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Skin Diaries This is Brave

This is Brave: Steve Hamilton

October 8th, 2006. I remember the day quite vividly. A week prior, I had been to my dermatologist to have a small bump on my head looked at. Not overly concerned since it didn’t have any of the typical signs of melanoma. My doctor scraped off enough for a biopsy and I went back to work. Then, on October 8th, I was in a conference room and my phone buzzed. It was my dermatologist’s office calling. I excused myself from the meeting and stepped into the hallway to take the call. It was my actual doctor and not the physician’s assistant. After an exchange of pleasantries, she paused, “I got the results of your biopsy. It’s cancerous. You have melanoma”. I was stunned by the gut punch. The rest of the day was a blur. At that moment, my cancer journey had officially begun.

Two months later in December, a surgical oncologist removed the tumor along with some adjacent lymph nodes on both sides of my neck. The tumor was deeper than expected and diagnosed as stage III melanoma, but it was removed. Margins were clear and I had no cancer activity in my lymph nodes. I felt fortunate and believed that I dodged a bullet.

In 2008, after two years of being NED (no evidence of disease), a follow-up routine chest X-ray showed shadowing and spots on my lungs. The melanoma had returned and had reached a stage IV diagnosis. Over the next 18 months, I had three lung surgeries to remove new tumor growths and wedge resection surgeries that took away 25% of my lungs. I tried to stay positive and committed to outrunning the cancer, literally. I took my exercise to a higher level, enhanced an already good diet, and made a conscious effort to mitigate the stress in my life.

After my third lung surgery, I completed 30 days of Interferon treatment (a form of chemo). It was challenging and I’d never felt worse in my life. Despite the steps I’d taken, by May of 2011, a CT scan revealed that I had tumors on both lungs, pancreas, liver and behind my heart. My stage IV diagnosis became more severe.

I met with my oncologist to map out a treatment plan. I wasn’t going down without a fight. Unfortunately, another surgery was not an option and my doctor didn’t know of any clinical trials. Basically, there was no plan. My doctor looked at me and said, “there is nothing more I can do for you”. Those words pierced the air. Emotions ran rampant, but reality had a way of setting in quickly. I had stage IV melanoma and there is no stage V.

After trying to fully comprehend the odds I was up against, I promised myself that I would find someone, somewhere to help. I wanted to give myself the absolute best chance for survival, so I sought out arguably the best place for cancer treatment – MD Anderson in Houston, TX. They are ranked No. 1 in cancer treatment year after year and are known for advanced cancer treatment options.

My wife and I flew from Atlanta to Houston and met with Dr. Patrick Hwu, a highly respected oncologist specializing in melanoma (today he is the Division Head of Cancer Medicine). When we met, it was clear that he had already reviewed my case as he said, “We’ve got a growing number of options in the melanoma treatment toolbox and I think we can help you. It’s never a good time to be diagnosed with melanoma, but if ever there was a time now is it”.

Amongst the options available, we talked a lot about a relatively new treatment category at the time called “immunotherapy” – training the cells of your immune system to seek out and destroy the cancer cells. After weeks and weeks of various testing, certain treatments were ruled out since my cells did not respond. Ultimately, the best option was a clinical immunotherapy trial that combined high dose IL-2 interleukin (a standard of care treatment option for melanoma at the time) with the Mage 3 vaccine. IL-2 by itself had a pretty low rate of response, but the clinical trial was to see if tying it to a vaccine would improve the response rate. The treatment had drawbacks – side effects, physical hardship, mental challenges, a long duration, and of course, the fact that the trial was new and nobody had completed it at that time.

To fulfill the inpatient treatment requirements, I would travel to MD Anderson in Houston for a week at a time, then return home for one to three weeks. I did this for about eight months. The biggest criterion of the trial protocol was that after each week of treatment I underwent a full CT and a brain MRI. If tumors were stable or shrunk, I continued with the trial. If they grew, then I was removed from the trial.

I started the first week of October 2011. The treatment was tough. Each time I was in intensive care hooked up to multiple machines monitoring every vital you can think of. I gained about 40 pounds of water weight each week and then would have to lose it before I was discharged. I experienced uncontrollable chills and muscular spasms. My heart rate would spike into the low 200’s after each dose of IL-2. My taste buds all but disappeared and I hardly ate. Somehow, in the haze of it all, my immune system responded, and my tumors began to slowly shrink. Week after week, month after month, my CT and MRI results showed progress and I kept going back to Houston for treatment.

