My Book Intro – Feedback Please!

Thank you to everyone who has taken the time to write me emails or make a comment at this website. I’m glad I have been able to support you on this journey. You have certainly been there for me, too. I am so grateful!

As of today, Stink is still doing awesome on the Intuniv. On a scale of 1 – 1o, I’d give his tics a 2. If you didn’t know he had T.S., you might not suspect a thing. Of course, if he plays computers a lot one day, his eye tics are more prominent. It’s just the nature of the beast. It’s an easy fix: Live a balanced life.

On another note, I have completely rewritten the intro to my book. What started out as a self-help manual – how to fix tics – became more of a journey of enlightenment: If you can’t fix the tics, fix yourself.

I am hardly a seasoned Buddhist. I am a card-carrying control freak Christian who lives in L.A. and wants everything as perfect as the scripts I used to write. Fade in: Life is kooky and unpredictable, but by the end? Fade out: Happiness.

Like my dreams of a wild affair with George Clooney – no such luck.

I’m hoping you can read this intro and tell me what you think. Honestly. Are you disappointed it’s not a book on how to get rid of tics 100%? Because, really, that’s what I wanted to write. But it’s not what happened. But something marvelous happened along the way, and while I still struggle, I’m a better person because of it. I’m hoping my story can inspire others to live with uncertainty also.

Can you give me some feedback? I’d really appreciate it. (Note: It’s not grammatically correct. Ahem, Margaret.)


My son, Stink, was diagnosed with Tourette Syndrome when he was four. Named for Georges Gilles de la Tourette in 1885, Tourettes consists of both vocal and physical tics that wax and wane in nature and last up to one year.  Though my son’s symptoms were fairly mild, my reaction was nothing less than mind blowing despair. Thanks to media and fear inducing websites, I was utterly convinced my son would bark, hump busses and scream the F-Word during circle time.

Looking back, I can cluck-cluck like a mother hen and chortle about how dramatically I reacted. But I was freaked out. With only the worse case scenarios presented, how did I know that a Tourettes diagnosis would not be a curse (no pun intended) but instead the biggest gift a mother could be given? That gift was none other than one giant invitation to live life on life’s terms, not my own. It was an opportunity to let go of preconceived notions of a trouble-free childhood. Like bottle of soda, it was my chance to shake up a routinely packaged life and watch with wonder as new challenges exploded over my ideas, drowning my soul with the mess and stick of fear, anger, joy and excitement. I could finally relinquish fast held ideals about what I wanted for my son’s life, and instead nurture the life that he was supposed to live.

In the subconscious recesses of my mind, I knew that Tourettes was a present, but that didn’t keep me from spending the next five years looking for the gift receipt. “Thank you, but no thank you,” was my reply. “I appreciate the thought, but I’d like to return this for something else. Perhaps a good case of musical genius, a pitchers arm, or the ability to burp the Ave Maria.”

No such luck. Tourettes was here to stay. I didn’t have to like it, but I could learn to accept it. Taking a clue from the Serenity Prayer, I vowed to accept the tics I could not change, change the tics I could, and have the wisdom to know the difference. What choice did I have other than to stress out my marriage, drink away my sorrows, or curl up in a fetal position in the geranium bushes out front? With two out of three being checked off that list, it soon became apparent that my son’s disorder would remain regardless of my response to it.

Taking a clue from my son, whose reaction to his twitches were nothing shy of unadulterated acceptance (“I love my tics! They are part of me!”) it was clear that I would have to love them also. After all, if they didn’t bother my son, and they didn’t bother his friends, and they didn’t bother his sister, his father, his teachers, his grandparents, cousins and even that random group of Girl Scouts who heard him cough his way through the The Tooth Fairy movie, why should they bother me? Oh, that’s right. I was narcissist.

