Hi Friends,

This is Birdie again. As Pete hasn't felt up to writing a blog like he originally intended, I will share with you what I understand of yesterday's surgery, for those who are anxious to know where we're at in this process. Happily, Pete is still sleeping soundly after a very long day at the hospital yesterday. He feels like he has a 2x4 nailed to his neck, so he was anxious about getting sleep last night. (Obviously, we figured out the right combination of pillows!)

We originally went in for surgery on Monday, but after the radioactive isotope injection, they were not able to find a sentinal node to biopsy. So we went back again yesterday. And after 4 hours of searching, they thought they might have found one in two possible places. The reason for a lymphoscintigram is to find microscopic cancer cells in the lymph nodes that a PET scan would not be able to find. The PET scan can only find masses of 1cm or more.

Unfortunately, what they thought might be lymph nodes were not. Therefore, we will not be able to get a biopsy of the lymph nodes, and thus, no complete staging of the cancer. The surgeon believes that there is no sentinal node due to the radiation Pete received 20 years ago.

However, they did remove the tumor and there will be a pathology report in about a week to let us know how far the cancer has spread. The good news is that after the tumor was removed, there was no more radioactivity in the surrounding area. Thus, we can hope that the cancer cells were encapsulated within the area they removed.

The sad bit of this, is that desmoplastic melanoma is tricky. It can spread through the blood stream, the nervous system and the lymph system, ending up anywhere in the body. In our surgeon's experience desmoplastic melanoma doesn't stick to statistics. That is why it scares him. It can show up later, anywhere in the body, bones, organs, etc.

When first analyzing melanoma, it doesn't matter how large the surface is, it is the depth that matters. The pathology report will tell us how deep the cancer cells have gone. If they have gone deeper than what they found in the original biopsy, then a PET scan might be the next step to try and look for it in other parts of the party. The doctors will confer on this.

This is all we know for now. We want to thank you again for all of your kind words, your encouragement and your prayers. Thank you for watching our dog, for bringing us food, and for cleaning our house. I sure haven't been up to any of it. (I'm just trying to learn how to dress a grown man who can't move his neck. It's tricky!)

We love you all and we'll keep you updated as we know anything.
To our dear friends and family,

This is a humbling plea for help from our community. As many of you know, Pete had Hodgkin's Lymphoma in his early 20s, and through radiation and removal of some lymph nodes, he beat it. However, Pete has now been diagnosed with another type of cancer known as dismoplastic melanoma. The oncologist tells us that this is a rare form of cancer and that there is no cure once it has spread. Chemo and radiation will not work and will not be used to fight it. At this point, we know that Pete is in stage two out of four. We should know how far it has gone after surgery.

Pete goes into surgery next week and will have a second biopsy taken from his neck that will result in a 3 1/4" long ellipse taken from his neck. The depth of tissue that will be taken out is unknown until they go into surgery, but the doctor assures us that he will take out everything down to the muscle tissue. They will also inject a radioactive isotope in order to see where the cancer has traveled through his lymph system and if any more lymph nodes need to be removed. From this surgery, we will know how far the cancer has spread and what Pete's chances are for survival. The best case scenario will be to find out that the cancer has not spread. At that point he may be able to take an immuno-builder that will help him fight future cancer cells. If it has spread, there will be no remission and he will need to be checked regularly, as this cancer travels along the nervous system and can end up anywhere in his body.

At this point, we don't know what the future entails, but we hope to face each phase of this transformative process with grace and the strength of your love. Pete has been working every day of the week to keep us afloat while I've been in grad school and we are worried about the fact that he won't be able to work for, at least, a couple of weeks. We are selling our house and though we will most likely not make any money from the sale, we are downsizing so that Pete doesn't have to keep working so hard.

I must admit, it is very awkward and uncomfortable to ask this of you. My plea to you is this: We will not have enough income to cover the doctor/hospital bills that are already accumulating, or our mortgage in February (hopefully, our house will sell sooner than later). I am asking for any help that you can give us (and ONLY if you can afford it, as I know that many of you have been struggling, just as we have, in this economy) to help us cover our bills so that we might have a little breathing room to deal with this. We could only return our complete and utter gratitude.
Pete will soon start a blog on his website,, so that his friends can simply check in and see how he's doing on a regular basis.

We can use your prayers!

Thanks for your love,


Organized by Rebecca Krebs

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We've set up an account for Pete's medical bills here. This is a very secure site and works through Paypal. Donations can be made even if you don't have an account on Paypal. We are not able to ensure that everyone who has donated at this site will receive a tax deduction. You may choose instead, to donate to The Jeremy Wilson Foundation for a tax deduction at website or better yet, to avoid a credit charge, send a check made out to The Jeremy Wilson Foundation ATT: Pete Krebs Fund 1028 SE Water Ave STE 230 Portland, OR 97214

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