October 2011 Rads

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  • pam53
    pam53 Member Posts: 131
    edited November 2011

    kay1963--  I had similar skin issues.  Very red, no blisters, no peeling.  I heard one woman who had been prescribed hydrocortisine cream.  I asked for it.  The RO was reluctant, didn't think it would help much but he still prescribed it--2.5%.  It worked wonders--went from red to light pink over night.  I am still using it.  They had given me two days off before and I am not getting stopped again!  I want this over!!!

    Little fatigued tonight--I am hoping it is the time change and not radiation.  FIrst boost tomorrow.  Electron type.  They put a device on the radiation machine and put it within an inch of the breast.  It is a little eriee but not too bad.  Don't know how long the zap takes will find out tomorrow.

    Here's to Madame Curie!

    Dancetrainer--I work in outpatients so not as strenuous.  I try to favor my left side--am right dominant.  I only had a lumpectomy and it was at the 11:00 position.  SNB--only one superfical one. So, I was lucky--was only out of work five days. 

  • bedo
    bedo Member Posts: 1,866
    edited November 2011

    I finished rads about 3 weeks ago? maybe 2? it's all a blur. My skin looks SO much better.  Not so much difference in nipple color and the redness is gone.  At this point the main thing that is most obvious is the scar from the lumpectomy around my nipple, but I keep it moist with aquaphor or anything else. (a tip from a plastic surgery nurse) She told me that keeping it moist allows the skin cells to "travel" across the scar easier and leave it flatter and more invisible. I still have some bruising from surgery but the end is in sight, keep focused on your goals. Stilll tired but getting a little better every day.

  • Ceeztheday
    Ceeztheday Member Posts: 403
    edited November 2011

    Natters-I lost almost all my armpit hair, except a little at the top edge. I also had a pretty bad armpit burn, so hopefully they are not getting your armpit so much. Fingers crossed.

  • marthah
    marthah Member Posts: 322
    edited November 2011

    dawmson, My appetite has been pretty strong, but I can't attribute it to any one thing. I've been rather indulgent since finishing my chemo. And yes, I think your "blah" feeling is probably your fatigue catching up to you. Be kind to yourself and get plenty of rest.

    Joan, you'll do just fine! Kay is right...it goes very quickly. I've actually counted down my treatments, and it's roughly 35 seconds; move the machine to the other side and then another 35 seconds. 

    Natters, my tumor was on the right side, so they have me position my head looking to the left each time. And yes, I've lost hair in the bottom half of my right armpit. I wish I could shave too...seems hair regrowth is winning out under my arms, so I have NO hair on the lower half and 3/4" long hair on the top half! It looks ridiculous! And I'll kvetch right along with you -- I think I've ruined a $30 sweater because I can't seem to get the perspiration odor out of the underarm of the sleeves! Ruining work clothes is going to piss me off! I went to K-Mart this weekend and bought 3 inexpensive turtleneck sweaters. I needed them to rock my new look (sans wig since Friday), and figured I wouldn't care as much if I ruined them...paid about $13 each. 

    Kay, we are really close to the same schedule...^5 on being so close to being done! Waaaa-hoooooo!!

    Have a great night, everyone...get some sleep!

  • 5kidsMom
    5kidsMom Member Posts: 118
    edited November 2011

    Havent been here in a while and I feel like I can't even catch up!!  My skin is really suffering these days.  Who was asking about the bolus--I'm still having it, every treatment!  I have a big red square on my chest and most of it isn't bad.  There is an area on my MX scar that is open, but fortunately for me, in the "numb zone" after surgery :)  I have a really sore place in my armpit though, and a whole pharmacy of creams they have given me.  It hurts just to put on the creams, and so far, none are really helping.  It looks like the skin will crack and separate, right at the crease in the armpit--yikes!!  Nurse looked at it yesterday, gave me a new cream that doesn't seem to do much but sting.  The doc looked at it and said my "current regimine" would change in 2 days and they'd give me new skincare at that time.  My mind was spinning, and he was in a hurry.  Don't have any idea what they mean unless I'm to start boosts in 2 days.  That would stink, since I'm supposed to have 12 more days of treatment.  Not sure I could do 10 boosts, if that will be more painful. At this point, can't lift my arm above shoulder level, and just positioning for rads is really painful. 

