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Tammy Needs Our Help!

Tammy Smith has been living with a rare disease called Langerhans cell histiocytosis for over 20 years, and there is no cure. After years of progression, her only hope for survival is a double lung transplant. Tammy was listed for transplant in the beginning of 2017 and now she needs our help.

Tammy grew up in Berwick, Pennsylvania, graduated from Columbia-Montour Vo-Tech. High School, and married her sweetheart, Joe. She worked as a machinist until they started a family. She was a stay-at-home homeschooling mother of four children: Nichole, Kristen, Danyell, and Joey. She worked hard to make sure her family had a happy and healthy home. When her youngest reached high school, Tammy decided to start working as a nurse’s aide, and then completed nursing school.

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