Fall 2013 Rads

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  • MsPharoah
    MsPharoah Member Posts: 1,034
    edited November 2013


    Batcatlady..(love that name). I had 6 cycles of TC and I see you had the same chemo. I had absolutely no fatigue from radiation. I too was afraid of that because when I was on chemo, I felt like I was the headliner in a tractor pull and I was pulling the tractor! Everyone is different, though. I upped my water intake and power walked every morning. Not sure if that helped, but it made me feel like I was doing something. Good luck and keep us posted.


    Wyo, congratulations are in order. Not only have you graduated, but you are magna cum laude in the radiance department in my book. You are so smart and logical and shine so brightly to others. Have a wonderful, healing holiday, hon.


    Ladies in healing, make sure to stay in your lounge clothes tomorrow and let your loved ones comfort you. You are beloved. Happy thanksgiving.


    MsP

  • LisaSp
    LisaSp Member Posts: 253
    edited November 2013


    Hello Batcatlady, welcome back. As for your question with the comparison of chemo fatigue vs. rads fatigue, for me at least, chemo is far, far, far worse. We both have had T/C and as I remember from your posting on the chemo boards, you had even more intense reactions than I.


    But the side effects for rads for me have been very minimal. Just started having minor aches in the boob being radiated, some skin darkening ( under my arm) and some fatigue late afternoon which is taken care of by a brief rest. Chemo fatigue by contrast was so bad sometimes I need two or three extra hours of sleep a day to barely function. And that nasty achy feeling in my joints is gone!!! And the chemo taste yay! And my hair is growing back!!


    Anyway, PM me anytime if you have questions. And good luck!


    Bluebird I am so sorry. Sigh the comment about Chernobyl victims really got to me. I hope that you might be considering second opinions at this point. I hate what has happened to you. Gentle hugs, and please try to have a restful Thanksgiving.


    Delirium Pie, congrats for finishing! And wyo, congrats for being so close to the end! So nice of you to bring your ROs office a basket. I brought my techs some TJs choc covered almonds the other day. I've got choc truffles from Costco and other TJ stuff I'll make into a basket to give to them my last day.


    PRB, the decision is your choice of course but please don't let your fears prevent you from doing this. Rads are really very easy and fast to get through and the SEs are so minimal for the vast majority. Particularly when compared to rad tx for other cancers. We are all here, hanging on as best we can, trying to save our lives. I'm sure you can do it too. Pretty soon this will be a bump in the road in the rear view mirror and we can all get on to living the best we can!


    Happy Thanksgiving (or Thanksgivakah!) everyone! I go in today for 23 of 33 today, only 10 left!

  • PRB1956
    PRB1956 Member Posts: 444
    edited November 2013


    Well, if I don't die from the cancer, I will surely die from the stress! Thank you all for the many responses. I certainly appreciate hearing from so many of you. You really are a caring bunch of women, and it does help to know I am not alone.


    My worries are many... mostly because I research everything too much. I guess I will just list them here and then maybe it will be more clear as to why I am melting from indecision.


    Possible radiation side-effects:


    1) Thyroid problems: I already have Hashimoto's and don't need more problems there.


    2) Fatigue: With my existing thyroid problems, this could get ugly...and I've read some women never fully recover.


    3) Lymphedema: I have a mild case of lympedema and cording from the lumpectomy. Will it get worse with rads?


    4) Possible lung issues/infections: I have had pnemonia in the past and am now super sensitive to 'smells' and caustic things...to the point they make my lungs hurt if I am in an area that has a strong odor (like glue). This one really scares me.


    5) I had endometrial cancer 3 years ago. All that was required was surgery, but I worry that excess radiation will just increase my chances for another cancer. I feel like I have a target on my back.


    I have never trusted the medical community. I had to demand a biopsy when I was having issues that eventually led to my hysterectomy. I also had to go against my gynocologist's advice on who should do the surgery...she wanted to do it, but I insisted on a gyn/oncologist because the biopsy was pre-cancerous. It turns out that I made the right decision..but it certainly is hard to be your own advocate while trying to navigate the medical world.


