Why am I writing this blog?

Euclid (Cleveland), Ohio, United States
Here I share the amazing spiritual journey I began on July 19, 2007. I received the diagnosis of a golf-ball-sized tumor on top of the left parietal lobe (motor functions) of my brain. I had severe symptoms all up and down the right side of my body and had received an MRI scan of my brain. In August 2007, I learned that my diagnosis was a Glioblastoma Multiforme (GBM). This is a common form of fast-growing brain cancer with a challenging prognosis. That's the external story about that moment in time. In the spiritual world I found (actually more like it found me) what I came to call the Fact-Based Spirit-Guided Path, and I began an amazing journey. After October of 2008, I lost the use of my right arm, and in early 2009, my cognitive abilities were struggling, and treatment options ended. My wife, Susanne, then began doing most of the blog postings, with my review and input whenever possible. I continued to apply the Fact-Based Spirit-Guided Path as the adventure continued. My soul then flew to the Kingdom of God on July 1, 2009. Thanks for your interest in my journey. Craig

Susanne's Perspective

During this entire journey, my wife, Susanne, had an entirely different kind of experience. Initially she added comments to some of my posts describing her experience of the moments I discussed and offerred perspectives on our relationship. In the latter stage of this journey, she is writing the blog, as I am no longer able to do so. I am truly delighted that she is doing so. Susanne and I work together as marriage educators/relationship coaches and she has written many books on preparing for and strengthening marriages so you can count on her comments to be insightful and poignant.

Thursday, October 4, 2007

Treatment Starts: Monday, October 1

The first treatment was smooth and uneventful. I have developed what I think will generally be my morning routine around the 6 weeks of chemo/radiation treatments:
  1. Eat breakfast before 8 AM to allow 2 hours, per pharmacist recommendation, before taking the chemo pill.
  2. Listen to the 1/2 hour tape from my hypno-therapy session starting at about 9:30 AM to get me fully connected with my “PLAN”.
  3. Take the chemo pill at 10 AM welcoming it to do its healing work. When we had originally spoken to the oncologist about the timing relative to the radiation treatment, he indicated that it did not matter. When Susanne pointed out research literature that indicated the optimal timing was 1 hour prior to the radiation, they agreed, and we may have helped with refining what they will be recommending to future Glioblastoma patients.
  4. Depart for the hospital for 11 AM radiation appointment.
  5. During the radiation treatment have the beautiful musical rendition of the "Long Healing Prayer" from the Writings of the Bahá’í Faith playing. I had neglected to mention during the post on preparation for radiology begins that I had played this CD during the MRI and the technician was so taken with it that she asked permission to make a copy. The site I’ve linked to above contains a free download of the music and shows the words. The artist, Allen Tyrone Johnson, also has audio gift cards available.

Each Monday, there will be a meeting with Dr. Einstein, the radiologist, and his nurse, Kathy. Susanne will be my driver that day to participate. The nurse basically goes through a set of questions to determine if any side effects are present. After she left, we reflected on how problem-oriented the questions are and that there are none to determine what positive state I’m in. We are now devising an alternate list of questions for her to ask me (the doctor has approved us working on this list), and we’ll post it next week when they are final. We had an excellent discussion with Dr. Einstein:

  1. I explained to him that I am doing visualization work to support the radiation treatment and that seeing exactly where they are targeting would be useful to me. He showed us a detailed mapping of my head and showed exactly where they are targeting. This targeting is based on analysis of all the MRI images taken over the last few weeks, including back to prior to the surgery so that it takes into account the full extent of possible cancer penetration. Based on these images, we agreed upon where I would be visualizing a layer of my white blood cells forming to surround it and remove the cancer cells.
  2. We inquired about the results of the MRI scan that was taken on September 20. He indicated that the swelling (edema) was significantly reduced and that there was no visible evidence of tumor re-growth. These are both very good pieces of news. You will recall that my visualization, prior to the surgery, was building a cocoon around the tumor so they could remove it in one piece. They/we were successful, so I’m not 100% convinced that there is anything left in there. The doctors have repeatedly assured me that, given the nature of the tumor, there are microscopic tumor particles that, at this point, would not show up on the MRI. Untreated, these will quickly grow into another tumor.
  3. He was very pleased with the progress on regaining the use of my right foot. He was very interested in Susanne’s theory about the role of the non-prescription anti-flammatory called Wobenzym I’ve been taking for my sprained ankle and asked what it was. He indicated that continuing to take it during radiation would be acceptable. Because it appears to have reduced brain swelling, it may reduce the future need for steroids (yay!).
  4. We discussed care of my scalp and hair. The standard recommendations for products to use to protect both don’t make the best sense to us, so he has agreed that we can use alternative products instead of theirs. It’s amazing to us that cancer patients are given/encouraged to use substances containing petroleum byproducts, formaldehyde, various chemicals, and products that promote itching.
  5. At the end of our meeting, he complimented us on the proactive, positive attitude with which we are approaching the treatment and to keep it up. We told him that it was our understanding that more “difficult” and questioning patients tend to live longer. That prompted a good laugh!

Today was the first day I was able to work since July 19th, and I put in a productive 3 hours catching up on my email and getting organized to get back in the saddle. Felt good!

5 comments:

Natalie said...

Go Craig!! Congratulations on getting back to work and making such wonderful progress so far! You are awesome. Give that blastoma what it's got coming to it!!! -Natalie

Anonymous said...

BE DIFFICULT!!! LOL! Be a total pain in the patoot and heal, heal, heal. And please keep writing about your process. It is confirming, soothing, and inspiring to read about your journey.

HuGo said...

Wow, very nice site! Continue your great job.

http://gohugodowntown.blogspot.com/

Anonymous said...

You are amazing Craig. The same attitude and drive that makes you special has allowed you to take on this illness and beat it. You are an inspiration. As your colleague, it felt good to have you pushing buttons again. You are important to our success. We all missed you.
Susanne, we are a witness to the strength a solid marriage/partnership brings. Thank you.

Anonymous said...

The rest of the story…

I admit it’s fun shaking up the normal flow of the doctor’s routine with our proactive approach! We will look for opportunities to give feedback to the oncology team at the hospital about ways to improve the program. Craig and I are usually in the mode of promoting beneficial systemic change…whatever the topic is!