Our precious little girl, Rhema, was born on 8/9/10 and was diagnosed with severe Myelomeningocele , Hydrocephalus and Clubfoot at birth.  The month of October we will be doing several posts about Spina Bifida and also specifically about Rhema’s journey.  Our goal has been the same since Rhema entered the world: boldly proclaim what the Lord has done and is doing in Rhema’s life, be an encouragement to families on the same journey, and to bring awareness to our community about Spina Bifida.  If you are new to our page, we encourage you to go into our archives to learn more about our precious girl we proudly call our Rhema Miracle, we encourage you to click on the links at the bottom of our page to learn the medical facts about Spina Bifida and we ultimately encourage you to visit the Spina Bifida Association of America.