    I have seen 2 breast surgeons, a MO, and the RO.. All are saying "do the radiation"...that a mastectomy isn't necessary. One minute I believe them, the next I think... but what if? What if I am in that low percentage of people who have problems? I had a 2% chance of getting 2 cancers in my lifetime, and I managed to fit into that statistic... so why wouldn't I get radiation side effects too?


    My last thought on this is this.... I read somewhere that radiation does not increase your survival time, it just reduces the chance of a local recurrence. If that's the case, why not just get another lumpectomy if it recurrs? Recurrence after radiation means a mastectomy the majority of the time. Then what? Chemo too? I do not want chemo...ever.


    So there you have it. Pretty obvious that I am one messed up chick. Hmmm chick.. I haven't thought of myself as a chick in quite some time. I feel old, and as each day ticks by, I feel like I am delaying my treatment and sealing my own fate. I wonder if there a point of no return for rads? How many weeks can a person go after surgery before it is too late to do radiation?


    OK.. signing off. Thank you again for the kind words...it really did help.


    Pat

  • LizzyinMI
    LizzyinMI Member Posts: 43
    edited November 2013


    23 of 33 done today. My husband drove me in since he's not working today and felt he couldn't lay in bed while I had to get up and out by 6:20am! Then he treated me to breakfast.


    Batcat - I did 5 months of chemo, finished Sept 5. For me the rads are way more fatiguing. I think part of it is because I have to be up by 5:45 since I made my appt for 7:20 so I don't interrupt my work schedule and I do have an hour drive in nasty traffic. But I'm in bed by 9 almost every night and I sleep well. So long as I am physically moving or doing something other than work I'm pretty ok but as soon as I sit down, Wham! I hit a wall. So needless to say sitting at my computer all day trying to work is a bit difficult. Though now I'm at the point with only two weeks to go I can see the end and if I don't accomplish much work wise, so be it. As my husband says, it's all about me right now.


    Can't wait for 12/12 when I'll to be totally done with all this cancer crap. Well, except for the Arimidex.... (fingers crossed!) What a year it's been!

  • Rainyday2013
    Rainyday2013 Member Posts: 20
    edited November 2013
    Dear Pat..I know that all of your fears are very real and only you can make the decision to have radiation or not. I want you to know that I also went through a lot of "What ifs". I have some medical issues that I was afraid were going to make this very difficult. Come to find out, as always, it was okay and I am fine. Keep in mind, the reason you are having radiation is to kill any cancer cells that may be floating around in your breast. If you don't take this precaution and you get a new lump, it will probably be a more serious situation and you Will have chemo then. So, please think about it. Just because the tumor is gone, that doesn't mean that you are in the clear.I guess we have to choose between worrying about other health issues that could be affected or wanting to survive our cancer. For me the anser was clear. It became more clear when I saw this quote:
    If you fixate on the worse-case scenario and it actually happens, you’ve lived it twice.” Michael J. Fox.
    This is a matter of saving your life and like they say, you don't know how strong you can be until that's the only choice you have.
    Please do the radiation.
  • PRB1956
    PRB1956 Member Posts: 444
    edited November 2013


    Thanks Libra. Even if I do the rads...now we're heading into the Holidays. I wonder if the delays make the radiation less effective. It's always something.

  • Rainyday2013
    Rainyday2013 Member Posts: 20
    edited November 2013
    From what I understand, there is a window after your lumpectomy that radiation must happen in. I'm not sure what that is. I read somewhere that 6 weeks is the optimal time frame. But that doesn't mean it won't be effective after that. I started mine 7 weeks after my lumpectomy because of some delays. I had to do gated breathing and my insurance had to approve that. You may want to ask your RO if you can wait until the holidays are over. You might be perfectly okay to wait. Let's hope so.
    Have a great Thanksgiving! And don't worry!!
  • MsPharoah
    MsPharoah Member Posts: 1,034
    edited November 2013


    PRB, below are my thoughts on your concerns. For whatever it is worth.....


