Synergy Children’s Therapy

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Synergy Children’s Therapy Welcome to Synergy Children's Therapy, providing Speech and Language Therapy for Children

As a Speech-Language Pathologist, there are so many things I TRULY LOVE about my job!  And the moments that I witness wi...
10/13/2026

As a Speech-Language Pathologist, there are so many things I TRULY LOVE about my job! And the moments that I witness with families as their children learn to communicate more effectively and efficiently are humbling and soooo rewarding. BUT, today I was part of a special moment in my dad’s life! He has been deaf in one ear for 12 years and hearing impaired in the other. It has taken away social opportunities, made him struggle to comprehend information, and even strained some social and family relationships. But today, through the power of technology my daddy received a COCHLEAR IMPLANT! It was sooo amazing to be part of this day when you saw his eyes light up and he could hear again!!! ❤️. We still have several more days of learning, training, and adjusting-but he’s off to a great start! Thank you to all the families that shared prayers and positive thoughts over him! It is much appreciated and I’ll see everyone soon ❤️

Amazing story of finding one’s place!
10/08/2026

Amazing story of finding one’s place!

Claire-Marie was born on December 8, 1984. Shortly afterward, she was left behind at the hospital.
Doctors had already told her biological mother that the baby would have Down syndrome, and according to Claire-Marie's later account, she had even been advised not to continue the pregnancy.
Claire-Marie was born anyway.
At around 8 months old, she was adopted and finally had a family of her own. Her childhood unfolded between France and Poland, surrounded by the faith that would eventually become one of the strongest parts of her identity. 🙏
As she grew older, Claire-Marie became increasingly aware that people sometimes saw her disability before they saw her.
Her response was never to hide it.
In 2013, she formally consecrated her life to Jesus, becoming a consecrated woman in the Catholic Church. She later moved to Lourdes, where she became involved in visiting sick people, welcoming pilgrims and speaking with groups of young people about faith, happiness and what it means to value every human life.
Claire-Marie can sometimes speak to hundreds of young people at a time.
And she doesn't pretend that having Down syndrome means life has always been simple.
She simply refuses to describe herself only through what she cannot do.
“I thank the Lord because I have a disability, but I still have two arms, two legs; I can walk, talk, pray,” she once said.
In 2022, her journey brought her to the Vatican as part of a synodal gathering involving people with disabilities from around the world. There, she spoke about creating a Church where people with disabilities are not simply cared for, but are also given meaningful roles and a voice of their own. ⛪
At the end of a general audience, Claire-Marie had the chance to meet Pope Francis.
She hugged him.
He asked her to pray for him.
She immediately promised that she would.
Today, Claire-Marie continues her life in Lourdes and remains involved with Pôle de Lumière, an association supporting families of children with Down syndrome.
Her story began with a baby who was left in a hospital.
More than four decades later, that same woman stands in front of young people, pilgrims and church leaders telling them something she has repeated for years:
“Life is a gift.”
How much can a person's story change when someone chooses to see possibility where others initially saw only limitation?

Amazing opportunity for parents!! FREE!!
09/24/2026

Amazing opportunity for parents!! FREE!!

32 autism experts share their knowledge with parents of autistic children

09/23/2026

As a child who grew up nonverbal until the age of eight, I learned early that compliance was often prioritized over connection within my speech therapy sessions. I internalized this. Completely.

I was expected to remain in my chair. I completed drill after drill. I was taught, directly and indirectly, that I needed to control my body, ignore my discomfort, and appear ready before I could be seen as ready to learn. In many ways, I had to learn how to mask before I was given the chance to learn how to speak. I want you to sit on that for a moment.

I was born with childhood apraxia of speech, and I desperately wanted to communicate. I wanted people to know what I was thinking. I wanted to connect with the world around me because I was trapped in my brain. My desire to speak was greater than what I was feeling during those sessions, so I pushed through. I did what was expected of me because speech felt like something I had to earn.

That approach may have helped me develop spoken speech with the direct method of motor planning itself, and I will always be grateful for the treatment and support that helped me fight for my voice. But gratitude and honesty can exist together. I can appreciate the skills I gained while also acknowledging the lasting consequences of how I was expected to gain them.

For years, I blamed myself. I wondered why sitting still was so hard. I wondered why I could not simply fit in or behave like everyone else. I thought my sensory needs, movement, distress, and differences were personal failures. Looking back now, I understand that none of that was my fault. I was a child trying to participate in an environment that did not fully accommodate the way my body and brain worked.

