This is my journey to healing from a rare and ugly disease. I hope to be an advocate for all rare diseases that are often misdiagnosed or worse left to think it is not real.
My Reason
My sweet Elijah has used every wish, every prayer, every day to ask for my complete healing. I knew in 2008 because God told me when I first started getting really sick that things were going to get much worse but He would heal me only when His timing is right and He receives the glory for my healing. For those of you that do not know, I have Idiopathic Gastroparesis caused by a genetic condition known as Autonomic Dysfunction. I am currently on IV nutrition through a central line and on several medications. I had a gastric pacer implanted in 2010 to alleviate some of my symptoms and it worked well for 6 months but my nerves quit responding and I finally had it removed this January. In other words it did get much worse. I start this blog now because I know God will not let my baby's faith die.
Thursday, December 18, 2014
Time for a miracle
This blog entry is going to be different. I want to ask everyone to pray and re-post this to everyone you know. We are praying for an honest to goodness creation miracle. This disease I have is incurable, and genetic. The root cause of all my problems is the fact that I am missing some neurons. I was born with this. Now as I pray, I ask everyone to pray that God will create neurons where they should have been but never were. Please join with me and ask for a miracle healing because there is nothing more the doctors can do. I am ready to stop existing and truly live. Live the life God created me to live. Please pray and share!
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