I would never be free again.

Oddly enough, during this period, I always felt most at peace when I was laying in my hospital bed, surrounded by medical personnel. These were the people I now saw the most; who understood me; who I never had to cancel plans on, and who never blamed me for ruining their good times. They were intrigued, not confused when I told them the problematic intricate details of my urinary tract system.

I was more caught up on the gossip of their lives than my own friends. The handsome Jewish gastrointestinal surgeon was having his fourth child: he admitted to me he preferred work because home was too loud. And when my adorable, Austrian urologist told me he was moving back to Europe, I felt like my heart broke in two.

During this period, I always felt most at peace when I was laying in my hospital bed, surrounded by medical personnel.

The nurses on the floor thought me as “the fun patient.” I tried to make them laugh whenever I could, telling them stories only a fellow nurse would find funny. They opened up to me: I remember a young blonde nurse holding my hand when I was crying in pain, and tearing up when she told me about her own mother’s stage 3 breast cancer.

I saw resident doctors become fellows, and fellows graduate on to become attending physicians. I felt proud of them.

After eight years of battling with my ureter, my newest (and possibly sweetest) urologist suggested we try and remove the stent and keep it out. He knew my quality of life was suffering. Although this procedure had been tried three times before, he assured me this time it would be different. “Your kidney is dead, you can’t go on like this,” he argued.  I hesitantly agreed.

It was a snowy January morning when I left the hospital without my stent. At first I was nervous, but two weeks went by and everything in my body seemed to be working. Even so, I couldn’t believe I was done with stents.

A month after my stent was removed, I had a follow-up appointment with my urologist.

A pretty woman in her 40s with a head scarf sips a coke with lemon in it.
The author, Liz Montgomery, today lives a stent-free life, but still misses her medical team.

“See? I knew it would work,” he said. “You’re free, Liz.”

I couldn’t believe it. “Really, that’s it?”

It was. Just like that, my whole life changed. I suddenly had more free time than I had in years. I was able to reconnect with friends I hadn’t been able to see for a while. I exercised daily, without pain; I was able to work full-time. Dinners with friends in SoHo were a weekly outing. I started dating. A girls’ trip to Italy was even a success.

I couldn’t believe it, I had my life back.

But a few months into my stent-free world, I felt a sudden pang of loneliness. I didn’t know why I was feeling sad, but something just didn’t feel right.

One night as I laid in bed, it dawned on me. I missed my family. Not my biological family, but my hospital family.

One night as I laid in bed, it dawned on me. I missed my family. Not my biological family, but my hospital family.

I had never lost so many “friends” all at once as I did when I stopped being sick. The eight years I spent in and out of the hospital were excruciating, but the people who had nursed me back to health had become an important part of my life. I felt like an orphaned chimpanzee who was sent back to the jungle alone after being raised in a sanctuary: sad, elated, and free, all at once.

Every now and then, I check the hospital website to see if my doctors are still there and see who the new urology residents are. It connects me to a world I don’t miss, filled with people I do. And I can only hope that when IO go to work every day, I make as much of a positive impact on my patient’s lives as they did on mine.

Cancer Chronic Illness

Why The ‘Saw’ Films Are Relatable To Anyone Who Is Chronically Ill

The series' titular serial killer might be a monster, but part of what turned him into one was our broken, unfair healthcare system.

The Saw movies are regularly classified as torture porn, on account of the extremely graphic deaths that occur throughout the franchise. But it’s actually rare to find a series of films so committed to exploring healthcare, a life-changing diagnosis, and what living a meaningful life really means when you’re faced with your own mortality. They’re not everyone’s cup of tea, but for those of us who know the real torture of trying to navigate the modern healthcare system while chronically ill, the Saw series of films can, in their own way, be a guilty tonic.

In the Saw series, a murderer going by the name of Jigsaw (Tobin Bell) places people in elaborate traps, forcing them to fight for their lives. As the authorities try to track the enigmatic killer down, his schemes only get more sophisticated. Jigsaw’s catchphrase, revealed in Saw II, sums up his core motivation for killing—“Those who don’t appreciate life do not deserve life.” But what strikes me about Jigsaw is that he’s not “just” a monster: he’s also chronically ill himself, and outraged by issues such as the unfairness and impenetrability of our health insurance system, as well as larger issues around healthcare equality.

For those of us who know the real torture of trying to navigate the modern healthcare system while chronically ill, the Saw series of films can, in their own way, be a guilty tonic.

Over the course of seven Saw movies, and the recently rebooted Jigsaw, we learn about the man behind the mask—John Kramer—and what drives him to play quite so many games, along with his handmade companion, Billy the Puppet. The reason, it turns out, is his own diagnosis with colon cancer, which metastasizes into an inoperable frontal lobe tumor. But instead of using cancer as a cheap plot point the way that many movies do, the Saw films use the condition as their main character’s greatest motivator. Kramer realizes that he’s been given a second chance at life, and is intent on making others appreciate what they have, too—albeit, using clearly deranged methods.

I don’t have cancer, and can’t speak to what that’s like (I have my own smörgåsbord of health issues), but my mom passed away from metastatic bowel cancer three years ago. Mom wanted as much life as she could possibly get, and in this one small way, John Kramer reminds me of her.  

A photo of the killer from the Saw movies, John Kramer, as well as his creepy puppet, Billy.
John Kramer, aka ‘Jigsaw’, and his creepy puppet, Billy.

One of Jigsaw’s most relatable moments happens in 2005’s Saw II, when Kramer explains the moment he realized his mortality was achingly close: “Can you imagine what it feels like for someone to sit you down and tell you that you’re dying? The gravity of that. The clock’s ticking for you. In a split second, your world’s cracked open. You look at things differently. You smell things differently. You savor everything be it a glass of water or a walk in the park. But most people have the luxury of not knowing when that clock’s going to go off. And the irony of it is that keeps them from really living their life.”

While Jigsaw takes his own epiphany too literally, leading him to place victims in murderous situations, any diagnosis can be a life-altering shift.

