Guest guest Posted September 21, 2006 Report Share Posted September 21, 2006 Hi all, My name is Sue and my daughter's name is Kaylee. We live in Rochester, NY!!! We noticed Kaylee wasn't talking at an early age, but her pediatrician wasn't that concerned. It wasn't till she was 20 months old that she introduced us to the early intervention program. After all the tests she started having speech therapy 2 x 60. Eventually it swithced to group 1 x 90 with individual therapy 1 x 60, weekly. When she turned three, we changed agencies. Just before we changed they mentioned that she may have Apraxia. Her brother started in therapy at that time too. Kaylee is now " 3 " and is " 2 " . After a year with this agency, Kaylee has made great strides. We still have some problem understanding her, but for the most part, she is doing very well. Her brother, who also had a speech delay, is doing great!!! No mention of apraxia with him.. Althogh, he has a list of other problems. I was just wondering, Kaylee wore a helmet as an infant for an extremely flat head. I'm sure this has nothing to do with her speech delay, but is it possible? She has had her hearing tested, and everything is normal. She is also a very smart child who has no problem understanding you. Is there anything further we should be doing that would improve her speech? Any suggestions would be greatly appreciated. Thanks. Sue Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 21, 2006 Report Share Posted September 21, 2006 > > I was just wondering, Kaylee wore a helmet as an infant for an > extremely flat head. I'm sure this has nothing to do with her speech > delay, but is it possible? She has had her hearing tested, and > everything is normal. She is also a very smart child who has no > problem understanding you. MMMMM...Kaden had plagiocephaly and is a STARband graduate...also with apraxia???? ~ Married to the world's greatest guy, & SAHM to; Mikayla (14) World's greatest teenager, compassionate, sensitive and a National Junior Honor Society member, Rilea (13) Energetic, funny, and impulsive. Believing for a breakthrough regarding her ADHD, Central Auditory Processing Disorder & Dyslexia, Jonathon (6) My miracle boy. My amazing, autistic, one-eyed wonder with a host of issues and struggles: Heightened sensitivity to corn, casein, gluten, red dye #40 & all adhesive material. Aortic Root Dilation, Band Keratopathy Right Eye, Bruxism, Choridal and Retinal Detachment Right Eye (Blind), Chronic Lung Disorder, Congenital Nystagmus/Legally Blind, Cornea Adhered to Pupil Right Eye, G-Tube Dependant/Oral Aversion, Gastro Paresis, GERD, Gross Global and Neuro-Developmental Delays, History of PDA, Incontinent, Increased Ocular Pressure (15/16 both eyes), Myopia (-14L), Retinopathy of Prematurity, Seasonal Affective Disorder, Sensory Integration Disorder and Vasomotor Rhinitis. A definite over comer and a true testament to God's mercy and grace, and Kaden (2) Momma's little wild man. My other autistic wonder, struggling with apraxia. Heightened sensitivity to mold, tomatoes, oranges & strawberries. Congenital Muscular Torticollis, GERD, Perennial Allergic Rhinitis, Reactive Airway Disease, STARband Graduate (11/9/04 - 2/9/05) and Sensory Integration Disorder. The happiest little boy with the biggest brown eyes and another testament to God's grace and mercy - believing for yet one more miracle! http://childrenofpromise.net/harriskids.html (and my dear Lizzie, who is now 9, and although not physically part of our family any more, a definite part of our lives, hearts and prayers) http://childrenofpromise.net/lizzie.html http://my.waiora.com/340124 Quote Link to comment Share on other sites More sharing options...
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