Wednesday, June 11, 2008

2 steps forward...

I am staying the night in the hospital with Paul and I can't sleep. This cot they let me use is not the most comfortable thing in the world and there is actually some guy a couple doors down moaning and crying. That is pretty much how I feel right now but thankfully Paul is still asleep.

On Tuesday evening we were visited by Dr. Koreth who is the head of the bone marrow transplant team. He came to really fill us in on what they hope to accomplish with the transplant and the risks. Unfortunately there are so many risks it is too depressing right now to list them. The biggest obstacle will be infections and what is called Graft versus Host Disease (GvHD). GvHD is where the donor's cells start attacking Paul's body because it doesn't recognize it. They search for the best match possible but not everything would be exact which then causes issues. Dr. Koreth's prognosis was disheartening and not exactly as high as we would have liked. He said there is about 50% chance of survival and coping with the issues of GvHD and then 50% chance Paul would not make it. But all of the doctors agree, this is his best chance at long term survival. If they didn't attempt the bone marrow transplant the Leukemia will certainly return and would become resistant to the chemo.

They are going to begin searching for a match and would like to get the transplant done within the next 2-3 months. He will be in the hospital for another four weeks during that time. We have received many wonderful offers from family and friends to test to be a match for Paul. The doctors say they have millions in their registry now and have a 70% chance of finding a good match for Paul. If we have enough offers (50 -100) of people willing to test they can hold a bone marrow drive for us. If you would truly be interested please email me at paw10198@aol.com. Thank you so much - and please continue to keep us in your thoughts and prayers.


4 comments:

The Stewart Stuff said...

I'm there for you in any way possible! You will find the donor you need and all will be right again!
Have faith!!! I'm so very proud of you!

Love, Jen

Lisa O. said...

Have faith, Amanda. The doctors have to tell us all the scary parts and we have to believe they won't become reality. Paul will get what he needs and be done with this. The family down here feels kind of frustrated since the distance prevents us from being any real kind of help. Your blog allows us to feel connected and I am in awe of your strength and ability to keep a clear perspective. If there is something more we can do, just name it. (Even if it's just a basket full of chocolate!) Every little bit helps.
Love & Hugs,
Lisa & Jeff

Jason and Jenn said...

Hi Amanda,
I hope you got the e-mail I sent you. I know how hard it is to hear all the crazy things the doctors tell you. We've been there with my dad. Keep that positive attitude and you will see all will be just fine.
We're here if you need anything.

Talk to you again.
Love, Jenn, Jason, Matthew,& Kaylee

Anonymous said...

Hi Amanda, You are amazing. Just keep up the positive attitudes...please know we are praying for you all!!
Love,
Chris and George