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Tourette Syndrome Awareness Month: A Conversation with Brad Cohen and Kid Author Dylan Peters

June 10th, 2010

Double Click Flyer to Enlarge and Read

The call with Brad Cohen and kid author Dylan Peters will be on Saturday, June 12th at noon/EST and will last 1 hour. Learn how children can become advocates for themselves and how one boy decided to not only tell his classmates, but tell the world about TS through his book, Tic Talk: Living with Touretre Syndrome, A 9-year-old boy’s story in his own words.  

Feel free to email us questions to read during the call. The conference call is free to the public.

E-mail us and ask for calling numbers and access codes for the conference call. When you email us, an auto-respond email will be sent to you with instructions: tsawareness@bradcohentourettefoundation.com

You can also click here to learn more about TS Awareness Month

Feel free to share this information with anyone who may be interested. Education about Tourette Syndrome will continue to make a difference for those who live with the condition daily. This event is sponsored by The Brad Cohen Tourette Foundation. Thanks for the support of Tourette Syndrome Awareness Month!

Cheers, Brad


Tourette Syndrome Awareness Month: A Conversation with Brad Cohen and author Sheryl Pruitt

June 1st, 2010

Double Click Flyer to Enlarge so you can Read

The call with Brad Cohen and educational consultant/author Sheryl Pruitt (Teaching the Tiger) on Thursday, June 3rd at 7pm/EST will last 1 hour. Learn about the co-morbid conditions that go along with Tourette syndrome as well as other education strategies for the classroom. Feel free to email us questions to read during the call. The conference call is free to the public.

E-mail us and ask for calling numbers and access codes for the conference call. When you email us, an auto-respond email will be sent to you with instructions: tsawareness@bradcohentourettefoundation.com

You can also click here to learn more about TS Awareness Month

Feel free to share this information with anyone who may be interested. Education about Tourette Syndrome will continue to make a difference for those who live with the condition daily. This event is sponsored by The Brad Cohen Tourette Foundation. Thanks for the support of Tourette Syndrome Awareness Month!

Cheers, Brad


Tourette Syndrome Awareness Month: A Conversation with Brad Cohen and actor Jimmy Wolk

May 23rd, 2010

Double Click Here to View Flyer of Event

The call with Brad Cohen and actor Jimmy Wolk (Front of the Class) on May 25th at 7pm/EST will last 1 hour. Learn more about what happened behind the scenes on the set of the movie. Understand how an actor portrays someone with TS successfully. Feel free to email us questions to read during the call. The conference call is free to the public.

E-mail us and ask for calling numbers and access codes for the conference call.  When you email us, an auto-respond email will be sent to you with instructions: tsawareness@bradcohentourettefoundation.com

You can also click here to learn more about TS Awareness Month

Feel free to share this information with anyone who may be interested.  Education about Tourette Syndrome will continue to make a difference for those who live with the condition daily.  This event is sponsored by The Brad Cohen Tourette Foundation.  Thanks for the support!

Cheers, Brad


Tourette Syndrome Awareness Month

May 11th, 2010

Double Click to Enlarge Flyer

 

Join Brad Cohen during Tourette Syndrome Awareness Month for some conference calls with guests to create awareness for Tourette Syndrome. This series is titled “Talking Tourette with Brad Cohen and Guests.” Brad will be speaking with the following people on these dates:

May 17th 7pm/EST Brad’s mother, Ellen speaking from a mother’s point of view
May 25th 7pm/EST Jimmy Wolk, actor from Front of the Class -get the inside scoop from the movie
June 3rd 7pm/EST Sheryl Pruitt, author and educational specialist on Tourette syndrome-learn more about the co-morbid conditions of TS and educational strategies in the classroom
June 12th noon/EST Dylan Peters, author of the book Tic Talk speaking from a child’s point of view on advocacy

Click here to learn more about TS Awareness Month

E-mail us and ask for calling numbers and access codes for the conference calls: tsawareness@bradcohentourettefoundation.com

Each call will last 1 hour. Feel free to email us questions to read during the call. All four conference calls are free to the public.

