Monday is my birthday. I will be 38 but the only thing I want is a prayer service next Saturday. I am so ready for God's healing but I can only hope it is His time. Welcome to the weekend everyone, I hope I have more interesting things to say later because I think my mind is still asleep.
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.
Friday, September 6, 2013
Day 234
Today is Hope's first performance at a game. I am so proud if her and all she is doing. I am also so proud of Noah and I must say I miss him like crazy. You know I am proud of my sweet Elijah, this school year has him so excited. He has always been such a sponge for learning but with this new curriculum he is going to be so far ahead of the pack. His science alone is Botany. Not many second graders learn about botany.
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