<div class="FTQUOTE"><begin quote><i>Originally posted by: <b>Mom2Brinly</b></i>
Follow up-
Thank you to those for your kind words of support- umm... for the rest of you! ;(
The organization is run through the city therefore the ADA act is in place. I will of course not take that route because i cannot waste anymore energy on this! She is only 7years old and reasonable accomodations must be made. I am NOT asking them to shorten the football game time because my child can't breath. jeez! If she had low fevs and couldn't jump do you really think i would ask the moon to be moved! It is in the hands of the parks and recreation director. The director has called the coach /ex friend and told her that if Brinly does need to eat and take breaks etc. then she needs to let her! I am sorry i am going to be an advocate for her til the end! SHE DOES HAVE SPECIAL NEEDS and just like we got to ride the front fast pass at Disney for every single line she will get what she needs!
There are many other parents on the squad with no CF issues and the head coach/ex-friend has been totally out of line with. She basically has called hard rules and does not follw them herself. She sends out the wrong field locations and then penalizes the child to sit out and not cheer because the parents took the cheer child to the wrong field in which she instructed. I could go on but it is too much.
Brinly just ABSOLUTELY loves cheer and i am stepping aside a bit until the 2 games that are left are over then she will get a ear full!
Blythe
Mom to Brinly 7 w/CF
don't mess with momma bear- lol</end quote></div><br>Like I said before, I sympathize with you here. <br>I think for the people that posted that were a little more critical of the situation, you have to understand you're looking at the balance of a parents perspective (yours) and the experience of an adult cfer (us). <br>All I can say, again from experience, is be very careful about your approach regarding this, esp in front of your daughter. Your disney/line comment in particular hit a nerve. You're right, of course-I get a letter from my doctor also when we go there for the same reason.<br>But, when parents voice this, sometimes it creates an 'i deserve this' mentality. Even though its bc of her health, thats still not good. Believe me, I've had to work really hard to realize that even though I have cf, I'm still not going to get everyone to understand and I'm not going to be able to snap my fingers and get accommodated all the time.<br>I'm not saying you're sending that message, my mom wasn't either. But thats what happens with kids. Especially when you throw peers and other kids into the mix. <br>Just an adult cfers perspective.<br>