Any April/May 2012 rad girls out there?
Comments
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Others have inflammation? I am still a little swollen - only in the breast area, not lymphedema down my arm at all. I just feel so stretched and tender. Months ago, I had this feeling on my left side and it was called costochondritis...this feels a lot the same, and is an inflammation of the cartilage in my rib cage. Hurts to take a deep breath. Hurts to cough or sneeze. Anyone else having issues like this? How long does the inflammation last?
Hope everyone is doing okay otherwise...
Andi
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Sounds like everyone is doing pretty well and I am so thrilled that we seem to be through the worst of it. I am saying that because I keep praying our after-effects will be non-existent! I still have pain in my shoulder blade area and am hoping it is just muscular. Saw 3 doctors last week (RO, rheumatologist and PC) no one could tell me what I am feeling. The RO did tell me that if it continues I should make sure the MO orders an MRI, x-ray or PT. And the saga continues...
It was bittersweet to be "cut loose" by the RO. I really do like her a lot. However, as I told her, I hope I never have to see her again! I am sure everyone can relate to that. I am just glad the skin is back to decent condition. She did tell me that the thicker skin by the nipple will eventually be normal. Yay for me!
Hope you all had a great weekend. Will check this board again soon. Miss keeping in touch as much as we did during our treatment, but it's great that we are past the active part of that. Hugs...Linda
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Well not much here either my skin is healing but seems very slow proses. one little raw spot yet but other then that just peeling and does not hurt or itch except the little raw part. Anyway yes linnyopp it is a bittersweet, I find that I have nothing to do now that I don't go some where every day kinda board and don't no what to do with myself anymore. I only get seen now every 3 weeks for herceptin seems strange not going in for blood work or something.. And just found out that herceptin will be over in Dec or Jan ..
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Saw my docs yesterday and another one today. Has anyone had to have physical therapy due to muscle cording? Apparently, my treated side is cramping up in reaction to rads, even 4 weeks out! Weird. I have to go to get PT and am told I will not like it. My doc did a little massage yesterday to determine what was wrong and I was in tears. I'm having chest pain like can't cough, sneeze, lift, etc. Feels good to stretch it. She said the PT will hurt but help and is necessary if I am going to maintain mobility.
Anyone had this? Forgive me but I'm sitting here in tears, not wanting to make the call. I know I have to, but it is so tender and painful. CRAP! Yet another leg of an awfully long journey.
On the upside, my skin is actually great and my PO has said that as soon as we see how I respond to PT, I can talk about my surgery to swap out the expanders. Can't WAIT to be rid of them. Hoping for a September surgery for that...which would be perfect since my daughter is HOPING for a December wedding! AHHH! At least I will have hair, even if it is short and will have my new boobs!
Hope everyone is having a good day.
Andi
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Andimom03,
Sorry to hear about the cording and the chest pain you are having. I hope the PT will give you relief ASAP! I too, had my fair share of recovery from the rads. After being on antibiotics for 5 weeks, I was finally given the clear yesterday that the cellulitis on my breast had cleared. Please take good care of yourself and let your family (and/or friends) help you out. For me, one of the hardest things in this journey, has been letting go and having others take care of me.
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I am more than 2 months post-rads, and I still have a good deal of swelling, and more tenderness than I did during tx. I have had a consult with a lymphedema PT, but the focus of that meeting was on my arm - we didn't really talk about the breast because it didn't bother me at the time. I see him for my first session next week, so we'll see what's up then.
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Thanks, mamglam. I am ready to get a move on with the PT, but don't like the idea of pain! I'm a wimp I guess. We will see what she says tomorrow. I am just consistently struck with how much longer this all is than I expected, even though I was told! They still always qualify it by saying they really don't know how each individual will react...so true!
Andi
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Andi
I went to PT during rads for lack range of motion and it was not painful at all just do to your comfort level and gets better every time. I am starting back,had to stop for rad burns. -
Andi I really hate it when they get you all worked up thinking something will be worse.
I went through pt after mastectomy during chemo. It consisted off some simple stretching exercizes. Followed by short massage to the pec musxle. It, was never morethan I could tolerate.
