Weight loss during radiation

netter43
netter43 Posts: 110 Member
edited December 16 in Social Groups
Good day everyone!! - I'm newly diagnosed (2/2012) - lumpectomy 3/2012 - just had my CT scan today for mapping my radiation and will be waiting to hear when treatment will start - sometime in mid to end of April - did anyone have any luck with losing weight during radiation treatments or did you all just concentrate on getting through?

I really don't think my body likes the Tamoxifen I've recently started either - I just feel bloated, tired, etc...I know, I'm a whiner.....not really, just feel too tired to even get up and go other than what I have to do to get through my day....

any tips of any kind would be greatly appreciated -

Hugs to all - Danette :)

Replies

  • Gorger
    Gorger Posts: 100 Member
    Hello Danette! Welcome! I'm glad you joined our group.
    Yes, you can still lose weight when you are doing the radiation. A good way is to increase your protein. You will feel more energy.
    The other day I had liver (yuk!) and vegetables for lunch and I felt so energetic! It was amazing. I don't generally eat organ meats but my girlfriend told me that was the answer to her abundant energy (and she has tons) and it worked for me too. I had lots of energy all day.
    To answer your question, the Tamoxifen made me feel as though I was dragging a truck behind me. My solution was to get the smaller dose pills and take 1/2 in the morning and 1/2 at night. You can ask your pharmacist about that. It is not a nice drug to have to take. I managed to take it for 2 years and then quit because it started to affect my eyes. Get your eyes checked when you start the pills and every 6 months afterwards.
    When I was diagnosed with breast cancer I immediately went on a diet and lost my excess weight and to do that I basically ate only 4 things: Fruit, Vegetables, Whole Grains and Beans, ( plus someFish and some Chicken). I learned to cook very well with those food for years. Then I started to drive through McDonalds again and guess what? The cancer came back. Food, weight, exercise are very important. What you have to remember is that it's not how much you eat, it's WHAT you eat. I eat tons of food all day long and am not fat anymore. The trick is to get your bowels moving and that gets rid of the excess estrogen. If you aren't moving your bowels everyday you won't lose weight so easily and you are not eating enough vegetable fibre.
    First...
    What I did is I went through my house and got rid of all the packaged junk food, took it to the food bank.
    If it's not in the house you can't eat it.
    Then on the way home I went to the store.
    I bought fresh apples and vegetables and made a salad that was big enough for 20 people and put it in my fridge.
    Every time I opened the door I ate the salad. I made it delicious. So I wanted to eat it.
    Breakfast was 2 toast (Squirlley bread) and coffee. That is the fiber that you need to get things moving. (I used avocado or sliced banana instead of butter).
    Snack was fruit. As much as you want. (Who can eat an orange, apple and a banana at 10 a.m. ?) That's only 200+ calories.
    Lunch was a huge bowel of salad. No lettuce, I just chopped up 5 or 6 different vegetables and then threw a handful of cranberries or dried cherries and very few nuts or sun dried tomatoes or something good that I liked on top. I'd eat 3 bowls of it. Supper would be four bowls of vegetable soup. (hence the name Gorger!) (Heart smart soup). I'd eat and eat and eat vegetables. And I very seldom have my calories go over 1300. No matter which way you spin it, you can't over eat calories that way. It works and it's good and it's fulfilling.
    I chose the lowest calories foods. Yukkie... Oysters have basically no calories, and today I ate boiled cauliflower with sun dried tomatoes and goats cheese. It was so good and I ate two bowls full. You can eat! And you will feel good when you eat this way. Dieting needs only to be- replacing that which you are addicted to- with something that is better for you. That's it. If you start doing that you will lose weight. Noodles and pasta and white garbage make me feel tired, bloated, and like there is cement in my gut.
    I eat nothing that is white and nothing that is beige and every time I put food in my mouth I ask myself the question..."Is this a fruit, vegetable, whole grain or bean? Is this good for me?". I find new vegetable receipes to try. I eat very little dairy and take calcium. Sometimes I have a tablespoon of zero fat greek vanilla yogurt on top of my fruit. (Try this if you want sweets....get a pie plate and put a bag of frozen raspberries in it, stir in sugar, add a couple tablespoons of flour to thicken and bake as a pie with no crust. When it is warm, put a blob of greek yogurt on top of it. You can eat the whole darned thing and if you count the calories you will wonder why you ever ate anything else. It hits the sugar spot. And then walk. What I do is think of who I want to phone. Then I put on my running shoes and head out the door with the dog and my phone. I dial the number. By the time I've walked a half hour, the call has ended and I'm back home and I never noticed that I walked. Also, instead of meeting a friend for lunch, meet them for a walk. Even if you are tired. First time 5 minutes, second time 10, pretty soon 40 minutes. Eat to live. Not live to eat. Hope this helps you! People will resist and discourage you. Don't listen to them. Whoever is giving you the advice, take a long look at them. Are they overweight? Why would you listen? Make socializing to be not food focused. Also get a Vitamin D blood test. Breast cancer patients seem to be deficient. Same with M.S. patients. So....go get 3 huge tomatoes, cut them in half, put a small piece of cheese on each one and put under the broiler. Then walk away from the table smiling because you are stuffed and full and ate very few calories. I'll be you can't eat all three! You won't ever feel deprived. Eating apples means you can eat all day long. Tell yourself that you can eat the horrid and unhealthy thing that you are craving, but not until you have eaten 9 1/2 cups of fruits and vegetables that day. Believe me... You will never get to the junk that you were craving.
  • netter43
    netter43 Posts: 110 Member
    Thank you Gorger - No one has ever just spelled it all out - really does sound simple doesn't it - Unfortunately guess what sorts of foods I hate - vegetables - I'm not kidding - well as an adult I've learned to eat more of them and obviously need to keep at it - I just want to thank you for such a detailed response - it really does help motivate me to be better and yes, getting my body in motion is the majority of the battle right now - thanks again and please be good to you!!!
  • 1953Judith
    1953Judith Posts: 325 Member
    OP, I don't know if this is the right course of action for you, but my doctor and I determined that I should work to maintain my weight through chemo and radiation. The radiation was touching my heart and we wanted to minimize changes and adjustments during the radiation. I have lost 70 lbs in the five years since.

