July 2012 Radiation
Comments
-
Ladies! Please stay out of the sun when your done! I finished my rad's back in mid-April and I have started outings like swimming, parks, etc... and now my entire area that was penetrated by the sun ray's is ithing like crazy!!! I itch all day and I itch all night!!! BTW-Ra'd were easy, no burns! Just this crazy ithing....wonder how long it stay's in you???
-
Thanks Teacup, I started today at 8:45 hoping for a later time. I have a half hour drive and don't like to get up early. I got my 3 tats to day also, they weren't too bad. 1 down 29 to go!
-
First session complete! It went really well. They said I could bring my own music which I did and that was relaxing. Afterwards, the nutritionist wanted to meet with me to go over supplements and diet. It's great that they provide that service too. I said my affirmation before the treatment and put my lotion on after treatment before I got dressed. Hope everyone else's first day goes well too!
Grace
-
Hi Graced, so happy to hear your first rad treatment went smoothly. Thanks for sharing and making me feel less nervous about Wednesday. I like the idea about music and I think I'll do it! I did it went I had my first surgery...my boyfriend brought my Ipad in with headphones, so as I was recovering those first two days in the hospital I could listen and relax. I hadn't thought about it for the radiation part...thanks!
Butterfly (Sharon)
-
Sharon, I had to bring a CD that they would play on their stereo. I can't wear the headphones during tx because I'm doing prone and laying on my side/ear. So bring both depending on your setup. You'll do great! Let us know!
-
Have my first appt with radiologist tomorrow morning - no idea if this is just a meet and greet or they will actually do something.
Everyone who got zapped today, hope it went smoothly!
-
Hi Ladies
Well it doesn't sound like anyone was too traumatized today with their first treatment. Thanks for checking in Grace, Jag and Julz.
Oh Julz, this is such an emotional roller-coaster. I think being emotional is just part of the craziness of the entire experience. Be kind to yourself, and just cry when you need to. I know it's hard when our children see our emotions, but we are real people after all..even if we are "mom".
I didn't have a treatment today after all...I got a call this morning and the machine was "down". I wonder how often that happens.
Kim - I went to my first RO appointment, just expecting a consult, and he was ready to get going with the exam, ct scan and everything. I was still doing chemo, so he put off the ct scan. So it's hard to say what will happen at your appointment tomorrow. I guess you just need to go in open minded and go with the flow. As I say that I have to laugh, because my first question is always "what can I expect today?". My daughter says I'm a control freak..... hmmmmm..... anyway, good luck tomorrow.
take care
-
Cheers for a smooth start & Cheers for the others about to start!
All went good today! The RADS nurse was very specific as to what she wants me to use. Calendula lotion by Boiron. She gave me a bottle told me to use it very Liberally 2x's a day & she would give me a bottle as I need it....don't skimp on it! Dove unscented soap only & as I'm not getting treatments to my axillary area I can use a tiny bit of deodorant Dove unscented also. She will let me know when I am to use anything else! I went to Wally World & got pack of 3 all cotton shelf Jog bras in size 40 band size. I'm a 36 so it's plenty big & I won't be falling out the bottom of it. They give some support but are over-sized enough to be outside the area of target. I also got my last Tattoo today. What a breeze & I didn't feel a thing. Right at the edge of the areola....not sure why the other tatoos hurt so much & this one not a bit.
Onvacation I'm sure every place is a little different. But my first time they told me ALL about Radiation & the treatments. The nurse took an in depth medical history, & did an exam of my breast as I had had surgery. I guess most of us do before RADS. They brought me back last Monday to do the Simulation & it took them a week to do the planning. I think the RADS ONC works with 2 or 3 others to plan my treatment. My first appointment was 1 1/2 hours with the Dr. & his Nurse.
Butterflylady sending sending extra soothing thoughts as my emotions have been all over the place for the past few days. I hope yours goes over in the blink of an eye just like mine did! In fact they were all please & thought mine was super fast for the first time!
Thanks Vacationbound for the heads up on the Natural Rays! My RADS nurse said I could use Hydrocortisone cream mixed with the Calendula cream she gave me today. She said women tend to get very itchy between their girls, the cleavage area. As always ask your Dr. if they haven't said you could use it.