    1) Thyroid problems: I already have Hashimoto's and don't need more problems there. Check with your radiologist. It doesn't look to me that you would be getting radiation in the supraclavicle area and if that is true, you should not have to worry about your thyroid being impacted. If they want to radiate that area, find out why.


    2) Fatigue: With my existing thyroid problems, this could get ugly...and I've read some women never fully recover. Most women do not have debilitating fatigue. Yes it can happen and if it does, you will have to put your health and well being first by resting. But it is unlikely that you will have a big problem with that due to radiation.


    3) Lymphedema: I have a mild case of lympedema and cording from the lumpectomy. Will it get worse with rads? If you are not getting radiation in the axilla region, your risk of having more problems with lymphadema is very small. You had negative nodes, so there should be no reason for your underarm area to be radiated.


    4) Possible lung issues/infections: I have had pnemonia in the past and am now super sensitive to 'smells' and caustic things...to the point they make my lungs hurt if I am in an area that has a strong odor (like glue). This one really scares me. Check with your radiologist. I did my radiation in the prone position to reduce exposure to the lungs. Not everyone is a candidate...ask!


    5) I had endometrial cancer 3 years ago. All that was required was surgery, but I worry that excess radiation will just increase my chances for another cancer. I feel like I have a target on my back. I'm so sorry that you have had to deal with this twice and that you had a bad experience with your doctors......but you are a smart lady and when you had your previous cancer, you made good choices and you will do that again with this. You are fortunate that you were able to have a lumpectomy. That surgical choice means radiation unless you are over age 70, because that is the standard of care. You can skip radiation, but in my humble opinion, you may be opting out of the very treatment that means you can take that target off your back and be happy.


    We love you and wish the best for you.


    MsP

  • Bounce
    Bounce Member Posts: 574
    edited November 2013


    For radiation I was told 6 weeks to 12 weeks after lumpectomy.

  • PRB1956
    PRB1956 Member Posts: 444
    edited November 2013


    Thank you all again. I am so miserable these days....and have decided to go visit my sister for Thanksgiving (3 hour drive into the winter wonderland..ugh). I really need to get out of my house and out of my 'funk'. We will play games and laugh and maybe I will be able to forget about all of this for a bit. Not much of a fan of traveling on the busiest day of the year, but it is what it is.


    Happy Thanksgiving everyone.


    Pat

  • Kruise
    Kruise Member Posts: 330
    edited November 2013


    hello Radiated ones! It has been a while since I've been on. So glad to see you are still here and active MsP, and wow what a time you have been thru Bluebird & Summergal. Catching up on all these posts - what an amazing and incredible bunch of ladies you all are. So happy for those that have finished, sending lots of love to those going through treatment and about to start.


    I finished my rads on 11/11 and am mostly doing ok. I have been to see a naturopath to help recovery and have to take about 10 drops of iodine at moment dropping down to 5 after 4 weeks. This is to help combat the radiation exposure. I am also diligently doing the 'No sugar No dairy' diet and have done one week, plus stepped up my exercise. I have come away from my home this week to my holiday house to organise it for Christmas and catch up with family. In New Zealand we don't really celebrate Thanksgiving in the way USA does - but on saying that my sister-in-law is cooking a thanksgiving dinner tonight (it's Thurs 28 already here in NZ) for some friends (one is American) and I'm invited! :) she was asking me if I knew what else was incorporated in a traditional thanksgiving dinner beside pecan pie and turkey and I told her she should google it - but perhaps you lovely ladies could help? A moment to think about food instead of boobs? Lol


    Wyo - I was in Hawaii about the same time as you were. I went for a week after chemo and before rads. Loved it! My first time there.


    Love to all. Xxx

  • MsPharoah
    MsPharoah Member Posts: 1,034
    edited November 2013


    Hi Kruise! We missed you. My hair is still growing and I blow it dry every day hoping that soon I will look like you! I did have bed head this morning, first time. LOL


    My family's traditional feast includes:


    Turkey, Bread stuffing, mashed potatoes and gravy, cranberry sauce, asparagus, fruit salad and for dessert, pumpkin pie. I hope you enjoy your feast and have all the blessings of the holiday.