    Will ask tomorrow, so tired tonight!!  Feel like a crybaby but I'm just SO DONE!  Apparently I must be faking it well. . . . lots of my friends don't seem to realize I'm still in treatment.  My first chemo was 2/25 of this year and I can't tell you how tired I am of cancer!  At the same time I'm so scared of it coming back, I'm just a mess.  Hubby was all set for us to go out of town mid Dec, after a few weeks of recovery from rads.  Not sure I really want to go :(  Been having lots of anxiety, every night as I fix dinner for the family.  Very weird.  Haven't mentioned it to the docs, cause I feel like they'll just offer another pill, and I'm really done with that. 

    ugh.  So now I've unloaded, how is every one else doing?  So glad for this cheap therapy!!  After a year of cancer treatment, who can afford real therapy?!

  • abatellik
    abatellik Member Posts: 80
    edited November 2011

    5kidsmom, So sorry you are having such a rough time right now. It has been coming and going for me as well. I ordered that After Breast Cancer book that people were talking about. Wondering if that will talk about some of the post-cancer anxiety... The unknown is so hard. The cancer they diagnosed me with (although I may not have that kind; I'll never know) is quite likely to recur although the ones that don't recur are the ones with my kind of path report... so I definitely know what you are talking about. Plus facing cancer 5 days a week at rads really stinks. I try to remind myself that the cancer is gone now and God has gotten me through this much, I know he'll carry me through the rest as well. But there are definitely bad days. I personally think the evenings are the worst- more time to think! You are not a crybaby in the least; we are running a marathon, and sometimes we just hit a wall. But we'll keep going anyway.... You'll be in my prayers.

    Kay- They are still using my bolus every day, but I'm only a bit pink and bumpy so far (16 more to go for me). I also have the "advantage" of having numb skin after the mx (not really an advantage but I'm trying to think positively here...). I think they plan on using mine the whole time though. They've never radiated without it.

     Dancetrancer- What did you decie about rads? My experience was probably one you would not have because I was a very difficult radiation for them to plan (and this is at a huge university hospital). The part she had trouble with was the electron beams at the end- they have to line up the cut-outs to overlap the radiation correctly. And I have to hold my breath while they do it! She just couldn't get it right and had me hold to my limit over and over again. It was really quite rude. But this only happened the one time, and like I said, you probably would never be in that situation. I talked to them about it and will not have her again.

    Hope every has good days today!

  • dancetrancer
    dancetrancer Member Posts: 4,039
    edited November 2011

    abatellik, I haven't decided yet.  I am getting a 3rd opinion at another large university hospital.  If I do get radiation, it would be bilateral, because they found an unexpected cancer on my R supposedly prophy side, too, and it also had < 2 mm margins.  Rads after BMX for DCIS is uncommon (let alone bilat rads), the research is limited, and the recommendations I've found are for the decision to be made on a case by case basis.  The two recommendations I've received thus far are opposing.  Uggh!  It will be a few weeks before I have to decide b/c I have to have another surgery to remove the areola on the L b/c DCIS was found behind it.  Thank you for sharing your experience - that does sound rough and so glad you won't have her again! 

    BTW all, what have you heard in terms of how long you can wait to have rads?  My BMX was 9/20, so I'm quite a ways out, but one doc told me I could wait 4 months if I needed to...thinking about it...as my plastic surgeon said if he can get one more fat graft in before rads, I might not need another graft (multiple surgeries would be needed if done after rads).   

  • Kay_G
    Kay_G Member Posts: 3,345
    edited November 2011

    abatellik, I am numb too.  The only place I am sore is right on my collar bone where the nurse told me my skin is the thinnest.  Also a little itchy around the breast, but my breast is numb and so is my armpit.  I had MX and ALND Aug. 17.  Not sure if I'll ever get the feeling back or not, but I agree, right now it may be a plus.  Like you, trying to think positively here.

