folfox club treatment #4
Comments
-
You've both been on my mind
You've both been on my mind today, I'm sorry so rough for you both! )o:
Jack is doing great, happy as a lark that he is not getting chemo till the 1st, me, not so much....I am horrible to be worried that he feels good. I want those cancer cells killed, I don't want to give them time to hang around...hmph.
I will be thinking about you two daily! Please know that my prayers are with you to stay strong and feel better!
Chriss0 -
Hey Lou
Sorry you're having tough time. Thanks for the udate. I think of you and your treatmetns and am glad to hear from you
I am having very rought time today. Oxy pins and needle started before infusion even done instead of day after so typing is hard. NO REACTION this time with double benadryl push! woo hoo! But, started feeling bad and slept during infusion and came home and slept. Usually don't do that. And I started having back, hip and leg pains pretty bad yesterday and still hurting today ins spite of pain meds that I finally broke down and took. Hope it's not those damn "spots" from my scans acting up.
Hang in there Lou. HUGS
PS: If they handed me a menu of side effects .. I'd just say .. no thank you I'm on a diet!0 -
Sorry
Sorry you two are having to play the side effects game! The nausea/vomiting was the worst for me at first ( The Sancuso Patch helped along with Emend pills...both very expensive ) For the Trots I usually stayed near a bathroom, but my meds for nausea caused constipation...so I would get the severe cramping and couldn't "go"! I decided the Trots were a better alternative for me!
As for picking Folfox side effects.....That would be hard. It seems like they change as time goes on. My peripheral neuropathy really didn't kick in until the last few treatments and has gotten worse in the last month! I slept better when I was having Chemo ( my Doc was suprised by this, but I am a low energy person and slept alot prior to chemo!)
I am so mean....I really wish there was a way to have my family/friends understand how bad you feel from the side effects.
Glad we have a place to talk about all of this crap ( literally ) where everyone understands what you are going through!
Take Care.....
Barb0 -
sorry LoriLori-S said:Hey Lou
Sorry you're having tough time. Thanks for the udate. I think of you and your treatmetns and am glad to hear from you
I am having very rought time today. Oxy pins and needle started before infusion even done instead of day after so typing is hard. NO REACTION this time with double benadryl push! woo hoo! But, started feeling bad and slept during infusion and came home and slept. Usually don't do that. And I started having back, hip and leg pains pretty bad yesterday and still hurting today ins spite of pain meds that I finally broke down and took. Hope it's not those damn "spots" from my scans acting up.
Hang in there Lou. HUGS
PS: If they handed me a menu of side effects .. I'd just say .. no thank you I'm on a diet!
Sorry Lori wish there was something I could do for what your going through? You are amazing you have it worst than I yet never a down moment? I don't take pain or many other meds much either. I think with all this medication I'm starting to rattle when I walk. I usually have back pains an hour or so after they end the oxi/folinic acid and start the 5-flu pump so I don't know which drug to blame. Still the pain comes and goes and right now last about a day. I do know when they disconnect and they give me the Neulasta shot for white blood cells the back pain does return but not as bad or for long. As far as those spots from your scan I want them acting up...I want that cancer to scream in pain dying like it should. I know its sadistic but it brings a little smile to my face to visualize cancer's death. I can take it if I know my cancer is suffering too...I know you can too kid! Hugs Lou0 -
I'm with youokthen said:You've both been on my mind
You've both been on my mind today, I'm sorry so rough for you both! )o:
Jack is doing great, happy as a lark that he is not getting chemo till the 1st, me, not so much....I am horrible to be worried that he feels good. I want those cancer cells killed, I don't want to give them time to hang around...hmph.
I will be thinking about you two daily! Please know that my prayers are with you to stay strong and feel better!
