Having a scan? Waiting on results? The waiting room is open!
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Picked up the report from my CT scan at lunchtime. Everything is STABLE!
Having bone scan on Friday.
(BTW, for the first time ever, the barium "milkshake" caused major gas and explosive diarrhea. I made it to the clinic restroom in time after the scan, but wow--what a mess I had to try to clean up.)
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Great news Tina!
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Stable is great. HOW AWESOME.
>Z<
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You go Tina!
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To clarify, "stable" for me indicates NED. The mets in my lungs show on the scan, but haven't changed significantly in years. There's a thoracic issue that's probably COPD and a several cysts in my liver and kidneys. The last sentence states "No identifiable metastatic disease or recurrent neoplasm."
I'll take it!
Tina
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Great news Tina!!!
I will receive cat scan results tomorrow. I am finding myself to be a nervous wreck today. Last scan was two months ago and there appeared to be small progression on two lung nodules but the others were stable. Doc didn't want to wait 3 to 4 months for next scan so I just had one which was at 2 months. I am having a pretty difficult day. Very anxious of results and what they could mean.
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hang in there singlemom. be ready for the possibility of an ambiguous report that takes a few weeks to sort out. seems quite common. let us know how it goes ..
>Z<
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I am new to this board as far as posting go. I read a lot, but post very little.
But now that I am nearing my lung scan on July 25 to take a looks at the noducle that was found on my pre-op X-Ray I am starting to be really stressed.
If that wasn`t enough to stress me to the limit, I went in to have some test done on my heart because I have been having some chest discomfort.
Well after two abnormal ECGs the cardiologist decided I need to have a chemical stress test. That will happen on Thursday of this week.
That`s not all of the fear factor. During the heart scan they saw some hypo densities in my liver, although they feel the are benign.
This will be my third lung scan, but the last two were only 1 month apart. Both reports then was they felt it`s scar tissue.
This is the first time I have gone for 6 months between scans. I am a total wreck now.
Any good thoughts are appreciated.
I do hope this post make sense as I am almost to stressed to even think...I hate cancer.
It killed my mom and only sibling. -
holding you close to my heart.
Brenda E
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tuckersmimi - it's not clear from your post, but it seems this is a scan that will tell you whether or not you are stage IV for the first time. this time was an emotional bottom for most people on this forum. shock, trauma, terror. there is an article in BCO that shows that most of us end up with PTSD symptoms. it's that bad. nothing much to do about it but go through it. we are here, we've been through it and whatever you need to talk about this is the place.
i hope so so very much your scans are fine. the waiting is terrible. once you know, either way, things settle down and you start to deal with it and that alone makes things better. however, know that, for the first time in years, stage IV breast cancer has improving options and odds. if you do end up here, you will find yourself among a lot women fighting in a different environment than your mother and your sibling. we don't expect a cure, but we are a hopeful bunch and fighting hard to have many more years and a good quality of life. we had a recent flurry of members celebrate their 5th year after diagnosis.
>Z<
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Great news Tina! Woohoo, Here's a Happy Dance for you! (Although sorry about the desperate rush to the bathroom.....that must have been a heart pounding event.Now that it is over and you have a chance to BREATHE, Go celebrate!
Great post Z, you are such a positive influence. I agree with everything you said.
tuckersmimi, I definitely felt shelled shocked by my Dx and definite PTSD which still has lingering symptoms. Random things can send me into a tailspin. Including some bad medical reports I have had so far. But then I regroup and dust myself off. There really is no other choice if you want to live well during this time. This is the best place to come and get information and support. Most times just reading others experiences and how they cope helps me calm down tremendously.
As Z says, it is a different era than just a few years ago. I have many friends and acquaintances who are amazed at how well I am doing a year later on just AI drugs. There are many more in the pipeline. As hard as I know it is, I feel 100% better when I try and take it one day at time. I stay busy and try to do fun things to keep my mind occupied which helps immensely. I know a time will come when things get more difficult and I hope I am able to adapt. For now I am grateful for being mobile and able bodied. I hope your scans go well too. From some of the things you said, it does not sound like anything earth shattering will happen. As far as chest discomfort, I can tell you from experience that stress alone can cause chest pains that mimic heart trouble. I hope all of this is true. Best luck to you and please check back to let us know how you are doing.
