Second Round of Chemo is Done!

Steve’s surgery last week was a success.  The spine surgeons were able to remove the tumors that were compressing Steve’s spinal cord without having to insert the titanium rods.  His bones were surprisingly strong.  They did insert a little cement into the spine where they removed the tumors, just to give it a little more strength. Because they didn’t have to insert the rods, the recovery was much easier.  Steve was up walking around the following day and then doing the stairs a day later. Two days after his surgery, his heart rate was still high – it was running 115-120.   Come to find out it was because he has a blood clot in his lungs.  He was at a high risk for getting one,…

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 has been having a lot more back pain.  It started to get worse last Thursday night.  He had a hard time getting comfortable and could barely move.  It was so hard to see him in so much pain.  Friday morning when I spoke with the doctor, he told him to double up on the pain meds he prescribed him and if it got really out of control to go to the hospital to get something stronger to give him relief.  He was scheduled to have a bone scan on Monday (yesterday) and CT Scan Tuesday (today) so he said we’d talk after those scans to see what was going on. After doubling up on the pain meds when needed, he felt better and got…

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.

Today was Steve’s 3rd Chemo Treatment.  It’s crazy how fast the last 6 weeks have gone by since we first found out he had cancer. Last time there was no issue with the port and the IV went right in with no problems.  This week we had a problem again.  Not getting the IV in, but getting the blood to flow out of the IV.  You see, when they put a port in, sometimes your body realizes this foreign object is in there and doesn’t like it.  So it sort of forms like a blood clot so nothing will flow.  I’m not sure of the exact terms they use but basically it blocks it.  When this happens you can get stuff into the IV, like…

Steve is at Rhode Island hospital and he’s scheduled to have surgery today.  And he’s still smiling… He’s not going to give up easily and without a smile on his face.  I admire that about him so much!