Starting Rads in March 2017

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  • javamama
    javamama Member Posts: 119
    edited March 2017

    My start date got pushed back to the 27th. Ugh

  • Cowboy-Up
    Cowboy-Up Member Posts: 211
    edited March 2017

    Just finished my simulation. Was a bit uncomfortable because I am ready to start my cycle and after the reduction, the girls are really sore at that time of the month. I am on my stomach so the "good" one is smashed. Was very quick though. Met some ladies in the waiting room and although I was definitely the youngest there, they made me feel welcome. There were volunteers there handing out water and chcolates. I can do this

  • Sorella
    Sorella Member Posts: 107
    edited March 2017

    Meet my radiologist next week. Will get schedule then. Finished chemo Feb 27th. Trying to enjoy being done one rough road before I start the next!


  • ILSunrise
    ILSunrise Member Posts: 130
    edited March 2017

    Looks like several have started treatments and so far so good.

    I had my marking session and simulation yesterday. My RO does not use tats, so I have 5 black Sharpie ink marks in a few places. Basically, the marks are for lining me up in the machine (around belly, on sides and on my sternum). We practiced the breathing technique where I would hold my breath to keep my heart out of the way of the radiation dose. I have to wait 5 to 7 days before I get my radiation schedule. I'm hoping to go in the afternoons so I don't have to go back to work after the treatments. I was told not too apply lotion over my breast 4 hours before treatment. Also, I'm not to wear deodorant under my left arm for the 6.5 weeks of treatment. I was told I could use corn starch instead.

    LynnieRich - sorry to hear you are battling lymphedema already. I hope the PT is helping.

    Lovey222 - thanks for the suggestion of Lansinoh cream I think I'm going to try it.

    Coupon

    - thanks for the suggestion of the Lindi skin cooling roller. Where did you find it - Amazon?

    Sounds like there are a lot of good options for creams, etc. to help with skin breakdown.

    Hang in there everyone....we've got this!

  • LynnieRich
    LynnieRich Member Posts: 28
    edited March 2017

    ILSunrise- no deodorant?! Eek! They told me no deodorant with aluminum. So I bought Toms for my left arm and use my regular deodorant on my right!!


    I had my second treatment today. It's itching but this seems WAY too early for any side effects... maybe it's the cream I put on it? Anyone else?

    Also I can't remember if I'm allowed to shave under my arm. I'm assuming not?


  • Coupon
    Coupon Member Posts: 29
    edited March 2017

    ILSunrise, I got the Lindi cooler roll and soothing balm from their website:

    http://www.lindiskin.com/shop/by-concern/radiation...

    I bought 2 cooler rolls but 1 should be enough. The cooler roll can be cut to size and can also be re-used. The soothing balm is not greasy at all! The radiated has been warmer than the other side since day 1, although the radiation therapist said it's way too early to have any side effects from rads, applying this cooler roll soothes a lot.

    I already had 7 out of 25 rads, and today start feeling tightness around the chest + develop some coughs. It doesn't bother me but will definitely bring it to my RO on my next review.

  • Not-happening-68
    Not-happening-68 Member Posts: 5
    edited March 2017

    I've completed 6 of 21 radiation treatments thus far. No problems with pain or redness. Just mildly tired in the evenings. I'm just wondering how much lung tissue the rads are hitting? And hopefully none to minimal of my heart tissue since it's right sided!! Today I will have a checkup with my radiation oncologist and will ask how much collateral damage is being done . I'm thinking the dr should know the answer since she set up the treatment plan ?

  • Mama2BC
    Mama2BC Member Posts: 12
    edited March 2017

    Morning everyone!!


