My name is Gentry and I am not your average girl. I am fully aware that most people will tell you the exact same thing, and I'm glad that they do. No one should feel as though they are just another carbon copy of someone that came before them. So here's why I'm different. I was diagnosed with Vascular Ehlers Danlos Syndrome (VEDS) in September of 2015. I am also currently a Children's Ministry Director as well as a full time college student looking towards Graduate school next year to get my masters in Speech Language Pathology. I started this blog in the hopes of giving people a new outlook on life or to help people better understand life with VEDS. Now, please don't think that VEDS completely defines my life. I'm still who I was before I was diagnosed, I just have to do some things a little differently. God is still God and He is still in control, so what on this earth do I have to fear?