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WOW...I think I see new names & sisters sharing lots of good info, as always! I agree Artist....I had more than 1 electrocardiogram when I was having trouble breathing. I was sure it was lung mets...but "just" anxiety-big time. I was driving to the dentist & thought it was a heart attack...it's all ptsd...and it's just starting to subside a bit...after 3.5 years of stable. My onc said on Monday that he doesn't see a need to scan...my last one was 11 months, 1 week ago!!! He said other Drs may call it irresponsible but from my physical shape & TMs say there's no need...unless I want one...ugh. A big part of me says no thanks....another part says yes please. But, like others, he says if there is something....it would be so insignificant, prob stay on same tx....kind of what you're saying, Artist...right? So, my decision is...no decision. Right now, Prozac & acupuncture are my calming forces!!! Graman...I did your same tx for 22 months. It worked very well....and it took that long before I really started feeling like I was in chemo. I had tanking wbc, but neulasta did its job. Tina...I only ever had the clear liquid...the other stuff sounds awful...but oh so happy for NED!
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RonnieKay, I have had a history of shortness of breath problems and chest pains. I think it all started in pre-menopause. I have had a couple of echos when I too wondered if I was having a heart attack, but it was always called "anxiety". It also took me a long time but it is slowly subsiding. Nothing like a bigger problem to take your mind off of the previous one right!? Haha! Wow, 11 months seems like a good stretch without a scan, but I think I would lean on the side of the Dr. on that one, as we all know that scans aren't good for us either. Just curious but what treatment are you on now? Last night we went to a James Taylor concert which brought me great happiness! One of my favorite things to do is a live concert.
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Oh My God...JAMES TAYLOR!!!! I am so fricken jealous, Artist!!!! He was in Seattle about 1.5 yrs ago & my (young) nurse told me she had bought tkts for her parents coming to visit from Minnesota. She was bummed her mom (a little younger than me...prob your age!), didn't know who he was. I begged her to take me :-) He is pure magic...and Carole King...I could die ever so happy!!!! I'm on Herceptin & letrozole now (for exactly a year now, July '15, when onc took me off Perjeta and chemo ended Oct '14...after 22 mos). Praying to stay stable until immunotherapy heals us all!!!! On our way to eastern Washington (5 hr drive from Seattle) to great niece's hs grad party. I'm loving DH driving so I can blog!!! Just saw on tv at McDonald's (salad for lunch stop) that Turkey has a coup...Ebru, thinking of you....so much sadness going on in the world...sorry to politic, but PEACE & HEALING to the world & us :-)
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Artist and RonnieKay - I've had anxiety attacks since I was pregnant with my first son..... I used to wake up in the night gasping for air and convinced I was dying. OR Id be driving and out of the blue - same thing. No rhyme or reason as to why I would have them...I am sure subcounscious stress working it's way out. When I have mine all the air literally leaves my windpipes... it's like my heart stops for several beats and then goes again, and suddenly my lungs realize there is no air. It's terrible. Anyway - just wanted to add my two cents on the whole topic. I still get them (OBVIOUSLY) but no more frequently than I used to. And wow RonnieKay - I find it amazing that your doctor said you don't have to be scanned. I'm sort of jealous! I am still getting CT and Bone every six months, although I have also been stable for 3.5 years and TM's are always in normal range. Maybe I should talk to my oncologist about that. My next one is in September.
Love and hugs to both of you and to everyone else here!
XOXO
Andi
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RonnieKay, Live concerts are such a thrill and I have loved James Taylor's music since a teen. I have seen about 200 big names since I was 16. Last night we saw Sting and Peter Gabriel in South Lake Tahoe. A much different and more raucous and exciting show than James. But I love both kind. It was fantastic. James and Jackson Browne, my personal favorite, are playing together in Fenway park soon. Would I love to see that! There is nothing more thrilling than waiting for the lights to go on, the roar of the crowd and then the music to start. I love when my DH drives too so I can multi-task in the car! We just got a nice newer car too so am always brainstorming an excuse to go somewhere. With my CD's plugged in! Hahaha...Have a great time up there in Eastern Washington! I missed my nieces grad in Seattle last month and now wish I had gone. I've never been that far North. All this stuff going on going on in the world is very unsettling and scary.
Andi, Mine frequently came at bed time when I would lie down and get a shaky quivering feeling and just escalate from there. I would also get a "fluttery" feeling in my heart area. It was so scary. sometimes the only way to stop it was to take a Xanex and fall asleep for awhile. But then I would be groggy. It has finally gotten better only to start up on meds that cause other similar sensations.
