Bone Scan is Clean!

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…

My families world was turned upside down in June 2014.  I’ve decided to share it here on our family blog to possibly help someone going through the same thing.  I’ve searched high and low for months for support groups and finally found one online.  I have so many questions and concerns that really only someone who’s gone through this, can help with. Here is our story: On Friday May 30, 2014 my husband Steve came home complaining of chest pains.  He was thinking he had gas and then ate dinner.  After dinner it didn’t get any better so he stayed home while I took Holly to her softball game.  I made him promise me that if it got worse, he’d take an aspirin.  He assured…

Steve had his 8th round of chemo this week and he’s pretty happy it’s over because he has a break and won’t be back to the infusion center for 4 weeks. Why the break?  He needed it for so many reasons and without it, going forward would have been way too hard. First of all, his CEA number is down to 11.  So that’s GREAT!  So if he’s going to take a break, now is a good time to do it since the number is still going down and the chemo is still working. But the real reason for the break is because he needs it physically and mentally.  Even with the reduction in the 5-FU, he’s still getting the mouth sores, but not as…

Last week was great.  Steve went to work, no doctor’s appointments, the girls fought like normal, I felt anxious about the girls fighting and Max pooped in the house.  It was a normal week and it felt good. I think we needed that break from “cancer”.   Just to realize that we are all still here and need to move along as normal as we can.  It was nice.  It recharged us for another week of Chemo.  Dr. Sam told us that we “can’t change what is happening to Steve.  We can only live each day as best as we can so we have no regrets.”  And he is right.  And while it’s hard to think that way every second of every day, we try…

Today we met with the Oncologist to get Steve’s CT Scan results and his latest CEA number.  The appointment wasn’t what we hoped for last week going into the CT Scan.  Steve and I both had different ideas of what to expect and neither of those expectations happened. First of all I’m very happy to tell you that his CEA number is 21.  Last time it was 64 so this was a nice drop and we were very happy to see it so low. That was good. Next is the size of the tumors.  They’ve decreased significantly in both his lungs and liver.  Which is great news!  But, Honestly this is where I was surprised as I assumed that one of his organs would be…

Steve had the port placed today.  It went well with no problems.  He’s sore and groggy and is actually taking the pain meds. Step 1 – DONE.