I had a child at an early age. I found out when she was 1 year of age Ashley was born with MPS I. Ashley Passed away in 2014. She put up a good fight and I did as well. The worst feeling in the world is to lose a child.
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The mission of the National MPS Society is to fund research and provide support for families affected by MPS and related diseases.
Please help our family and support the National MPS Society. Every donation will make a difference in the lives of those affected by MPS and related diseases. Please visit www.mpssociety.org for more information.
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