6 Month CT Scan Results
Comments
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Thanks, Jane. I appreciatecheerful said:Hi Kim:
I am sorry to hear about your small nodule. Your doctor can treat it as it was found early. I wish you all the best. I will keep you in my prayers.
Going through a Pet Scan I feel is easier than going through a Cat Scan. I went through my first Pet Scan in October. Good luck with your Pet Scan on Wednesday.
Please keep us informed.
Cheerful
a/k/a Jane
Thanks, Jane. I appreciate that info on the PET (this will be my first) and will let you know what I find out. My follow-up isn't until the following Thursday (12/22) so will send out an update then.
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Thanks, Soup. I couldn'tSoup52 said:Oh Kim I'm so sorry:( This is
Oh Kim I'm so sorry:( This is what we all fear, but as others have said it is small, so there is hope and as always you have a great attitude. I can relate to this all as my treatments have taken over a similar time period to yours. My prayers are with you.
Thanks, Soup. I couldn't believe it when I saw the doctor's name come across my phone yesterday. The dread while answering it was very physical but it subsided quickly once they told me what it was they saw. Keeping my fingers crossed that it's nothing serious!
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Thanks, Eldri! Keeping busyEZLiving66 said:I'm so sorry, Kim! But, as
I'm so sorry, Kim! But, as everyone has pointed out, it's very small and it's been discovered really early so it can be treated. The waiting is the worst but I like your attitude - let the doctors worry. Sending you all my good vibs and positive thoughts.
Love,
Eldri
Thanks, Eldri! Keeping busy is the very best way for me to keep my mind from wandering to the "dark side".
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Thanks, Becca! Stayingbeccabtown said:Sorry to hear this
So sorry to hear this, Kim. I hope you can focus on other things until you have more information and a plan for treatment. I know your positive attitude will make a big difference.
Thanks, Becca! Staying positive has worked so far so I intend to keep it up as long as possible!
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Thanks, Janae! I'm working onjanaes said:Im so sorry. Not the news i
Im so sorry. Not the news i wanted to hear but i hope you can find peace as you wait for your pet scan. Hope it turns out to be nothing
Thanks, Janae! I'm working on it. Like everyone says, the waiting is really the worst part of this whole process.
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Thank you, derMaus. It doesderMaus said:Kim, I always love seeing
Kim, I always love seeing your picture and your posts although this one, not so much. But as a friend once told me, everyone with cancer focuses on being *cured*, i.e. surgery, treatment, etc., then getting back to your 'normal' life. She said that for her, cancer is more of a process; she focused on the long term and expected bumps along the way. I don't know if this is of any help or not but, as the others have noted 4 mm is a very small bump along your way. Be well, my online friend. B
Thank you, derMaus. It does help. It's easy for me to get ahead of myself and to think that it was all over once I got that first NED when that was really just one sign post on a long journey. I think that when my gyn-onc told me that my frontline would either work 100 percent or zero percent on this aggressive disease that I just figured it had worked 100 percent. Truth be told, the jury is still out on this one.
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I agree, MAbound. Not fair atMAbound said:Ahh ladies
This is so hard to hear: nodule, mass, 1st or subsequent recurrences....it's all not what any of us want to hear. Why is it all so stubborn to make go away? Not fair! Not fair! Not fair!
I agree, MAbound. Not fair at all but if this ends up being something serious I will not give up and will fight this bugger to the very end!
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Thinking of you
Kim and Old Beauty, I am thinking of you. So sorry you both have to go through this. But as Editgirl indicated 4 mm is very tiny. For reference, I have a soft tissue mass which is PET low-level positive that is 5.4 cm. x 2.2 cm. I get PET scans frequently to keep tabs on it.
In measureable terms, 5.4 cm is equal to 2.1 inches. 4 mm is equal to 0.15748 inches.
Keeping all of you in my prayers.
Kathy
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Correction on size - cm not mm
I was finally able to access the radiology report online today and here is what it says under the chest section: "In the anterior mediastinum in the region of the thymus, there is new soft tissue present measuring 3.8 x 2.3 x 4.1 cm. Lymph node enlargement is suspected."
I guess my chemo brain made me hear millimeter instead of centimeter when speaking with the doctor's office last week. Oh well, this really doesn't change anything. I just wanted to correct the record. Thanks again to everyone for your support!
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Hang in there Kim!!! Staying
Hang in there Kim!!! Staying positive does make a huge difference. Keeping u in my prayers that all will be ok. Many warm hugs to u! Maryanne
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PET scan is much easier.
PET scan is much easier. What other tests do we have where you basically get to be a slug the day before and then spend an hour in a darkened room, resting, before they do the scan? Small blessings, but nonetheless...
I, too, hope the scan gives you a better idea of what you're dealing with. I'll be thinking of you tomorrow.
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Kim thinking of you tonight
Hope you are resting and that tomorrow you have peace during the PET scan- it was easy for me too and I was so glad they had approved it so we could KNOW what was going on in there- amazing they have that technology! Prayers for you tonight and tomorrow (((HUGS)))
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Kim, Thanks for posting. I
Kim, Thanks for posting. I was thinking about you earlier today! Looking forward to hearing your results and hoping that it will be the best of news.
Love and Hugs,
Cindi
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KIm, Not the news I was
KIm, Not the news I was expecting to hear from you. This MMMT cancer sucks but we are both strong and will get through what ever they throw at us. I am sending HUGS and prayers.
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Looks like I dodged a bullet!
I heard from the gyn-onc's office today about the results of the PET scan and signs point to it being a benign "thymic rebound" although malignancy cannot be completely excluded since there was some metabolic activity noted. I may still need a biopsy to confirm that it is benign and will find out for sure on Thursday at my next appointment.
From my research, it appears that thymic rebound is usually seen in children who have gone through chemo or some other extreme stress inducing trauma but it is not unheard of in adults who have gone through strong chemo, too. It tends to resolve itself within a few years without intervention.
So, I will be celebrating this good news all weekend long and hope that you all do, too! Keep the hope and don't ever, ever give up!!
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