I'm sort of jealous about the scan thing too. I'm having another in August. yikes
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Artist- James Taylor AND Sting? Wowzers! I have loved Sting since the Dream of the Blue Turtle days. I'm sure I was the only 12 year old rocking out to Moon over Bourbon Street! I saw him once solo and once with The Police. Wish I would have spring for the Sting/Peter Gabriel tickets. I bet it was fantastic!
My favorite Pandora station is my Carol King station. It's heavy on JT and Fleetwood Mac and CCR. I think I live permanently in the 70's/80's!
Just scheduled my August scans (CT, bone, echo) and suddenly feeling uneasy. The area where I had a hip met has been reminding me that it is there...not really pain just a small ache off and on. I've been trying to exercise more, so I'm blaming it on that. TMs are still low, so expecting good news from scans, and trying to squash the little voice in my head that says "but what if...?".
Best wishes to all who are waiting...
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Thanks Shutterbug, It was a great night. Sting is one sexy man! LOL! CCR is one of my favorites too. John Fogerty in concert is fabulous! So my liver enzymes are going dwon on my week off of Ibrance but my TM's rose a little again......crud. I have a scan in August too and get the feeling Arimidex is not working. Maybe just the "dread in my head" response but I'm scared. I find it is pretty hard to "squash the little voice" sometimes......I start 75 mg Ibrance soon and hope the enzymes finally behave. I just want something to work for awhile. I'm wishing the best for all of your scans. Exercise can certainly aggravate an area where you have mets so try not to stress too much Shutter.
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May 18, 2016 08:10PM NineTwelve wrote:
Hi everyone. I haven't posted in a while, because my family situation blew up, in a big way. Currently my mom is in hospice, after her stroke. My dad, brother, and I go visit her daily, though she can't speak or swallow. It's horrible to watch, but it's what she wanted. She insisted on the feeding tube. She really wants to keep going. I don't understand it, but it is her will.
I had a new PET scan yesterday and I will get the results on Friday. I really feel like my cancer is back, and I can't shake the feeling.
Hello, again. I posted the above back in May when I had my PET scan. My oncologist wasn't worried when we got the results, showing activity in the main tumor sites (right breast and armpit), but he referred me for a new mammogram and sonogram. With everything going on in my family, and no one to remind me, I forgot about the mammo. Two months later, my oncologist's nurse called me to say where were those mammogram results? I had to say, no one called me to schedule, and I just forgot about it.
I thought the PET scan showed everything still stable... Fast forward to this morning...
Today was my mammogram and sonogram. The radiologist said it looks like there is a tumor on the chest wall, under the primary tumor, which is why it wasn't seen on the PET.
I don't know what to do now. I guess my oncologist will call me?
what happens now?
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Hello NineTwelve, I'm sure your Onc will call, but if not soon I would call them just to push it along. Nothing worse than waiting through a stressful situation. You will feel more calm when they get your treatment plan in place. I'm so sorry you got such crummy bad news along with everything you went through with your Mom.....Life just seems to throw curveballs at an alarming rate sometimes. Let us know how you're doing....
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Thanks, artistatheart. I just got off the phone with my oncologist. Progression. We are switching to Ibrance (which he calls "Imbrance") and Faslodex. Still no question of surgery; he ruled that out. It's just as well, though, because I have no one to help me through the recovery. And I need my work, because it keeps me from spinning those worry wheels. It keeps me distracted. Helps me feel like I'm valued.
I am more calm now, though the tears are falling. I am numb.
Funny how you don't just get the bad news once, with this disease. You get to do it over and over. Fun times.
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NineTwelve -There is a period where you will just cry and shake periodically. Nothing much to do about it but go through it. According to one study we all end up with PTSD symptoms for at least a few months.
Come join Tribe Ibrance on the Ibrance thread. You will find we are all fairly hopeful and happy bunch, even as we complain about the side effects and worry about our scans. Ibrance is a promising if still experimental treatment. There are others coming along.
When I need to feel a little more in control, I read Anti Cancer a New Way of Life. There is a lot we can do to improve our odds. This book got me through the first few months.
You will figure this out over time, as we all have. You've already identified one key to your long term healing - your job.