    Pam53, thanks for the tip on hydrocortisone cream.  They actually gave me 1% hydrocortizone cream a few weeks ago to put where I was itchy.  RO and nurse said to use it only on the itchy areas, which I have been doing.  Is yours a stronger cream?  I know you can buy the 1% over the counter. 

    Marthah, hurray, we're almost done!

    Oops, I am at cancer center and they just called me to go back, so will check in later.  Only 3 more to go after this.

    Hang in there everyone.

  • Natters
    Natters Member Posts: 361
    edited November 2011

    5kidsmom - do you have an expensive deductible and/or copay for therapy? I just had a tiny little spot of DCIS and I am not raising any kids but I started to just basically fall apart as rads approached. So I started going to therapy once a week. In therapy, you don't have to act strong and calm and like you are all over everything. It's perfectly ok to bawl your eyes out and voice all your worries and concerns. I highly recommend it if you can afford it - maybe you can double-check to see if it's as expensive as you think? 

    Thinking of you today and hoping you feel less anxious tonight.

    Nat 

  • 5kidsMom
    5kidsMom Member Posts: 118
    edited November 2011

    thanks for all your kind words :)  Things always look better in the morning don't they?! 

    Natters: I haven't even looked into medical coverage for therapy.  I'm just so sick of doctors, referrals, co-pays etc etc!  My hubby went for therapy years ago and had a negative experience with the person he was referred to.  We have an HMO (a good one, but an HMO) and I'm not sure how much choice I'd have.  I'm really tired of people who have not gone through cancer treatment, telling me how they think I should cope/deal with things.  I just don't feel like I have the energy to go through all of that.  Just keeping up with my kids is a full time job Wink

    Dance: good luck to you and good job on getting the 3rd opinion!!  We need to be sure of our decisions for treatment!  I had my MX 5/25, then 3 mos of chemo.  My MO wanted me to start rads right away after chemo, but I waited a few more weeks, maybe a month after chemo before I started. 

    Abatellik: The after cancer book does talk about the post cancer anxiety/blues etc etc.  I found it very helpful.  I completely understand what you are saying about facing cancer 5 days/week.  I HATE walking under the big "ONCOLOGY CENTER" sign every day.  Makes it so real.  I find that "controlled denial" works so well, and having that stripped is rough.  The thing that makes it doable for me, is how very kind everyone is at rads.  The receptionist will open the door if she sees me coming and uses my name to greet me and say goodbye EVERY DAY.  The therapists themselves have tons of compassion for me, and have a great sense of humor.  They seem to have the goal of making me smile every day.  When I cried over the tatoos at the beginning, they hugged me, held me and let me cry.  They at least act like they get it.  The first few chapters of the after cancer book talk all about the roller coaster of feelings, and I'm reading those chapters again :) 

    May you all have short waiting times, and better skin reactions today!!

  • Kay_G
    Kay_G Member Posts: 3,345
    edited November 2011

    5kidsMom, glad you have such great people at your cancer center.  That really does make a big difference.  Sorry you're having the rollercoaster of feelings.  I go up and down with it too.  So looking forward to being done with rads, but wonder if I will feel the anxiety I hear about when you're done active treatment.  Since Herceptin will still be on-going through May, maybe it won't hit me until then. 

    Wishing everyone short waiting times and better skin reactions too.

  • pam53
    pam53 Member Posts: 131
    edited November 2011
    Kay1963--I also had the 1% for itching. But then they prescribed  2.5% (can't get that strength over the counter).  That strength made the difference in the redness of my skin and has me back in the game.  28 down, 6 to go!
  • lovetosail
    lovetosail Member Posts: 544
    edited November 2011

    Good morning everyone - I just finished 7 of 35 ... slowly it gets done.

