Michael trip to MPS conference 8/16

Monique Whitaker is organizing this fundraiser.

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Michael lives with a none cureable disease called Mucopolysaccharidosis type II (MPS II) also known as Hunter Syndrome Disease. We would like to attend the National MPS Annual Family Conference this year in August in Columbus, Ohio. This conference allows us to fellowship with MPS families from all over the & give us the opportunity to build life long realationships. I was skeptical about doing a go fund me because we have never been sucessfull, but Michael told me he want to go, so we reaching out for help. Please help us reach our goal so we can attend the conference this year. Even if you can't help please share, share, share! Thanks in advance & God bless you all!