    Love, MsP

  • flaviarose
    flaviarose Member Posts: 442
    edited November 2013


    Re; Fatigue in chemo vs. radiation. For me, I had extreme fatigue during chemo which was due to extremely low blood counts. My hemoglobin was 8.3 at one point - they would have considered a transfusion if it fell below 8. I couldn't climb a flight of stairs without getting short of breath. My last chemo was Oct.21. I started rads Nov 11. Today my hemoglobin was 10.7, which is why I'm feeling a lot more energetic than during chemo. I'm not sure if I will keep getting stronger the further away I am from chemo, or if the fatigue from radiation toward the end of treatment will happen, but so far, radiation is much easier than chemo for me.

  • flaviarose
    flaviarose Member Posts: 442
    edited November 2013


    HI Pat, I too agonized about the decision to have radiation. In my own case, I think that the fact that I had annual mammograms for 35 years (first breast lump at age 23) could have been a contributing factor to my getting cancer. Radiation scares the hell out of me. My dad had radiation for prostate cancer, and some years later got bladder cancer, probably as a result of the radiation. In my case, I had an aggressive cancer with a positive node, so I knew I had to treat it aggressively. so, I put on my big girl panties and am doing radiation, after doing nasty chemo. I'm also an alternative medicine crunchy granola kind of person, so to go 100% mainstream western medicine was also against my typical way of dealing with health. If I had your diagnosis, Pat, Grade 1, no nodes, I might have had a harder time making the decision to get radiation. You have a good chance that your cancer will not recur, but there is a chance that it will, and radiation is supposed to lessen that chance. As far as bad long term negative side effects of radiation - my view was that I hope to be lucky to live long enough to see those long term effects. I think that if I didn't treat my cancer I'd be dead in a couple of years. That all said, I think that people like Kruise who have altered their diet and exercise program are taking charge, so Pat, if you do decide against rads and/or chemo down the road, there are still a LOT of things that you can do to prevent a recurrence. And Kruise, my mom used to make this great mashed sweet potato recipe - boil the sweet potatoes - mash - add butter, brown sugar and bourbon, top with marshmallows and bake. sinful.

  • Lav
    Lav Member Posts: 65
    edited November 2013


    Hello sister !Im finally done 30/30 it was kind of emotional all my techs wishing me good luck and hoping they dont see me there again on an official basis. They actually cheered me before I could start the last booster telling me this is it and your officially on holiday! An old man I knw who was doing radiation with me and has metastatic cancer hugged me and wished me all the best and blessed me that this should be the last of it all. So sweet including my RO who told me to keep in touch and if I jad any issues with skin to whatsapp him or call him hes given me his cell number too!


    Went in to see my oncologist and since its d season of giving I convinced him to start my tamox after the new years since my husband has surprised me by booking us for a 1 week cruise and orlando trip after. So for now everything seems good.


    Bluebird I think you should go to a skin specialist and get your skin checked out. What your going thru is not normal! As for the holidays I went thru the same for our christmas which was 1st week nov and my daughter had to stay home instead of celebrate with d rest of the family. I infact encouraged her to go on without me but she refused to leave me aline on a special day since I was down with my ashthma problem . You should think of yourself and whats good for YOU. I feel sad though we started on d same day. Do please take care of yourself and try and go to a skin specialist they might be able to guide u better as to how to cure ur skin.


    Bounce Ive been lucky that way all the techs that treated me were super nice and caring. So much so they put a blanket over me because I could never stand the cold.


    All I can say is thank you. Thank you Msp Bluebird Bounce and to all the radiant ladies on this forum. You have been here for me thru out this time and understood me more than what my family or doctors could understand me. I wouldnt have been able to do it without you! Bluebird please keep us posted on how your doing and please pamper and rest up thruout the holidays. Happy Thanksgiving Sisters!

