Sunday, October 10, 2010

I’m Back!

10/9/2010

Sor ry for the long delay in my posts. 2010 has been a bit crazy. What I thought I would do today is have a catchup day. For you new followers I will give the readers digest/speed racer condensed version of my Cancer Journey. If you want the full story, please read my past posts from the beginning, which I encourage. Here is the quick chronological story:
12/27/2007 – You have an inner ear infection…ooops I mean Brain Tumor
1/29/2007 – Dr. Crute removes Tennis ball from my right temporal lobe in a quick 12 hour surgery. Friends and familysit in uncomfortable chairs in the waiting room and Lyle saves the day with Jimmy Johns. When pathology comes back we find out that I have a Glioblastoma multiforme IV,One asshole resident gives me 6-18 months and I said “wanna bet” and 34 months later I write to you today.
Q1 2008 – I recover quickly from the surgery and start a course of radiation 6 weeks 5x per week. I also start a cclinical trial of Chemo(Temodar)
March 2008 – the night I will never forget. After completing the first course of radiation, my buddy Marky – who comes in from Phoenix. Throws me an amazing surprise party see the post “a night to remember a night I will never forget to see how amazing. My keyboard is still dry at this point and if I write too much more about it, I will cry all over it.  Thanks again to everyone who came from far and near.
10/15/2009
After several clear MRIs, the Tumor comes back. Dr. Crute again performs a tumor resection. This time I had a little stroke during the surgery and spend2 weeks at inpatient rehab doing physical therapy, Occupational Therapy, and speech therapy along with 6-8 weeks of outpatient therapy.
11/2009 I start Avastin treatment before Thanksgiving evey two weeks.
3/29/2010
Its back again, but this time we do a non-invasive Stereotactic radiosurgery to NUKE the tumor. That works wonderfully and I get a clear MRI in May. Fast forward to 10/4/2010 – New MRI, get the results on 10/4
**********Current Day
MRI results Day – Its Back again. This time in 3 or 4 pieces. They cannot treat with Chemo or radiosurgery or crainiotomy. However, DEM SMART Doctors strike again. My Radiation oncologist, Dr. Roberts at UW, invented a new delivery method for radiation to allow for retreatment delivery of Radiation and its called Pulsed reduced dose rate Radiotherapy. It is the same dose delivered over longer period of time. I will begin this 10/12 and continue every weekday for 27 days.
Well folks, that brings us up to current day. There has been a lot of other things going on in the past few months, but I will save that for my next post that I will soon. The Fight goes on, and as always, I will never give up. Thanks for allowing me to express myself.

9 comments:

Bryttany said...

Steve your like are like a bouncy ball, never down for more than just a second and always right back up high as ever! :)
Your fight is an epic battle of life and you will come out on top I just know it! you are always in my thoughts! I love you!
Brytt-

Bryttany said...

Steve your like are like a bouncy ball, never down for more than just a second and always right back up high as ever! :)
Your fight is an epic battle of life and you will come out on top I just know it! you are always in my thoughts! I love you!
Brytt-

~Val said...

Well said, Bryttany...

wendy said...

I found out about you through a quilting blog and have been reading your story ever since you started this blog. I send you lots of best wishes and love from the UK
wendyx

Shahed Kasem said...
This comment has been removed by the author.
Shahed Kasem said...

Steve
Nothing can beat you ever. Shahed

mjwilcox said...

Steve, you have such a positive and transformative energy about you... Know that your friends, near and far, are connected to you in such a powerful way--one that transcends distance and overcomes the daily grind of life that keeps us so focused/distracted. We feel connected to you, believe in you, and pray for you.

Anonymous said...

Steve, you have a bunch of people who are proud to say they are your friends. I love the courage and confidence you display everyday. Please let me know if there is anything we can do to help you Steve.

Ken

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