This is about my daughter Emily Sells.
Emily was born on September 8th of 2008 and by the time she was just 4 months old she developed a rare intestinal disease. Emily's disease isnt like anything the drs have ever seen before, her treatments have been completely "experimental" most failing to help her. By the age of 1 Emily had undergone more procedures and been through more pain than any adult I know.
Emily received a stem cell transplant in June of 2013 (the first sct of its kind) in hopes to give her better quality of life. In October 2014 her disease made an appearance again and to this day she suffers with discomfort, taking daily meds, getting frequent blood draws, having monthly infusions and not having a childhood that she deserves. I am writing in hopes to get help.
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