Clint Kicks Cancer
  • Home
  • About Clint + His Family
  • How You Can Help


I've had a lot of people who care about me ask for an update on my health, which I haven't done in a while. I apologize for that! I have a hard time sharing news that isn't the greatest. Not to say that this is horrible, but it's not great.

What you need to know about the liver is that there are two lobes and 4 sections in each lobe for a total of 8 sections. I had 6 sections removed in November (75% removed) and then arteries and veins redirected to the 2 sections that are left. This promotes rapid regrowth of the remaining liver so I can get back to 100% quickly. 



The issue we have, even with the best technology ever, our imaging machines cannot see everything. So as we promoted the growth of my healthy cells within my remaining liver, we also promoted the growth of microscopic unhealthy cells, which we knew most likely existed. The plan had been to eliminate these remaining cancer cells as they popped up. The problem is that the popped up too quickly.

These tumors are very aggressive, already occupying over 50% of my liver. I was given a scary prognosis about a month ago, which I'm not comfortable sharing on this platform (Russians are watching). So we went to work and found a potential, cutting edge treatment known as a Living Donor Liver Transplant. It's exactly as it sounds. A sibling, cousin or close friend, meeting all the correct criteria, would donate a portion of their liver to me and my existing liver would be removed.

One critical qualifying component on my side is that there cannot be any disease existing outside of the liver.

Just as I was preparing to undergo a full examination to qualify, three "nodules" were found outside of my liver. So, we came up with a game plan.

We are targeting those three spots with a type of radiation (non-invasive) called SBRT or more commonly known as the cyber knife. It is so precise that it can target all three in a session and I can go about my day with minimal side effects. 

At the same time (already started) we'll treat my cancer with 6 months of systemic Chemo to ensure no further progression or recurrences outside of the liver. As the end of the 6 months approaches, I'll undergo the full examination and most likely be placed on the National Liver Transplant list. As soon as that happens, potential donors will call and undergo some initial phone screenings and if selected, undergo a full examination. 

I am not allowed to pick the donor or provide feedback on who should be the donor. We'll leave that to the experts.

A date for the surgeries will be scheduled and we'll travel to the Cleveland Clinic to have the procedures completed. 

It's my understanding that my insurance will pay for both surgeries and recoveries, but will not cover travel expenses. It's important to me to have both my family and the donor's family in Cleveland for as long as they want, which adds up when you're talking two whole families for an undetermined amount of time. Most likely 1 1/2 weeks for the donor and 2-3 weeks for me.

So that's it! It's a novel! Thanks for caring enough to ask Amy Christensen Cosby and Emily Martino Gold!

We're very optimistic about this plan and have already seen some positive responses from the Chemo we started! Got to make it through these next 6-8 months!

Thanks for all the thoughts, prayers, cards, meals, donations, and the list goes on.... they help tremendously and give me the energy I need!

Here are some pictures of a Vacation we were able to fit in! We had a blast and created memories to last a lifetime!











Rock & Roll HOF in Cleveland with my Dad!

0
Share


Within a few days of the 5K, we met with a local surgeon who is well known in Utah as the #1 liver transplant and resection surgeon in the State. My Ongologist had recommended we at least meet with him to see what his opinion was about my possibilities for a potential liver resection. A liver resection is crucial to a Stage IV Cancer Survivor with metastasis to the liver only, as it provides a path to a cure.

The Surgeon proceeded to explain the liver and it's function within the human anatomy. He explained the lobes and sections and the livers miraculous ability to regenerate. He described how, in resection cases, a patient needs to have at least two sections remaining (of 8) to live, and those two sections must be about 40 percent of the physical size of a normal liver after resection.

Then, he said something I'll never forget. "You're fortunate to have the Oncologist you have. Most wouldn't have even given you a chance for a consultation with me." He went on to explain that after careful examination of my imaging (CT and PET) that he believes I have my far two left lobe sections that are healthy enough for resection. He explained that he would need an MRI of my liver to confirm.

Within two days, I had the MRI done (really annoying, btw) and was back in his office. He showed Kim and I the images and confirmed that I was eligible, in his opinion, to have a liver resection. He recommended we do it ASAP, as he is not a fan of adding more toxicity to the liver through additional Chemotherapy. 

