Anyone starting chemo in Aug. 08?
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Copied and pasted from 'AOL ONLINE':
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ANTICANCER DIET
Seasonings:
Turmeric
Found in curry powder, this spice is the most powerful natural anti-inflammatory available today. It encourages cancer cell death, inhibits tumor growth, and even enhances the effectiveness of chemotherapy. Some research shows that turmeric is most effective in humans when it's mixed with black pepper and dissolved in oil (olive or canola, preferably). In store-bought curry mixes, turmeric represents only 20% of the total, so it's better to obtain ground turmeric directly from a spice shop.
How to Use It:
Mix a teaspoon of turmeric powder with a teaspoon of olive oil and a generous pinch of ground black pepper and add to vegetables, soups, and salad dressings. Use a tablespoon if you already have cancer. If it tastes too bitter for you, add a few drops of honey or agave nectar.
Ginger
Fresh ginger, or ginger root, is a powerful anti-inflammatory that combats certain cancer cells and helps slow tumor growth. A ginger infusion can also alleviate nausea from chemotherapy or radiotherapy.How to Use It:
Add grated fresh ginger to a vegetable stir-fry or fruit salad. Or, make an infusion by slicing a 1-inch piece of ginger and steeping it in boiling water for 10 to 15 minutes; drink hot or cold.
Japanese Green Tea
Green tea is rich in compounds called polyphenols, including catechins (and particularly EGCG), which reduce the growth of new blood vessels that feed tumors. It's also a powerful antioxidant and detoxifier (activating enzymes in the liver that eliminate toxins from the body), and it encourages cancer cell death. In the laboratory, it has even been shown to increase the effect of radiation on cancer cells.
How to Drink It:
Sip 2 to 3 cups a day within an hour of brewing. Green tea must be steeped for at least 5 to 8 minutes -- ideally 10 -- to release its catechins, but it loses its beneficial polyphenols after an hour or two.
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Enjoy!!!!
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Thankyou for sharing that Roya, Very cool info. I started greentea extract (pill form)a week or too ago, its supposed to help with weight loss too. Baby weight be gone
Chelli-I am so sorry to hear about your friend, and that your in the hospital (if still there) or were. I am thankfor you were able to get a laptop working in your room. Your in my prayers.
Anybody else getting red from rads? A bit intimidating, but not painful.
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Thanks for the info' on Woolite, Bette. I think I'll try that over the weekend. When I bought my wig, they told me it only needed washing every 20 or so wearings. I've worn it very infrequently -- a baseball cap just seemed more comfy to me -- and I haven't worn it for more than 2 or 3 hrs. at a time, like when we've gone out in the evening. But now that it's turned so cold this week, I've been wearing it more. (Just didn't want you all to think I've been wearing that thing since August without washing it!!! LOL!)
Roya, thanks for the anti-cancer diet info. I bought some curcumin capsules in a health food store because I'm not crazy about the taste of tumeric. Hopefully, they'll be just as good as cooking with it. I've also added green tea to my diet, but I didn't know about the ginger. Guess I'll have to remember to use that too now.
How's everyone doing with their holiday stuff? I was out shopping tonight and actually felt kind of "normal," (a great feeling!), although I still get tired more quickly than I would have pre-bc. Deanna
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I have all my presents except one that hasn't come wrapped and under the tree.
It is Saturday post chemo and so far so good. Just tired and achy, but Tom is here taking care of me . If we get through tomorrow with no fevers it will be a welcome milestone.
Bette
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Bette, how is the neuropathy in your feet healing? Mine seems to be getting worse before it gets better. My finger tips feel about the same.
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For all doing rads, or soon to be, I found some deodarants to use that are alluminum free (thanks to an old post on here). Crystal (which is what my dr recommended),,,Dr.Mist, Tom's of Main, and Alba-lavender. I read that Vitamin World, and Walmart carry some of these products. I am going to go look for the Dr's Mist, and Crystal tomorrow at Vitamin World. I am tired of stinking LOL. Its funny it has taken this long to get to me
I got a nice dress for Christmas,,,and would like to smell nice too
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I haven't started radiation quite yet, but since my mastectomy in June I've been using Adidas absorbent-deo. It doesn't have aluminum and seems to work pretty well.
