March 2009 Rads Group?

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  • towdoe
    towdoe Member Posts: 17
    edited April 2009

    #14 for me today & all of a sudden I feel like I have been hit by a ton of bricks!! I wasn't on here last week because I ended up having to have surgery & have my gallbladder removed. I was sick for 2 weeks before. So probably a combination on the surgery & rads has hit me. I don't know??

    Does anyone else have severe tiredness? Like you can hardly put one foot in front of the other?

  • Mary22
    Mary22 Member Posts: 779
    edited April 2009

    Yes I experienced severe tiredness, I can not even stay awake past 8pm. I had Tx#24 only 9 more.

  • bluedasher
    bluedasher Member Posts: 1,203
    edited April 2009

    The radiation tech told me that the last 5 of my 30 treatments are electron boosts so with number 13 tomorrow I'll be half way through the whole breast rads.

  • nelia48
    nelia48 Member Posts: 539
    edited April 2009

    I've been terribly tired lately.  Can't stay up much at all in the evenings.  But then, when I do go to bed, I can't sleep.  I'm on the Arimidex, and the night sweats keep me awake.  I'm sleeping with ice packs!!!!!

    Yesterday, the radiologist drew a big black circle on my chest, mostly around the scar area.  I asked if it would wash off, and he said, "It won't if you don't wash it!"  So what am I to do?????  Can't put cream on something if I can't wash it off before treatment.  I'll have to ask the girls today.  That man is useless!

    More blisters coming up today.  Glad it's Friday and we all get a rest this weekend!

     Cora

  • Anonymous
    Anonymous Member Posts: 1,376
    edited April 2009

    Hey nelia48...I have started on the Arimidex as well...2 weeks so far.  A couple of things that I noticed on the Arimidex group, some of the women who switched from taking the Arimidex at night to taking it in the morning had an easier time sleeping.  Also, I have noticed that I am getting the "night sweats" back (been there, done that years ago) however, I started drinking coffee again and think that might be contributing to the sweats.  Fortunately mine are not to bad and happen around 4:30 am.  Figure I will stop the coffee for 2 weeks to see if it makes any difference.  If the difference is negligable then I'm back on the coffee...cos I love my coffee!!!  

  • Mary22
    Mary22 Member Posts: 779
    edited April 2009

    I had #25 today, only 8 more to go. I am really excited about finishing. Today one of ladies at the cancer center gave me a bag of markers and colored pencils that someone donated to the center for my children. They come with me every morning.

  • nelia48
    nelia48 Member Posts: 539
    edited April 2009

    PurpleMe, I do take the Arimidex in the morning, and I only drink 1 mug of coffee per day.  I've tried different times of the day to take the pill, but it seems the longer I'm on the pill, the more consistent the night sweats are.  My dr. said there really isn't much out there to take, as most are hormone based and we can't have that.  Even the natural herbal stuff is stuff that stimulates the hormones.

    mfgibby, I had #24 today.  We're seeing the light at the end of the tunnel, aren't we??????  That was so nice of the cancer center to think of your kids like that. 

    Have a great weekend!  Two days off from Rads!

  • nelia48
    nelia48 Member Posts: 539
    edited April 2009

    I'm starting to have a really hard time of it.  I don't feel well at all -- dull headache, can't sleep, taste is way off, and the radiation site is reeally burned.  I have some nice big blisters, and the scar line is white and crusted, and very very sore.  I was hoping for a rest this weekend, but looks like I'll just be moaning and groaning to whoever will listen --- probably just my dog!

    Cora

  • TorchSong
    TorchSong Member Posts: 348
    edited April 2009

    Cora

    I'm so osrry you're having a rough time of it! I used to think they did rads just Monday through Friday because they didn't want to pay the techs overtime--now I think it's so we get a break. Rest up and take care of you.