While Jigsaw takes his own epiphany too literally, leading him to place victims in murderous situations, any diagnosis can be a life-altering shift. For instance, I made several major changes in my personal life following a diagnosis with MS in 2013, such as moving across the country and leaving a long-term relationship behind. Any illness or condition has the power to bring things into sharp focus, or blur them beyond all recognition.

As the series progresses, it’s eventually revealed that Kramer’s own diagnosis didn’t come as quickly as it could have. In 2017’s Jigsaw, Kramer tragically reveals: “Were it not for a careless mistake by a resident of the hospital I was in, my cancer could have been diagnosed a lot sooner. It was simply the wrong name on an X-ray.” This delay undoubtedly influenced the anger the antagonist felt at not receiving the appropriate care he required. Kramer laments in 2006’s Saw III, all patients “need a competent physician who looks them in the eye and treats them like human beings,” something he seems to have lacked. But rather than simply pursuing revenge, Kramer becomes a patient advocate of sorts, fighting on behalf of other chronically and terminally ill individuals (when he’s not busy setting traps, that is).

This is no more evident that in 2009’s Saw VI, which puts access to healthcare and insurance under a UV light. When seeking an experimental treatment for his cancer, Kramer is told by his insurance company, Umbrella Health, that the procedure will not be covered, mainly because it isn’t financially viable due to his age and prognosis. The algorithm used by the company makes a plethora of patients disqualified from treatments which could improve their conditions and potentially save their lives. This major injustice doesn’t sit well with Kramer.

A woman in a rusty torture device.
In the Saw movies, Jigsaw puts his victims in deadly contraptions and make them make impossible choices in order to live. It’s a metaphor for the chronically ill experience.

The desire to explore a universal topic, which continues to impact upon chronically and terminally ill individuals on a daily basis even now, shifted the focus of the horror franchise entirely. Rather than simply documenting the conquests of a deranged killer (which the movies still do, of course), Saw VI asked why all humans aren’t treated equally when it comes to the level of care they receive and the treatment they’re able to access. Money is at fault, too, with financial inequality viewed every bit as damning as an insurance company’s impersonal, lottery-like, algorithm.

Jigsaw’s solutions aren’t for the faint of heart, but his unwavering belief that life should be savored melts even the stone in my chest.

Kramer, of course, uses his insurance denial as another motivator, and a chance to examine the unjust areas of society he’s intent on adjusting. He exclaims, “Once you see death up close, then you know what the value of life is,” although his words aren’t enough to change the insurance company’s decision. Kramer sets traps for every Umbrella Health agent responsible for his denial from beyond the grave, by way of his ever-growing list of protégés, but healthcare inequality is insurmountable even for a prolific serial killer to tackle, sadly.

For all these reasons and more, I’m relieved that the Jigsaw Killer will reportedly be returning for a ninth instalment in the franchise. Gore that burns into your eye sockets, and blood-curdling traps aren’t for everyone. My mom hated gore, but she’d have loved John Kramer’s bad attitude and penchant for justice. Jigsaw’s solutions aren’t for the faint of heart, but his unwavering belief that life should be savored melts even the stone in my chest.

Cancer Chronic Illness

Chronic Illness When You’re Twins

Through cancer and celiac disease, these twins helped each other through their diagnoses.

Growing up, Robin Melamed and Tara Liebnick, now 45, were typical twins. They shared the same group of friends and more often than not, they completed each other’s sentences. In college, they joined the same sorority. Then, in their thirties and within a matter of months, the twins got the news—they both had cancer.

Facing a double mastectomy, they mulled over a procedure to rebuild their breasts. Melamed, who panics when she reads about health-related topics online, depended on Liebnick’s research to decide. During Liebnick’s chemo, Melamed flew to Dallas to help out and cheered on her nephew at his soccer games. Through hysterectomies, chemotherapy and lengthy hospital stays, the twins found solace in their relationship that’s like no other.

They’re not alone. Many twins with chronic illness have found that navigating their condition together has both grounded them and lifted them up.

Robin Melamed and Tara Liebnick are twins who navigated cancer diagnoses at the same time.

Cancer When You’re Twins

“What’s made it easier is having each other,” said Melamed, who lives in Houston. “It’s helpful we’re so much alike. We know how to be there for each other. We know what to say and what not to say. Going through this together has strengthened our relationship.”

Liebnick was the first to find out. She felt a lump in her breast. Cancer, her doctor said. Then, she tested positive for the BRCA1 gene mutation, which put her at a high risk for having both breast and ovarian cancer. Melamed was browsing the racks at Nordstrom’s in Houston when their dad called and broke the news about her sister’s diagnosis. She was devastated.

“It was a very scary time,” Melamed said. She also knew that if Tara had tested positive for the mutation, she would too. “I thought, fine, I’ll have preventative surgeries. At the time, it wasn’t on my mind I’d be dealing with cancer first-hand.” Melamed, who didn’t have any symptoms, still decided to have both breasts and her uterus removed. That’s when they discovered she too had cancer, in her abdomen.

“I don’t know how I would have gotten through [cancer] without her…”

As the months progressed, the sisters spoke multiple times a day and late into the night after their kids went to bed, on the phone, by text and over email. When Melamed had surgery to remove the cancer in her abdomen, then got an infection, Liebnick flew to Houston. She slept on a pull-out couch in Melamed’s hospital room for nine nights.

As Melamed lay there, moving in and out of consciousness, Liebnick knew how to bring a smile to her twin’s face. She played the Hamilton soundtrack for her on her phone and wheeled Melamed outside to get fresh air.

“I don’t know how I would have gotten through that without her,” Melamed said. When Melamed finally came home, she recovered in a rented recliner chair. The suggestion had come from her sister, who’d rented one after chemo.

Fraternal twins Jamie Serrano and Zach Friedlander were both diagnosed with celiac disease around the same time. 

Celiac When You’re Fraternal

Fraternal twins Jamie Serrano and Zach Friedlander, 29, have supported each other through chronic illness as well. The twins always had diverging interests. Serrano is more of a book worm; Friedlander was the physical twin. Having celiac disease has given them something to bond over.

Serrano was the first to get diagnosed. She was 16, volunteering in rural Mexico for the summer and wasn’t feeling quite right. Her stomach was off, but she assumed she had a virus or traveler’s diarrhea. She stuck to bland foods like flour tortillas and made do. Back in the U.S., doctors ran a blood test. It was positive for celiac. “An endoscopy showed my intestines were demolished,” she said.

