Hair loss on Oxiplatin/5fu
Anyoen loose there hair, doc said yes after 4 treatments, chemo nurses said after 10 days. I had my first treatment Sept 18th, still have my hair and it was my second treatment today, Oct 2nd. I get he oxiplatin infusion for 2 hours and then i leave with the 5fu for two days and them bring the pump back.
Please advise on who lost and who didn't.
Trying to get an average here.
thanks
Carolyn
cheeks917@comcast.net
Comments
-
Carolyn
I had hair thinning, none that people notice on the Oxy and Xeloda. I think the 5fu is just hair thinning as well.
Other may have had different affects. That's just mine. Here's hoping you get to keep your hair!!!!
Winter Marie0 -
hair lossabrub said:From my experience, most don't lose hair on Folfox
double post
Is folfox another form of oxiplatin? I had thinning the 5 fu when i did my first treatment in may I asked the doctor today and he said by the 4th treatment. And the nurse said by 10 to 14 days. I still have it. confused about the folfox. is it the same as oxiplatin/5fu?
please advise0 -
I didn't lose my hair on this,
although I was on an every three weeks cycle, so maybe slightly different? But from what I've seen and read, this isn't one of the big hair loss chemos. Hugs~Ann Alexandria
PS I believe that FOLFOX is 5-fu, oxaliplatin and Leucovorin, so similar to what you are on. Leucovorin isn't a chemo drug and doesn't affect the hair issue, as far as I know.0 -
Nope
Fortunately my hair only thinned, but it was thin before as I've got baby fine hair and thin hair. No one ever new I'd lost hair as no one could tell. Some loose more than others, but when you start out with thin hair and it thin's more your hair still can look normal. Good luck and hope you don't have much more than that.
Kim0 -
Thinned a little.Annabelle41415 said:Nope
Fortunately my hair only thinned, but it was thin before as I've got baby fine hair and thin hair. No one ever new I'd lost hair as no one could tell. Some loose more than others, but when you start out with thin hair and it thin's more your hair still can look normal. Good luck and hope you don't have much more than that.
Kim
Carolyn,
Thinned a little.
Carolyn, you are really stressed. I am so sorry. Try to meditate or try reiki.....it is awesome in how it relaxes you.0 -
Carolyn
I have had 6 of 12 treatments and haven't had any hair loss. We will see - 6 more awful treatments to go.
Sandy0 -
My hair thinned a little
My hair thinned a little during chemo. It started fairly early but did not get much worse after the third treatment. It does come back during recovery.
The worse symptoms are the loss of touch and eye sight. My sense of touch diminished quite a bit. I am exceptionally slow on a ladder. My sight diminshed a bit also. I have reading glasses and lost some distance also.
Best Always, mike0 -
Hair
When on Oxi and 5fu the only hair loss I had was when I cut my long hair to a "respectable" length. I'd planned on running for Congress in my District and figured I needed to get back to looking like a business man instead of a renegade biker. When they put me on Ironitecan in February of 2011 my hair did start falling out in patches. When it got to the unsightly stage, I shaved it all off. After moving to Utah, I started a new drano cocktail and the hair started to come back, but it only grows put to a certain length and stops. I haven't had a haircut in over a year now and it's still short enough that I could pass military inspection.0 -
Hair, Oxiliplatin, 5fu....
Greeting Carolyn
sadly, you'll learn that every question you ask a doctor and then a nurse and then online anywhere... each have different answers. The common answer to most questions: "well, every case is different and everyone reacts to the meds differently as everyone's cancer is different"
If I heard that once I've heard it a 100 times.
but, as for hair... you might lose it, it might thin out, or you might not lose it.
(you catching on?)
it stinks because its such a scary journey and we each want solid answers... and what I've learned is to reduce your expectations... so you're not disappointed.
not sure if this is the right way to attack this stuff... but it has worked for me.
Probably some profession psychologist would say that's negative thinking... when I am truly a Glass Is Half Full type of guy... on the outside. But, internally, it seems like I prepare myself for the bad news, and if the bad news doesn't happen...I feel pretty damn good about things. Well, at least that's how I handled things during the main part of my first rounds of treatments (Dec. 2011 through July 2012)
as for your question on Oxy and 5fu being referenced as FolFox.
I hope I answer this correctly, and if i do not... hopefully someone will chime in and correct me. I had FolFox 6 for 24 treatments. the drugs included Oxiliplatin, 5fu, Leucovorin, Fluorouracil, and then Erbitux was added (but that drug isn't part of the FolFox combination.
so, those two drugs that you are on, are part of the FolFox "Cocktail" of drugs.
google Folfox and you'll find a boat load of stuff. Its been around for a really long time, and they keep adding or improving it.
the Oxiliplatin has many side effects such as neuropathy and the 5fu has its share of side effects... again, EVERY side effect is different for EVERY patient. It's crazy, but its true. Weight loss is obvious one of them... as diarrhea and nausea are constant with all these chemo meds.
the main thing.... Keep you head up and keep your focus.
your objective is to take these meds, and worry about GETTING better!
