ROBPI for 14 years now
Posted: Tue Feb 20, 2007 1:58 pm
My daughter was born with ROBPI 14 years ago. Her dad left because he couldn't handle having a child that was less than perfect - his words... in my eyes my daughter was more than perfect. We've been in PT/OT since about 9 weeks old, had a muscle transfer at age 2, tendon release, and an osteotomy at age 10 with Dr. Waters in Boston. She has gained about 65% use of her right arm, but has endured years of pain and hard work to get there. Middle school was hell, and the kids were mean. She is struggling with being different. Now in High school her workload is ever increasing and she aches at the end of the day from so much writing. I work full time and have 2 other children at home, so this has not been easy..... OK that said, I am wondering
1) if anyone knows of anything else that can be done to increase the use of my daughter's arm.
2) is anyone else having issues with medical coverage for on-going therapy?
3) is there a peer group that she can join so she doesn't feel so isolated in this.
4) how do you deal with the medical bills that aren't covered by my medical?
1) if anyone knows of anything else that can be done to increase the use of my daughter's arm.
2) is anyone else having issues with medical coverage for on-going therapy?
3) is there a peer group that she can join so she doesn't feel so isolated in this.
4) how do you deal with the medical bills that aren't covered by my medical?