Serrano changed her diet, cut out gluten and focused on fruits, vegetables and proteins. She learned to navigate eating out—which restaurants were safe, what questions to ask to make sure she didn’t get “glutened.” She studied food labels and learned where hidden gluten can lurk.

Friedlander got tested at the time too, even though he had no symptoms. But, he was negative for celiac. So, he forged on, enjoying beers and burgers during his college years and indulging during regular visits to Taco Bell. Then, a few years ago he noticed he was getting light-headed and dizzy. He was anemic. It was celiac.

“It’s given us something to bond over.”

Soon after, Serrano went in for a regular endoscopy to check her intestines. Her brother set one up for the same day. Afterwards it was clear; they both had celiac. As nurses pushed them into the waiting room in wheelchairs, Friedlander told Serrano he wanted to have one last gluten-filled hurrah. Pizza, burgers, beer, cookies and cake. Serrano set him straight.

“She said ‘no you can’t do that,’” Friedlander said. “She told me stories about people who don’t follow the diet, what can happen to them.”

From then on, Serrano has served as her brother’s guide, facilitating his way into the world of gluten-free eating. After his diagnosis, Friedlander regularly snapped photos of food labels and texted them to his sister to screen for gluten. When he moved back home to Chicago from Indiana, she showed him the best gluten-free friendly restaurants, and at grocery stores, pointed out the tastiest gluten-free cookies and crackers.

“It’s given us something to bond over,” Serrano says. “I’ve helped him navigate everything, and we enjoy sharing gluten free food together.”

The twins talk more today than they did in the past, Friedlander said. “It’s been a big help having her,” he said, “and I know she’s enjoyed helping me and having someone who can relate to her. We talk more now. We’re more open and we’re closer because of it.”

Cancer Chronic Illness

Cancer Was My Crucible, And It Made Me More Compassionate

The tragedies of illness can be agonizing to endure, but oftentimes, we come out the other side more loving people than when we went in.

If you saw my friend in the check out line at the grocery store with an expensive bottle of wine, you might feel envious. Jan is a traffic-stopper. Her facial features are perfectly symmetrical and her skin is dewy perfection. You might assume she’s on her way to a fancy dinner party with a better looking date than your husband.

When she came over yesterday, she wore a striking red tunic on her head with a matching red rose tucked behind her ear, a look only a movie star could pull off. It wasn’t one of those coverings that screams Breast Cancer in all caps like most head scarves do, no matter how cleverly they’re tied, piled, wrapped, or draped. Hers had the touch of a deliberate statement, a sense of style sported by a woman who can own any room she enters.

I couldn’t help contrasting her wrap with the one and only head cover I bought in anticipation of my own hair loss back when I got my diagnosis. The American Cancer Society website sold me a white cotton skullcap that looked good on the model, but I knew better than to have any faith in it even as I entered my credit card information. At the time, those scraps of cotton were offered at two for fifteen dollars or one for eleven, and I visualized an underpaid, overworked laborer cranking them out in a dimly lit factory for tightwads like me.

I’m not giving cancer an extra dime, I thought.

I’m not giving cancer an extra dime, I thought, and I ordered only one. It was comfortable but hideous, and I wore it all the time for nearly a year except when it was in the wash. My friend Rebecca sent me fun hats and a bright green wig, but I couldn’t find my playful side when it came to being bald, and trying to look glamorous hadn’t even occurred to me.

When Jan and her turban walked into my living room yesterday, I rushed to take her in my arms. We’ve met in person on only one other occasion, and it was just before she started treatment. Seeing her in person again overwhelmed me.

If it’s possible to touch grief, to taste it, to smell its fragrance, I would say that’s what I did when we embraced. After Jan’s first chemo session, she lost her child to suicide. On the morning of her daughter’s memorial service, Jan woke up with pneumonia. While we hugged, I brushed against the bottomless pit of her sorrow.

While we hugged, I brushed against the bottomless pit of her sorrow.

Looking at Jan’s manicured nails and curated outfit, no one would guess the depth of her suffering. It reminded me of a time in my life when I too endured a sustained season of grief.

During my twenties, my boss’s husband put a gun in his mouth and pulled the trigger. Then a friend with bi-polar disease killed his mother in a terrible psychotic episode. Shortly thereafter, my friend Bill, a guy who wore his homosexuality like a badge of honor, fatally overdosed on street drugs. My friend Kathy made an unsuccessful attempt on her life and then my friend Glenda lay down on the blind curve of a freeway until an unwitting motorist ended her painful existence. It seemed at the time that sadness had no floor, that my very survival required me to trudge through one brutal moment at a time. Most people saw the smile on my face and never knew about my struggle.

Sometimes back then I pictured God throwing rocks at me, his aim spot-on, his appetite unquenchable. I was in therapy for trauma I experienced as a child and the series of bad choices that trauma prompted me to take, choices that piled one miserable circumstance on another.

Now, I recognize that agonizing season developed my ability to feel compassion for others. The pain I endured then still helps me bond with others in need.

Now, I recognize that agonizing season developed my ability to feel compassion for others. The pain I endured then still helps me bond with others in need.

I don’t know how Jan will survive the loss of her daughter or the effort cancer demands from people it ensnares in its web. I only know that we have to be gentle, to love one another every chance we get.

First Corinthians reminds us that “Love bears all things, believes all things, hopes all things, endures all things. Love never fails.”

Sometimes love feels as thin as a strand of dental floss, but it’s there, as undeniable as the rising sun in the morning, the stars at night, and the toil of the days. Ultimately, it’s all we have, and I’ve come to believe, no matter how difficult it is sometimes, that somehow, it’s enough.


Cancer Can’t Keep The Cat Lady Down

After stage 3 colorectal cancer, Samantha Martin is cancer free and ready to hit the road with her act, the Amazing Acro-Cats.

“It’s my gift in life to be able to figure out an animal’s mind and what motivates them,” says Samantha Martin.

