Two steps forward…one step back..
I just got back from visiting Travis. He was not as 'tip-top' as I had been lead to believe. He was in a great deal of pain and unable to verbally communicate to me (but through blinking and moaning I could get the picture he wanted and needed pain medication). He had previously been able to answer questions and had asked to see me but when I got there he was not doing so hot. I think it may have been the anxiety, pain and raw emotion all coming together and it was just way too much too soon. They administered quite a bit of pain medication and some to bring his blood pressure down as well. When I left a few minutes ago he was finally resting quietly.
Thank you all for the tremendous amount of support
However while in the ICU we ask that you do not visit or call his room as the nurses have told us this can be too much for him to handle at this time. I will let you all know as soon as he is moved from ICU to a regular surgery recovery floor and at that time will be allowed to have calls and visitors.
PLEASE continue to give him words of encouragement and support through this site
I am hoping for a better day tomorrow and that I can once again share this site with him.
Thanks again...be well,
Karla
p.s. sorry if any of these posts are hard to follow or don't make sense...I need sleep
What the surgeon said…..
So we have talked to Dr. A but I have not been able to see Trav yet. He is in recovery and will go for a baseline MRI soon. She said he is responding well and moving his right side well as of right now.
Dr. A thinks she got MOST of the tumor. This doesn't mean he is "cancer free" there will always be cancer cells and now we have to KILL them with radiation (to put it bluntly). Unfortunately there a high chance of recurrence with brain tumors but Travis will have MRI scans every three months to check for new growth or changes.
The tumor is currently in the hands of pathology and we should hear back in in 2 to 5 working days. The pathologist will tell us if the whole tumor is stage 3 or if there is any stage 4 lingering in there. This will determine if he gets radiation only or chemo therapy as-well (the chemo would be a pill for not the intravenous type you are used to)
I should get to go see him soon...another 45 minutes or so
Man it has been a LONG day! Thank you all for all of your support and kind words! It has been so wonderful to see throughout this ordeal.
Thanks again from the bottom of my heart!
Karla
Just got to talk to Travis….
They nurse just put me on speaker phone in the OR and I got to talk to Travis! It was really hard to hear each other but through the emotions I heard him say he is 'happy' and he is 'okay'. Dr. A had just showed him the tumor and told him she had gotten MOST of it and it had not infiltrated his primary motor function
That is a REALLY GOOD THING!!! The tumor will now be sent to pathology to see exactly what the next step will be. It was so great to hear him and even better to hear they got most of that damn tumor!!!
The nurse also said he has been in great spirits through-out surgery ...of course braggin' on his boys and i am SURE sharing several tid-bits about is GORGEOUS wife
(lol)
He should be out in a few hours....to be continued!!!
Surgery Day…..
Well we made it to check in on time this morning (see silly story below:)) 6:00 a.m. (too early) Travis actually slept some last night (I can always tell because he is snoring, lol) I didn't do so well sleeping but oh well.
He was taken back at 7:30 a.m. and I got the first update call at 9:30 a.m. that Dr. A has began her incision. They said they will call me every couple hours
Funny story- So we decided to go for a little walk last night around the buildings here at the Med Center. We wanted to go to the Gift Shop to look around (okay so I wanted to go to the gift shop to look around) any-hoots we only needed to go down ONE floor so Travis said "let's take the stairs I feel lazy when it is only ONE floor" so I said 'okay' so down the stairs we go.....we get to the door we need and it is LOCKED!!! Both of us were like "OH SH*T!" We tromped back up the flight to the door we had entered and LOCKED!!! I swear Travis was beginning to have a heart attack at this point. I then began to have several thoughts go through my mind like #1. I have my cell phone so we will be fine #2 crap what if I have no reception in these stairwells #3 we will have to start banging on the doors yelling "HELP" (while doing chest compressions on Travis because he seriously was FREAKING out on the inside. We went down to the bottom level and low-and-behold FREEDOM!!!
Thank GAWD! What a night we would have had stuck in a stairwell
Thanks again to you all for the support! I shall keep you all posted as this is a great outlet for me!
Karla.
MEG Test scheduled for tomorrow….
| January 29, 2010 | ||
| 12:00 pm | to | 6:00 pm |
Here is a link that describes what the MEG scan is and what it is used for. Travis starts this test tomorrow at noon and it should last 3-4 hours and then he has to undergo yet another MRI
(so much going on in that BIG head of his, lol ...love u honey)
Getting used to blogging…
Hi there it is me Karla. I am just learning the ins and outs of this blogging thing....bear with me

