Hi! My son was just diagnosed with apraxia (or dyspraxia). Anyone else out there that has gone through this? I'm just wondering if you have found any sources of info or good therapies out there? Thanks!
Our daughter, now 25 yrs old, was diagnosed with apraxia when she was 18 months old. She attended a special pre-school for babies/toddlers with language/speech problems. She also learned sign language so she could communicate (and we took classes, also) and had private speech and language lessons with a speech pathologist who specialized in infant speech development. When she went onto elementary school, she had speech three times a week. It was very tough and a very emotional time. However, she's 25 now, speaks normally, and is a wonderful girl! She still has some slight problems with understanding directions and will probably also have some slight problems with understanding speech. However, she is able to work as an administrative assistant (she's a whiz in the computer!) and commands a high salary as her computer skills are outstanding. She didn't have to talk to a computer. :) It's a tough road, but use all the resourses your county has to offer including special pre-schools, etc. All of our daughter's pre- schooling, speech and language classes, sign language, etc, were paid for by our state and county.
My 11 year old son has apraxia also, and the first web link posted - Apraxia-Kids.org is absolutely THE BEST resource out there for parents of apraxic kids. It's also an amazing site for kids with other speech or language disorders, or special needs in general.
John had one-on-one intensive speech therapy between 2 and 6 times per week for almost 7 years, occupational therapy for 3 years, music therapy and vision therapy for 2 years each. Apraxia is a very real problem...
joann23456
eileenlamp
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