Martin, 54, is the founder of the Amazing Acro-Cats and the Rock Cats, a traveling troupe made up of typical domestic short-haired cats, a groundhog, a chicken and two rats that perform jaw-dropping circus-like acts and even play music. “We’ve added a saxophone and a trumpet, so it’s taken on a free-form jazz feel,” explains Martin, who, outfitted in cat’s ears and either a catsuit or a ringmaster’s outfit, is a big part of the show.

Checking boxes off a seemingly endless to-do list before she departs, Martin is preparing to hit the road in her brand-new bus for a southwest tour. Before she brings the Acro-Cats on tour, though, Martin has one last appointment: getting her bloodwork done to make sure she is still cancer-free.

Meet the Acro-Cats.

Healing Cancer? Cats Can Help

Diagnosed in early 2018 with stage 3 colorectal cancer, Martin was forced to cut last year’s tour short to begin her treatment.After five-weeks of oral chemotherapy, Martin underwent one surgery to remove the cancer and a second seven weeks later to “reconnect” her. While the treatments had side effects, including fatigue, bowel issues, “chemo brain,” and post-operative pain, Martin was comforted by her animal companions, which include 27 cats, an African serval and two Labradors.

“The purring sound lowers blood pressure and helps people to heal, emotionally and physically,” she says. “It’s science.”

“The purring sound lowers blood pressure and helps people to heal, emotionally and physically,” she says. “It’s science.”

A self-described “outcast” with few friends, Martin discovered that she had an unusual rapport with animals early in life.

At the age of 10, she started training the family Lab, and when she was 16 years old, she caught a rat, smuggled it into her dorm room at military school and taught it to do tricks. “I was drawn to misfit animals like rats and snakes,” Martin says. “If nobody likes it, it must be special.”

Later, she enrolled in an animal behavior class at the local community college and ultimately earned a degree in animal service. After interning at a store that trained exotic animals to perform in film, television and live shows, Martin took a job running the rodent and reptile department at a local pet store.

Samantha Martin running a couple of her cats through a routine.

Finding Her Calling

One day, a movie production team stopped in and asked if she could train rodents to climb into a box for a key scene in their film. “I can train them to crawl in a box and answer a telephone,” she told them.

It turned out to be her big break. While she was on set, a WGN news crew showed up and filmed her, later airing a segment that got picked up by CNN and aired around the world. It led to a slew of television spots, including high-profile gigs on Geraldo and Inside Edition.

To supplement her film work, Martin worked as a wildlife educator, giving talks at schools, libraries and birthday parties. She turned her two-flat building in Chicago into a private “zoo,” with a reptile room in the basement and a space for farm animals out back. The whole house smelled like animals, she recalls, but she didn’t mind. “I started coming up with ways to teach them, so that I could demonstrate their abilities with cute tricks,” Martin says.

For example, after watching her coati, a relative of the raccoon with a long nose, dive headfirst into a laundry basket and fish out a pack of gum buried deep in a pants pocket, Martin started putting treats in other places. Eventually, the coati could open a mail box, take out a wallet, remove a rolled-up dollar bill and unroll it to find a treat. She likewise taught groundhogs to raise flags and raccoons to play basketball.

Two cats playing drum and guitar. The drums say "Rock Cats"

The Rock Cats, the Acro-Cats’ house band.

Founding The Acro-Cats

Not to mention her many cats. Weary of giving talks at schools (“I don’t care for children,” she says), in 2005, Martin put her cats to work, launching first the Rock Cats and then the Amazing Acro-Cats. “There are a million dog trainers, but very few cat trainers, and I like a challenge,” Martin says.

It wouldn’t be possible without clicker training, she explains, a method of pairing a clicking sound with a treat to encourage the desired behavior. Starting out with art gallery openings, night clubs and birthday parties, Martin eventually rented a theatre in Chicago for a six-week run. People showed up in droves. “The cats sucked, but people loved the act so much,” Martin says, remembering their first performances.

“The cats sucked, but people loved the act so much,” Martin says, remembering their first performances.

Over the years, Martin’s cats have appeared on Animal Planet’s Pet Star, Must Love Cats and Animal Witness. Her favorite one, Tuna, now deceased, also starred in the independent movie, Zeke. Most recently, Martin and her feline friends appeared on the Late Show with Stephen Colbert, where Martin says they “bombed.” “I’m terrified of public speaking, and the cats feel your stress,” Martin explains.

A woman with dark hair in a circus ringmaster's outfit standing proudly in front of posing cats.

Martin is proud of what she’s been able to accomplish with her cats.

Fur-Ever A Feline Foster Mom

Not just an entertainer, Martin has made it her mission to foster cats as well. She’ll take on an entire litter, train them all and keep the most talented for the act. Those that remain are available for adoption, a service she runs out of the front of her tour bus. Over the past decade, Martin has found “fur-ever” homes for 228 felines.

“You’ve already adopted a cat that has developed a relationship with people, a cat that will meet you at the door and give you a high five,” she says. I can’t save the world, but I can help people build a relationship with their cat.”

“I’m one of the luckiest people alive… because I’ve had all these animals giving me all this unconditional love.”

Martin knows all too well how impactful such relationships can be, offering companionship as a child and comfort in the wake of her cancer diagnosis. That said, she has plenty of human friends and supporters too, people who accept and even embrace her for her uniqueness. When her insurance policy denied a claim, for example, she launched a GoFundMe and raised $76,000, which allowed her to keep the lights and feed the animals on during her nine-month treatment.

“I’m one of the luckiest people alive,” Martin says. “Everybody has sad moments, but overall, I’m a pretty happy person, because I’ve had all these animals giving me all this unconditional love.”


How To Help Someone After Disability? Teach Them Tennis

Paralympian Kai Schraymer knows firsthand how becoming disabled can turn your world upside down. That's why he teaches newly disabled people the same sport that helped him.

In May of 1984, in a local tennis club in Brussels, Belgium, 16-year-old Kai Schrameyer sat in his wheelchair holding a tennis racket, looking at his father across a net. He had trained many many days on that very court, he had become good at tennis; he had fallen in love with it. But this time, everything–or at least one thing– was different: he’d had his left leg amputated above the knee a year earlier after a bout of bone cancer, and now he couldn’t chase down any balls that flew more than 3 feet away from him. He felt sad and frustrated.