He went on to describe how he would perform the procedure and the potential risks. One issue we have to solve is that the two sections that will remain and operate as my liver are the smallest sections and we would need to promote growth of these sections prior to resection.

We talked about three options to grow the sections. One was to have a Portal Vein Embolization. This is a procedure where a special type of glue is injected into the Portal Vein of lobe that is to be removed. This sends the nutrients used to promote healthy cell growth to the lobe that will remain, and it begins to grow. This is a process that promotes about 70% growth over a 4-5 week period. 

The second option is to open me up (gross!) and perform most of the cuts that would be used during the actual resection, minus the final cuts that would be used to remove the unwanted side of the liver. Then, the Portal Vein would be closed permanently on the right lobe. This is known as an ALPPS procedure (mentioned on a recent Greys Anatomy episode, btw). This promotes rapid growth of the remaining liver section over a 9-10 day period. I would be closed back up and wait in the hospital until the right amount of growth is achieved and then they would go back in to finish the resection.

The third option, also the option we chose, is to do the Portal Vein Embolization, and then, if needed, the ALPPS procedure. 

I had the Portal Vein Embolization done in mid-October and I've felt the liver growth over the last 4 weeks! 

The Dr. that performed the Portal Vein Embolization described my Surgeon's game plan as a "Heroic Plan". I said "Wait a second, Heroic as impossible?" And she said, "No, if anyone can do it, it's him and if it were me, I'd choose to do it as well!"

So, on November 22, 2017, I go in to get a liver resection! 

I'll keep everyone updated after the surgery. 

Thank you for for all the support, thoughts and prayers!

Love you all! Happy Thanksgiving!


5
Share
One month after diagnosis, I learned that a group of coworkers were organizing a 5K to help me in my battle with Cancer. I found out that they were meeting weekly to plan the event. A feeling of gratitude and humility overwhelms me as I think of their friendship and generosity!

We had the 5K on 10/07/17.

Hundreds of people attended, including friends from my childhood, mission, treatment and Goal Zero.

To raise money, my friends in this picture committed to carrying weight as they ran. Bill Harmon, in the vest, was originally the one designated to carry the load, but the donations quickly exceeded the weight of the vest, so my good friends and colleagues, Adam, Scott and Sterling took on the extra load!


Thanks guys for your willingness to literally and figuratively carry an extra burden during this trial of mine!

Thank to all those that could attend and to the well wishers that couldn't. I know I had the Atkin family participate from thousands of miles away while on vacation in Italy! 

Love you all!
1
Share
Hi All!

First off, I apologize for the gap between blogs. I hope to explain some of it now, but there is not a great excuse. I should be doing better at keeping everyone updated. I want you all to know how I'm doing!

I went down to MD Anderson on July 5 to meet with the GI Oncology Team and a Surgeon. It started off well, with the GI Oncologist talking about swinging for the fences, etc. Unfortnately, after having me get a new scan that evening, he wasn't so optomistic...

He met with me two days later to inform me that the Surgeon had an "emergency surgery" he had to go to, but that they had discussed my case and decided that I was not a candidate for Liver Resection, and would never be a candidate for Liver Resection.

It was my birthday, and I was devistated.... He did say that he thought I was tolerating my chemo really well and asked if I was willing to endure some more side effects, by adding a fourth cancer killing drug to the cocktail. Of course I said yes!

Best part of this trip was the Crawfish and the company I kept! Shout out to Kelly O'Donnel and Dean Chuang! Dean let me stay at his house! Also to my brother Greg who came down and hung out through the fourth of July in Galveston and went to my appointments with me! Love you guys! 




The next three months, I had a regiment of drugs commonly known as FolFoxIri. When the doctor mentioned additional side effects, he failed to mention that meant walking around like a zombie for the next three months. Honestly, those three months are cloudy.

Good news is, the regiment worked! We saw tremendous amounts of internal necrosis of the tumors (dead cancer inside), as well as shrinkage!

We decided to remove Oxaliplatin from the regiment after it's 10th cycle. Oxaliplatin causes the extreme neurothapy in my fingers and feet. They said that it is known to possibly cause permanent damage, if done more than 10 cycles, so we stopped.

