Thursday, 6/14/12

UPDATE: 

Thursday, 6/14/12

Happy Flag Day!!

Hank went in to see Al this morning.  Turned on the news and got the day started with the latest info.

I arrived in around 10am and got a morning update.
The doctor downgraded Al's condition today, meaning that he is able to be moved out of CCU and into the MEDSURGE area.  He will have a private room for at least two more days at CMH.  He had a refreshing dribble of OJ today.  He swirled it around his mouth like it was melting.  Then let out a huge AAAHHHHH.  His poor mouth has been so dry, his lips were cracked and peeling.  Now, with Carmex on hand and his body once again properly hydrated, he has more moisture for the sensitive areas. 

He is still in isolation, gowns and gloves needed.  He was on two types of antibiotics for the MRSA and only one worked, so the nurse started him on more of the good stuff to continue positive progess. I expect him to be moved Friday to the medsurge area.  He is tolerating his fluids and feeding tube very well, you can tell his body is strengthening everyday.

Alvin also pushed himself upright a little bit with his own strength, that is HUGE!!  The weakness of his arms has really taken a toll on him, so frustrating. 

He had a wonderful day yesterday....he told me so.  A very long day of visitors but he enjoyed every moment.  He is a very blessed man.  You, his friends and family are everything to him.  Everyday he tells me how much he loves Rik and his children.  It is truly beautiful.

Rik is with him this afternoon, so after talking with Hank, I have chosen to let them have some alone time.  I bet they will hold hands and watch a movie. 

Things are looks up!!  Your prayers, messages and visits mean alot. 
Over the next few days, I am going to take a tour of Clatsop Care Center where he will return and continue to recover.  I want to know what benefits are available to him and Rik.  Using the therapy balls or whatever else to help improve his strength is crucial and want to plan accordingly in addition to his regular therapy. I plan to spend a great portion of my day working with him, weather it be swallowing or taking him for strolls through the grounds. 

I am also looking into fixing some things around their house.  Alvin wants to be home very badly, so that is the goal.  If there are any suggestions to whom I should be contacting for supplies, housing issues, like bathroom area, ramps etc., please let me know.  I have a list already but the more the better.  I appreciate all info!!

My regular email is  isurfergirl2010@yahoo.com
My phone number is 503-791-5421 call/text


**Please note that when I refer to myself taking care of business, by no means am I doing this alone.  WE as in family and friends are doing this together.  We all appreciate input!  Please feel free to leave comments on this blog!!   A great way to have conversations all inclusive!

Thank you for all the positive feedback from our first post!  I hope this finds you all in good health!