6.03.2011

Strongly Moving Forward

Just a quick update...Pierce is now on the high-flow nasal cannula. The cannula is the next down from the cpap in breathing support. The next step from here is room air! They weren't going to try the nasal cannula on him until next week, but he was doing so well on the cpap. He did not have one brady (that is where his heart drops) all day yesterday. That is a really good sign. God continues to strengthen and bless Pierce. Thank you for your prayers and support. Please don't stop.





Grace and peace,



Nik, Lindsay, and Pierce
Posted by Nik, Lindsay and Pierce Franks

3 comments:

  1. JenJune 3, 2011 at 9:05 AM

    YAY for Pierce!!!! :) Keep it up!!

    ReplyDelete
  2. Andrew and Lauren HessJune 3, 2011 at 10:05 AM

    Way to go Pierce! Before you know it he will be just a regular "feeder/grower" in the NICU.

    ReplyDelete
  3. UnknownJune 3, 2011 at 8:21 PM

    YAY! Go Pierce, GO!!

    ReplyDelete

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