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surgery
Hi, I can't be much help because I did my surgery first followed by chemo. I know I have read other posts where there was chemo, surgery and then more chemo. I'm sure when somebody sees your post they can tell you something more helpful. Is there something you can take for you neuopathy. I know I've seen posts where some are taking something for that and it really helps. Maybe you could try something like that. Lots of good luck. Patty0 -
try maggagessofarstillhere said:surgery
Hi, I can't be much help because I did my surgery first followed by chemo. I know I have read other posts where there was chemo, surgery and then more chemo. I'm sure when somebody sees your post they can tell you something more helpful. Is there something you can take for you neuopathy. I know I've seen posts where some are taking something for that and it really helps. Maybe you could try something like that. Lots of good luck. Patty
my doctor just told me to try massaging my feet and to make sure to moisturize them, it seems to help some. also have you tried glutomine, i have heard it helps. I read that antidepressants also help some as well as neurontin. I do not like to take meds, so have not tried them, but the massing is helping some, by the way it has been a year since my last chemo and still have the neuropathy, but I am alive and i am thankful0 -
Chemo after surgeryazgrandma said:try maggages
my doctor just told me to try massaging my feet and to make sure to moisturize them, it seems to help some. also have you tried glutomine, i have heard it helps. I read that antidepressants also help some as well as neurontin. I do not like to take meds, so have not tried them, but the massing is helping some, by the way it has been a year since my last chemo and still have the neuropathy, but I am alive and i am thankful
I had three rounds of chemo prior to surgery (taxol/carboplatin)one infusion every three weeks. Had surgery about five weeks later than about five weeks after that had three more rounds of chemo consisting of three infusions per round. Day one taxol, day two cisplatin, day eight taxol again. Then same thing two weeks later. Day one and two were administered through a port in my abdoman and day eight intravenously. Surgery was 6/21/2010 and last chemo was 9/15/2010. I have nueropathy in hands and feet but not too bad. What is really bothering me is aches in my shoulders, knees and thighs.
Karen0 -
chemo after surgerykikz said:Chemo after surgery
I had three rounds of chemo prior to surgery (taxol/carboplatin)one infusion every three weeks. Had surgery about five weeks later than about five weeks after that had three more rounds of chemo consisting of three infusions per round. Day one taxol, day two cisplatin, day eight taxol again. Then same thing two weeks later. Day one and two were administered through a port in my abdoman and day eight intravenously. Surgery was 6/21/2010 and last chemo was 9/15/2010. I have nueropathy in hands and feet but not too bad. What is really bothering me is aches in my shoulders, knees and thighs.
Karen
Karen,
Thanks for the reply. You have had a lot of chemo. I'm glad to h ear your neuropathy is not too bad. When I had pains in my joints and in my legs, the doctor prescribed a Medrol dose pack. You take 6 pills the first day, then 5, then 4, etc. However, I took this after a chemo treatment so I don't know if it would work for you but you might want to ask the oncologist. I have read on the discussion board under Long Term Effects of chemo that these pains are one of the side effects of taxol/carbo. There was one suggestion that said to get a tempurpedic mattress and that will help you sleep. Do you take anything for the aches?
Chris0 -
Chris,
you might want to ask your doctor about using taxotere this time. It is reported to be a bit better for the neuropathy in some studies. I am a 31/2 year survivor and have had lot of chemo. I do have nueropathy in my feet, that is permanent. I do notice a difference when I can excersise regularly and get to have a break from chemo. I have chosen to get treatment in spite of the neuropathy. Fortunately, I don't have any pain, just a lot of clumsiness and tingling. I have tried many things including lyrica. Right now I am using a Japanese herb which seems to help a bit.
Wishing you wisdom as you decide about your treatment going forward.
kathleen0 -
Memory Foam is Great!cfont11 said:chemo after surgery
Karen,
Thanks for the reply. You have had a lot of chemo. I'm glad to h ear your neuropathy is not too bad. When I had pains in my joints and in my legs, the doctor prescribed a Medrol dose pack. You take 6 pills the first day, then 5, then 4, etc. However, I took this after a chemo treatment so I don't know if it would work for you but you might want to ask the oncologist. I have read on the discussion board under Long Term Effects of chemo that these pains are one of the side effects of taxol/carbo. There was one suggestion that said to get a tempurpedic mattress and that will help you sleep. Do you take anything for the aches?
Chris
Hi, Chris. My husband and I have been using a 2.5" memory foam mattress pad for years, and it has reduced many of our aches and pains. I highly recommend it. The pad is a lot less expensive than the entire mattress, but if you can afford it, then go for the whole thing. Even with the "marshmallow" bed, I was unable to sleep in a bed for the week following chemo. We bought a recliner, and that helped me a lot, as I could be on my back without the stress of lying flat. If you think a recliner might help, I suggest you find a store with a variety of brands and styles and try them out. I thought I knew what I wanted until I got into it.
DB0 -
Painkayandok said:Chris,
you might want to ask your doctor about using taxotere this time. It is reported to be a bit better for the neuropathy in some studies. I am a 31/2 year survivor and have had lot of chemo. I do have nueropathy in my feet, that is permanent. I do notice a difference when I can excersise regularly and get to have a break from chemo. I have chosen to get treatment in spite of the neuropathy. Fortunately, I don't have any pain, just a lot of clumsiness and tingling. I have tried many things including lyrica. Right now I am using a Japanese herb which seems to help a bit.
Wishing you wisdom as you decide about your treatment going forward.
kathleen
Chris,
I have only taken tylenol so far. I emailed my onco to ask for suggestions and she referred me to my primary saying it may be arthritis. I am a little confused by this because I did not have arthritis before, so is she now suggesting I suddenly have it in several areas of my body? I really do not want to take any drugs unless it gets intolerable. I think my body had enough with the chemo and after reading that it effects the liver I am less receptive to taking anything. But having said that I just took a couple of extra strength Tylenol and it states it can effect the liver. We can't win can we?
Karen0
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