Help us spread the word about this event to help create more awareness for Tourette Syndrome. This event is sponsored by The Brad Cohen Tourette Foundation. Tourette Syndrome Awareness Month is from May 15 – June 15 2010. Join us on Facebook too by clicking here!

Cheers, Brad


The Newest Addition to the Family: Dylan Louis Cohen

April 9th, 2010

Nancy and I are excited to announce the birth of our baby boy, Dylan Louis Cohen, born on March 25, 2010 at 6:40pm. He weighed 7 lbs 13 oz and was 19 inches long.

We are a happy family and we appreciate all the kind notes that have come in from so many of our fans.

We appreciate the support!
Cheers, Brad Cohen


Hallmark Channel Now Featuring Front of the Class

March 31st, 2010

What do Martha Stewart and Front of the Class have in common?

They will both be featured on the Hallmark Channel! The first viewing will be on Saturday, April 3rd at 9:00pm/est. Look for reruns to continue throughout the year.

Feel free to spread the word to those who missed it the first few times. This is your chance to learn more about Brad Cohen and Tourette syndrome. Check out Jimmy Wolk, Patricia Heaton, Treat Williams, Dominic Scott Kay and so many other wonderful actors as they help the world discover that dreams can come true!

Get updated on Brad’s new foundation too. The Brad Cohen Tourette Foundation is up and running. Sign up on this website for updates.

If you like the movie, be sure to check out the award winning book too. It makes for a great present to educators or anyone looking for an inspirational story. Buy the book or DVD now!

Cheers, Brad


Showtime! Front of the Class on CBS!

February 4th, 2010

Set your DVR’s now for an encore presentation of Front of the Class on CBS, Saturday, February 6th at 8pm (est). Please be sure to spread the word to friends and family members. This is one movie you will not want to miss. And if you have already seen it once, you know you’ll want to see it again.

If you have Tourette syndrome or you know someone who faces a challenge in life, this is a movie that could change your life. Teachers, don’t miss this movie! If you don’t believe me, that’s ok. I’m not bias. But this is my new favorite movie of all time!

If you do miss it or you’re interested in owning a copy of the DVD, you can find it in your local Hallmark store or feel free to buy an autograph copy from my website. Click here to learn more.

To learn more about the Brad Cohen Tourette Foundation, visit our new website: www.bradcohentourettefoundation.com

As always, I appreciate the support!

Cheers, Brad


American Idol Contestant, Dave Pittman, Shocks Doogie Howser Because He Has Tourette Syndrome…….But Why?

January 28th, 2010

Dave Pittman, American Idol Contestant

Did you watch American Idol? Did you hear the news? This is what I heard over and over through facebook, emails and when I got to work the next day. Many of them wanted to make sure I had seen Dave Pittman on American Idol because they knew I would be interested.

The answer is yes, I saw American Idol and yes, I heard the news. I was really excited when I saw that Dave was being open and honest about living with Tourette syndrome. My biggest fear was that he was going to be a poor singer and the judges and America would then make Tourette syndrome the punchline of another bad joke. But then we heard him sing. The judges were into Dave as they nodded their heads up and down as they enjoyed what Dave had to offer.

But then, Doogie Howser M.D. stepped up to the plate. Like any other doctor, he recognized that Dave had a medical condition called Tourette syndrome. I was excited Doogie knew about Tourette’s. He even addressed it on air. I was proud of that too. Dave stood tall and accepted Doogie’s comments and explained he had TS. As many of us Touretter’s know, when we are concentrated on something, we don’t tic nearly as much. The judges were a little shocked by this.

The part that was disturbing was that the judges were actually surprised that a person with Tourette syndrome could actually be such a good singer and do it without the tics disrupting the performance. People with TS or any other disability live with this perception on a daily basis. People don’t believe in us and think we can’t do certain things.

I can already tell that Dave is similar to me. He will, and has already stepped up to the challenge. You see when someone tells me I can’t do something, or even if they “think” I can’t do something, it just motivates me more to prove them wrong. Dave now has the stage to show the world his own talents, while at the same time be a great role model for the millions of people who are a little different.

I guess you now know who I will be rooting for in this years American Idol competition, and I hope you will root for him too. Because we need to show people that we all have talents and when given the right opportunities, we are able to shine.