    As an aside, I am about to leave for a Survivorship Series at the U of . Here are some of the topics.

    Future of Cancer Survivorship
    Staying healthy after cancer therapy
    Exercise for cancer surviors
    Cognitive function and cancer therapy
    Sexual health and cancer survivorship
    Maintaining a healthy heart
    Growin through the Narrow Spot in the Hourglass

    Maybe I'll post something on another topic when I get back.
  • Gorger
    Gorger Posts: 100 Member
    Seventy pounds! Congratulations. That is so wonderful.
  • Gorger
    Gorger Posts: 100 Member
    Vegetables are the least desirable things for me to eat too! I try to trick myself by using nuts instead of croutons and mashed cauliflower instead of mashed potatoes. Things like that.
    ...Best wishes with your radiation treatments. Please check in and let us all know how you are doing. If anyone is having difficulties coping let us know and we can totally arrange telephone support for each other. I'm as near as the phone. (Probably Gorging on something:)
  • weemuse
    weemuse Posts: 40
    Eat to live. Not live to eat.

    Gorger, your full response to netter this is the most detailed, practical and best advice I've seen EVER! I'm going to print the whole thing out and put it on my fridge.
  • weemuse
    weemuse Posts: 40
    Good day everyone!! - I'm newly diagnosed (2/2012) - lumpectomy 3/2012 - just had my CT scan today for mapping my radiation and will be waiting to hear when treatment will start - sometime in mid to end of April - did anyone have any luck with losing weight during radiation treatments or did you all just concentrate on getting through? I really don't think my body likes the Tamoxifen I've recently started either - I just feel bloated, tired, etc...I know, I'm a whiner.....not really, just feel too tired to even get up and go other than what I have to do to get through my day.... any tips of any kind would be greatly appreciated - Hugs to all - Danette :)

    Welcome, Danette. I'm at the same stage... two more chemo treatments then on to radiation (30 treatments). I start Tamoxifen next year, after Herceptin is finished. So, I thank you for posting these questions and I look forward to any and all advice you get back.

    Question though... had you heard that weight gain during radiation was normal? Because it's taking every ounce of strength and constant vigilance to PREVENT gain weight during chemo, let alone achieve a weight LOSS.