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Well girls I used Tom's of Maine when I was going through rads and it felt kinda sticky but it was better than nothing. I am not one of those girls who can go without!!! LOL Well I went to church yesterday with nothing on my head. Kids said I looked great so I went for it. Walked in and right off the bat some "old man" says LOUDLY "that is some kind of haircut" - I wasn't sure if I wanted to laugh or cry. My 13 year old daughter CAME UNGLUED. I told her not to worry about it and had to laugh and she said VERY louldy - "Old or not - that was rude and if he isn't sure of someones situation he should shut up"!!!!! My kids are VERY respectful to EVERYONE and I had to laugh cause I looked at her and said Ali - really it is ok I don't care what he thinks and she spouted off - I DON'T CARE WHAT HE THINKS EITHER - HE IS OLD, RUDE AND JUST PLAIN IGNORANT! Guys I have to tell you I wanted to yell at her but I just couldn't! I about died laughing cause I thought my 13 year old was going to whoop some behind right in the middle of church!!!! I finally got her clamed down and told her not to worry about it - the ONLY people I cared about what they thought was her, Gunner and my hubby and my family. They all said go for it and that was all that I cared about. Got a lot of other good compliments about how good I looked so it made up for it. Still felt great going out without anything to cover up my head!!!!!!!!!!!!! Had to share with you all cause I knew you would appreciate it!!!!! Loves to all..............
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Way to go, Alibug!! My DH would love me to do this. I am just not ready yet because of my work situation. I am off for two weeks now, so I hope to get some growth without wearing the wig around the house!!
Have any of you joined Susan Love's "Army of Women"? I sent out a message to all my girlfriends last night encouraging them to join. Google it and you will see what I mean.
~misty
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Thank you Lisa, Deanna & Misty for your support. I'm in tears today. Taxotere's got my joints so achy. I feel like $%!@. Also getting those hot flashes. I'm a mess.
I feel like you Lisa, my entire being is in God's hands and this thing can surely come up somewhere else. I don't want another surgery! (Nor the consequences). I'm done w/babies though so just need to decide.
Misty: I saw Dr. Susan's Love, Army of Women study and it's great. We definitley need to get a grip on this disease ASAP.
Love to all,
Jeannine
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Oh, Jeannine-sorry to hear you are having a bad time wtih the joints. How many more TXs do you have? I get the hot flashes over night. Last night, my DH was actually rubbing my cute 1/2" of hair and I started to get one. He couldn't believe how hot the top of my head got. After a moment, it went away. Have you been walking or working out? I know it sounds painful, but you might get some relief if you stay active. I hope they go away soon!!!! Take care!!!!
~Misty
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Jeannine ~ You have been through so much, and you are so strong. I know it's hard, but if you can, try to focus on how far you've gotten, and try to leave the next decision for after the holidays. No doubt your mind will still be working subconsciously to help you figure it out, but I think you need a break from all the mind-boggling "what if's..."
My sister, a bc-survivor and RT research administrator, keeps reminding me that it takes months to recover from chemo and surgery. The timing she often quotes is a month for every hour of surgery, and a month for every month of chemo. My chemo was Taxotere+Cytoxin, so I know what you mean about major body aches, some of which I'm still experiencing 10 weeks out. But I firmly believe our bodies will heal and renew themselves with time. My bc survivor friends all talk about how hard the first year after tx was for them, but none of them have any lingering SE's several years out.
Alibug ~ I loved your story. Those moments can be so funny -- when part of you wants to correct a child (or at least calm down their behavior), and the other part of you is falling apart laughing or trying not to laugh. Your daughter sounds fiercely protective of you! Did the folks @ church know about your bc?
Misty ~ Love the Army of Women -- great focus on finding the underlying causes of bc. Hey, are you still coming out here in March? I haven't heard a word from Gail. I guess I'll call her and see how she's doing. How did your holiday party go?
(((Hugs))) to all ~ Deanna
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Hi girls! Rough day here. We had to put our dog down today. We have had him for almost 13 years. Actually, he was born the day we got married (also dh's bday) and we got him 3 weeks later. He had been sick for 2.5 years with insulin dependent diabetes and had gone blind. He went into organ failure this weekend. Makes for a rough holiday.
