Welcome to "Hope Does Not Disappoint"


There are two key reasons I have finally decided to join the world of blogging:

First, my cancer has become active and there is a loving congregation and many family & friends who want to keep track of what is taking place. This provides a way for me to update them as often and with as much detail as they desire.

Second, the Lord often links Scripture with circumstances in life for a much more potent 1 - 2 punch. I have already found that to be true and I hope to share some of those lessons for those who are interested.

So almost every entry in this blog will have two parts to it: Body (what's happening physically with the treatments) and Spirit (what God is sharing as I open His Word).

Thanks for visiting. I hope some of the "Points Along The Road" in my journey are helpful and encouraging to you.

Dave




Thursday, May 13, 2010

PET scan update

It's Andrea, this time....a visiting "writer" to this blog. We're a little pressed for time tonight, since we have to be at Trumbull High soon. So while Dave is eating dinner, I am posting an update from our visit to the doctor this afternoon.

Dr. Cooper was disappointed to see that the PET scan showed that there was still a spot of cancer -- it's 80-90% gone, but there is still a spot that showed up on the PET scan. Usually, he says that by the 4th round of chemo, they don't find anything on the PET scan and then the 5th and 6th treatments are kind of like "clean up" chemos. Since there still is cancer there, he wants to change the last two treatments to a different kind of chemotherapy which uses different drugs. He said that the residual lymphoma cancer cells that are still there MAY be resistant to the other treatment he was on, and using the new drugs may prove to be effective on these resistant cells.

Treatment WAS going to be on Tuesday, as originally scheduled, but they want to have a port put in first so that giving the treatments from now on will be easier. -- The nurses who had a hard time finding a decent vein for the infusions will be happier, too! :) SO, we are supposed to get a call tomorrow, letting us know when the port will be put in next week and then they will tell us when the treatment will start. We are guessing Dr. Cooper wants to stay as close to the schedule as possible, so if he gets the port on Tuesday, we are thinking that he may have treatment on Wednesday. Stay tuned....!

This new treatment is a little different...instead of being given all in one day, like we have been used to, it will be given in 3 consecutive days. Then he will have a 2 or 3 week break before getting the last treatment. When we asked about side effects, he said it all depends....some people think it's the same as the other chemo, some think the chemo we are on now is worse, and others think the new chemo Dave will be having has worse side effects. Obviously, we continue to pray for healing of ALL the cancer and it would be really nice if the side effects are not any worse than what he has been experiencing.

The plan of action after these last two treatments is kind of like before.....after his blood cell counts "recover", they will harvest his stem cells. When they have enough, he'll have the 6-day- every-day chemo "blast" to "wipe out everything" (as the doctor says). Once that is done, they will put the stem cells back in and then do another PET scan. If it is all clear, he still wants to do radiation on the spot where the cancer was concentrated just to make sure there is nothing left.

The time frame of all this?? We really have no idea...but we know the Lord does and we continue to trust Him for each day and for His perfect timing and perfect will. Thanks SO much for all your prayers!

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