Laugh about your hair when or if you begin to lose it. try laughing. It helps.
try and be as positive and happy as you can... it makes this battle a lot easier.
i wish you the best in your continued battle.
you'll find a lot of info here... just remember, that each experience is different for each person.
cheers!
Joe0 -
Lost mine in patches on thejoemetz said:Hair, Oxiliplatin, 5fu....
Greeting Carolyn
sadly, you'll learn that every question you ask a doctor and then a nurse and then online anywhere... each have different answers. The common answer to most questions: "well, every case is different and everyone reacts to the meds differently as everyone's cancer is different"
If I heard that once I've heard it a 100 times.
but, as for hair... you might lose it, it might thin out, or you might not lose it.
(you catching on?)
it stinks because its such a scary journey and we each want solid answers... and what I've learned is to reduce your expectations... so you're not disappointed.
not sure if this is the right way to attack this stuff... but it has worked for me.
Probably some profession psychologist would say that's negative thinking... when I am truly a Glass Is Half Full type of guy... on the outside. But, internally, it seems like I prepare myself for the bad news, and if the bad news doesn't happen...I feel pretty damn good about things. Well, at least that's how I handled things during the main part of my first rounds of treatments (Dec. 2011 through July 2012)
as for your question on Oxy and 5fu being referenced as FolFox.
I hope I answer this correctly, and if i do not... hopefully someone will chime in and correct me. I had FolFox 6 for 24 treatments. the drugs included Oxiliplatin, 5fu, Leucovorin, Fluorouracil, and then Erbitux was added (but that drug isn't part of the FolFox combination.
so, those two drugs that you are on, are part of the FolFox "Cocktail" of drugs.
google Folfox and you'll find a boat load of stuff. Its been around for a really long time, and they keep adding or improving it.
the Oxiliplatin has many side effects such as neuropathy and the 5fu has its share of side effects... again, EVERY side effect is different for EVERY patient. It's crazy, but its true. Weight loss is obvious one of them... as diarrhea and nausea are constant with all these chemo meds.
the main thing.... Keep you head up and keep your focus.
your objective is to take these meds, and worry about GETTING better!
Laugh about your hair when or if you begin to lose it. try laughing. It helps.
try and be as positive and happy as you can... it makes this battle a lot easier.
i wish you the best in your continued battle.
you'll find a lot of info here... just remember, that each experience is different for each person.
cheers!
Joe
Lost mine in patches on the Irenotecan/avastin, no 5fu. So just shaved it all off. Was about 4th round.....Nothing like the nueropathy the 5fu caused prev treatments.0 -
Lost mine in patches on thejoemetz said:Hair, Oxiliplatin, 5fu....
Greeting Carolyn
sadly, you'll learn that every question you ask a doctor and then a nurse and then online anywhere... each have different answers. The common answer to most questions: "well, every case is different and everyone reacts to the meds differently as everyone's cancer is different"
If I heard that once I've heard it a 100 times.
but, as for hair... you might lose it, it might thin out, or you might not lose it.
(you catching on?)
it stinks because its such a scary journey and we each want solid answers... and what I've learned is to reduce your expectations... so you're not disappointed.
not sure if this is the right way to attack this stuff... but it has worked for me.
Probably some profession psychologist would say that's negative thinking... when I am truly a Glass Is Half Full type of guy... on the outside. But, internally, it seems like I prepare myself for the bad news, and if the bad news doesn't happen...I feel pretty damn good about things. Well, at least that's how I handled things during the main part of my first rounds of treatments (Dec. 2011 through July 2012)
as for your question on Oxy and 5fu being referenced as FolFox.
I hope I answer this correctly, and if i do not... hopefully someone will chime in and correct me. I had FolFox 6 for 24 treatments. the drugs included Oxiliplatin, 5fu, Leucovorin, Fluorouracil, and then Erbitux was added (but that drug isn't part of the FolFox combination.
so, those two drugs that you are on, are part of the FolFox "Cocktail" of drugs.
google Folfox and you'll find a boat load of stuff. Its been around for a really long time, and they keep adding or improving it.
the Oxiliplatin has many side effects such as neuropathy and the 5fu has its share of side effects... again, EVERY side effect is different for EVERY patient. It's crazy, but its true. Weight loss is obvious one of them... as diarrhea and nausea are constant with all these chemo meds.
the main thing.... Keep you head up and keep your focus.
your objective is to take these meds, and worry about GETTING better!
Laugh about your hair when or if you begin to lose it. try laughing. It helps.
try and be as positive and happy as you can... it makes this battle a lot easier.
i wish you the best in your continued battle.
you'll find a lot of info here... just remember, that each experience is different for each person.
cheers!
Joe
...oops, double post sorry. No delete button?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