What's the Point of Radiation Follow-Ups
I had DCIS - Stage 0, grade 3, estrogen +, lumpectomy, with 16 general radiation treatments and 4 focused.
I had few issues with the skin during treatment and the 1 month post treatment follow-up seemed like a waste of my time.
What's the point of 6-month/annual follow-ups with the radiation oncologist?
Comments
-
Hi Rebakoosh, and welcome to Breastcancer.org,
Thanks for posting! We're sure someone from our Community will be by shortly to weigh in with their experience and thoughts on this soon. In the meantime, please let us know if you need any help as you navigate the boards.
Welcome again!
--The Mods
-
I had the long course of radiation, 33 if I remember correctly. On the last day, I was told to call for an appointment if I had any lingering issues, otherwise I was good to go. I was happy because I didn't like the RO, and his substitute, who was there the last few weeks, looked and sounded like Jabba the Hutt, which made him look like he was leering.
-
Both times after the 1 month visit, I was released. Told to call if I had any problems I didn’t, and haven’t been back.
-
My RO said I didn't need a follow up unless I noticed any issues or had question. I haven't been back.
-
Yeah, I go yearly now and am not sure why. My follow up got cancelled because of covid....I haven't rescheduled yet because I see the surgeon in a couple of weeks and the MO in August. So what's she going to do. How many breast exams do I need in a 2 month period, you know?
-
I know I am supposed to have a one month follow up but haven't heard of going back to RO after that. My understanding is that it is to check for skin healing. Also RO is supposed to give the go ahead to start anti-estrogen meds. Those can interfere with healing and that's why docs usually have you wait to start them until after radiation.
-
I had the last visit with my RO a few days after the last radiation treatment. We chatted about how everything felt. He let me know how well everything went … his opinion. Then he wanted to do a breast exam to see, I said no. I didn't say it to him but I was done with popping my breasts out anytime someone said to. I had a follow-up with my oncologist the next week so I just said no, he said OK call if I have any issues and that was it.
Even during the weekly visits with the RO while I was having radiation, I would slip on a stretchy sports bra so he could see my skin without me completely exposing my breasts. I was very fortunate that I had minimal side effects. I started my anti-estrogen meds one week after my last radiation treatment.
-
The thing is - I loved my RO. Her exams beat out the plastic surgeon by miles. And my MO, who did great exams, retired. The replacement was perfunctory. My RO is also the one who diagnosed my lymphadema and sent me to a certified, trained LEPT before things got worse.
I agree - how many exams do you need. But I chose to skip some of the others and went to the RO every 6 months for 2 years. A good doc it hard to find & harder to give up.
-
Thanks for all the answers. I don't go back for my next follow up until September and I had gotten an e-mail notification that the RO wanted a follow-up at 6 months. I'll wait until I talk to my doctor and see if she can give me a compelling reason to do a follow-up with the RO.
-
I'm 6 months post radiation and scheduled for a mammogram and a follow up with my RO. My understanding is that this will be used as the new baseline post lumpectomy. My right breast, the one treated, is still sore and tender and different then before. I can feel some more dense, hardened areas, that could be scar tissue. Thing is I will sleep better once it is confirmed by the RO. After this, I will have yearly mammograms.
-
I finished (or quit early as the case was) radiation in March. I have an appointment scheduled with RO in August, he is running every test again (mammo, ultrasound, tons of blood tests and MRI) over two days then I meet with him on third day. The MD Anderson protocol with him is every 6 months for 18 months then if he thinks everything is fine he turns me back over to MO to order testing. This is the only doctor I do not like, he is an arrogant little jerk with no bedside manner, but is "world renowned." I have visited with patient advocate man times about him and will do the testing minus the MRI in August and meet with him, but not be undressing at all. I'm still not sure why I meet with him again since I have no skin issues that are repairable.
-
Rain88
Why would your RO diagnose anything that's not a skin issue? I had some thickened, sensitive tissue last winter and my MO was the one who ordered a mammogram and ultrasound and a follow-up with the breast surgeon.
-
I am about 1 1/2 years post radiation. After my last visit this past January she wants to see me next January. I'm happy to have her look at my skin as I had BC 2x. I don't see my breast surgeon as I now live in a different state. After so many people seeing my chest area I'm not bothered anymore as I no longer have real breasts.
Jaybird
-
I was very happy with my RO. I saw her 6 months and 1 year out. She said I could come back a year later, but it was not necessary as long as I was being checked regular (by MO, BS, etc).
-
Alice - my RO gave a very thorough breast exam. She was interested in me & any or all symptoms, and not just my skin. My new MO didn't & wasn't. That's why I stayed with her.
-
Alice, the RO will interpret my mammogram. (I didn't have any skin issues during or after rads.) I will see my MO again later on about how I'm doing on Tamoxifen. I can contact either one if I notice anything of concern.
-
I am eleven years out and I still see my RO and MO annually (even though I stopped tamoxifen 6 years ago). The RO orders my imaging and the MO says he wants to keep me an active patient, in case....
-
Rebakoosh - my RO and MO alternate their annual checkups, so that I see one of them every six months. That way I get a physical breast exam + a discussion of my scans twice a year. (I also have alternating mammograms and MRIs.) You might ask if you can schedule them that way so there's more value for you; I appreciate the opportunity to go over my test results.
-
Georgia1, I love your quote - gave me a laugh.
I'm in a slightly different place as I had radiation, but not to my breast. I had 3 palliative radiation treatments to my hip and spine and then 10 palliative treatments to my femur. My RO said to follow up with him in 3 months. I happen to really like this man. I met him 12 years ago with my first bout of cancer. I didn't have radiation at that time, but he still remembered me from then. Amazing! His concern is with the stability of the femur and the potential for a pathological or spontaneous fracture. He and my orthopedic oncologist are working together on my treatment plan. So, I'll probably keep seeing him even if he doesn't examine my one remaining breast.
