August 2011 rads
Comments
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Jeana, yes as much as I research as I do, I still think this is a guessing game. How about the knew news on how multivitamins may be hurting us??? We will always wonder if we should be doing more or taking different vitamins or eating differently but my docs don't really push anything in particular. Maybe they just don't want to scare us and want us to try to get back to "normal" so we feel well emotionally and mentally. I have to say that rads were easy for me emotionally as I was only on the table for less than 2 minutes. I can't believe how well I've healed after being so red and peeling. My breast looks almost normal except for one major thing....Has anyone else had a lumpectomy that caused their nipple to retract? My docs don't think it will ever come out again.
It doesn't look right but if that's my only battle scar (my scars are also healing nicely), I guess I can live with it (but I am single
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Thanks for the "tired" tip. I had way more energy when I was going through rads than I do now (3 weeks post rads). But I've also had some sleepless nights due to work and family issues. I need to get to bed earlier.
Pam - I still have the bumps on my skin. I also feel like I have to shave my legs more than I used to. The hair there is growing more quickly than the hair on my head.
Congrats to all who've crossed the finish line. Let's keep up the support for those still in the race. I think I'll go do some yoga now (on demand on my TV).
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Jeana-Congrats! I'm sure that they would not let you walk away if they had any fear that you had not had sufficient care (hey, they'd be afraid of a lawsuit, right...lol). Enjoy the weekend!!!!!!
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katfinn - I have the opposite problem - since my lumpectomy, I'm always "at attention" Need extra lining in the bra to cover it up. UG.
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Katfinn after two lumpectomies my nipple has retracted a little. I am hoping my surgery in December for implants and lifts will correct it.
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Hi All,
I was done with my 35 treatments on Wednesday and I really did crash for two days ... was so tired I was falling asleep every night on the couch! The RO was very pleased with the new skin that appeared as the burnt skin peeled away ... yay for emu oil!
Good luck everyone ... radiation does end and we will survive this like we survived all the other treatments before.
My oncologist had initially told me that I would start my hormone suppressant therapy in April 2012 after the Herceptin infusions stop, but yesterday she recommended starting in two weeks. Is anyone already doing this?
I'm off to check out the Arimedex boards in a little bit.
Stay strong, folks!
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Evelymarie++++++++ this is me clapping for you!
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CONGRADULATIONS EVELYNMARIE!!! I have not had chemo so I hope someone will come along and answer your questions. I am on tamoxifen and so far so good. Yeah!!! Mama V I had to laugh at your post. Mine is the same way. Surely they will settle down...
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Merilee and all - the pic of the lone woman almost at the light at the end of the tunnel, looking out at snow - I really don't like cold...perfect for the blues I'm feeling today. Such a beautiful visual, yet So glad to finish up four boosts this week, and be done with phase 2 (Herceptin until April I call phase 3) yet stepping out of the tunnel is cooooold - scary. Oof, I usually keep the blues at bay; it's a bit rough today. Sorry, ladies. One day at a time, eh?
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lrw333: I am going 2x a week. I go Monday to be measured/fitted for my custom sleeve/glove.
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Hi Jackifp, Sorry you are feeling down. Have you tried going for a walk. Sometimes that can change your mood. Congratulations you will be finished soon.
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Thanks, Kate, you're sweet. Just knowing y'all are out there, and understand these swings of ups and downs, helps. Sweet dreams to all, and a good start of the week tomorrow.
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Jackifp maybe this one is for you
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jackifp: We all feel down sometimes. We are all here for you. Sending lots of hugs your way.
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Thanks Sarahbob for answering my question... Merilee that is so pretty. jackfp it is true I think we all have been where your at. For myself slowly getting back to normal. It does take time though. I hope your doing better today. Thinking of you!!!
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IRW - I have to now put a swim suit cup inside my bra to cover up! Ridiculous! Of course, my DH thinks it awesome! Ha ha! (But I have a 15 year old son - can't walk around like that!)