In 1990 Kai saw the world’s top wheelchair tennis players compete in the Swiss Open in Geneva. The players’ smooth movement and flawless technique moved him. The event changed his life. He decided to dedicate himself to the sport. He got a coach willing to train him for cheap, and went to work, five days a week. By 1992 he was ranked #6 worldwide. That year, he beat some of the same players he had watched in Geneva to win a silver medal at the Paralympic Games in Barcelona. In 1993-94, Kai was the #1 ranked wheelchair tennis player in the world for 12 consecutive months.

That first day back on the court, Kai had been comparing himself to the player he had been before the amputation. It’s a common reaction, he says, but “not fair or helpful.” Now, as the National Coach for Wheelchair Tennis for the Canadian Tennis Association, he’s helping people new to their wheelchairs in Canada and around the world avoid the same mental trap — both on and off the court.

Kai Schraymer showing off his Silver Medal from the 1992 Paralympic Games in Barcelona.

The Tennis Association’s mandate is the development of tennis in general including of wheelchair tennis. In order to develop wheelchair tennis, Kai needs to recruit new athletes, so he works in a network of rehab centers all over Canada. The international tennis federation sends coaches and players to developing countries to help them set up tennis infrastructure, and Kai has been to Uruguay, Colombia, and Bolivia on such trips visiting rehab centers, helping local groups maintain recruiting pipelines from rehab facilities, and training able-bodied coaches for wheelchair tennis. We caught up with Kai to hear more about his work.

What exactly do you do when you go into a rehab center?

The rehab center is the first point of contact for somebody who has had a traumatic experience and finds themselves in a wheelchair. At that point, their whole life is upside down. That’s where we come in. The centers usually have a gym. We bring rackets and balls and set up mini nets. We have them hit the ball in a series of regular intervals a to see how it feels. Sessions are about 45 minutes to an hour. We introduce the idea: “you can be active.”

We are always looking to find future champions, someone who will win a medal for Canada.

We end up at the centers because maybe a physical therapist mentions that someone is asking about tennis, or because someone was already an athlete and might have potential. We’re introducing wheelchair tennis to be beneficial, recreational–not necessarily aiming for greatness or the paralympics. But also, we are always looking to find future champions, someone who will win a medal for Canada.

What is your experience of your work like?

Kai Schraymer embraced wheelchair tennis after losing a leg to bone cancer.

It’s an amazing feeling. You find someone who is new to their wheelchair and that’s usually after an illness or an injury, and that’s a pretty low moment. They’re in the process of reshuffling everything in their lives and coming to terms. But you can throw them a ball, and they hit it, and they’re having fun all of the sudden. That just literally makes my day every single time. That is why I do this work. It’s not a broad impact job. You’re not making a difference in millions of people’s lives. But you make a lasting and profound impact on people that you work with.

What does that impact look like?

It’s different case by case. It’s also not usually a linear pathway. You could have somebody who has not done any sports before their accident, so usually they struggle more because they don’t have physical literacy but maybe they saw wheelchair tennis on youtube and they’re more than happy to give it a shot. On the other hand, we have a young guy in Vancouver right now who used to be a great tennis player. He’s super coordinated and learning really fast. But he was really struggling when he came in. He wouldn’t always show up so I’d call him and ask him if he wanted to go out and hit some balls, and he’d say yes, but cancel 30 minutes before. He hasn’t come to terms with his new reality.

I get it, that’s what I did for a while too: I compared myself to the person I was before I lost the leg in so many ways…

And I get it, that’s what I did for a while too, I compared myself to the person I was before I lost the leg in so many ways, including being able to run and do all kinds of athletic things. That’s something that was taken from me, and that still sucks, but it is what it is. You have two choices. You can dwell on “I wish I could run around on two legs,” but that’s not going to move you to a better place; it’s just going to keep you stuck. Your other choice is to come to terms with it, make the best of it, and focus on the things you can do. But I just have to be patient. It might take that kid another year, some more psychological support. At some point, he might come back ready.

I met another young kid only a month after his accident and three years later he’s enrolled in a scholarship program at University of Alabama for wheelchair tennis. I got to see him from that ground zero moment through to thriving. Wheelchair tennis opened the door for him, and now he’s getting an education because of his talent. It feels super satisfying to be part of that journey.

How do you try to coach people beyond tennis to help them along in that journey?

If people ask me for it, I will give advice, but I try not to intrude and give it unsolicited. I just try to be patient and encourage them as players. If that helps, then great, but there are often unresolved identity issues that are above my pay grade.

I got my motivation when I started by seeing some of the best players in the world compete and I said, “are you kidding me? I want to be able to move as well as they do!” So I hope having success stories of other athletes in front of them helps them too.

Mostly it’s through the sport itself. Before wheelchair tennis, I started with basketball. That changed my world completely, changed my confidence level because I was able to do something competitively, to play for points, games, championships. It also helped me form a new community of like minded people. That’s also a super important component because as I see often in my work, people tend to withdraw after their accidents or illnesses; they isolate themselves. It helps them to create a support system in other areas of their lives. That’s true for sports regardless of disabilities.

There is also the physical aspect: practicing the sport helps build strength and explosiveness that transfers to everyday skills.

Kai training one of his students.

When you are teaching able-bodied coaches, what do you teach them about working with people in wheelchairs?

We really want people to understand that wheelchair tennis is not just for people that are in a wheelchair in their everyday lives. Wheelchair tennis is a sport and the chair is a piece of sports equipment. Internationally top players are people with a minimal disability like a blown out knee and they’re eligible. Amputees like me, because of the good prosthetics, they can run around a court with a prosthesis but they can also play wheelchair tennis. Even able bodied people, like some coaches love playing in a wheelchair.

Wheelchair tennis is a sport and the chair is a piece of sports equipment.

I don’t teach coaches how to relate to people in wheelchairs. They are coaches and actually, my main message to them is: this is still tennis. The only difference is that going from a to b is not through running or shuffling but through pushing the wheelchair. So a large chunk of the course is teaching them about efficient movement in the chair. Rather than teaching them about people in wheelchairs, I tell them tell them to let people indicate to them what their limitations are, to wait for the, “hey coach, I don’t have full core muscles, so that move is hard for me.” But basically, they should not be treating the athletes differently.