  • McKatherine
    McKatherine Member Posts: 300
    edited November 2013


    *McKatherine walks into the room, squinting at the bright lights and rubbing the bed-head cowlicks to try and fix them*. Hi everyone. :)


    Fighting a nap today. Not sure if it's because of all the travel last week (we got to take our boys to our alma mater for a football game) or if it's the tamoxifen (one week in) or still the rads - but I'm still so tired. I've taken a nap every day. Good thing we're with my parents - my Mom is loving time with her grandsons! On a happier note, my skin looks great! You can't even see most of the "tan lines" anymore. Peeling is all done, no more itchiness - it's amazing how fast your skin heals once the zaps stop!


    I forgot who asked - but I still have my port - had it all through radiation.


    PRB - Ms Pharoah said lots of what I would say. I do want to add one thought: take that list to your MO and don't leave until you are happy with his / her answers. Both the ROs I met were absolute nerds - and LOVED talking about the science behind what they do. If the RO tries to brush you off - find another one who can convince you why rads are or are not best for you. (Beyond the "we do it for everyone" response).


    Kruise - turkey, cornbread dressing, cranberry sauce, mashed potatoes, peas, green beans, sweet potato casserole, corn casserole, deviled eggs, rolls, pumpkin pie and pecan pie. Clearly, my family is all about the carbs. :)


    Hope all you radiant ladies have a wonderful Thanksgiving!!

  • MsPharoah
    MsPharoah Member Posts: 1,034
    edited November 2013


    Lav, you are so radiant today and we are all so thankful for your glow. Congratulations and thank you for being on this board and helping everyone get through. You are a sweetie pie.


    McKatherine, so good to hear from you and know that you are getting better every day.


    Shine on, MsP

  • L2girl
    L2girl Member Posts: 113
    edited November 2013


    Well, another one crosses the finish line!


    I also just had my last radiation treatment today. I did 10 weeks in total! (30 each side, for a total of 60, but overlapped somewhere in the middle) Woohoo! I am finished! The whole staff applauded as I walked out after changing, while they played the graduation march in the background, (I think it is called pomp and circumstance?). I gave them all hugs and thanked them. They gave me a certificate and card, which they all signed and wrote some really nice things to me. And they gave me a goodie bag. Everyone there was always so kind and caring to me. I think I am going to miss them. (wipes away a tear). My RO was also very nice. Overall, I would have to say I couldn't have asked for a better experience going through this whole cancer thing.


    Tomorrow I can truly celebrate, for I feel I have more to be thankful for this year than ever before. Even though this past 6 months or so has been quite an ordeal, I am thankful for all the good care and great people I have met along the way. I am thankful my side effects have been minimal. And most of all, I am thankful I am still here.


    Love to all, and thank you for all your support. Couldn't have done it without you!

  • MsPharoah
    MsPharoah Member Posts: 1,034
    edited November 2013


    L2, we are also thankful for you, especially now that you are exuding so much radiance. Congratulations! Yes you are still here and better than ever.


    Love, MsP

  • Kruise
    Kruise Member Posts: 330
    edited November 2013


    yummmmm - thanks for the suggestions MsP and McKatherine. I have told my sis-in-law that sounds like she has to do mashed potatoes! :)


    MsP you make me laugh about the hair - mine is still growing away albeit slowly - but it looks like a hairstyle now as opposed to when it first started growing back. I used to have long dark hair and now I have short ash-blond hair! Lol. Good job I had lots of different wigs throughout treatment so people got used to my different guises.


    Happy Thanksgiving to you all!


    If any of you find yourselves traveling to NZ in the future - would love to have you stay.


    Kia Kaha (stay strong) x

  • Kruise
    Kruise Member Posts: 330
    edited November 2013


    congrats on finishing L2 girl - woo hoo! Can hear you all the way over this side of the world

  • bikergirl
    bikergirl Member Posts: 112
    edited November 2013


    Congrats on finishing L2. I had 26 whole breast treatments, today had 1/8 boosts. Breast just pink, no broken skin. Weird thing is the other side of my back and under my breast is painful. The RO said from laying in the same position Mon-Fri and I also probably was lifting more with my unaffected side.


