January 2012 rads

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  • lisalock
    lisalock Member Posts: 45
    edited January 2012

    Never had radiation the first time I was diagnosed, but with the bone mets I'm having 15 treatments to my sternum...halfway through!!

    Lisa

  • twistedsteel
    twistedsteel Member Posts: 156
    edited January 2012

    Ann

    I have Miaderm and it has fragrance which bummed me out big time so I used it once and not again. Just FYI

  • mags20487
    mags20487 Member Posts: 1,591
    edited January 2012

    Ralston--no TE's for me yet...waiting til treatment done.  The RO showed me the "range" of the beam on the body.  It covers where the lymph nodes were but not the actual armpit.  Took his word for it not sure where they actually were.  I am getting 30 treatments and 5 boosts to the scar on the left (cancer) side.

    Maggie

  • ptdreamers
    ptdreamers Member Posts: 1,080
    edited January 2012

    Annalive what  is the exercise you are doing? Can you describe it?

    Ppatrictia, Be sure to use some hydorcortisone cream 1% if you aren't allergic and some aquaphor to help with the redness.

    Ladies steal you husband, boyfriend's or get some old ratty t-shirts to wear after rads. You won't mind slathering on your creams etc. and will be happy to throw them out at the end.

    Put on a bra for the first time in two plus months. Making progress!

  • Patrithia
    Patrithia Member Posts: 19
    edited January 2012

    Hi, 

    I wasn't going to get the tatoos thinking that they would be obvious; however, after a week of the "stickers" I changed my mind (trying to be careful in shower, etc.). The tatoos were like a tiny dot (like a freckel) and I'm so glad I did them.

    Patrithia 

  • Ralsper
    Ralsper Member Posts: 352
    edited January 2012

    I also have a complete lymph node dissecton (22 of them were healthy nodes!!) I still do not know my RO plan, but I will email him with all this questions. I do not have enough data, so I need to see more information before I let them radiate my nodes. I have mild LE and is already killing me... I care alot about the quality of my life after this.

  • AnnAlive
    AnnAlive Member Posts: 450
    edited January 2012

    twistedsteel - Uh oh, I just looked and see fragrance as the last ingredient in Miaderm. I hope that means there's very little of it, and so I'll try it anyway. I don't seem to have trouble with fragrance as an ingredient in lotions. Is it toxicity or allergy that concerns you? I bought Miaderm after searching other rads threads for creams that ROs recommend. My RO didn't mention any brands.

    ptdreamers - Manual lymphatic drainage (MLD) involves light circular strokes on the skin to redirect lymph fluid from the affected to the unaffected side. It starts in the supraclavicular area, moves on to arms, chest, and inguinal areas, and is specific about the order to make the drainage work. It's probably best to be shown the technique by a physical therapist. 

  • Ralsper
    Ralsper Member Posts: 352
    edited January 2012

    I am using Cethapil Fragance Free Moisturizing Cream and Aloe Vera (Lily of the Desert Gel 99%). A friend gave them to me because she used them 1 year ago during radiation (30 rads) and these products worked great for her, but she had a lumpectomy, so let's see if with MX work.  I am planning to wear cotton t-shirts and no bra. Still waiting to hear from my RO.

  • chef127
    chef127 Member Posts: 891
    edited January 2012

    Hello ladies,

    I thought I'd post because I need your inspiration. Yesterday I had my first rad tx. 1 of 25, plus 10 boosts. I was pretty scared. It was sooooooo easy. I hope it stays that way. I did ask the techs and the RO about creams and maybe a diet to help with all that raiation my body will absorb. no real answer. "We'll cross that bridge that when we come to it." Really. I will moisterize my skin and add more greens and protien to my diet.

    It's so nice to be here and I wish you all a easy trip down the radiation trail.

    Maureen

  • itsjustme10
    itsjustme10 Member Posts: 796
    edited January 2012

    Hi.  I started my radiation treatments on the 10th.  I have to have 25 of them.

     Other than having to stay still the whole time, it doesn't seem all that bad so far.  I'm using the Aquaphor at night, but from what I understand, it's too early to worry about skin problems, anyway.  I just hate the consistency of the stuff.  Ick.

     Good luck to everyone!!  Hope it goes easy for you. Smile

  • Ossa
    Ossa Member Posts: 919
    edited January 2012

    Morning Ladies

    Was supposed to have my radiation planning today, but the machine broke down.. so have to wait until Monday... That happens to be my birthday,53, and I get to spend it at the hospital for planning.... but then again.. glad it is getting done.. the sooner I start the sooner I will be done..

