Peter Hoffman Hope For Peter

First post: Mar 19, 2019 Latest post: May 3, 2022
Peter is a fun, rambunctious, loving, big-hearted little guy. We love him to pieces, and we're glad you do too. Peter also has MPS II, aka Hunter Syndrome, a rare genetic disease. He doesn't make an enzyme his cells need to recycle complex sugars, and they build up in his tissues causing damage over time. We're doing all we can to help Peter. More on that in the Journal. Thanks for visiting and supporting Peter & our family. We couldn't do it without wonderful support from our family & friends! Love, Katey, Andrew, Maddie, & Peter

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