Update
March 23, 2017: It's been a great day for Mr. Blanton. He continues to amaze the doctors and nurses everyday with his determination and progress, but to his family and friends we just smile and say, "that's Andrew". Every time he pushes a little harder or says, "sure, I'll try" we are thankful and blessed for Gods grace in his healing and strength. He had 2 round rounds of occupation therapy today and then on his own decided he wanted to try and stand up....and well, he did it (of course with help, but he took the initiative) 13 days here and he has made more progress than other patients that have been here over a month. The nurses wish all their patients could be like Andrew. 1 week from today is our "Andrew goes to Shepherd" day. He even asks I have it in my phone on the calendar (his OCD is still in full effect) Each day with therapy, we see just exactly where his biggest struggles are. Leg raises, leaning on his elbows, kicking his leg out side to side are all new and trying movements for him. Some are easy, some are hard and some he can't quite understand what he is being asked to do. He doesn't quit though and his eyes and face show that he is fighting hard and wants to get there.
Today, he was at Dekalb Medical Center but knew he was in a hospital, knew the year and could read the words "brain injury" written on the white board. "Brain Injury" he would randomly say. For lunch I thought I'd get him a sweet potato as a treat and see if he could eat it....well He also managed to eat 1/2 of my piece of pizza and drink my tea. I've never been so happy in my life to share my piece of pizza. That's love y'all.
Going to bathroom has been an issue, so we got him a portable seat to sit next to the bed. Check. Did that. Later on in the day, he said, "I'm going to the bathroom." I said, "ok. One second let me get...." couldn't even finish my sentence and he says "That bathroom over there" and points to his bathroom and started to push himself to stand. So I called Chad, his nurse and we went with it....Check. He did it. They have this cool "Rascal" looking scooter thing that can maneuver him around and really helps get him from he bed to the recliner or to the bathroom. He's always wanted a Rascal.
Andrew and Annika had a wonderful surprise from some of the girls and boys from the Mill Creek golf team tonight. He couldn't stop talking about scores, tee times and courses they had to play. He must have asked them 20 times, who played today and what their tee times were tomorrow. The best thing he said to these kids he's known for years is, "Good luck, have fun and be silly" That's Andrew. He wanted them all to go home and rest and be ready for the morning and to have dinner and good breakfast. He says there's a cookout at Heather's tomorrow at 12pm and we can grill whatever. Lol...maybe not tomorrow but yes, eventually we will have that cookout. No matter what kids he knows, supports or how he knows them, his heart genuinely cares about all of them and wants hem to succeed.....that's why we all love him. By the end of he day he was exhausted. We still had a nice quick game of "Andrew Uno" with our good friend Hank Annika and Layne.
Andrew's Neurologist stopped into today to check in. He is extremely hopeful and while he is excited for Andrew's progress, he still will mention the slow and long recovery road he has ahead. That gentle reminder that there will be 2-3 good days and then there may be 2-3 bad days. Even though we know this, we still need to to hear it. 1 month, 6 months, 1 year or 10 years....even if it's forever. He's got this. We got this.
Since we are trying to get Andrew on a schedule with eating and sleep times.... if you would like to visit, the best times are probably around 12pm, 3pm or 6pm. Just message or text us before coming up so we can let you know how he is that day.
Hope everyone has a great Friday and thank you again for all the love, support and prayers. Without y'all, we couldn't get thru this and be #stronglikeandrew.
XOXOXOXO