Monday, December 17, 2012

Interview With Author Matt Cavallo*

I recently read “The Dog Story” by Matt Cavallo.  Matt was diagnosed with multiple sclerosis (MS) at the age of 28. 

I’ve invited Matt here today to tell you a little bit about himself and his book. 

First off, can you tell my readers a little bit about yourself?

MC: Hi Leslie! Thank you so much for having me! As a fellow complicated patient and Master of Public Health, I enjoy your blog immensely. My master’s degree is all about using technology and public health policy to solve the types of challenges solving the coordination of care with multiple specialists as you pose in your, “There’s No I In Team” blog post. My day job is training doctors, nurses and therapists on hospital EMR systems. I was in your neck of the woods at Botsford Medical Center in Farmington Hills, MI earlier this year.

As for me, I’m thirty six years old and live with my wife, Jocelyn, two boys, Mason and Colby, and our neurotic Wheaton Terrier, Ted.  At age twenty-eight, I was diagnosed with Multiple Sclerosis. Seemingly overnight I went from a fully-functioning, healthy man to someone who was numb from the waist down and unable to walk.  I wrote my story of being diagnosed and overcoming the physical and emotional challenges associated with having a chronic disease in my memoir, The Dog Story: A Journey into a New Life with Multiple Sclerosis. As a result of my diagnosis, I have dedicated my life and career to healthcare and the fight against MS.

What made you decide to write a book about your experience with MS?

MC: When I was diagnosed with MS, I went into a deep depression. I didn’t want to accept that at 28 years old my fate would be to have a progressive disabling disease. My friends, family and even my wife, tried to connect with me, but I felt isolated. To snap me out of my depression and to feel reconnected, I wanted to read another patient’s experience. I found myself in the aisles of Barnes and Noble flipping through books that were either scientific and clinical, focused on the power of positive thought or holistic “eat these leaves and you’ll be cured” books on the shelves.

I wanted something different. I needed a story that captured the fear and emotion of the unknown that I experienced alone, in my hospital bed. I left the store without buying anything and feeling more isolated and alone than ever. Then, I got home and started flipping through a journal I had been keeping in a green, spiral notebook. Because this experience was new and scary, I had wanted to make sure that I remembered everything, so I wrote it down. Writing also helped me cope with the depression and other emotions I was experiencing at that time.

As I flipped through the pages, I realized that my story was the type of story that I needed. That I had a responsibility to other patients to write an honest story that they could relate, too. I also made a pact with myself to be honest, open and to not be afraid to be vulnerable. It is difficult to share a personal story that lets the reader into intimate scenes of your life, but when it comes to personal health, that is the only way to be true to your audience. By doing this, I knew my story could become a vehicle to raise awareness to the devastating effects of chronic illness.

I definitely agree with you about the importance of truth and authenticity when sharing your personal health story with others.  In the book, you seem to use humor to help you cope, but it doesn’t seem like the people around you, including medical personnel, were all that amused.  Did humor help you cope, and how did you deal with those around you?

MC: My sense of humor was off the mark in the hospital. The nurses and doctors were so serious that my jokes fell flat as I tried to lighten the mood. I also think I was using humor to mask my fear. It was difficult to maintain a sense of humor because those closest to me were all doom and gloom. As I lay in my hospital bed watching my mom and dad fall apart, I knew that I had to be the strong one.

It is interesting how people close to you act when you are diagnosed with a chronic illness. My mom was crying, saying it was her fault for having me. My dad all of a sudden met a hundred people with MS that were playing tennis and hiking mountains. I even had a friend tell me that drinking Pedialite would somehow help regenerate spinal fluid after my spinal tap.

While people were trying to help and sympathize with my situation, all of their help was making it worse. So, when I could walk again well enough to leave the house on my own, I hopped in my truck and headed to the beach. I wanted to do a mental flush. With all the people around me having trouble coping with my condition, I never had a chance to process what actually was happening to me. During this time, I had an epiphany about the song, Moon Shadow by Cat Stevens. This epiphany eventually led me to start writing The Dog Story.

Eight years later, the way that I have handled my diagnosis and the way I fought through my many relapses and recoveries has served as inspiration for others. My sense of humor has encouraged other patients like me to find the humor in their own situation and appreciate the life they still have. Laughter continues to be the best medicine for my MS.

Can you talk a bit about the timeline of the book?  It actually covers a relatively short period of time, right?  I know it probably felt like forever to you.

MC: I’m glad you brought up the timeline as it was a challenge for me to capture. The first part of the book is essentially a daily journal. It follows me from my initial onset of symptoms, to the hospital and eventual discharge.

Once I am discharged from the hospital, I am severely affected by spinal headaches and pain meds, so the period in between the discharge and diagnosis spans about a month. This is a collection of scenes that transition from the everyday journal, but keeps a similar format.

The book concludes a month later with me starting to come to terms with my diagnosis and how I coped with my fate. The dates in the story actually happened in my life from May to July of 2005, so about a three month span.

So I am often “accused” of sharing too much on my blog – TMI – if you know what I mean.  And there are some pretty intimate moments that you share in your book.  How/why did you decide to include those?

