hey Disdaddoc
I know what it is like to have admistrators try to discontinue services, Having had two boys who where born premature,both at different times. We (more ike DW) spent way too much time in DR's offices trying to get diagnosis after diagnosis,especiay on my oldest one, he was born at 28 weeks and spent about 130 days in the NICU, they think he suffered a brain bleed in utero thatn had a possibe stroke in the first few hours of life. After finally getting a CP diagnosis and heading into special ed, only to discover that because he walks normal and had normal thinking patterns, and the only visibe problem was a speech delay...the "admin" people didn't think anything was needed, THANK GOD for DW...she was the fighter and it was trying times...finally getting people to see the CP diagnosis...and the horribe leg pains that they owuld say where growing pains...BS!...we eventually had a great case worker who saw through everything and went to bat for us....NOW...on the second boy who has speech issues and was born at 34 weeks we had a better understanding how the "SYSTEM" worked and were able to figure it out....THERE is always a brite side, the oldest after 7 years was able to get off the special ed list and has no other IEP's .....there is the fact that he can't run as fast or play organized sports that well like his bud's but that to me is no big deal, his legs still hurt after long wallks or running around, but he is vry intelegent and figure stuff much better than his 42 yo dad....Thanks for sounding off here we will always listen....as the 4 yo he is just plain crazy.......
Where in CT????