Can't go without head cover yet as it is too cold. My dh and bro in law both said I looked like Sinead O'Connor. It was said lovingly so I had to crack up. My youngest dd told me today that I had a buzz cut!
Halfway mark with rads and really no problems yet. I will go tomorrow and Wed. then get a break until Monday due to the holiday.
I am having some rather painful joints and muscles after TAC. Feels like arthritis or like I am 90 instead of 38!! I need to start working out. I did pick up golf clubs for the first time in 14 years on Saturday. Felt really rusty, but great at the same time. Especially when I picked up an oversized driver for the first time ever and did better than my dh!!
Hugs to all!
Stacy
**If you are on facebook look me up Stacy VanDermeer Robinson and I will add you to my friend list! It is a great way to keep up outside of bc!
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So sorry to hear about your dog, Stacy. I can empathize because we had the same experience about a year ago. They really are a part of the family, especially when you've had them that long.
I'm empathizing with the joint & muscle aches, too, which Jeannine also mentioned dealing with, as are some gals on the TC board. Yikes, I'll be glad when we are all past this stuff and back to whatever the new normal is going to be, which I hope and pray will NOT include any of these aches and pains. I just think it takes more time than anyone told us to get all of this stuff out of our bodies and get them built back up again from the damage done by the chemo. I guess we can start thinking of 2009 as the year of rebuilding.
Love your new avatar! Deanna
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Oh, STacy, I am so sorry about your dog. I'll be thinking about you. Your new pic is great!! Good for you for getting out there with golf. I think any type of exercise will help you feel better.
Deanna, yes I am still coming out to Palm Desert on 4/1 (evening). We'll touch base about this soon-haven't heard from Gail in a while.
Hope everyone is getting ready for the holidays!! Should be a good one this year.
`misty
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Bumping us up...Thanks for the wishes for our sweet Trouble dog! We do miss him!
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Stacy I'm so sorry about your dog. We had to have our old dog put to sleep about a year and a half ago. I stll expect to see her lying on the floor.
I went for my radiation set up this morning. It went well and quickly. I'm still not sure when I'm starting - I was given an appointment for the 1st one on Jan 7th, but by the time I got home there was a message saying they gave me the wrong date and to call back, I called and just got voicemail. They're probably off for the holidays now!!
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Bump!
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Hi y'all, Just wanted to sign in. Been praying for all of us. Start my Herceptin only on Monday. Also starting Tamoxifen. i was told that Tamoxifen causes severe hotflashes. Is anyone here on that and what are you doing about the flashes? I was also asked if I wanted to be on a trial of bosphosphinates. Is anyone here in that trial and what are you experiencing for SE's/ Going to a friends tonight for Christmas Eve and staying home where my kids come to see me tomorrow. i want to wish everyone a VERY MERRY CHRISTMAS!!! Love to you all, Corinne
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Just released from the hospital on Christmas Eve! What a great present!
This was a three-day stay for neutropenia. Tom has been great, sitting up with me all nights with fevers and body aches and transporting me to the ER and keeping me company through those long hours.
I am finding also that my body aches from the Taxotere I got last week. I do not feel like doing much, so it is good the Christmas stuff was completed last week.
My plan tonight is to hang out on the couch and let others take care of me. Maybe next year I can be a gracious hostess once more.
Most of all, I will be still before God, and celebrate the coming of Christ quietly and joyfully, as God has brought me safely through so much this year.
A blessed Christmas to all.
Bette
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Jeannine, don't hesitate to ask your doc for pain meds if you need them. I asked for something and I got something similar to what you call Vicodin in the US. I had already been using vitamin B and other remedies but sometimes we need more. You should not have to suffer!!!!!I know that those can get very very intolerable!
Lisahugs, sending much love and many blessings to your little Ella...her very first Christmas!!!
Stacy, I am so sorry about the loss of your dog. I agree with Deanna, in that it is really like losing a family member.
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Wishing you peace, love & joy.
