December 2010 Rads

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  • Lynn18
    Lynn18 Member Posts: 416
    edited February 2011

    Latte:  Sorry to hear you have bad burns and are in pain.  Don't know if this will make you feel any better, but my doctor said they want to see redness on your skin. . .mine wasn't red at first and I was worried.  I'm plenty red now!

    I finished about a week ago and was wondering.  How many times a day are we supposed to put the lotion on? 

  • jo1955
    jo1955 Member Posts: 8,543
    edited February 2011
    Lynn - When I finished rads, I continued to use my creams for about 2 more weeks - 3X a day.  I was told I would continue to cook for that long.  When the redness was gone, I went back to my usual stuff.
  • Latte
    Latte Member Posts: 1,072
    edited February 2011

    i'm finished!!!!!

    thanks everyone for your support :-)

    the rad onc gave me silverdene cream today - i wasn't allowed to use it during rads, but now it is a good thing to use apparently. i read about it on the internet, and it is for 2nd and 3rd degreee burns. my neck, armpit, cleavage, and under my breast are these raw weeping sore areas - need to get them healed up quickly.

    were raincitygirl and i the last ones to finish?

  • Lynn18
    Lynn18 Member Posts: 416
    edited February 2011

    jo1955:  Thank you, 3 times a day sounds good.  

    Latte:  Congrats on finishing and I hope you heal quickly!

  • Sherryc
    Sherryc Member Posts: 5,938
    edited February 2011

    Lynn18 you can ask your RO but mine told me to use my same stuff just like I had for 2 weeks then he wants me to switch to a good vitamin E cream for three months.  So I am using that now and only using it morning and night.

    Latte-hope the silvadene works and you heal quickly

  • jo1955
    jo1955 Member Posts: 8,543
    edited February 2011

    latte - CONGRATS ON FINISHING RADS!

     

  • MrsNice
    MrsNice Member Posts: 258
    edited February 2011

    Gosh, Latte - my burns have not been as bad as yours and I'm still whining.   The silvadene cream has worked wonders for me - sure hope it does the same for you.  Keep it glopped on those raw spots for as long and as often as you can.  So glad you're done and can focus on healing.  I have 2 more boosts - Thurs & Fri - then I'm done too.  I glop on the silvadene before I go to bed and just let it stay there all night.  My RO's nurse also gave me some non-stick dressings which I use during the day if I want to put the cream on; i put the non-stick dressing between my skin and my prosthesis so the cream has a chance to soak in.

    Hi to everyone - just dropping by to check in.  My last 2 boosts are tomorrow and Friday; so glad to be one the road to done.  Having an oophorectomy on March 11th, the I'm REALLY done.  No recon for now; if I decide to do something, it won't be until after August 2011, so I'll have several months off with only a couple of follow-ups.

    Hope everyone is doing well; haven't been able to read back and catch up.

  • jo1955
    jo1955 Member Posts: 8,543
    edited February 2011

    MrsNice - So glad to hear you are almost at the finish line.  We will be waiting for you so we can do the happy dance with you.

  • Teklya
    Teklya Member Posts: 435
    edited February 2011

    Congratulations to all the sisters who managed to make their way to the end of these treatments.  You are all rock stars!!!!

    Teklya

  • Sherryc
    Sherryc Member Posts: 5,938
    edited February 2011

    Mrs. Nice you are almost done!!!!!!!!!!!!!

  • Latte
    Latte Member Posts: 1,072
    edited February 2011

    hi Mrs Nice - hope the last tx go well! i am having my ooph on march 16, just after you, and then i plan to be done too :-)

  • singletona80
    singletona80 Member Posts: 224
    edited February 2011

    Hey ladies its been a while for me cuz Ive been sort of "busy" . . . . .  Hmmm lets see

    Well I came back from Hawaii, went to Pro Bowl had a great time.!!!! Glad I went . . .  needed the vacation . .  didnt want to come back home.  lol !!!!

    Neways I had just finished rads the day b4 I left for Hawaii. . . so My skin was burnt crisp, black !! It started to hurt and blister in Hawaii but I had my rad cream to put on it . . Im sure the bra and prothesis I was wearing didnt help but I refused to walk around flat chested !!!!

    When I came back from Hawaii my skin really started to break down, blister and peel.  I actually started back taking my pain pills.  My skin is still peeling but now it is a dry peel and it feels sooooooooooo much better !!! Plus I walk around the house flat chested.  I now know what burn victims feel like, cuz my skin looks just like a burn victim. 

    So all this happened after I finished rads on 1/25 !!!!!! 

