Taking Zinc supplement for regeneration of taste
For me, during treatment I did not take the zinc because it is a heavy metal and in conjunction with my Cisplatin (platinum) chemo I was concerned about interaction during IMRT. But, post treatment I am taking 50mg. per day and I think it has helped. I am only 3 months out and my taste has recovered to about 50-60% of pre-treatment. And, it continues to improve. I frequently find new things that taste similar to what they used to. Very encouraging.
Has anyone else heard of or tried Zinc supplements to accelerate taste recovery?
Comments
-
Please remember that every single one of us experiences fear at one time or another. And usually more than once. IT IS HUMAN NATURE. I am a fairly Newbie in that my tonsil cancer was found last July and I had 35 IMRT's and 7 Cisplatin chemos last Sept-Oct. BUT, I can tell you you will get through it. I would love to help you and offer you whatever benefit there might be of my experience(s) but I don't want to tie up the boards here. So, please email me directly by clicking on the small email icon in the lower left of this message box. Also, please check your CSN email and I will send you one directly. Hang in there.......you will beat this.......JKmom674 said:I am about to start chemo(cisplatin) and radiation next week. i had surgery last month. i will ask about zinc post treatment.
ps. really scared.0 -
It has been suggested through direct email to me that you and "we" should correspond here on the boards so that others can contribute and/or benefit. I think that is a great idea. So, please tell us about yourself and your cancer so that we may be somewhat specific in advice and tips. We'll electronically hold hands and go through this together. Trust me, that is what really made a difference for me..........tremendous support from total strangers who had "been there done that". Of course now I consider them close friends even though we have never met. OK........TALK TO US MOM!!mom674 said:I am about to start chemo(cisplatin) and radiation next week. i had surgery last month. i will ask about zinc post treatment.
ps. really scared.0 -
Yes,
I heard that from one doctor.... And saw some things on the internet...
On a related note, found one that said 'green tea extract' did likewise for salivary glands.
Haven't noticed a difference/change.
My 'taste' - I would put it about 50% of what it was before as well. Somethings more than others - e.g. I can taste cucumbers like nothing is wrong - as you know - other tastes - e.g. coffee - barely.
Saliva - maybe about 10% of what it was before.
There is drug that helps 'protect' the salivary glands during radiation. My doc told me that there were 'side-effects' that they don't like using it for that reason. Kinda wish I looked at that more closely at the time.
Best to all.0 -
BTW... CAUTION with ZInc.....stevelfun said:Yes,
I heard that from one doctor.... And saw some things on the internet...
On a related note, found one that said 'green tea extract' did likewise for salivary glands.
Haven't noticed a difference/change.
My 'taste' - I would put it about 50% of what it was before as well. Somethings more than others - e.g. I can taste cucumbers like nothing is wrong - as you know - other tastes - e.g. coffee - barely.
Saliva - maybe about 10% of what it was before.
There is drug that helps 'protect' the salivary glands during radiation. My doc told me that there were 'side-effects' that they don't like using it for that reason. Kinda wish I looked at that more closely at the time.
Best to all.
BTW - DO NOT mega dose zinc or any heavy metal. They are toxic in such dosages!!!!
Sometimes people feel if one is good - two is better - ten is GREAT!!!
NO!!! NO!!!! NO!!!!
Just like the chemo - side effects - too much zinc (or any heavy metal supplement) will have the same effects - hair loss, finger nail weakness/loss, etc...
I think if you do - 50 mg you are all good (daily recommended allowance 15mg) 100 or 200 is probably 'safe' - yet if a doctor didn't tell me to do it - I wouldn't. Anything more than that - I would really question.
Just my opinion - feelings.0
Discussion Boards
- All Discussion Boards
- 6 CSN Information
- 6 Welcome to CSN
- 121.9K Cancer specific
- 2.8K Anal Cancer
- 446 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
- 671 Leukemia
- 794 Liver Cancer
- 4.1K Lung Cancer
- 5.1K Lymphoma (Hodgkin and Non-Hodgkin)
- 237 Multiple Myeloma
- 7.1K Ovarian Cancer
- 63 Pancreatic Cancer
- 487 Peritoneal Cancer
- 5.5K Prostate Cancer
- 1.2K Rare and Other Cancers
- 540 Sarcoma
- 734 Skin Cancer
- 653 Stomach Cancer
- 191 Testicular Cancer
- 1.5K Thyroid Cancer
- 5.8K Uterine/Endometrial Cancer
- 6.3K Lifestyle Discussion Boards