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I can't even wear a bra yet. It is really bad for me. Walking around in all the loose fitting clothes. It is embarrassing, but you have to laugh... haha I hope everyone is having a good day with RADS... Thinking of you!
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lrw333: I just started wearing my boobs again over the weekend. I didn't wear them for almost 3 weeks. Since I had a double mx, it's not like I HAD to wear a bra.....no boobs to be bouncing and jiggling! LOL!
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IRW....I have not been able to wear a bra in a few weeks. I rarely go out of the house. I can tolerate a sports bra just for short periods of time.
jackifp....I am so sorry you are experiencing the blues. I know this is perfectly normal but when you are experiencing it, well, it sucks. Come here and vent away. Don't hold it in becasue we all understand. We can at least let you know we care hon. This is a rough rough road. You will be well one day, but bad days are going to happen. I am sure I can speak for everyone here and let you know we are here for you anytime, and we truly care. Very gentle healing hugs to you.
Mamav...I laughed when I read your post about the nipple being at attention. What is up with that? Mine too. This has been so weird with my bad burn and swelling. Okay, before surgery I was a C cup. Always fit fine. After I healed, before rads I noticed my right breast was just slightly smaller. There was a small amount of room left in the cup, but nothing very noticeable except to me. So I sort of decided the new right breast was a B-. LOL. Then after the rads and I burned so badly, the right breast began swelling. It felt liked it weighed 50 pounds! It became impossible to even walk much. I told my nurse I felt like I needed a cart to carry the heavy breast in! Last night the pain got very bad again. The burns in that armpit area are still open and weepy. I stood in front of the bathroom mirror naked and stared at them. I figure now the right breast is a good sold D cup! I tell you this is an interesting adventure. I talked to the nurse last week and she noticed the swelling. She said because those underarm burns are so hard to heal (arm movement makes it very difficult for the skin to close). The lymph glands just produce more fluid, hence the swelling.
I have to have surgery next Tuesday, one week from today. The surgeon is removing my right thyroid node in order to do a proper biopsy on the nodules. He thinks the chance they are cancerous is fairly low, at about 20%. It will be outpatient surgery in the hospital, if I get the early morning time slot I will be home by late afternoon. (sigh)...another hiccup and just hope this is uneventful. The only places I have gone in this past month are doctors, pharmacies, and radiation, and more doctors and hospitals. It is kind of interesting to me that this new thyroid issue was discovered only because of the BC. I had a CT scan when I had the pleurisy attack. That routine scan discovered the nodules on the thyroid. So here I go...off on yet another new adventure!
I hope all of you are doing better every day. Each day is one more day toward being healed. Hang in there all of you. Gentle hugs to all!
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Janis I think I caught up with you on the other boards except for the nipple thing - LOL. Always an adventure!
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Vicky know I was trying to catch up, it takes awhile. So glad you are doing better, I hope it continues to improve.
I am having such a problem with fatigue today. My sister is a nurse in Colorado. She called this afternoon with all new instructions for me, after talking to her favorite RO. This RO said I should not have burned this badly. She told Susan of a specific oil they give all their patients to use before and all through rads. They get it at a health food store. The RO also gave Susan a sample of some burn cream for me. Sue got the name of the oil and will pick some up and send it to me, along with the sample med. My baby sis is taking great care of me. She is a real doll. Also this RO told Susan bed rest only for me to prevent the arm from moving, This will help the healing as the arm movement just aggravates that burn up there. It was bleeding this morning.
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Thanks, all, for empathy and support. The burden of keeping up a good front wears and tears, doesn't it?
Merilee, usually, that tunnel would be perfect for me; I don't know what was wrong with me that day...oh, yeah, the keeping up a good front thing, now I 'member. The new one hit me perfectly that day, so thanks much.
Two days of rads left, and I be done! Except for Herceptin til April, but the daily extra hour drive and zap of rads will be done, hurray! Best to all of us finishing up, and those of us with the road still in front. -
Thanks, all, for empathy and support. The burden of keeping up a good front wears and tears, doesn't it?
