(continued from above....)
Then came the time a year or so later that we ultimately did decide to medicate her. Nothing else helped. The therapy ,the social skills group. And meds were always our last resort. What broke the camels back with this was DD got injured. She did a BHS and her foot jammed into something and never said ANYTHING to the coach at all. It was at the end of practice and when it ended 15 min. later she suddenly hops on one foot, CRYING to me and her father. She tells us what happened and how she hurt herself. Because of her SM she did not tell the coach she did this and was in pain and never said a word.

Turns out we took her to the ER and she hyperextended her knee or her leg (can't remember). So for her safety we had to look into medicating her to just help take some of the edge off (there were other things that happened as well out of the gym in which she didn't speak up when should have). We figured we'll put her on it for short-term in hopes it'll help take the edge off to have her not be so scared to speak. When we did medicate her, we also let her coach know as well in case there were any changes and adjustments DDs body/behaviour was making from the meds. About 10 mos. later DD requested to be off of the meds so we had to wean her. Boy, that was an awful experience. So, again...I felt we should let coach know what was going on....she's being weaned off it'll take a couple weeks and keep me posted if she is sluggish, headache, etc.
So basically what I'm saying is that like some others have posted, I DID keep the info. to myself until I felt a situation was warranted in which I needed to tell the coach. I sat back and observed and when I seen things I said we need to let her coach know. It was only fair to the coach and to my child. In the beginning I felt kinda odd telling coach about all of DDs issues. I'm saying to myself...my god she's gonna think my DD has all these issues and that it's odd, etc. But I felt comfortable with it after a while. Till this day I keep her updated on any types of changes and we have a very open communication about it. I'm so glad I did let her in on what's going on.
Now fast forward, she's doing level 6/7 this season. She currently has ticks with her eyes, and her arms she does this weird thing where she straightens them straight out then pulls them back in. It has come to the point where her teammates and school mates has asked her how come you do that with your eyes or how come you talk like that. But lemme tell ya, once she's doing her gymnastics (floor routine, on the beam, etc.), it all goes away even if it's just during her event. She's focused and has made us so proud. As for the SM, it will prob always be an issue. She is a very shy girl, and she will talk to some people but never speaks to her coaches unless they talk first.

It's kinda sad, but they understand. She's at the point where she tells me I want to talk to them so bad mommy, but if i do now it's gonna be weird and they never seen me talk and I just can't. And I TOTALLY GET what she's saying cuz i found out 30 yrs. later I had SM growing up and I remember feeling that SAME way.

And it's normal for kids with SM to feel that way as they get older....it becomes a learned behaviour at this point. Oh well. They love her to death and she's an extremely talented gymnast. I feel with her unique and "special" ways about her, that has helped make her the wonderful gymnast that she is.
I also would like to add that by her having these "special qualities" about her, it hasn't affected how she performs at all. As a matter of fact, she's known that when she is in front of the judge she really turns it up! You would think she would fall apart in front of judges cuz of her anxiety-based issues but she does quite the opposite!! She is a two-time state champion!!! Level 4 state champ in 2010 and Level 5 state champ this year, she holds a Level 4 state record on bars, and this is the 2nd year she made it to National Testing. this year made it to Tops A and last year Tops B. She is amazing, and I tell her all the time she is my hero. <3 So my DD is proof that no matter what type of disability or special needs you have, anything is possible. It's all about their drive and determination.
Thanks for letting me share my story.
PS. Her almost 7 yr. old sister is special needs, and is classified so through her school as well as she even has an IEP at her school (she's in a special ed class). She has apraxia and is a bit delayed (she's more like a 5 yr. old). She enjoys her rec gymnastics 1 hr a week, although I feel so bad when she asks me what level she is in and when she can compete like her sister. How do you tell your kid that's just not going to happen? You can't. It's not like I don't have faith in her, but it just will never happen.

Ugh, sometimes it's so hard being a parent.... I wish they had a competitive team for special needs kids for my 6 1/2 yr. old...that will be perfect! But she goes to her rec class with a smile on her face as always.....
