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 Although CranialTech works hard to continue the strong reputation we have, you don’t need to hear it from us. Our best spokespeople are the families we’ve treated for the last 20 years. All of their stories are unique and may very well be a situation that sounds just like your family.
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Hear from some of our newest grads!
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Your baby's plagiocephaly journey might just be beginning, but here's what some of our recent DOC Band families have to say about their treatment experience.
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From the first couple of weeks that my children were in the NICU, several different neonatologists spoke with us about the probability of our quadruplets needing cranial bands in the near future. My pediatrician agreed and was VERY adamant that we ONLY use Cranial Technologies in Dallas.
 Our treatment experience was amazing. The staff at CranialTech was SO positive and helpful—from the ladies behind the front desk to the therapists. The therapists were very thorough and quick—they were always great about getting us in and out! And when driving 60 minutes across town with quadruplets, we were MORE than grateful for their efficiency.
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 When Keller was about 4 months old, I noticed that the back of his head was flatter than it used to be. I was concerned and began to reposition him while he slept. He seemed to prefer to lay with his head to one side. I realized later this was because of some tightening of his neck muscles.
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 Dylan's family traveled from almost five hours each way for treatment at CranialTech's Pasadena clinic!
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 I remember the anxiety and fear that came with putting our daughter in her first DOC Band. Should we? Shouldn’t we? If I didn’t, would she forgive me? If I did, what if it didn’t work? I almost worried myself sick. In the end, my husband and I decided that we had a very limited amount of time to correct her head shape, and we wanted her to know we did everything we could to ensure she felt “normal” when she looks in the mirror.
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 Aiden was born 5 weeks premature on November 18, 2006. He had severe plagiocephaly with a cephalic index of 116. It was so bad that his head literally went flat right behind his right ear. In late May 2007 he was fitted with a helmet from our local provider, Orthotic & Prosthetic Lab, Inc. He did receive some initial good results: his CI went down to 96.
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When we adopted our son, Samson, from China, the day that we met him was the most amazing day of our lives! But there was one thing for which we were not prepared. The few photos of him that were provided us during the adoption process were taken directly from the front. But meeting Samson in person, and spending so much time with him during that very first day together as a family, we realized he had a strikingly flat spot at the back of his head! What did this mean, we asked ourselves? Many worried thoughts dashed through our heads.
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Our son had plagiocephaly and wore a DOC Band for three months. His treatment results were excellent, and the team of well-trained and concerned technicians at Cranial Technologies impressed us with his individualized plan of care.
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 From almost birth, I noticed that my girl twin Olivia had a funny shaped head, an asymmetrical face and that she always looked to her left. However, I was unaware that any of those were reasons to be concerned. In fact, I placed Olivia on the side of the car that allowed her to look to the left thinking I was helping her. I read so many baby books and none of them even mentioned the words torticollis or plagiocephaly.
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I was referred by the State of Florida to Cranial Technologies; before going, I read the blogs and testimonials posted on their Web site. I was drawn to the many stories of mothers fighting for their children. I made an appointment and decided to meet with the team at their Miami location to get further information and to see if we could form a relationship so that my son, Jayden, could receive treatment.
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 Sitting at the dining room table, I was stunned. My son had plagiocephaly and needed a cranial band. It wasn’t fair. I had done everything right. I was overwhelmed. I didn’t know what to do. That all changed after my first visit to Cranial Technologies.
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 Jeanne,
I really don't know how to begin to thank you for everything CranialTech (Angela and Leslie in Annandale especially) have done for our baby. I could talk facts and how much research I did on plagio trying to seek treatment for Dominick, but I think it is more important for you to hear how you have affected our lives.
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