Cancer Diet and Supplements, etc.
Greetings all, Am a month into my diagnosis (ILC, ER-, PR-, Her2+, Oncotype DX 37%, two tumors 2.5 cm and 8 cm area of calcification) and am searching for a family diet and supplements to go with my chemo. Is there a source where I may find information on transitioning my family to a diet similar to a cancer diet that they will actually eat?
Also, curious about wigs. Are they really necessary?
Is there a list of Chemo drugs? Why is one chosen over another with hundreds available?
Blessings ![]()
Comments
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There are soooo many great resources available. Two of my favorites are Beating Cancer with Nutrition by Patrick Quillin and Anti-Cancer. Both can be found at Amazon.com. Most oncologists will discourage you for taking certain nutriants during chemo because they are concerned that they will protect the cancer cells. However, they may not discourage eating nutrient rich foods. It is best to check with them about specific things to avoid.
I did not have chemo, but several of my friend did. There are beautiful wigs available but whether you need one is a matter of choice. Some find that the scarfs and hats available are a good choice while others prefer to have a wig or two. Before my onco test results, I did some window shopping for wigs online and found some beauties that I would have ordered if chemo was ordered.
Hopefully, you will hear from some of our post chemo sisters who can give you personal experiences.
Roseann
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Hi SamsMom,
Just wanted to say hello. I had wigs, hats, and scarves, and used them all during chemo. It depended a lot on how much I wanted to not attract attention. I wore the wig if I wanted to be inconspicuous ( not often ), but most of the time I relied on hats and scarves. They were just so much more comfortable.
I'm afraid I'm not that informed about diets and supplements to take during chemo. It seems that we are discouraged from taking certain ones, so best to check with the oncologist before taking anything. Hope you get the help you need on that from others.
I know that the chemo drugs are chosen according to the characteristics of your breast cancer. Your oncologist can explain to you why he/she has chosen a particular regimen for you. Some of us get second opinions, too, to see if another oncologist would agree.
There is a lot to learn at first. Ask lots of questions! Hugs.
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Sams_MominGA -
I'm so sorry you are joining this club but I'd like to add my welcome to the boards. I hope you've taken some time to look around at the different forums. There are a lot of women and a lot of information.
Check with your oncologist's office or cancer center to see if they have a nutrionist on site. Many do. And I concur with the others that oncs are very careful with what you are taking during chemo. Don't want interactions or anything that might interfer with the chemo or bone marrow's production of platelets, red cells and white cells.
I really can't write more since I have to get ready for my weekly chemo appt. Hopefully this will be my last and I'm going to be on cloud 9 later today. We'll see.
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Christy (AnacortesGirl), I hope SamsMom doesn't mind, but I am going to use her thread to write to you. I just wanted to say that I am hoping that your final MRI shows that the chemo did its job. ILC usually doesn't go away completely, but I am anticipating that you had a fantastic response. It's so great that you got a drug against EGFR/VEGF2 along with your mix. You are absolutely hitting this with everything. Guess they will be letting you rest up and recover before surgery. Let us know how you are doing. All the very best. G.
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I am just starting to check out dietary stuff myself. Books that have been recommended to me on different threads by multiple women are What Your Doctor Doesn't Know About Nutrition...by Ray Strand. Real Food by Nina Planck. Anticancer A New Way of Life by David Servan-Schreiber. Beating Cancer with Nutrition by Patrick Quillin. Worlds Healthiest Foods by Mateljan. I am very cheap, so I checked my local library system on line today and they have all of those books available in one of the county libraries. I've placed a hold on copies (which means that they will send a copy to my local branch and call me when it arrives). I figured I may actually want to buy some, but probably not all. Hope that helps...
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Sams_MominGa -
I'm back to add a few more thoughts.
Your chemo regimen really depends on two things. First, how the cancer presents itself in your breast. Each of us can have slight varitions (amount lymph nodes, which nodes, vascular invasion, amount of diffusion, etc.) that need to be evaluated by the onc. Then he (or she!) is going to recommend a regimen that he's comfortable with and feels is appropriate to get the best results for your presentation. But at this point it is very reasonable and very comforting to get a second opinion. The onc should expect it. You have all the diagnostic information so the 2nd onc can review and either concur with the first or propose a different regimen. In both cases ask the oncs why they feel this is the best regimen. This also gives you an opportunity to find out if you are really comfortable with the onc -- it's a long process and you need to have confidence that you can communicate with the doc and that they relate to your way of thinking and approach to treatment.
Consider a trial if it fits your approach. I was dead set against a trial when I was initially dx'ed. Since then I learned that you always get standard of care during a trial. But, depending on the trial and the phase it is in, you may always get the investigational part of it or you may be randomized. I'm in a phase II so everyone gets the investigation drug -- no blind arm where you don't know.
As for wigs. It really depends on your chemo. A lot of the drugs will cause you to lose your hair. I got one wig through American Cancer Society's TLC catalog. But it doesn't fit that good and the color & style weren't great for me. Many insurances will cover the cost if you have a doc's prescription. Mine doesn't. I went to a wig store and they had lots to try on. I settled for a synthetic and it cost me $125. I've been very happy with it and get lots of compliments (people would walk up to me and tell me they liked my new style!). But, I'm pretty tired of wearing a wig so sometimes I just go the scarf/ball cap route. There are a lot of topics on hair and wigs on the boards.
Gitane -
Thanks for comments. Unfortunately I didn't get my last chemo yesterday. Platelets were at 51. So next Monday is either the last one or, if counts are still low, then I'm finished. I've already met the trial requirements so my data will be included. It was disappointing but the ladies in the stage 3 forum really cheered me up. And I am looking forward to that last PET/MRI so I can find out how much the cancer has been reduced. I'm sure it won't be a complete pathological response but it will be a lot less then the original dx. I'm happy I did the trial.
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