    I had a bilateral mastectomy with TE on 1/18. Pathology results showed one of the lymph nodes removed had cancer. Long story short, I have received 2 opinions and both doctors are recommending radiation. That's fine. However, I am struggling because one doctor thinks I should do the whole chest wall, while the other believes I should localize the radiation under my arm. I just don't know what to do! The physician that recommended the whole chest wall, has indicated this is a proactive approach to reduce recurrence. Which I like. But I am also aware that there are some risks involved with doing more radiation. I guess I am primarily concerned about reconstruction issues. My plastic surgeon has already started filling my TE's in preparation for radiation. I am leaning towards the whole chest wall, even though there are more risks. That being said, when I met with both doctors, I still like the personality of the one that recommended the more localized treatment. Anyone else in a similar boat? How did you decide what to do? Has anyone ever spoken to a doctor about their 2nd opinions and wanting to still treat with their doctor, but do something based on another doctors recommendation?


    Thanks!!

  • Kinnie88
    Kinnie88 Member Posts: 9
    edited March 2017

    Radiation has been easy compared to chemo, I did have a little nausea. After the third day the Tomotherapy equipment malfunction, so instead of two day weekend without it will be three. They are not concerned about this. Using Aloe Vera plant juices really does the trick for me.

  • Cowboy-Up
    Cowboy-Up Member Posts: 211
    edited March 2017

    LynnieRich, I had my second day yesterday and I too was itching a little bit. Had a tiny bit of pink too. Thank goodness for the weekend to have a couple of days off.

    I was told I could keep shaving until it started burning. If it wasn't red, I could keep shaving.

  • Emily2008
    Emily2008 Member Posts: 605
    edited March 2017

    Hi ladies,

    Just popping in here to give you my personal experience. I finished 30 rad treatments yesterday (yahoo!), and I have had very little trouble with my skin. My rad onc and nurses recommended using Gold Bond powder under my arm and breast fold on the treated side (in the morning), no deodorant, no shaving. Right after treatment (before getting dressed again), I covered the area in Aquaphor. It's sticky, so I trashed a number of t-shirts and camis, but it's a small price to pay. Then at night, Hydrocortisone cream on the treated areas. That's it! I ended up with a red, somewhat itchy patch on my chest, and a slightly pink breast. Nothing more! The itchy chest is solved by a second application of Hydrocortisone cream. I feel some nerve pain mostly under the armpit and some breast tenderness, but it's not too bad. And my skin is doing great considering how many sessions I had.

    So, just my experience, which I think has been successful in terms of skin. Hope you all do as well!

  • CeliaC
    CeliaC Member Posts: 1,320
    edited March 2017

    Hi, everyone. Thought I would share my experiences thus far. Yesterday was 13/16 whole breast zaps & setup for 4 boost zaps concentrated at tumor bed, for a total 20 zaps. Got 4 more marks for the boosts. Skin effects were a big concern due to very fair skin that sunburns easily. Started using the Dr/Nurse recommended Miaderm (not greasy, spreads easily) one week before rads and use it 4x daily. Could not use Aquaphor as petrolatum bothers my skin. Skin a little pink, especially nipple. Like Emily2008, some nerve pain under armpit and breast tenderness. Prescribed Lidocaine ointment working well to relieve nipple & armpit effects. Also using prescribed Mometasone Furoate cream on sensitive areas. My advice: Use creams! Do not wait until "effects" start. Also, make sure you let a Rad Nurse/Dr know when you need more "help" with your skin. Cancer Center I go to always has a Rad Nurse/Dr on duty & you can speak to them even if it's not your "scheduled" day to be seen by them. My rads are after work - helps to be distracted during the day & Center to home is a 6 min trip. Managing to wear normal business casual at work by wearing a cotton tank with a "stretched out" bra over it so rad area is not irritated. Saw this "tank tip" somewhere on the internet. (shopping hint: at Target, currently 3/$24) Hope some of this info is helpful to fellow rad ladies.


  • ILSunrise
    ILSunrise Member Posts: 130
    edited March 2017

    Emily2008 and CeliaC - thanks for sharing your experience for those of us just starting rads as well as the advice and tips on creams, tank tops, etc. We're all a but nervous and are just looking forward to having this chapter behind us.

    Coupon - thanks for the link to the Lindi cooler roll. I need to get online and order one.

