Anyone have light headedness from chemo (folfirinox)?

Now my husband is on Abrax/Gem and it is definitely easier than the folfirinox. However... severe light headedness when he stands up. The doctor prescribed duloxetine for neuropathy and I'm wondering if it could be a side effect for that drug. Hoping it gets better as there have been near falls a couple times. He is getting his vitamin D checked as someone said that also could be a possibility if it is low.

sorry to hear of your husband's temporary set back. My husband had a bad couple weeks midway through his 12 treatments, and though he was not hospitalized, they did delay his treatment because of poor blood test results. Still not sure why it hit him as bad at that time, but we have gone in for lots of extra hydration since then thinking that may have been part of the problem. It hasn't been easy since then... but better than in March. I don't think he realizes or recognizes how serious it was at that time. But hydration has helped in his case.

He’s improved, but still having some memory issues. There are a few days just prior to his hospitalization that he cannot recall at all. The hospitalist said it could take a few weeks before he’s back to his usual self. Unfortunately, he was too ill to have his scheduled treatment. It will be delayed 2 weeks.

@jbnc23, a good reminder. How is your husband doing now? Will he be able to have the next chemo treatment?

Thank you. My husband will be happy to hear that he can get back to "normal" with time. I know it has been disturbing for him to spend all of his time on the couch or in bed. Not like him at all, but just too tired to move. He just finished chemo #12 so I know he is looking forward already to having more energy.

I was VERY fit and healthy before my chemo. I eased back into exercising by first buying & riding an electric bike....saved my sanity. The physical recovery followed but does take awhile. I always said to my friends, I need to adapt to "my new body". Well, with time, that new body became as fit as my old body....keeping in mind that my body is also aging and will not be the same....like everyone else.

My husband is currently in the hospital being treated for dehydration and slightly high ammonia levels. The doctor explained that only 1/3 of IV fluids will get into the blood vessels so it’s extremely important to drink at least 2 liters of water each day, not sodas or other sugary drinks, which are bad for pancreatic cancer patients anyway. He had had a fluids infusion the day prior to our ER visit so I was surprised when they said he was dehydrated. Now I understand why.

Thank you. He got the pump off yesterday, and today is feeling better it seems than he has for a while. I think just the idea that he is done with that series of treatments gave him some relief. They did lower the dosage of one of the drugs slightly because he had had more neuropathy in his feet, so possibly that made it slightly easier. But I think it is psychological that he doesn't have any more of the "whole kitchen sink" of drugs to face again.

@sheridanb, here is the discussion that @lisn started:
- Vertigo and Folfirinox?
https://connect.mayoclinic.org/discussion/vertigo-and-folfirinox/
How is your husband doing with treatment number 12?

Thank you again for sharing your experience. Before chemo Dan had exercised daily for decades and was in great shape. So it is now hard for him to barely be able to stand or walk. A year ago he was white water kayaking on big water, but June started all the tests for diagnosis, then chemo for mis diagnosis. Then more tests, CA19-9 number at 39000. Then started folfirinox. Hoping after #12 he can regain some of what he has lost. I'll check into Liquid IV. Thanks again.