Radiation Machine Down for Past 3 days
Well the radiation machine that Don uses (tomography) has been broken since Wednesday - so this is the third day of no rads.
Has anyone else experienced this and what do they do - add the days to the end or would they do 'makeup' radiation sessions on the weekends? What are the potential issues with this happening, if any?
Also - thanks to all of you pioneers for the advice on the nausea meds - taking them the night of chemo and following through for the next few days seems to have helped with this last chemo treatment. Don is also getting IV fluids starting this week for 2 times a week for hydration - chemo doc made that call Wednesday - so he seems to be proactive in this department, and I was happy that he suggested doing that rather than waiting for Don to ask.
Thanks,
Judy
Comments
-
It does suck
because we are all geared up to get this done, and now its hurry up and wait. This will NOT, however, do any harm in the long run. Routinely, on holidays like XMas and 4th of July, they shut the machines down and we wait until they open again on Monday. They will simply add these days onto the end of treatment.
Best to you.0 -
add it to the endlongtermsurvivor said:It does suck
because we are all geared up to get this done, and now its hurry up and wait. This will NOT, however, do any harm in the long run. Routinely, on holidays like XMas and 4th of July, they shut the machines down and we wait until they open again on Monday. They will simply add these days onto the end of treatment.
Best to you.
my radiation machine was broken for a couple of days and it was a welcome time off for me and all was added at the end.
I wish you the best!!
Jim0 -
happened to us toounknown said:This comment has been removed by the Moderator
Judy, Keith "broke" the machine once and we attributed it to his superhero power. It made me terribly anxious but they can add it in to the protocol. Please remember this is a cumulative process so is the total amount of "gray" or whatever it is called that they get. Still, psychologically it is scary. Even though Don has missed a few days of treatment, the radiation he has in him right now is still working in conjunction with his chemo. But I do understand your concern. When our machine broke, they had it fixed within a day and Keith went back in- but again- it truly is the cumulative dose that matters. You just think though if they have people on call all the time for getting the internet up and running they could get the machine fixed faster than 3 days. But it is truly more the emotionally inconvenience than if he misses a few days. I just hope it's smooth sailing ahead cuz every little thing that doesn't go just right is a source for worry with cancer and a lot of isn't gonna make a difference. And you are correct that in adenocarcinoma the chemotherapy is the sensitizer to help the radiation work better to shrink and kill as much as possible so the surgeon has as little of work to do when the time comes to get rid of that THING! Also, Ericalynn knows a lot about radiology so if you have any specific questions, she is a great resource and very generous with her knowledge.
Cora0 -
Holiday Break
I was undergoing radiation during Thanksgiving of 2009. They took a break and I had radiation on the Sunday before Thanksgiving and didn't have any radiation over the 4-day break, so I only had 4 days that week followed by 4 days off. As far as I know, it created no problems for me.
Melinda0 -
For nausea, Bill gets zofranCora11 said:meds
a p.s. about the meds. There are newer anti-nausea meds that are given IV on the day of chemo that last about 3 days. If Don isn't getting those, do ask as they make a world of a difference.
Cora
For nausea, Bill gets zofran by IV when he is getting chemo. He also has oral anti nausea meds that the nurse said to start taking about 6 hours after he finishes chemo at the hospital. He takes it regularly every 6 hours until about 24 hours after the 48 hour FU pump is disconnects. So far he has not suffered much nausea.0 -
My understanding...
IS that breaks in the radiation are actually needed. Being off of the radiation for a small while (even a week) won't quell the effectiveness. And, I was also given to understand that the radiation has a direct effect on shrinking the tumor, while chemo shrinks the tumor as well as rounds up any suspicious outliers.
I wasn't given an 80/20, but remember, different oncologists say different things. My feelings are... No worries mate. You'll get the necessary dosage.
--Jerry0 -
Rads added
Hi Judy
That happened to me one day, and they added it at the end. I was away from home in Texas getting tx, and wanted it to be over asap. But things happen. I don't think the machine was broken, but I believe it was being serviced. Something like that.
Try not to worry.
I was happy to read that Don is doing better with nausea. Glad that some of the suggestions have helped. Just remember that many nausea meds cause constipation and it is better to prevent it, than to try and treat it after the fact.
Lisha0 -
Radiation machine broken
They called yesterday and have Don set up for radiation tomorrow (Sunday) but they will call if the machine is not repaired prior to his appointment. Thank you all so much for your responses - very reassuring to say the least - the support you provide is so appreciated.
Hydration and taking nausea meds seems to be key things for Don as many of you have suggested - our chemo onco seems to be right on top of the latest and somehow he manages to 'read my mind' and know what we'll be asking of him.
Don's tastebuds are all over the place and smells still bothersome - hearing from all of you on that subject is also reassuring. Seems to be very 'normal' with our EC group.
Thanks to all of you for your continued prayers and thoughts. We'll keep you posted as treatment progresses.
Hugs to all,
Judy & Don0 -
back on trackJReed said:Radiation machine broken
silly site
Hi Judy, hope you are feeling better that the radiation is scheduled now. Hydration is a BIG thing and really helps, too bad my hubby was stubborn with this, I know it would have been easier on him, he just got so sick of being "poked".
Julie0 -
Glad to hear things are back on scheduleJReed said:Radiation machine broken
They called yesterday and have Don set up for radiation tomorrow (Sunday) but they will call if the machine is not repaired prior to his appointment. Thank you all so much for your responses - very reassuring to say the least - the support you provide is so appreciated.