-
Thanks for the info on what to expect on my first appt! I guess I will just tell work I will be back when I'm back! I hope they do get things moving so I can start soon! I kept telling myself I would be done by football season! When I told my MO this, he just laughed, don't think he is a football fan! LOL
-
Teacup what a big LET DOWN! You spend all that engergy Mentally Prepairing yourself then poof! I'll be thinking of you tomorrow & hope all is up & in working order!
Thanks Teacup crying does help & I really haven't let myself do much of it! Even though I have treatments every day now it's just been not stop go with everything else this beast puts us through! Life has kept me busy also & I guess now that I'm getting back into a routine post surgery, back at work. It's hitting me some how!
Lyrics from Hootie & the Blowfish come to mind.....Let her cry...if the tears fall down like rain
Let her sing...if it eases all her pain.... -
Hello. I am halfway through my radiation. I do not have to have chemo, PTL. Good luck to you.
-
My treatments are nothing really. I just lie there positioned on the table (the position depends on the location of your treatment area) with my arms over my head on a form they made for me. They move me and adjust my position to match the computerized positioning coordinates. I'm only there a very short time. It takes me longer to get there than the treatments themselves.
The first week I had no side effects at all. The second week the skin on my chest (below the collar bone to my cleavage) started to have something akin to a heat rash or shingles. They have cream for the itching. I have very sensitive skin so that may make a difference. I know some that have gone all the way through treatments with no rash or itching at all. I've also had a little fatigue and a dry cough, but nothing overwhelming, I drive myself to and from treatments.
I agree with the poster above about the sun. I seem to be highly sensitive to the sun now even under normal circumstances. I get hot more quickly and it will definitely aggravate the itching if you have any. Be sure to use your lotion at least twice a day (1x after treatment and 1x in the evening) during your treatments and use sunscreen when outside.
Good Luck!
-
My 25 radiations finished on Friday July 6. The whole area is red, and I have an area on my chest and one in my armpit which are beginning to peel. It is not too bad though. My underarm skin feels tight, and it is uncomfortable when I stretch my arm out above my head. The rad onc prescribed some Flamazine (for burn wounds) which I must apply twice daily after I've held a cold, moistened washcloth to the area for ten minutes. I am not supposed to use anything else, but my skin is now quite dry, and the Flamazine is not moisturising it. Maybe I must also apply Lubriderm once a day. Any thoughts on that?
Is anybody experiencing swollen feet? My feet have been swelling every day since I finished radiation. It goes down during the night, but comes back as the day wears on. Maybe it has something to do with the neuropathy I still have after Taxotere.
The rad techs warned me that the side-effects will be at their worst one week after finishing radiation. At the moment I don't have the fatique that may come as radiation ends, so I'm waiting to see what will happen. For those of you still getting radiation, hang in there. It passes quicker than you think.
-
Thanks for all your advice. Funny, I worked for BBW for 10 years (just quit about 2 years ago), but I have recommended the shea butter balm for other things, but not that. I spoke w/my sister this weekend, who is a radiation oncology therapist, and she recommended the aloe gel from WM as well as aquafor. I am for trying ANY and EVERYTHING to prevent burns. Thanks for your advice. Happen to have some in my stash.
-
#5/34 done today. The process seems less scary now and almost routine.
Some of you may remember me posting that my first RO left the practice without telling me. He did all of my planning and then left. I had a "meet and greet" with my new RO last Monday (1st day of tx) but didn't really get to talk to her for very long. My first "real" appointment was with her today. I like her but she is a temporary RO until they get a replacement. I was told that she most likely will be there throughout my treatments. Needless to say, I am having trust issues but it is too late to go somewhere else.
Here's my problem. My first RO was open to using a variety of creams and oils. My new RO instructed to me to use only olive oil and Aquaphor. I have already gathered together various kinds of creams and oils in preparation of the SE of rads. Do I follow her advice or should I use the stuff the women of breastcancer.org talk about? I am so tired of making decisions regarding my treatment. BC sucks.
Olive Oil!!?!! I will feel like a garden salad.
-
Babette you edged ahead of me with my treatment cancelled today. I have the same issue trying to figure out which creams to use. My RO says only 100% aloe Vera. I don't feel like that's enough moisture. But I am apprehensive to use anything else. I did buy calendula and have used it a few times. I'm not sure what I'll do as we move forward. Olive oil does seem strange but it seems many women on other rads threads use coconut oil. It's just really hard to know what to do. I agree BC sucks. Big time.
