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Mito Kids Rock! LOL ( Not Fobi related just a bragging mom)

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Forgive me if this is a double post I sent it once with too many pictures I think so it never showed up. shows his project this year for the Science fair. He took first at his school site level and then at district he took Blue in his division and then Top honors this year He is 11 years old. We are so proud of him. As you can see he is working on educating people about Mito. His goal is to be a researcher. He tells Dr. Boles all the time he wants to find the cure for Mito. We say Go Baby!

shows his Blue!This is Krisalynn's project this year. She took first at her school level and for the first time was old enough to compete at the district level and took blue (1st) at the district level. We are so proud of her as well. She did hers on the chemical reaction between baking soda and vinegar and blew the cork clean off her test bottle! LOL below she is talking to her judge and then she is showing off her Blue with her Principal.

Thanks for letting me brag! It sure is nice when we can celebrate good things around here. worked on his project for a little over six months. I am so glad we started early this year with as sick as he has been these past few months with the NVD Nurovascular Dystrophy. We did kind of pre warn him this year that he had placed at the district level, we didn't tell him what he got just he had placed. To try and take some of the stress off of him so the adrenaline didn't build up so much while he waited to hear at the awards part. Dr. Boles had highly recommended this to try and avoid another melt down. I had asked my principal if it was possible if we could know if he placed or not ahead of time so we could do this to avoid him passing out like he did last time from the adrenaline build up and the disautonomia issues. Poor kid, last time he got an award, walked up and got it and then passed out on his way off the stage. They were great about it and said most definitely they would. I don't think they wanted another issue either! LOL Anyway we say go MITO kids! Who says this dumb disease has to stop us! LOL They have now recommended we send to a magnet Science school. Yikes! Now that is something that can stop us! Mito kids parents don't have the money for that!!!!! Anybody know someone who would want to sponsor a budding researcher?

HUGS!

O and crew - Kira,, and Krisalynn Mitochondrial Myopathy-MIDS Maternally Inherited Dysautonomia and dad Enrique

Visit our web page: WWW. caringbridge.org/ca/mitooggo

Help support my sister in her new business at : Come and see what's NEW! http://www.youravon.com/elleenmiller Your AVON representative (Sign in passcode: ElleensAVON if you are signing in for the first time :-)

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