Okay, I know that fall hasn’t officially started yet, but I’m in need of a refresh. I’ve dug the fall décor out of the attic and am slowly putting it out on display. I’m doing a purge of the closet again, if I didn’t wear it this summer and if it’s older than 5 years it is time for it to go. All this newfound closet space has left me the ability to do one of my favorite things, shopping! I even convinced the hubs to head out to the Gilroy Outlet Stores for some fun in the sun and maybe pick up a few things.
Why the sudden need for a refresh you ask? You see last week I got some news that punched me in the gut. I got the results of my PET Scan and found out that the chemotherapy that I have been on for the last year or so, has officially failed. The spot on my lung that we treated with radiation looks like it has stabilized, but it decided to grow a new friend. The new spot on my lung isn’t very big, but big enough to cause concern. My poor little adrenal glands seem to be throwing a cancer party again. The spots that were there last year have returned. And just to add some extra cancer confetti to the mix, I’ve got spots on my left and right pelvis and a spot on my right collar bone. For the icing on the cake a few of the lymph nodes on my chest wall are inflamed, possibly with cancer activity. I’m big on listening to my gut instincts. The day of my appointment my gut told me that I needed to prepare for some not so friendly news. Normally the results of the PET Scan is released pretty quickly to My Chart online so I can review it. This time it never showed up. Also, my lower back had started to give me issues, just like when the cancer flared in my spine last year. So, things were just adding up to not being the best of news to come. I did my best not to dwell and to practice mind over matter. I put on a cute outfit and a face of make-up so I wouldn’t want to cry. But, I also tried to prep myself for what could be next. The doc and I have been talking about the possibility of changing chemotherapies for the last few months. So, it’s not like it’s a huge surprise. Trodelvy had been showing signs of not bringing it’s A game, but we had hoped that by increasing the dose and the jolt of radiation to my lung would give it a burst of life. But alas, it is now game over for Trodelvy. The plus side is we already had a plan lined up. Way back when they did the biopsy on the tumor on my lung, we found out that while I’m a still technically Triple Negative, the tumor was producing a little, teeny, tiny amount of HER2. This is good news! Just out of clinical trials with excellent results, were people like me using the chemotherapy Enhurtu. For me to use the drug, it would be considered “off label”, so a whole lot of approvals would be needed. My doc did all of that while we were hoping the Trodelvy would still work. We weren’t sure if the insurance company would approve it, so I started filling out financial assistance paperwork at the same time. Whatever I needed to do to get this medication I was going to do. Well, the stars must have aligned and the day after meeting with the doc I received a call from the insurance company approving Enhurtu. Dance of joy happened, and maybe another shopping trip to celebrate. Once the celebrating was done, the prep work must start. First up a Echo with Doppler on my heart. Chemo is pretty hard on your body and some chemos effect different parts more than others. The downside of Enhurtu is that is can cause some heart issues. The plus side is they tend to go away if treatment is paused a few weeks. I’ll be doing echos throughout treatment now, so they want to get a base reading. The stars aligned again and I was able to get an appointment this week. After that some basic lab work will need to be done just to see how my red and white blood cells are doing. If all goes to plan I’ll do my first infusion on Friday. In reading the details of Enhurtu it sounds promising, but I’m still nervous. Not knowing how the side effects will affect me has my anxiety going on overdrive. I’m trying my best to focus on the positive and what we do know. Big plus, I will only have to infuse it every 21 days. That means I will have more free time to play, hopefully. Another plus is that it shows signs of crossing the threshold to the brain. Fingers crossed that it will keep these little spots that keep showing up on my brain in check and banishing them. I was hoping to get some hair out of this, but it looks like I’m destined to be bald. Oh well! Good thing I have a nice shaped head. Keep your fingers crossed for smooth sailing on Friday.
4 Comments
Karen Bertolini
9/19/2024 09:57:33 pm
Hi there Dawn…we are still praying for you and will especially pray for you tomorrow as you begin this new treatment. Praying for peace and healing as you go through this storm. Kristy and your Mom have kept us informed and it’s a reminder of the preciousness of each day. 🙏🙏🙏
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Evelyn Israel
9/20/2024 05:47:04 am
Dawn. Today is Friday. A new day! A big day for YOU. You can do this. You are a Total Warrior and one strong Woman and YOU are the most inspiring!
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Akanesi Maileseni
9/20/2024 08:10:42 am
My friends ( here & abroad) will commit to pray for you daily, Dawn. With much love & prayers 🙏💖🙏
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Sandra Schoppert
9/20/2024 11:56:33 am
Go Dawn! I am so inspired by your courage and positive attitude which is a big part of the battle. Keep fighting 🙇🏻♀️💜
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