April 2010 Rads Group

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suzieq60
suzieq60 Member Posts: 6,059

I'm starting rads on 6th April. I know it's early to post this topic but I'm having my planing session today while I'm still well (before my last TCH treatment on Wednesday). I decided to get it all organised so we can have a short holiday before the next part of my journey begins.

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  • BossyRenee
    BossyRenee Member Posts: 77
    edited March 2010

    I'll be starting rads the 1st week of April. My 6th and final TC tx is on 3/16. I am sooo ready to get past the extreme fatigue days I experience about the 4th day out.

  • suzieq60
    suzieq60 Member Posts: 6,059
    edited March 2010

    Hi Renee,

    Welcome. I was starting to get worried I was a bit early with this. Had my tats done yesterday - didn't feel a thing. When do you have Easter over there? I'm starting on the 6th April because the 5th is Easter Monday in Australia.

    Sue

  • sweatyspice
    sweatyspice Member Posts: 922
    edited March 2010

    I start April 5th.  Perhaps I'll bring some chocolate Easter bunnies to bribe the staff so they'll like me from the beginning.  Had myself tattooed on Tuesday, I thought it was simply a consult but I misunderstood.....

    I also got a complimentary bottle of Calendula lotion.

    The resident asked me what my thoughts about radiation were.  Dumb question.  I said that I thought it was something I wanted absolutely no part of, but that I should do anyway.

    Here we go.....

  • suzieq60
    suzieq60 Member Posts: 6,059
    edited March 2010

    I had the consult at a different centre - the place where I'll be having treatment. Had to go to another private hospital for the tats as they are set up for it there. I finally found 3 little spots. I have lots of small spots so it was hard to pick them out.

    Chemo all done as of Wednesday but I'm not excited that it's over yet. In a week or I'll be happier after I feel better. Still have 11 herceptin treatments to go though.

    You're right about the radiation - don't want to do it but don't really have a choice.

    I'm glad you've joined us for the April rads.

    Sue

  • sweatyspice
    sweatyspice Member Posts: 922
    edited March 2010

    I'd scheduled my rads for 8:30am, and then got laid off yesterday.  I hate the idea of having to get up that early just for rads.  It will be about an hour's commute.  BAH! 

    I'm tempted to switch the time, but if I get another job I'm afraid I won't be able to quickly switch back to what is one of the most desireable (pre-workday) slots!

    Hopefully I'll get used to it and enjoy having ny whole day still ahead of me.  Or just get a new job really fast.

  • suzieq60
    suzieq60 Member Posts: 6,059
    edited March 2010

    Sorry you lost your job, that must be so hard. I'm lucky I had insurance and don't have to rush back to work. I don't know what time they've scheduled only the first one at 12:10. I did ask for early morning to just get it over with but I'll have to wait until I show up for the first one to find out the times. We've got to fit it in around the herceptin treatments too.

    Good luck in finding a new job (((HUGS)))

    Sue

  • sweatyspice
    sweatyspice Member Posts: 922
    edited March 2010

    I'm happy to have a break from work, right now BC is one of the easier things in my life to deal with.  Although the financial reality will probably hit in about an hour, as soon as I pay my bills.

    When the s**t hit the fan, it really does, and all over the place, too!!

    I was able to pick my rads schedule ahead of time, that's one of the reasons I waited an extra week or so, to get the slot I wanted.  My rad onc was fine with it.

    I don't have to do anything besides surgery, rads and tamoxifen - so good luck with your Herceptin treatments!!!! 

    (((HUGS)))) back!

  • kmid
    kmid Member Posts: 23
    edited March 2010

    Starting Mar. 29.  Had simulation yesterday.  Still hope to get another med onc consultation about chemo in the major city where I had my lumpectomy.  This process is so consuming and frustrating.  You need to be your own researcher, advocate, decision maker, etc.  I think I will have 28 doses and 6 boosters.  Want to start today but they said no opening until Mar. 29.  Welcome all!

  • BossyRenee
    BossyRenee Member Posts: 77
    edited March 2010

    Finally finished chemo on the 16th. So happy to be done with that part. Appt with Rad Onc on 4/1. During initial consult in Nov. she said probably 30 with 6 boosts. Hoping that changes since chemo. Onc says my chemo was just "mop-up" so hopefully won't need as many rad tx. good luck to all in this next phase.

  • kmid
    kmid Member Posts: 23
    edited March 2010

    Had simulation Mon.  Went to breast surgeon yesterday in a large city for 1+ month f/u.  All well at 1st, though area above/below scar looks like a golf hole.  Surgeon found a "M& M" size lump under my left arm-not the right, cancer side.   Due to see a med. onc. there next week and now scheduled for ultrasound on previously unaffected breast area. Dr. said not to worry, most likely nothing, etc.  Reminded me of when I started this last Aug.  Am pretty freaked out but trying to be positive.  Anyone had this experience?  Supposed to start radiation daily Mar. 29. Breathing deeply!