  • WenchLori
    WenchLori Member Posts: 1,558
    edited March 2017

    Cowboy-Up, I was told I could shave but only with an electric razor. I'll have to use the electric razor for the rest of my life due to having 13 lymph nodes removed. Nicking myself with a blade razor could cause lymphodemia to develop and that terrifies me!

    Not-happening, does your radiation team do x-rays with every treatment? Mine does and so far no signs of lung or heart damage (15 of 33). My cancer is on the left side so I'm very nervous about them zapping my heart even with the breath hold. I'm having the chest wall and arm pit treated as there is no breast tissue left to treat (I hope!).

    Coupon, thank you for the cooler roll information. I wonder if I can use it? I was told no cold or heat in the treatment areas. I'll ask my RO if he thinks the cooler rolls would be safe for me to use when I see him tomorrow. I've developed a cough too and I was given a prescription for ?!. They are little tiny balls and I take one 3xs a day. It's works wonders. The tightness in my chest started at about treatment #8. My RO is able to treat under my TEs so I won't have to have my TE emptied and then start expansion all over again.

    Emily, congratulations on finishing your radiation treatments! Yay!

    Celia C, thank you for sharing your experiences and all the tips on tank tops etc. I can use A&D ointment at night only so I have old night gowns that handles the greasy sticky stuff. I have to shower to get the A&D off in the mornings or it'd still be there for my treatments. I even use it on my horses for all the scrapes and cuts they show up with at the barn. It even gets the hair to grow back on their scars. Pretty potent stuff. Hopefully I won't have any hair show up on my chest. That would be horrible!

    Until next time

  • SCGirl50
    SCGirl50 Member Posts: 43
    edited March 2017

    Met my RO last week for consult. Absolutely love her. She spent an hour with me explaining everything and asking me many questions about me. A change from most docs who are all about getting it done. CT/planning is scheduled for 3/28. Will do simulation the following week and begin 25 treatments. I am facinated with the science behind radiation. I will probably drive them crazy with all my questions.

  • Ruby3813
    Ruby3813 Member Posts: 96
    edited March 2017

    Good Morning!

    My initial appt with the MO is tomorrow morning. I guess I'll find out then what my course of treatment will be. I don't see the RO until next Thursday (23rd), so it's looking like rads won't start until April. Looks like I'll be moving to the April Rads Group. We're supposed to leave for Vegas the evening of April 21st. I sure hope I can get a reprieve from rads for 2 days!

    Good luck and prayers for everyone!

  • Cowboy-Up
    Cowboy-Up Member Posts: 211
    edited March 2017

    WenchLori, I do have X-rays every time. Mine is on my right side so less chance of heart issues.

    So far so good. 5 down, 26 more to go

  • ILSunrise
    ILSunrise Member Posts: 130
    edited March 2017

    I start rads on Monday. I plan to go shopping this weekend for some tank tops and have bought a soft front hook bra and some radiation cream. So I guess I'm ready as I'll ever be for this step.

  • Leslie2016
    Leslie2016 Member Posts: 316
    edited March 2017

    Had my first one today. Simple, and short.

    Anyone know how they decide how many treatments we get? I just find it interesting that it seems we all have a different amount of rad treatments.

  • misslil
    misslil Member Posts: 260
    edited March 2017

    It's looking like I will be starting partial breast radiation treatments on the 27th, after they did measurements or whatever it was today and I go back next week for a revisit and their rehearsal.

    Still up in the air what plan of attack -- could be 3 weeks twice daily, or the more conventional 30 sessions once daily.

  • WenchLori
    WenchLori Member Posts: 1,558
    edited March 2017

    Ruby, my rads was supposed to start the week after chemo ended (12/27) I asked if I could put it off until the beginning of February without doing any extra harm by the delay? I was told I'd have more energy to get thru rads if I took a longer break. All ROs are different but ask, it's your body. I spent January in Austin/San Antonio TX with my kids and grandkids. I slept the first 2 weeks but my kids were able to see that I was ok and fighting this BC with everything I have. My RO was surprised how good I felt when I got back to my treatments

    Cowboy-Up, cheering you on!! I'm 20 down with 13 more to go. So far I've got some redness and I hurt like crazy after waking up laying on my radiated left side. You got this!

