November 2011 Rads
Comments
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Congrats natters! You are beautiful! thanks for sharing the photo! I am so very happy for you. Congrats to you too RealtorJackie! I am so very happy for you.
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Congratulations to Natters and RealtorJackie
Natters, what a great celebration picture!
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Natters - congrats! Glad this is over for you. Hope your partner is feeling better to.
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Congrats...Jackie & Nat !!!!!!!!!!!!!!!!!!!!!!!!!!!!! I have 2 more....
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Anandagram, I know what you mean about needing a month off from appointments. I carved out December as a month to be free from doctors. The appointments start up again in January, but I am enjoying this month immensely.
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An appointment-free month is an awesome idea. I think I'll designate February. It should work out fine as I'll finish rads on 1/12 and I have an MO appointment on the 23rd, I think. I haven't had a free month since June 2010. I think I am overdue!!!
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I wish I could join in on the doctor-free month idea, but I'm taking care of an 87-year-old mother in declining health. I've been fitting in her doctor's appointments between mine.
I seem to remember one of you complaining of an itchy, bumpy rash which appeared after rads. It's happening on my chest and I wonder if it was ever explained?
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I had an itchy bumpy rash, after chemo, just above my port incision. Never figured out what it was, but it did go away b4 rads....
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Thank you for the compliments everyone. I did have some good moments this weekend celebrating the end of rads. My skin continues to worsen and I am just hoping I can make it through this week without having to go back to the hospital for their help with my burns.
LuvRVing - you are WAY, WAY overdue! Hope you get a nice break to spend the holiday with your family soon, and not have that long drive back and forth to rads.
Congrats to everyone finishing up like JACKIE who started this thread and rn4babies, and tvacrat and dsnydawn
Good luck to everyone else who is spending hours and hours every week getting healthy thru rads, when I'm sure they'd be happier getting ready for the holidays and spending time with family and friends. You too will finish up soon, even though I know it feels like it is just taking forever.
I am hopeful 2012 will be a much better year for all of us.
Nat
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Hello All!
Haven't been on in awhile. I finished RADS last Wednesday! Congrats to all that have finished or are about to cross the finish line.
I do have severe burns under my arm (sentinal node scar), neck and under the breast. So bad, that all of the skin has come off in these areas. They are now open and pink and I'm just waiting for them to heal. Using wound wash, domeboro soaks, silvadene, aquafor and neosporin. I pray this all clears up soon -- under my arm is the worst as it's a big open, pink area about 5 inches across. Blech.
If anyone has any other remedies to help clear this up, I'm all for it! The RO's say that this is ok and will just take time to heal. These burns didn't happen until right up until the last week of treatment.
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I have the big, open pink burns, too, Chrys, and my RO didn't seem fazed and gave me nothing. One of the nurses gave me Xeroform but the other one told me not to use them often, just let it air out as much as possible. I can't believe how different they approach our burns but how nothing seems to help except time, apparently
. I'm going back in this week if it gets too much worse.
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Oh Natters -- I'm sorry to hear you are going through this too. I have THREE open pink burns. Neck, underarm and under breast. The one under my arm is the worst. It looks like raw meat or like I'm a walking dead zombie.
My RO says, Aquafor, Aquafor, Aquafor. I keep pads or gauze on it and I try to air it out as much as I can, but as you know -- it's quite painful to sometimes put my arm down!!! Are you in much pain now? My center also provided me with Lidocaine gel and that helps somewhat. Most of the pain is gone -- it was really bad when the skin was literally burning off my body. Most of the skin in my areas is now gone, so it's not as painful.
As you said; time seems to be the big factor. Keep the area clean; I purchased some sterile saline 'wound wash' and I use that about 3x's a day. I was doing the soaks (Domeboro -- you can find the packets at Walgreens or RiteAid). They are an astringent that helps soak off the dead skin. You just mix it in 16oz of water. It's very soothing to use. I was doing that 4x's a day to get all the dead skin off -- gross!
Let me know if you need anything or if I can help in any way -- since we are both going thru this.
Feel better!!!
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Mine started under my arm and kept growing until it started snaking under my breast. I'm afraid to put Aquaphor or anything on it! I put some Sweeney cream on it once and it stung so bad! So I asked the nurse and she said that there was no need to out anything on it. The other nurse told me that they don't think anything really helps except time, so maybe that's why they take such a minimalist approach?
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Natters and Chry23 so sorry you are hurting! Prayers that you will heal quickly with little pain.