I could talk a big game about nurturing my child’s individuality, but truth be told, it was all about my own fragile ego. When my golden haired wonder boy would create marvelous stories or put together complicated puzzles in ten minutes or less, clearly it was due to my emotional and intellectual nurturing.  By the same token, every minor gulp, throat clear and tongue click were magnified as LOUD! RICOCHETING! EXPLOSIONS!  They boomed like ringing fog horns in my ears, taunting me that “My child’s life is O-V-E-R. AND IT’S ALL YOUR FAULT.” 

Tourettes might have been my son’s diagnosis, but co-dependence was clearly mine. My son’s symptoms, which were ever changing and often unpredictable, served as my emotional pendulum, which didn’t exactly create a peaceful living environment. “No shoulder shrugs or tongue clicks this week? Woo hoo! Let’s go to the library and join the book club and hear a talk about emperor and gentoo penguins!” …”Oh, crap. Head nods and humming? Let’s go to the library anyway because God dammit no T.S. is going to keep my kid from living a normal life but so help me if he gets one stare from some elitist botox mom whose kid is named after a French painter and has hair down to his designer jeans I will kick her to the North Pole so fast it will make a polar bear’s nuts freeze off.”

In retrospect, my reaction seemed extreme. But at the time, I was in pain. I was in shock over a syndrome I never saw coming. I was in grief over saying goodbye to the childhood I thought my son would have. And I was in denial about my ability to fix those tics. Tourettes might not have a cure, but that didn’t stop me from spending hours on the internet researching natural cures and remedies. And while a steady diet of magnesium and Epsom salt baths, coupled with a healthy diet, helped – it did not eradicate tics altogether. For an A – personality type like myself, nothing short of complete symptom elimination would do.

Insanity is often described as hitting your head against the wall over and over and expecting different results each time. I would agree with that definition, but I didn’t see myself as crazy. I saw myself as head heels in love with my son who would do anything to alleviate his ails. And it’s hardly like I was hitting my head against the wall the same way every time. I used a helmets to soften the blows. I went about slamming against the wall with different intensities. From homeopathic visits, dietary changes, acupuncture, neurologists, online ordered vitamins, support groups, books, habit reversal training, psychologists and psychiatrists and ultimately medication, I did everything in my power to “normalize” my son.

For a few weeks, even months at a time, my efforts seemed to pay off. Sure, I had bad hair from exhaustion and wearing all those helmets, but sometimes those tics would dissipate. But just when I’d let my guard down, they’d come back. And then the insanity of head banging would begin again. It was exhausting, and those bumps hurt, but until I got rid of those tics, I’d simply have to live with the pain.

Peda Chodron, a world renown Buddhist teacher who practices awakefulness, fearlessness, and gentleness, speaks often about the futile attempts of changing others to make oneself feel better. In a lecture entitled “This Lousy World” she reveals a list a mile long of things that annoy people to no end, including, but not limited to, the weather, the government and scent assaulting perfume. She then offers an analogy borrowed from another teacher: “It’s like being barefooted and walking across blazing hot sand or across cut glass or in a field with thorns and your feet are bare and you say, ‘Oh, this is really hurting. It’s terrible. It’s too sharp. It’s too painful. It’s too hot. Do I have a great idea! Everywhere I go, I am going to cover it with leather. And then it won’t hurt my feet anymore.’ That’s like saying, ‘I’m going to get rid of her and get rid of him and get the temperature right, and I’m going to ban perfume in the world and there will be nothing that bothers me anywhere. I am going to get rid of everything – including mosquitoes – that bothers me  anywhere the world, and then I will be a happy, content person.’”

Chodron could have replaced “him” and “her” and “mosquitoes” with the word “tic” and describe me 100%. In the aftermath of a devastating and unexpected diagnosis, I was too emotional to do the logical thing. I wasn’t able to see past my anguish and simply wrap leather around my feet – instead of the desert – and walk pain free across a desert of uncertainty.