    Happy Thanksgiving to all!

  • wyo
    wyo Member Posts: 541
    edited November 2013


    Woo hoo Radiant Ladies- I finished my last treatment today!! I brought in my goody bag for the techs and honestly they were so taken aback hugging me and thanking me I thought- wow don't these people ever get gifts or a warm-hearted thank-you? They said I would miss me and I will actually miss them too just not the radiation.


    btw- no bell ringing or anything like that but the certificate they gave me- its a purple heart award. I really liked that because as we all know it takes incredible valor and bravery to hop up on that table each day.


    The crazy news was the MO office called and said I needed to be seen within 2-weeks of rads finishing so I said well I am available now til the 10th then avail on the 23rd and on. She says- oh well the schedules are impacted and the drs are on vacation- so PS my appt is January 2nd. I was feeling somewhat snarky and said " that is a bit more than 2-weeks after today" she says" well I know they have schedule issues" hmmmmm I thought a bit more and said "I want you to send her a message and let her know that you can't schedule me until January 2nd because of your schedule not mine"- I am going to email her myself anyway. I don't know that it is a big rush to start tamoxifen but I kinda thought I could get it going over the holidays to see how I do.


    Thanksgiving- hmmm mashed potatoes are a staple for sure to go with turkey and stuffing (if you are not familiar with stuffing its cubes of bread or croutons with sauteed celery and onions all bound together with chicken broth- then you can add sausage, apples etc. My personal favorite is adding fresh oysters- ummm


    For veg my mom made squash and turnip- I don't ugh. Also this fun corn pudding which is frozen corn, eggs, milk and cheddar cheese. It all bakes like a yummy casserole/souffle.


    Desert is pumpkin praline pie I am making it this year for christmas glad I ate before posting all this my stomach is growling hahaha


    I am Thankful for all the friends I have met on this site- enjoy the day with loved ones and travel safe.

  • McKatherine
    McKatherine Member Posts: 300
    edited November 2013


    congrats wyo and L2!!!

  • Teachersbc123
    Teachersbc123 Member Posts: 34
    edited November 2013


    MsP,


    You are a vat of knowledge. Thank you for sharing your research.


    PRB,


    This is as much an emotional and psychological journey as a physical one. Please take care of your head as well as your body. My cancer center has a team of social services. They are there to listen and point you in the right direction for appropriate help. You don't have to desl with these feelings and decisions on your own. Hugs!

  • summergal
    summergal Member Posts: 208
    edited November 2013


    L2grl - way to go. So happy for you! Hope you have a wonderful day tomorrow!

  • rosecal954
    rosecal954 Member Posts: 79
    edited November 2013


    This is my first post in this thread and pretty new to the forum. I have gained so much information reading the posts. Thank you -- for sure we are not alone! I had my lumpectomy about 11 weeks ago and will start 30 radiation treatments soon. Will have the simulation most likely next week. I have been fairly anxious since my breast cancer diagnosis three months and am wondering if my anxiety will make side-effects worse. I have dropped about 12 lbs. since my DX and I was not over-weight to begin with. Had a Oncotype score of 21 and no chemo. Everything has gone smoothly so far except for the anxiety which I seem I cannot control. Sometimes I just start crying for no other reason than just plain fear -- maybe of the unknown? Anyone else out there feeling the same way or thought anxiety led to more severe side-effects?

  • wyo
    wyo Member Posts: 541
    edited November 2013


    Symphony for a Hungry Old Man


    I found this to use for my Thanksgiving wish that, whatever your present circumstances, you will be able to sing like a cardinal and not squawk like a blue jay. Its appropriate for what we are dealing with in our lives I think. Happy Thanksgiving!


    The blue jay and the cardinal made their livings in the park at the outskirts of the old village. Every day, they sat in the low branches of the maple tree, near the wooden bridge where a small stream twisted back upon itself, gurgling over rocks that God had planted before memory to teach the stream patience. The morning sun transformed the little brook's crystalline surface into a dance floor for angels, their wings all a-shimmer as they pirouetted across the liquid ripples.


