Mayo Clinic Connect
I am just curious. How many of you have been misdiagnosed by a radiologist. Was it on your mamo or an MRI…or something else? How many were told you did not have breast cancer when you did?
Liked by Christine Huyber
I was not misdiagnosed by a radiologist but was told by my oncologist in February 2018 during a routine exam that I had a "cyst" in my left breast. When I asked my doctor several times if she was sure, she said yes, that she thought it would be gone by the time I had the mammogram she was going to order for "due diligence". I suspected that she was being less than honest; as it turns out, I had a second breast cancer. I dropped her immediately. To accept that your oncologist would intentionally lie to you after knowing you for several years and seeming to take such a sincere and personal interest was devastating. But–I contacted her informed her that I was requesting another oncologist and moved on.
Liked by trixie1313, trivia
Yes, 2 years before I had Stage 3, I felt three lumps and a mammogram and an ultrasound. I was told to monitor then and come back in 6 months. I did and they said the same thing. Then another 9 months I had Stage 3. Totally misdiagnosed.
Liked by trixie1313
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I am so sorry you went through that. Stay strong.
Liked by trivia
Unfortunately, maybe she just isn't that bright. Good that you are moving to another oncologist. I didn't feel comfortable with mine and switched out. Always follow your gut.
Liked by dthayer, trivia
Absolutely! Thankfully, this was nearly three years ago and I have great trust in my current oncologist. 🙂
That's horrible! Why wasn't a biopsy performed right away? I have learned to be quite assertive in my treatment. I have even considered checking out Stanford University if I need care in the future. I wish you all the best.
I wish I knew why the two radiologists who looked at the test results didn’t suggest a biopsy. Of course, I know better now but back then I didn’t know that much about breast cancer. Can’t go back and change it. Now I’m Stage 4 Metastatic Breast Cancer, which they guess now that I was Stage 4 when they first diagnosed me. It was too small to see the lesions in my liver back then.
I am so sorry you have gone through all of this. It is so difficult when you expect those with knowledge to guide you. Because I kept worrying about my other breast, I had asked the oncologist and my regular doctor for an MRI of the breast which they both told me was not necessary. It was my breast surgeon who I asked following my lumpectomy who said she didn't see why not to alleviate my worry, and it was at that MRI they noted another lesion on the opposite side of the affected breast which turned out to be a neuroendocrine cancer. I thank goodness I had decided to go to the other facility as had I not, that second lesion would have spread like wildfire. Stay strong Trivia, look out for yourself and keep questioning.
Liked by elizm
The beast cancer clinic at University of San Francisco is fantastic for the support and the knowledge. When I went there with a friend they tape the whole conversation with the doctors and the team and not only gave it to her on a CD/DVD but there was a typed out record of everything discussed
Oh that is great to have a record of the discussion as you get overwhelmed with information and thoughts.
Liked by lucky1038
It would seem an easy thing. But apparently sometimes, the medical establishment is more about covering their tracks and dealing with what insurance companies will cover rather than the good of the patient.
I was diagnosed with breast cancer 1992. A routine mammo showed calcifications. Biopsy showed cancer. Because of the size I had a mastectomy and chemo. No lymph nodes. I was supposed to return the mammograms to the radiologist and decided to take a look first. What shocked me was the report from previous mammo 15 months earlier stated all normal, but this one compared the calcifications to the ones on previous mammogram. In other words, it was there more than a year earlier. The surgeon agreed with my findings.
I have been fine and no recurrence. However, I realize now how the chemotherapy affected my health. I got chemo brain- foggy etc. I was also very susceptible to infections. 20 years later I was diagnosed with autoimmune gastrointestinal inflammation, caused by severe GI reaction I had to chemo. I had this for years before diagnosis- I finally got treated with immunosuppressant medication and it’s gone. However, I’m exhausted, brain fatigue etc.
My point is- a missed diagnosis follows you- even though I have been cancer free my health has suffered.
Sorry for your hard experience. It’s true we are still plagued years later by the standard protocol from the medical community. I asked my Natureopath yesterday why aren’t they focused on why we have cancer so we can get to the root of the problem. There lies the cure! It’s probably all related to gut flora which controls the absorbing of key nutrients which allows your body to fight the abnormal cell production.
Liked by Ingegerd Enscoe, Volunteer Mentor
In my view, researchers are totally focused on causes (which appear to be numerous). Following genetic testing (which was free of known genes which cause breast cancer and others), with no family history of breast cancer, and with my level of physical fitness, my oncologist (who is well-connected to the major medical research organizations) concluded that the cause of my breast cancer was prior years on hormone replacement therapy for menopause… which makes complete sense for my situation. Each of us has different factors at play.
Drugs approved by the FDA are simply taking a natural substance and patent a portion of it for financial gain. No matter what caused your cancer, our bodies made it. It’s part of us. Now take that information and see what you can do about it. You are your best defense against disease.
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