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Ashley Allen


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.

Thanks for visiting my page. Please help me with my fundraising by contributing to this great cause.

Making a donation is easy and safe- simply click the “Donate Online” button in the upper right to donate.

Make sure to bookmark this page and come back often to check on my progress.

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 for more information.


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