Children should not have to hide their needs to prove that they are capable of learning. A child having a disability does not mean they can not learn, instead, we need to adjust the learning environment to meet their unique needs.

Connection is not a reward that comes after compliance. Connection is what makes learning accessible. When a child feels safe, understood, and respected, they are more able to engage, communicate, and build trust with their provider.

If we do not build a connection with the child, respect their autonomy, support their sensory needs, and provide the accommodations they need to participate, we are setting them up for failure. We cannot call a child “noncompliant” when the session itself is inaccessible. We cannot assume a child is unwilling to learn when their body may be communicating that they are overwhelmed, uncomfortable, dysregulated, afraid, or exhausted.

Participation does not have to mean sitting still in a chair. Attention does not always look like eye contact or a "quiet body" (I dislike this term). Progress should not require a child to suppress natural movement, tolerate distress, or disconnect from their own body. A child can learn while standing, moving, taking breaks, using AAC, avoiding eye contact, or engaging through an interest that feels meaningful to them.

Our job is not to make children look less disabled. It is not to train them to appear compliant for the comfort of adults. The goal should be to help each child communicate in ways that are authentic, accessible, and meaningful to them.

This requires providers to ask different questions. Instead of asking, “How do we make this child comply?” we should ask, “What is this child communicating through their behavior?” Instead of asking, “How do we keep them in the chair?” we should ask, “What would make this environment more accessible?” Instead of measuring success only by completed trials, we should also consider whether the child felt safe, had choices, trusted the provider, and left the session with their autonomy intact.

I am sharing this because many speech-language pathologists follow my work, and many parents take what they learn from me back to their child’s SLP. I want us to have honest conversations about what therapy can look like and how it can improve. This is not about blaming every provider or dismissing the value of speech therapy. It is about recognizing that good intentions do not automatically prevent harm, and that we can do better when we listen to people with lived experience.

I will always value the support that helped me learn to speak. I also have a responsibility to tell the whole truth: communication should never come at the cost of a child’s sense of safety, identity, or worth.

Children deserve therapy built on trust. They deserve choices, accommodations, movement, breaks, sensory support, and access to every form of communication that works for them. Most of all, they deserve to know that they are not broken, difficult, or failing.

I was never broken nor will I ever be; and today as an adult I finally know that.

- Jordan Christian LeVan

Families, we need your help and support! There’s a link in the following article for families to use to share their stor...
09/23/2026

Families, we need your help and support! There’s a link in the following article for families to use to share their story about the impact speech therapy services have had in your lives and in the lives of your children and the importance of these continued services. If rates are reduced our availability and ability to provide the services with excellent care is severely compromised! Please take the time to respond. Your support is greatly appreciated!

https://www.facebook.com/share/1Ed2Zrh2Je/?mibextid=wwXIfr

Speech therapists pushing back against billing changes https://whnt.com/news/huntsville/speech-therapists-pushing-back-against-billing-changes/

So true for so many kiddos!  Really good read for perspective ❤️
09/11/2026

So true for so many kiddos! Really good read for perspective ❤️

I was labeled nonverbal until I was eight years old; and this is something I wish everyone knew when I was growing up.

Because I couldn’t speak, people often made assumptions about me. Some assumed I couldn’t hear. Others assumed that because I couldn’t communicate with spoken words, I couldn’t think, understand, learn, or have something meaningful to say….

But I could.

I was there.

I was listening. I was thinking. I was learning. I was observing. I had opinions, feelings, ideas, and an entire world happening inside of me.

However, my diagnosis of childhood apraxia of speech made it extremely difficult for me to turn the words I had in my head into spoken words. My inability to speak was not an inability to think.

…and when people failed to understand that distinction, I felt even more trapped inside of my own body.

Imagine knowing what you want to say but not being able to make your mouth say it.

Imagine watching people talk around you while wondering if they even realize you understand everything they’re saying.

Imagine being treated as though you aren’t capable of learning simply because you communicate differently.

That was my reality.

There were times when I would be at extended family members’ houses during the holidays and feel like I wasn’t really being included. There were times when I sat by myself at lunch.

I don’t share those memories for sympathy. I don’t want your sympathy. I don’t share them because I want anyone to feel sorry for me. I share them because this was my real life & these experiences had consequences.

When a child repeatedly experiences people assuming they cannot understand, cannot learn, or cannot participate, those assumptions can become another barrier on top of the disability they already have.