Cancer Chronic Illness

How Music Heals

A new partnership between the National Institutes of Health and the John F. Kennedy Center for the Performing Arts explores the many ways music can heal the body and mind.

It has long been suspected that music can strengthen and improve the body and mind. But it is only in recent decades, with advancements in brain measuring technologies like fMRIs, that science has been able to prove how. One recently launched initiative, which straddles the border between the scientific and creative worlds, hopes to educate and inspire more research into the topic. Called Sound Health: Music and the Mind, it explores how listening to, performing or creating music involves brain circuitry that can be harnessed to improve health and well-being. It is a partnership between the National Institutes of Health (NIH), the largest public funder of biomedical research in the world, and the John F. Kennedy Center for the Perfoming Arts, a renowned creative arts institution in Washington D.C.

Heavily involved in the initiative is renowned soprano Renée Fleming, a 2013 National Medal of Arts winner and artistic advisor to the Kennedy Center (most recently, she sang at John McCain’s funeral). “The first goal is to move music therapy forward as a discipline,” she says of the initiative. “The second is to educate the public and enlighten people about the power of music to heal.”

In supporting the initiative, Fleming has been giving talks about it at her performances (nineteen thus far), often including local music therapists or researchers. She has also taken part in a brain imaging experiment focused on creativity and improvisation, where she spent hours inside an fMRI machine under the guidance of an NIH researcher. It was the exact kind of research which Sound Health encourages. In the machine, she was given three different instructions: to sing, to imagine singing, and to listen to music. “In my case the findings were a little bit surprising because the most powerful of the three in terms of brain activation was imagining singing,” she says.

We reached out to Fleming and NIH Director Dr. Francis Collins to hear more about this fascinating project.

What are some findings or impacts of the initiative thus far?

Francis Collins

Francis Collins: Over the last few years, I’ve been hearing some interesting reports about researchers using music to improve people’s health. But these were mostly anecdotes, and what was really needed for the field to grow and expand was scientific evidence. NIH, with its mission to improve health and ample funding, is in an ideal position to help build that evidence. And the fact that Renée Fleming and the Kennedy Center were interested in the intersection between music and health was a good indication to me that this topic could get people excited about scientific research and the future of medicine. So we joined forces to create this important partnership.

Music can help Parkinson’s patients walk with a steady gait, help stroke survivors recover the ability to speak, and give cancer patients relief from chronic pain.

Out first goal with the Sound Health partnership was to educate each other and the public on what we’ve learned from research in this area so far. We held an unprecedented scientific workshop at the NIH with some of the world’s leading music and health researchers. Some were investigating how music could help Parkinson’s patients walk with a steady gait, help stroke survivors recover the ability to speak, and give cancer patients relief from chronic pain. It was clear that there was some exciting research in this space.  We’ve since held two public events at the Kennedy Center to share this science with everyone. You can see recordings of the scientific workshop on the NIH website and read a summary here.  Recordings of some segments of this year’s Kennedy Center event are posted on YouTube.

Based on what we’ve learned, the NIH is supporting future research on this promising topic. We’ve announced the availability of $5 million in funding in fiscal year 2019 to support a wide range of research into the effects of music therapy on various health conditions. Because that research hasn’t been done yet, the most exciting results are yet to come.

How is music beneficial to young minds?

Renée Fleming.

Renée Fleming: Music activates more parts of the brain than any other activity, which is amazing. For education one of the things they’ve proven is that children benefit from learning a musical instrument; some of the reasons are obvious: the discipline, the practice. But the scientific piece is that eye-hand coordination through the ear helps them develop academically, with better aural comprehension and better academic outcomes overtime. It seems to be very powerful. It’s a fascinating project and there’s an endless number of things we can explore with it.

What do you hope the initiative will accomplish?

FC: I hope Sound Health will help determine whether and how music could be an effective part of a doctor’s toolkit. At the NIH, our goal is to better understand how our bodies work, then to use that understanding to help people live longer, healthier lives.  And we do that through research. We just issued these funding opportunity announcements about music and health to encourage scientists to submit their best research ideas.

I also hope that our partnership with the Kennedy Center and the National Endowment for the Arts will get people excited about this topic and the role science plays in it. So many people have made music a part of their daily lives, and they’re curious about why it has this profound effect on them. The public events at the Kennedy Center, which you can watch online, will help you learn more about yourself and share in our excitement about how music may play an important role in medicine.

What are some questions you’ve always had about music and its impacts?

RF: This potential of music to connect us with our emotional life. That’s valuable and not really well understood. Also the connection to music and memory. Our senses are hardwired to be used in terms of memory and music is one of the most powerful of these triggers.

As a health official, what interests you most about music and its impact on the mind and body?

FC: I’m fascinated by the ways that music overlaps with other processes in the brain. When you sing or play an instrument, it doesn’t just activate one part of your brain: a whole constellation of brain areas becomes active. And some of these musical areas are partially shared with activities like speaking, which if disrupted can have devastating consequences.  An amazing thing about this overlap is that when the normal speech pathway in the brain is damaged, music can sometimes be used as an alternate path.

When you sing or play an instrument, it doesn’t just activate one part of your brain: a whole constellation of brain areas becomes active.

This finding inspired something called “melodic intonation therapy.” When someone has a stroke that damages the left side of the brain, it can cut off the normal language pathway and make it hard for the person to speak. Therapists will work with stroke patients to sing phrases like “I am thirsty” to use that alternate, musical path instead of the damaged one. It takes a lot of work and practice, like using a different muscle, but stroke survivors have used this technique to learn to speak again.

Scientists have been working hard to understand the complex pathways in the human brain. And here is a payoff where we might use these pathways to improve mental health without drugs or brain stimulation. What’s more, music doesn’t just overlap with language: it also shares brain areas with movement, memory, motivation and reward. These things are hugely important to mental health, and researchers are trying to use this same concept of an alternate pathway to address new categories of mental disorders. If they’re successful, that would be a significant breakthrough for patients around the world.


