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!
Nathaniel's Story

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.
Tanner's Story

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 thankfulElla's Story
I wanted my daughter to talk. I watched and learned from several speech therapists. I would do the homework with Ella, and frustration after frustration left me researching for something more. All I wanted was for Ella to talk! I found some information online about oral motor therapy- this sounded interesting to me since Ella was diagnosed with low muscle tone. Jenn described Oral Motor Therapy as "physical therapy for the mouth"- slam dunk! This was what we needed.
When we first started with Jenn 2 years ago, Ella would make more progress in her 1 hour with Jenn, than she would with 5 or more sessions of traditional speech therapy! Two years later, Ella SPEAKS! AND to top it off- her traditional speech therapy sessions are more productive because of the oral motor therapy component. Jenn has written homework and exchanged emails with our traditional therapist to help her be more productive with Ella as well. 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.Claire's Story

Devon's Story

Vital Stimulation Therapy (swallowing therapy) is never something to look forward to but I would definitely recommend the experience offered by Jennifer Buck.
It took a perseverance to find Jenn and get the necessary approvals from insurance; the experience at her clinic was WELL worth the effort. At Jabbermouths, patients get a great sense of individual attention with the one on one therapy. Parking is easy! Scheduling was a breeze. Jennifer is very professional and really great with kids and equally great with parents. Jenn even set up Devon's follow up swallow tests to accommodate our busy schedule.
We saw marked improvement every two weeks as we crept down in thicknesses until we could celebrate with un-thickened juice boxes! Jenn made something that could be very traumatic for my child more like playful, fun lunch dates! Thanks Jenn!
-Michael & Maritza K.
Collin's Story
My son has a diagnosis of autism and apraxia of speech. He is essentially considered “non-verbal.” As a parent, it is my dream to one day be able to have a full verbal conversation with him. Jennifer Buck at Jabbermouths is helping us achieve that dream! When I realized that traditional speech therapy was not what he needed to help him get his words out, I went on a hunt to find what could really help him.After finding out about his real deficits in regards to oral motor, I was thrilled to be able to have him accepted to Jenn’s caseload! We have seen him go from having literally no sounds, to now imitating sounds on command at a rapid pace. He can even form words, when prompted, that are made up of all of the sounds he has mastered. Needless to say, it is very exciting! The program is intensive, but fun to do. I personally like having a specific program with a hierarchy of goals.

Emily's Story

Emily was born in April 2003. Since her birth, she has had pneumonia at least once a month. After several tests at Phoenix Children's Hospital Emily was diagnosed with Dysphgia on Feb. 5, 2009. Dysphgia is a swallowing disorder which required Emily to have thickener in all of her drinks. This is definitely not pleasant for anyone, especial
ly a 2nd grader! The only solution to resolve this issue, in Emily's case, was Vital Stimulation Therapy. We were placed on a waiting list at Phoenix Children's Hospital for the therapy, but were advised that we should seek therapy outside of the hospital, due to the long wait list.
We found Jenn in April 2010 and quickly started therapy in May. The atmosphere at Jabbermouths is very relaxing. Scheduling is very flexible. Jenn managed to work with my busy schedule and Emily’s school schedule.

Jenn has the patience of a saint. Getting a 7 year old to cooperate at times can be very
challenging. After 7 months, Emily has successfully completed her therapy and just had a normal modified barium swallow test. She does not require thickener in her beverages any longer and has been discharged from therapy. We are so grateful to have found Jenn! She will always hold a special place in our family.
-Don & Andrea H.
Ryan's Story
Hugh's Story