    ILSinshine, wishing you smooth sailing! Cheering you on also! You can do it!

    Leslie, my RO loaded the results of my pathology report into the NCN website and the program told him/us the best treatment program to follow. I don't know if all ROs and MOs use this program but seeing that it's a national database they might??

    Hello to All I may have missed! Praying you all have a wonderful day today!

  • CeliaC
    CeliaC Member Posts: 1,320
    edited March 2017

    Leslie2016 - Agree it is confusing how number of treatments is determined. Believe it is case by case, depending on type, stage, grade, node involvement, etc. RO scheduled me for 16 whole breast + 4 boosts to tumor bed, total 20. Have heard mostly 25 or 30 treatments, so I was happy when it was only 20. Came across something about "typical" dosage: 100-200 rads or centiGrays each, 4000-5000 centiGrays over 5 weeks (5 treatments per week) plus an additional 1000-2000 centiGrays for 1 week (5 treatments) as a boost. Saw my dosage info @ latest RO visit on 3/15: 4256 centiGrays total for the 16 treatments + 1000 centiGrays for 4 boosts, total 5256.

    Only have 2 boosts and then done! Now that whole breast is done, only minor pinkness in underarm & near sentinel node scar - nipple no longer irritated & I have very fair skin. Hope things go as well for everyone else. Hugs all around.

  • Leslie2016
    Leslie2016 Member Posts: 316
    edited March 2017

    Thanks ladies. I'm very glad that they seem to be able to help tailor make our treatments as much as possible. It just makes me curious about how they arrive at things. :)

  • WenchLori
    WenchLori Member Posts: 1,558
    edited March 2017

    Celia, I'm getting 33 treatments of 180 centiGrays every day. No mention of boosts at this time so I'm sure it's not on my treatment plan. Maybe it's due to the type of surgery we chose? I had a DBMX and those that have mentioned getting boosts had lumpectomies? Do you know how they determine boosts?Things that make me go hhmmm.


  • CeliaC
    CeliaC Member Posts: 1,320
    edited March 2017

    Since boosts go to the tumor bed, which is where they removed tumor during lumpectomy - my guess is they pertain to lumpectomies. Maybe someone can ask at their next scheduled RO visit? RO said I will not have another visit after last Thurs., since only 2 boosts.

  • WenchLori
    WenchLori Member Posts: 1,558
    edited March 2017

    Celia, I'll have to remember to ask my RO on Tuesday... IF Ican remember, my chemo brain still runs my life 🙁

  • Coupon
    Coupon Member Posts: 29
    edited March 2017

    My RO told me boosts only apply to those who had lumpectomy, not mastectomy.

  • WenchLori
    WenchLori Member Posts: 1,558
    edited March 2017

    Coupon, thank you, now I don't have to remember to ask my RO tomorrow. Chemobrain at its worst for me

  • Ruby3813
    Ruby3813 Member Posts: 96
    edited March 2017

    Morning Ladies!

    WenchLori - thanks for your info! I'm definitely going to ask about fitting my vacation in when I see the RO tomorrow morning.

    I saw my MO for the first time on Friday. He gave me a very positive prognosis, but the best thing he said was NO CHEMO. Thank God. I feel for all of you women going thru it and you're in my prayers daily.

    I guess I'll find out tomorrow how many rad rounds I'll have, then I can start to see the end of the road. The MO said I don't need to come back until October to see him, and he already sent out my prescription for Arimidex. He said I don't need to pick it up yet. Said to start it 2 - 4 wks after rads are finished. Oh, and he told me 5 yrs only. I'm 65.

    Have a blessed day!

  • WenchLori
    WenchLori Member Posts: 1,558
    edited March 2017

    Ruby, great news on no Chemo! I'm doing the happy dance for you!

    My RO original told me 33 days of rads but the techs just told me only 28 were ordered. I'm waiting to see him now so I'm keeping my fingers crossed for the 28 instead of 33!

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