The Magic Healing Power Of A Miniature Therapy Horse

Who says Magic isn't real? This special therapy horse has provided comfort to terminally ill children, and the victims of the Sandy Hook and Pulse Nightclub.

The hospital elevator doors open and out walks Magic, an 11-year-old American miniature therapy horse. Worried faces break out in smiles. Loved ones and hospital staff do a double take.

A little girl, about age seven, tells Magic’s handler that her face hurt from smiling so much. She recently underwent a heart transplant and is fighting leukemia. Nearby, a little boy who was losing his sight because of a brain tumor put his face up against Magic’s so he could always remember what she looked like.

Another little boy with a terminal illness laughs so hard when he sees Magic that his mom begins to cry. She told Debbie Garcia-Bengochea, co-founder of Gentle Carousel Miniature Therapy Horses and Magic’s handler: “We never had a happy day and now we’ll always have a happy day.”

Debbie Garcia-Bengochea, Magic’s handler and co-founder of Gentle Carousel Miniature Therapy Horses, says: “Sometimes you can’t fix things, but you can give someone a happy day.” We spoke with her to learn more.

Debbie Garcia-Begochea, Magic’s handler and co-founder of Gentle Carousel Miniature Therapy Horses

When did you start Gentle Carousel Miniature Therapy Horses and why?

Twenty years ago; back then, there were therapy dog programs and a few therapy horseback riding programs. I was a school principal with experience working with children with special needs. I saw a need. And there’s something magical about horses. People are used to seeing dogs indoors, but not horses and definitely not miniature horses.

Our horses go through a two-year training program. They’re taught to be in tight spaces like an elevator or a hospital room. They learn how to go up and down stairs. They’re toilet trained. We don’t teach them tricks or ride them. Our horses offer emotional support. They know how to approach people.

And they know how to stay calm. People take out their cameras, flashes go off, and hospital alarms make noise. The training keeps them safe.

Magic knows who to approach and when. She can sense who needs her. She’ll approach, let the person pet her, sometimes, she’ll lay her head on someone’s lap. She’s 26 ½ inches tall and very approachable.

Where does Magic work?

Magic has visited children and families at Sandy Hook Elementary School, the Pulse Nightclub, Emanuel AME Church in Charleston, and other places where trauma was front and center. In addition to the victims, Magic and the other horses in the program have comforted medical professionals, law enforcement, and families.

The medical staff working with the Pulse Nightclub bodies worked so hard and didn’t have a moment’s rest. When they saw Magic with her deep blue eyes, they smiled. Some even laughed. It’s like she gave them permission.

When Magic isn’t on the road, she works at local hospitals, hospices, and assisted living centers. Her schedule, like the other horses in the program, are two days of work and a week of being a horse. Horses are herd animals and need to be around other horses. Our horses get to run and play.

Our home base is Florida and we’ve traveled to about 30 states and have about 20 volunteers.

Magic visiting a young boy at Ronald McDonald House.

Is Gentle Carousel mostly run by volunteers?

Yes. We depend on them. We have a group of women who sew beautiful homemade toy horses, which we leave on hospital beds. We do a reading program where our horses hoof-a-graph books. We dip their hoofs in ink and stamp the books, which we give away when we get to the hospital or trauma center.

How many people have you helped?

Since we started, about 25,000. We also have a team of volunteers and horses in Europe. Many work in hospitals and orphanages.

You have 21 horses in your program. Why does Magic stand out?

All of our horses are special and everyone has their favorite. Magic has this special ability to find the one person in the room who needs her the most. At a camp, she approached and stood by one little boy who didn’t speak much. He just learned his cancer returned.

Some of our horses work well with children and others prefer older adults. Magic works well with everyone.

One elderly woman in an assisted living home didn’t talk to anyone until she saw Magic. She hadn’t left her room in six months. When she heard Magic was coming, she got up early to wait. She held an old black and white photo of her as a child sitting on a pony. When I arrived, Magic approached and this woman who had not spoken to anyone in a long while, told everyone how beautiful Magic was.

I didn’t know she didn’t talk to anyone. The staff told me. They had tears in their eyes. Now she talks to the staff and the other patients.

A little girl named Caroline takes Magic for a walk.

Tell me about American miniatures.

There’s a wide range of looks and sizes; they can be as large as 34 inches at the shoulder. That’s pony size. Our horses are around 26 inches tall. They can weigh 100 pounds or less. Magic’s jet black with ¾ apron (white) face and deep blue eyes. Our other horses come in all white, tan, a mixture of white and black or tan and white, or they can be spotted. They all have their own personalities. And they all get along. Horses need to be around other horses.

You’ve probably heard that horses can sleep standing up. While that’s true to get true REM sleep, they should lie down. They do that when they feel safe, when other horses are around. They’re prey animals and in a herd some animals stand guard.

American miniatures can live well into their 30s and they can work as long as they’re happy and healthy.

How do you travel with the horses?

We have a horse trailer, which is tricky to park when we’re in a busy city. Often we need police assistance to help us with parking. Our goal is to get a custom minivan to transport the horses.

What makes Magic happy?

Magic has a big ego. She loves getting attention from children and adults. And if there’s a challenging situation, Magic is the horse who can be counted on.


When Health Insurance Is No Assurance At All

What does it say about our system when you can scarcely afford a routine medical procedure even after spending $12,000 a year on health insurance?

Lying in a flowerbed with bark chips poking my shoulder wasn’t the best way to start my 57th birthday. My husband Bob and I had taken the day off from our respective consulting businesses—he was a private investigator, I was a speaker coach—to head up the Southern California coast to Encinitas to shop for a beach coverup, have lunch at the organic paleo café, and take a walk through the Self-Realization Fellowship Gardens. Then my gynecologist’s office called. They wanted me in for another test. I scheduled it first thing, thinking we could head north afterwards.

Instead, thirty minutes after the procedure I found myself in the fetal position at the edge of the medical center parking lot, halfway between chunky mulch and pavement. My body was unclear what it wanted. Pass out? Throw up? Both? I’d sent my husband back up to the doctor’s office for a wheelchair and was trying to slow my panicky breathing. I felt the eyes of the freshly scrubbed parking valet on me. I sent him this silent command, “Please don’t call 911.” We had pitiful insurance. I couldn’t afford an ambulance.