    Hugs

    Martha

  • kristifromsandiego
    kristifromsandiego Member Posts: 271
    edited April 2009

    Hi guys,  Well everyone is a bit in front of me.  I finished #9 on Friday and I like many of you are so happy that it is the weekend.  It is great to have two days off.  My skin looks OK but underneath the arm is a little red and sore.  I cannot imagine what 28 of these are going to be like.

    I have booked a cruise for June 20th so I am hoping that I will have enough energy to enjoy it.  I here that you get tired after radiation more so than during it.  I have met 3 other women that are going through this, I hope to have coffee with them and discuss our different treatment plans, which seem quite different.

     Hope everyone keeps their spirits up, remember this is a piece of cake compared to chemo!  I gardened today, enjoyed coffee with friends and lived life to its fullest.  ENJOY!

  • nelia48
    nelia48 Member Posts: 539
    edited April 2009

    Oh, My!!!!!  I hate to whine and complain here, but I'm really having a hard time.  My chest is soooo red and blistered, and the surgery scar is all scabby and crusty and hurts terribly when I move.  It doesn't help that I have this magic marker black circle drawn on me now, and I'm not supposed to wash that off.  How can I use any cream or ointment if I can't wash it.  It's already starting to run, fade, and get lighter.  I had the most miserable night last night as that scar hurts terribly!  Anyone with any suggestions?????

  • TorchSong
    TorchSong Member Posts: 348
    edited April 2009

    Oh wow, nelia! I am so sorry you're having such a rough time! Did they really tell you not to wash off the marks? My onc drew the lines, but then a tech traced them onto a template and told me I could wash...ended up with marker all over my bra...

    Ask the techs tomorrow--it doesn't seem right to me. They tell us to put lotions and creams on it, but then if you can't wash....

    Hope you get it sorted out soon!

    Hugs

    Martha

  • nelia48
    nelia48 Member Posts: 539
    edited April 2009

    Martha, they said to be careful over the weekend not to wash off the ink markings.  I could put the cream on inside the circle and outside the circle, but not to get it on the lines.  But I'm wondering how I'm supposed to wash it all before Monday's treatment?  I may just retrace the lines myself. 

  • bluedasher
    bluedasher Member Posts: 1,203
    edited April 2009

    Did they tell you that you need to wash off the cream before treatment? They told me to not put anything on for the two hours before, but they didn't say anything about washing off what is there. It is well absorbed in by then.

  • Mary22
    Mary22 Member Posts: 779
    edited April 2009

    I was told to wash any cream or deodorant before treatment as well. Not a problem for me since my appt is first thing in the morning.

    Nelia, why did they draw a circle on your chest? I had 5 or 6 pin point tatoos, to line up the radiation machine. Also after treastment #25 I only have a bit of redness around the scar. I have 8 more treatments to go.

    Good Luck.

  • nelia48
    nelia48 Member Posts: 539
    edited April 2009

    Yes, I was told to wash off any powder, deodorant and/or creams before all rad treatments. 

    Mfgibby, I'm not sure why I had the circle on my chest.  I also had the tatoos up until treatment #24, and then the radiologist drew the circle around my scar, I think for the boosters???? 

  • bluedasher
    bluedasher Member Posts: 1,203
    edited April 2009

    It is odd how the instructions differ. Mine said nothing about washing off the lotions. I use aloe vera and Eucerin Daily Replenishing lotion. My appointment is mid-day so washing off before it would be really inconvenient. The only deoderant I'm allowed to use is Tom's of Maine and they didn't say anything about washing that off either.

    When they did my initial simulation, they had a wire taped to my scar so they would know where it is from the X-rays. I wonder if my onc will need to draw some marks on or whether the X-ray plus my 3 tattoos will be good enough to line it up.

