Dealing with constipation from chemo?
Anyone have any advice?
Comments
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Jen
I'm the same way. I'm on Folfox too and I will have diarrhea one day and not go for 5-6 days and worry about another obstruction. Then I will go. It has been 13 weeks since surgery. I talked to my dr and he said it will take time. I try to drink water but it is so hard to drink anything because the taste from chemo. Sometimes I feel so hungry and havent gone in 5 days and wonder where all the food is going. I actually gained 3 lbs this week on chemo.
Sandy0 -
I get the diarrea followed
I get the diarrea followed by constipation for a couple of days. Staying more hydrated helps... I need to pick up some miralax for the next round. I am on Folfox too with the take home pump. I also get Neulasta for my low WBC ...took some pain meds for the bone pain...that did not help the constipation.
Alex0 -
Partial?
Jen, sounds like it could be the beginnings of a partial obstruction. With the types of things he's doing, it should be working a little bit better.
When I got out of rectal surgery, I had a few issues...and one of them was the development of inside and outside hemi's, which made passing stool almost unbearable...like heart stopping...straining so hard you saw stars and almost passed out..sweating profusely etc. etc.
My surgeon examined me and saw the problem with the hemi's...he wondered how I even went at all...we did another surgery and cleared that problem up.
The other thing you could try would be a couple of those Fleet enemas...found at the drug store...usually contain two tubes of saline...insert the liquid...hold it...etc. etc.
If things don't noticably improve, I'd sure consider having them x-ray or scan the area to check for a partial blockage.
If he continues to lose weight at this rate, you're both going to find yourselves in the ER getting fluids at the least.
If he can't get nutrition or keep anything down...they can insert a nasal feeding tube to help him....they are small and go in the nose like a cannula and into the stomach.
Don't wait too long...maybe make some phone calls while you wait to his health providers, explaining the situation.
-Craig0 -
Chemo constipated me. I
Chemo constipated me. I took senna and colace regularly starting a couple of days before.
However, when I was really stopped up, the dr gave me Lactulose, which works fairly quickly.
It is a matter of balance. I never had the diarrhea portion. Most people suffer from both. I didn't, so take the advice that best fits his situation.
Alice0 -
Polyvinylglycolabrub said:Chemo constipated me. I
Chemo constipated me. I took senna and colace regularly starting a couple of days before.
However, when I was really stopped up, the dr gave me Lactulose, which works fairly quickly.
It is a matter of balance. I never had the diarrhea portion. Most people suffer from both. I didn't, so take the advice that best fits his situation.
Alice
or Miralax mixed with water as a drink it will soften stool ...normally for me after 4 days of constipation I started having diarhhea issues.....0 -
I have a transverse
I have a transverse colostomy, so my experience is likely a little different. I have had 5 tx with FOLFOX (last 4 with Avastin) and I swing from firm to loose stools, but no constipation or real diarrhea. I have the colostomy because my colon was 90% obstructed and they weren't able to do a resection on me. I was initially on colace and miralax, but now don't take anything except the occasional compazine as needed for nausea.
Edited to add that I lost 45 pounds within the first 6-8 weeks after my surgery, but I needed to lose that weight anyway. I'm now at 200 lbs and 6' tall.
Tedd0 -
Thanks everyone for the
Thanks everyone for the great advice. He has his 2nd treatment this Friday and I think his mind will at least be at ease that it's normal and not a blockage. I guess it's a learning process that we'll have to learn as we go, but you are all so great about sharing your experiences. I appreciate it very much!
For the first treatment - it was on Friday and by Wed he finally felt better. Wonder if that will get better, stay the same or get worse??0 -
jen2012jen2012 said:well...no blockage
Now its diarrhea. I feel so bad for him...hes in and out of the bathroom constantly. I guess its all going to take some getting used to and figuring out what may help.
Thank you all for taking the time to reply and for your suggestions.
Get some script fob LOMOTIL. It is the strongest available to stop diarrhea. Good luck!!0 -
Same for mejen2012 said:Thanks everyone for the
Thanks everyone for the great advice. He has his 2nd treatment this Friday and I think his mind will at least be at ease that it's normal and not a blockage. I guess it's a learning process that we'll have to learn as we go, but you are all so great about sharing your experiences. I appreciate it very much!
For the first treatment - it was on Friday and by Wed he finally felt better. Wonder if that will get better, stay the same or get worse??
I had the same problem. During chemo, I had a lot of diarrhea and then bouts of constipation. I was admitted to the hospital three times because of it. My anal opening had narrowed a lot after my colon resection. They kept going in via colonoscopy to stretch the opening. I started taking Miralax regularly after the last one (sometimes in the morning and in the evening) and that helped when I was "backed up". Good luck to your dad!0 -
hey Jen
Hey Jen, I know how your husband is feeling, i was constipated during my first round of Chemo to and found some stool softners, they took a few days to kick in but i take them eveynight and they really seem to help me have better bowel movements. I have also lost about 20lbs since i started and i was afraid to eat to, but i also found that if i eat more often but smaller meals throughout the day i actually felt better. Not that i was 100% because i eneded up in the hospital a few times for dehydration and other issues. Keep hanging in there!
