Leah’s Story

Site created on July 19, 2021

Welcome to my CaringBridge! I was diagnosed with invasive ductal carcinoma (IDC) PR/ER+, HER2- breast cancer in July of 2021. Scans show that the cancer has metastasized to my lymph nodes. At this time, cancer is not showing up on scans any other place in my body. After that, I will undergo reconstruction and then deciding the route for hormone therapy. My plan will be adjusted as needed.

A little info about myself…..
I was born and raised on NW Iowa but moved to San Antonio in July of 99 to student teach and never left! I live in New Braunfels with my husband, Tony, and our 11-year old twin daughters, Ainsley and Brinley. I also have a bonus daughter Sierra and a son-in-law Mario. I am Gigi to their almost 3-year old daughter Melanie and their 6-year old son William. They only live a few minutes from us so we see them often. I am in my 23rd year of education and am currently the Lead Counselor at Clemens High School in Schertz, about 20 minutes from our house. My campus serves about 2600 students in 9th-12th grade. I am able to take our daughters with me to my district which is very convenient and they are only a few minutes away from me. Tony works for Comal County here in New Braunfels.


For those who have asked how to help, my friend/teammate set up a meal train: https://mealtrain.com/0o5599
Thank you to all of those who have donated, brought meals, given gifts and gift cards and sent cards. Most importantly, your prayers are coveted. We are humbled by the outpouring of love and support. Please know that every message and text is read and means so much. I often re-read them especially when I’m having a rough time.

Together we fight!

Leah 💗

Newest Update

Journal entry by Leah Salas

This week I had several appointments so here’s a little update on all of them. On Monday I made the trip back to Houston to MD Anderson. I had an appt to see my plastic surgeon. I was mostly concerned about a large area of fat necrosis on my cancer side that has developed over the past few months. The dr looked at it and he thinks it should break up and soften some more as time goes on. If it becomes painful, then we should act on it. He said it would be best to leave it alone if possible since we could have issues with future fat transfers. Since the skin was subjected to radiation, it will never be the same as the non-cancer side. He did say we could go in and try to match sides a bit more closer. He left it up to me but after talking things through a bit more, I think we’re going to leave it alone for now. I’m also having some discomfort by my belly button and they don’t believe it to be a hernia. We’re going to give that more time to settle down as well. Hopefully, both areas will improve some more. I then went to have the ultrasound on my thyroid. I didn’t get those results until I had my Zoom follow up on Tuesday afternoon with the neck and head oncologist. I was expecting her to tell me that we were going to keep monitoring the nodules on my thyroid. But this time, she told me she thinks we may need to move forward in the future with removing it. The biggest one on the right side is getting bigger. She first said maybe only removing the right side but then said it would be best to remove the whole thing because there are several nodules on both sides. I asked what happens when the thyroid is removed and she said I would have to take a pill for the rest of my life to do the job that the thyroid does. We didn’t decide anything definitively but I’m kind of leaning towards just having it out so I don’t have to continue to worry about what the nodules are doing. 

Tuesday afternoon I also had an appointment with my oncologist. I hadn’t seen her since February so I caught her up on a few things. One other appt that I had a few weeks ago was my regular PA. She has noticed that my kidney function has been decreasing according to my blood work and would like me to see an nephrologist. My oncologist suspects it could be related to my Verzenio but she thinks I should see the nephrologist just to make sure. I have an appt next week. I should be done with taking Verzenio this fall. We talked briefly about what next. She is hoping to get me on a trial drug for high risk of reoccurrence patients but said we would discuss it more later. She feels taking out the thyroid might be a good idea as well. She asked where we with the back pain. I have to get another Zometa infusion in 2 weeks but then I don’t have to go back until July. 

I had an appt on Friday with a spine dr. He went over my imaging that I had done in January and March. He thinks physical therapy is a good place to start to see if we can strengthen my back but he does think it’s going to take some time. He also agreed with what the neurologist thought about having kyphosis. I told him I’m just desperate to feel better. He asked me how I found out about my cancer and what kind of treatment I had been through. He was familiar with the DIEP flap surgery I had. He was very kind and compassionate. I will go back for a follow up in a couple months. 

I will keep moving forward. The end of the school year is coming to a close in a few weeks and I’m looking to summer break. We have a few things planned for the summer. My sister is going to come for a visit, we are going to Iowa, we have a trip to the beach planned and of course we will be going to Schlitterbahn often. 

Thanks for your continued prayers, support and love! 🩷

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