    I'm having unbelieveable success in finding radiation-themed songs.  Sorry Natters, but very few are ballads.  I'm trying to get a variety of genres of music - a sampling (and I found all of these on YouTube if you're interested to hear any of them):

    Gavin DeGraw "Radiation"; Lady Sovereign "Drunk on Radiation"; Fountains of Wayne "Radiation Vibe"; The Black Seeds "Love is a Radiation"; Goldfrapp "We Radiate"; REM "Electron Blue"; Strontium 90 "Electron Romance"; Kings of Leon "Radioactive"; Kraftwerk "Radioactivity"; Army of Lovers "The Ballad of Marie Curie"

    so the last one is a ballad, the others are uptempo and a mix of rock, reggae, electronica and rap.  I also found some "Norwegian experimental black metal" (Code - "Radium") but even I couldn't take that. And, random factoid of the day - Strontium 90 is what the Police (w/ Sting etc.) called themselves before they became the Police.

    I'm totally making a CD soundtrack to give to my techs on my last visit ;)

  • Kay_G
    Kay_G Member Posts: 3,345
    edited November 2011

    The techs always have a CD on when I get tx.  Today had Adele Someone Like You On.  Such a pretty ballad, even if it has nothing to do with radiation.  Okay, time to leave.  See you all later.

  • Natters
    Natters Member Posts: 361
    edited November 2011

    5kidsmom, I have an HMO too, I think - but there were a lot of therapists in my network that I could choose. Not sure if you would have that many options, but maybe. One of my friends has a BS who is a survivor and one of my coworkers is a therapist herself (LCSW) who is a survivor, so maybe you could find a therapist who has gone through breast cancer herself. My copays are only $15, and they are well worth it. I'm sorry your husband had such a crappy experience but I think therapists are like DRs in that you might have to try 1-2 different ones until you find the right fit for your situation.

    lovetosail - thanks for the song suggestions! Some of those titles crack me up. And are you still getting out on the water? I bet it's nice and warm where you live. We had unseasonably warm weather here this past weekend so I paddled on Saturday and Sunday in short sleeves. But I did wear a Farmer Jane (neoprene wetsuit that looks like overalls) when I went out by myself because the water is already < 50F.

    Besides the skin reaction, I am also getting swelling. My cancer boob is my smaller one, and after the lumpectomy it got even smaller, but now it's all swollen and my bra feels too tight. I am about to close my office door and undress so I can apply the Miaderm (my life has changed so much, sheesh) and I plan to change my bra before I put it back on, so that it's on the very last hooks. Dunno when I am going to find the time to go shopping for larger bras and/or camis.

    Nat 

  • lovetosail
    lovetosail Member Posts: 544
    edited November 2011

    Natters I am still getting on the water, in fact did a regatta last Sat. Our ocean is always cold, even in summer, but air temps are still warm-ish in the daytime.  Sailing season will wind down not b/c of temps but b/c the wind kind of shuts down over winter, unless a storm rolls through and then you wouldn't want to be on the water anyway.  by "paddling" I assume you mean kayaking?  Sounds like fun!

    I'm getting a little bit of swelling on the radiated breast also.  I've given up on bras and am just wearing camis or men's tank-style t-shirts under my tops now.  I work at a University, so I am lucky that the dress code is pretty lax ;)

  • marthah
    marthah Member Posts: 322
    edited November 2011

    5kidsmom, I'm so sorry you're having such a rough time of it right now. Some other options for talking would be a BC support group, your church, or any group of women with whom you feel comfortable. I think the primary thing for you to do is to talk about it, though, with whatever audience you can find.

    Everyone I know, knows. Coworkers, my church family, my family, neighbors, friends, people I know through various clubs and volunteer work I do. I told them, initially, because I had to take a hiatus from my responsibilities. I have found, however, that when I talk about it, people are really gracious, pray for me, spoil me, care for me, and tell me their own survival stories. This type of sharing has been very cathartic for me, and for them too, I think. It eases everyone's fears. 

    For now, I'm nearly through the worst of it (chemo of the summer being the absolute worst). I'm planning on having a joyful period of growth from when I finish rads till my first cancerversary. It is my intention!  I need to spend some time in introspection and figure out what I've learned from all of this, and how I can put it to good use! 