-
Babette, the herbal ointment I am using is in a base of olive oil. I think the ROs mean very well but can only recommend what they are familiar with. Different ROs have experience with different products so we know there is more than one option for people. My thought is, if I know other women have succesfully used it during rads, and it's all natural, then I'm using it and they don't have to know about it. Trust your instinct! If you already have the cream in the house, see how you feel when you hold it. Your body will tell you if it's good for you.
-
I was using a cocoa butter that someone I know swears by, but I found the Aquaphor to work better. I never heard olive oil mentioned but I do use it on my dry skin in the winter. If you use it be sure to get plain olive oil not the pressed virgin or extra virgin oils.
-
A coconut oil might be good. I never thought about that. I think as long as it is a heavy-duty lotion w/o alcohol you're good. I know some like Eucerin and Lubriderm. I've started to use aloe to cool my skin and help the itching and burning after treatment and the Aquaphor to moisturize. Since I've used the Aquaphor in combination with the aloe vera the irritation is less and the itching and burning seems much better than just using the lotion by itself.
-
I'm not doing so good. I went to work last night & a little over an hour after I arrived I started really getting nauseated! The whole night I really felt yucky. When I went in for my treatment today the nurse looked at me & said whats wrong. I told her about the nausea & she said that's too early for that to happen. Quietly as if she were talking to herself. No one has the the Bug at home or work. She asked if I had any anti nausea meds at home. I do & am to take them & let her know how I'm doing tomorrow. I've only slep 4 hours today & have to work tonight! I took a pill before I went to sleep. I woke up & am still nauseated! If I have some weird side effect.....the next 6 weeks are gonna be YUCK! Don't feel like eating anything!!!! Just gingerale & ice chips!!!! I guess it's a good thing I'm 28 pounds over weight! Down 4 in one night!
Babette I've done reading here & the most "popular" creams used seem to be the Calendula, Aquaphor, & Aloe. I think my nurse wants me to save the later 2 for the big guns. Wait to see if I need them. Go with your gut. Maybe mix a little Calendula with the olive oil. It's a tough call. As you don't want to tick em off...because you have to deal with them for a while longer.
I'm gonna go & try to sleep some more. It's gonna be a long night! Then I have 4 off! Yeah! -
Hello ladies...tomorrow is my first appointment with radiology oncologist...one more scarey thing to deal with but it is now 2 1/2 months since my diagnosis and I am almost over the shock, if one ever becomes "over" it.
Julz4, I spoke with you when I first came on here May 29th....we had surgery about the same time. My rad treatment is a little late starting as I was transferred to Barrie (40 minute drive as opposed to 1 1/2 hrs to my other centre) and the Barrie centre just opened yesterday. Sorry that you are feeling so poorly & I guess sympathy is all I can give you.
-
Isabelle: I go on Thursday for my consult. We should compare "notes".
My sister said wheat germ oil is great, but is hard to find...Maybe health food stores. Expensive, but more moisturizing than olive oil. Again, aquafor highly recommended with aloe--Fruit of the Earth from WM.
Julz: Hope you're feeling better soon.
-
Hello kjiberty..I only ever use olive oil on my face as I am allergic to many skin creams....will let you know what is recommended to me. I would be happy to go on this next journey with you.
-
Thanks Isabelle2! Looking forward to having a "sister" to go through this with me!
-
I met with my RO today, more of a consult and what to expect. He said I should tolerate the treatment very well and no need to pre- treat my skin. I still think i will start lubing it up to keep it moisturized! I go in Monday for simulation and mapping, hoping I will find out more infor then. Going to be a long 6 weeks!
-
#6/34 done today.
I had my first x-ray check. They do an x-ray after every 5 treatments to check alignment. Mine was off by 5 mm so they needed to re-draw the marks on my chest before zapping me. I was told that swelling and gaining/losing weight can cause this to happen. The techs said it was nothing to worry about--easy for them to say. They are not getting hit with massive doses of radiation. I'm still amazed that I am trusting these strangers to do this to my body. I tell myself to take a deep breath. This will be over soon.
Teacup2012 - If this was a horserace, I would have you by a nose. I'm sorry that your machine was down today. I hope that doesn't happen to me. I only have two "cushion days" before the start of school. I don't want to take more sick leave unless absolutely necessary.
graced - Thanks for for giving me your opinion about using creams/oils instead of the olive oil recommended by my RO. I agree with you totally about trusting my instinct. My gut feeling is to use the stuff suggested by my BC sisters who have "walked the walk."
julz4 - I hope you are feeling better and that you are not experiencing early SEs. Doing rads is difficult on a good day, I can't imagine feeling nauseated.
