The Port is In Place!

Yesterday  (7/21/14) Steve and I received some really good news about his Stage 4 Colon Cancer.  His CEA number, which is the tumor marker in his blood, was lower – a lot lower!  When he was in the hospital the first week of June it was 536.  Then a few weeks later it was up to 834.8.  Yesterday it was 263.1.   Needless to say we both cried when I gave him the good news. That means the chemo is working. We saw the doctor today and he was very happy as well with the results.   He said the drop in his CEA is great after only 2 treatments.  I asked him if he expects that number to go to zero at some point, if…

Steve had another CT Scan last week and it showed that unfortunately the cancer is still spreading in his lungs.  The liver is stable.  He also has some pretty swollen Lympnodes near his lungs.  His CEA is the same as it’s been the last 3 months – 11. We had a really good conversation with the doctor about what is happening and what we should do next.   So here is the plan right now: 1.  We are going to go to Dana Faber and talk to them about clinical trials.  It’s not very likely Steve will do a trail, but we at least want to talk to them about it. 2.  Steve will continue on the chemo he is on right now for 6 weeks…

I had to take Steve to the hospital today. His breathing hasn’t been very good and I just knew it needed to be addressed. I’m so glad we went because his oxygen level was VERY low. They did a CT scan to check for a new blood clot, but found nothing. There is a little fluid in his lung but the doctor thinks it’s old and doesn’t believe it is related to this. They did hear some crackling in one of his lungs so perhaps it’s a little collapsed but again, he didn’t think it would cause this much distress. There is some progression of disease in his lungs so it could be a combination of everything. They admitted him and have him on oxygen…

Steve saw his Oncologist today and his CEA is still going up, slowly but it’s going up.  Today it was 20.  In March it was 17 and in February it was 12.  So it’s moving up but that’s not the direction the doctor wants to see it go.  That means the cancer is also growing.  So it’s time to change chemo treatments. We are going on another family trip this month, this time out to California to Disneyland!!  The girls are VERY excited.  The doctor is going to wait until after our trip to change his chemo.  Tomorrow will be his last one on this type of chemo and then he’ll take a break so he’ll feel great on our trip. It’ll actually be a…

Well friends…..It’s with a very heavy heart that I have to write the post I never wanted to write, nor did I expect to be writing it anytime soon. Steve came home today with Hospice. Unfortunately the tumors in his lungs have spread more and have taken over about 80% of his lung capacity, which leaves him with about 20% to breath. The doctor doesn’t really know how much more time he has, but from the looks of how much of the cancer that has grown in his lungs over the past month, his guess is about 2 weeks give or take. He’s on oxygen and Morphine to help him be more comfortable. He’s happy to be home and in a place where he can…