So what is the biggest shock? Is it that Doogie brought up the elephant in the room? Is it that Dave has a good voice? Could it be that a person with Tourette syndrome can find success when given a chance? Or could it be that dreams CAN come true when given a chance?

Step up to the plate America and turn your TV sets to this season’s American Idol on Fox. Let’s all hope that we can embrace Dave’s challenge and root for him because of his true talents. Vote the way you want, at least you know what I’ll be doing.

Get caught up with the latest news from the Brad Cohen Tourette Foundation by visiting www.bradcohentourettefoundation.com

Read the book or see the movie Front of the Class to learn more about Brad Cohen.

Cheers, Brad


Just a Reminder!

January 16th, 2010

Today, I had a little girl email me a simple question: How do you live with Tourette syndrome….with all the people saying stuff?

She went on to tell me she received the movie Front of the Class, and it was the best thing she got for Christmas.

It was just a simple reminder that kids are still figuring out the game of life. So with that, I remind everyone what has helped me overcome the challenges of living with Tourette syndrome. I hope these ideas help others move forward to follow their dreams.

1) Keep that positive attitude
2) Focus on your strengths…….show the world what makes you shine
3) Educate everyone who will listen and tell them about Tourette syndrome and the challenges you face
4) Never give up……every time someone tells you that you can’t do something, prove them wrong! Show them not only can you do it, but you can do it better than others
5) Surround yourself with people who believe in you
6) Don’t make excuses, because the first excuse will lead to another, after another, after another
7) Find your passion in life and go for it
8 Last but not least……….Don’t let Tourette syndrome win! Don’t allow any of your weaknesses in life get the best of you!

While we are talking about Tourette Syndrome, you can help support the National Tourette Syndrome Association by clicking on the link below and vote to help them win $1 million in the Chase Community Giving Contest. Spread the word. Each person gets five votes and be sure to place one with TSA. Thanks for the support!

http://apps.facebook.com/chasecommunitygiving/charities/744837

Don’t forget, Front of the Class will be on CBS the evening of February 6, 2010.

You can also learn more about the Brad Cohen Tourette Foundation, Inc at www.bradcohentourettefoundation.com

Cheers, Brad


Camp Twitch and Shout- The Movie

December 28th, 2009

Camp Twitch and Shout logo

I’m excited to share two video clips with you. Camp Twitch and Shout-The Movie (a 30 minute documentary) and a 7 minute preview of what Camp Twitch and Shout is all about. They were put together by Emmett “Butch” Williams, one of my former counselors from Camp Sabra when I was growing up. Emmett spent a week with us at Camp Twitch and Shout to film what we were all about.

These movies will give you insight of what it is like to have Tourette syndrome and what we deal with on a daily basis. At the same time, it will show you why Camp Twitch and Shout needs to be supported and the difference we are making in the lives of children and adults with TS.

Camp Twitch and Shout provides an opportunity for children with Tourette syndrome to join others who are similar to themselves and just have fun for one week. Our goal, is that those memories made will stick with everyone for a lifetime. I believe these movies will show you what happened for one week and how that week changed lives forever!

This is why I have also started The Brad Cohen Tourette Foundation, Inc. To raise money to help support Camp Twitch and Shout and other camps and programs like this for children with Tourette syndrome around the country. If you are interested in making a donation, visit www.bradcohentourettefoundation.com

June 27-July 2, 2010 will be the dates for this year’s Camp Twitch and Shout, located just outside of Atlanta, GA. Applications will be ready around February 1st. We will be looking for both campers and volunteers from around the country to attend.

Enjoy the movies and as always, thanks for the support!

Cheers, Brad


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Testimonials
"Brad Cohen is a walking billboard for the idea of living positively. He is like a cold drink on a hot day--refreshing, energizing, and likely to put a smile on your face."
Tim Shriver - Chairman of Special Olympics

"I have observed the magic of Brad Cohen in the classroom. He has turned Tourette Syndrome into an asset, and his life into inspiration."
Senator Johnny Isakson, Georgia

"Brad Cohen's story is a triumph of hope, determination, will and relentless good humor."
Peter J. Hollenbeck, Ph.D., Professor and
Associate Head of Biological Sciences,
Purdue University


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