Day 22 here at Johns Hopkins, and things are going great.
Krysten is breathing very well, and should be on minimum to no oxygen by
tomorrow. Her respiratory rate is around 30 tonight, So LORD willing by morning
should be down in the twenty’s. The surgeon told me earlier today they
would take her chest tube out tomorrow. Then, she should be on her way out of
the MICU. Also, speech therapy evaluated Krysten today, she is able to eat ice
chips and drink teaspoons of water. Tomorrow should bring a better diet. Today
has been a great day, and I can’t wait to see wait to see what the LORD has for
tomorrow. I also wanted to thank everyone who donated to Krysten’s Great Strides
walk to help support the cure for Cystic Fibrosis. She is going to be blown
away by all of the love and support she is getting. If anyone would like to
help support the cure, and Krysten this is the link to her donation page. http://www.cff.org/great_strides/KrystenHanneken/
We continue to praise GOD for our journey and the support we have had through all of this. Krysten and I cant wait to be able to share this with as many people as possible, we know that with HIS strength anything is possible. We will continue to Praise HIM for every step we have taken.
Patrick
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