Starting Radiation October 2017

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DodgersGirl
DodgersGirl Member Posts: 2,382

I have been thru chemo and surgery and was just scheduled to see my RO for mapping next week. So it looks like rads will be starting for me this month.

Anyone else starting rads in October??

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  • LoJo100
    LoJo100 Member Posts: 123
    edited October 2017

    Hi DodgersGirl!

    Yes, I started rads this week. Just finished #3 today. So far, so good!

    I'm using Miaderm right after the treatment and then a couple more times a day.

    I also finished chemo a couple weeks ago and am now in radiation. The good news is, each day feels better because I'm still coming out of the chemo haze!

    The mapping wasn't too bad, just a long time with my arms over my head. The tattoos they gave me are so small, they look like freckles. I barely see them! The techs have all been amazing. I find the machine and the science of it all quite fascinating.

    I hope your set-up is easy. Thank you for setting up a group for those of us starting in October!

    -LoJo

  • Teach70
    Teach70 Member Posts: 64
    edited October 2017

    I had my mapping done last Thursday. I should have my simulation next week. I currently have marker covered with clear stickers. They won't tattoo me until the third treatment. I'm not sure why.

  • DodgersGirl
    DodgersGirl Member Posts: 2,382
    edited October 2017

    LoJo- glad to have someone else starting rads in October!

    How many rad treatments will you have?

    Glad to hear so far so good for you!!

  • DodgersGirl
    DodgersGirl Member Posts: 2,382
    edited October 2017

    Teach70 - another October member!

    What is the difference between mapping and simulation?

    So far, I have an appointment with RO on 10/10 and will start the process. Am not sure what that means yet.

    I haven't had physical therapy yet after surgery so worried about being ready to hold my arm over my head for a length of time.

  • LoJo100
    LoJo100 Member Posts: 123
    edited October 2017

    Hi Teach70!

    I don't know why they won't tattoo until the 3rd treatment for you. Interesting. Maybe it's just the way they do it. I've found out one thing on these boards... everybody's team is a bit different! :-)

    DodgersGirl - I have 28 treatments scheduled at this time, no boosts. They may add boosts at the end, but as of now, the consensus is I don't need them due to the wide margins I got from the BMX.

    Now, that being said, even though it did not spread to the lymph nodes, we are doing a full lymph node treatment, up to the clavicle. I had a larger tumor, so they want to make sure that if a cell decided to have a party in a lymph node, they get it. I'm all for it, and due to my chest shape, the increased odds of lung dose stay very low, so there really is no reason not to do it this way. Oh, and it's on the right side, so heart dose is not expected to be a factor.

    Do you know how many treatments you will receive (both DodgersGirl and Teach70)?

  • DodgersGirl
    DodgersGirl Member Posts: 2,382
    edited October 2017

    LoJo100- when I met RO back in April, he said I would be getting 35 treatments. Hope to be done before Thanksgiving.

    Will see next week if that is still the plan.

  • Teese
    Teese Member Posts: 379
    edited October 2017

    Hi ladies, I won't be starting till Nov but will be following your thread to learn what it's all about. I have my first RO appointment 10/19.

    Theresa

  • DodgersGirl
    DodgersGirl Member Posts: 2,382
    edited October 2017

    Teese-- welcome.

    I haven't read up on rads too much yet. Taking this cancer journey one step at a time. Curious as to what RO will recommend regarding creams or lotions (or whatever the term is for skin ointments for rads)

  • Teese
    Teese Member Posts: 379
    edited October 2017

    Dodgersgirl, the lotion thing is my biggest question and seems so variable. I wonder what my RO will suggest. I know one gal who just finished up recently posted shewas strongly advised not to use anything because it's the creams that cause the issues. She had no skin issues at all. Makes me wonder....


  • Castigame
    Castigame Member Posts: 752
    edited October 2017

    sisters,

    I am just chiming in.

    I used cool aloe gel only (non aloe gel was about 5 times total) and no bra no top as much as possible. Walked min 30 min everyday. During radiation, I had min 2 appts every day. At least 25% of days I did not get to moisturize till about late afternoon. Did 30 zappings. Only faint pink at half way. Everything including fatigue accelerated after half way mark. Sudden sleep coming over was big for me. When it was done I had two small blisters appeared one at a time. Yea my underarm was raw from rad. Rawness peaked for a week right after completion. Last rad was 09/14. All effects from rads are gone except trace of greyish brownish skin in radiated area. Yea I am hoping I never have to shave radiated right armpit. After two weeks, I even felt sudden drop of general swelling.