Isabelle2 and kjiberty - Good luck at your appointments. As I am slightly ahead of you, I can assure you that the consultation, mapping, and simulation appointments are stressful but uneventful. The worst part is the waiting. We all want this part of our journey to be over.
-
Grace - I like your logic on the lotions, I'm still struggling with what to use. I guess I really need to just trust my body, and do what I feel is right regardless of what the RO says. I really like the California baby calendula cream (target).
Mini1 - thanks for your suggestions also, aquaphor seems to be a favorite on the other rads boards.
Julz, sorry you are not feeling well. I didn't realize that was a possible SE. I hope you feel better soon. Take care of yourself.
Welcome Isabelle2 - Good luck today with the RO. BC diagnosis is quite a shock. I was diagnosed in November of 2010 and there are days I still feel "in shock". All we can do is take one treatment at a time, on day at a time. We are all here to go on this rads journey together and to help each other is one of us stumbles.
Babette - I had an X ray on Friday, but no one shared any information with me. Did your techs share the fact it was off by 5 mm, or did you have to ask? I didn't even think to ask. I know what you mean about trusting the techs. I think we choose our doctors carefully, but really have no control over the techs who have such an important job! One thing I've learned with this BC journey, and in life is that there is really very little I have control over. (but that doesn't mean I don't try!)
I'm gearing up for my vacation next week. My favorite sister is coming tomorrow to spend the week with my family. I haven't seen her since my surgery in December, I am so excited! I started planning this vacation while I was in the middle of my AC chemo, and it seemed so far away, and now it's here. I am so ready for a week off work and off treatments. I have worked 3/4 time throughout my treatment with the exception of a couple weeks after my surgery. So I might be MIA for a few days, but you will be in my thoughts and I will be back!
-
teacup2012 - The techs told me that if after the xray something was "off," they would come in and re-arrange me. So, when they showed up, they moved me around a little bit. I believe they took another xray and then my tx continued. While they were adjusting me, I asked questions about being "off", what it means, is it serious, etc. They shared with me that 5 mm is nothing to be concerned about. It happens all the time and if it had been a couple of cm, they would have contacted the RO. I will admit it was a bit unnerving but I have to trust that they know what they are doing.
I know what you mean about getting excited about seeing your sister. I also have a favorite sister who has been gone on vacation for nearly 3 weeks. She doesn't know it yet, but I plan to go see her this weekend and spend the night. I need my "sister fix." She lives 1.5 hours away.
Have a great time. Put breast cancer in a box and put the lid on tightly. Don't open it up until your vacation is over.
-
I had my 3rd tx today and apparently wednesdays are the day I will meet with the RO afterwards and have blood drawn, etc. He asked me what product I normally used on my skin and I told him what I normally use and what I was using on my breast for the rads (the herbal ointment w olive oil). He was AOK with it. He said as long as it didn't have alcohol in it. The nurse chimed in when I said it had calendula in it that that was good. My RO is an older man and has been doing this for a long time. He used to run the department but has scaled back now. I hope this helps those of you struggling with what to use.
Teacup, have a great vacation! Relax for all of us :-)
Smooth sailing to those starting today & tomorrow.
-
1st Rad treatment in 2 hours. I'm ready to go! Don't get me wrong, I'm not excited about it, but I'm better then I thought I'd be. Friend is going with me. I'll be taking a little Xanax though and Benadryl for my allergies. The Xanax is the lowest dosage, just to take edge off a bit. Hearing about Rad experiences from everyone on this site has helped me to feel more relaxed. And Graced, I'll be saying..."The Radiation is helping me, I feel my spirit lighter and relaxed because I know I am being healed..Amen". Thanks everyone for sharing....because that sharing helps others. This is a wonderful site for all us BC girls who need to know we are not alone.
Categories
- All Categories
- 679 Advocacy and Fund-Raising
- 289 Advocacy
- 68 I've Donated to Breastcancer.org in honor of....
