Friday, August 1, 2008

Day 47 - August 1 - Baby steps!

Another day draws to a close. It amazes me that it's August, and I'm still in Fresno. Oh, and I still think too much.

Today had some good things in it! Connor was able to stay on his speaking valve for over 20 minutes today, and was much less exhausted at the end. The physical therapist said that, if he stays healthy and on this bed, she will start swallowing therapy the first part of next week. She told him that if he can safely swallow thin liquids, she'd bring him a Jamba Juice (his favorite). He responded "OK, now I've got a goal!"

Also, today he complained to his nurse that his arm was asleep, and was tingly on the whole length of it. She manipulated it and the feeling went away. And tonight, JoƩlle was massaging his feet while he and I were talking, when Connor suddenly told her that he had felt her touch! She had been poking his feet with her fingertips, and she found a spot near his toes that he said he could feel. Since he could see his feet, we asked him to close his eyes and open them when we touched the spot. He nailed it five out of five times! So, we called his nurse, but then were unable to duplicate it when she came in.

Connor did run a fever for a while this morning, raising concerns of another infection. The RTs came in and took specimens from his lungs this afternoon to culture, so they are worried about infection as well. We have been praying specifically against infection for a few days, and are confident that the cultures will return clean. Please continue to pray for that result, and that Connor would remain protected against any infections whatsoever.

The boy went to sleep tonight in better spirits, and we continue to pray for rest for him - he hasn't been sleeping well lately. Neither have we, but looking back over the last 47 days, we see God's steady provision for us in every single need, every single day.

Thank you all for your faithfulness to us and to God. You honor us. Goodnight.

9 Comments:

At August 1, 2008 10:35 PM , Anonymous Anonymous said...

Sounds like a good day overall! Hope he enjoys his upcoming Jamba Juice thoroughly :-)!! Connor remains in our thoughts and prayers, and so do all of you. Baby steps are still steps!

iamjustone

 
At August 1, 2008 10:48 PM , Anonymous Anonymous said...

Thank you again for sharing this journey with us and allowing us the blessing of coming before the throne of God with our prayers on Connor's behalf.

Just a word of encouragement - When I experienced nerve damage from toxic chemotherapy, I was told that it could take 6 months (maybe as long as a year) before I would know the extent of healing and improvement neurologically. And that was from man's perspective, not Gods! Do not despair at the slow progress.

 
At August 1, 2008 11:29 PM , Anonymous Anonymous said...

Praying for much needed restful sleep for all of you tonight!

~Becca

 
At August 1, 2008 11:31 PM , Anonymous Anonymous said...

And now I'm also praying that the enjoyment of Jamba Juice would be able to come soon! (My favorite too) =D

~Becca

 
At August 1, 2008 11:47 PM , Blogger Linda said...

"My presence shall go with thee, and I will give thee rest"
Exodus 33:14

Thank you Lord for your promises

Lord Bless You And Keep You Always, Connor and Family

Praying in Downey!

 
At August 2, 2008 12:13 AM , Anonymous Anonymous said...

This is all SO exciting! I must can't wait, every day, to see what God has done! Thanks for sharing the baby steps.

 
At August 2, 2008 10:13 AM , Blogger Kimberly said...

Very exciting! San told me to say that we are praying he can come back to relieve the lousy replacement drummer on worship team...and we certainly don't mean David! ;)

One question from a rusty rehab speech therapist: why are they starting him on thin liquids and increasing to thick? Usually it starts the opposite way, but like I said I haven't worked in a hospital setting for a few years. Just curious...

 
At August 2, 2008 11:13 AM , Anonymous Anonymous said...

More questions, from someone totally ignorant about these situations....hope they aren't too invasive, but I've been wondering...

Have they been "feeding" Connor only through IV?
Have they been stretching and exercising his limbs?

 
At August 2, 2008 9:50 PM , Anonymous Anonymous said...

Hi Williamson's...
We think about you everyday...often throughout the day ..God puts you on my heart and we pray for you..We can't imagine your journey.. This is very very difficult..So lonely and so exhausting.. For each one of you..The only comfort i get is that God is with you and we see the work of His hands in your lives.. we are trusting Him for more and more miracles big and small. We are thankful for every sign of God.. We love you and we are believing...
Love..
The MacPhails

 

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