    Lastly, I do remember not moisturizing for about 24 hrs after rad completion again I was busy w drs appt. This helped scabbing raw underarm. This was 1 wk to 10 days post rads. You will know when the entire sore spots scab. Moisturized as little as possible for the secod week. Someone said it took her two weeks after rad completion. It seems no matter what everyone's DX is, rad healing takes about two weeks.




  • Teach70
    Teach70 Member Posts: 64
    edited October 2017

    Dodgersgirl- the mapping is when they use the ct scan and make all kinds of drawings on you. I still have little x’s covered with sticky tape. It will be sent away for calculation and should be back soon. They will then do a test run or simulation to make sure all my markings are correct. On day two they will actually use radiation and if everything is correct, they will make the tattoo marks on day three. That’s is how the tech explained it to me. However, after having the stickies on my skin for over a week, two of the five washed off. She told me I could shower as normal. She said they will remark me anyhow when I go for my simulation. It is funny how everyone’s treatment is slightly different in how it is dibe

  • DodgersGirl
    DodgersGirl Member Posts: 2,382
    edited October 2017

    Teach70- thanks for the explanation!

    It is strange how the rad process differs from place to place. I realize equipment could be different but would think recommendations on gels and such would be more similar

  • DodgersGirl
    DodgersGirl Member Posts: 2,382
    edited October 2017

    Castigame- did you do the green tea pads or spray during your rad sessions

  • l_brain
    l_brain Member Posts: 71
    edited October 2017

    Started this week. Number 4 will be today. 15 regular and 5 boosts. To use cream or not seems to be the question. I'm going to use what I have once a day and just see what happens. Doc thought the third week I may see irritation start.

  • Castigame
    Castigame Member Posts: 752
    edited October 2017

    I tried total of 5 non aloe gel. One or two was cool green tea and two or three was acquaphor. Cool green tea was good but I liked Aloe better. Also doing just one was simpler for me to remember.

    I am thinking even keeping your choice of creams in fridge may not be a bad idea. Your entire upper body will get sooo hottttt. So almost anything to lower body temp helps.

  • DodgersGirl
    DodgersGirl Member Posts: 2,382
    edited October 2017

    castigame- thanks. I remembered reading about how you kept aloe in the fridge to apply. I ordered aloe yesterday from Amazon. I am buying green tea bafs this weekend as I hope RO will it is ok to use. Some ROs say no to green tea. If mine says no to green tea then I will just drink it after rads are over! Haven't bought anything else waiting to see what happens at RO appointment

  • utjoy
    utjoy Member Posts: 56
    edited October 2017

    I start the 23rd...28 zaps. Will get the clavicle, too...I'm really dreading rads! I had 4/6 nodes positive after chemo which has been really hard to deal with emotionally, I also have full-blown osteoporosis...due to early menopause they say. I'm 56. MO wants to start me on Arimidex asap, have appt to see dentist tomorrow.

    I was given the ok to use the green tea...RO said he'd heard of it, but, yet to have a patient who tried it. Said he wants to see red skin as he then knows it's working!? I'll use aloe, too...idk what else?

  • Teach70
    Teach70 Member Posts: 64
    edited October 2017

    My RO's office called. I go tomorrow for my simulation and start rads on Monday. 25 whole breast and 5 boosts. I ordered miaderm and also bought pure aloe gel and have it in the fridge. I have been using emu oil twice a day since I had my stitches removed. I thought I would try to get ahead with the softening of the skin. Plus emu oil helps heal and fade the scar. Also bought deodorant without aluminum and dove soap. I hope I am prepared! Good luck to all that is starting soon.

  • DodgersGirl
    DodgersGirl Member Posts: 2,382
    edited October 2017

    utjoy- rads scare me more than pre-surgery and pre-chemo. Hoping having a group of us all going thru this at the same time and sharing tips and such will provide comfort as threads on chemo and surgery have done.

    I still have all my steri strips from my mastectomy. They seem to like being there and don't show any signs of coming off. Maybe RO will remove them next week? I feel like I can't possibly be ready for rads yet. Scary.

    Have you had your mapping ?

    Please let us know how the green tea works for you.

    My MO wants me on AIs asap but said RO will want to wait til rads have been completed so I am scheduled to start AIs after rads at this point.

  • DodgersGirl
    DodgersGirl Member Posts: 2,382
    edited October 2017

    Travel70- starting tomorrow... best of luck to you. Will keep you in my prayers.

    While I am nervous to start, my rational side knows the sooner I start, the sooner this step can be behind me.


  • utjoy
    utjoy Member Posts: 56
    edited October 2017

    Dodger... I wonder if the 'fear' is simply due to being very tired of it all? We both have husbands who are dealing with serious health issues, too, that likely plays a big part in our reluctance to take another step? lol...I hope yours is healing! Mine has had complications, but, is sloooowly getting better. He was dx'd with a movement disorder 4 years ago....come to find out it was all from his neck! Alas, he lost a lot of muscle, balance & strength along with permanent nerve damage that we won't know the extent of for some time yet.