Hard Decisions During Open Enrollment

I sent him this silent command, “Please don’t call 911.” We had pitiful insurance. I couldn’t afford an ambulance.

I’d worked since age 15. I’d always had health coverage through my job or my husband’s. By 2015, both of us were working from home. As self-employed workers we still paid our taxes and social security, but now had to run the gauntlet of private insurance. I was grateful for the Affordable Care Act’s provision for pre-existing conditions, as it meant we could no longer be turned down for coverage. That didn’t make it affordable. Our high deductibles covered little of our care. In 2017 two flu shots and a mammogram were the only care covered at 100%, yet our premiums were over $14,000. Every year I had to weigh the importance of continuity of care against the steep premiums of plans which covered my two specialists. I hadn’t had a primary care doctor or annual physical for ten years.

During open enrollment last November, with both of us in our late 50s, we debated whether we should skip health insurance and pay the penalty. Our 2018 deductible—the cheapest plan—was slated to come in over $12,000. We were healthy at the moment, working hard to watch our weight, eat right, and exercise. Could we risk it? If something happened we’d wipe out our savings, maybe lose our house. We bought in, unwilling to court disaster.

An Unwelcome Birthday Present

All was well until six weeks prior when I started spotting. I’d been on hormone replacement therapy to manage my menopause symptoms. A little blood could be normal, but it kept happening. I ignored it because seeing the doctor and the tests she’d order wouldn’t be covered. I told myself it was because I’d forgotten to change my estrogen patch on time. One day, the flow too heavy to ignore, I called my gynecologist’s office. They scheduled an ultrasound. I paid for the $250 test out of pocket, not covered because it’s diagnostic.

If something happened we’d wipe out our savings, maybe lose our house. We bought in, unwilling to court disaster.

When they called back with my results, they said I needed a uterine biopsy to check for abnormal cells. They warned me it would be uncomfortable. I took the first available appointment on my birthday, not wanting to wait. They wouldn’t be calling for another test so soon if nothing was wrong.

Before she did the procedure, my gynecologist explained that my ultrasound had revealed my uterine wall was thicker than it should be post-menopause, 7.5 mm instead of 5 mm or less. That thickness could be a side effect of the HRT, pre-cancerous cells, or endometrial cancer. Trying to quell my fears at hearing the C-word she said, “If you do have it, it’s the best kind. We almost always catch it early. We do a hysterectomy and then it’s gone. There’s rarely a need for chemo or radiation.”

Treatment I Couldn’t Afford

My first thought was that I couldn’t afford surgery. I knew my doctor was out of network and so was her hospital. If it turned out I needed this operation, she would have to refer me to a doctor I didn’t know.

She told me the biopsy might hurt, as the cervix is uncooperative my age. “If we can’t get the sample we need, then we have to schedule you for the procedure under anesthesia.” I knew I couldn’t afford that. I had to do it there.

When a doctor tells you a procedure will be uncomfortable, have a strong hand to hold. I tried to breathe through it. I tried not to flinch. I told myself to gut it out as tears squeezed out the edges of my eyelids. Finally, it was over. My doctor got what she needed and promised to call as soon as the results were in.

When a doctor tells you a procedure will be uncomfortable, have a strong hand to hold.

On the way downstairs in the elevator I felt light-headed. Bob sat me down in the lobby. Unsure of how to help, he came back with cold water, ginger ale, and a protein bar. He held my hand. He got me outside to a bench for air. He got me to the flowerbed because I thought I might hurl. He left me on the ground when I asked him to, because I knew I should go back upstairs to see a nurse. I hoped they wouldn’t charge me extra for coming back.

An Uncomfortable Procedure

Once I was wheeled upstairs, my blood pressure and pulse were so low they couldn’t get a reading. I heard the nurse explain to Bob I was having vasovagal syncope, an overreaction to the test that happens occasionally, causing my heart rate and blood pressure to drop suddenly. It looked serious but wasn’t a medical concern. My body needed time to right itself.

I suddenly needed the bathroom right away. Bob hustled me over there just in time. He asked if I was feeling better? Not quite. It turned out my stomach did need to empty itself after all. That finally did the trick.

Now that I could stand, he walked me back to the exam room. My pulse was now 45, my blood pressure coming up. The color came back into my always-pale face. They declared me safe to leave. Bob deposited me back on the same bench outside while he fetched the car. I looked at the flowerbed where I’d left my dignity, wondering how, in a building full of doctors, care was still nearly out of reach.

I looked at the flowerbed where I’d left my dignity, wondering how, in a building full of doctors, care was still nearly out of reach.

Once in the car, Bob and I agreed that my 57th birthday deserved a do-over. He drove me home for a two-hour nap. I made myself a birthday treat that night: fudgy chocolate cake with fluffy marshmallow frosting.

A Birthday Do-Over

The next day we headed up to a store where I found khaki Capris and a white linen shirt. I pushed away thoughts about my future as I pulled on clothes in the dressing room. I wondered whether I would be having major surgery with a doctor I didn’t know, and if hysterectomies were inpatient or outpatient procedures these days. We drove to Encinitas for organic Thai chicken salads for lunch. I ate chocolate cake for dessert at home.

My doctor called four days later. “How are you feeling now? Were you able to enjoy your birthday after all? It’s good news, we saw no abnormal cells. I’m going to lower your dose of estrogen. That should balance things out.” I felt the tension I’d been holding in my shoulders start to leave my body.

It feels like a terrible compromise,  to spend so much on a policy that covers so little.

I was thrilled I don’t have cancer, and that if I did, my insurance would have covered at least a portion of my treatment. But it still feels like a terrible compromise, to spend so much on a policy that covers so little. A car accident or major illness could wreak havoc in our lives. As Congress chips away at the Affordable Care Act’s protective provisions, we will see a rate increase of $3,300 next year. If they revoke the provision for pre-existing conditions, I’ll be without insurance altogether. For both those reasons I plan to trade off self-care with activism for the foreseeable future. With occasional slices of cake.