Makenzie & Isabella Hardesty

Story

Our family was told when the girls were two and three that they suffered a reare genetic disease called MPS VI, Mucopolysaccharidosis. At that time they had said that children did not live past the age of five.

Today, almost 10 years later – Makenzie and Isabella are still with us. My oldest niece is about to turn 13. These girls are my inspiration and I love them dearly.

Please help us and donate to the National MPS Society. I am hosting an online auction through ebay selling baby dolls. Our goal is to reach $1,000.00. We hope you can help us. Please visit the auction by clicking ???

$1,000

$833

$667

$500

$333

$167

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