This blog will chronicle my experiences dealing with Stage IV,rare, Neuroendocrine Cancer (also called Carcinoid) from my diagnosis in June 2012 until ...
Showing posts with label Scanxiety. Show all posts
Showing posts with label Scanxiety. Show all posts
Wednesday, February 4, 2015
Scanxiety...
Google Scanxiety and you will actually get a definition: Anxiety suffered while waiting for the results of an important medical scan.
My definition: Anxiety suffered while waiting to get the scan!
I met with my oncologist yesterday and while everything seems fine, he did say that I should have a scan now rather than wait. I was a little surprised because at our last visit he said I could wait as long as my tumor markers remained "normal." This time he said he wouldn't want me to go longer than a year, which it has been as of Monday.
I am actually relieved to be getting a scan. Even though my markers and other blood work are good, I still want to "see" what is going on, if anything. Better to know that I am still stable than to wonder if I am. I don't trust tumor markers to show everything. However, even with the relief, there is anxiety. You just never know. He also told me I could get it within the next couple of weeks, like no hurry. Then he told the nurse to schedule it "now." NOW? Did he feel something when he palpated my abdomen and just didn't want to say anything? Then I remembered that we discussed getting the scan before he examined me. I'm sure he just told her to go ahead and schedule it now, not meaning urgent but to get it done since I may have had to wait a couple of weeks to get in. Well... that ain't the case. I go in Monday morning at, gulp, 7am! I'm not too thrilled about that but at least I'll be done early and can get to work. This is at a different hospital than I've had my other scans. This is at the hospital where I had my mammogram. Its a nice place and I'm sure it will be fine.
Keep your fingers crossed for good results!
Also, today is World Cancer Day.
Tuesday, January 28, 2014
One month and counting down...
One month until my CT scan! Seems weird to be counting down to a scan! I am somewhat regretting my decision to wait 7 months between scans instead of the usual 6 months! I've said before that this is the longest I've gone between scans since my diagnosis. Most have been no more than 4 months apart. That was, in part, due to liver surgery and the issue I had after. See my post from 4/5/2013.
My scan is scheduled for the end of Feb. with my Oncologist appointment the following week. I have always seen my reports before my doctor (except for my very first scan--I didn't know I could get the written report online). I've never really felt Scanxiety before but I am feeling it now. Even though I tell myself that nothing will have changed, this is a slow-growing cancer, I still have that anxiety of all the "what if". What if they've grown? What if there are new tumors in my liver? What if they've taken over my liver? What if they are now popping up everywhere? I know that this is very unlikely. I will genuinely be surprised if I am not still dancing with Stable Mable! Even with that said, I am still going to worry.
I will be getting my blood work done next week so if anything is truly amiss, it should show up there. I don't have to wait long for most of my test results. Only that damn pancreastatin that takes 3 weeks to get back! That is why I'm getting it so early. I want the results to be back before I see my doc!
Now I'm throwing another wrench into the "plan". There is a clinical trial at NIH (National Institute of Health) in Bethesda, MD for the Gallaim 68 Dotatate Pet/CT Scan. I am not sure that getting the Gallium scan right now would be that helpful (unless there is new stuff going on) but you go back every year for five years for a follow-up scan and this could be VERY helpful. The Gallium scan is so much better at "seeing" NET tumors than either CT, MRI, or Octreotide Scans are. It is not approved by the FDA yet so most patients end up paying the costs themselves to get this scan (anywhere from $4,000-$6,000. This trial is free! The only thing I would have to pay for is my first flight out and back. Returning flights are reimbursed. I can stay in-patient and not pay for room or board.
Clinical Trial at NIH
If I'm accepted into the trial, depending on when they would want me there, I will have to have an octreotide scan, CT scan and then the Gallium scan (unless my last octreotide and CT scan is within six weeks and it's been 20 months since my O-scan and you know how long since my CT scan). That would be a lot of scans and radiation in a very short amount of time. I think you stay for 3 or 4 days.
