need some in put switched my chemo and im in bad shape

I am on the same, except
I am on the same, except avastin. Are you hydrated? It is really important. The last thing i want to do is drink water...
But it helps. I force it. Try it and see if it works. When you are disconnted you really want to flush your system.
Take care.

I'm sorry to read that you are having such a hard time...
when I was on FOLFOX I had horrible side effects that didn't start to improve for five or six days after infusion. I had serious diarrhea and the only thing that worked for me was lomotil, which is a prescription medication. And it didn't work when I took it as directed, so on the advice of a chemo nurse I would take 6 pills all at once, and then two more about a half-hour later if the diarrhea continued. This was the only thing that helped me, and I tried pretty much every other possible treatment, including tincture of opium! And as others have said, you really do have to watch out for dehydration. I found out only after a trip to the ER that I could have gone into the infusion center to get IV hydration. If that's available to you, I would definitely take advantage of it if you feel like you might be not getting enough to drink. Sending hugs and strength-Ann

I just had my first Folfox
I just had my first Folfox on Monday...also disconnected on Wednesday. I was not able to do anything for the last 3 days...constipation...then diarrea and vomitting...no appetite and mouth sores. Drinking water and magic mouthwash has helped. I still have a little of the "big D"... but i feel human again. I slept most of thurs & fri. I guess some of us arejust more sensitive tothe treatment. I can deal with most of it...when i know that there are going to be good days. I am justconcerned about developing the neuropathy...like Jimthebassist posted about in another post.

Alex

Momof2plusteentwins said:

Same problem
I had this week off, it has been nice. But last week it took until Sunday- to not feel like I was hit by a truck. I dread getting treatment #2. I know it will be 5 days of feeling like crap. The bad thing is, I can't sleep during the day, can't eat, drink, just lay there and moan. I hope it gets better, I don't know if I can do this through December.
Sandy

Sandy...we are pretty much
Sandy...we are pretty much on the same schedule...we can lay on the sofa and moan together. I think the hardest part has been on my kids...they are only 10 & 11...this is not summer of fun that we had planned.

Alex

FOLFOX vs FOLFIRI/FOLFURI
I believe (but not 100% sure) folfuri is the same as folfiri which, like folfox, is made up of 3 drugs, two of which are F-5u and folinic acid. the difference being that folfox includes oxaliplatin where folfiri uses irinotecan(camptosar). You can verify, but I think the irinotecan is causing the diarrhea.

Your oncology office needs to be apprised of your condition and how long it lasts. My wife was beaten down for many days after each treatment. each of 12 cycles was with folfox. the worst period was the 3 or 4 days after coming off the pump. could never work or do normal activities. so get advise. If your ONC can't help get advise from a palliative care specialist and have your doctor help refer you to one.

Hi glinka
I did the folfiri for 2 years then switched from the 5fu to xeloda (pills that work the same way as the 5fu). I found this combination much easier to tolerate than the 5fu. The 2-3 days after disconnecting are the most difficult. Drink lots of water to flush your system. Water with lemon juice helped me with the yucky taste in my mouth and is also very good to help cleanse your liver.

All the best to you

barbebarb said:

Folfox-not fun
I am on last round of folfox and hope I will get a break after the scan to follow.
I had two surgeries and chemo was broken up before and after-this is treatment eight. Neuropathy concentrated in between left foot big toe and ball of right foot. Also feel like my left kidney hurts during and after infusion.
Going to mention to my oncologist this week.

It is not fun. Feel awful the first 3 to 4 days and take Xeloda too. Appetite is very suppressed and I have to force myself with liquids. I have lost 30 pounds and try to really eat well the week I am off Xeloda...
I don't get nausea but each time I get some different discomfort.

I don't know how others endure all the chemo treatments. I guess one day at a time. Ugh...

Kidneys
I'm glad you mentioned the pain in your kidney. Last week when the onc increased my 5-FU by 20% both of my kidneys had a dull ache similar to after getting a big adrenaline rush. It went away after about half an hour, but it was real misery while it lasted. My thought was that it was the increased amount of fluid (I had a large bag of magnesium as well) that was causing it. Now I'm thinking it might be because the larger dose of 5-FU.