-
Thanks for sharing, Sunshine 99. Seeing an empathetic health professional helps a lot - we're people, not just patients.
-
This thread just caught my eye. I am 17 years out from my original diagnosis, 14 years out from my first metastasis (polyp on my cervix), and a year out from my second metastatic diagnosis (liver and bones.)
I LOVED my RO for my first diagnosis. She was caring, intelligent, involved -- just terrific. No RO really involved in first metastasis. This time around, I had the liver diagnosis and it was pretty clearcut. The bones -- not so much. Now there are things going on with my bones and the radiologists (different ones each time) are having some different opinions on bone metastasis over the last six months and so I wanted a comprehensive review of my scans over the last year or so so that ONE person can give me a coherent radiologist's perspective. I asked my MO. Guess who I am going back to? My RO from my original diagnosis.
I guess I'm posting this because even though it seems that you don't need a certain type of doc in your pocket, you actually may, down the road. I'm happy to go back to this doc bc of who she is -- so if you find a good doc, hold onto his or her telephone number! You may need it in the future.
-
Hi. I have been reading your experiences with your respective ROs. I consulted my first RO but I didn't like her from the start. She was cold and gave me the necessary information to justify treatment. However, since I was diagnosed with BC, I just made a search of information about RT; I came from nuclear medicine and I worked in diagnostics using radioisotopes. The information I got from my search was really awesome, and helped me to confront her and give me the unmentionable like necrosis of the skin, secondary cancers, and other permanent ailments. Well, to make things brief, I consulted another RO. This other doc was warm and gentle but she also attached to the 28-35 RT rounds. I considered that amount of radiation excessively high. My skin is so sensitive that I didn't want to expose myself to a secondary RT cancer. In Puerto Rico, the ROs are extremely retrograde in terms of therapy. Since I am a Medicare patient, they only want to give me conventional therapy while there are other most modern types of external RT which are more precise and less dangerous. One of you mentioned she only had 16 fractions (16 sessions of RT); you are really lucky. That was what I wanted but the ROs I visited didn't like the option. The second RO said that was an incomplete treatment option. (Since Medicare only pays the minimum for a service, the ROs won't offer another type of RT to us old cancer patients. Capitalism; I already accepted that fact.)
I liked the attitude and decision of JDB1965. We are not supposed to yield to everything under the MDs' heaven. We are persons and sometimes I feel they treat us like trophies. When my PS told me he wanted to take my breast recosntruction photo, I said no. First, I am not delighted with his work and it is causing me mental and physical pain. Second, I am not willing to expose myself to videos and photos not even for the wealth of science. How can I be sure they are using them for that only purpose? That's why I never went back to the new PS (the first one does not accept my health insurance anymore); in the papers I was given to sign, he obliged me to accept to filming the operation for educational purposes. The only doc that checks me is the BS because I have another nodule in my left breast and the radiologist in the mammogram and sonogram just say the nodule is almost the same as before. No more information.
Thank you for hearing me.
-
In my case, I've decided to have my RO follow up on all breast care (and she had offered). My BS is a great surgeon but other than that, I would prefer never to deal with him or his staff again. My RO is completely different, fully present in every visit I've had with her and just all around great.
-
My BS retired, I had one visit with someone else in his practice, and she said I could keep going to her or not and I decided not to. I still see both my MO and RO every six months--still on an AI and honestly I'd be hesitant to give up my RO--I really really enjoy her. For some reason she has been the one to order my annual mammo. I happen to have an appt with her tomorrow--I'm wondering if she'll suggest going to once a year. I gotta say I don't mind having another MD look at my hooters whenever I have an opportunity--just a little bit of comfort hearing another "all clear."
-
I think who you see once you stop active treatment is a personal choice. I see my PCP annually and my MO semiannually (will probably go to annual once I finish with the AI) and my dermatologist annually. I don’t see my RO or my breast surgeon and haven’t seen my plastic surgeon since my follow up post final surgery (didn’t go back at 6 months).
My MO orders my mammogram but my PCP can do that too. My PCP orders blood work and occasionally my MO does.
-
My RO just seemed to be going thru the motions at the end but she was 34+ weeks pregnant. I like my BS and the only doc I really clicked with thru this experience.
My MO is ok but he is always running 1-2 hours behind and isn't interested in doing anything beyond the meds. I still have another 8 weeks before I get thru all my scheduled appointments including dermatologist. Then I'll revisit whether I want to see the RO.
-
I had partial breast radiation but I believe even then there can be problems from radiation that aren’t just skin related. The radiation can cause bone, lung and heart problems. Maybe that’s why they suggest you see an RO.
-
For the folks seeing an RO regularly, are they specializing in just BC?
My treatment was at the hospital that had 2 RO's on staff, but they did all cancers. With one machine. It was a mad house. I did a 3 month follow up, had a consult afterwards with a lady to see if I was interested in signing up for 2 studies I qualified for, but I declined and moved on to the MO. I still see my BS though. Not sure when she will release me.
-
I think my RO treats other kinds of cancer, but she's one of the three MDs on the care team specifically for BC.
-
Hi, I finished RT almost three weeks ago. I would like to know what type of follow-up does the RO do. Is it a clinical breast exam? Or is it a radiation-wise exam, meaning to check on the skin, long-term side effects? Do ROs order tests? Isn't the BS more qualified to do breast exams? My RO doesn't even specialize in breasts, so I'm quite confused.
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