I'm gathering my info. to send in to see if they will accept me. I am not sure I would be able to participate though since I have no money to pay for the initial flight out and back. It's looking like between $500-$1,000 for a round trip ticket. Argh. I just figure I'll worry about that hurdle after I get accepted. I don't know if I should talk to my doc about it. I'm sure he'd be 100% for it since it would save the insurance co. money on my next scan! I could skip my Feb. scan if they wanted me out there before that -- they will send him all results. I just honestly don't know what to do. I would be going alone and that just sounds crappy. I mean, I wouldn't want to make someone sit around for four days being bored to death while I'm getting scanned. I am the only one who can stay in the hospital. You can't have anyone stay with you. It just sounds so lonely though. Of course, my ex lives nearby so I could always ask him if he wanted to come and see me. Show me the sites. You can leave the hospital. You don't have to stay 24 hours a day.
The only thing I don't have is my surgery notes. I think I can get them from my oncologist. I know they have EVERYTHING in my file... I'm going to ask when I go in for my blood draw and shot. I'll keep you posted.
My scan is scheduled for the end of Feb. with my Oncologist appointment the following week. I have always seen my reports before my doctor (except for my very first scan--I didn't know I could get the written report online). I've never really felt Scanxiety before but I am feeling it now. Even though I tell myself that nothing will have changed, this is a slow-growing cancer, I still have that anxiety of all the "what if". What if they've grown? What if there are new tumors in my liver? What if they've taken over my liver? What if they are now popping up everywhere? I know that this is very unlikely. I will genuinely be surprised if I am not still dancing with Stable Mable! Even with that said, I am still going to worry.
I will be getting my blood work done next week so if anything is truly amiss, it should show up there. I don't have to wait long for most of my test results. Only that damn pancreastatin that takes 3 weeks to get back! That is why I'm getting it so early. I want the results to be back before I see my doc!
Now I'm throwing another wrench into the "plan". There is a clinical trial at NIH (National Institute of Health) in Bethesda, MD for the Gallaim 68 Dotatate Pet/CT Scan. I am not sure that getting the Gallium scan right now would be that helpful (unless there is new stuff going on) but you go back every year for five years for a follow-up scan and this could be VERY helpful. The Gallium scan is so much better at "seeing" NET tumors than either CT, MRI, or Octreotide Scans are. It is not approved by the FDA yet so most patients end up paying the costs themselves to get this scan (anywhere from $4,000-$6,000. This trial is free! The only thing I would have to pay for is my first flight out and back. Returning flights are reimbursed. I can stay in-patient and not pay for room or board.
Clinical Trial at NIH
If I'm accepted into the trial, depending on when they would want me there, I will have to have an octreotide scan, CT scan and then the Gallium scan (unless my last octreotide and CT scan is within six weeks and it's been 20 months since my O-scan and you know how long since my CT scan). That would be a lot of scans and radiation in a very short amount of time. I think you stay for 3 or 4 days.
I'm gathering my info. to send in to see if they will accept me. I am not sure I would be able to participate though since I have no money to pay for the initial flight out and back. It's looking like between $500-$1,000 for a round trip ticket. Argh. I just figure I'll worry about that hurdle after I get accepted. I don't know if I should talk to my doc about it. I'm sure he'd be 100% for it since it would save the insurance co. money on my next scan! I could skip my Feb. scan if they wanted me out there before that -- they will send him all results. I just honestly don't know what to do. I would be going alone and that just sounds crappy. I mean, I wouldn't want to make someone sit around for four days being bored to death while I'm getting scanned. I am the only one who can stay in the hospital. You can't have anyone stay with you. It just sounds so lonely though. Of course, my ex lives nearby so I could always ask him if he wanted to come and see me. Show me the sites. You can leave the hospital. You don't have to stay 24 hours a day.
The only thing I don't have is my surgery notes. I think I can get them from my oncologist. I know they have EVERYTHING in my file... I'm going to ask when I go in for my blood draw and shot. I'll keep you posted.
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