Physical Therapy Patient Spotlight — Olivia

Olivia is an adorable 17-month-old girl who was born 6.5 weeks early with a diagnosis of Trisomy 2 (duplication of part of chromosome #2). Olivia spent her first few months in the NICU and had a tracheostomy placed at 7 months of age. Due to Olivia’s rare diagnosis, she has low muscle tone, which contributes to feeding difficulties, problems with breathing, and delayed development of motor skills such as sitting, standing, and walking. Olivia’s physical therapy treatment over the past 2-3 months has focused on helping her to become indepent and  focuses on mobility. Olivia’s most recent accomplishments are transitioning into sit all on her own and commando crawling! Go Baby Go! Oliva’s therapist, Heather Pitner, PT, and a group of THERAPY 2000 therapists attended a workshop to learn how to modify toy power vehicles t hrough GoBabyGo!  This program started several years ago at the University of Delaware by Cole Galloway, PhD, PT. After studying infant behavior, Dr. Galloway became interested in closing what he calls “the exploration gap.”  This is the gap that we see between children with typical mobility and those who experience mobility impairments such as cerebral palsy, spina bifida, and Down syndrome. When an infant or toddler reaches for an object, scoots across the carpet, or learns to walk around the room, she’s learning to interact with her environment in a way that forges new connections. A mobile child learns how to explore a room and approach other children. Go Baby Go! provides powered toy cars to developmentally disabled children from 8 months to 4 years old. This enables these children to move themselves similarly to typically developing children. Research has shown that early mobility opportunities lead to an increase in social interaction and cognitive development.   New Surroundings The moment Olivia was placed in her […]


Read More

Speech Therapy Patient Spotlight: Josue

Josue is a very happy 4-year-old boy who loves Lightning McQueen, playing games with his little sister and friends, and watching movies. Josue was diagnosed with a Specific Developmental Disorder of Motor Function and a Mixed Receptive-Expressive Language Disorder. He started receiving speech therapy services with Therapy 2000 in May of 2018. When therapy began, Josue had a vocabulary of approximately 5 words, could not follow simple 1-2 step directions, and only communicated via gestures and single word utterances at times. Ashley Jarrett met Josue when she was shadowing physical therapist Emily Parks, as a new employee.  Josue had been waiting for ST services for approximately 2 years, although he was out of her treatment are Ashely wanted to work with Josue over the summer.  After only 2 and a half months of services, Josue is now able to speak in three to four-word utterances, identify all his body parts, label common objects, follow 2-step directions, request help, and communicate wants/needs in English and Spanish. Josue has come a long way in such a short amount of time due to his hard work, mom’s willingness and motivation to work with him daily, and a physical therapist who went above and beyond to recommend speech/language services to help this awesome kid and family! Ashley is so proud of all the progress they were able to make and the goals they were able to accomplish in such a short time! Ashley Jarrett, M.S. CCC-SLP   After Ashley started working with Josue, Emily was able to notice a huge increase in his talking during physical therapy sessions. Josue was able to name all the colors for the toys that we typically play with. Also, instead of pointing at the toy he wanted to play with, he would say words such as “block”, “ball”, […]