    Oh, I also started taking Tamofixen on 2/1

  • toni30
    toni30 Member Posts: 252
    edited February 2011

    Latte - congrats! Doing the happy dance.

    Mrs. Nice - gettng ready to dance for you too.

  • jo1955
    jo1955 Member Posts: 8,543
    edited February 2011

    singleton - So glad you had a good time in Hawaii (I'm jealous) and at the Super Bowl.  So sorry to hear about the skin issues and hope you heal real soon.

    Sendng gentle ((HUGS)) 

  • Sherryc
    Sherryc Member Posts: 5,938
    edited February 2011

    Singleton so glad u had a great trip and r back. Sorry about the skin issues and hope u heal quickly

  • jo1955
    jo1955 Member Posts: 8,543
    edited February 2011
                        
  • MVRobbins
    MVRobbins Member Posts: 4
    edited February 2011

    Anybody else experiencing Radiation Pneumonitis

    I finished my radiation 01/18/2011. I felt terrific.  Almost back to 100%.  I was thinking, "Wow!  I made it!  Now I'm cruising!"  Well, just 2 weeks later a dry cough and tightness in the lungs appeared. I figured it was just the start of a chest cold and I started a regimen of the typical over the counter meds.  I didn't develop any other cold symptoms like runny nose, congestion, or achiness.  Just this continued tightness, and it was becoming harder to breath deeply - especially exhaling.  Nothing I did was making any change in my condition so yesterday I decided to call in the pros before the start of the weekend.  I stopped at our neighborhood walk-in clinic on the way home from work. (Remember, at this point, I'm not connecting the dots.  I'm still thinking that this is just some stubbon type of cold or bronchitis that normal people get.)  I got there at 7:30pm and they close at 8:00pm. They did an EKG (normal), Blood Ox by finger (98), temp (normal), blood pressure 140/80 (my normal is more like 115/70).  Doc didn't hear anything in the lungs but opted to do a chest xRay.  He thinks it shows some pnemonia in the right lung (won't be read by a radiologist until Monday).  He prescribes predisone and antibiotics and instructs me to follow up with my doctor who I will see on Monday while I'm getting my herceptin therapy.  Today I called my sister, who happens to be an ER nurse for 35 years, and told her about the diagnosis.  It was she who gave me the words Radiation Pneumonitis - first I heard of it.  Now I feel like such a dope.  My radiation was to the entire right breast area.  Is my inability to connect the dots a form of denial?  I don't want to be that patient who every time I get a boo-boo immediately jumps to cancer.  Even cancer survivors can get run-of-the-mill colds.  Anyway, after doing some research this evening and getting a better understanding of the symptoms I think she's right.  The good news is that the clinic's ER Doc ended up prescribing the same drugs needed.  It just looks like the dose will have to be higher and last longer.  I'll call my Radiation Oncologist first thing Monday morning and we'll get on the war path.  So maybe the finish line is a little further away than I thought but I'm taking 3Monstmama's approach.  I won't accept these things that lower my quality of life.  I'll walk farther, I'll walk faster, and I'll show you Big C - that I can't be beat!

  • jo1955
    jo1955 Member Posts: 8,543
    edited February 2011

    MVRobbins - YES!  I am right now.  I finished rads on Dec 3rd and mine started about 3 weeks after and I still have it.  My rad onc is such a moron - he tells me not to worry about it - it will eventually go away.  Another thing you might find interesting.  I recently had a CT & Bone scan done - ordered by my BS - and guess what?  I also have lung damage from radiation.  Imagine that.  My RO did not even tell me there was a possibility of lung damage and my rads were on the left.  Now I have to see a lung specialist this week.

    Think I am a bit angry?  You bet I am.  Sorry to vent. 

  • MVRobbins
    MVRobbins Member Posts: 4
    edited February 2011

    jo1955 - We've done all the treatments. Surgery to remove the cancer. Chemo to kill any renegade soldiers. Radiation to lower the risk of recurrence.  NOW we get on the merry go round of dealing with the side effects.  Those treatments will probably lead to more side effects and then more treatments...etc. Just a vicious circle.  I keep hoping that each detour is the last one and I can get off the constant doctor visits and let something more fun occupy my free time.

  • Sandeeonherown
    Sandeeonherown Member Posts: 1,946
    edited February 2011

    I ended up with a sinus infection within four days of surgery and was on antibiotics for a week....the dr. barely looked at my throat and did not eveyn look at my ears but asked if I anted him to look at my breast incision....uh...NO?!!! just give me the damn prescription...what is with people? As for nothing connecting the dots..perfectly normal. why would you? chest infections can happen without cancer, right? We are just more susceptible after surgery. Be well

  • jo1955
    jo1955 Member Posts: 8,543
    edited February 2011

    MVRobbins - I so agree with you.  That is exactly what I am trying to do now.

