FAQ/Help |
Calendar |
Search |
Today's Posts |
|
![]() |
#1 | ||
|
|||
Junior Member
|
New to site. Found this forum out of frustration. Had chemo for breast cancer. The lump was right on the size line between chemo or no chemo needed. I was scared and confused at the time and I feel the doctors pushed me right into it. Half way thru I started getting numbness in hands and feet. Was told not to worry, that was normal and it would all go away after treatment To make a long and painful story shorter, it is now 5 months after chemo and not much improvement. The doc is still saying "don't worry, be happy - it will all go away in 6 months after treatment"
This is all going away in another month ? I don't think so !!! My face, head & back all feel like I am wearing a latex glove (can feel most things but not the light surface touch). Fingers are slightly numb (the only part of my body that has improved a bit). Feet are lumpy and legs from ankle to above the knees are surface numb. Take b vitamins but I don't know how much it is helping - afraid to stop to see if it gets worse. I can handle lumpy feet & fingers that don't feel quite right - I just want all the surface numbness to go away. |
||
![]() |
![]() |
![]() |
#2 | |||
|
||||
Wisest Elder Ever
|
There are studies showing that acetyl carnitine may be helpful during and after chemo treatments.
Some doctors know this and others not, or don't believe it and don't offer it. I also know two women which breast cancer who used flax oil mixed with cottage cheese (to provide amino acids with sulfur), to make the chemo less damaging, and one of them used this to prevent a metastasis. Here is one post from ~Pansy~ http://neurotalk.psychcentral.com/sh...967#post238967 The dose of acetyl carnitine (which is over the counter) is often 2 grams a day. Take in divided doses. This helps with the DNA damage from the chemo which occurs in your good cells, including nerves, so that the mitochondria can work better. This is just one of many articles about it: Quote:
You can Google acetyl carnitine chemotherapy induced neuropathy and read more.
__________________
All truths are easy to understand once they are discovered; the point is to discover them.-- Galileo Galilei ************************************ . Weezie looking at petunias 8.25.2017 **************************** These forums are for mutual support and information sharing only. The forums are not a substitute for medical advice, diagnosis or treatment provided by a qualified health care provider. Always consult your doctor before trying anything you read here.
|
|||
![]() |
![]() |
"Thanks for this!" says: | MelodyL (07-05-2013) |
![]() |
#3 | ||
|
|||
Junior Member
|
Thanks, I have never heard of that one. I do eat a lot of cottage cheese. Never thought to add flax. Will pick up others at drug store tomorrow. I am ready to try anything !!!
|
||
![]() |
![]() |
![]() |
#4 | |||
|
||||
Wisest Elder Ever
|
Flax oil (not capsules) typically is not in drug stores.
Mostly health food stores, in the frig. Capsules are more expensive, since you are going to use about 2 tablespoonfuls at a time. You can also make salad dressings with the oil, and also smoothies. Acetyl Carnitine will be much less expensive online (sometimes more than 1/2 the cost online compared to local stores). NOW makes a good affordable type. This tends to be pricey however, so expect that. The most expensive you will probably find locally is at GNC...so you want to avoid that if possible. You can check iherb.com or Amazon for some savings.
__________________
All truths are easy to understand once they are discovered; the point is to discover them.-- Galileo Galilei ************************************ . Weezie looking at petunias 8.25.2017 **************************** These forums are for mutual support and information sharing only. The forums are not a substitute for medical advice, diagnosis or treatment provided by a qualified health care provider. Always consult your doctor before trying anything you read here.
|
|||
![]() |
![]() |
![]() |
#5 | |||
|
||||
Member
|
I had hand foot syndrome ALL over my body. Numbness, clumsy, lost every nail, peeled like a bad sunburn ALL over. The numbness is pretty much gone, last treatment was Oct 16. Good luck!!!!
__________________
Barb |
|||
![]() |
![]() |
![]() |
#6 | ||
|
|||
Junior Member
|
Barb - Thank you, thank you, thank you - No one else at the clinic had numbness as bad mine. Doctors act like I am faking it. They are (or pretend to be) totally clueless about how bad they fried me. My last chemo was Feb. 15th.
Did the worst go away gradually or all at once? The docs keep telling me it will ALL be gone in in another month or two. There has been very little improvement in the first 4 1/2 months. Did yours continue to improve after the 6 month window for most improvement? I seem to take 2 steps forward and one (sometimes 2) steps back. I never know what I will feel like when I get up in the morning. Any information or stories you could tell me would be greatly appreciated. I really need someone to talk to that understands. |
||
![]() |
![]() |
![]() |
#7 | ||
|
|||
Junior Member
|
lol - I forgot to mention the fingernails. Walked around with band aids taped around mine so they wouldn't come off before the new growth got a good start.
|
||
![]() |
![]() |
Reply |
|
|
![]() |
||||
Thread | Forum | |||
Health Advice for Peripheral Neuropathy & Drug Induced/ Toxic Neuropathy | Peripheral Neuropathy | |||
Hubby has neuropathy of feet due to chemo... | Peripheral Neuropathy | |||
Chemo Neuropathy | New Member Introductions | |||
Chemo neuropathy | Peripheral Neuropathy | |||
Neuropathy from Chemo | New Member Introductions |