Zach0 -
Hi Deena,Deena11 said:Same for me
I had the same problem. During chemo, I had a lot of diarrhea and then bouts of constipation. I was admitted to the hospital three times because of it. My anal opening had narrowed a lot after my colon resection. They kept going in via colonoscopy to stretch the opening. I started taking Miralax regularly after the last one (sometimes in the morning and in the evening) and that helped when I was "backed up". Good luck to your dad!
Sorry you've had
Hi Deena,
Sorry you've had the same problems. I hope all is looking better now!0 -
Hi Zach - you gotta keepbigman4christ said:hey Jen
Hey Jen, I know how your husband is feeling, i was constipated during my first round of Chemo to and found some stool softners, they took a few days to kick in but i take them eveynight and they really seem to help me have better bowel movements. I have also lost about 20lbs since i started and i was afraid to eat to, but i also found that if i eat more often but smaller meals throughout the day i actually felt better. Not that i was 100% because i eneded up in the hospital a few times for dehydration and other issues. Keep hanging in there!
Zach
Hi Zach - you gotta keep drinking (water) and stay out of the hospital! My husband has done much better since that first treatment - we figured out that the steroid was causing more problems than the chemo so they cut the dose in half. He had his 5th treatment and things are going okay so far.
How are your treatments going? When are they doing a scan next?0 -
3 months or sojen2012 said:Hi Zach - you gotta keep
Hi Zach - you gotta keep drinking (water) and stay out of the hospital! My husband has done much better since that first treatment - we figured out that the steroid was causing more problems than the chemo so they cut the dose in half. He had his 5th treatment and things are going okay so far.
How are your treatments going? When are they doing a scan next?
Hey Jen, i know i gotta keep the water intake up but it is hard when i am not used to drinking that much water everyday. But i have been slowly getting better at drinking more I believe my next scan will be in about 3 months or so. The Dr. want to do at least 4 rounds of Camptosar, Xeloda, and Avastin. After that they are going to see how everything is working and go from there. Is your husbands treatment working for him? how long do the dr think he will be on chemo?0 -
When I had chemo. over abigman4christ said:3 months or so
Hey Jen, i know i gotta keep the water intake up but it is hard when i am not used to drinking that much water everyday. But i have been slowly getting better at drinking more I believe my next scan will be in about 3 months or so. The Dr. want to do at least 4 rounds of Camptosar, Xeloda, and Avastin. After that they are going to see how everything is working and go from there. Is your husbands treatment working for him? how long do the dr think he will be on chemo?
When I had chemo. over a year ago it gave me the big D, and I was popping anti-dirarrhea pills constantly. This time around it's leaning to the opposite direction. I mentioned this to my onc.s nurse and she said it was one of the side effects of one of the pre-meds, (I can't recall which one she said, it's either dexamethasone or onedesterone) ....she recommended senna, I've seen senna tea at the health food store.....but one of our fellow members on here suggested increasing pro-biotics....so I've been eating more yogurt and that's helped a lot. I've been afraid to try anything else because of my experience last year and I just don't want to throw things into a direction of where I'm having to run to the bathroom constantly and popping anti-diarrhea meds.0 -
It was the dexa that gave mysmokeyjoe said:When I had chemo. over a
When I had chemo. over a year ago it gave me the big D, and I was popping anti-dirarrhea pills constantly. This time around it's leaning to the opposite direction. I mentioned this to my onc.s nurse and she said it was one of the side effects of one of the pre-meds, (I can't recall which one she said, it's either dexamethasone or onedesterone) ....she recommended senna, I've seen senna tea at the health food store.....but one of our fellow members on here suggested increasing pro-biotics....so I've been eating more yogurt and that's helped a lot. I've been afraid to try anything else because of my experience last year and I just don't want to throw things into a direction of where I'm having to run to the bathroom constantly and popping anti-diarrhea meds.
It was the dexa that gave my husband problems. I think he was taking 8 Mg for 4 days and they cut it to 4 Mg a day and he hasn't.had any issues.0 -
I know Zach ...I don't.drinkbigman4christ said:3 months or so
Hey Jen, i know i gotta keep the water intake up but it is hard when i am not used to drinking that much water everyday. But i have been slowly getting better at drinking more I believe my next scan will be in about 3 months or so. The Dr. want to do at least 4 rounds of Camptosar, Xeloda, and Avastin. After that they are going to see how everything is working and go from there. Is your husbands treatment working for him? how long do the dr think he will be on chemo?
I know Zach ...I don't.drink enough water either so I can imagine how hard it if you aren't feeling great. Dr office just called today to set up his first scan ...Nov 30th. Ive been kind of freaked out about it all day....worried. some ways I wish we could wait til after Christmas . We haven't even thought about what comes after the folfox avastin surgery.
Your wife looks so much like our neighbor I do a double take every time I see your picture!0
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