My cording was in elbow and did go away -
Andimom ~ Sorry you are having problems with cording. I feel for you knowing you will have discomfort/pain, but you are strong and will make it through. Hey, look how far we have all come...you never know how strong you are til you don't have a choice, right? One of the teachers I work with whose wife has been dealing with BC ignored what she needed to do for the cording and lymphedema...not a pretty sight. I will think positive thoughts for you that your treatment will go as GFLislander and fredntan...gotta pace yourself! You are NOT a wimp. Like the rest of us you have been through so much that still having to deal with another rotten issue sometimes is just almost too much to think about. Don't be so hard on yourself, girl! So true about the length of time all of these treatment takes...however, I honestly can't believe how far everyone has come and for me the time (as I look back from diagnosis last August) has actually flown by. Not so much on the days I felt rotten from the chemo...LOL! But now it seems unreal that almost a year has passed and so much has taken place. It definitely gives one a different perspective on how to live life fully every day!
MizMarie ~ Hope the breast swelling resolves quickly. I had a consult with the PT who specializes in lymphedema as well. My MO said I had to be seen and get fitted with a sleeve and gauntlet before I fly at the end of this month to try and avoid swelling as I don't have an obvious problem right now.. I sure hope it works! Hoping you won't have any big "L" issues as well.
Mamglam ~ Happy to hear your cellulitis issue is resolving. I so agree with the hardest part being the "letting go." Just the other day a friend said she really wanted to help me during this time, but knew I was trying to handle it with the least amount of interruption in the lives of my family and friends. She is right. I think that sometimes women get so used to being the "caretakers" that we are uncomfortable being taken care of by others. In hindsight I do wish I had let people do more for me since I now know it would have been gracious to accept what they offered and would have made them feel more accepted and appreciated. I guess that's what they mean when they say...live and learn.
To all...take care and it's so good to check in with our group and see that in spite of all we have been through, we are moving on in a positive way!
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We have been done with radiation for longer than we did radiation! It's still tough not to walk out of work 45 minutes early. The only good thing about Rads really. I've managed to get back to the swimming pool. Started back July 1 with the RO's blessing. It feels so good to be back to the water walking. I think I had my last LE session yesterday. The insurance is unlikely to approve more, and I'm doing somewhat OK with my sleeve and my MLD. But I will miss my treatments. They really feel good, and really do help.
Oh yeah and you ladies! You were/are a great thing about radiation. i glad I didn't have to do this alone!
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Thanks for the support, ladies. This morning as I was going to have a shower, I noticed my affected nipple to have turned black!! I got some saline and removed the crusting that had formed (sorry TMI!!) and now my whole breast is really sore. I placed in a call to the RO but not sure when she will call back (or if she even will!!). Has anyone here experienced this?? This whole ordeal has been difficult and emotionally exhausting. It seems that I move on and then something new comes up. Just frustrated and venting...
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Thanks so much for all the encouragement, everyone. I loved my PT and she was very gentle, gave me some exercises, told me I needed to be doing nothing on that side for now...lifting no more than a pound, no major stretching since things are so tender. Just need to let it rest. Hard to do when I'm just doing normal stuff! Everyone is helpful, and I am thankful it didn't hurt too much. I look forward to when the pain is all gone.
Mamglam, I had a bunch of black/grey skin under my breast and in my armpit. When it peeled, it was tender but new skin. I used Silvadeen cream on it, or Aquaphor. It took a couple of days to not be too tender, but then healed nicely. I don' t have any nipples! So, I don't know if there is something else you should be doing, but just baby it. It is very exhausting! Each step has its challenges, but linnyhopp is right! We have come a long way, dealing with things we never imagined...and there is no such thing as TMI here!
Enjoy the rest of the weekend!
Andi
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Andimom03,
Glad to hear that your PT appt. went well and that you are resting.
I had an emotionally exhausting day today. I was crying and was upset about the return of cellulitis and the fact that the RO never bothered to call back. I made a trip to the ER and was seen by a very compassionate physician who has put me back on antibiotics. The ER Dr. wants to me to follow up with the RO but I am thinking that I will go to my MO instead. My MO is sympathetic and has straightforward answers to my questions.
Have a great Sunday!
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I'm sorry you have had a tough day. I'm emotional for no good reason at all! Alot! I hope you get some very satisfying answers. Sometimes, it is just in voicing it and having someone listen where I find the help. Keep us posted.
This week, only 2 dr. appts. My regular doc for a routine check, and my PT on Friday. Otherwise, just focusing on resting and NOT using this pectoral muscle!
Andi
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Hi There Ladies,
I don't post often, but I have a concern and am looking for some guidance. I had a right breast lumpectomy (12/2/11) and 0 node involvement. Did 8 dense dose chemo and 6 weeks of Rads which I just finished end of May. I am experiencing some intense pain in a rib that is a couple of inches below the node incision. If I sleep on it it is too much to bear and forget touching it. I just saw my surgeon for a follow up to having my port out 3 weeks ago. He checked it out and he wants me to have a chest xray done. I am going tomorrow morning at 7:30am. He also advised me to call my chemo doc and advise him of the issue in case he wants to do any tests. Has anyone else gone through something similar? I am a little beside myself here. Thank you in advance.