  • suzieq60
    suzieq60 Member Posts: 6,059
    edited March 2010

    kmid: I hope the lump turns out to be nothing (((HUGS)))

    Sue

  • ebethnp
    ebethnp Member Posts: 3
    edited March 2010

    Hi there,

    Good luck with this next stage of your treatment.  My best friend has just finished all of her treatment for breast cancer.  She had aggressive chemo and very aggressive radiation.  She was super high risk for having skin problems during her radiation.  My other good friend had radiation and some problems with her skin so the two of us (I am a nurse practitioner who specializes in skin) decided to create a skin cream for her.  Anyway, to make a long story short, we hooked up with a lab and did tons and tons of reserach and formulated a cream that she used before, during and after (she still uses it) the radiation.  She just did phenomenally well.  Her radiologist was shocked.  It worked so well that we have produced it.  The website is called www.epicureskincare.com.  It's quite different than other stuff out there.  We really did our homework on this.  The website also talks about how to take care of your skin in general during radiation.  My friends both were not given very much info on what to do so we wanted to give people as much info as possible.  I am uncomfortable with any kind of "salesperson" thing and I hope that I'm not coming across that way.  I truly believe this cream can help people, which was the point of the whole thing. Our website has only been up for two weeks. Good luck to everyone.  I have such respect for all of you after watching my friends go thru this.

  • whippetmom
    whippetmom Member Posts: 6,920
    edited March 2010

    ebethnp:

    You are in violation of the following rules of bc.org:

    You agree not to advertise or promote any goods or services in the Discussion Boards or Chat Rooms. "Junk mail", "spamming," "chain letters," "pyramid schemes" and similar activities are strictly prohibited.You agree not to solicit anyone to buy or sell products or services, or to make donations of any kind, without our express written approval.
  • cwbagne79
    cwbagne79 Member Posts: 9
    edited March 2010

    Simulation on Good Friday and start PBI (3-D conformal) for 1 week, April 5 - 9 with treatments 2X per day for a total of 10 ... can't wait for it to be done.  Anyone else having the one week treatment?

  • dsj
    dsj Member Posts: 277
    edited March 2010

    I had my simulation on Friday and will start 5 weeks of radiation plus boost on April 12.  Unfortunately, I won't know what time slots are available til I come in on April 9 for my "dry run."  I thought I wouldn't have a problem with radiation, because it seemed, in prospect, the least stressful part of the whole experience (surgery done, pathology read, decisions made), but when I went in on Friday for the simulation I really got kind of upset (inside); it all seemed more real and more serious than I had realized.  

  • suzieq60
    suzieq60 Member Posts: 6,059
    edited April 2010

    Welcome dsj. Don't worry too much about having the radiation. Everyone I've spoken to says it's not too bad. Remember, it doesn't take long each time.

    I start on Tuesday, I'll let you know how it goes. When I went for my herceptin treatment yesterday, I saw a girl from the radiation centre and she remembered I start next week. That was nice, as it's a month since I went to see the rad oncologist.

    Sue

  • BossyRenee
    BossyRenee Member Posts: 77
    edited April 2010

    Went to see the rad onc today. Thought I was gonna get set up for my sim however due to having previous lung issues she had me scheduled for a CT scan of the chest this coming Monday instead. Once they get the results back then they will do the sim. I am so ready to get started and done. MY plan was to be finished by the 2nd week of May. Now it will probably be close to the last week of May. UGH...

  • CTMOM1234
    CTMOM1234 Member Posts: 633
    edited April 2010

    Welcome. As a member of the MARCH 2010 RADS GROUP I am happy to report that it gets easier. I just had zap session #19 and am way less stressed out now than I was when I was going though the simulation-dry run-first week period! I remember reading the Jan. and Feb. rad group posts to "prepare" myself for what was to come (haha, as if anything can prepare us for this head spinning process since initial diagnosis).

    Good luck you all.

    And fyi, I suggest you report the post by ebethnp as I have done -- awful to abuse the purpose of this board.

  • willheal
    willheal Member Posts: 12
    edited April 2010

    I was supposed to start Wednesday, March 31 but it has been delayed because insurance didn't approve IMRT.  It is what the rad. oncologist felt was best for my left breast dcis.  I believe doctor will appeal. I had gone for the simulation on Tuesday and was given the "go ahead" to start next day.  I had spoken to billing person 2 weeks prior and asked her to get it approved.  Before leaving Tues. I asked if everything was a "go" with insurance and nothing had been done to get authorization.  Miscommunication between the employees there (to my detriment) because treatment has been further delayed.  I was diagnosed in Jan. and lumpectomy in Feb.  Here it is April already.  I've been very positive until this.  The radiation therapist is nice but seems inexperienced.  She alone did CT scan last week and tatooed me (4 marks).  When I went in Tuesday for simulation, a more experienced therapist helped her reposition me and they placed a temporary mark next to the tatoo mark between my breasts.  This has clear tape over it.  The therapist who did the CT scan said since I will be going every day that it would be ok???? Is this normal (permanent and temporary daily mark with tape over it??? I wonder if she placed the permanent tatoo mark in the wrong spot.  Any thoughts?  Also is anyone having IMRT for left breast dcis?  Is anyone having conventional radiation for left breast IMRT?