    Kathy
  • weemuse
    weemuse Posts: 40
    70 lbs, Judith! Way to go!
  • Gorger
    Gorger Posts: 100 Member
    Thank you so much!
    When I first joined MFP, I couldn't help but study the diets of the anorexics on this interesting and informative diet site. ...(You know how some people let you read their diaries). ...Well, there are some people on MFP that are trying to gain weight and some that want to lose weight and some that are tracking their sodium or sugar intake etc. So I made a point to snoop at the diaries of those who were having problems with gaining. Most notably some underweight people eat quite a lot of food and often times they eat in front of their loved ones to cover up the fact that they are anorexic.
    I noticed that some were eating Body Wise bread. (50 calories a slice). So in other words, it looks to their families as though they eat 2 pieces of toast for breakfast or in their sandwich when really they are only eating 100 calories. So, there is no deprivation. And they also eat no calories to speak of. So....That's the key.
    Then I also noticed that some of these people I was following also ate apples quite a bit. (Apples also stop cancer). So, by mid-day these thin people had only consumed 150 calories even though they ate the same amounts of food that I ate. They just simply ate differently. Lunch would be a lovely salad and a piece of meat and so would supper. And again there was the apple in the afternoon, big juicy and delicious and people saw them eating so the alarm bells weren't going off. They certainly weren't starving themselves. But there were reducing calories on purpose. So, 2 toast, 1 apple, a huge salad, a piece of salmon, another apple, more salad and a fruit in the evening and wahoo! A grand total of 700 calories a day! They also used that low calorie mayonnaise and on it went.
    So, today I ate 2 Body Wise Toast at breakfast, two at mid morning snack, I made a vegetable soup with a hot and sour soup base mix and put avocado on top to get the texture of meat so I didn't feel deprived and then I ate the soup again for supper and I even ate a 400 calorie treat at 3 p.m. a cinnamon scone and my total calorie for today is a whopping 1000 and I sure am not hungry.
    I have just learned to cook vegetables in a way to make them delicious. It takes time. But if you make lots, you can take them to work with an apple. The difference between a fat person and a thin person is not much. The heavy person eats the same as the thin person except they only eat one more sandwich than the thin person every day. That adds up to a 52 pound gain over one year. With just the extra sandwich. Thats why heavy people say they don't eat much because often they don't. The thin person eats the same as the heavy person except they don't eat the sandwich before they go to bed and they also replace a couple of foods a day with lower calories substitutes. That's it. Simple. Everyone is noticing that I have lost weight. Yet I am eating to battle this disease with healthy foods. I eat way too much. Yet I am losing weight. I also listened to Matt Cutt's 30 day challenge. Here is the link. It so motivated me! http://www.ted.com/talks/matt_cutts_try_something_new_for_30_days.html
  • netter43
    netter43 Posts: 110 Member
    Well I actually called the radiaton therapist yesterday as I have not even started treatment yet, but feel like a big fat blob and wanted to know if I can workout/try to lose weight again since I'm now 3 weeks out from surgery....

    She suggested no, that I should work on maintaining my weight....because I'm all marked and ready for treatments and if there is too much of a change in my breasts and or measurements that it would alter my treatment....

    I went for a long one hour walk last nigh with the neighbor lady and thought I was going to have to call 9-1-1 - can't believe how out of shape I have gotten again - YIKES - my goal is once that damn radiation is done, I'm walking - I don't care if it is 5 minutes or 5 miles - I'm walking every day!!!! - I don't ever want to feel or look like this again in my entire life!!! - I'm disgusted (can you tell - LOL)!!

    The other thing - Tamoxifen is kicking my *kitten* - I'm more forgetful, agitated, cranky, don't want anybody barely to talk to me - that is not me - I'm social, talkative and one of the most outgoing people in this world.....is anyone else struggling with Tamoxifen?

    Gorger - You are a wealth of information and I truly appreciate everything you share with us!!!! - Hugs and prayers sent your way!!!

    Weemuse - You hang in there girl - I shouldn't be complaining - I don't have to have chemo - I give you all the props in the world and sending lots of hugs and prayers for you to stay strong in your continued battle during your treatments!!!! -

    To all of us woman battling this disease and any other out there - BE GOOD TO YOU!!!!
  • Gorger
    Gorger Posts: 100 Member
    Wow! You are right about the markings for the radiation. (Although, I don't think I could lose enough weight in 3 weeks to mess that up anyway. haha )... oh dear! I seem to like to eat lately. If I didn't eat my vegetables I would weigh 4000 pounds!