I can tell you that after 6 weeks without it, my neuropathy is the worst it's been. I cannot feel my feet and it feels like what I imagine it would feel like to walk on stilts or with prosthetic feet. So I look like I'm a 95 year old walking around. Typing without being able to feel your finger tips is also a talent I've learned over the last few weeks.

Good news is that they say that the side effects are accumulative and that it should be the worst right now and get better soon.... I guess we'll see.

I've got some more updates on what's next, and will be posting about that soon!

Clint
1
Share

We're excited about the Clint Kicks Cancer 5K Fundraiser coming up in less than a month! Here are some important updates to make note of, including a location change. Make sure to register before Sept. 16th to secure your spot (and tshirt!) before the price increases.

0
Share
We're really excited to announce a wonderful fundraiser that some pretty amazing people have put together to benefit Clint's family. Mark your calendars for the Clint Kicks Cancer Run/Walk in Draper, Utah on October 7th. All ages and participation levels are welcome! This will be a fun, uplifting family event. Whether you're an avid runner or a sidelines cheerleader, we hope you'll join us to offer our love and support to Clint, Kim, and their children. Click the picture below to read more about participating and to sign up! There is an individual and family rate, as well as a pancake breakfast option for anyone who just wants to be there and show their support.

Please share this with your friends and spread the word. It really is an event that everyone can enjoy! Let's show Clint he's not fighting this battle alone.


1
Share


While I was in substance abuse treatment at Odyssey House of Utah, I discovered many things about myself that contributed to my addiction. One of these discoveries is that I struggle with being genuine and/or authentic. In short, I tend to outwardly present my life in the most positive light as possible, regardless of what is actually going on. I've learned that being honest, vulnerable, and real is the best way to show the most authentic version of myself. I truly believe that people will connect with me on a more personal level the more genuine and authentic I am. I promise that my posts, to date, have been genuine and authentic. I've actually delayed posting to the blog a few extra days than normal, because I was struggling with wanting to be disingenuous.

With that spirit in mind, last week was rough... In fact, I'd say it sucked!

The fatigue and nausea set in much quicker than the previous rounds. By 1:00 p.m. on Wednesday, I found myself falling asleep in a meeting with my boss! I woke up on Thursday unable to identify what was wrong with me, but knew that something was wrong.

This isn't anything that is unexpected. My Oncologist has prescribed a handful of medications for such situations. My problem is that I have no idea how to pin down exactly what my problem is, communicate it, and then use the tools provided me to combat the symptoms.

The result, is an unpleasant Clint. I believe anyone else would call me a Jerk, or even worse.

I apologize to all of those who encountered such a version of me last week, and I commit to ensuring that I am communicating with Kim and others exactly what is going on with me to ensure that I'm staying ahead of my symptoms and not allowing them to get the best of me.

Today, I feel great! My energy is back, and my mind is clear. I remain optimistic about the treatment plan I have, and am excited about being able to get some time with the folks at MD Anderson in Houston, TX in a couple of weeks!

Again, I appreciate every body's support and I love you all!


7
Share
Older Posts Home

About Clint

Clint was diagnosed with colon cancer out of the blue on Easter 2017. But he can tell his story better than I can, so I hope you'll read along. #clintkickscancer

Clint Kicks Cancer Run/Walk

Clint Kicks Cancer Run/Walk
Let's show Clint he's not fighting this battle alone. Sign up today for the Clint Kicks Cancer Run/Walk going on October 7th in Draper, Utah. Help spread the word!

GoFundMe Page

GoFundMe Page
With cancer comes necessary medical expenses. Although Clint has health insurance, some of his procedures haven't been covered as expected. We'd like to help relieve some of their financial stress by coming together to help and appreciate anything you are able to give!

Clint's Story Starts Here...

Clint's Story Starts Here...

Search This Blog

Popular Posts

  • Heroic Plan!
    Within a few days of the 5K, we met with a local surgeon who is well known in Utah as the #1 liver transplant and resection surgeon ...
  • Long Time... No Blog
    Hi All! First off, I apologize for the gap between blogs. I hope to explain some of it now, but there is not a great excuse. I should...
Copyright © 2015 Clint Kicks Cancer

Created By ThemeXpose