    :::hugs::: 5kidsmom

  • Natters
    Natters Member Posts: 361
    edited November 2011

    lovetosail - I paddle canoes, actually - dragonboat (which are giant 40' 20-person canoes) and outrigger canoes. You should have both out in LA. I went to a Db race nearby once, in Long Beach. It wasn't in the ocean so the water wasn't cold there. The DBs rarely flip, but it is possible to capsize in an OC, although also fairly rare. But that's why I was dressed to swim on Sunday, in a Farmer Jane and PFD. When the water is under 50F, I guess it can get bad quickly, especially if your head goes underwater. How was your regatta? My last race was just before I started rads and I miss the distraction and soon I will miss being out on the water at all. When does your wind shut down? I work at a university, too. I do research, not clinical work, so I don't usually wear a suit but I do tend to wear dress pants and fitted blouses and sweaters. I'm not comfortable coming to work without a bra because I am fairly busty and my work tops are more form-fitting. When I have been going out in the evening, after rads, I have been leaving the bra off and wearing huge, baggy old sweaters and hoodies.  Not so attractive but certainly comfortable!

  • 5kidsMom
    5kidsMom Member Posts: 118
    edited November 2011

    Discussed the rest of my tx plan with the nurse today. . . . now more questions!  I have one more "regular treatment" then 7-10 boosts. . . . that was one thing I didn't get clarified.  She mentioned that while I have the boosts, at least some of the other areas can heal.  My scarline (except for the ugly open area) is in good condition, so I'm hoping we can just motor through the last bit.  Any tips on the boosts?

  • Paintingmywaythru
    Paintingmywaythru Member Posts: 317
    edited November 2011

    5kidsmom...I'm at treatment 26 and I feel so sore and itchy and red and brown and done... My breast looks hot pink with brown spots at every pore and under my breast..yuck..and then the skin on my nipple comes off in little flakes ...haven't worn a bra since I started and I tell you I jsut heard that the radiation keeps on giving for 2 weeks after you're done...but whoa ...and now the books say the depression hits when you are done with treatment....well...cancer sucks big time...so I hear you..but also know we are all strong and will deal deal deal...until we are are out of this place!!!

    So i am hanging in there and rubbing stuff on my breast all the time..even have these ice gels from the RO...

  • MostlySew
    MostlySew Member Posts: 1,418
    edited November 2011

    5kids,

    The boosts for lots of women are actually much easier than the regular tx. I, however had them from 3 locations instead of the usual two though, so didnt find them any easier. Apparently they target the tumor bed itself rather than the whole breast and the rads aren't as intense, although I thought the machine was on as Long as usual. They did miss some of the previous areas though, so that skin definitely did start healing immediately. It's possible I started feeling less tired, but know at the very end I was more emotional (if that's even possible)!



    I also went thru terrible depression and a severe low time just before my boosts. The Dr made me take a few days off, and I was just devastated. I wasnt sure how I was going to make it thru the rest of the tx. However.......I did and the end is so worth it! I love not having any dr appts on my calendar. The fatigue is definitely lessening and I'm feeling like a normal person. All this after just 6 days finished. The mental relief is amazing.



    Pam53

    I so glad the hydrocortisone is working for you. That's what got me thru also. I did actually have a "super hydrocortisone" which is Clobetasol Opionate" which you can only use for a max of 2 weeks. I ended up needing it for 10 days, 4 of which were after completing rads. My burn is looking great. It's amazing how fast our bodies can heal. You can keep that name in your bag of tricks, but it sounds as though you'll make it with the regime you've got going.



    Keep on looking up ladies. You're hitting the hard part of the hill, but you'll soon make it and feel so elated to be All Done! Good luck to all of you......

  • dawmson
    dawmson Member Posts: 75
    edited November 2011

    #20 done, 13 to go! I feel a lot less blah today. I'm trying to focus on that countdown getting smaller and smaller every day I go. 