  • NancySchoen
    NancySchoen Member Posts: 32
    edited April 2009

    I have not posted in a few days but I have been reading all the posts. I have had 26 tx and 3 boosts with 4 more left. I had the original tatoos and black marks with clear round tape on the black marks. I was told no deodorant only cornstarch and not 2 hours before treatment. Also only the radiation cream and that could not be used two hours before treatment. I was so excited the day I had my last regular treatment as they said I would get to remove the black marks and the tape. Much to my surprise on the day of my first boost they changed the whole look of the machine with a long tube that comes to within an inch of my scar. At the end of the tube is a metal shield with the shape of my tumor cut into it. But the part that really surprised me was that they were tracing around my scar so that it was centered on this sheild. When I got to the dressing room to change I now had this wonderful BLUE circle all around the scar. So much for getting rid of the black marks. They said do not wash this off while we do the 7 boosts. When I  shower  I just rinse around the mark. I wash everything else. If it fades some they can just trace it again. I think it is easier for them if they do not have to trace and set up each time. I can't wait until Thursday. That will be my last boost. My breast is very red but the cream is working. I have been so careful with not using a wash cloth or towel on that breast. I air dry with the hair dryer. Also only dove soap for sensitive skin. Apply with my hand and rinse with tepid water. I don't think I have ever been so careful with anything in my life. But after reading so many bad things I just wanted to get through with no break downs. Hope this info helps. The reason for the new marks is that the boosts are only to the tumor area. You recieve the same amount of radiation but is is Electron instead of Photon. Which really does not mean much to me. But apparently the electron does not go as deep?  Good luck to everyone this week. Nancy

  • Mamie2
    Mamie2 Member Posts: 108
    edited April 2009

    @$$d!! Anyway I finished nine rads and will have four more this coming week, (our machine is goofy too so they gave me Mon. off), then the following week, I finish up with three more. I'm doing the Canadian shortened version and so far I'm doing ok.

    I'm the sensitive type that felt it the very first day, and twinged pink the first day too. I'm just using pure aloe gel, and when I shower I use pure aloe soap but I really use the soap sparingly on my right breast. I only use all natural products and creams. No parabens.

    I think someone asked about those a couple posts back. To quote from Dr Servan Schreiber's book, Anticancer A New Way of Life, page 78, "some xenoestrogens simply come from certain plastics and some by-products of industrial waste disposal we are regularly exposed to. They are even widely found in beauty and household products." Avoid parabens and phthlates in cosmetics and skin care products that contain estrogens or placental by-products." This may not be a concern if your tumor was/is ER negative. But my tissue was found positive for ER receptors. And xenoestrogens (pollutants) are hormonal disruptors and imitate structures of certain human hormones - which can set off a chain reaction sparking the growth of cancerous cells.

    So do your research ladies. Breathe, exercise, eat organic clean healthy food, be good to yourselves, and look in the mirror and tell yourself how beautiful you are.  

  • CindaD
    CindaD Member Posts: 120
    edited April 2009

    Cora, I feel your pain, I too am having skin breakdown, today is tx21 for me and I want to go to get the damn thing over with but then I want to take a break!  My incisions actually turned a dark red almost brown over the weekend, I have a rash and the skin under my breast broke down and is now an open sore, they gave me new cream on Friday (silvadean) and it helped but I'm not completely healed!  I'm thinking of taking next week off from work to just heal both mentally and physically, my bras are killing me!  This is still easier than chemo, but still a pain (literally)

    On a good note, my hair is growing in, my bald spots are almost covered, I'm so excited about that!  I'm now wearing just baseball caps to work instead of scarves and I'm never wearing my wig again!

    I hope your tx goes ok today, I don't know what to tell you about the circle, but I'd ask about what to put on your open sores......good luck.... the finish line is in sight!

    Cinda

  • bluedasher
    bluedasher Member Posts: 1,203
    edited April 2009

    Mamie, it was beautiful here yesterday. It has been sunny but the days were still cool and sometimes windy but yesterday it was calm and warm.

    After the weekend off, my skin is just barely pink. The outside is doing well but my breast feels very tender inside. Today will be #14 of 25 whole breast Tx then there will be 5 boosts. Nancy, my boosts will be electron too.

    I hope everyone was helped by the weekend off.

