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Showing posts with label Feeding Disorder. Show all posts
Showing posts with label Feeding Disorder. Show all posts

Owen's Story:

When our son Owen was a newborn, he had trouble choking while nursing and drinking milk from a bottle. We went to a lactation consultant, tried nursing shields, various nursing positions, the slowest-flow nipples we could find, but nothing stopped the choking. Owen’s GI ordered a modified barium swallow (MBS) at4 months, and he was diagnosed with laryngeal penetration. We started feeding him honey thick liquids and were told he would eventually outgrow the condition.We were optimistic his 3 subsequent MBS’s would show progress, but sadly we were still at honey thick consistency and extremely discouraged. One of the speech language pathologists at Phoenix Children’s Hospital suggested we look into VitalStim therapy. We immediately discussed VitalStim with Owen’s pediatrician. He had never heard of the therapy, and therefore didn’t feel like he could recommend it to us. We respect our pediatrician very much, and were hesitant to try a new therapy without his recommendation. Still, we wanted to know more. Jennifer Buck at Jabbermouths was very responsive to our initial inquiry, and answered our numerous questions regarding the therapy, costs, and expected results. Her thorough explanations and case studies really helped clear up some of our confusion and hesitation to try the therapy.

Happily, Owen responded immediately to VitalStim, and especially to Jenn’s warm, loving approach. Within the first few sessions, Jenn began moving him to thinner consistencies. She also coached us about thickening at home as we progressed through therapy. He had very little choking during therapy and never once became ill. By our last two sessions, he successfully drank un-thickened milk and apple juice! After all this effort, we are optimistic that our tedious days of thickening and expensive MBS procedures may be over forever. Buh-bye, thickeners… and thank you Jenn!

- Lindsay W.

Nathaniel's Story

Our son Nathaniel was born at 23 weeks gestation and is a true miracle! He spent the first 4.5 months of his life in the NICU, and developed subglottic stenosis in his airway from being intubated. Nathaniel had to be trached at 3 months of age in order to get him off the ventilator, and he was successfully decannulated in May of 2010. After his first reconstructive airway surgery in August of 2008, Nathaniel stopped eating and drinking due to a plastic stent that had to remain in his airway for 6 weeks post surgery. Three months later in October of 2008 after slow weight gain and reduced oral intake, he received a g-tube.


We started working with Jenn in November of 2008 and initially Jenn's
goals for Nathaniel focused on normalizing responses to input in his mouth, building his oral motor movements to an age appropriate level, and creating positive food experiences. He has since mastered these areas and now our goals focus on increasing oral volume at mealtimes and keeping Nathaniel interested in food/eating orally until we can start weaning him off the g-tube.


Nathaniel's speech was late to develop due to being a micro-preemie and also from having a trach the first 3 years of his life. Jenn has also been working with Nathaniel on his speech, and he is doing wonderful! He has gone from signing with a few vocalizations to using all age appropriate sounds in just 5months.

Jenn has been a Godsend to Nathaniel and our family, in fact we consider her part of the family! Her dedication, enthusiasm, patience, and love for children and for what she does is truly amazing and inspiring! Nathaniel instantly connected with Jenn and she has been instrumental in Nathaniel's amazing progress over the last 2.5 years.

We love her, and are truly thankful to have her in our lives.

- Nancy G.

Tanner's Story


Our son, Tanner, who is now 3 & 1/2 years old, first started having problems with feeding around 15 months old. It started with drooling & oral feeding difficulties. Soon after these began, he was diagnosed with dysphasia/swallowing difficulties & we were told that Vital stim therapy would be the best treatment for him.

We tried going thru our local children's hospital, but their wait was over a year long! I soon found Jenn Buck & am so thankful we did. She got us started very quickly & ALWAYS worked with our schedule (including an hour drive time to therapy). Within a few weeks, we went from having only a few foods in his repertoire to having a variety of foods he would actually eat! His dysphagia & drooling also improved dramatically with Vital stim therapy.

Jenn was always so patient & energetic. She is a pleasure to be around & truly cares for all her patients as if they were family. Anytime I have a question about other speech or feeding issues she is prompt to return my inquiries & always knows the answer. I am truly thankful
to have such an experienced speech & language pathologist in our lives! She has made my son's quality of life so much better with her knowledge, experience & sweet spirit!

-Gina B.

Christian's Story

Our precious son Christian was born with Down syndrome in August of 2007. The first 6 months were filled with the greatest love for our son, as well as the overwhelming task of finding all of the right therapies, tools and programs to help him develop into a happy, healthy toddler. Our family is very fortunate to have found Jenn Buck and she is unquestionably a perfect addition to our son’s “team.”

Jenn’s knowledge of Down syndrome and her extensive background in different oral motor techniques have been extremely beneficial for Christian. One of the things Jenn taught us was how to start Christian on a straw. He started straw drinking at 7 months old and by the time he turned 1, he was able to use the same straws and straw cups as our 3 year old daughter. I have had several other parents and therapist comment on his lip closure, straw drinking and tone around

him mouth. I truly believe the techniques Jenn taught our family have provided Christian with an invaluable opportunity which will turn into better communication and clearer speech patterns as he becomes an older child/adult.

Jenn also provides support for our family as we learn about Down syndrome and decide on the best programs and therapies for our son. She is extremely patient and I feel she tailors our oral motor program based on Christian’s individual needs as well as our family’s comfort level with implementing it. Her professionalism, responsiveness and energetic attitude are exceptional and I always leave therapy feeling confident I have the best tools and techniques to help our son progress each week. -Karen S.