Hi everyone,
I recently joined this site and I'm loving all the info here. So far it's my favorite of all the autism websites I've been looking at.
My name is Laura and I have 3 children. My middle child, a 5-year-old girl, was just diagnosed with autism a week and a half ago.
I'd always felt that she was 'different', from a very young age. Probably from infancy. She was a late talker and was diagnosed as having a language delay when she was a toddler. However, I felt there was something more going on besides a language delay. When she was 4, she had some assessments done by a pediatrician and the pediatrician said that she had a cognitive delay in addition to the language delay and was therefore 'globally delayed'. Whenever I raised the subject of autism, the pediatrician always dismissed my concerns. She seemed to have 'old school' ideas about what autism was and probably only recognised the severe cases.
So I got my daughter to see some other specialists for a second opinion. She ended up seeing one of the top autism specialists in my city, who diagnosed her with autism. She was also diagnosed with a severe receptive language delay. Her expressive language is only mildly delayed now - she speaks pretty well. It's hard to get people to understand sometimes that a child can speak well but have a lot of trouble understanding what other people are saying!
At the moment I'm waiting for the pediatrician's official report with the diagnosis and then I'll be put in touch with some early intervention programs.
All in all, I'm accepting of my daughter's diagnosis. She is what she is, I say. I think, when it came to diagnoses, that the 'not knowing' was worse than the 'knowing'. I'm glad I finally know what she has. I just want to make sure that I can get her whatever help she needs to make her life easier in the years to come.
Cheers,
Laura