    My steri strips like me, too! PS did remove and replace them twice now...I had my first fill on Monday, not bad at all...a little tender down my armpit, he said if the strips come off to not worry about it. My next appt with the RO is the 17th for mapping. He told me that he'd rather I was not on AI's until after radiation, however, he said it's really just the old tradition and to go ahead with it if my MO recommended it. MO does still...

    I'm looking at December as being my fresh start to freedom...for awhile!

    God Bless all...

  • DodgersGirl
    DodgersGirl Member Posts: 2,382
    edited October 2017

    utjoy- I think you may be right..... I am tired of this trip. Hubby is recovering. He is in rehab 3X a week. They are still working to get his meds right, especially the Coumadin.

    Glad to know steri strips hand around for someone else.

    I am supposed to have a bone density test, a colonoscopy, and hysterectomy before I am thru with this journey.

    I did have a PET scan last week since they found cancer in a few nodes during surgery. Results of that showed no cancer at surgery site, lymph nodes, or other places in my body so at least for now, I can say I am NED. Just gotta learn to live in the moment and not worry about mets

  • DodgersGirl
    DodgersGirl Member Posts: 2,382
    edited October 2017

    I_Brain- welcome to our group!

    Good luck with #4 today. Sounds like you and LoJo100 started about the same time so you two will be our early explorers of this trip. Hope you will share what you learn and experience.

    What time of day is your appointment? Wondering if afternoons or mornings are better?

  • dmjmom
    dmjmom Member Posts: 79
    edited October 2017

    Dodgersgirl, thanks for giving us an Oct Rads Thread! I had my CT-simulation last week on the day of my last chemo. I have my first rads on the 11th. I am scheduled for 33 treatments. I've got three green X's covered in clear tape, will get my tattoos on the 11th.

    I was worried about shoulder pain due to a couple rotator cuff tears and some other shoulder issues, but it wasn't too uncomfortable. The techs were very compassionate and did what they could to help me get comfortable.

    Debby

  • Spinning11
    Spinning11 Member Posts: 2
    edited October 2017

    I'm new to the group and so glad I found this thread...im sitting in treatment now getting my herceptin infusion. I see the RO on October 16th so I assume ill be starting before month end. My mastectomy was September 11th and has healed nicely, I had staples not steri strips

  • DodgersGirl
    DodgersGirl Member Posts: 2,382
    edited October 2017

    dmjmom- welcome!

    Happy to read your comments about shoulder discomfort. Hope my experience is similar to yours.

    I see my RO next Tuesday so assume I will have a start date at that point

    Wish you the best during your 33 treatments.

  • DodgersGirl
    DodgersGirl Member Posts: 2,382
    edited October 2017

    spinning11- welcome!

    I, too, had mastectomy on 9/11. Makes me feel better about this journey knowing you had surgery at the same time. We can do this !!

  • l_brain
    l_brain Member Posts: 71
    edited October 2017

    Dodgers girl,

    Most of mine are around 9 a.m. I think it's good to get it over with, but hard to get going in the morning. Not sure there is a good time simply because being there everyday is a pain. I'll let you know how things go as I progress. A few twinges her and there, but no discomfort or redness at this early stage.

  • l_brain
    l_brain Member Posts: 71
    edited October 2017

    My doctor said that woman that exercised not only had less fatigue, but less skin reaction as well. They didn't know why, but studies showed that to be true. The fatigue I knew, but the skin part came as a surprise to me.








  • LoJo100
    LoJo100 Member Posts: 123
    edited October 2017

    Hi All!

    I had rad #4 today. I do see a little pink in the area, but it feels fine (it is very faint). I am faithfully using miaderm three times a day (right after treatment, afternoon and evening). My RO recommends Miaderm, Calendula First Aid or Eucerin. I went with Miaderm as I had read great things about it and it feels the best on my skin. It is expensive, but I figure, if there ever were a time to spend $$ on something, this is it!

    As far as the procedures go, they have been easy. Most of the appt. time is lining me up, I think actual radiation time is 2-3 minutes. I'm drinking lots of water every day, and walking at least 2-3 miles everyday, up to 5 miles or so on some days. So far, so good. Still take an afternoon power nap, but think some of this is from chemo (I'm only 2 weeks PFC).

    They ask me each day how I'm doing, and right now, each day is better than the last because the chemo SE's are wearing off. My dream is that the chemo SE's leaving will keep going until the end of radiation so the rads SE's feel minimal. It's good to dream!


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