I finally completed the inpatient portion of the trial over the eight-month period. Although extremely happy to finish, I wasn’t done. I continued head, neck, chest and pelvic CTs and brain MRIs immediately prior to each return trip to Houston. Every three months, then every six months to get lab work done, meet with my research nurse to answer a litany of questions about how I was doing physically and mentally, meet with Dr. Hwu and, of course, get my vaccine. On February 14th, 2014, in Houston for my checkup and scan results, I received the news I had been dreaming about. My scans and MRI showed no tumor activity. I was in remission. 

After that landmark day, I continued getting CT scans, MRIs and the vaccines for another year. In July 2015, after 4+ years of countless hours in the ICU and flying back forth from Atlanta to Houston for the vaccine, I become the first patient to complete the IL-2 & MAGE 3 clinical trial.

It’s now May 2020 and I am 13+ years removed from my original melanoma diagnosis. I’ve had a combination of 16 major and minor surgeries. But most importantly…I’ve been cancer-free for six years.

My advice to you after all of this is to accept the facts and realize that no one is immune. More people are diagnosed with skin cancer each year in the U.S. than all other cancers combined.

Melanoma is the third most common cancer among men and women ages 20-39, and on age-related cancers, melanoma is the #1 most diagnosed cancer among 25 to 29-year old’s in the United States. So be smart! PLEASE wear sunscreen and sun protective clothing, check your entire body for changes in your skin and see your dermatologist regularly. Most importantly…enjoy life and take care of your body – it’s the only one you get!

For those still battling cancer – keep the faith, keep fighting and don’t ever give up. Above all, always believe that miracles are possible.

Peace!

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Skin Diaries This is Brave

This is Brave: Marit Peterson

My journey started almost fourteen years ago when my mom noticed a raised pink bump on the base of my right ring finger. I was only a year old at the time. For many months, my mom took me to numerous doctors to try and find answers. Each one told her it was nothing; however, she thought otherwise. She thought it looked like a melanoma lesion my grandfather had years prior. Her continual pestering to doctors finally worked, and I was called in for a 30-minute “cosmetic” surgery to just remove the bump. The 30-minute surgery turned into two hours, and afterwards the doctors sent the tissue they removed to be biopsied at several leading cancer centers. All of the results came back inconclusive. After weeks of back and forth, I was finally referred to MD Anderson Cancer Center. It was there that my melanoma was confirmed, and my cancer journey began.

Being that melanoma was known as an old person disease, people didn’t take me seriously. One time, someone told my mom to get me out of the melanoma clinic because children weren’t allowed to be there. Little did they know that I was the patient.

At MD Anderson, I met the doctor that saved my life, Dr. Jeffrey E. Lee. At this point in time, for a melanoma diagnosis like mine, the life expectancy was just six months. And this was for adults – I was only a toddler. However, that was not the plan for me, and I write this 156 months after my diagnosis, living life to the fullest because I wasn’t even supposed to have a life at all.

Following my surgeries, I had a port put in and year-long treatment with interferon. For a solid year, I experienced extremely high fevers (up to 105!), night terrors and was a very sick little girl. But, I survived, and for that I am grateful.

Surprisingly, I have no memories from my cancer treatments. It must be God’s way of protecting me from those bad memories.

Although my family and I were thrown down a path that no one would ever want to go, we decided to make the best of it. In the year following my treatment, my mom and grandfather, the one who had a melanoma like mine, established the Marit Liv Peterson Fund for Melanoma Research with the goal of raising half a million dollars to support melanoma research at MD Anderson Cancer Center. We began by asking family and friends to contribute, but half a million dollars proved to be too difficult of an amount to raise with them alone. That’s when we decided to hold our first golf tournament to help raise money. Since we began, 100% of every dollar raised has gone directly to Dr. Lee and his melanoma research team. And every year, Dr. Lee and his team join us for free skin screenings and to report back on the research that was funded by the golf tournament. To date, we have raised over two million dollars and have caught five melanomas and numerous other skin cancers on our players through the skin screenings.

Although my melanoma was likely genetic, I do all in my power to help educate others on melanoma prevention. In 2016, the Melanoma Research Foundation (MRF) reached out to me and my family and invited us to go out to Washington, D.C., to advocate for melanoma research. We were taught about needs in the melanoma community such as funding and education. Then, the next day, we went to Capitol Hill and spoke with our senators and representatives about these topics relating to melanoma. We have been going to D.C. for the past four years and through this, we have connected with Coolibar! When I was in 8th grade, I was invited to go to the MRF’s Pediatric Summit in Colorado Springs, Colorado, where I took place in a mini fashion show wearing Coolibar clothes. It was super fun for me and all the little kids there.