To all of you who have finished congrats! Here's to a better New Year.
I got measured for my boosts today. It's a little freaky having the attachment on the machine. It comes so much closer to me. I was surprised when I talked to the doctor that she said the boosts were not treating as deep along the scar as the regular treatments on the rest of my chest. She also told me that the changes in my skin would continue for a week after treatments before any healing took place. Sooooo ready for this to be done. 8 more to go.
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Natters -- Try the Aquafor, it really does help! I hope you can get relief soon. Also, Lidocaine Spray can help soothe it.
Thank you Nans; you are well on your way!!!
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DCIS Stage 1 Grade 1 Lumpectomy HERS2 negative hormone receptors progesterone estrogten positive. I am 56 yrs old.
My treatment center is pleasant and welcoming in appearance. The staff is very nice and pleasant. The lobby is decorated in a comfortable atmosphere with a puzzle table area (rotated by theme or season) soft lighting on another side with a Kureg drink station with tea, coffee and graham crackers available. Another area is more brightly lit and all area are available for those awaiting appointments or therapy.The treatment center has issued their patients a photo ID card with a barcode. What I call my speed pass which I present under a scaner,and enter through an automated handicapped opened door to the 4 room dressing area, to gown and wait my turn for radiation.
Does anyone have Syndrome and Fibromyalga?
I began my radiation therapy on 28 November 2011. Had my facility walk through, tattoo guides placed and set up (mold fitting) and treatment walk through stretched out 2 weeks prior while awaiting HERS2 results which was negative, (one less therapy) Yeah!
Into day 17 of 30 treatments. I was given the Bard brand skin care cream provided my radiation treatment center of which I began applying prior to my radiation treatments. I am doing well considering my other medical history. At first the treatments felt like they were taking forever. The colorful markings are a conversation piece as I am not embarrassed that they show when I wear some tops. Recently I have begun to go bra less with just a cotton Camey and over sized sweaters. My right breast is now sore and beginning to turn a light to medium pink with a definite light brown tan pattern line above and below my breast as well as a darker nipple and areola. My radiation treatments are seemingly feeling like they are going by more quickly even with radiation films check. I see my doctor every 2 weeks and the staff is helpful in answering most concerning questions. The one they cant answer is my autoimmune body reactions to radiation. My rheumatoogist hasn't a clue as well as the radiation onocologist and I feel like a hot potato being tossed back and forth. I have a follow up with my onocologist in 3 weeks.
Has anyone experienced severe abdominal pain? In ER last night intestinal blockage. Sjogrens and Fibromyalgia causes me fatigue and some IBS issues anyway. I can tell an increase in fatigue level with increasing intensity is a side effect from the radiation therapy treatments. I was told by a ER staff nurse her opinion this was a possibility in my body's reaction to treatments due to my autoimmune diseases.The ER doctor did not elaborate to my question but was detailed in clarification of all my test and discharge instructions. I try to stay as hydrated as I can to the best of my ability but realize this is a problem at times with my autoimmune issues. Has anyone had this problem in their treatment?
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mkmware: I,too, have an autoimmune disease--sarcoidosis. I have felt much muscle pain during rads. Getting my sarc checked again in a few weeks. I have been tired, but not nearly as much as during chemo. I was finished with the whole 33 treatments on Friday!
I want to congratulate everyone who is finishing up this week. What a great Christmas gift! I can't believe how quickly my skin is starting to heal. I am still using Aquafor 3-4 times/day, and drinking Juven.
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Jackie and mkmware, I don't think I have an autoimmune disease but there is so much in my family (lupus, Ra, sarcoidosis) that I asked my RO if rads might trigger it if I was susceptible. He said no way but he dismissed all my other concerns, too. He was determined I complete rads. I was lucky I didn't develop abdominal or joint pain, in the end. -
Mkmware - I have IBS and it was really bad during chemo. Its all back to normal now and I am lucky that I can get things "normal" by taking Metamucil. Your treatment center sounds exactly like mine except for the card id. My center has the puzzle too and snacks.
Getting tired and pink. But no real burn yet.
Saw a male patient (accompanied by his wife) at treatment today. This man has throat cancer. He has 3 very large tumors on his neck that are very visable. While speaking with his wife, I had to excuse myself and run to the bathroom and cry. My heart goes out to him. I don't think he will make it. I cried as I am so lucky to have this type of cancer...if one has to have cancer. My heart goes out to him. I don't know his name, but PLEASE say a prayer for him and his wife. I will not complain.... it could be so much worse.