Merilee, usually, that tunnel would be perfect for me; I don't know what was wrong with me that day...oh, yeah, the keeping up a good front thing, now I 'member. The new one hit me perfectly that day, so thanks much.
Two days of rads left, and I be done! Except for Herceptin til April, but the daily extra hour drive and zap of rads will be done, hurray! Best to all of us finishing up, and those of us with the road still in front. -
Yeah Jacki! Almost done!
Janis I am so sorry your RO didn't give you something better! I hardly even turned pink so can't imagine what you are going through. But so sorry
I'm so glad you have your sister watching out for you. Sisters can be amazing can't they? Mine cooked dinner for us 4 nights/week from January until just last week!
If you are fatigued, then sleep, sleep, sleep! It's your body telling you it needs rest to heal!
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Better yet rest and have someone rub your feet LOL
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Dear Juliana - you are truly an inspiration - Thanks! I had chemo first, then a lumpectomy and SNB on 9/26. All went well - I felt very positive and strong up to that point, but I know the journey is far from over - I will have rad mapping on 10/25. I just want to get started and be done. My surgery went well and my SNB was negative, however, upon reading my path report, I find that my Nottingham score is 8 - in other words, very high risk for reoccurence. Due to this finding, the Tumor Review Board at my hospital invited me to join a research study - which I joined. So, following six weeks of rads, I will be taking a daily low-dose of cytoxan and rheumatrix for 16 weeks and have two years of intense follow-up. Even if the meds do not work, my arthritis will probably hurt less due to the arthritis med and at least I will feel like I am still fighting.
Sher
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Hi all! Boy, despite hearing it could go otherwise, I really expected to feel better after the rads stopped. So wrong! I'm really sore, weeping, peeling - all of that! I did want to come on and tell you what my husband did for me! He cut a circle from cardboard (like from a cereal box), maybe 4 inches in diameter, then twisted into a cone and glued it. Then it cut the tip off. I wore it while I couldn't stand even my light t-shirt touching my nipple - it helped SO MUCH!!! (Yes, it looked WEIRD).
Yesterday I came down with a big ol' fever and slept and moaned for 30 hours. Better today. Probably unrelated, or just my body saying SLEEP. You are right, jackifp, keeping up the front, even when you feel like you aren't - it wears us out. Good lesson for us for when our friends are going through this, as some of them probably will.
We're all on quite the ride. And now comes the Tamoxifen question. I know all about it, and I don't want to take it. So glad to hear a few people who are tolerating it just fine. What about weight gain? I'm so bummed I didn't lose a pound on radiation - could use about 8 off.
I'm with you on the path,
Jeana
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MamaV...I am so sad my sister is so far away. So are my kids. We had to move here for my hubby's health. The elevation was too high and he has emphysema and COPD. We had to choose someplace to live with a lower elevation. So here we are, 900 miles away. It is tough.
I did finally get some good burn ointment today. Hoping healing will be a bit quicker now.
jackifp...you'll be done tomorrow! I know you can't wait. I am really happy for you!
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Jeana-I am so sorry that you are feeling bad. I know how you feel and it sxxcks! I am hoping that you will feel better very soon! FYI, I have been on Tamoxifen since Aug. 4 and I have had very little SE's (just a little bit of night sweats). I have not gained any weight, even lost a few pounds. Perhaps there will be more SE's to come, but so far so good.
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Janis-Could I ask what brand of burn ointment you are trying now? Is your armpit doing better? I thought mine was healing, but today it seemed worse.
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Ceeze.....it is prescription, called Vasolex. The RO had originally prescribed Xenaderm but it was too expensive at $67 so I could not get it. Vasolex has the same ingredients and it was $24. It is prescription too.
My armpit is better but still has a couple bad spots. I got out of the shower and it was bleeding where the skin had sloughed off. This was before I got the new med so hoping it will finally heal. This med promotes the skin cells to heal and can help prevent infection.
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