Chriss
Chriss Chemo is hard but if I could have started it the day after surgery I would have. My Onc believes in the ability to kill cancer when it spreads. I believe kill the beast before it spreads or spreads beyond where it is. If I had listened to my ONC when my CEA went up to 14.6 I have no doubt it would have gone beyond my three localized to site nodes to who knows where ( of course it may have who knows). ONC wanted to wait 6 more weeks after a CEA reading of 14.6? I kid you not "to give it time to grow so we can see it better". I don't think so. Fortunately my persoanl doctor didn't think so either and ordered a colonoscopy. The tumor and nodes were located and removed within three weeks which saved me three weeks of growth and spread. Could my ONC be right that it would not have made any difference? Maybe... but I'm the one facing a bad outcome if he's wrong not him. I don't blame Jack for not wanting to do chemo. It like shooting yourself in the foot to check to see if the gun is loaded. The gun needs to be loaded so you can kill what's trying to kill you. But crap that's my foot I'm shooting. But I see where Jack is coming from-soon or later it has to be done putting it off may mean you have to shoot the other foot later. Sorry about the metaphor, it late and I'm on my chemo brain pump. I will post the good and bad as I go through this as I'm sure Lori will to hope it helps. Lou0 -
folfox club no one wants to belongjararno said:Sorry
Sorry you two are having to play the side effects game! The nausea/vomiting was the worst for me at first ( The Sancuso Patch helped along with Emend pills...both very expensive ) For the Trots I usually stayed near a bathroom, but my meds for nausea caused constipation...so I would get the severe cramping and couldn't "go"! I decided the Trots were a better alternative for me!
As for picking Folfox side effects.....That would be hard. It seems like they change as time goes on. My peripheral neuropathy really didn't kick in until the last few treatments and has gotten worse in the last month! I slept better when I was having Chemo ( my Doc was suprised by this, but I am a low energy person and slept alot prior to chemo!)
I am so mean....I really wish there was a way to have my family/friends understand how bad you feel from the side effects.
Glad we have a place to talk about all of this crap ( literally ) where everyone understands what you are going through!
Take Care.....
Barb
I agree it hard to be nice when you deal with people who don't understand. Since I get hit with chemo yester day and for me my worst time is the day after disconnect from the pump though the next 3-4 days. In those days I want to be left alone to handle my situation. My family decided since I would be too sick for Thanskgiving they showed up Sunday for Thanksgiving. Of course I was have a severe bout of stomach cramps. I was so angry at my wife for allowing this. What I should have done was considered why they wanted to do this. What was best for me wasn't best for them so it took a lot from me to struggle through the situation and the guilt of directing my anger at her.
Low Energy I really understand. I'm finding as soon as I can after disconnect I start flushing the chemo out not to the level of diarrhea but as much as I can. This seems to bright back my engery quicker. Maybe it's just a placebo effect but for me it seems to work maybe just in my head.
I don't take medication for nausea any more. My Onc PA put me onto tums which helps when it gets bad. Doesn't always work but works enough to get me through the very bad times.
Take Care
Lou0 -
each treatment, in a cumulative sort of way, not like 1+1=2+1=3+1=4 etc but as 1+1=3+1=6+1=11,etc. The effects of the oxi are worse on you than the other components of the FOLFOX. Just hope it destroys all the cancer cells to make it worthwhile.....Hope all goes well for you and others dealing with this.....steveLOUSWIFT said:folfox club no one wants to belong
I agree it hard to be nice when you deal with people who don't understand. Since I get hit with chemo yester day and for me my worst time is the day after disconnect from the pump though the next 3-4 days. In those days I want to be left alone to handle my situation. My family decided since I would be too sick for Thanskgiving they showed up Sunday for Thanksgiving. Of course I was have a severe bout of stomach cramps. I was so angry at my wife for allowing this. What I should have done was considered why they wanted to do this. What was best for me wasn't best for them so it took a lot from me to struggle through the situation and the guilt of directing my anger at her.
Low Energy I really understand. I'm finding as soon as I can after disconnect I start flushing the chemo out not to the level of diarrhea but as much as I can. This seems to bright back my engery quicker. Maybe it's just a placebo effect but for me it seems to work maybe just in my head.
I don't take medication for nausea any more. My Onc PA put me onto tums which helps when it gets bad. Doesn't always work but works enough to get me through the very bad times.
