I’m meeting with a surgical oncologist on Wednesday which was the “next step” after finding out I have HDGC. Between being sore from the race and thinking about my upcoming appointment Wednesday, I couldn’t sleep last night. I rarely have sleeping issues. Matter of fact, I can sleep almost anywhere. Something has to be really bugging me for me to lose sleep.
I’m excited about today, however, because I have a call today with the founder of No Stomach For Cancer. I’m excited to hear her feedback. She wants to give me tips and information about things I should know before my appointment tomorrow. I feel at peace speaking with people who have done this before. She went down this road 10 years ago and created No Stomach For Cancer because there was such little information and help during her diagnosis. Thank God for her. I can’t imagine figuring this out without nostomachforcancer.org
I’m starting to accept the fact that I’m going to have to get my stomach removed. It still sounds crazy to me. It also sounds crazy to people when I tell them what’s going on. They say things like, “Can’t you just live a healthy lifestyle?”. I wish it were that easy. According to the publications, I have been reading, my gene mutation has created a situation that a healthy lifestyle cannot prevent. I’m trying to figure out how to educate those around me without being too much of a nerd. I also know that this is a tough topic and difficult to understand.
Hopeful for a great meeting tomorrow.
I just finished an Olympic distance triathlon at Kiawah Island, SC. My time was about 9 min slower than my goal but the waters (ocean swim) were super rough which made the swim very hard for me (motion sickness). The bike part was great and I improved from last year. The run was brutal as the heat was 90ish degrees with 95% humidity. So, the heat index was 101. I just couldn’t run fast without feeling like I was going to pass out.
Last week was bizarre. That is the only way I know how to explain it. I felt a strange peace about the genetic testing so when the Genetic Counselor (GC) told me I tested positive for CDH1 Gene Mutation, I didn’t know what to say. I also had been telling my wife, Melissa, to not read up on CDH1 Gene Mutation as the information out there was scary and we didn’t need to rush into knowing anything until we found out if I was positive/negative. I thought that was a good plan, but maybe not. Now she is playing catch up but seems to be in great spirits.
We have an appointment with the surgical oncologist on Wednesday, which I’m happy I didn’t have to wait long. I did learn through a connection that he does have at least one experience with HDGC and CDH1 Gene Mutation. That is important as I start this journey because HDGC is not common so I want to get advice from those who have seen it the most.
If you want to learn more about HDGC and my CDH1 Gene Mutation, you can learn more at the page called “Learn about HDGC” at the top right of this website.
Thanks for reading,
10/4/2017 – Learned I have the CDH1 Gene Mutation
I learned I’m a carrier of the CDH1 Gene Mutation. Learn more here: https://www.nostomachforcancer.org/about/hereditary-diffuse-gastric-cancer
The same exact gene mutation that killed two of Mom’s cousins and that Mom and my Uncle have. It’s most likely the same thing that killed my other Uncle in 1990, but we will never know for sure. All the things point to it though (rare cancer, undetectable until very late, etc).
I’m still processing everything and because there isn’t a super strong history of early onset, I don’t know if anything will change in the short term. I’m going to try and figure out how to eat much more healthy to prevent any cancer growth in my body. (Update – I now know this is pointless based on the type of disease. A healthy diet doesn’t prevent cancer from forming based on the gene mutation).
My biggest concern, and as I feared, my wife is very upset. She is sad and concerned. I totally understand. I feel kind of emotionless at this point. She mentioned the kids (we have three), and how they might be impacted. I get it. It’s a lot to take in. I’m just trying to take one step at a time. The next step is to meet with the local surgical oncologist and listen to his recommendations. I wonder if he has ever seen this before? I’m going to try to do some research and figure out who has the most research out there. I need to figure out how to be there for her.
Listen, I want to be cautious and safe but I’m feeling really good at 32. I’m about to finish a half-ironman which does require a good amount of fitness (1.2m swim, 56m bike, and 13.1m run). I’m not saying that I’m immune or anything, but because my family history seems to show onset in the 60’s in most cases, I don’t believe I have to make drastic changes in my life just yet. (Update – I now know this is inaccurate and the CDH1 Gene Mutation is different for everyone. There is no pattern with onset age, but – the gene mutation is creating cancerous cells. I just don’t know how many or how much).
I’m married with three wonderful children. At the age of 32, I found out my Mother was a carrier of a rare gene mutation in her CDH1 Gene. It was the same gene mutation that caused stomach cancer in three of my mothers family members. Being a carrier of this gene mutation gave me an 80%+ chance of developing stomach cancer. On top of that, once cancer is formed, it’s extremely hard to detect and almost always fatal.
I was given a choice: 1) monitor the situation and get scans/scopes/biopsies a few times a year to try and “catch” cancer early, or 2) have a prophylactic total gastrectomy (total removal of the stomach). The end goal: Live a very long life. I didn’t like either option, to be honest, but option two seemed to have the best chance for me living a long life. It is also the recommendations of doctors familiar with this disease.
I created this blog to document my journey. Others in my situation have done the same, and I found it very encouraging as I tried to learn about my disease. I’m hopeful I can pass the torch. I’m having surgery January 6, 2018. Wish me luck!