FOLFOX #1


Gail
Comments
-
Oh Gail:
Fear of the unknown and how this chemo will affect you is so very human. Very difficult sitting there watching the infusion, try and nap or read or simply talk to others in the lab and it will be over before you know it. Get lots of rest and fluids when you get home. I sincerely hope the side effects are minimal for you. Reading our experiences will prepare you for any side effects.
Wishing you continued healing - Tina & George0 -
Good luck
You'll do fine. Thanks to this site you won't be caught off guard with the possible side effect symptoms. I'll be hoping for an uneventful and easy round for you. Hydrate, hydrate, hydrate. That seems to be what most end up in the ER with when it comes to chemo - dehydration. Just be careful not to drink anything cold! And watch you first bite of food. Some have a sudden jaw pain with it but, if you keep chewing it goes away. And above all ... stay warm especially hands and feet. HUGS0 -
Folfox
As others mentioned hydrate well. The side effects aren't so bad at first, except for the intolerance to cold, especially cold liquids, and the first bite syndrome ( the jaw spasm). I found that by clenching my jaw first before chewing the fbs wasn't so bad. I hope you live in a warm state. I'm in Minnesota so it was pretty much covering everything up when going outside. The side effects do become more cumulative, especially the numbness in the hands and feet but be sure to talk to your onc as you go along and she/he can help.
Keep at it, ****0 -
Treatment
Hope that it all goes well for you. You can do it, I'm sure of it. If by chance you get vision problems that can happen too but it will get better.
Kim0 -
Folfox Club
Welcome to the Folfox Club where no one wants to be. React to your side effects as they come don't be a tough about it. Folfox has a way of changing side effects on you just as you get use to the ones you had. Let the adventure begin and start killing the beast. Hugs Lou0 -
oxy ClubLOUSWIFT said:Folfox Club
Welcome to the Folfox Club where no one wants to be. React to your side effects as they come don't be a tough about it. Folfox has a way of changing side effects on you just as you get use to the ones you had. Let the adventure begin and start killing the beast. Hugs Lou
Lou do you have to be a current user of the drug oxy to belong to the club.
I am one and onehalf years out of oxy and I would like to apply for membership please
lol.....you must need some old timers......
Christmas Hugs....
maggie0 -
Welcome to the club
Take a good book.
I took my laptop and did some posts while getting infused.
Then I feel asleep.
Hope it goes well.
Pete0 -
Gail, good luck and don't think aboutpete43lost_at_sea said:Welcome to the club
Take a good book.
I took my laptop and did some posts while getting infused.
Then I feel asleep.
Hope it goes well.
Pete
side effects,I was on Folfox last year and was manageable to me!.
Cheers and Hugs!0
Discussion Boards
- All Discussion Boards
- 6 CSN Information
- 6 Welcome to CSN
- 122.1K Cancer specific
- 2.8K Anal Cancer
- 448 Bladder Cancer
- 309 Bone Cancers
- 1.6K Brain Cancer
- 28.5K Breast Cancer
- 398 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
- 673 Leukemia
- 795 Liver Cancer
- 4.1K Lung Cancer
- 5.1K Lymphoma (Hodgkin and Non-Hodgkin)
- 239 Multiple Myeloma
- 7.2K Ovarian Cancer
- 65 Pancreatic Cancer
- 490 Peritoneal Cancer
- 5.5K Prostate Cancer
- 1.2K Rare and Other Cancers
- 543 Sarcoma
- 738 Skin Cancer
- 658 Stomach Cancer
- 192 Testicular Cancer
- 1.5K Thyroid Cancer
- 5.9K Uterine/Endometrial Cancer
- 6.3K Lifestyle Discussion Boards