  • Momine
    Momine Member Posts: 7,859
    edited January 2012

    Chef, my zap-doc gave me a cream with cortisone and vitamins and wants me to use 2X a day for the duration. I started rads Monday, and used other creams, because the steroids scared me. But today the doc sort of yelled at me and insisted that I must use the special cream.

  • J-Bug
    J-Bug Member Posts: 626
    edited January 2012

    chef127: As far as diet is concerned, my RO told me not to go out of my way to get extra antioxidants beyond the normal diet because that could disrupt the effects of chemo. They want to destroy those bad cells and if we have an excess of antioxidants, our bodies would be repairing them. Crazy stuff! She didn't say to eat poorly of course, just not OD'ing on the antioxidants. That is the only thing I have been told about diet so far.

    My RO gave me a burn gel to use but said that I didn't really have to use it until I started seeing skin changes. She said that I could use lotion if I wanted, but it is not necessary yet either. She will have an appointment for me with a nurse about skin care in a week or two. I just finished my 4th appointment today. Momine: kind of funny that you are getting yelled at for not using the "special cream" and I have no special cream recommended yet. But, I will eventually.

  • Momine
    Momine Member Posts: 7,859
    edited January 2012

    J-bug, yes, it is a little funny. It seems like docs are all over the map on this one. I am too scared to look though, so probably better to use the cream instead of waiting for changes, lol.

  • mags20487
    mags20487 Member Posts: 1,591
    edited January 2012

    Wow so many docs and so many opinions.  Mine said use whatever you want for moisturizing.  Will address cortisone cream if necessary during treatment.  Cannot wait to get on with this phase.  Sim/mapping on Tuesday and then MO appt Wed to get results of blood work and pet scan from today.  Then Thursday leaving for Vegas for franchise conference for my store.  Busy Busy...feels good though to be doing something.

    Maggie

  • Ralsper
    Ralsper Member Posts: 352
    edited January 2012
    Well... Someone with more experience than me said that it is not about the cream, but to make sure to apply it constantly (at least 3 times a day) and everyday. Surprised
  • Ralsper
    Ralsper Member Posts: 352
    edited January 2012

    Okay.  So I feel a bit better knowing others have had the rads with the tissue expander in and my PS will not need to deflated. Still waiting to know which day next week I will have my first treatment (1 of 25).

  • Rockym
    Rockym Member Posts: 1,261
    edited January 2012

    I had #8 today and all is well.  It's very quiet in my RO's office.  It's a very different experience then chemo.  Chemo was kinda social since there were a lot of chairs/people in my MO's office and the nurses were around to chat with, etc.  With RADS, I walk in and take off my shirt immediately, put my things in a locker and then I walk back to the rad suite.  I say a few words to the techs, they say a few words to me and then I lay there for the 10 minutes.  It's kinda lonely.

    I'm scheduled for 27 treatments with 9 boosts.  I'll have to ask my RO what determines the number of tx and boosts.  Anyone know the specifics?

  • chef127
    chef127 Member Posts: 891
    edited January 2012

    Rockym,

    Yes it is a lonely Tx. When my first Tx was done I asked the tech what the burning smell was during the zaps. She looked at me almost terrified. And I thought I was being funny. Today I had my #2 Tx and before we started I asked her to zap the hairs on my chin. They both laughed. They need to ease up on the assembly line attitude. I'm lying there, half naked, with my mutilated breast exposed, for all to oogle. Lets lighten up a little.

    I'm having 25 zaps and 10 Boosts. I thought it was because of the large tumor area, but I see your Tumor was a lot smaller. Curious question. are you having 27 TX PLUS 9 BOOSTS? or 27 total?

    Maureen

  • rjbaby69
    rjbaby69 Member Posts: 349
    edited January 2012

    Hello ladies.  Had my 5th of 30 treatments today.  So far, everything has been uneventful.  It takes me longer to drive there (45 minutes) than it does to get the radiation (10 minutes).  LOL!  I did visit with my nurse yesterday about skin care and she told me that they prefer that I do not use anything on my breasts and that if I needed something, they would give me some special cream.

    So far, radiation is turning out to be a walk in the park compared to the chemo.  I just try to remember there is an end in sight.  My last treatment should be February 22.  Yippee!

    Hope you all do well with your radiation treatments.  I will check in soon.

    HUGS!

