This blog is meant to provide a place for family and friends to follow Olivia's progress in her fight to defeat her Alagille Syndrome. ---
Feel free to post any comments and questions.
We are the proud parents of Olivia & Amelia Huelsbergen. Olivia Anne came into our lives in Feb. 2009, diagnosed with Alagille Syndrome at 3 months old and sadly succumbed to complications from AGS shortly before turning 6 months old. Her story can be read at Oliva's Big Adventure.
Amelia Anne was welcomed into our family in Oct 2010, hale and hearty, with Olivia as her personal guardian angel.
Just heard from the nurse, that Olivia is doing well under anesthesia, still doing the Laproscopic procedure, haven't made a determination about the need for a Kasai procedure or not.
I dont like waiting for anything. I am sure you feel the same about lil Peanut. But, I like you am waiting to hear. Please tell us good news next post. I cannot get the lil Peanut out of my thoughts.
I dont like waiting for anything. I am sure you feel the same about lil Peanut. But, I like you am waiting to hear. Please tell us good news next post. I cannot get the lil Peanut out of my thoughts.
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