The Isaac Foundation was formed to find a cure for my son's progressive and very rare disease, MPS VI. For more information, please visit us at www.theisaacfoundation.com.
Just received this quick video of Isaac presenting the 2011 Lifetime Impact Award at our Gala For A Cure, right after the video presentation we made. Super Cute!
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purestpartofme reblogged this from theisaacfoundation and added:
Somehow I missed this....is growing up… a good thing!
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imnotlostjustundiscovered reblogged this from theisaacfoundation and added:
So unbelievably cute! :) “and I will mail...mail for him.”
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pialuta said:
Aww… Conguadulathonson!
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mimimph reblogged this from theisaacfoundation and added:
Isaac, you are one precious, wonderful boy! Love You!!!!!!
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