The path that someone takes when presented with a challenge can say a lot about who they are as a person. When my family and I were presented with cancer, we decided to make the most of it. As weird as it sounds, my cancer has given me so many amazing opportunities that have given me a greater look on life and how I should appreciate every day that I have.

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Skin Diaries Together We Will

The Inspiration Behind the Enright Melanoma Foundation

By: Mark I. Zimmerman, MD, Founding President Enright Melanoma Foundation

On the 20th anniversary of the Enright Melanoma Foundation, I’m retelling the story of a friend I lost over 20 years ago to rekindle the passion of a foundation that continues to work in his name.

It started with four of us…

Rich Nelson and Peter Colucio were young physicians at the Summit Medical Group (NJ) when Joe Enright and I joined them in 1991. The four of us quickly became friends. Pete was a confirmed bachelor (and scratch golfer), and Rich, Joe and I were married with growing families. We ate lunch together, we played golf, and we often met up at Joe and his wife Kathy’s house for birthdays and barbecues. While Joe coordinated what he fondly called “male bonding weekends”, our wives often took a “spa” vacation together. Life was good.

Shelley, Joe’s 3-year-old daughter, scratched a mole on Joe, which bled. He saw his physician and the biopsy revealed melanoma. Joe went back for the “wide and deep” surgery that was hopefully going to remove all of the melanoma. It didn’t. Over time, while life continued and little Shelley got a new brother Nicholas, we learned the melanoma had metastasized.

Joe and Kathy went to MD Anderson Medical Center in Houston for what was the most promising treatment option at that time – interferon. To support him, I collected the signatures of close to 500 coworkers on a “get well soon” banner and Rich and I flew to Houston to be with our friend. While he went through a brutal interferon treatment, we watched the Superbowl together. Even as physicians, it was painful for us to see what this treatment was doing to our friend.

When Joe came home, it was clear that he only had a short time left. The four of us played a final round of golf even though Joe could barely hold a club, but he never complained. I arranged for a “make-a-wish” type of event and we met one of Joe’s favorite teams, the New York Rangers. Joe took pictures with his favorite players (including Mark Messier!) and got a hockey stick signed by the players. It was great to see a moment of joy on the face of my friend who was rapidly losing weight, and his battle.

Through it all, Joe maintained his courage and what appeared to be an inner peace. He never gave up, and he would not let the melanoma define him. My last memory of Joe was of him lying on his couch and apologizing to me for “not getting up and seeing me to the door” when it was time for me to leave. We lost Joe in 1996. Joe’s death was devastating to me. I had experience dealing with death as a physician, but I had never lost someone as close to me as a brother.

I thought about the things I learned from Joe – his loyalty, courage, dedication, calm demeanor, his love of family and friends, stoicism, and his love of life. But it was the quirky things that have stuck with me. Joe taught me…

  1. It is okay not to shave every day. 
  2. You don’t have to wear a tie all the time.
  3. It’s okay to leave your wallet in the car and let your friends pay for lunch!

Joe was loved by his family, friends and patients and I wanted the world to remember him. I wanted his children to grow up and learn about who their father was and what he meant to his friends and coworkers. And most of all, I wanted to do something so that no one else would lose someone in the prime of their life from something that is both preventable and curable if caught early enough.

Rich and I, along with co-workers at the Summit Medical Group, started the Joseph E. Enright Foundation in 1999 to raise funds to contribute to worthy causes in Joe’s name. Over the past 20 years, our passionate Board of Trustees has evolved and we have narrowed our focus and the redefined Enright Melanoma Foundation’s vision—to live in a world free of melanoma. Our mission is to raise sun-safety awareness and help prevent melanoma through education and early detection.

Over the years, the Foundation has held a variety of fund-raising events including golf outings and bike treks. Joe’s mom, Catherine, has always been at these events and was my “walking” partner. She could not have been prouder of the work the Foundation had done which in some way, had eased the pain of losing her son.

Everyone involved with the Enright Melanoma Foundation has been touched by this devastating illness in some way.  We understand the need to be vigilant, both in terms of sun protection and skin checks. Since starting this foundation, my own father has had four separate melanomas removed simply because of my insistence on a skin exam.

Our ask is that you become an advocate for your friends, family, teammates and coworkers – become a free member of our foundation, take our sun safety course, do business with our sponsors and business partners, donate time and money, network and spread our message.  Help prevent this from happening to someone you know and love.

To learn more about the Enright Melanoma Foundation, please watch the 20th anniversary video below, then visit: www.enrightmelanomafoundation.org/.

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