- Test
- 322 Walks, Runs and Fundraising Events for Breastcancer.org
- 5.6K Community Connections
- 282 Middle Age 40-60(ish) Years Old With Breast Cancer
- 53 Australians and New Zealanders Affected by Breast Cancer
- 208 Black Women or Men With Breast Cancer
- 684 Canadians Affected by Breast Cancer
- 1.5K Caring for Someone with Breast cancer
- 455 Caring for Someone with Stage IV or Mets
- 260 High Risk of Recurrence or Second Breast Cancer
- 22 International, Non-English Speakers With Breast Cancer
- 16 Latinas/Hispanics With Breast Cancer
- 189 LGBTQA+ With Breast Cancer
- 152 May Their Memory Live On
- 85 Member Matchup & Virtual Support Meetups
- 375 Members by Location
- 291 Older Than 60 Years Old With Breast Cancer
- 177 Singles With Breast Cancer
- 869 Young With Breast Cancer
- 50.4K Connecting With Others Who Have a Similar Diagnosis
- 204 Breast Cancer with Another Diagnosis or Comorbidity
- 4K DCIS (Ductal Carcinoma In Situ)
- 79 DCIS plus HER2-positive Microinvasion
- 529 Genetic Testing
- 2.2K HER2+ (Positive) Breast Cancer
- 1.5K IBC (Inflammatory Breast Cancer)
- 3.4K IDC (Invasive Ductal Carcinoma)
- 1.5K ILC (Invasive Lobular Carcinoma)
- 999 Just Diagnosed With a Recurrence or Metastasis
- 652 LCIS (Lobular Carcinoma In Situ)
- 193 Less Common Types of Breast Cancer
- 252 Male Breast Cancer
- 86 Mixed Type Breast Cancer
- 3.1K Not Diagnosed With a Recurrence or Metastases but Concerned
- 189 Palliative Therapy/Hospice Care
- 488 Second or Third Breast Cancer
- 1.2K Stage I Breast Cancer
- 313 Stage II Breast Cancer
- 3.8K Stage III Breast Cancer
- 2.5K Triple-Negative Breast Cancer
- 13.1K Day-to-Day Matters
- 132 All things COVID-19 or coronavirus
- 87 BCO Free-Cycle: Give or Trade Items Related to Breast Cancer
- 5.9K Clinical Trials, Research News, Podcasts, and Study Results
- 86 Coping with Holidays, Special Days and Anniversaries
- 828 Employment, Insurance, and Other Financial Issues
- 101 Family and Family Planning Matters
- Family Issues for Those Who Have Breast Cancer
- 26 Furry friends
- 1.8K Humor and Games
- 1.6K Mental Health: Because Cancer Doesn't Just Affect Your Breasts
- 706 Recipe Swap for Healthy Living
- 704 Recommend Your Resources
- 171 Sex & Relationship Matters
- 9 The Political Corner
- 874 Working on Your Fitness
- 4.5K Moving On & Finding Inspiration After Breast Cancer
- 394 Bonded by Breast Cancer
- 3.1K Life After Breast Cancer
- 806 Prayers and Spiritual Support
- 285 Who or What Inspires You?
- 28.7K Not Diagnosed But Concerned
- 1K Benign Breast Conditions
- 2.3K High Risk for Breast Cancer
- 18K Not Diagnosed But Worried
- 7.4K Waiting for Test Results
- 603 Site News and Announcements
- 560 Comments, Suggestions, Feature Requests
- 39 Mod Announcements, Breastcancer.org News, Blog Entries, Podcasts
- 4 Survey, Interview and Participant Requests: Need your Help!
- 61.9K Tests, Treatments & Side Effects
- 586 Alternative Medicine
- 255 Bone Health and Bone Loss
- 11.4K Breast Reconstruction
- 7.9K Chemotherapy - Before, During, and After
- 2.7K Complementary and Holistic Medicine and Treatment
- 775 Diagnosed and Waiting for Test Results
- 7.8K Hormonal Therapy - Before, During, and After
- 50 Immunotherapy - Before, During, and After
- 7.4K Just Diagnosed
- 1.4K Living Without Reconstruction After a Mastectomy
- 5.2K Lymphedema
- 3.6K Managing Side Effects of Breast Cancer and Its Treatment
- 591 Pain
- 3.9K Radiation Therapy - Before, During, and After
- 8.4K Surgery - Before, During, and After
- 109 Welcome to Breastcancer.org
- 98 Acknowledging and honoring our Community
- 11 Info & Resources for New Patients & Members From the Team