If only someone out there could have told me what I know now: That Tourettes isn’t a death sentence. Not only would my son go on to defy any ridiculous stereotypes of what it means to have a tic disorder, but he would develop a soul far stronger and richer than I would have imagined. His ability to transcend his label was not due to thriving despite uncomfortable and dire circumstances, because my son never saw his disorder as tragic. Ticking was just a small facet of who he was. Instead of being Stink, the kid with Tourette Symptom, my son quickly showed me, and the world, that he was silly Stink, the kid who cracked jokes and loved karate and told fabulous stories and read everything he could get his hands on and made babies laugh and adored his sister and held my hand even in the third grade and was fearless in tumbling class and thought each one of his three biological grandmas were the most awesome women on the planet and oh, in addition to these endearing characteristics, he had Tourette Syndrome.

As a woman who had lived her entire life judging herself on what she did, instead of who she was, it took a long time for Stink’s philosophy to sink in. I still struggle with it, but like Chodron’s desert analogy, I have learned to accept that I can’t change the tics, but I can change myself. This includes letting go of expectations of what I want, and becoming more comfortable with what is. And some days, when he’s ticking a bit more than I’m comfortable with, I still freak out. But instead of judging myself for my reaction, I am willing to look at myself with compassion. Like my son’s face, that occasionally decides to eye roll or nose scrunch, I’m not perfect. I am perfectly human. And that is enough.

One of my favorite all time stories about special  needs is called “Welcome to Holland.” I took the liberty of adapting it for my experience with Tourettes.

One day a family of five boarded a plane headed for London. It was winter, which meant their luggage was filled with sweaters, thick wooly socks, mittens and scarves. The mother, who had dreamed of this vacation ever since she had children ten years prior, had planned out the entire trip in painstaking detail. They would have tea near Buckingham Palace after shopping at Harrods. They would tour the Tate and take a family Christmas  photo in front of Big Ben.  They would catch a show in the West End and go to mass at St. Paul’s.

After two hours on the plane, she looked over at her three children who had magically fallen asleep in the seats between herself and her handsome husband. She grabbed her mate’s strong hand, smiling at how perfectly everything had fallen into place.

At one point the captain’s voice streamed over the P.A. system.  “Ladies and Gentlemen, thank you for flying with us today. Due to some unexpected orders from the ground crew, this plane will no longer be flying to England. We will be changing directions entirely and landing in Africa. I can’t give you much information other than we cannot alter our course. You will have no choice but to make the best of the new arrangement. We’re not sure when we’ll be able to get you back home but you all seem like capable people who can wing it just fine. So, with that in mind, enjoy your new destination!”

Understandably, the mother was horrified at this news. Her husband remained cool and collected. She was both grateful, and horrified, that he wasn’t as freaked out as she was. How could he be so calm??! How could this enormous error happen? She wasn’t prepared for this abrupt switch of plans! This was not the way her dream vacation was supposed to go! The remainder of the flight was spent in abject misery as she ruminated, sulked, cried, moaned, hollered and generally cursed her fate.

By the time the plane landed, she was in quite a quandary. While this was one of the most unsettling experiences of her life, she also knew that falling apart would not help anyone. She’d have to be strong for the kids. She’d have lean on her husband when she could. But mostly, she’d have to lean on herself. She’d attempt to make the best of it. What choice did she have?

Once on the ground, the luggage never arrived. Everyone was sweltering in their woolen sweaters and itchy pants. What could she do? She borrowed a pair of scissors from a taxi driver and cut off the sleeves which they used as headbands. She turned their pants into shorts and hailed a taxi.

As this disheveled family of five crowded into a cab, the driver had a good laugh at their outfits. It turns out he spoke English and asked what happened. Against her normally private nature, she told him. He invited her family home to his home and she said yes. Clearly she needed help and couldn’t rely on herself anymore.

For the next two weeks, her family  did not shop. They did not tour museums. They did not eat at restaurants.

They ate home cooked meals around a plain wooden table with the taxi driver’s wife, her sisters, their kids and 20 other people with names  she could barely pronounce on Day 1 but by Day 20 knew as well as her own family’s names.

The kids ran around  barefoot  with children who didn’t speak their language but sure knew how to laugh.