The most important thing someone could have given me wasn’t pity.

It was patience.

Taking the time to communicate with me.

Giving me opportunities to demonstrate what I knew.

Allowing me to participate instead of deciding for me that I couldn’t.

It was presuming competence.

The reason I talk about my childhood today is because there are children experiencing this right now.

Children sitting at lunch alone.

Children being excluded from conversations.

Children being underestimated in classrooms.

Children being spoken about instead of spoken to.

Children being treated as though their inability to speak means they don’t have anything to say.

We have to do better.

Give children time.

Give them access to communication.

Give them opportunities to learn.

Give them opportunities to prove what they know.

Because the child who can’t speak may have an entire world inside of them that you haven’t taken the time to discover yet.

I know.

I was that child.

- Jordan Christian LeVan

08/27/2026

Texas has officially expanded the age limit for its Children’s Autism Program, meaning eligible autistic Texans can now receive services through age 21. The new rules took effect August 25.

Under the updated rules, the Texas Health and Human Services Commission now defines a “child” in the program as an autistic person younger than 22. The changes also expand who can qualify as a professional providing diagnostic documentation, adding nurse practitioners and physician assistants alongside physicians and psychologists.

Officials said the age expansion brings the autism program in line with another state children’s program, while commenters welcomed the chance for young people to keep receiving support for longer. Importantly, this change applies specifically to Texas HHSC’s Children’s Autism Program, rather than every autism service in the state.

For Texas families, how much difference could five additional years of eligibility make during the transition into adulthood? 👇

Source: Texas Register / Texas Health and Human Services Commission, August 21, 2026
Official Texas adopted rules⁠

I haven’t taken this class, but I sounds really interesting! https://emily-hamblin.com/class/?fbclid=IwcGRvZgVmZGlkFlDNM...
08/20/2026

I haven’t taken this class, but I sounds really interesting!

https://emily-hamblin.com/class/?fbclid=IwcGRvZgVmZGlkFlDNMBiy-tsp3mpDj05xv5Wl2Qc2E7xleHRuA2FlbQEwAGFkaWQBqy93sfvBWnNydGMGYXBwX2lkCjY2Mjg1NjgzNzkAAR4tBCPjijevpgrzlYA1ehs2aZr_Ft5TjPbFb3FiZmjvK1oA03DlpZkB6AJ9CQ_aem_rONJYQVfUVTSKmxRY0rxZw&utm_medium=paid&utm_source=fb&utm_id=120242006159520074&utm_content=120242006159500074&utm_term=120242006159510074&utm_campaign=120242006159520074

FREE Masterclass for parents: Emotional Regulation for Neurodivergent Kids The step-by-step masterclass to help you teach your amazing, uniquely wired kid how to regulate their emotions – without harming your relationship In this NEW free class for parents, you’ll discover: ✅ The 2 Biggest Par...

This is awesome!!!!  If you’re heading to NY-check out the schedule!
08/01/2026

This is awesome!!!! If you’re heading to NY-check out the schedule!

For one afternoon last Sunday, an entire Broadway theater belonged to autism families.

That’s not a figure of speech. For its Autism Friendly Performances, TDF buys every single seat in the house, then makes them available at discounted prices only to families, schools and groups that include autistic people. No stranger behind you sighing. No one to apologize to.

Inside, the show itself changes. Sudden loud noises, strobes and spotlights are reduced. The house lights stay dimmed but on. Break areas staffed by autism specialists sit just outside, so anyone who needs to step out can, and come back when they’re ready. Families can download visual guides beforehand showing the theater and the characters, so nothing arrives as a surprise.

Sunday’s show was Ragtime at Lincoln Center, the first autism-friendly performance in that production’s history. It sold out.

And it was only the opening of TDF’s largest season yet, ten productions in all. Six are announced so far: Hadestown on August 23, The Great Gatsby on September 27, Maybe Happy Ending on October 25, the Christmas Spectacular with the Rockettes on November 8, and The Lion King on January 31. Four more come next spring.

This isn’t new, either. The program started in 2011 with The Lion King and has quietly run for fifteen seasons.

Details are on TDF’s site for anyone who wants them.

Source: TDF

Address

8045 FM 359 Suite 103
Fulshear, TX
77441

Opening Hours

Monday 9am - 6pm
Tuesday 9am - 6pm
Wednesday 9am - 6pm
Thursday 9am - 6pm
Friday 9am - 6pm

Telephone

+18325291593

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