  • sweatyspice
    sweatyspice Member Posts: 922
    edited April 2010

    I take the plunge on Monday.  Not sure if I get zapped or if it's just a dry run.

    *quaking in fear and trepidation*

    Oh well, whatever.  Let's do this already.

  • dsj
    dsj Member Posts: 277
    edited April 2010

    willheal, I had my simulation last week and got tatoos.  He said that they would also put sharpy marks on me when I had the radiation that would be covered with tape.  All kinds of cautions about how to wash, etc.  So I think (from my limited experience and from reading) that tattoos and temporary marks with tape are frequently used together.

  • willheal
    willheal Member Posts: 12
    edited April 2010
    Thank you, dsj.  It looks like you and I got similar diagnoses and on similar dates.  I was diagnosed with DCIS on Jan. 28, 2010 (biopsy on Jan. 26) My stage is between 2 and 3 so I say 2 and 1/2.  It is unsettling how many of us are diagnosed all the time.  It seems like a plague. There has to be a strong environmental component (nothing new) to this as well as our own body's vulnerability to developing this.  I think though, that environmental factors of our industrialized, polluted, animal-hormone and pesticide-abundant society plays the major role. I am actually a positive thinker.  But seeing all these stories about how many of us are affected makes me wonder why so many of us? What are we being exposed to that stimulates the development of cancer in so many.
  • MNLinda
    MNLinda Member Posts: 204
    edited April 2010

    I'm expecting to be starting in April, but haven't had the simulation or anything yet.  I just had a drain removed last week and have had some seroma issues, so they're giving me a little extra healing time.

    Does anyone have experience with autoimmune disorders and radiation?  The RO says it's usually not a problem unless it's scleroderma.  Mine isn't, but I've had so many skin problems and rashes in the past I'm kind of concerned that I'll develop some kind of horrible chronic skin condition.

    willheal,  I share your concern about environmental factors.  I think endocrine disruptors probably play a major role.  And one web site I found had a statistic that a woman living in an urban area has twice the breast cancer risk of a woman living in a rural area.  Gives one pause.

    Thanks for starting the group, Sue.

  • kmid
    kmid Member Posts: 23
    edited April 2010

    Hi! Started radiation this past Mon-4 down and 30 to go! Had to wait 2 weeks after sim to start-so busy there.  Everyone very nice. No scans with sim, though. Came down with very sore throat and laryngitis last weekend.  They said come anyway. Not bad at all yet. Rad.Onc. doesn't believe in using creams before problems start.  Makes me a bit nervous. Had aloe plant, etc. ready to go.  Anyone had this experience? Good luck to all as we move through this process. Still teaching full time but will change that if needed.  Still sick and exhausted from week, though.

  • suzieq60
    suzieq60 Member Posts: 6,059
    edited April 2010

    Well, tomorrow is the first day - wish me luck. Luckily the treatment centre is only a 10 or 15 minute drive but I'm sure I'll be sick of it after 6 weeks. And I get free parking!!! if I can find a space. If not, I can park on the next level as it's the same building as my oncology is done.

    Sue

  • hymil
    hymil Member Posts: 826
    edited April 2010

    Got my tattoos, Starting with you on tuesday. Have to say i have found the information from previous sets very helpful, Thank you! but still a bit confused, should i use cream beforehand or wait and see.

  • sweatyspice
    sweatyspice Member Posts: 922
    edited April 2010

    Suepen, we both start tomorrow!!  Even though, since you're in Australia and I'm in New York City, they're probably actually different days.....

    Good luck!

  • suzieq60
    suzieq60 Member Posts: 6,059
    edited April 2010

    Hymil: DO NOT put any cream on before. One lady in the rads forum had nasty consequences. Others told her you are not to put anything on within 4 hours of treatment. Read all of the posts here:

    http://community.breastcancer.org/forum/70/topic/750530?page=1#idx_16

    I'll be ahead of you both so I'll write and tell you how it goes.

  • KatieMom
    KatieMom Member Posts: 127
    edited April 2010

    I started rads today.  The tech was really nice, although I have Sharpie marks ALL OVER my best and booby.  All fine.  33 more to go.

    Katie 

  • suzieq60
    suzieq60 Member Posts: 6,059
    edited April 2010

    Katie,

    Didn't you get tatoos - it didn't hurt. Hope they don't use pens on me as well as I now have a green permanent marker stain on the white bra I wore for the planning session. I go for my first one in about 5 hours - feeling a bit nervous at the moment, but I do know it will be fine.

    Sue

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