Love and hugs to you all.
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Jackie - Congrats! You did it --- and thanks again for getting us together to help, support, laugh and cry TOGETHER. Who else in the world would want to hear about our peeling skin?
Nat - So glad you are done! Nice photo!
Congrats to Chrys, too!
And for all November ladies who are done....Gotta party!!!Hugs to all,
Joan
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Chrys - you were right! Aquapor does not sting or burn the wounds
I steeled myself last night and gingerly applied it right before bed. So glad there is something I can use on that area and I'm really hoping this helps me heal up before the new year. The rest of my breast is actually looking better. Went from an angry bright red to a less obvious red and looking almost like it's starting to be a tan instead of a burn. My breast is less sensitive and tender and slightly less swollen, I think, too.
Joan - thanks for the image - it's a woohoo moment indeed to finish rads
And would you believe I am still wearing the camis you suggested when I go out? Inside the house, I try to give my skin a break from any pressure and go all loosey-goosey under baggy sweaters and hoodies and fleeces.
MrsMot, I saw lots of older men and also some elderly and infirm women at my rads center. I think a lot of them were there for throat and tongue cancers. There were and are high rates of smoking in Pittsburgh, so it's not surprising. One of my team-mates recently had surgery to remove part of his tongue and then did rads. Another team-mate privately confided in me that she had had colon cancer years and years ago. She wanted to let me know that there were a lot worse places to be radiated than your breast, and she was right...
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Did not mean to be Debbie Downer yesterday. Just that man effected me so. The realities of cancer can be difficult. Lost my dad to cancer, my mother-in-law and countless coworkers to cancer.
Love the new photo Natters - Hope your wounds heal fast.
Congrats to all that finish this week. What a Christmas gift! #15 today...half way done.
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Stick a fork in me.....I'm done (& burnt) 28 today....although I look like I have been through a nuclear attack..my skin held up!!!
Mrs Mot....I left my center a few times like that........hey that's what we are here for...to lean on and you all have been wonderful.........
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Congrats to all those who are finishing rads this week. May your burns heal quickly!
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Natters- I'm glad you're finally done as well! Things should heal up quickly now. I saw your BS, Dr. Rubin on "The Doctors" the other day. Did you see that segment? Suzanne Somers was on there discussing her breast reconstruction that was part of a clinical trial. I hope things turn around for you for the holidays. I think the holidays are stressful as it is and adding dealing with BC and relationship issues sure doesn't help. My NSDH (not so dear husband) is creating much added stress on me as well..... I think I'd rather just be alone.
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Rn4babies - I didn't see Dr Rubin on TV! I wonder if I can find and tape it....?
My NSDP is crapping all over my Xmas as well. We're probably going to spend the weekend apart - I'm going to see my family in VA alone. At least THEY love and support me!
Hope you get some Downtime in the coming week. My mom was a nurse and I know you guys don't always get all the time off you deserve. You sound as stressed out as me and you have a lot to figure out, too. -
Natters: So glad you tried the Aquafor! Keep using it as much as you can; even on the nipple!!
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Rn- I saw it online and it's not the same Dr Rubin - there are 2 surgeons at UPMC with that name. That guy is a PS. I only had a BS because I didn't need recon. I think my surgeon does other onc surgery but no plastic work....the fat grafting is very interesting to me, though, as a possibility of improving MX concavity and maybe just creating tiny breasts.
Am I the only one who got a lump that's already planning for a potential BMX in the future? I don't even have all that high chance if a recurrence, if I can tolerate the Tamox, but it's still a lot higher than my chances of initially being dx and I feel like my luck has run out these days. -
Natters. ....Sorry, I thought he was the one. Why are you considering BMX in the future? I have pretty much the same DX as you plus an extremely strong family hx. I am going to wait it out. Believe it or not, I'm strongly considering refusing the Tamox. I see my gyne on Thurs and my MO next week. I know they're not going to be happy about it.
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Joan: Thank you and every one elso for being here with me! I did the happy dance in the hospital corridor and waiting room. Now back to Fox Chase tomorrow to see my onc. Hopefully, everything will check out OK. Bone scans and CAT in Jan. I had originally been diagnosed with mets at another hospital. It wasn't until late summer that I went to Fox Chase,and was found to be NED. That is why I started rads so long after surgery and chemo. I had been written off by my last onc. I have my Christmas miracle. Praying to stay NED for a LONG Time!
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