MC: Thank you for bringing this up, Leslie. I’ll try not to blush! When I lost functionality from the waist down, I didn’t just lose my ability to walk...I lost my ability to use everything. This was also during a period when my wife and I were planning on starting a family. I feared that I would never be able to have children.  Sexual dysfunction is a subject that is difficult for most people to discuss. So, I challenged myself that if I was going to write an honest book, I would have to write about, well, everything.

Sexual dysfunction is a common problem for people with MS. According to the National MS Society, 91% of men and 72% of women with Multiple Sclerosis experience sexual problems. While ignoring these problems can lead to depression, self-esteem issues and reduced quality of life, the topic is awkward to bring up in casual conversations. Even talking to your doctor about your sex life can be painfully embarrassing. So, I figured if I was going to write an honest book that I was going to have to address what happened to me.

My readers have connected with my openness. I have received emails from all over the world about my courage to discuss uncomfortable subjects and how they feel less alone. I think that my story also gives my readers the strength to talk about these topics without feeling embarrassed. Plus, my story has a silver lining. Two years later after I went through all of this, we were finally able to conceive a healthy baby. Today we have two beautiful boys, which back then I didn’t think would be possible.

Sorry for making you blush, Matt!  I really did appreciate your honesty on those topics.  I think for me, one of the hardest parts of the book to read is when you are talking about the experience you had getting a spinal tap. To be honest, I’ve never had one, but that is one of the few things that really scare me still. 

MC: I hope you never have to get a spinal tap, Leslie! I try not to relive that scene in my life. The pain, the recurring crippling headaches, the helpless feeling that it would never end still ranks up there with the worst thing that ever happened to me. I broke my neck in 201o as a result of the damage from the Transverse Myelitis. I had to wear a hard collar, plus get used to the idea of swallowing with a titanium plate in my throat. While that ranks up there, the pure torture of the spinal tap still is the worst thing that has ever happened to me!

As a writer, I wanted to capture the gut-wrenching emotion involved with my spinal tap to evoke a visceral reaction to the scene. People have written me, saying that reading my spinal tap scene actually caused them to feel back pain. I think that I have done a good job as a writer if readers can experience the pain of a spinal tap without actually having the needle driven through their spine.

I certainly had a visceral reaction to it.  Are you well now (relatively speaking)?  How do you stay healthy?  Do you think you’ll get seriously ill again?

MC: MS is a lot like what you go through with RA, Leslie. I’ll have periods of calm, but I always know it is there. After the Transverse Myelitis, I had Optic Neuritis, which caused me to go blind in my right eye. Then, I had a cognitive relapse which affected my memory like an early-stage dementia patient. All of these symptoms were treated and resolved.

Today, I feel like Cinderella at the ball. In 2007, I was switched over to a risky, new treatment which killed people in clinical trials called Tysabri. I haven’t had a relapse since starting the new medication, except in 2010 when I had a neck surgery.

After surgery, I was sick of the fight and stayed off the treatment for over ninety days. As a result, all my MS symptoms came rushing back and I had a major relapse. I needed IV steroids before I could resume my Tysabri treatment. I knew then, that I was married to my medicine and that I only had about ninety days of my current quality of life before my MS symptoms overtake my body. Taking a risky medication is a tradeoff that I make so that I can work to support my family and be the husband and dad that I want to be.

What have you learned from your experiences?

MC: I learned to never take one moment for granted. Since going through the experience of being diagnosed with MS, I have experienced a lot of loss. Experiencing losing my ability to walk helps me to appreciate every step that I take. This is why that even on days where I feel weak and tired, I force myself to get up and walk my dog, Ted. This was a promise that I made back in the summer of 2005 when I got Ted. It has been eight years and I still have not broken that promise.

What do you hope readers will get from your book?

MC: Readers will finish my book with a sense of hope. They will realize that if I can overcome what has happened to me, that they can too. That using humor in the face of great adversity can help to keep their spirits high and to do the best they can with what they’ve got, no matter the situation.
Your story is similar to other young patients, myself included, even though we have different illnesses. You were at the top of your game, your life was settling in, and then you were diagnosed with MS.  What advice would you give to others like you?

MC: When I worked at the neuroscience clinic, helping patients like me and you, I would find myself talking to people that had seemingly given up the fight. They would recall how they used to be before becoming ill. I would tell them, we have eyes in the front of our head because we were never meant to look back. Focus on being the best you can be today. Just because the circumstances are different, that doesn’t mean you can’t enjoy life.

What’s next for you?

MC: Right now my kids are small and my health is good, so I plan on playing with them and being as involved as I can be in their lives. I am also going to continue to use my story to help spread awareness and to help other patients like me. I have been doing a lot of motivational lectures and would like to expand my speaking opportunities to reach more people. My readers have asked me to keep writing and tell more of my adventures as a continuation to The Dog Story.

Thank you again for having me, Leslie!

Thanks, Matt, for sharing your story!  And thanks for stopping by Getting Closer to Myself today. 

For more information, head over to, and say “hi” to Matt!

*I received a free copy of this book from the publisher.  However, my choice to have Matt as a guest blogger was my choice, and had to do with my personal opinion of the book.

1 comment:

  1. Thanks for this great post & your brilliant blog, Leslie. I don't think I could handle reading about Matt's spinal tap myself, but I love how he says 'we have eyes at the front of our head so we don't look back.' A good one for us lupies to remember. All the very best for 2013. X