    Summer days, people sat on the banks watching the angels dance and listening to the lullaby of the brook cascading over the rocks - and to the symphony of the birds. The blue jay and the cardinal made a comfortable living serenading the picnickers, who shared crusts from their meat pies; the young lovers, who tossed bits of bread and cheese; the rangers, who always had delicious seeds and bits of dried fruit; and the old man, who feasted them with chunks of the heavy black bread he made in his own oven.


    Life was good for the birds, plump and content up on their branch. It was beyond their comprehension that upheavals in the world outside this little haven could someday impinge upon them. So they were slow to notice the changes when they occurred. How the picnickers stopped bringing pies, then stopped coming altogether. How the young lovers walked briskly, heads down and hands in pockets, without stopping to gaze at the brook or listen to the birds.


    How more often than not, instead of bringing fruits to share, the rangers came foraging themselves, digging up roots and dropping them into the limp satchels at their sides. How thin the old man had become, and how his meager bread had lost the taste and the texture of the old days. The blue jay and the cardinal could now be seen with the ordinary birds, picking through the dead grass of the meadow and chasing bugs in the tree branches.


    "What have I done to deserve this hunger," the blue jay squawked. "I sing as beautifully as ever, but they don't appreciate me anymore." His trills no longer drifted down from the tree branches; when the old man sat on his bench, the jay just screeched at him, vainly demanding food.


    But every afternoon the cardinal took his place on the branch. He was scrawny now, and his once regal plumage showed scars from the daily struggle for food. But when he puffed his chest and cocked his head, he regained his ancient majesty. And then he filled the old man's ears with the symphony of his heart. For that brief eternity, the hungry little bird and the hungry old man danced with the angels across the stream, floating beyond time and care.

  • wyo
    wyo Member Posts: 541
    edited November 2013


    big hugs to you rosecal- so glad you came here and posted.


    From my own experience its been a lot of emotional ups and downs and tears for no reason just "because" Other days I am just a little to "perky" and wonder about that too.


    Many on this site have had good experiences taking medication for anxiety to face their journey. Perhaps that is an avenue for you to explore as you get into the radiation part of your treatment?


    I think radiation is a bit of a head game for me. Every day you get up to go have a treatment that reminds you - oh yeah you do have cancer. No matter what else you are doing that day- your once constant reminder is there. Though the positive is- every day you are having treatment you are working to beat the odds against cancer so its in investment in the future. I finished today and now on to Tamoxifen- no chemo.


    If you find that your level of anxiety is getting in the way of you being able to carry out your normal activities of daily living or severely interrupting sleep- probably best to intervene with anything from exercise, to meditation to support groups or medication. Its not "weak" to need help getting through this its strong admitting you need support for the journey.

  • Bounce
    Bounce Member Posts: 574
    edited November 2013


    wyo - Thanks for the story - its a perfect reminder to me to start "singing" more.

    We can't control what happens but we can control how we react.  Smile

    Rosecal 954 - I agree with everything wyo said - especially trying to help the tension through exercise, meditation and a support group.

    You should ask at your cancer center where you will be getting radiation if they have an exercise group and a  psychologist you can meet with.  These psychologists can usully help quite quickly as they understand what you are going through.

    To answer your specific question - I don't think that feeling stressed will make a big difference to your side effects but it will make a difference in how you perceive the side effects and in how well you cope with them.

    Having a little pain or discomfort is not a big deal when you are calm and happy - it can be ignored and overcome - but dealing with the same level of pain can be overwhelming when you are scared and upset.

    My first 2 weeks of radiation were much harder than the third week because of my fear and anxiety at the beginning.  Not to mention my control issues!

    You deserve to feel as good as possible and its worth getting some professional help - even though it is natural to have a certain amount of stress and mental unease.  Your unwanted weight loss is perhaps a sign of distress beyond the usual.

    Feel free to share here too. 

    Hugs

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