  • elf_song
    elf_song Member Posts: 163
    edited April 2009

    Hi, ladies~~    I started my rad end of march and 25 more to go..(out of 30)  so far not to bad, it starting to sore and tired but nothing new since chemo..  what is that boosts everybody talking about??  I don't remember my doctor mentioned..  or I for got...  maybe I gotta ask one of the tech.. 

  • Rachel_BC
    Rachel_BC Member Posts: 1,386
    edited April 2009

    Hiya gals, looks like this here's my train too.  I came here all freaked out (right, like everyone) and you helped me a lot.  A lot.  A previous poster said it better- how I feel humbled in the presence of my sisters who went through chemo.  Like I shouldn't even speak I am so lucky.  But thanks to you, I got help I needed, then I helped someone else, so I promised myself to post here and let you know.  It was SO empowering to be able to help someone else- that's the me I know, pre-cancer. Being able to do something for someone who has cancer and being able to see myself as me again is just a total frikin high.  They stopped me at the hospital entrance today, I think because I looked so happy that I didn't belong there- but I do.  And leaving, I saw a boy in a wheelchair with his parents, that makes me the most angry at cancer.  OK OK, I should stick to the subject at hand.

     My oncotype is 17 - so I escaped chemo just barely.  I also have a 1 year old and I am a single mother at 48.  OK right, back to the subject. 

    How I got help from you- well a lot of things in this thread.  My FIRST day of radiation (I need to learn all the abbreviations) I had big side effects.

     I am a 36 D in am underwire sport bra (so first thanks to all the big boobed ladies for sharing, I have to wear a bra of some sort.  I looked into corsets at one point, reasoning that their support comes from the belly, not the "band" of a bra that's right under the boob.  I am too fat to pull off a corset, but anyone interested, try orchard corsets, they are really nice and helpful and have all sorts of boobery stuff.

    Then I got some vests from the Levis Store.  They have two kinds, a denim look and a white one with thin red stripes.  The denim is actually stretch material, but both shrink when washed, even if dried alone.  My plan was to wear the vests with nice soft t shirts- perhaps inside out if need be for support and modesty, and wore the denim ones to bed even before starting to get used to it.    I got size L, I wear like a sized 14, and they are really tight.  

    So that first day, actually the morning after, I wake up with Pamela Anderson's boob.  I thought it was funny, remembered how I had read women asking to have their other boob radiated after the instant boob job, I had the same thought.  But I thought it was supposed to take a while to happen, not just one treatment. Then the exhaustion hit me- like a ton of bricks.  This was not what I had planned so carefully in terms of child care or life etc... if I was already exhausted with ONE day, and its cumulative, what would it be after another day, a week, 6 weeks?  The good news is that it all went away the next day.  For that day, even the vest wasn't hiding my very lopsidedness.  

    The nurse practicioner said I should go ahead and wear my underwire bra, I need the support, and the wire doesn't come near my incision.  This is a good thing because I have had very droopy boobs since I was 8, and going another month without a bra would probably send them to my knees.  But going to bed the weight of my boob was pulling on my scar, so I put back on one of the ill-fitting wireless bras. (As a techno geek, I get a kick out of calling them "wireless" bras, as if they were bluetooth).  Next morning I had the usual marks from where the wireless bra cuts into my skin, then i put back on my underwire bra.  That was this past Thursday.  On Sunday  I walked with my father for about 5 miles that day, had a great great day, then when I was getting ready for bed, I took off the underwire bra to put on the wireless, and saw this huge red bra mark on my treated boob- and nothing on my untreated boob.  I ASSumed it was from the wireless bra, having seen it that morning, and freaked out.  I emailed my doc (she's amazing) and she could not say it was not permanent.  

    Well of course that blew my mind so I hit the Internet, the ACS, the NIH, never found anything about permanent disfigurement, so I ended up here.  Although no one had these problems (thank heavens), it helped me a lot to see how other women felt the same way as I do.  You have all gone through so much more, and are much better patients than I am, and yet nearly everything you wrote I could have written.  So that was the first way you helped me.  

