Diagnosed with DCIS: How do I decide on treatment?
I was diagnosed with DCIS. I have to go in for a breast MRI with contrast tomorrow to see how active the cancer is. If it’s contained and not very active, do I have to have a lumpectomy?
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What if indeed❣️ I can only tell you my story and my families stories. Two brothers a cousin and myself all had radiation. Mine was 20 years ago and does not even resemble what they do now. My cousin had 5 weeks and my husband had 6 weeks (prostrate) my brother had 3 weeks (lung) overwhelmingly the side effect was fatigue. Then recovery from fatigue. In my case it was a small part of treatment and frankly the easiest, of the multiple surgeries, chemo, radiation and endocrine therapy program.
When it did recur, I did not have to ask myself if I had done everything I could to prevent it. I was 35 and quite a few family have died young from cancer, I didn’t want to join them.
If I was given your choice I would take the radiation because it is short duration and done, unlike the endocrine therapy which can go on for years. Also I could save that tool in the box for later if I needed it.
I could feel like I covered that “what if” without a significant disruption to my quality of life.
Are you an active person? Do you have family you can discuss this with?
My Cancer is very similar... I had 1.9mm invasive cancer(too small to do onco test), also DCIS, I had lumpectomy on left breast and double reconstruction. I did radiation for 15 days. I started Anastrozole right after radiation and started having side effects in about 4-6 weeks. I stopped taking it. I am starting to feel better after about 10 days. BUT... while on anastrozole, I had Brain MRI due to headaches, got a breast infection in both breasts and now just found a cyst in left breast. I am having a MRI on breast in a couple weeks.
I am looking for good information on how to proceed. Doctor has suggested a different Hormone blocker-that was prior to cyst being found. I am currently reading Anti Cancer Living. I agree about healthy eating and exercising 100%
Can you share a link to your research on DCIS Cancer?
Thanks for sharing!
I was diagnosed with DCIS No invasive cancer low to medium grade DCIS In January couldn’t clear margins and went for another surgery to clear.
The surgeon didn’t clear margins. I had a second opinion after my first surgery and the surgeon said she would have never suggested surgery. My calcifications hadn’t changed in 5 years. She didn’t recommend any estrogen blockers. Mammograms will always pick up calcification which I have. She suggested ultrasound which will pick up invasive cancer. I changed my diet, vegetables, less meat, juicing , soy milk, exercise, green tea, and fasting.
The original surgeon won’t give me an ultrasound without a mammogram.
I prefer not to get a mammogram because I know the results calcification.
Going to get a Sonocine ultrasound which scans the whole breast not just one area. It will pick up 3 mm invasive cancer
Why treat DCIS like cancer it may never turn into cancer?
I have done a lot of research since my diagnosis and decided to wait before I have another surgery and take estrogen blockers
Yes I am also waiting- got a nutrition referral-genetic testing-pending and that’s that - time to get on with it instead of mentally anguishing for the what if
I understand your anguish. I have had my third surgery for DCIS. Intermediate grade. First two surgeries could not get a clear margin. Waiting 3 weeks for the path report on this last surgery. I am also very confused on the treatment of this. The first surgeon told me it will definitely turn into an invasive cancer. How does he know that? The surgeries were not bad and I did prefer removing it rather than working about it being there, but three surgeries!
I’m sorry you are going through this and ugh, I hear ya!
I will also be having my 3rd surgery coming up. My surgeon said I had clear margins and would not need to take anymore out and then I met with my Radiation and Medical Oncologist’s and they both agree my margins are way too close and do need more taken out before I can start Radiation.
I have had a couple complications from the other 2 surgeries and I am actually not too impressed with a few things my surgeon has done, so I have an appointment with a different one on Monday for a consultation. Hopefully it goes well and this is the last surgery!
I really hope you get your Path results soon. The waiting is the worst!
And praying you now have clear margins!
I feel for you too. That seems kind of ridiculous that the surgeon would give you clear margin and then the others would not concur. Very frustrating. The only thing is knowing that your not alone with these conflicting diagnoses.
Yes I am also concerned about the conflicting opinions!
Possibly the surgeon I have been using just doesn’t have enough experience and that is why? She had a surgery opening last week, but I declined and decided on getting a second opinion.
The surgeon that I am meeting with tomorrow is the one I had initially wanted (he was on sabbatical when this all started so I couldn’t see him) and he has lots of experience and is supposed to be the best.
Fingers crossed I made the right decision!
I think you did. After the first surgeon could not get it the 1st 2 times for me. I went with a more experienced surgeon. I pray this is it for me. Will research the radiation after I get a clear margin.
According to the Mayo Clinic DCIS IS cancer. "Ductal carcinoma in situ (DCIS) is the presence of abnormal cells inside a milk duct in the breast.
DCIS is considered the earliest form of breast cancer. DCIS is noninvasive, meaning it hasn't spread out of the milk duct and has a low risk of becoming invasive." Source: https://www.mayoclinic.org/diseases-conditions/dcis/symptoms-causes/syc-20371889