Dr. Montgomery was more than excited about Sadie's progress, since our last evaluation......at which time he had noted that everything with her seemed poised and ready, but patience might be best....he seemed confident, then, that it would be a matter of time before she started reaching some of the expectations he has for her.........we had begun to grow very concerned and anxious.
After this weeks evaluation, he described her progress as 'explosive' and referred to her as now being considered as 'stimulable' (in a nutshell, more aware and respsonsive), which is huge, with respect to how she will be perceived by therapists, etc.! Being 'stimulable' and still being in the more formidable age range, should help us secure more aggressive therapies, through school, etc. He referred to her as an ideal candidate for the new, Pilot program (Reverse Mainstreaming), that we have her set for at Birdneck Elementary this year, and encourages us to continue everything that Lisa has focused on (ie, Assistive Technology devices around the house to help with communication).
He's a great doctor, who is optimistic and realistic.......and loves Sadie......and seemed genuinely excited about where she is now and who she may develop into to, over the next few years.
Daddy.
Our life, our experience, our history, about my daughter with a rare chromosome disorder. She is missing a small portion of her 8th chromosome, which is called a deletion. She also has a small part of XP added to that. Her karotype or diagnosis is deletion 8p23.3 with extra xp22.2 to the terminal deletion (a new chromosome test summer 2011 changed her karotype to deletion 8p23.2 with extra xp 22.12, essentially meaning more missing chromosome 8 and more added xp). #herrarelife
Sunday, August 23, 2009
Time is a Thief
I don't remember the first time I heard the sentiment, "time is a thief." Recently it is heavy on my mind. I haven't post...
-
and the flu panic begins... http://www.cloroxclassrooms.com/downloads/teacher_brochure.pdf
-
Sadie has been having spasm type clinch arm and mouth type movements that last about 2 seconds randomly starting in June. For the past mont...
-
Today I was feeling the need to read other stories about other children with chromosome disorders. I googled blogspot to see if I could find...