    The second was someone writing about removing the wire from her underwire bras.  While I was reading all these posts I was reminded to re-apply the cream I use.  (btw, my doc says there have been reliable tests to show the best product is calendula, so that's what I use.  I also use aloe, because I figure that can't possibly hurt anything.  My doc prefers not even corn starch, no powders at all, but suggested I use a piece of cotton from a cut up t shirt under my boobs to collect the sweat instead.  Works great- and it also holds some of the creams on. )  So when I went to put the cream on- the mark was GONE.  Turns out it was from the underwire bra.  I guess it was sitting funny on that boob, or the exercise or something made it push into the swollen skin.  I was grateful for the near miss- but haunted by my doc saying she couldn't say it wasn't permanent.  I figure this was a warning.

    So what do I do, I need the support but fear the underwire for marks and whatever else.  So I remembered what that poster said about taking out the underwire.  Today, Pamela Anderson's boob came back, and I had no way to disguise it.  I took otu the underwire on ONE side of the bra, put it back on and voilá, droopy boob supported enough to nearly match radiated Pamela Anderson boob.  So that was the second way you helped me.  I will post next how I helped someone else, just in case this is too many words for one post. 

  • nelia48
    nelia48 Member Posts: 539
    edited April 2009

    Rachel, you are priceless!!!!   Your post was just what I needed today.  I'm so sorry you have to go through all this, but I was still smiling as I read your post!

    I, too, have been so helped by all the gals here.  I felt so alone going through all this until I found this group.

    The end of this radiation thing is getting really hard.  I nearly broke down and cried today as I got my treatment.  My skin around the scar line is completely broken down, open and weepy.  Dr. won't be in until tomorrow, and I'm NOT leaving until I get something else to put on this.  It feels like hot knives in my chest all the time now.  I had a terrible time with chemo, felt half dead most of the time, but for some reason, this is over the top for me.  Maybe it's cumulative emotions from the whole journey --- I don't know, but this radiation thing has pushed me over the edge!

  • Rachel_BC
    Rachel_BC Member Posts: 1,386
    edited April 2009

    I was reading in one of my two favorite BC books (Five Lessons I Didn't Learn from Breast Cancer) how one gal was a bit germophobic, especially after chemo, how she wore gloves in radiation because she wasn't sure how often they cleaned the handle bar.  I thought that was brilliant, being a germophobe myself.  I also usually wear velvet gloves anyway in the winter, I sort of collected them over the years.  My first day of radiation one of the tech complimented my velvet gloves, so I figured what the heck, and I wore them for treatment.  It was my little piece of control, of me, I know you know what I mean.  I handle this stuff with comedy- and research.  For example, when I had my colonoscopy I put a temporary tattoo of a Van Gogh masterpiece sideways on my arse.  I figured they should have something nice to look at back there.  But it was really my way of exerting control over the situation... like, yes, you have me knocked out and vulnerable and exposed on a table ... but I am still present.  I really wanted to wear a stripper's tassle on my boob for surgery, but I was afraid they'd leave it on when they wrapped me up... anyway...

    Also, my radiation place lets me bring my own music on ipod or CD for treatments.  So we had a bunch of fun that day and each day since I try to wear a different pair of cool gloves and the techs are so nice and comment on them.  In the old days I would have tried to wear stilettos to match.  Now I am a mommy and I have to get that exercise in so I wear walking shoes.

    Yesterday I was chatting with some people who were there to support their friend on her first day of radiation and they noticed my gloves and we had a laugh about it.  Then their friend came back, she was just before me.  I had my treatment and when I came back I heard the techs talking to this woman who had been before me, and asking her if she felt ready to try again.  She had freaked out.  She didn't know it was  going to take so long and she was most disturbed that there was "no communication" she was left alone (we know you have to be, can't be radiating the techs all day every day) and it was cold etc.  

