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Michaels Rare Disease Fund

Organized by: Melissa Everett

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Michael update
February 29, 2016

Michael update: his mouth lymphatic malformation is growing at an exceptional rate now. Dr Magit explained to me today that Michaels situation See More

THE STORY:

Michael was born in Southern California with a lymphatic malformation in his jaw and neck. He was treated at San Diego children's hospital using a schlerosing agent called OK-432. Seven years later it came back and is now in Michaels mouth and throat. He had his mouth lasered in September however the mass has already started to grow back. Since we now live on the east coast and what he has is so rare we have to fly to San Diego to get the medical attention he needs. Our family has decided to move back to California. However, the timeframe is moved up now and we have to leave soon than my finances allow. I'm asking for help from the community and friends to get Michael back to his hospital so he has be treated regularly. Any amount helps. Thank you.

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Organized by

Melissa Everett

This is a direct to organizer fundraiser.

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Melissa is still setting up this fundraiser so please check back so you can support Michaels Rare Disease Fund .

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