>Z<
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Gang, I have a question--does anyone else get anxiety for the month or so leading up to their tests? In some ways, I wish I'd had a mastectomy just to end this hell. My mammogram is tomorrow, and an MRI in a month. I feel like these tests ruin my summer, and I have to medicate myself with Xanax just to muddle through. It is sheer misery. Today is a wash, I am shaking, feel sick to my stomach, and have to force myself out the door for meetings.
I was a Stage 1 node-neg patient, but I was young, so I always feel like the axe will fall.
I just wonder if I should be seeking more in terms of counseling and medication. This is ridiculous and such a robber of my time.
Edited to add: I will be six years out this summer.
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Sorry, friends, I posted in the wrong section--apologies if anyone read my post.
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Hi zarovka, thank you for the words of support. I've been spending hours poring over the Ibrance and Faslodex (and the Ibrance & Faslodex) threads. I feel better today. (Fuck you, Cancer, I'm not dead yet.)
I have the book you mentioned. I'm also getting some help from the book Breast Cancer: 50 Essential Things to Do. Something that really resonates, as I deal with my helpless dysfunctional parents, is the foreword, written by Dr. Christine Northrop. She describes the Adverse Childhood Experience (ACE) study, that concluded unmet childhood needs set the stage for future illnesses. She goes on to quote Lewis Thomas, "I have come to believe that cancer is the physical metaphor for the extreme need to grow."
Maybe that's a topic for a separate thread - because things can get pretty heated when we start talking about cancer as a metaphor (journey, war, wake-up call, etc). So I won't go there. It means different things to us at different times, I guess.
One thing that's not controversial: without this forum I would be so lost. Thank you all, again. I can never say that enough times.
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NineTwelve, Well that stinks for sure. I'm sorry you are dealing with this at all not to mention alone. That makes it twice as hard for sure. That is probably the worst part of all of this; constantly waiting to see if the news is good or bad. Talk about stress. I have had a few blows already and it is a emotional circus for me too, so I totally get it. Work keeps me distracted as well, although it can be stressful and sucks up most of the free time I would love to have for other things. I go back and forth about "retiring". Luckily I get summers off for 8 weeks so was able to get some things done. But I could still use 8 more! Anyway, you are valued here as well. I hope things settle down as your new treatment starts up. Keep checking in with us! Hugs....
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NineTwelve - Funny that you should mention that relationship between your childhood emotional "journey" (forgive me) and cancer. I am sure that many people on this forum had wonderful parents and still ended up with cancer. However, that very emotional post-diagnosis period brought up a lot parental issues for me. I had about 25 sessions with a coach/therapist/spiritual guide during that period to work through it. Certainly the cancer feels like a metaphor for a lot of pain and disfunction that I need to get rid of.
When the side effects of my treatment aren't getting me down, I find myself oddly happy these days. Today I spent the afternoon biking around after pokemon and giggling with my daughter. I ran into someone concerned about my cancer, and I had the strange feeling of not being serious or concerned enough in the face of their sincere concern for me.
I believe that this odd happiness is a result of taking advantage of that extremely emotional time to access and release some fears and experience that normally are not available to me. You seem to have some awareness of emotions and pains. You might do well to work through the relationship, metaphorical or otherwise between the cancer and your personal history. At a minimum I feel free of a lot of emotional pain as result of that process and that has got to help with my healing. It is one of these strange opportunities that the cancer experience provides. In any case, I encourage you to pull the thread on that insight you had Lewis Thomas's words.
>Z<
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sigh, parental issues, at some point I need to deal with that too.
So here we go again, scan and echo tomorrow, after 6 short BUT great weeks. Dr sees me doing so well, that proposed postponing scan for 3 more weeks but I told her how I've quickly adapted to the living scan to scan routine and can't postpone this one. She understands.
I get so much motivation and inspiration from BCO, that I'm trying to live as much as possible everyday. After my last scan, I was able to go "home"/Puerto Rico and have a great vacation with my mother/sister/nephew and hubby. A week later Mom/nephew joined us in Atlanta and stayed for 3 weeks! Lots of fun including baseball games, camping, tubing down the Chattahoochee, etc. And I'm still working full time...come on treatment, now is time to start kicking this cancer's butt!!!
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Good luck on your scan today, gramen. Sounds like you're making the most of your life right now, even with all the worry and - wow - a scan every six weeks! I guess I could get used to that, but it blows my mind. The courage I see here really inspires me.
Yes, now is the time for treatment to kick that cancer to the curb!
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Gramen, I am with you in spirit with a virtual hug today as you have your scans. I hope the news is really good.
Lynne
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