    I just made a vegetable sandwich. One piece of bread with low calorie mayonnaise, mustard, layers of tomatoes and cucumbers, red onions and avocado. The onions make it tasty. I am so full because I had two huge servings (total of 2 breads). That was 400 calories and I am stuffed. If I ate that much of any other kind of sandwich I'd be as big as a horse. ( I need to stop eating so much.) I need another hobby.:)

    As for the Tamoxifen, I had problems too and so was prescribed the 1/2 dose, twice a day pills. It reduced the side effects for me.
    When I was on that drug it felt as though I was dragging a wheel barrel full of lead behind me when I walked. It's nasty.

    The thing to do is to eat healthy stuff. It's so important in this battle. Make sure you get enough Vitamin D. I likely now - am being diagnosed with M.S. as well as the breast cancer. MS can be related to a vitamin D deficiency. Same with some cancers. I either have M.S. or I've had a stroke from the Letrozole and Tamoxifen I was on. ( I have more medical problems than our local hospital :)
    I am losing my balance when I walk. And I continue to have flashing lights in my right eye. Numbness on my left side of my face, blurred vision, tingling, tightness and muscle spasms in my legs, word searching problems when I speak and sometimes my words come out like a drunk person. Slurred speech. God help me.

    A sense of humour helps me cope.

    Good food, laughter, love and heath to all of you.
  • Danette - How are you coming along in your treatments? I did not have whole breast radiation due to my mastectomy, but had to have radiation to my rib as my breast cancer had cropped up there too. I coupled radiation and chemotherapy and found that I was absolutely exhausted. It was also during the Christmas holiday season. I had lost about 35 lbs before my diagnosis in July 2010 (the reason I was able to find the lump in my breast) and found that as I went through all my treatments (4 AC, 12 Taxol & a year of Herceptin followed by Tamoxifen which I'm still on) my lost weight slowly found it's way back plus some. Steroids seemed to put the weight gain on overdrive. I waited for my reconstruction to be done with all my treatments other than Tamoxifen. I wanted to be declared NED since I was a stage 4, there was not a great outlook. Anyway, I'm almost 2 weeks post reconstruction and although it was a long difficult process I feel more like myself than ever, so I'm thankful I did it. We have so much to focus on while beating this disease. My Onc looks at me like I'm crazy any time I complain about the weight. So do your best to eat well (healthy) and move (exercise), but try not to obsess. I ran 5Ks before diagnosis and now can only walk them. It is okay though, as I heal I will get it back. I have faith you will reach your goals too!
  • Hi Itzmeshel I'm am new to this group. I was diagnosed with Triple Negative BC March 2011. 4 x ACT and 4 x Taxoll both every two weeks followed by 7 weeks of radiation. Finished with chemo in September but still experiencing side effects, peripheral neuropathy. I love to elk but find that after more than 30 minutes my feet burn. Glad to be on this site to keep me motivated.
  • netter43
    netter43 Posts: 110 Member
    OK people - I have been missing in action and I am sorry - I have 7 treatments left (started with 32) - it seemed so daunting and now I am amazed I have only 7 treatments left - I am burnt of course and my skin is peeling like crazy but overall I have had one melt down day where the staff at my cancer treatment center treated me like I was the most important thing at that moment and they all pulled me through my day - of course I continued to cry at work and that day was just chalked up to a bad day - but....I'm a fighter and a survivor and this too shall pass.....my family and friends pulled me through and now I can see the light at the end of the tunnel. As far as my eating and exercising - well, lets just say that is the last thing on my mind - I know, I know...I should be focusing on it all, but I just want to get through the days - I'm tired and hurt and I just want to get through a day of work....

    If no one has heard of Mepilex and you are going through radiation therapy - get you some!!! - It is a tacky foam that you can cut to fit and put anyway on your burns and you can even keep it on during radiation if it does not fall off - I look like a patch work doll on my left side....it is covering under my breast as I have a line of blisters there and under my arm where my bra rubs - I am a 44DDD so of course I cannot find any nice comfy cotton bras out there....and I even have a square patch over my nipple....it is a miracle helper....then at night I goop up with lidocaine jelly and Xclair cream.....all I can say is I'm ready to be done and put this behind me....

