Diagnosed with breast cancer & primary lung cancer: Next steps?
Hi. I’m Barbara. I was diagnosed with breast cancer in October. At the pre op I had a slight cough. I was diagnosed with pneumonia and breast lumpectomy surgery was rescheduled. Cough didn’t resolve so further testing was ordered. I was diagnosed with Lung cancer also at Christmas. Had lumpectomy and lymph node removal Jan 7 and just started radiation. In meantime my case has been presented to the tumor board and I should hear treatment recommendations for the lung cancer by end of week. Dr ordered a pulmonary function test for tomorrow and said it’s looking like surgery may be best option.
Interested in more discussions like this? Go to the Lung Cancer Support Group.
Connect

@bdurel checking in on how you're doing...
-
Like -
Helpful -
Hug
1 ReactionIs the lung & breast cancer on the same side? The reason I ask is that I had my first abnormal mammogram a few months ago in my left breast - I go back to recheck the spot in July. My lung cancer was in the right lung …?
I just had a RLL lobectomy Monday morning. I’m doing fairly well - taking all the pathology and new information in …
-
Like -
Helpful -
Hug
2 Reactions@bdurel you are truly fortunate to have EGFR and option of Tagrisso. We were hoping for that mutation in Guardant 360 results, but got ERBB2 w/Exon 20. Then a new drug Hernexeos came out for that!! Keytruda & platinum chemo not much hair loss. Maybe you can consult a hairdresser for permanent extensions or a fall? You’re beautiful either way! Hang in there!! Outcomes are all at least 10-15 years outdated and Keytruda (pembro) and Tagrisso are both game changers! You will beat this!!
-
Like -
Helpful -
Hug
2 Reactions@bdurel Hi Barbara I can only imagine how you feel with so much coming at you at the same time. I believe in God and I know he is able. He sees you and already knows how our stories, past, present and future. Be strong, we can only do what’s in our control. You’ve got a lot going on but you’ve had a lot of wins too. Even while you’re going through this try to fine some joy and peace. Laugh smile when you can and always advocate for yourself. You keep mentioning a second option, I’m doing the same. I reach to second hospital and go my self scheduled. I pray that happens for you as well. It’s going to feel good to heard what two different professionals recommend. Wishing you the BEST on this journey.
-
Like -
Helpful -
Hug
1 ReactionWelcome @lisawolub, I hope your surgical recovery continues to go well.
Mammograms aren’t perfect, especially if you have dense tissue. A follow up is a good idea. If they were overly concerned they likely would have recommended a different type of scan, ultrasound or MRI.
I was diagnosed with lung cancer in 2020 (left and metastatic), and a completely separate breast cancer in 2024 (right side).
Density can make the mammogram images more difficult to read. Sometimes an ultrasound may be helpful after that second mammogram check. Have you been told that your tissue is dense?
-
Like -
Helpful -
Hug
2 Reactions@lls8000 Hi ✋ Thank you for the reply. Yes on both - I have dense tissue, and am having ultrasounds. I guess if we have a genetic predisposition/vulnerability to cancers, multiple diagnosis would be unrelated to one another.
My recovery from RLL lobectomy is going pretty well. My path came back EGFR (19 mutation), tumor 3.7cm, VPI, adenocarcinoma. My oncologist is of course talking about 3years on osimertinib and possibly chemo. I meet with the surgeon and oncologist on the 22nd. So glad to find this group. Any other sites for connecting with others?
-
Like -
Helpful -
Hug
3 Reactions@lisawolub In response to your last question. Facebook has a private group for Tagrisso (osimertinib) patients and caregivers. There are frequent posts and lots of good info for patients on Tagrisso. -Rose
-
Like -
Helpful -
Hug
2 Reactions@bdurel Hi, I don’t have any answers either but wanted to reach out and say hi! and you are in my thoughts and prayers. I’m in Chico, CA and I had surgery at UCSF for ILC, last Nov. they are monitoring a spot on my lung currently. I hope the second opinion referral happens soon. Take care, Tawny
@mamajite
I just read this. I had long red curly hair my whole adult life. 40 years. I got Taxol/Carboplatin and my Medical oncologist suggest i just cut my haor. Cold capping does not always work. Easy for others to say that. I had asked after hoe many infusions would my hair would fall out. I had 12rounds, for 12 weeks. The 2nd week i had my hair cut to my shoulders. One week later I asked my sister to do very short. I had 2 wigs. One i just saw picture on Facebook and it looked good. Many people thought i cut my hair. I WORE HATS, IT WAS COVID TIME AND I went to headcovers.com and bought rosette hats. Beanie caps. It looks 2 years about for my hair to hit my shoulders.
Ha in Sept 2023 i was diagnosed with MDS. My hematology oncologist said i would not lose my haor. HA HA. My nurses there said yes, you will. I had a bone marrow transplant and the chemo was melphalan. For just a minute i ask God if he was kidding. Lose my hair twice? Yep, I did, but for fun, a nurse said to me 26 days past transplant i may not have red hair because of my donor's blood cells. Ha! 2 years after it is red curly to my shoulders.
-
Like -
Helpful -
Hug
4 Reactions@katgob wow - you experienced the full gamut of treatment associated hair loss twice!! I'm delighted that your hair returned unaltered. I'm still not feeling great about mine. They told me initially I wouldn't lose my hair on Tagrisso. To be fair, it was only about half. I just started a treatment pause and I'm hoping it will help my hair, but my oncologist couldn't tell me if my hair would improve or not.
-
Like -
Helpful -
Hug
1 Reaction