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I have not had that exact issue, but don't underestimate how much radiation affects you...and for how long. It's cumulative. I just started physical therapy for pectoral muscle and cording issues and I am almost 6 weeks out. My PT told me that she has folks come to her 2-3 months after being done radiation, and just beginning with some reaction to the radiation. I am constantly reminded how LONG this journey is. Maybe it is just some irritation or inflammation in the rib cartilage from the radiation...I will be eager to hear what they find out! I also had something called costo-chondritis, which is just that...inflammation of the cartilage. Don't let your mind wander too far too fast.
Please keep us posted!
Andi
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Hi Andi, I had physical therapy after surgery and then again during rads -- I am going to go back. I did have cording but that cleared up but have shoulder pain -- things were good for awhile but aggrevated easily. I do the exercises that I was given but it has flared again. You are right -- it is cumulative and is ongoing ....
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I have healed up nicely it's weird it kind of itches now under arm & part of my breast but it is all healed except the nipple area still darker and dry pealing. I have not used anything now for about a week or two it's almost like never even had rads yeah!!
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So how are the April/May girls doing? I go in for my 6 month mammogram on Wednesday and follow up with the RO on Thursday, and I have to admit I scared. I have several "things" in my breast. PCP says they are cysts and nothing to worry about, but of course, I worry. I'm doing OK with my tamoxifen, not too many SE's. I do have a sore heel that I need to have looked at...
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I get my squeezing on monday! Saw my gyn today. What fun. Good news is i dont have to worry about birth control anymore!!
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Good luck!
Radiologist says my pictures look good. I see the RO and PCP tomorrow, hopefully they will agree.
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Hi everyone it's been awhile hope all you are doing OK. Got a question for you all . I am 2 months out of rads and I am all of a sudden my breast is hurting and so is my ribs by my breast and under it , is this normal? has any of you got this after rads? I do sleep on my sides always have it sure has been a pain in you know what since all this but I just can't change the way I always slept.
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ang7894-do let your doctor know this is going on. It could be nothing or it could be something that needs to me dealt with, like le (some drs claim lymphadema doesn't hurt, but that's so not true)
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Hi, all. I saw my oncologist today after finishing radiation in early May. I have a lump where I had radiation. He says this happens sometimes and we'll just need to watch it. Have any of you had this happen post rads. It has me a little unnerved after all I've already been through.
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Boy it has been awhile. Sorry I haven't been in here much. Doing pretty well, and the arm/pec muscle issue is MUCH better thanks to PT. My surgery for swapping out expanders and getting my port out is on Sept. 19th. Can't WAIT to have them out! Overall, my energy level is getting better all the time and skin looks great. Moving on, and still have some little issues that are lingering but time is beginning to heal all things. Still checking in with my docs every 3 months, and things are forward motion. Hang in there, ladies! Hope you are doing well and healing and living without fear. Trust what we have all been doing over the last several months! Keep kicking cancer in its butt!
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Andi - glad things are going well for you! I hope your swap goes smoothly.
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Andimom-do your expanders hurt? Mine has allways been uncomofortable. I am so sick of it. doesnt hurt much, just enough to be pain is arse.
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My right side was a problem after radiation since my pec muscle got inflamed and swollen. Couldn't sneeze or cough...PT helped a lot and I haven't been lifting anything more than a pound on that side for almost 2 months! MUCH better now, but tight. the expanders are just a pain...I AGREE! And can't wait to get them out. Now they are just annoying and I have told my doc they feel like hubcaps under my skin! Or like half a bowling ball stuck to my chest. Or like a heavyduty immoveable underwire bra/cage that I can't adjust! So I am very much looking forward to Sept. 19th!
Definite pain in the butt!
Andi
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Well, I hope that the lack of posts on this thread means that we all have healed up and moved on.....
Andimom, sounds like you are doing better!
Cindyl, glad your pic are good!
mamglam, how are you doing?Can't believe it has been 3 months since the end of my rads. My scars are still a little tight and sore, especially since I've gotton a pocket bra and a small prosthesis to fill in the lumpectomy space to round out and equal things out; must be the extra pressure on them. ROM is good, I always stretch my shoulder out fully in the shower -- still.
Started hormone therapy and having very little SEs -- taking extra vitamin Bs as I had a little intermittent hand numbness for a while, but resolved now.
Hope everyone had a great summer!
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