Jaw pain
Tim
Comments
-
Hi Tim,
Yes, I was on Folfox 4, and my jaws would almost lock at times. It would go away after a few seconds, but it was scary at first. I took the entire 12 treatments and am happy to say that I have no lasting side effects. I just celebrated my one year mark post chemo!
Kay0 -
Oh yeah Tim,
I've totally had that. It's from the oxaliplatin, and it's very unpredictable. Sometimes when I start to eat something or drink something quickly, my jaw gets really crampy, near the back of the jaw, and then it goes away after a few seconds. It's a weird side effect, but I have had it before so don't think you are alone!
Rodney0 -
Yes. Exactly as you describe. I call it a jaw spasm. Last just a few seconds. It's a side effect of the oxaliplatin. For me, it starts on day 1 of oxalitplatin, and lasts for a few days after the infusion (as least, so far -- I'm only on tx #4). I get it every time I first take a bite or sip -- doesn't seem to matter what food/drink. But, if I am having a whole meal, it is only that first bite. It suprises me every time (I'm a slow learner!). Oddly, my oncologist never mentioned this to me -- I had to mention it to him.
Good luck with it.
Tara0 -
Thanks for your responses all, thought it was a little weird. Also, did you all have the sensation to cold ? if so when did it set in ? I haven't noticed it yet, maybe i will get lucky on that one. Take care all.
Tim0 -
Tim:
That happened to me too. I noticed it occurred to me right after my infusion. It seems to me that it only lasted a day or two and things returned to normal, until my dose...
Buster0 -
Hi Tim -Firefighter35 said:Thanks for your responses all, thought it was a little weird. Also, did you all have the sensation to cold ? if so when did it set in ? I haven't noticed it yet, maybe i will get lucky on that one. Take care all.
Tim
As everyone else has said, the oxaliplatin does cause the sensation you describe. Very wierd.
I experienced virtually no cold sensitivity after my first treatment. However, just had my second treatment this past Monday and the cold sensitivity is MUCH more pronounced.
One of the nurses told me of a patient who went home after treatment and ate a Klondike bar - his face froze up so much he almost couldn't talk!
Betsy0 -
Hi Tim, that oxaliplatin was the pain in the butt for me caused jaw pain teeth pain sores in month tingling and numbness(sp) in hands and feet neuralgia(sp) of the face high blood pressure, burning eyes and inside of my nose. If I cried the pain was terrible to make a tear. Boy I tell you every other week I had a different side effect from this drug, They subsided in a few days still have tingling and numbness of hands and feet. Reason I know oxi caused the problems is because I had all the other drugs before and didn't have any side effects. But remeber everyone is different.0
-
I'm finishing up round 4 and haven't had the sensation to cold yet (well, hardly -- an occasional twinge but nothing to speak ot). I'm avoiding cold food/drinks during and after the chemo just in case.Firefighter35 said:Thanks for your responses all, thought it was a little weird. Also, did you all have the sensation to cold ? if so when did it set in ? I haven't noticed it yet, maybe i will get lucky on that one. Take care all.
Tim
Tara0 -
Yeppers
On the jaw pain when I was on Oxi for the first few bites, and yes on the cold sensation, some people are lucky on the cold thing, apparently you're one of the lucky ones!!0 -
Jaw Pain
i know there haven’t been any recent post on this topic but I was glad to see the post still here about jaw pain. I have had 2 FolFox sessions and I am having the same pains with the first few bites of food. Knowing it is going to happen helps to work through it.
0 -
CommonFolfox1 said:Jaw Pain
i know there haven’t been any recent post on this topic but I was glad to see the post still here about jaw pain. I have had 2 FolFox sessions and I am having the same pains with the first few bites of food. Knowing it is going to happen helps to work through it.
It's common and very annoying at times. It gets better after stopping treatment but after 10 years once in awhile I'll still get it and have to pucker up to stop the chills from going down me. It would be nice if you could start a new thread and introduce yourself. Welcome to the board.
Kim
0
Discussion Boards
- All Discussion Boards
- 6 CSN Information
- 6 Welcome to CSN
- 121.8K Cancer specific
- 2.8K Anal Cancer
- 446 Bladder Cancer
- 309 Bone Cancers
- 1.6K Brain Cancer
- 28.5K Breast Cancer
- 397 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
- 671 Leukemia
- 792 Liver Cancer
- 4.1K Lung Cancer
- 5.1K Lymphoma (Hodgkin and Non-Hodgkin)
- 237 Multiple Myeloma
- 7.1K Ovarian Cancer
- 61 Pancreatic Cancer
- 487 Peritoneal Cancer
- 5.5K Prostate Cancer
- 1.2K Rare and Other Cancers
- 539 Sarcoma
- 730 Skin Cancer
- 653 Stomach Cancer
- 191 Testicular Cancer
- 1.5K Thyroid Cancer
- 5.8K Uterine/Endometrial Cancer
- 6.3K Lifestyle Discussion Boards