    Oddly, my skin looks less pink today than it did over the weekend. I haven't changed anything about my skin care. I'm still doing Miaderm 4x a day. I tried Aquaphor over the weekend and it was just way too sticky. The nurse at my RO said one trick she'd heard was to warm up the Aquaphor a bit so it's more liquidy before you put it on. I might try that - maybe take a small amount and microwave at low heat for a few seconds (and test the temp before I apply!).

    Paintingmywaythru - I have feelings like yours a lot. Driving home today I started to wonder what it will feel like to not have this daily treatment anymore. On the one hand it'll be a relief to not have to face my cancer every single day but on the other hand, there's a lot of comfort that you are doing something to actively fight this beast and then at the end, there's just ... waiting and hoping.

    Mostlysew - thanks for checking back in and letting us know how you're doing! So glad to hear yo are feeling good and healing well.  

  • 5kidsMom
    5kidsMom Member Posts: 118
    edited November 2011

    Mostly sew thanks for the info on the boosts.  One of the therapists today did suggest that I could have a few days off.  I told them I'd rather blast right through and get it done!  They agreed that if I could stand it, that would be best.  So happy for you being done--sounds great :)

    Painting, I've heard that about depression and anxiety too when you are done.  Hubby and I were planning a little getaway that I thought might help with that.  Not sure what the timing will be though. . . . I'd hate to go away and still have my skin be painful!  I read that it's nice to mark the end of your intensive therapy, get away, make a kind of "new start" with your marriage. . . . I KNOW we could use all of that. 

  • Joan811
    Joan811 Member Posts: 2,672
    edited November 2011
    Kay, I am finally feeling like I can do this simulation thing.  I found a drug combo that is working just today - am hoping it will carry me through the week.
    Wow you are getting close to the treatment finish line!  Nice way to celebrate.
    Natters, I have asked about my tiny iPod but so far they said they had their own....but I want it in my ears.  I'll have to see how it goes.  I'd also like a camelpak so I can sip water as needed (haha fat chance).  I found a natural vapor rub with eucalyptus, peppermint and wintergreen oils.  I can use that to help me breathe and relax. 
    Natters, are you lying face down for rads?  How do they determine where to put your head?  No one has been able to answer that for me. I just want to know what I'll have to do.
    Hairy armpit - can I not remove hair during rads?  Nobody has told me anything.
    Kvetch away, Natters!  You seem to be hanging in there and a bit less stressed.
    I can't decide about music....I love trivia and word puzzles. there are a few audio CDs that have games on them.  Am thinking that would work for me.
    Best wishes and hugs to everyone here.
    Joan
  • Natters
    Natters Member Posts: 361
    edited November 2011

    They just have me on my back with with my head in a support, but not fixed or anything. Sometimes my head is turned away to the side, but not always. Atmy center, they don't want you to shave that armpit, not even with an electric razor, just in case you nick yourself. Although my armpit is apparently hardly getting any rads. And I have to wear natural deodorant, no anti-persperant. Joan, maybe they will give you more instructions at your next visit. One of the most anxiety-provoking things about this whole business for me is not being told what to expect, hardly ever. I'm amazed at some of the info other women on here seem to have about their tx. I was doing better but yesterday I shed a few tears on the way home because it was "picture day" and I had to hold still. Lot longer so they could take films. I never knew when it was going to be over. And just the thought that I'm going to have 2/5 weekdays with longer visits like that was frustrating. Today is "Dr" day where I'll have to wait around to be weighed (ugh) then see the nurse then the Dr,

  • 5kidsMom
    5kidsMom Member Posts: 118
    edited November 2011

    Natters and Joan, you were both talking about not getting as much info as others. . . . I'm finding that overall, lots of people don't *want* to know, so the nurses/docs/therapists have gotten into a habit of giving just minimal info.  Once I start asking, they open up.  I know for some people they just don't want to know, it's a kind of denial defense mechanism.  Just let them know you would feel so much better with MORE info than less, and ask when you could come in and have a longer appointment. Yesterday I did that with the nurse. . . . she was re-stocking some cabinets so I asked if she had 10-15 minutes to explain some things to me.  She was delighted, and I think would have made us some tea if I didn't need to go for my treatment LOL! 

