I'm Here (waving)

As most of you know my life barely ever stops for a tea break, or even a "pee" break for that matter. I can not believe how the time has flown by. It actually make me really sad that time flies by so fast. Before I know it, my kids will be graduating and off on their own with an agenda to be conquered. Ugh.

So anyways, I'm sure many of you are asking, "where have you been?" This is where I've been.....

~Last weekend, Carson and Cooper turned 4 yrs old (see what I mean about the time flying by?)

~Last Tuesday, Our friend Katie had her chiari surgery and I am happy to announce that she is home and doing well.

~Last Wednesday, Keegan and I were in Madison. He had an LP done with his neurologist. He did really well. We got home around 8:30pm

~ Last Thursday, My self, my mom, Riley, and Carson ,headed down to Madison at 4:30 am for Carson MRI and bladder/kidney ultra sound at 830a. Then we sat around and waited for Riley's MRI at 1:30p. We 4 girls lived in a post op waiting room which was probably like 10X10 for a total of 11 hours that day. Mean while, at 10am I got a call from Matt that Keegan is struggling with head pain and need to be picked up from school. Great. I made my phone call to the neurologist and she explains to me that he probably is having a spinal headache from a CSF leak. He is to lay completely flat for 48 hours and pump the fluids.

~ Last Friday, Neither child goes to school and I am home with all 4. 3 that are over tired and 1 that is not supposed to be lifting his head up at all. RIGHT! Come evening time the pain is so bad, I call the "on call" nurse and she insists that I take him to the ER immediately. He and I packed up, I SO broke the law by letting him lay on the floor of the van Vs his eyes popping out of his head by sitting in his car seat but shhh, don't tell. We get to the ER, they get him in right away, we explain everything, they get an IV started with some fluids, good pain meds, and caffeine. We were there for about 3 hours and then they told us he "should" be better by the morning.

~ Saturday morning arrives and he is NOT doing any better. This time I call his neurologist in Madison in hopes they will do something more for him. They send us back to the ER, the ER doc and the neurologist speak, and we are admitted, hooked up to an IV, and laying flat. Life is good while laying flat, but once he is up, the pain is back. We were told that with the IV we would be there at least until Monday. Swell.


~ Today, IV meds aren't doing it. They asked if we wanted to be at home laying flat or in the hospital laying flat until Wednesday. Keegan I both voted to go home. Now, we will lay flat until Wednesday and hope to god that things get better. If not, Wednesday we will contact the neurologist and we will go from there.

So.....that is where I've been. How about you???