Meet Our Kids
Dylan White was born on July 4th, 2008. Dylan overcame many difficult challenges at birth. He was born prematurely at 32 weeks without a recorded heart rate for first 11 minutes and 52 seconds of life. Dylan stayed nearly 3 months in Sutter Memorial Neonatal intensive care unit. He underwent multiple life-saving surgeries during his stay due to prematurity and oxygen loss. Dylan's oxygen loss left him with moderate hearing loss in both ears. Dylan began wearing traditional hearing aids when he was 5 months old.
In January 2011, we discovered the services provided at CCHAT after a chance encounter with another parent. Dylan began attending CCHAT within 2 weeks and we noticed a significant improvement in Dylan's verbal communication right away.Within 6 weeks of attending CCHAT, Dylan began vocalizing his wants and needs more and crying less out of frustation. After 2 + years at CCHAT, Dylan is catching up to his older brothers and giving them an earful on daily basis. CCHAT has given Dylan a fighting chance at a life of normalcy we did not expect to happen prior to CCHAT. There is no way we could ever thank CCHAT enough for what they have given Dylan and our family. ~ The White Family
What a great teacher taught me...
The best teachers are said to be those who can think outside the box. At the CCHAT Center, sometimes this means getting in the box...literally. No matter how grumpy a child might be, through the magical power of a cardboard box (or an amazing teacher), a jump into Diane's mysterious attitude adjustment box always results in a smiling face and positive attitude.
Diane teaches with her heart. She is passionate, caring, alive, present, inspiring, real and possesses a love for what she is teaching. Teaching a profoundly deaf child to listen and speak takes skill, patience, creativity and a leap of faith. Diane genuinely believes every child with hearing loss is capable of learning to listen and talk. This expectation creates a self-fulfilling prophecy. The children, parents and staff sense her confidence and work to make it happen.
Diane begrudgingly tolerates the massive amounts of paperwork and testing now required of teachers in special education. She rolls her eyes at fancy, expensive materials and technology. She firmly believes her time is best spent with her students and that she can do her lesson with old fashioned balloons. She makes classroom experiences exciting and memorable. Think tactile, unexpected, movement-oriented, and a little bit crazy...and you will be on the right track. She celebrates the smallest student successes, shows compassion for struggling parents, laughs at her own mistakes and isn't afraid to be imperfectly human in front of her students.
I feel privileged to have worked with someone who reminds me on a daily basis to believe in children, to be compassionate, to laugh and to make decisions with my heart. Diane, thank you for your unwavering conviction that every child deserves both a chance and our respect and for your constant support and belief in me. You made a difference. ~ with much appreciation, Laura
It wasn't until Reagan turned 3 that we found out she was moderately/severely deaf in both ears. We were shocked to receive this news as Reagan and her twin brother, Reid, both had passed their newborn hearing tests. However, we were determined to meet this challenge head-on by quickly getting her fitted with hearing aids, enrolling her in a pre-school program and taking her to one-hour speech therapy sessions twice a week. Because of her severe and undetected hearing loss, Reagan had missed out on valuable years of listening, learning and language skills.
Even though her hearing aids assisted her ability to perceive voices and sound, Reagan would continue to 'shut down,' become introverted, and often times display bouts of anxiety and frustation with others because she did not truly understand what was said to her, nor did she have the capability to communicate her needs, ideas and feelings in return. She had always been a hard-worker at home and at school, but it was apparent that, despite all that we had been doing for her to get her caught up to her hearing peers, Reagan needed additional assistance provided by audiology experts within the educational field.
Our journey with CCHAT began in July 2012, during its three-week summer school program. The entire CCHAT staff, teachers, teacher's aides and former students welcomed Reagan and her twin brother with open arms. Surrounded by warm smiles and an enormous amount of enthusiasm each day, it was clear to us that CCHAT was the perfect educational and social environment for our twins to thrive. Remarkably, in this short amount of time during summer school, Reagan began to evolve in to a completely different child. Participating in a classroom filled with other students that wear hearing aids and cochlear implants helped Reagan to truly understand that she is not alone on this life-long passage. With this new found sense of camaraderie with her peers, Reagan's confidence began to soar. Friends and family members that hadn't seen her in a while noticed immediately. She smiled more, and became more outspoken and expressive with her ideas and experiences. Reagan began to shine!
In the fall of 2012, Reid and Reagan enetered their first year at CCHAT, and we are forever grateful. Every day, they wake up thrilled to go to school! Leah is an extraordinary teacher -- she is so patient, compassionate and encouraging to all the students. Reid and Reagan are actually reading and writing...we love Leah! And Matt is always so helpful and fun with all of the kids...it's an outstanding classroom!
Every day, Reagan attends speech therapy with Lisa, and words cannot fully express our heartfelt gratitude towards her. She has given Reagan the confidence, self-advocacy and the invaluable tools to process spoken language, allowing Reagan's receptive and expressive skills to thrive beyond measure. During our time at CCHAT, Lisa has not only become Reagan's greatest champion, she has also become a dear friend to our family.
From the moment we first walked through the doors at CCHAT, Licia took our family under her wing. She has always been a positive, genuine and honest friend, and we feel incredibly relieved to know that Licia will always stand shoulder to shoulder with us - as a life-long friend and mentor - as we continue to move forward on our journey!
This fall, Reid and Reagan will be transitioning to our local public elementary school. Thank you CCHAT! Our hearts continue to melt each and every day as we watch our beautiful Reagan continue to blossom into an assertive, ambitious and amazing little girl. We are deeply grateful to Leah, Lisa, Licia and Laura for always having our back...YOU ROCK! The entire staff at CCHAT is incredible, and they continue to serve as an inspiration to our family. We are forever in your debt. ~ The Wilson family.
A Beautiful Journey We Never Imagined
When we were told that our 9-day-old son, Cruz, suffered from bilateral sensorineural severe to profound hearing loss, it was difficult to process or even understand that our son was deaf.
We were welcomed at the CCHAT Center a couple of hours after receiving his diagnosis. The moment we walked in the door, we were treated like family. We were greeted with, "We understand, we get it, we are here for you." We could have never imagined the amount of support and guidance that we have been provided. CCHAT has helped in the process of finding our surgeon; provided a support group; speech therapy; and face-to-face contact with others that truly get what we are experiencing. Because of CCHAT, we no longer fear our son's deafness as a disability, but accept it as 'A beautiful journey we never imagined.'
~ The Cordova Family.