TEAM TYLER~ Supporting The Beyond Batten Disease Foundation

TEAM TYLER~ Supporting The Beyond Batten Disease Foundation TEAM TYLER: Beyond Batten Disease. Tyler was diagnosed with Juvenile Batten Disease in 2009; he pass It began to rob him of all he had and continues to do so.

www.teamtylerallman.com
Tyler was once just like any of your children. He could read, write, play with his friends and enjoy all that life had to offer. That was until Tyler was diagnosed in June of 2009 with Batten Disease. Batten Disease is a neurodegenerative disorder that is fatal. Tyler is missing an enzyme that takes all of the bad proteins out of his brain, therefore the proteins have now

here to go and it is slowly killing his brain. This in turn has caused Tyler to become blind, suffer from seizures, as well the loss of his fine and gross motor skills. Tyler was a natural athlete and had hopes and dreams of being a business man like his dad. Batten Disease has taken all of Tyler's hopes and dream and smashed them. Batten Disease affects only 500 children in the United States and 1,200 Worldwide. Since there are so few affected, Federal Funding is sparse. It is up to us as his parents, family and friends to help slow or stop progression and ultimately find a cure. I work closely with Beyond Batten Disease Foundation and there IS hope! Because of the promising hope we cannot stop in our efforts to spread awareness like wild fire so we can BURN Batten! Every penny counts and will help us in our mission. Beyond Batten Disease Foundation (BBDF) is a 501(c)(3) and Tyler has a direct site in his honor to donate with all proceeds going to research. Please visit www.beyondbatten.org. We will also use this page as a place for you to follow along in Tyler's fight against Batten's and our mission to raise funds to help eradicate Batten Disease for ALL children. We will also use this page as a positive place to support Tyler and for you to follow and see what an amazing, strong-willed and loving child that Tyler is. Tyler has Juvenile Batten Disease which puts his life span at late teens to early 20's. Tyler is now 11...we have to fight hard; plain and simple. We thank you for your support! Love, Royer, Heather, Tyler and Ryan

03/01/2026

This is "The Allman Family" by Beyond Batten Disease Foundation on Vimeo, the home for high quality videos and the people who love them.

~2024~SIX YEARS ~ right now~ I’m not sure where the time goes. I just remember when Royer and I went to bed 6  years ago...
01/22/2024

~2024~SIX YEARS ~ right now~ I’m not sure where the time goes. I just remember when Royer and I went to bed 6 years ago and we said “what in the hell just happened?”
One minute Tyler was here; the next minute gone forever. 💔🙏🏼💙
We knew the community would be shaken the next morning. The kids at school would learn that their sweet SHARKBOY had gone to Heaven…that was the most devastating to us.

~2018~Unaware; I woke up to give Tyler his last morning kiss. Later, I had just given Tyler his final meds for the night. This is actually a video but I just took pictures from it. I truly believe he started to transition at 8:08pm, which Tyler would always say was his bed time. It’s the time that “Sharkboy” went to bed. So every night, Tyler went to bed “at 8:08”. In true Tyler style, that’s when he went to sleep for the last time on this earth. 💙💔❤️😇🙏🏼🦈❤️‍🩹

01/17/2024

Normal: Nothing is nothing normal after you lose a child. BUT… helping, talking or sharing about your child; and with anyone that has lost a child is invaluable. Not only invaluable; but it also helps speak for your child that can’t. It helps you spread love for your child that can’t. It helps spread the faith for your child that can’t. It helps family’s that have been affected that are suffering and can’t. It sadly helps you speak and share beautiful memories about that your child can’t. This next week I will be sharing Tyler’s legacy as I should because thankfully… I can.
💙😇🙏🏼❤️

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Austin, TX
78720

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