Hydration and taking nausea meds seems to be key things for Don as many of you have suggested - our chemo onco seems to be right on top of the latest and somehow he manages to 'read my mind' and know what we'll be asking of him.
Don's tastebuds are all over the place and smells still bothersome - hearing from all of you on that subject is also reassuring. Seems to be very 'normal' with our EC group.
Thanks to all of you for your continued prayers and thoughts. We'll keep you posted as treatment progresses.
Hugs to all,
Judy & Don
Judy,
I am sure there is somewhere else Don would rather be on Sunday than inside that machine, but each time there is one less time.
I remember after my second chemo cycle, things started to taste "metallic" to me. I was careful not to eat things I really liked because I had been told that you should avoid things that you really liked because after chemo you would associate the bad taste with those foods. Not sure if it was a good idea but I avoided pizza until after I finished chemo and my "celebration" dinner after I finished treatment was "guess what???"
Tell Don to hang in there, we are all praying and pulling for him.
Best Regards,
Paul Adams
McCormick, South Carolina
DX 10/22/2009 T2N1M0 Stage IIB
12/03/2009 Ivor Lewis
2/8 through 6/14/2010 Adjuvant Chemo Cisplatin, Epirubicin, 5 FU
Two year survivor
Life may not be the party we hoped for, but while we are here we might as well dance!0 -
Glad to see an update!JReed said:Radiation machine broken
They called yesterday and have Don set up for radiation tomorrow (Sunday) but they will call if the machine is not repaired prior to his appointment. Thank you all so much for your responses - very reassuring to say the least - the support you provide is so appreciated.
Hydration and taking nausea meds seems to be key things for Don as many of you have suggested - our chemo onco seems to be right on top of the latest and somehow he manages to 'read my mind' and know what we'll be asking of him.
Don's tastebuds are all over the place and smells still bothersome - hearing from all of you on that subject is also reassuring. Seems to be very 'normal' with our EC group.
Thanks to all of you for your continued prayers and thoughts. We'll keep you posted as treatment progresses.
Hugs to all,
Judy & Don
Thanks for keeping us in the loop, Judy.
Sounds like things are going decent for you two. Glad of that. When Nick got the "go-ahead" for surgery, his surgeon said "don't worry, surgery is easier than treatment". Got to say I agree with him after being beside Nick.
Here's hopes & prayers that treatment continues to go well and that your oncologist stays on top of things for you.
Love & Hugs,
Terry0 -
Terry! I needed to hear that todayTerryV said:Glad to see an update!
Thanks for keeping us in the loop, Judy.
Sounds like things are going decent for you two. Glad of that. When Nick got the "go-ahead" for surgery, his surgeon said "don't worry, surgery is easier than treatment". Got to say I agree with him after being beside Nick.
Here's hopes & prayers that treatment continues to go well and that your oncologist stays on top of things for you.
Love & Hugs,
Terry
Thank you and hugs to you Terry!
Yours is the first time I've heard that surgery is easier than treatment and MAN did I need to hear that today! I did not realize that we have at least three of you going through the surgery at the same time. Jeff, JeffT and Nick - wow - it's good that you all have each other to compare notes with and the other pioneers to check in with too.
But do keep us not-so-newbies-now posted on your progress. Love to hear from everyone - hope you're taking care of Terry during this time also!
Love and Hugs,
Judy0 -
Here's our "class" of 8 and Surgery datesJReed said:Terry! I needed to hear that today
Thank you and hugs to you Terry!
Yours is the first time I've heard that surgery is easier than treatment and MAN did I need to hear that today! I did not realize that we have at least three of you going through the surgery at the same time. Jeff, JeffT and Nick - wow - it's good that you all have each other to compare notes with and the other pioneers to check in with too.
But do keep us not-so-newbies-now posted on your progress. Love to hear from everyone - hope you're taking care of Terry during this time also!
Love and Hugs,
Judy
Bill and Kim (Kateel) - August 28th, I think - Kim recently lost Bill to aspiration
Luis and Laura (Laura23) - Aug 30th
Jeff and Niki (NikiMo) - Sept 6th
Jeff Thomas (JeffT) - Sept 8th
Nick and Terry - Sept 8th
John and Erica (EricaLynn) - Sept 9th
Michael (Hopper52) - Michael sadly didn't make it to surgery. His cancer was more advanced than anyone realized
Bob Haze (BobHaze) - early Sept
We were a mix of Stage 1's to Stage 3's. Sadly, I think Michael was actually a Stage 4. I haven't seen much of Jeff Thomas lately. I know he had a rough surgery. Jeff's MIE turned into an Ivor Lewis with an extended hospital stay. But everyone else (other than Michael) had very successful surgeries. and is making a full recovery. Those surgery dates will give you a reference if you want to try and find posts of our "real time" experiences.
It did help to have a large group going through this together. We all bounced ideas off each other and gauged progress against others that went just before. Sure gave us all a sense of security knowing that someone from the group was just ahead and doing well.
I know the same will be true for you and Don. Your journey so far sounds much like ours - and I consider that a good thing. Life is 85% back to normal and getting better every day.
and Yes I'm taking good care of me. Behind Nick and behind the littles Then me! LOL
Love & Hugs!
Terry0
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