tag:blogger.com,1999:blog-1947957832192035290.post1139608667257408087..comments2018-01-03T19:29:43.283-06:00Comments on FPIES & Mud Pies: Our Boys, Our Journey, Our New World...: Dinner as a family....Joyhttp://www.blogger.com/profile/05801049405099115795noreply@blogger.comBlogger1125tag:blogger.com,1999:blog-1947957832192035290.post-18567912316472181762011-10-04T09:28:50.754-05:002011-10-04T09:28:50.754-05:00I just stumbled upon your blog as I was doing an F...I just stumbled upon your blog as I was doing an FPIES search....and began to cry as I read. We're there too with our 20 month old. She is not diagnosed FPIES, but neither was her sister who is now 5 years old. Her only food passes are white potatoes, canola oil and salt. Our pediatrician doesn't really "get" FPIES and honestly, I am tired of doctors. We took our older daughter to every doctor imaginable in 3 different states when she was a baby to try and find out what was "wrong" with her....they never figured it out...but I did. :) <br />I just wanted to post to say it is nice to read about a fellow mom who understands, because as you know, with our children it is hard to find anyone nearby with our same issues and concerns. Hears hoping to food passes soon for our little ones!Tracy Williamshttps://www.blogger.com/profile/16832464825725025116noreply@blogger.com