    I started walking last night with my sister-in-law - believe it or not we are doing the American Cancer Walk for my county this Friday night - I may not be first, but I will damn well finish....

    God's blessings to all and please - BE GOOD TO YOU!!!!
  • weemuse
    weemuse Posts: 40
    Welcome TrinaMargaret. Hope you are well. What does "triple negative" mean? How did you find the radiation treatments? I start next week, 30 in all, and am a bit nervous about it all. Burns are the worst! The women in this room are awesome! So much to learn... Kathy
  • weemuse
    weemuse Posts: 40
    Netter, I had been wondering how you were doing through your radiation treatments. Sounds painful. I'm about to start mine, and will look for that Mepilex... I may not find it as I'm in Canada. Did you have your meltdown due to pain, or was it stress, or both? Sounds like you have good people at your radiation clinic! Good luck on the walk. Kathy
  • Gorger
    Gorger Posts: 100 Member
    Welcome to our group!
    I had breast cancer in 2001, then again in 2010, then I just about went blind in January from Angle Closure Glaucoma, ( a silent thing I got from the cataracts that were caused by the Tamoxifen. After which I just got diagnosed with M.S. Go figure? Bad luck or what! All I can say is to eat 3 to 4 heaping plates of vegetables everyday. I think it's whats stopped me from getting metastases.
    I don't even know what I'm supposed to be doing right now. hahaha. I have more doctors than our local hospital!!!! The thing I do to cope is just block out the illness and continue my life just as it was. There's nothing else I can do otherwise I would be so depressed. Somehow I have reached inside for my inner strength and have just kept going. I'm still working full time, I have no other choice right now. I have no pension and no disability insurance and I am on my own. I'm kind of thinking about the fact that I lived 1/2 block from a hospital incinerator when I was a kid. They burned bio hazard material and there was always black dust on our windows etc. Dioxins and other chemicals is likely what was created. All the people that I keep in touch with that lived in the area seem to be getting auto immune disorders. It makes me wonder... What's going to come to us from the radiation of cell towers!
  • fancyladyJeri
    fancyladyJeri Posts: 1,319 Member
    Good morning everyone. We all have our stories to tell.

    It is almost 1 yr since I was diagnosed. I've had my lumpectomy and radiation. I finished in November. My affected breast is still recovering. Is anyone consideriing plastic surgery?

    Jeri
  • 1953Judith
    1953Judith Posts: 325 Member
    Thanks for reminding me about the mipilex (silacone self-adhesive then wound covering that you could wear through radiation). During my time in 2008, the thin version that was acceptable to wear through radiation was somewhat new. It saved me so much pain.

    Over a month ago my L3 disk in the spine burst. No precipitating event. My specialist thinks that the chemo in late 2007 may have been a contributing factor. It is amazing the tentacles that the cancer treatment has. I have been working hard to maintain my weight, but my exercise has turned to physical therapy instead.
  • Hi Weemuse thank you for the greeting . I copied some information that better explains tnbc

    These subtypes of breast cancer are generally diagnosed based upon the presence, or lack of, three "receptors" known to fuel most breast cancers: estrogen receptors, progesterone receptors and human epidermal growth factor receptor 2 (HER2). The most successful treatments for breast cancer target these receptors.
    Unfortunately, none of these receptors are found in women with triple negative breast cancer. In other words, a triple negative breast cancer diagnosis means that the offending tumor is estrogen receptor-negative, progesterone receptor-negative and HER2-negative, thus giving rise to the name "triple negative breast cancer." On a positive note, this type of breast cancer is typically responsive to chemotherapy. Because of its triple negative status, however, triple negative tumors generally do not respond to receptor targeted treatments. Depending on the stage of its diagnosis, triple negative breast cancer can be particularly aggressive, and more likely to recur than other subtypes of breast cancer.

    TNBC Foundation® is devoted to finding targeted treatment for triple negative breast cancer. With your help, we will find a cure.

    Download a PDF of the Guide to Understanding Triple Negative Breast Cancer, developed in collaboration with Living Beyond Breast Cancer.

    http://www.tnbcfoundation.org/understandingtnbc.htm
  • cmb0267
    cmb0267 Posts: 7
    Hi netter, I guess your treatments should all be done by this time: Congratulations!

