What is Tourette Syndrome? To people who do not have it, it is probably not what they think. To fully understand this baffling disorder you must be afflicted with it. There is no other way. Even then, there are no guarantees. The everyday feelings and urges to perform the tics that are symptoms of TS are unlike any that a person without TS could imagine.
There are as many cases of TS as there are people who have it. No two cases are exactly alike. This book was put together in order to raise awareness for TS. After reading them you will not totally understand TS. That is a given. It is my hope that the readers will understand it just a little bit better. Even if just one person learns more about TS or gains a greater understanding of TS as a result of reading this book, it will be well-worth the time and effort it took to write it.
Tourette’s Syndrome is an often, misunderstood neurological disorder. The main symptoms are what are called “tics”. A tic is defined as an involuntary, sudden, rapid, repetitive, unbalanced, motor movement or vocalization. The tics occur many times a day, nearly every day.
The most common motor tics are rapid eye blinking, shoulder shrugging, squinting, and facial grimacing. Some of the less common tics include grinding teeth, neck jerking, flailing arms, biting nails, and toe curling.
The most common vocal tics are throat clearing, sniffing, grunting, coughing, and stuttering or stammering.
There are a few important facts about TS that are important know. Up to one in 100 schoolboys have some form of TS. Three to four males have it for every female. The diagnosis is often missed. TS symptoms usually decrease with age. TS is an inherited disorder. Learning disorders, panic attacks, school phobias, speech problems, and sleeping problems are common too.
People with TS usually also have either ADHD (Attention Deficit Hyperactivity Disorder, or OCD (Obsessive Compulsive Disorder). Many people with Tourette’s have both of these accompanying disorders.
When most people think of TS they think of the disorder where people with it swear uncontrollably and profusely.
This symptom of TS (coprolalia) is the easiest symptom to recognize, but it is also the rarest. It is important to remember that coprolalia is present in less than thirty percent of TS patients.
Most people with TS, when describing a tic, say that they feel a sudden tension building up that must be relieved by performing the tic. Tics are suppressible for varying lengths of time. The longer the tics are suppressed the more the tension builds up and the more there is a need to release them.
Another major characteristic of TS is a waxing and waning of the symptoms. This includes both a change from one tic to another, to the complete disappearance of symptoms for varying periods of time.
The tics usually begin during the ages of five through nine, but symptoms can start as late as twenty years of age.
While motor and vocal tics are the main symptoms used to make a diagnosis, and they are what are most identified with TS, there are many other problems that can be associated with it, the main of which are behavior related.
The people with TS who suffer from these behaviors are often angry, argumentative, and confrontational. Everything has to be their way or is someone else’s fault. One minute they’ll be fine and the next minute they’ll be in a rage. They tease their siblings relentlessly. They have a short temper, smart mouth, talk back, throw temper tantrums over nothing, and won’t take “no” for an answer. Many of them lie and steal too. Of course it is difficult to tell if a person’s TS is causing these behaviors or something else is, but many studies of TS patients have shown that these behaviors are much more common in them than in people without it.
Very few people with TS have symptoms that require medication. Medication is usually only prescribed when a person’s symptoms prevent them from doing routine activities. Just like no two TS patients cases are the same, either are the treatments.
Medication must be carefully monitored and doctors’ instructions must be followed precisely to benefit from the medications. Almost all of the medications have side effects, some of them many and some of them major. Many TS patients decide to live with their many symptoms, and stop taking medication, because living with the side effects is more than they can bear.
This book will probably make you laugh. It will probably also make you cry. I have told my story in a brutally honest way. Even though there is almost no chance of you walking in my shoes I have told my story the best way I know how to help you understand what people like me go through every day of our lives. I am proud to present to you my book about what makes me “tic.
What Makes Me Tic: Living With Tourette Syndrome Description:
This is not a Medical Book. It’s the story of a Man’s Life. A Man with a lot of talent, a man with some challenges. A Man perhaps very much like you, a Man named Chris Mason. This Man has had a life much like any other man, but from time to time his life has been punctuated by Tics resultant from a disorder known as Tourette’s Syndrome.
Usually, Tourette’s is more a puzzling phenomenon that is only sometimes traumatic, than a dreaded disease. Mr. Mason relates experiences of his life from childhood through adulthood that can help both Tourette’s Sufferers and Parents to better understand this Syndrome.
The quirks and conundrums of the Human Mind and the Human Experience are always present all around us, but are sometimes more visible and interesting in the case of a Tourette’s Sufferer.
As the author explains, his book pulls no punches.
“Readers will laugh, they will cry; they’ll be shocked at what they didn’t know and be ashamed by their previous assumptions. In all, I tell a brutally-honest story that attempts to put readers in my shoes,” says Mason, a prolific writer.
Continuing, “I am proud of who I am and am blessed to be in a position to help raise awareness on behalf of the millions of Tourette Syndrome sufferers around the world. If I can change how just one person thinks, it will all be worth my time. However, I intend to enlighten the masses – it’s time attitudes changed!”
Amusing and sorrowful, all interested readers are urged to purchase their copies as soon as possible.
‘What Makes Me Tic: Living With Tourette Syndrome’ is available now: http://amzn.to/1a2hemB.
About the Author:
My name is Chris Mason. I am a forty-three-year-old male. I live in San Francisco, CA. I have Tourette Syndrome and Obsessive Compulsive Disorder. I began having symptoms of both disorders at the age of six, but I wasn’t diagnosed until age twenty. For fourteen years I wondered why I had these strange symptoms and why I was different than everyone else. I had trouble in school because of behavior problems and learning disorders. I also have some undiagnosed mental illnesses.
I am now on medication, which has totally rid me of all my tics, but at a price. The medication has many side effects that I have been dealing with and trying to control, with no avail, for the twenty-three years I have been taking it. I know that unless there is a cure I will be on medication for the rest of my life. This is my second book. My first book (Touretties) was published in 2011. It is an anthology that includes twenty-one true short stories, including my own, about people who have or have a family member who has Tourette Syndrome and its associated disorders.
Contact:
Chris Mason
My website: www.facebook.com/cdm230
My e-mail: cmason@astound.net
Link to buy my ebook on Amazon: http://amzn.to/1a2hemB