Read More
Father and Downs Syndrome son with laptop

PATIENT SUCCESS STORY: GRACIE

This is Gracie, an amazing three-year-old in Amarillo that THERAPY 2000 provides both speech and physical therapy services. Gracie was born with a very rare condition called Birk-Barel syndrome which is characterized by intellectual disability, hypotonia, hyperactivity, and unusual facial features. She had severe feeding issues and airway difficulties at birth but has already been discharged from feeding therapy because she has met all her goals. Gracie, her family and her feeding/speech therapist, Val Betts, worked very hard and now she can enjoy a meal with her family. Gracie’s diagnosis places her at one of only twenty-five in the world and the only one in Texas with the condition. Kristy, Gracie’s mom along with her dad and three older siblings feel she has the special gift of bringing all of them even closer together since she was born. Gracie’s parents were told about T2K in Amarillo from one of her many professionals she sees in Dallas. Dr. Elizabeth Sperry of the International Craniofacial Institute had seen a lot of success with her patients she had referred to T2K in the Dallas/Ft. Worth area over the years. Gracie had her first of many surgeries at five weeks of age in Dallas and has had numerous returning trips over her three short years. She is a very hard working, happy and social little girl that enriches everyone’s lives that have the pleasure of meeting her! She currently receives PT services with Ashleigh Wilson and ST services with Val Betts. Gracie loves them both. Her mom Kristy says they both therapists are very loving but push her to work hard to reach her goals. She also says they are like family and genuinely care about Gracie. Mom states from day one the therapists really listened to her and took the time to “learn […]


Read More
Father and Downs Syndrome son with laptop

PATIENT SUCCESS STORY: GRACIE

This is Gracie, an amazing three-year-old in Amarillo that THERAPY 2000 provides both speech and physical therapy services. Gracie was born with a very rare condition called Birk-Barel syndrome which is characterized by intellectual disability, hypotonia, hyperactivity, and unusual facial features. She had severe feeding issues and airway difficulties at birth but has already been discharged from feeding therapy because she has met all her goals. Gracie, her family and her feeding/speech therapist, Val Betts, worked very hard and now she can enjoy a meal with her family. Gracie’s diagnosis places her at one of only twenty-five in the world and the only one in Texas with the condition. Kristy, Gracie’s mom along with her dad and three older siblings feel she has the special gift of bringing all of them even closer together since she was born. Gracie’s parents were told about T2K in Amarillo from one of her many professionals she sees in Dallas. Dr. Elizabeth Sperry of the International Craniofacial Institute had seen a lot of success with her patients she had referred to T2K in the Dallas/Ft. Worth area over the years. Gracie had her first of many surgeries at five weeks of age in Dallas and has had numerous returning trips over her three short years. She is a very hard working, happy and social little girl that enriches everyone’s lives that have the pleasure of meeting her! She currently receives PT services with Ashleigh Wilson and ST services with Val Betts. Gracie loves them both. Her mom Kristy says they both therapists are very loving but push her to work hard to reach her goals. She also says they are like family and genuinely care about Gracie. Mom states from day one the therapists really listened to her and took the time to “learn […]


Read More
courtni

Patient Success Story- Harper

PATIENT SUCCESS STORY- All therapists want to make a difference! With pediatric patients we not only receive the immense joy of seeing the progress in our patients, but on the faces of their parents as well. Approximately one year ago, I began working with an adorable little girl named Harper. She was born at 25 weeks with Chronic Lung Disease, and multiple other diagnoses that come with being a micro preemie. When I started treating Harper, she was 14 months old and still only taking liquids from a bottle. Harper demonstrated a severe oral aversion to foods, her suck/ swallow/breathe pattern was disorganized, and she exhibited multiple signs of aspiration. Harper would gag and retch, so we started slowly with the introduction of purees from a gloved finger. We slowly built her response while simultaneously using techniques to decrease oral aversion. Within six months, Harper was able to eat purees from a spoon and had integrated her suck/swallow/breathe pattern successfully. During her modified barium swallow study, Harper demonstrated some aspiration and penetration due to muscle fatigue and was recommended to begin NMES (Neuromuscular Electrical Stimulation). In the beginning, Harper did not enjoy NMES and required multiple verbal cues throughout the session, but soon began demonstrating an increased chewing pattern while expanding her variety of food and textures. Our goal was to maintain Harper’s calorie intake without supplementing with Pediasure, so Harper’s mother was encouraged to talk to her gastroenterologist about medications for reflux and a diet plan. Harper is now successfully taking all liquids via sippy cup and eating a variety of food such as broccoli, cauliflower, cheese and crackers, and many more. Harper continues to demonstrate some difficulty with coarse meats and requires extra chewing during these times. Since she began speech therapy, Harper has decreased upper respiratory infections, […]


Read More