    Since I had already had my freak out, I asked if I could be any help to the newbie. Her friends had told her about my gloves.   I offered her to try my gloves- I was wearing red velvet at the time, and she didn't want to be a bother, she said she only needed one, because one hand was cold.  I said hey, I have a selection, and showed her the weeks supply of colors I had brought.  She picked a gold striped pair, smiled and completed her treatment.  When she was back we were all laughing and joking.

    So if it helps anyone, you can try wearing gloves during treatment!

    I've been so excited about this I haven't even been tired today!

    Today is day 6 for me, I have Pamela Anderson's boob, it's red and swollen, sometimes some little pains, sleeping on my back, drinking at least 1.5 liters of water a day, walking to appointments.  Swelling and fatigue seem to come and go. Alternating between the one-wired underwire bras and vests as applicable, no powders, using cut t shirts instead, using only calendula and aloe, but frequently and remembering to slather my underarm and underboob.

    Thanks, I'll shut up now! (for a while, anyway) 

  • Rachel_BC
    Rachel_BC Member Posts: 1,386
    edited April 2009

    To nelia-

    I am SO happy if I was able to anything to lighten your load- I have been following your story (I read the whole thread before I posted) and I gotta tell you, it's a durn good thing (hey, I am from NYC, so you know "durn" is not the word I would usually choose) that I don't know who your doctor is, and that I am tethered to NYC for the next month, because I would hunt them down and do them serious damage. (eek, I hope that doesn't get me thrown off the board).  I am only holding my tongue because you are nearly done.  

    Your spirit is amazing.  You have handled this !(!!U&!~)#!@**! protocol and the !(!@!**$$ hyperthermia treatments with an incredible grace and aplomb. 

    If there is ANYTHING I can do to put a smile on your face, I am doing it.  I am serious about that.

    You are 1000% right to stand up for yourself in terms of demanding pain management.  That's frikin hooey.

    I know very little compared to you, and I only know about my stuff, so I am avoiding saying anything that would be counter-productive and worse, incorrect.  I did read - in that same book- how many women get the blue after it's all over.

    Like at least before you were in the struggle fighting, but once the treatment ends, where do you land a punch?  Not to mention the over-the-top pain you have endured- like you said, chemo was supposed to be the worst part, now they do this?  And top if off with beating yourself up for not being happy that it's ending.  

    I want to give you advice, tell you to think about how you will celebrate once these burns and blisters heal, give yourself a break, allow yourself to feel how you feel blah blah but wtf do I know?  You know so much more than I do, and you handle it so beautifully.  So instead of that, I will try to entertain you with some thoughts I have had regarding breast cancer ...

     My definitions for boob sizery: When I woke up on the first day with Pamela Anderson's boob, I was afraid the next day would be like... Anna Nicole Smith.  I began to make up my own scales for boob-dom.. the next size would be Dolly Parton.

    My definitions for breast cancer staging:  I call DCIS the Sheryl Crow version and Stage II the Melissa Etheridge version.

     Wink

    Jeez, nelia, I would do just about anything to keep that smile on your face.  Seriously. 

  • TorchSong
    TorchSong Member Posts: 348
    edited April 2009

    Hey Rachel, I like the idea of having Stage Melissa Etheridge! Sounds much better!

    You are great--I've been having trouble feeling very upbeat and you just lifted me. Thank you!

    Nelia, Hope they listened to you and you got what you need. Sometimes it takes forcefulness.

    Hey, I can pull my hair now--it's long enough, at least in back, to grab a bit of in my fingers and tug it a bit! Whee! All grey though--no wheee for that!

    Had #16 today....tomorrow I will be half-way through (if you can be half-way through an odd number). I've noticed my skin is darker--like a really good tan, which I never get, I burn and then tan.

    I STILL don't have the durn compression sleeve I need for my LE. The first authorization form was lost, so we tried again and the doc was supposed to sign it Friday, still hadn't today...they hunted him down this morning and MADE him sign it. I think they thought they were going to have a patient in tears if they didn't.... I was pretty frustrated.

