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Our mission is to raise funding and awareness so that we may help find a way to Build a Bridge over this devastating disease. 

Young men with Duchenne typically live into their late teens. Today there is no cure, and very minimal treatment but that can change and has been changing greatly over the past 4 years.


Goofing off as usual

What is Braedan thinking???? Would love to know....

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Trip to Cabela's in Dundee MI to get Braedan geared up for his first deer hunt. Cabela's treated him like a king. Thanks so much to all!!!

John Owen, whom also has Duchenne and Braedan at the JOA (John Owens Adventure) picnic held in North Royalton, OH. 

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Meeting Clay Matthews was a special treat in 2012. We had tickets but were given side line passes to watch the guys practice and the hopes to meet Clay. Simply Incredible!!!

The Wheeling Sportsmens Club and NWTF organized a turkey hunt for all interested that have disabilities.  

The Wheeling Sportsmen and NWTF are forever in our family!

    Braedan's first Wild Hog.       Truly a Amazing experience to share this with him. He absolutely has a passion for hunting like no other.

Braedan and his Black Bear hunt with a Great group of guys that were involved.

Braedan and his Black Bear hunt with a Great group of guys that were involved.

In New Mexico hunting Mountain Lion with Eric. Along the way, finding this great tresure.

In New Mexico hunting Mountain Lion with Eric. Along the way, finding this great tresure.

Our Son, Braedan 10 years old

Braedans Bridge, a non profit 501(c) (3) ogranization was started by Braedan's parent's Scott and Tammy Henegar to help raise funding and awareness for Duchenne Muscular Dystrophy. In March 2011, we received news that our son was diagnosed with duchenne. Like many parents would feel, our world felt like it crumbled beneath us. We decided we would not give up our HOPE and FAITH and push forth in whatever we had to do to make his life an amazing one. Our endeavor in life, not only to make our children happy but we are helping to find a drug that will alter the path way of this disease so that our son and many of other boys with this disease will live a long happy and healthy life. The drugs to alter this are out there, and they are just within reach but yet so far away for us families that live with this. "It is probably the hardest thing any parent can go through, watching their child slowly waste away and not being able to stop it." says The Henegar Family. We will not stand by and not TRY to do something about this. We will continue to raise funding and awareness as long as duchenne continues to make its presence in the world. We will not give up our

HOPE and FAITH.

                                           IN MEMORY OF TRAVIS T DOGG COLL

                                           IN MEMORY OF TRAVIS T DOGG COLL

Our hearts weigh heavy as it is still so hard to understand that you are gone...  

until we meet again.

Travis T Dogg Coll fought his battle with Duchenne until his lord and savior called him home  February 2015.  Travis was a Godly Man that was always sharing his faith. Travis and his parents were active in helping us make our ALL IN FOR DUCHENNE the success it is today. We will continue to keep fighting and raising funds for research so that we can find a way to alter this muscle monster.  

RIP Travis Coll.

                                 Braedan dreaming of a World without Duchenne

                                 Braedan dreaming of a World without Duchenne

April 25, 2015 Braedan shot his 1st Ohio Long Beard. The Northwestern Ohio Wheeling Sportsmen and the NWTF granted Braedan a very special guide for his hunt.  He was accompanied not only by his dad, but they had Michael  Waddell "The Bone Collector" assisting in calling in the turkeys, and it only took Braedan 1 shot to take him down.

Amazing weekend that our little hunter will never forget!

Follow us on a trip of a Lifetime Braedan's Make A Wish was so graciously granted and we are about to go on an adventure like no other.

Braedan's Make a Wish was to go to South Africa and see the animals in their habitat. Braedan enjoys watching animals and not all of them are animals that he would choose to hunt. He does understand however the importance of God's Renewable resources. Here are a couple pictures from the trip. It was simply incredible!!!

With your help, we can fight this disease.

With your Help

We can

"Build a Bridge over Duchenne."

Vacation to Yeallowstone National Park 2014. Best trip ever!!!

Getting read for his first Deer Hunt in 2014 at Maumee Bay State Park with the Wheeling Sportsmens Club.

Braedan and Tom Sulfaro Jett Ride 2013

Tom Sulfaro also has Duchenne. He is one of the oldest survivors in the US and a true inspiration to our family. Him and his family are our family!

Braedan and Jackson McNutt, 6 yrs old with Duchenne MD

Braedan out Mudding on his 4-wheeler. One of his favorite things to do out doors.

 

 

Braedan and Michael Waddell "The Bone Collector" in April 2015. Braedan shot his first Turkey that day.

An Awesome day!!!

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Braedan and Ted Nugent at Sunrize Acres while Wild Hog hunting. We all had an amazing time at his ranch.

Braedan and his First 8 Point Buck that he shot in Williams County Ohio.

Braedan and his First 8 Point Buck that he shot in Williams County Ohio.

Braedan and BIlly "Catfish" Parker clowning around while gator hunting in March 2016. Braedan and Billy are so much fun together.

Braedan and BIlly "Catfish" Parker clowning around while gator hunting in March 2016. Braedan and Billy are so much fun together.