    I began rads on 7 June and will be undergoing treatment roughly through the end of July.

    I was diagnosed ER+/HER2- BC in November 2011, lumpectomy December 2011, completed chemo in mid-May. I opted for chemo instead of Tamoxifen because I didn't want to deal with the TMF side effects, but wound up in chemo-induced menopause just the same. Needless to say, I'm furious about this but there's nothing to do about it except wait and hope it's temporary.

    The chemo drugs I was given induced a weight gain of some 20 pounds over 3 months. I'm beside myself with frustration, not to mention shame and a whole slew of body image issues (as if BC and breast surgery don't engender their own set of body image issues as it is!), all of which are exacerbated by my onco's insistence I not lose weight during radiation. She says "It's just a few more weeks, deal with it later" but this is hard medicine to take. The rationale, of course, is that rads depletes the body's energy stores during treatment, so if any weight loss does occur it comes from lean muscle mass and not adipose tissue. What's kicking my butt at the moment is that as my mind and energy levels return post-chemo - and, oh, by the way, it's now summer - I want to do something to shift the weight but at the same time not deplete the lean muscle. I'm told that although I have energy now, I'll feel depleted as rads continues. My nutritionist had me sign up here to track what I'm eating, suggesting 1800 calories, 120g protein per day in order to keep on top of things. I'm concerned that that is going to backfire on me and I'll have to buy more fat pants before this is all over. Worse, I'm freaked out that with the menopause now happening my metabolism will have changed and I won't even be able to lose the weight at all.

    Who else has been in this situation? What did you do and how did it work out? I'm terrified that I'm destined to be a fat old lady now and don't see being cancer-free as a worthwhile trade for it.
  • Gorger
    Gorger Posts: 100 Member
    Hi there. Don't fret. You will lose the weight.
    I'm in menopause and yes, dieting still works. I do notice more- that my skin suffers from the menopause. .. I am starting to get the chicken skin looking kind of neck. I find that using olive oil on my skin at night seems to help a lot and keeps it soft.

    I thought the same...that I would be a fat old lady too. I did manage to lose my extra weight. It changed my life.
    I went out last night to see live music at a local pub and it was amazing. I had men smiling at me and one even asked me out on a date. Before I lost weight, no man would give me any eye contact or smile back. Now... They can't figure out why I say no to a date. ( It's pretty hard to accept a date when you've had a mastectomy.) I am 55 and the guy that asked me out on a date guessed that I was 35. Weight makes a huge difference. Unbelievable.

    Losing weight almost makes me feel normal again. The more weight I lose the less I notice that one boob is bigger than the other.
    Claiming power over weight is rejuvenating in a world in which we don't have a lot of control.
    Remember that all you have to do is cut back for awhile and then you will be normal again. You don't even need to cut back much on the amount you eat. The secret is... It's what you eat, not how much you eat.
    Boil up a big plate of yummy vegetables and eat them 3 times a day. They have no calories. Throw away all the bad food. Soon you will be thin again and much healthier.

    Remember this...dieting is very difficult, but only for the first two days. Then you start to feel powerful and have energy and then the weight loss starts happening.
  • weemuse
    weemuse Posts: 40
    ..it is covering under my breast as I have a line of blisters there and under my arm where my bra rubs - I am a 44DDD so of course I cannot find any nice comfy cotton bras out there....and I even have a square patch over my nipple....it is a miracle helper....then at night I goop up with lidocaine jelly and Xclair cream.....all I can say is I'm ready to be done and put this behind me....

    Did you continue to get worse for 2 weeks after your radiation stopped, netter? That's what they're telling me now. I have 2 left and they said the worst is yet to come. Yikes! I'm already scarlet with at least 2 spots about to break.
  • SuzieQ430
    SuzieQ430 Posts: 44 Member
    It's been a while since anyone has posted on this topic, so I thought I would.

    How is everyone doing? I have only 6 radiation treatments left and herceptin until next June. I start tamoxifen in November. I am really scared about gaining weight on the taxomixfen. My doctor has warned me that I WILL gain weight! Sigh, I just want to lose the extra weight, not put it back on! What has everyone's experience been with weight gain and tamoxifen? I hope everyone is doing well.
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