In a comment, not long ago, about getting a second opinion, Tall_Allen suggested/gave out the name of a well known female Oncologist/Researcher in Chicago. I live here and want to give it a try. This past week called to her office and the receptionist took a long time to complete what she called an 'intake' so much time that I had to tell her I needed to go back to my desk as it have been more than a half an hour. The questionnaire started by asking what time of cancer and when I got diagnosed, I answer that. Then she goes, have you had a biopsy done, I said yes, she is like where and what were was it done and what were the results, I was honest and told her that I was diagnosed in 2018 and that I had a biopsy done, she almost interrupted me and said, 'well you are going to need to get a copy of the biopsy and results, translated into English' Dr such and such won't see you without that information, I explained to her that getting those documents is impossible as in Ecuador the public health insurance, where I had the procedure, diagnosis, and following treatments, is chaotic to say the least. Then it felt like alarms went on over there at the receptionist office, she put me on a long hold, came back and said wait some more as she was discussing this with her supervisor? Finally she came back and said she definitely needs to complete an 'intake' form before even looking at her calendar to see what appointments were available. This is when I told her I needed to get back to work, she told me to callback when I get more time as there were a lot of questions she has to ask. I called the next day during my one hour lunch time, the line was 'busy' the entire time. I called again the day after that and finally she picked up the call, it didn't take long for her to identify me, this time she started by asking about my Insurance, she checked and checked to make sure they will accept it. Then we went to the 'intake' she kept making remarks about how my biopsy was done in Ecuador, I tried to tell her repeatedly that now I do have an oncologist and that I am on treatment here in Chicago ,she is like ' I don't know how they are even seeing you without the biopsy results and even less, how they put you on a treatment' Then she started asking what kind of radiology scans have been done, I answered to that. And once again she asked me the name of the urologist who diagnosed prostate cancer! I said I can't remember his name, he is in Ecuador. The she proceeded to ask about contact information and then she said the Dr. Such and such will review the 'intake' to decide if she wanted to see me or not! The receptionist said it'll take a few days before I get and answer, then only then she would start looking for a day and time, I said I don't understand why it is so hard to get this appointment scheduled and that what I am looking for is a second opinion. OMG, all hell broke loose, she raised her voice and said 'the doctor doesn't see people for second opinion, it is either you are accepted as a permanent patient or not! I replied, then I'll switch my care to this office. Before hanging up, she said this is all we can do today, just wait for us to contact you!
I can't help to have this very strange feeling of being discriminated against based on my ancestry and my accent. Could it be so? Has anyone experienced this kind of behavior?
I was hoping to get to see the MO before seeing my MO this coming Tuesday, where I am not entirely happy with their procedures, such as seeing the oncologist without having lab work results as the blood samples are only taken a few minutes before I walk in his office. It is very hard to discuss a new treatment with him, he always says I call you back to let you know what is next regarding you starting a new treatment based on the lab work.
I will also get my fourth Lupron injection that I am getting every four months. And that is it.