My friend, Christa West, became the happy mommy of a beautiful little girl, Nevaeh, this year. Nevaeh has Short Gut Syndrome. This has led Christa on an adventure as she has learned all about living with this. Christa recently asked the Nana's Ninas to join her in a crusade to let other families with Short Gut Syndrome know what resources are available for them. One of the things needed is a pad of some sort to protect the tummy where the tube comes out. That was where the Nina's came in. Christa brought one over; I "reinvented" it , and the Nina's began to crank them out. We made over 50 of them. Then Christa came, and we put together packets for families dealing with this syndrome. The highlight for the girls was when we went to Egleston Hospital (the children's part of Emory Hospital in Atlanta) and met the surgeon who performs the surgery to put the tubes in the infants and children who need to be fed from a tube. Christa bought us all shirts, arranged the visit, then took the girls out to Varsity afterwards. It was a wonderful experience for them to see first hand how their service will benefit others. What a blessed Nana I am to have my Ninas! Thank you Christa for this wonderful opportunity!

The surgeon took time from his busy schedule to meet with us and showed the girls how the tube works. He was so impressed with them and kept thanking them for making a difference in the lives of others.
I was impressed with the way the girls acted. They
shook hands with the surgeon and introduced themselves. They paid attention and asked questions.
In this picture you see the surgeon, Christa and Nevaeh and all the Ninas.
from left: Dr. Matthew Clifton, Carleigh, Rhys, Christa, Nevaeh, Me. Front Row: Ryleigh and Swaye. Thank you to our photographer Susie Futral Mohler!
This is how the colorful, flannel "tubie hoopie" (our own name for it) fits around the feeding tube.