Kerri’s Story

Site created on July 23, 2021

Welcome to my CaringBridge website. Tyler and I are using it to keep family and friends updated in one place. We appreciate your support and positivity. Thank you for visiting and please remember my #1 rule, don't tell me sorry!  :)  It won't change the results, is slightly depressing to hear, and I am staying positive!

On July 6th, Tyler (yes, Tyler) noticed a lump on my right breast, aka the shitty titty, and asked me to have it checked out.  When I couldn't get into see my primary doc in a timely manner, I reached out to a friend who does mammograms.  With some guidance, I tried to get in sooner, but was unable to.  This friend was then able to get me in on short notice on the 8th.  By EOD on the 8th, I was scheduled for an ultrasound of the area on the 12th.  On the 12th, the doctor looked at the images and due to some jagged edges wanted me to get it biopsied and another area near this lump.  Their first available was on the 13th, so I took it.  The biopsy was done and the wait was on.  On Friday the 16th, I was leaving a work meeting and found my car tire to be totally flat and also saw my biopsy results were in.  I figured this wasn't a good sign, but waited to get the call.  I drove 3 hours on a donut to get right tire and while I was in the lobby waiting to get my tire changed, I got the call.  I had breast cancer. 

The nurse navigator called me a few minutes later and she was already working to set up my appointments for the following week with a radiologist, medical oncologist, and a surgeon.  She got me in Monday, Tuesday, and Friday, respectively.  

I didn't know what questions to ask when I got those initial calls, so I didn't know any information about my cancer when I let close family and friends know.  On Saturday, I started reaching out and letting friends and extended family know and messaged a family member of Tyler's.  Little did I know, this family member works for a company the specializes in cancer.  After sending them the biopsy results, this family member sat on the phone with Tyler and I and explained SO MUCH and also gave me my specific cancer: Invasive Ductal Carcinoma and I had Triple Negative Breast Cancer.  While negative sounds good, it isn't.  This is an aggressive cancer.  However, I later found out the good of the bad, which is that it is in stage 1a.  We caught it VERY early!

Moving forward - We are heading out on vacation and  when we come back, I will have an MRI and an ECHO done on the 30th, my port placed Aug 2nd, and my first round of chemo begins Aug 3rd.  Chemo will be every other week for now and then there will be surgery and possible radiation.  The outlook is fantastic for me and I will beat this!  The road is going to be long, but we are on it and we can't change the results.  Tyler or I will update along the way, typically when we are at the hospital for treatments and open to any questions you may have along the way too!  Your support and positive thoughts are VERY appreciated.

Newest Update

Journal entry by Kerri Gortmaker

It's been another month and lots of good stuff going on.

Let's start with the medical updates:

  • We were able to get the MRI's approved by insurance and I ended up having 2 of them, and then insurance approved the CT.  The spot they wanted to look at appears to just be just some trapped fluid.  Everything looked good and they want to do a follow-up MRI in 3-6 months to ensure stability.  
  • I finished my LAST round of chemo pills on August 3rd.  What was crazy, it that was exactly 1 year to the date from when I was headed in for my very first chemo infusion!  I was incredibly lucky to be surrounded by a few friends and the Barbells for Boobs team to take that last pill.  We went live from Madison, WI since I was there for the CrossFit Games (as a spectator).  It was a large rollercoaster of emotions that whole day.  I literally was going from laughing to crying.  I am so grateful to be done and also for everything this past year has taught me.
  • Moving forward I will have visits with lab work with Dr. T every 3 months for the first little bit and then we will gradually spread those visits out until I am at 5 years.  I also have a Survivorship appointment next month on the 19th, where I will meet with a handful of different specialists to discuss survivorship and things to do moving forward.  I will also get to RING THE BELL that day!  Luckily it is in the afternoon, so Tyler will be able to join me for that moment too.
  • I will have another follow up in Dec/Jan with my plastic surgeon and then I won't see her for 4 more years when we will start doing MRI's to check my implants,
  • For those that have asked, there are no follow-up scans to make sure I am clear.  They removed the tumor in December with clear margins, so the assumption is that I do not have Cancer anymore.  The chemo pills were due to there being active cancer cells still in the tumor that the chemo infusions didn't completely kill.  So the pills were to catch any super small cancer cell that could possibly still be floating around somewhere that we didn't know about.  Since I have implants, I will never have another mammogram and the only way to check for anything is by touch or MRI.  We will continue to monitor my blood work and will do scans if we notice anything abnormal or different in blood work or any new/weird bumps forming at my breasts (yes, there can still be new cancer bumps at the skin level or under the implant).  But I'm not even the slightest bit worried about it.  Because, as I said from the beginning, it's nothing until it is something.  There is zero point or benefit in worrying about it.

Some other fun things that have happened.  As I mentioned, I was at the CrossFit Games.  This was such an experience.  I was able to participate on the "Demo Stage" for a workout during a panel discussion regarding CrossFit and Cancer.  They were discussing how those of us with Cancer can still move and will move, it's all about asking questions and scaling appropriately.  Then, I was asked to talk with the CrossFit Journal/CrossFit Training team as they wanted to do a little article.  Because of that, I was able to do a 1:1 session with a CrossFit Training from HQ while the Journal photographer snapped some pictures.  It was pretty cool and the article was perfect.  She actually confirmed with me that I said "I am glad I got cancer".  Which I did, and I am.  It has given me so many bright spots, moments, and wonderful people in my life that I can't be upset.  Yes it sucked, No I don't want to do it again, but I am glad.  As crazy as that sounds.  I have a lot to be thankful for and even more people in my life that I appreciate so much.  Additionally, I have a whole new perspective that I didn't have before and I appreciate some things more than before.

I hope none of you have to go through this, ever.  But if you do, know I am here if you want me to be a sounding board, share stories, or just sit in silence as we process the facts.  I hope that sharing my story helps you or someone you love through this, if that happens.  My cancer likely won't be the same as yours, but know that if you look for the positives, even in the suckiest of moments, and stay active - you will and can fight it.  I am 100% certain that attitude and movement are huge parts of what got me through this chapter of life.   From a t-rex costume at treatment to walking 5 minutes when I felt the least like doing anything.

My last plug, here, is to encourage you all to come to Sheyenne River CrossFit in West Fargo on October 23rd, starting at 9am.  We are hosing a Barbells for Boobs fundraiser.  We will have silent auction items, a workout (you don't HAVE to do it, but you should try!), raffle items, and a brunch following a VERY SPECIAL heat workout (approx time of 10:15) that will be only for breast cancer patients and survivors.  We are still looking for event sponsors too, if you or someone you know is interested.  Please reach out!

With that, I think this is the last post, the final page; unless I post a few pics from the bell ringing here.  Yes, there will still be some lasting side effects that I will, and am, learning to manage, but all I can hope for from here is smoothing sailing and continued clear blood work and scans.  It's crazy to think that a year ago there was so many unknowns and I had no idea what I was getting into.  But now, it's crazy to think of that 5 year moment.  I can't wait to see what is next.  Thank you ALL for being here for me for the past year, your support, love, and laughter was just what I needed.  

Don't forget to make someone smile today.0

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