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To all my bc sisters here ... Just stopping by to wish you all a beautiful Christmas (or Chanukah), and more than anything, the blessings of love and good health in the coming year ~ Deanna
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Merry Christmas everyone! Here's to feeling good all day! Love, Deen
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Hey All!! A Merry Christmas to all of the wonderful women here. I have enjoyed making so many new friends this year.
Corinne-You will love getting the Herceptin by itself-I treat it like going to a spa for 90 min. I read, relax, and catch up with the nurses! I have been on the Tamox for exactly four weeks. I do get some hot flashes over night. But, they are not too bad. I wake up for a bit, but then fall back to sleep. There are some nights I do not get them at all. Good luck!!! I go for my next Herceptin dose tomorrow.
~Misty
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Merry Christmas to all my Hot Baldy Beautiful Sisters!
Well I've got the flu! Yuk...
That explains some of the joint, achy pain I had. Achiness has subsided. Now it's this nagging cough. Spent X-mas Eve at home watching movies. Also not going no where tonight. Too cold in CA! BUT I am headed to Las Vegas this weekend and I'm going to enjoy everything!
I'm happy you're home Bette. And YES Roya, I've got my Vicodin!
Wishing everyone a blessed Christmas, and HEALTHY 2009!
Love,
Jeannine
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Merry Christmas everybody! Hope you had a nice Christmas Day. I've had a quiet one, stayed home with my daughter while hubby went visiting his side of the family. Mine is coming here today.
Hubby's already invited everybody to our place for next year, we should be in a big new house by then!!
I've noticed achy muscles in my legs the last few days, not sure if it's fromChristmas shopping or Taxotere, I hope it's not the flu coming on - didn't get my flu shot yet!!! Jeannine, hope you feel better and maybe Las Vegas will dry out your cough - have fun!
Bette, I hope you're doing better and were able to enjoy the day.
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Happy Holidays BC Sisters! I hope everyone had a good one. Many blessings and best wishes to all. Stacy so sorry about your lost. Deanna your an amazing woman and very strong mentally I really admire that. As for me girls I still have swollen hands and ache joints and I don't think i'm getting the flu. Lots Of Love, Karen
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Hello all!
Tom and I celebrated our Christmas today. We had breakfast out, picked up our wedding invitations (it's in print!) and came home to a long lazy afternoon of openiing presents and enjoying a meal together.
I had a minor meltdown on Christmas when I saw some pictures my brother took of me and family. I've changed so much! Significant weight gain, pale puffy face with no eyebrows. It's no wonder my mother didn't recognize me(who's that man over there?)
Today I compounded the injury by deciding to measure myself to order some clothing online. I burst into tears and ran straight into Tom's arms, where I stayed, being comforted the rest of the evening.
We decided on a plan of action. He will start walking with me on a daily basis whenever he is here. I will use the fitness center on the off days. AND tomorrow I am going to weigh in and restart Weight Watchers Online. It worked really well for me two years ago. I am going to work it again.
Now that I am finished with the steroids, perhaps I can lose some of this puffiness. And Yes, sick as I was, I should have put on makeup and drawn on some eyebrows for the pictures.
Chemo is over. I have to look forward and do the best I can to overcome some of the effects it has had on me.
But I am definitely showing some peach fuzz. Straight down the middle of my head and on the sides. If it grows in that way I will have a natural "chemo mohawk"!
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Bettelou68 it's been about 3 months since my last chemo and I know how you feel. I haven't lost any weight and I also have cried and feel very bad that i'm not my self. I know that we should be happy that we are alive they say but they just don't understand how we feel. My hair is growing it's about 1 inch long and get this, it's coming out white!! I know that i had a couple of white hairs but OMG 80% is white. I know that all this is temporary but it still hurts. Last week I saw a male friend at the gym and he just walked by me because he didn't recognize me. I felt so awful that I never went back. I also see people I know and they say Oh I didn't know that was you. We need to stay strong and all this will soon be behind us sooner or later. God willing! When my hair started growing, I didn't shave my legs for a long time because i was so happy to have hair. Then it got to scary so I had to shave them. I hope that you start to feel better soon!!!
Lots Of Love, Karen
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