  • findingsolace
    findingsolace Member Posts: 17
    edited January 2012

    Hi Everyone! Went for my mapping today. It was uneventful. One thing I was curious about was the weekly "quality assurrance" scans they do. I was worried about the extra radiation from them and if they were really necessary to keep them on track since they have marked me up so good. I asked how often they change something based on these weekly scans and she said "about once every 6 months". I then wondered if I was getting more radiation each week because of these scans. She started writing dosage levels and all this other stuff down on paper for me to understand and essentially what she explained was that they figure the dosing from these once a week scans and minus it from the dosing that day to treat you so you are getting the same dose each day, even if you get the scan one day and not the next.  The total radiation dosing is the same and the scan counts as the body burden for the radiation treatment. I don't know if I explained this clearly enough but it made me feel better about the quality assurrance radiation I was getting weekly to make sure there markings were still accurate.  I tried to joke a bit too but my guy was really concentrating on giving me the tattoos and stickers and getting me out of there on time. Geez!

  • tnhelen
    tnhelen Member Posts: 63
    edited January 2012

    I had my 13th treatment today.  23 more to go.  My breast is red and sore so the RO wrote me a prescription for motrin.  He can't seem to understand the pinkness because I came in with it before I started rads so he thinks it could be a flare in my lupus panniculitis. 

    I use the cream they provided, it is prescription.  The radiation is very easy and takes very little time.  But I have been having a few episodes of fatigue.....it sort of washes over me like a wave and stays for awhile and I have to rest.  Odd, but not unbearable.  I just sleep a little more. Things are going well.

  • Rockym
    Rockym Member Posts: 1,261
    edited January 2012

    Maureen, the printout they gave me showed 27 reg tx and an additional 9 boosts.  He originally said 33 tx and I never really asked how they figure out the number, boosts, etc.  I was definitely more on my game a few weeks back.

    I still joke around a bit, but it's all so quick.  There really isn't time to talk much or get to know these guys.  With chemo, I got to know the nurses and even had a couple of ladies that I chatted with while in the chair.  Of course I would have preferred only rads, but I'm 47, had 2 positive nodes, an Oncotype dx of 22 and I have young children.  I couldn't afford not to give it everything.  Love the burning smell joke :-).  I may just have to borrow that one.

  • Terry71
    Terry71 Member Posts: 293
    edited January 2012

    I started my rads on the 12th and have 25 of them..... Can anyone tell me what to expect? did 18 weeks of chemo, finished Nov 17th, had mx on dec 14th and started rads 3 days ago..... Thanks ladies

  • chef127
    chef127 Member Posts: 891
    edited January 2012

    Terry71,

    It is impossible to predict  what side effects we will suffer, if any. We are all different. The tx themselves are very easy to take. From what I've read it takes approx. 3 weeks of tx. before you get a reaction. burning skin and fatigue. Thats it. But like I said we are all different. We can only take 1 tx at a time.Good Luck to you and all of us.

    Maureen

  • HJMom
    HJMom Member Posts: 1
    edited January 2012

    I am 9 treatments in out of 30. So far it is easy going. Takes more time for prep than the actual radiation. I was recommended to use Miaderm 3x/day for the duration of the treatments to prevent skin irritation and assit in healing. It does have a floral smell which I dont enjoy but my usually sensitive skin is not reacting negatively in any way to the perfume in it. No fatigue - just a slight skin sensitivity like being in the sun too long on a spring day when you weren't expecting the sun to be strong yet. All very bearable so far! 

  • Ralsper
    Ralsper Member Posts: 352
    edited January 2012

    Rockym- Did you have a lumpectomy or a mastectomy?

  • Rockym
    Rockym Member Posts: 1,261
    edited January 2012
    Ralston, I had a lumpectomy.  My mass was very close to my left armpit.  Good for preserving the look of my breast and having a very small scar practically under my arm, bad for the node situation.
  • lifechanging2011
    lifechanging2011 Member Posts: 48
    edited January 2012

    Hi all,

    I had a lumpectomy on 12/27. Luckily, I don't need chemo. I met with my radiation oncologist last Wednesday and I go for mapping on Monday. I've been stressed out about this whole radiation process. At this point, it seems that the surgery was the easy part. I  also have rheumatoid arthritis, so I already suffer from fatigue and the medication I take for that makes my skin sensitive. I don't know what to expect from radiation. I can't imagine doing that 5 days a week for the next 6 weeks. I guess I need to be willing to do  anything that will protect me from the cancer...but I'm stressed out about the next part of the treatment process.

    Traci

  • lifechanging2011
    lifechanging2011 Member Posts: 48
    edited January 2012

    Hi Maureen,

    Thanks for your post. I haven't started my radiation treatment yet, although I get mapped on Monday so I'm assuming my treatments start this week.  I asked my radiation oncologist about diet and he suggested a healthy diet but emphasized exercise to stay strong.  I was curious why you deleted earlier posts? Just curious.

    Traci

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