Skip to main content

Scan Results

I've been getting some of my results over the past few days. I hoped I would have gotten them earlier, but I didn't. The big test result I've been anxious to see was the MRI, and I finally received it this morning. The test results I got are the CT scan, and the MRI, but no bone scan.

Let's start with the MRI results because that's what I'm sure you've been waiting for too. I read the report, and from what I can tell, everything looks good. What's left of Jimmy didn't absorb much of the contrast dye meaning the cells aren't active. There was less absorbed this time on the outside, and little to none on the inside. It's like an empty shell. My surgeon said that this happens sometimes. When they take Jimmy out, they are going to run tests on the cells of the tumor to find the necrosis percentage which is the percentage of the tumor that is dead. She said that in cases like mine that they are a lot of times close to 100%, which is awesome! Hoping for that 100% necrosis percentage. The bone marrow in my arm also didn't absorb nearly as much as it did on the original scan. And most importantly, Jimmy shrunk SIGNIFICANTLY! Here's a chart displaying the original dimensions, and the current dimensions.
 

That's an 81% decrease right there folks! No wonder why my arm feels so much better than it did in July. There's like nothing there now. It's still kind of long, but the width, and height decreased a lot which is what saved me when calculating the volume.


Now onto the CT scan. There was a 2 mm nodule in my right lung, but my oncologist said that it's nothing to worry about, but we're gonna keep an eye on it just to be safe. It wasn't on the last scan, so it kind of freaked me out when I saw it on the results. I called, and didn't get a call back for a few hours. It wasn't fun. I was more afraid about this little 2 mm nodule, than I was back in July when I was being diagnosed with this because I know how bad this cancer spreading to your lung can be. Then I talked to one of his nurses, and she explained that it's nothing to worry about, and it's very small. Like so small that its barely detectable by a CT scan. I'm doing better now, but I'm still a little scared about it. I'll feel better after my next CT scan if it doesn't change in size, or shrinks. I mean it might not even be Ewing's Sarcoma at all.

So I'm still waiting for bone scan, but I'm not too worried about that one. I don't think it's going to show anything. I'm pretty sure it would have shown on the PET scan that I had before I started treatment.


So what have I been doing with my time during this wonderful break that I have you may ask? Well, a lot actually. I had some friends over on Saturday. It was great seeing everyone. It was fun crushing my friends in Madden! They couldn't handle my awesomeness. On Sunday I went to church, and received the Sacrament of the Anointing of the Sick. Thanks Father Gerry! I also enjoyed dinner at one of my favorite restaurants. Banko's! I got the orange roughy. Never had it before, and I thought it was really tasty. It was a really fun night out with my family. On Monday, I just rested at home. Didn't do much. I feel like I should have been somewhere that day. Oh yeah I forgot, I would normally be getting chemo, but not this time. Yesterday I had another friend over. It was a good visit. Played some 2k, and talked about sneakers. I don't think I've mentioned this before, but I love retro sneakers, and so does my friend. We're sneakerheads! My favorite sneakers are the Penny Hardaway retro's because he's my favorite player of all time.

Today I'm just resting. Getting my body ready for my favorite holiday tomorrow...Thanksgiving! I can't wait to see everyone tomorrow. It's going to be a great day! 


Lastly, thank you everyone for the prayers. They definitely help, and the proof is in the numbers. Keep praying for my healing of this rotten disease. Also for all of the other children battling cancer.

Me being a goof at Banko's





Comments

Popular posts from this blog

First Entry!

Today is my first post on my blog about my battle with Ewing's Sarcoma. The main purpose of this post is to get my readers to know a little bit about me, and to provide a little background of this cancer that I have. First and foremost I am 19 years old, live in a family of 5 with two great younger brothers, and loving parents. I love to play sports, video games, and I'm very passionate about technology. I don't really have a favorite sports team because I don't like to watch sports, but my favorite sport to play is basketball. I'm not much of a bragger, but I am very good at basketball because I'm very athletic. I can dunk easily. Check it out...  mike's dunks on youtube . I am a sophomore student at Penn State University majoring in Computer Science. I'm also from Pennsylvania, in the small Mountaintop area.  Personally, I am a very reserved person, I like to keep to myself. It might be surprising to you that someone that is so reserved would mak...

10 Year Survivor

Hi everyone, its been a while. I think this might be the largest time gap between posts. I've had a tough time with this entry, coming back to it from time to time over the last several months. Every time I finished editing I just did not like it and scrapped it. Hopefully take 4 is the charm, lets get into it. Late in 2023 I became a 10 year survivor and also turned 30. It was a deep time of reflection for me. There were many questions I asked myself, but the most challenging ones included:  Why am I still here?  Am I happy?  What changes do I need to make to become happier?  Am I ready to make those changes?  What are my goals?  What has gone well these last 10 years?  What do I want to do better going forward? Very deep, uncomfortable topics and questions I had been stressing about, but avoiding for years. It was both empowering and deeply saddening to reflect on these topics. I hated to admit it at the time, but I was very unhappy. I was going thro...

It's Back Again

Since my last post I have had two sets of scans.  I had my first scan in March, and with that came uncertainty. It appeared to have grown on the scan, but my primary oncologist, and surgeon from last summer remained skeptical of this being a recurrence. My oncologist in Cleveland believed it to be a recurrence. His opinion was that it would need to be taken care of sometime this summer. My most recent scan has now put both of my oncologists in agreement. It's now 99.9% likely to be another recurrence. It is now measured at 9x8 mm, up from 6.8x6 mm in December. Luckily it is growing slow for Ewing's, and at least nothing else has come up on the scans yet, but it is still terrible news. This will need to be taken of, and will be soon. The best option for me after consultation with both of my oncologists is to enroll in the Vigil trial ( https://clinicaltrials.gov/ct2/show/NCT03495921 ).  It was originally slated to start taking patients at the end of June, but has ...