    I know relationship seminars always talk about good communication, and I've decided that it applies in my relationships with my docs :)  Yes, they want to cover their butts--no one wants to be sued, and heaven knows people sue for everything!!  Me asking questions, but at the same time being respectful of their time has gotten me SO much farther, in getting the info I want/need

    just my little 2c worth today.

  • MostlySew
    MostlySew Member Posts: 1,418
    edited November 2011

    Natters, was this the first time they did the x-rays? My first ones took quite awhile too, but after that it only lengthened my treatment by about 30 seconds, if that. The first time they had to do the, from lots of angles, verify all their settings and get the Dr to look at them right then. Hope this helps

  • marthah
    marthah Member Posts: 322
    edited November 2011

    5kidsmom,

    That's great advice!  You sound like you're in a better place than you were a few days ago...good for you! I think most of us feel more empowered when we have more information; at least that's what I find here on this website, but perhaps it's because of the kind of "inquiring minds" who are drawn here in the first place. 

    #22 of 31 for me today. Yippee! I'm into the single digits, gals. My skin is holding it's ground too, with the Miaderm. I'm still applying it 3x/day...sometimes I think I could have gone 4x. I'm usually a little tender by bed time, but slathering it up and getting out the bra seems to help, too. 

    I've switched to entirely cotton bras, and they are all different styles, so things lay a little different. I try not to wear the same style 2 days in a row, and that seems to help. 

    Sure wish I could shave the top half of my underarm...it's starting to look a little like Gene Shalit under there!

    gene shalit

  • Natters
    Natters Member Posts: 361
    edited November 2011

    marthah - ha, that pic reminds me of my RO just a little, although to be fair his hair and mustache are not THAT unruly...but yeah, he is that sexy, ladies. I have been applying my Miaderm faithfully 4 times a day since Day 1. And my whole left underarm is getting hairy, it's super attractive. And I'm so anal that I keep shaving my other one so I'm all lopsided. But hey, I figure I can at least be less sweaty on that one side. hey, congrats on getting so many done already and being in the single digits, Martha! You can see the light at the end of the tunnel now.

    5kidsmom, thank you for the good advice! I just may do that Smile Most of the rad techs/nurses are sweethearts and they are really patient with my questions. I get that a lot of people don't want to know, but I do research for a living because I have a burning desire to know everything. I have a much better relationship with my BS and MO, and I have decided to try and be more patient with my RO. I hope he takes my skin seriously today, because even the MO was concerned when he examined me this morning. As he put it, I still have a long ways to go! He said to make sure I saw the RO and worked with him to minimize SEs.

    MostlySew, I think this was the 2nd time they did Xrays. But they have moved my center dot 3 times in the past week so maybe they needed more views to figure out if I was getting zaps in the right places? I dunno. I am hoping it will just be 30 seconds longer next Tue. At least next Tue, I will be mentally prepared to spend more time there. It was just hectic for me to get home in rush hour traffic and then try to clean my house and prep for a birthday dinner we were hosting. 

  • Robyn6463
    Robyn6463 Member Posts: 167
    edited November 2011

    I'm up for number 2 today. Yesterday went pretty well all in all. I still don't really like my rad tech, she's very young, and can be snide and sarcastic when she doesn't have an audience. I'll mention that to the dr when I get a chance. Secretary and nurse have confirmed that I'm not the first to feel this way. Not fair - you need to have the right kind of disposition for that job!

    My breast felt really warm last night. I don't know if that's normal, but otherwise, I'd never know they'd done anything to me at all. I don't have a lot of information though, I'm getting most of what I need to know from here! 

    I've finally found a positive in the chemo s/e's. I don't have to worry about shaving my armpits at all yet:-) And I'm told that the radiation will keep the hair regrowth in the affected armpit at a minimum, if there's any at all. 

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