Lost, confused! No treatment plan!!!!!!!!
Hi,
My mother diagnosed on 14 August with IDC. The surgeon decided lumpectomy as her tumor is 1.4cm. I didn’t get full explanation from him. Many doctors I asked they are with lumpectomy not mastectomy. So I agreed with the lumpectomy. The doctor said from the ultrasound that the lymph node looks normal not affected and he said she looks stage 1B. The tumor is ER + and PR + both 95% HER2 is negative. The ki67 is 5%. Her age is 68 years old. I have no idea what to expect after the lumpectomy? How painful it is after the surgery? How long she needs to heal? They didn’t do any MRI or Pet scan for her.. what if there are another tumors? Why they didn’t do PET scan? If she has 1 node with cancer. Is this mean maybe she will get chemo? If all her nodes are clear, can we skip radiation? I read very scaring things here about the side effects of radiation. The doctor didn’t even check with us if she might have cardiac problem. I feel lost Without having potential treatment plan with scenarios. Is it normal they don’t tell till after the sur
Comments
-
Your best plan is to see an oncologist before surgery. They can guide you through the chemo questions and hormone blocking therapy. I didn't have a lumpectomy so I can't answer those questions for you. They may be planning on doing a sentinel node biopsy at the time of lumpectomy to check the lymph nodes. Not everything shows up on the scans. You usually get radiation after a lumpectomy verses a mastectomy where you don't unless the lymphs are involved. As far as pain and recovery go it varies greatly from person to person. Chemo was hard on me but radiation just made me very tired. Others had much better or worse experiences. Just keep asking the drs questions until you're satisfied with the answers you get.
-
Im 68 and had a lumpectomy in July (and a re-excision to get clean margins in August). The surgery wasn't terribly painful, I took a prescription pain pill that night at home and I think once the next day. Most women don't see an oncologist until after the lumpectomy because until the doctors have the final pathology after surgery, they can't plan a course of treatment. It would all be hypothetical until then.
-
Hi Dana...After the surgery she'll be referred to an Oncologist who will order the necessary tests
Lumpectomy was easy for me. I didn't take any pain killers...just uncomfortable for the first couple of days.Everybody reacts differently I wish her the best
Good Luck to your mother. We're here for you.
Sending hugs
Sheila
-
Hi, what they said to you after the surgery
-
you won't get the full treatment plan until after the lumpectomy. They'll need to test the tumor and lymph nodes. after my lumpectomy I met with the Radiation Oncologisgt, Medical Oncologist, and Breast surgeon to discuss treatment plan. My hospital has a tumor board, where all the docs meet to review each case and plan treatment. Typically you will have radiation after lumpectomy. They want to kill any stray cancer cells. Perhaps they will not recommend radiation due to your mother's age, I don't know. I had no major problems with the radiation. They typically won't do a PET scan unless there is some sign that the cancer hasn't spread. I have never had one. This is really the hardest part of this whole ordeal, the waiting and wondering. Try to be patient
-
Hi...yes after surgery and some healing I met my Oncologist who ordered all the necessary tests.
I never had a pet scan .....After that port was placed because I have very tiny veins.
I had chemo first follow by radiation and 5 year of Femara
-
I agree with seeing an oncologist prior to surgery. I had my port put in (I was HER2+++ so I knew chemo was on the table) and had a node biopsy during the port surgery. So I knew right away I was node negative. I also had an MRI, MRI biopsy and two additional ultrasounds to look for additional cancer spots. No PET scans.
Once I had my original mammogram and they found cancer, my primary doctor wanted me in surgery ASAP. Since my primary and the cancer center I wanted were in two different hospitals, I was already listening to my cancer centers advice. I ended up having chemo, lumpectomy (twice, once for re-excision for clear margins) and radiation (and more chemo because of the HER2) and NOT just jumping into the surgery for which I am very thankful.
I was told (by my radiologist, ironically, who I met with at the very beginning) that I had two months from diagnosis to make up my mind about treatment. I was diagnosed on December 8th and started chemo on January 23rd. While it can be, for me, cancer is not an emergency. I wanted ALL of my facts and wouldn't let anyone rush me. Ask a million questions. It's your body and their job. If you don't like the answers, change doctors.
And the lumpectomy surgery was easier than the node biopsy, quite frankly. Two ibuprofen three times a day for two days and I was fine. I also took the advice of taking it easy.
-
Danaqtr , I'm 74 and had a lumpectomy in July. The surgery wasn't bad at all and not very painful. The doctor prescribed very strong pain killers. I took them on the first day but they really made me spaced out, so I took only Tylenol thereafter.
It took a couple of weeks to heal. Most pain (not bad pain) was where they removed the nodes. The pain subsided in about six weeks though I can sometimes still feel it very slightly.
I started radiation last Thursday. I felt fine the first day but was fatigued and a little shaky after the second treatment and spent a good part of the day in bed yesterday. I was told fatigue would begin about the second week of treatment, so was surprised that it hit me after two days. I don't think this is typical and have no idea if the same thing will happen after my third treatment this Monday and thereafter. I've been told some people go right to work after treatment.
The treatment takes about five minutes, though they will take X-rays and reevaluate the markings every Monday and Thursday. They said it wouldn't take very long.
Prior to treatment I had a Radiation Planning Session. Article at this site: The Radiation Planning Session (Simulation), which took just over an hour. The day of my first treatment took longer because they needed to take x-rays and add additional markings.
One of the reasons they are very precise with the markings and recheck twice a week is to protect the heart.
I apply moisturize three times a day. Another helpful article: Skin Care Tips
I wish your mother well! My daughter has been a huge support for me.
-
My mom had a lumpectomy for Stage 1 cancer at age 80 for a 1.6 cm tumor. She was at the casino the next day, and truly had no pain..
She absolutely breezed through it. I would agree to go see an Oncologist now.
-
tThanks. I was reading here some ladies got radiation immediately with the lumpectomy which is before closing I think it is called IORT instead of traditional sessions. Have you asked about it???
-
wow. Your mum is great!!
-
Danaqtr, yes it is called IORT and it is essentially a single dose of radiation while the patient remains sedated from the lumpectomy. It's still considered experimental so very few hospitals do it and eligibility is strict. If it's being offered to your mom it is well worth considering. (I looked into it but wasn't eligible.)
-
if IORT is safe. I will ask the surgeon about it.
-
Denise-G, it is wonderful to read that your mom had a lumpectomy and breezed through it. I have friends that have breezed through it. We all react differently. I pray that it goes as well for Danaqtr's mom!!
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