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This fundraiser ended on 04/12/12

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The family of Hannah Ortega is rasing money to help with travel expenses related to Hannah's healthcare.

My daughter, Hannah Faith Ortega is 17 months old. 2 weeks ago she was diagnosed with Russell Silver Syndrome, a rare form of Dwarfism.
Hannah has had multiple health issues since she was born. Projectile vomitting from acid reflux, inability to gain weight (now labeled with Failure to thrive), lack of growth.
Upon seeing Dr, Machester is when we got the diagnoses of Russell Silver Syndrome. It turns out that all of Hannah's issues(past and most presnt) are all related to Russell Silverr Syndrome.
In addition to this she has a low functioning thyriod.
Russell Silver Syndrome is so rare that not to many doctors know much about it. My hope is that the money donated through this site can help her father and I get to the National Convention so we can learn more to better help Hannah. The funds will also be used to help fund trips to Denver when Hannah has to see the specialist there.
For a daily/weekly update on Hannah visit
Please contact me at for mailing address (if needed) or if you would like more information on Hannah.
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