    Now I can get a fitting appointment and hopefully in a week or so, have the sleeve/gauntlet/whatever.

    And the weather is getting warmer--maybe I will dare to put my porch furniture out this weekend.

    Hugs all--we are making it!

  • Rachel_BC
    Rachel_BC Member Posts: 1,386
    edited April 2009

    TorchSong, thank you so much for starting this train... er thread... Cool

    Did you see Melissa Etheridge's return on the Grammies?<---that should be a link to the video on youtube

    Aside from everything else, how often do you see a bald woman just finished chemo completely and unintentially outsexing and outperforming a long haired vixen like Joss Stone half her age?

    Hmmmm? 

    Big congratulations on the hair!  I am learning by reading this thread to look for the women with about that much hair in the waiting room, so I'll kind of know where they are at in radiation treatment.  Thank you for that head's up too. 

    Today I met a woman at radiation who wears a wig for religious reasons.  In the waiting room, I think all the chemo patients must think she's had chemo. I did.  Imagine that, not having to wear a wig and having to wear it anyway.  

    On the "patient in tears" thing, I say, go for it.  If that's what it takes to  get whoever's head out of where its at and puts it where it should be: getting you your cuff, why not "play the cancer card".

    You've been patient, diligent and reasonable. You're being given the runaround. Why not throw a hissy fit?

    You've earned a helluva hissy fit, and no one could possibly blame you.  Maybe they'll ask you to speak to a social worker- and that's fine too.  Maybe they can work it out.

    Mind you, I have little idea what the compression cuff is about.  

    Again, thanks for the ride :) 

  • BooBee
    BooBee Member Posts: 860
    edited April 2009

    Welcome Rachael.  You make me smile.

    Martha......Me too on the hair thing.  Not much on top but lots on the sides.

    Interesting observation today.  I'm day 14 and I asked my rad onco why I had a rash on my collar bone and neck, she said I was getting rads all the way to the top of my shoulder.  I didn't know this or I would have applied the pure vit E oil there as well.  So it looks like I performed my own single blind, phase 1 trial.  No problem with the boob except for mild looking sun burn.

     This is what I do.  Pure vit E oil goes on like honey so it stays there for a long time.  Then I put on a cotton sports bra that holds the oil on the treated area.  Warning: the oil doesn't come out of the bra.  I also put a terry cloth wash cloth (rolled up) under my boob due to a fold from feeling 3 children.  When I get home from rads I take a shower, lube up an then put on a old t-shirt to help with the goo.  My boob is still greasy the next day.

    Anyone want to share how they are doing and what has worked for them?  What day you're on is helpfull too.

  • TorchSong
    TorchSong Member Posts: 348
    edited April 2009

    Renee-- Here`s my routine...I shower before I go to rads, because I usually have to go right from there to work or appointments or meetings... So I take along my tube of Burt`s Bees Radiance Skin Cream (and thanks for turning me on to this, Deb C.!), and after my treatment, slather it on. Like you, Renee, I was getting some sort of spots--like the Dex rash I used to get in chemo--on my shoulder and neck, so I`m been putting the lotion there too. Then I put on my bamboo bra and head off. End of the day, before I go to bed, I slather on the emu oil. It`s pretty greasy, so I wear an old tshirt to bed. The Burt`s Bees smells a lot better than the emu oil, which is why I use it in the morning. So far ir seems to be working--like I said, just a tanning, no redness or blsters...knock wood!

    I loved ME doing the bald thing! She just rocks. 

    I`m stopping by my friend the stylist`s salon later this week to se if he thinks it`s worth trimming what I`ve got--I`m thinking I might as well wait a couple more weeks, as long as I don`t look too mangy.

    Today will be number 17--officially halfway through AND my birthday! Hope you all have wonderful days, too!

    Hugs

    Martha

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