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Hi Jenny and welcome! My son is now 5, he will be 6 Oct 25. He was dx'ed just before he turned 2. He has had many complications, but early intervention has been the key! He has been in therapy for OT/PT-ST since he was 10 months old. He is still delayed by about 2 yrs, give and take in some areas. I am hear, so any support you need or just another parent that has been there, I am here! I look forward to hearing from you and getting to know your little one. Where do you live? I am in NE Washington, I say it that way because no one knows where our home town is, it is Hunters, population 200-. We are 85 or so miles one way to Spokane, and this is where Devon sees his specialists. He has a very complicated health history, and has required several surgeries and procedures..
Hope to hear from you soon!
April
Mary Hearing <momofalex031505@...> wrote:
Mary Hearing <momofalex031505@...> wrote:
My son is 2 1/2 and was diagnosed at 8 months. he has done pretty well over the last couple of years with all the different therapies. He still doesn't talk, but we can communicate with him pretty well. He is fairly aggressive and has some sensory issues that are a little challenging right now. He is a happy boy and enjoys playing with his sister and anything that has a motor in it. How is your son doing? Where are you from? We are in Portland, OR. Do you have a good support system? I would love to talk to you. Hope to hear from you soon.Mary
Jenny <myjenny_80@yahoo.com> wrote:My son is 3 and was diagnosed with Weavers at an early age. We've
talked to doctors,teachers and therapists but it would be nice to talk
to another parent. Hope to hear from someone soon.
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