Her husband helped reupholster  taxi driver’s car which earned the family some extra money which they turned around and used for goodbye feast when the time came to finally fly back home.

With bellies full of food and hearts full of gratitude, they said their tearful goodbyes and boarded the plane.  As they flew back, the mother couldn’t help but think that Africa was a far cry from England. It wasn’t as civilized. It wasn’t as comfortable. But it was exotic. It was different. And her family bonded more in that two-week unplanned adventure in an African village than they ever would have in pristine London hotel.

That mama, despite feeling like she was going to drown in despair, faked a good attitude until a true, authentic joy bubbled up from the pit of her soul. Despite signing up for it, she made the best of it and had an adventure of a lifetime.

You will, too. Grab your TS passport. TS is an adventure. It might seem scary, but let this book be your road map.

Let me be your tour guide.

It’s going to be a bumpy ride, but I promise you’ll land safely and have the time of your life.

Buckle your seatbelt. It’s time to Happily Tick Off.


14 thoughts on “My Book Intro – Feedback Please!”

  1. WOW! You are really an amazing writer, Andrea!! This is really good.

    It totally addresses the heart of the matter for moms. It gets to the only real way to be ok and have peace no matter what. I think it is just what anxious mommies need to read.

    LOVE, LOVE, LOVE it!!!! I want to read more!

    (I will let the grammatical stuff slide for now. 🙂

  2. Grammer aside….and the fact that I don’t like reading….I think its great and can’t wait for the first chapter….only thing I may tweak is the definition because as we all know it clearly lasts longer than a year but a newbie may be like cool 1 year and it will go away rather than crap now it can be diagnosed 🙂

  3. Perfect intro- You couldn’t have written your original book- THIS is the book that gives you the TRUE answer to Tourette’s: there isn’t any – but you can still have peace, and a happy, well adjusted child. Very engaging and funny- the gift receipt part almost made me spit coffee on my laptop.

  4. @ Everyone – Thank you. I appreciate it. I’m so ready to have done! I will delete this post in a few days just so it’s still private until I get it done

  5. I love it !! “Thank you but no thank you” was so funny. Exactly how I feel. I am a control freak as well and still in the early stages of all of this. Your book is so needed for us, and all the families out there with TS. We need humor and encouragment and to feel like someone “gets it.” Keep writing !!!! 🙂

  6. You know I love anything you write Andrea! I have said it before…your writing is a gift….and you need to write this book! I love it.

  7. Andrea,

    This is a really good intro. I think I might agree with your friend who said you could keep some of the great details out of it.
    For me, writing the book the way you did (vs. the definite answer to TS) is brilliant, because it now appeals to those who have a child with TS, another diagnosis, or no diagnosis at all. I’m interested in reading it, for example, because your journey is inspirational. Everyone can relate to your story without having to live through similar details. Good work! -Adelia

  8. Andrea,
    What wonderful writing. I admire you using your experience to help other people. Keep up the great work!

  9. My initial thought was this intro is pretty long as in wow this is a short story within the book…if that makes sense. I think its great and it keeps my interest and is a fast read but I do agree with your friend..it kinda feels like it did when I read romeo and juliet in high school….bear with me…we read the whole thing and got to the end and the last 2 pages summarized the whole thing without me having to read the book…in this case it feels like I’ve read the book and haven’t started

    1. Oh oh oh…or like the movie trailers that give ya the whole movie in the trailer….really wish I knew what the chapters say so I could be of more assistance 🙂 and know if I’m off base

  10. @ Lisa and Adelia – I really appreciate your comments. I know that I have a LOT of stuff in the book that the intro doesn’t cover, but if as a reader, it feels like it’s being given away, then I have to think about that. My main thing is I want everyone to have hope. LIke you, LIsa – you have T.S., and you have a girlfriend and a job and kids and a good life. It wasn’t a death sentence for you. I want people to know it’s going to be okay. THANK YOU ALL! And Judy, thank you!

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