    Sandee - We did have other ailments before cancer and will have them long after cancer.  Doctors need to stop focusing on that one word and treat the whole body. 

  • Sandeeonherown
    Sandeeonherown Member Posts: 1,946
    edited February 2011

    Jo1955- Amen to that...whole person....staying well all over should be the priority but soooo hard to do. Told someone I had not seen in 2 years that I had had breast cancer and surgery etc...she looked shocked but gave the perfect answer "Well you are strong. That is such a good thing that you are strong"...and smiled and I thought "Yes!! Now that is a response I can live with, May tell more people and see what happens...more people who know the more who will go for mammograms, right?

  • jo1955
    jo1955 Member Posts: 8,543
    edited February 2011

    Sandee - I tell everyone these days I am a firm believer in mammograms since that is how my tumor was found.  I had missed the year before but will never do it again.

  • spark
    spark Member Posts: 130
    edited February 2011

    Hey all, I have not posted in forever. I finished rads last week. Tomorrow will be 1 official week from my last one. under my armpit is painful. I am peeling and raw! i was prescribed silvedene (sp?) and my RO told me to use Domeboro as an astringent to clean it first, then use the cream. ugh, then i get these shooting pains. when will the peeling stop and my skin not hurt?? anything else i should do besides the domeboro and the silvadene??

  • Latte
    Latte Member Posts: 1,072
    edited February 2011

    hi spark, glad to hear you finished. I'm just using the silverdene (a very thick layer) and it is amazing how quickly it is working for me. i can see the raw areas getting smaller every day (the peeling is another issue, but that doesn't hurt like the rawness so it bothers me less). i'm one week out from finishing and i think that in a few more days the raw areas will be all healed. i also have the shooting pains after i put the cream, but it usually goes away quickly. in the beginning i was on painkillers all the time, but I'm not taking any anymore. hope you heal soon too.

    mrs nice - not sure if i congratulated you on finishing up - so here you go - well done! (in all senses of the term - i told my friends after i finished that i wasn't done, I was well done like a steak!)

  • jo1955
    jo1955 Member Posts: 8,543
    edited February 2011

    Spark - Congrats on finishing rads and hope you heal quickly.  Hang in there, I does get better

  • lizzyanne
    lizzyanne Member Posts: 73
    edited February 2011

    Hi Spark

    It took me about 2 weeks to finish cooking and start to heal. I feel much better now and am just dealing with  some "chording" in my right arm. Going to ask the Onc on Thursday if I could get a referral to a PT to work that out. 

    Congrats - I still have herceptin every 3 weeks until September, an exchange to do and some cosmetic matching...it has been a long year. 

  • Sherryc
    Sherryc Member Posts: 5,938
    edited February 2011

    spark CONGRATS I am doing the Happy Dance for you!!!!!!!!!!!! hope you start healing quickly

  • soulswithin
    soulswithin Member Posts: 154
    edited February 2011

    Hi everyone, so happy to see most all of you are finished! I had a fairly hard time, split some lymph node scar open, had a pretty good frying, on the last of 10 more, my dad was dying so I had to stop and came back to finish. Then my Dad died, and I had to go north again, so I just quit 2 days early. Gruelling trip and had to take care of my mother in a wheelchair too, so I came back really beat and sore. Doc said I did look worse than most, so I just quit.

    Your assessments of what we go through are so accurate. This whole thing becomes so bizarre, with each treatment risks. And then reading the side effects later, only the doc denying you might have that. I came back with a bad cold. Worried because I had tight lungs before I went up north.

    I'm on ABX now. I often wonder what the heck my first mamo after cancer will look like and my lungs too. Just had to see a dentist, two teeth fell apart and I was considering a grafted tooth. He immediately was concerned about my bone loss with the next BIGGY treatment, Femara. Does this end? I don't think so. My Rad docs and techs were great though. I miss them.

    Take care and I meant to say, 2 weeks later the boob is healing! OMG what will it be like to be normal for awhile??? And now I need a mole taken off the breast. That mole was painful all along, and I have had melanoma before. This Rad stuff is not friendly to melanoma, so I'm having this mole taken off soon! I do NOT want to worry about it later!

    Sweet month ahead to all of you!!

  • spark
    spark Member Posts: 130
    edited February 2011

    thank you all for your kind words!! ok, so i am exactly 1 week out. i will keep up the silverdene. and cross my fingers!

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