Our Goal

The purpose of this blog is first and foremost to bring all glory and honor to Christ through our actions and words. Though this blog helps those who view it to follow the life of my amazing little brother I write this blog primarily to unite the body of Christ through prayer and thanksgiving. Samuel and I love sharing the beauty of our Lord with you. May you feel the healing touch of the Savior in your daily lives.
-Kaitlyn

Samuel's Celebration of Life DVD

Here it is guys. This is the service we had for Samuel on 10/13/10. This is for you guys. You have been such a help and support. We want to thank every prayer warrior and follower who has journeyed alongside us and Samuel.

If anyone would like a copy of the DVD, you may e-mail me at kaitlyn@contractcallers.com .

We hope you are as blessed by Mike’s work as we have been.

Samuel's Celebration of Life- Part 1/6

Samuel's Celebration of Life- Part 2/6

Samuel's Celebration of Life- Part 3/6

Samuel's Celebration of Life- Part 4/6

Samuel's Celebration of Life- Part 5/6

Samuel's Celebration of Life- Part 6/6

A Walk with Samuel

These are the videos that show you glimpses of Samuel's life. We hope you enjoy them.

Samuel's Third DVD

Fearfully and Wonderfully Made- Samuel's Second DVD

A Video for Samuel by his big sister Kaitlyn

Thursday, June 18, 2009

9th Update

Samuel has had some ups and downs since my last update. Today he is doing well in all areas, except still no gag reflex. In my last update I spoke about trying to remove the ventilator and see how he tolerates it and replace if needed. They were slowly weaning his breathing and had lowered it to a rate of 14 breaths per minute. Samuel decided he was really comfortable with that rate, got lazy and decided he was just going to let the vent breathe for him. The last few days he has been very inconsistent with his breathing. They did another EEG to see if Samuel was getting into a sleep cycle which caused him not to breathe over the vent. The results didn’t show definite sleep cycles, so we again started the discussions with the doctor about the tracheotomy and G-tube surgery. Last night he decided he didn’t like those discussions, so he did well breathing thru the night. This morning he was still doing well, so the doctor decided to lower the support rate to 10 breathes per min and he is doing well with it. We are back to talking about removing the vent in the next couple of days…

Main prayer requests: Gag reflex and swallowing, consistent breathing – especially when we remove the vent, and healing of the brain areas.

Today we spoke with an organization called Footprints. One of their many services includes professional photos of the baby and family. We are going to try to coordinate these photos at the same time we remove the vent and if Samuel decides to cooperate with our plans, I will have Anita post them on the blog.

As always I thank you for your prayers and support. If anyone on this list is in need of our prayers, we will gladly lift them up with ours.

Yancy

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