Official Interview: Mark Unger
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Official Interview: Mark Unger

Official Review
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1. What do you do when you aren't writing?
I own and run a family business with my two brothers in Connecticut. We manufacture commercial and retail window cleaning products – squeegees, buckets, scrapers, poles under the "Unger" name. You will see our products in Home Depot, Amazon and many commercial cleaning distributors throughout the world. My mother and father started the business in 1964 and we continue to produce high-quality cleaning tools that meet our homeowner and professional customers' needs. (www.ungerglobal.com)
In my free time, I love to play golf, snowmobile, work around the house and travel with my wife and family.
2. Who has been most influential in your life?
My father had the most influence on my direction in life. He built the family business from nothing to a worldwide leader in window cleaning equipment. His hard work, personal drive to succeed and iron will were always front and center as he raised us. He always had high expectations of me, and I was motivated to succeed just as he had. His stubborn and no-quit traits had a huge influence during the treatment of our son, Louis during his battle against cancer. Although he passed away in 1996 his presence drove me to never quit and push through boundaries to help save Louis.
Mel, my wife of 29 years, is forever the love and anchor in my life. She has guided me and our sons Harry and Louis through periods of joy, growth, challenges, and hardship. She supported my book ambitions and helped me craft the story although it brought up feelings we had all tried to suppress after treatments were over. Without her my book would still be floating around my brain today – rather than being in print.
3. Let's discuss your book First Survivor: The Impossible Childhood Cancer Breakthrough. This book is about your son and his journey with cancer. How difficult was it for you to write the book?
The simple answer is that it was one of the greatest challenges of my life. I am not a professional author and had no ambitions of being one. I had a burning desire to tell Louis's incredible story to keep a detailed record of what we went through to save his life. I wanted to write a quick-paced story that takes readers on a real-life roller coaster ride they won't forget. My goal is to engage and inspire the reader to understand the power of advocacy while never losing hope even if a diagnosis is very poor.
4. The book comes from journals you kept at the time, correct? Was there anything from your journal that didn't make it to the book?
When Louis was first diagnosed I found myself in an altered reality. Never had I experienced the medical world with this urgency and intensity. I was literally lost, without any points of reference to provide me with some footing. In order to understand what was happening to our 3 year old boy in those first few days and weeks, I started asking questions and taking notes. I continued taking notes and journaling my son's treatment path until he was declared free of his cancer – 7 years later. These notes helped my wife and I keep track of all the information, test results, treatment options, doctors' thoughts and online information. They also served as the foundation of my book. I would highly recommend that anyone who is faced with a serious medical situation – take notes – lots of them and ask lots of questions of the doctors and nurses.
5. How does Lou feel about the book?
Louis is very proud and appreciative of the book as it tells his remarkable story with a lot of insights and details that bring depth and color to our journey. He told me that the book helps him understand what he and our family went through as he was only 3 years old when he was diagnosed. He simply does not remember much of what happened and was never aware (we never told him) of his "zero chance of survival" diagnosis at the time.
Now that he reflects on what happened and knows the details of what our family went through, he is happy that others will benefit from the story. He also feels proud of his strength and determination to battle the "bad cells" and be the "first survivor". He hopes that readers will be engrossed as they read his story and leave them inspired and hopeful.
6. You founded the Carrot Seed Foundation. Can you tell us more about that?
My wife and I started the CSF to fund medical research and clinical trials for children stricken by the same cancer Louis had – Neuroblastoma. All proceeds from the sale of First Survivor go to the Carrot Seed Foundation. In addition, we receive donations and contribute our own funds to various charitable organizations that support children and families going through cancer treatment who are in need. Please visit our website for more information: www.carrotseedfoundation.org
7. This book is a memoir. Are there things that parents going through a similar situation can learn? What do you most want them to know?
During the first few weeks the shock and stress of a critical diagnosis makes it very hard to think clearly. The stress is enormous - my wife and I both lost 20 pounds in the first 2 months. The needs of your child or loved one will control your life 24/7. You are immersed in the world of hospital critical care and forced to get up to speed fast. You have no choice. Nurses are there to help your child and provide round-the-clock care. Lean on them to help you stay informed and teach you how to take care of your loved one. We formed close and lasting relationships with Louis's nurses over the years. They are truly empathetic and loving professionals.
Once the initial shock settles, begin to do research on the diagnosis and start to ask the doctors questions about the treatment plan, what their experience is with the disease, survival rates of the institution. Go online and learn about the diagnosed disease – there will be a lot of information. Search for Foundations that specialize in your child's or loved one's illness and call them. Many of them are run by families, like ours, that have 1st hand experience with the illness and are supporting ongoing medical research. You will find comfort in speaking to someone who has lived through it before. They are eager to help you and answer all the questions you have.
As you search, you will see hospitals advertising their experience with the specific disease you searched for. Bookmark these pages as you will want to study their capabilities, specialized doctors, treatment options and survival statistics as you progress with the treatment. Some hospitals will have a larger team of doctors who only treat the specialized disease you are looking for. These will most likely have more experience and resources than those that do not have this specialization. We had to change hospitals for our son's illness which helped to save his life.
Strongly advocate on behalf of your child or loved one to ensure they receive proper care. Don't be afraid to ask questions – even hard ones, like: How many children have you treated with this disease last year / What is your overall survival rate for these children? You only get information if you ask for it. Don't be satisfied if you don't get a straight answer – keep asking. Remember that endurance and resilience are needed as the treatment is underway. There will be a lot of up and downs during the long process of curing a critical illness. Our motto was "every day is a great day". Never give up hope.
I like to end with fun questions.
8. Are you a cat person or a dog person?
Dogs for sure – we have had dogs since my wife and I married 30 years ago.
9. What's your favorite vacation spot?
Our beach house on the shores of the Atlantic Ocean in Connecticut.
10. What's on or in your beside table?
I am currently reading Blind Man's Bluff a nonfiction book that tells the story of secret U.S. Navy submarine missions during the Cold War
11. How do you unwind?
I love to play golf as it takes my mind off everything else.
—Neil Gaiman
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