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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

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>

> 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

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