Back Surgery is Scheduled for Today

On June 18th, we saw the Oncologist and he told us the bone scan was clean and there is no cancer in his bones.  First good news we had received!  I thought for sure it would be so I was pretty happy to hear that. The plan was to start chemo on Wednesday, June 25, 2014 and the doctor planned for the first scans to be done probably in September to see it’s working.   They will be doing blood work weekly or biweekly to make sure the chemo isn’t affecting his white/red blood cells and platelets.  If it does, the doctor will readjust. Really hoping we can put this in remission for a long time.  Only time will tell.

Steve is doing great.  He’s just tired.  But he feels fine. The side effects from Chemo can come on at anytime but he’s doing really well so that helps.  He had trouble sleeping last night because one of the meds is a steroid – the nurse warned us about it. Steve is also having some back problems which is completely unrelated to the cancer, thankfully.  So his back was also very sore.  After he finally listened to me and took the pain pills they gave him at 2am, he was able to fall asleep and slept through till 10am! Who knew I actually knew what I was talking about! He’s tired still and has napped a few times but in general, he still feels great. …

Today began round 6 of chemo.   It was the fastest and smoothest one yet.  We had one of our favorite nurses Erin (she was actually our first so that maybe why we like her so much).  The port worked great and Erin got the IV in right away with a perfect blood return!  So we were off to a great start. Steve feels good today, his appetite is up and he’s just in a good mood.  He’s been unhappy the past week due to another sore on his tongue.  When he gets these sores he can’t eat much or even drink much.  So think about it, would you be miserable?  I know I would!!  So it was a tough week but yesterday he started feeling…

I’ve received so many texts, IM’s and messages with words of encouragement, love and support and I appreciate it so much! But please know that I am OKAY.  We’ve expected his treatment to take this turn at some point and honestly, we thought it would be 2 months ago. I posted this on Facebook today but I know not everyone is on Facebook…… Thank you everyone for your prayers, thoughts and positive vibes. We are so lucky to have so many amazing people in our lives. I do feel blessed, considering the situation. The time we’ve had since his diagnosis has been a gift, a gift that one day the girls will realize was one of the best gifts ever. Right before Steve starts the…

We received the results of the CT Scan today.  The doctor says that after looking at the ct scan himself, there has been a small reduction in the tumors.  It’s not as big as the last time but he feels they are all slightly smaller.  He did point out that they are measuring them in mm and not cm so we are looking at something very small in size. Tomorrow is Steve’s first treatment in the next chemo regimen and it will be less the Oxaliplatin.  The doctor is going to monitor his CEA number closely and if he sees any change then he’ll likely change up his entire chemo prescription and use some different drugs. At this point the doctor is looking at it…

It’s been about a month since I updated and I realize some of you are thinking something is up since I haven’t updated. I’m here to tell you NO, nothing is “UP”… all is good. Steve took a cycle off from Chemo and ultimately had a month break. It was a nice break and Steve bounced back amazingly and we took full advantage of it. We went to Disney with the girls! We surprised them with a trip. It was a trip we all needed. You see, we love going to Disney as a family. We go every other year and it’s the biggest thing we do. And the girls love it. We all love it actually. It’s our “family thing” to do that we…