The Parker Lee Project

The Parker Lee Project started right before my daughter, Parker Lee Reynolds passed away on October 20, 2012. Parker was born June 30, 2010 with Lissencephaly and Microcephaly. Over her short life she acquired many more diagnosis, equipment, and supplies. When she passed away she was tube fed dependent, had a trach, and was on oxygen full time. Her bedroom looked like a hospital room. During her time as an angel on earth I struggling, argued, and screamed at doctor offices, insurance companies, and DME companies more times than I can count.
I know first hand how hard it is try to get all the equipment and supplies that you need for your special needs child. As well as the struggle of finding agencies to help with these things or therapies. I learned more than my fair share through diligent research, caring for my daughter, and watching all my friends do the same for their children. At no cost to parents we would like to accept equipment and supplies that are no longer needed and provide them to new families who do for free.