Take Care
Lou0 -
cumulative effectcoloCan said:each treatment, in a cumulative sort of way, not like 1+1=2+1=3+1=4 etc but as 1+1=3+1=6+1=11,etc. The effects of the oxi are worse on you than the other components of the FOLFOX. Just hope it destroys all the cancer cells to make it worthwhile.....Hope all goes well for you and others dealing with this.....steve
Thanks Steve
Yes I know the cumulative effect and the retaining effects of our bodies to "keep" oxi and 5fu in our systems for a long period of time perhaps better expressed in these terms where X=number of treatments; M=molarity(infusion rate of Chemo in solution); T=time; N=ned; V=variable (individual side effects) then the formula would be (X+M)x T=N-V math or algerbra it sucks!!!! I just wish as with my menu idea that there was a C=constant or non-variable. In other words what side effect(s) we can expect as an absolute as we do folfox instead of not knowing or getting unwelcomed surprises. It would thus allow preparation at least. I know too much to ask. Perhaps the greatest unknown is we endure all this and there already be no cancer left alive or worst chemo doesn't work. I know they are working on nano molecular cell killers but in my view the trouble is creating the homing device so the nano killer cells know what to direct to kill. We have this biologically in white blood cells but it gets turned off by cancer. So in a sense there is likely just a protein and amino thread away from a vaccine and maybe a cure. Problem is as always money and profit. I am hoping to do 8 treatments of folfox but if they keep reducing the "M" they may extend it beyond 8 to 12. Just can't get the platelets to increase with their 4-8 day survival rates.
Take Care
Lou0 -
folfox clubLOUSWIFT said:folfox club no one wants to belong
I agree it hard to be nice when you deal with people who don't understand. Since I get hit with chemo yester day and for me my worst time is the day after disconnect from the pump though the next 3-4 days. In those days I want to be left alone to handle my situation. My family decided since I would be too sick for Thanskgiving they showed up Sunday for Thanksgiving. Of course I was have a severe bout of stomach cramps. I was so angry at my wife for allowing this. What I should have done was considered why they wanted to do this. What was best for me wasn't best for them so it took a lot from me to struggle through the situation and the guilt of directing my anger at her.
Low Energy I really understand. I'm finding as soon as I can after disconnect I start flushing the chemo out not to the level of diarrhea but as much as I can. This seems to bright back my engery quicker. Maybe it's just a placebo effect but for me it seems to work maybe just in my head.
I don't take medication for nausea any more. My Onc PA put me onto tums which helps when it gets bad. Doesn't always work but works enough to get me through the very bad times.
Take Care
Lou
I just wanted to say, my thoughts are with you both and everyone going thru chemo. Reading you posts reminds me that I had not found this site and knew no one else who was experiencing folfox when I was going thru it. The only positive I can come up with is that you have others to relate too. To me it was hell and I only made it thru 7. Bless you both, cumulative is for sure. Thoughts and best to all who are going thru their various chemos and procedures, you have to experience it to understand it. May the new year be the year of advancement in a cure for this and other cancers. Bless you all..Pat0 -
7 treatmentsLifeisajourney said:folfox club
I just wanted to say, my thoughts are with you both and everyone going thru chemo. Reading you posts reminds me that I had not found this site and knew no one else who was experiencing folfox when I was going thru it. The only positive I can come up with is that you have others to relate too. To me it was hell and I only made it thru 7. Bless you both, cumulative is for sure. Thoughts and best to all who are going thru their various chemos and procedures, you have to experience it to understand it. May the new year be the year of advancement in a cure for this and other cancers. Bless you all..Pat
I hope I can make it at least thru 8 so my insurance will okay a CT/Pet scan and maybe see what is going on. If they show nothing then I'm done. I know I'm a reoccurrence of sorts different type of cancer in different area of colon but this time with 3 localized nodes my onc wants twelve. I feel right now he can do the remaining four. Thanks Pat Lou0 -
Sorry
Sorry you are having such problems. The folfox is a hard chemo to deal with and the oxy is a bear. Hope that your counts go back up.
Kim0 -
You are so rightAnnabelle41415 said:Sorry
Sorry you are having such problems. The folfox is a hard chemo to deal with and the oxy is a bear. Hope that your counts go back up.
Kim
They disconnected my pump today. We walked outside the hospital and the cold air (Michigan today in upper 20's). My face froze like frostbite. It was kind of like when your mom tells you "if you keep making that face it will stay that way". Well the warm of the car returned my face back to normal whatever it has become with the chemo. The hands still have not thawed out and I was wearing gloves. Another new adventure with Folfox. Anyway the fatigue has not hit me yet maybe the reduced dose helped. Still I've had about eight hours sleep in the last three days. Still always good to get the pump off it just gets annoying. Take Care Lou0 -
New member of folfox club finished 2 of 12LOUSWIFT said:You are so right
They disconnected my pump today. We walked outside the hospital and the cold air (Michigan today in upper 20's). My face froze like frostbite. It was kind of like when your mom tells you "if you keep making that face it will stay that way". Well the warm of the car returned my face back to normal whatever it has become with the chemo. The hands still have not thawed out and I was wearing gloves. Another new adventure with Folfox. Anyway the fatigue has not hit me yet maybe the reduced dose helped. Still I've had about eight hours sleep in the last three days. Still always good to get the pump off it just gets annoying. Take Care Lou
I hope we all get through the folfox test! The comments make me nervous about what maybe ahead. At least downunder its summer and the issues with the cold are not so bad. Except now its so warm I have to put my vegies in the fridge so they don't go off. The catch is on the treatment days I needed gloves to get them out of the fridge to make my veg juice and then I had to wait for the juice to warmup before I could drink it. I have been up late reading posts and cannot sleep and suspect I am about to be knocked over by the folfox express this weekend. I got really tired and dizzy four days after treatment on the first dose.
