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.
I think Olivia must like all the attention. Roman could not wait to get out of there. We can just call her the little Diva. She knows how to milk it for all it is worth. Hopefully, she can bust the joint in the next couple of days. Kelleyn
Glad to hear you guys are finally getting some rest. Give big cuddles and kisses to the little one. Shes a fighter, dont EVER tell her she cant do something...she is amazing!
Thank you. I was worried. Now a sigh of relief. Be good lil Peanut.
ReplyDeleteI think Olivia must like all the attention. Roman could not wait to get out of there. We can just call her the little Diva. She knows how to milk it for all it is worth. Hopefully, she can bust the joint in the next couple of days. Kelleyn
ReplyDeleteKeep the good news coming! Thanks for the updates, which we read daily. You all are in our thoughts and prayers. Love, Tom and Marie
ReplyDeleteGlad to hear you guys are finally getting some rest. Give big cuddles and kisses to the little one. Shes a fighter, dont EVER tell her she cant do something...she is amazing!
ReplyDeleteSweet dreams........
ReplyDeletehugs
M
Thank's so much for the updates. You are in my thoughts and prayers. Glad to hear all the good news.
ReplyDeleteMary