Saturday

Your attitude must be like my own,

for I, the Messiah, did not come to be served,

but to serve and to give my life.

~Matthew 20:28 (LB)~

Stacey Scarle

Stacey had her last radiation today. Thank God that part is over. Next phase is the oral chemo which shouldn’t be too bad. Now she is burned pretty bad and has several blisters. She should start healing soon. Thanks for your prayers, thoughts, cards and calls they have really been appreciated. Please keep her in your prayers. as she still has a way to go. Love to you all. Joan

Jadan’s Story

Hospital Day 3

Posted: 03 Jun 2011 01:01 PM PDT

Things are not looking to great for me. I’m still having alot of seizures. The only change is the intensity of them. They are going to give me the steroid tonight and tomorrow morning. If they haven’t decreased by then we will be coming home a day early. So there you go another medicine that did not work. I don’t know what to do anymore. We are so tired of watching me have seizures everyday of my life. I guess we have to be thankful for the progress I’m making and pray that I will continue to develop. Maybe one day we will have some control of these horrible things. Our next step in my journey is to go to Boston at the end of the month. By that time I will be on enough lamictal to know if it is working. We will then wean vimpat and start vagabatrin when we get back. This is the medicine that can effect my eyes. I really didn’t want to try this medicine but it is only fair to try it for a month and see if it will help. Please pray for me and my family!!!

CaringBridge: Logan Watts

FRIDAY, JUNE 3, 2011 6:43 PM, CDT

We finally just got to our room. The hospital has been full so we have been waiting all day. I miss the PICU so much they were all so good to Logan and Jonathan and I. Logan has been really agitated since we have been up here. He keeps moving his left leg and kind of groaning. We had become so used to how things work in ICU and its not the case up here. We want to give a big shout out to all the PICU staff who took such great care of my lil man. I can’t wait to walk my lil man thru yalls door in a year from now and show yall how much he has improved and to see the look on the neuro Dr’s faces. We thank God for all of his “baby steps” and please do NOT stop praying now. We will have a long, difficult road ahead and we have come to far to be satisfied. PLEASE CONTINUE PRAYING FOR LOGAN!!

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FRIDAY, JUNE 3, 2011 9:15 AM, CDT

Well its a big day of celebration for our lil boy. He is getting moved to a real room. Here comes the PICU going away party. So I will post our room number when we get it. Hopefully he gets transferred to New Orleans soon cause everyone is saying the sooner he can start therapy/rehab the better. PLEASE CONTINUE TO PRAY FOR LOGAN!!

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THURSDAY, JUNE 2, 2011 10:58 PM, CDT

Not much to update but he is doing good off of the vent. They actually removed the machine from his room earlier today. He was put on oxygen which they just removed as well. We are so thankful for this progress but at the same time a nervous wreck since he can not swallow. I’m so scared he’s gonna choke or aspirate. They say he may never learn to swallow but there is a also a chance he can so we are staying hopeful. PLEASE CONTINUE TO PRAY FOR MY SWEET LOGAN!

FRIDAY, JUNE 3, 2011 6:43 PM, CDT

FRIDAY, JUNE 3, 2011 9:15 AM, CDT

THURSDAY, JUNE 2, 2011 10:58 PM, CDT

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