Best wishes from downunder ( Sydney , Australia ),
Pete0 -
Welcome Pete!pete43lost_at_sea said:New member of folfox club finished 2 of 12
I hope we all get through the folfox test! The comments make me nervous about what maybe ahead. At least downunder its summer and the issues with the cold are not so bad. Except now its so warm I have to put my vegies in the fridge so they don't go off. The catch is on the treatment days I needed gloves to get them out of the fridge to make my veg juice and then I had to wait for the juice to warmup before I could drink it. I have been up late reading posts and cannot sleep and suspect I am about to be knocked over by the folfox express this weekend. I got really tired and dizzy four days after treatment on the first dose.
Best wishes from downunder ( Sydney , Australia ),
Pete
Welcome to this forum; I hope you will find it very helpful! Ron50 is from downunder also. Best of luck with your treatments.0 -
Let the weekend last!....AnneCan said:Welcome Pete!
Welcome to this forum; I hope you will find it very helpful! Ron50 is from downunder also. Best of luck with your treatments.
Reading all this has me dreading next week. In for #3, was nice getting a extra week off.0 -
Next TuedayKenny H. said:Let the weekend last!....
Reading all this has me dreading next week. In for #3, was nice getting a extra week off.
I start my chemo next Tuesday for the first time and after reading all of the above I feel like running away. I already have neuropathy in my right foot and it is not fun! Oxy. side affects sound horrible and VERY EXPENSIVE! My insurance is changing Jan. 1 and they will not be paying as much as they did for chemo. This cancer thing is for the birds! Poor birds I wouldn't wish this on them.
Anyway, I hope you all get releif soon!
Hugs to all, prayers too!
I dread next week too!
I hope it goes well with you Kenny.
Diane0 -
DianeOGammy01 said:Next Tueday
I start my chemo next Tuesday for the first time and after reading all of the above I feel like running away. I already have neuropathy in my right foot and it is not fun! Oxy. side affects sound horrible and VERY EXPENSIVE! My insurance is changing Jan. 1 and they will not be paying as much as they did for chemo. This cancer thing is for the birds! Poor birds I wouldn't wish this on them.
Anyway, I hope you all get releif soon!
Hugs to all, prayers too!
I dread next week too!
I hope it goes well with you Kenny.
Diane
Remember everyone's experience is different. You may not have the difficulties that some have. Try to take everything one day at a time. Good luck!0
Discussion Boards
- All Discussion Boards
- 6 CSN Information
- 6 Welcome to CSN
- 122.3K Cancer specific
- 2.8K Anal Cancer
- 451 Bladder Cancer
- 310 Bone Cancers
- 1.6K Brain Cancer
- 28.5K Breast Cancer
- 399 Childhood Cancers
- 27.9K Colorectal Cancer
- 4.6K Esophageal Cancer
- 1.2K Gynecological Cancers (other than ovarian and uterine)
- 13K Head and Neck Cancer
- 6.4K Kidney Cancer
- 677 Leukemia
- 799 Liver Cancer
- 4.2K Lung Cancer
- 5.1K Lymphoma (Hodgkin and Non-Hodgkin)
- 240 Multiple Myeloma
- 7.2K Ovarian Cancer
- 65 Pancreatic Cancer
- 492 Peritoneal Cancer
- 5.6K Prostate Cancer
- 1.2K Rare and Other Cancers
- 544 Sarcoma
- 740 Skin Cancer
- 658 Stomach Cancer
- 192 Testicular Cancer
- 1.5K Thyroid Cancer
- 5.9K Uterine/Endometrial Cancer
- 6.3K Lifestyle Discussion Boards