We do not have a time yet, we'll post as soon as we know.
We'll also have some other tidbits to pass on & talk about Tetralogy of Fallot / Pulmonary Atresia Anatomy a bit.
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.
Hi! You do not know me, but I found your blog. I just want you to know that our hearts and prayers are with your family. I am a mom of a little boy with TOF with Pulmonary stenosis. Wishing Olivia a fast recovery. BTW we use to live in Michigan. If you ever need anyone to talk with you can contact us at our blog or at kelleynr@yahoo.com
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