Patient profiling is the practice of regarding particular patients as more likely to have certain behaviors or illnesses based on their appearance, race, gender, financial status, or other observable characteristics. Profiling disproportionately impacts patients with chronic pain, mental illness, the uninsured, and patients of color. Like racial profiling by police, patient profiling by physicians is more common than you think.
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I wondering about that I got copies of my medicail from my cardiolist 5 years ago .recently I exprenced puting me off for an apointment 2 times and showed up then they said that could find me on the the appointment had to come back for 2 or 3 hours later .Then it was a bad stress test .The doctor wants to do a angiogram was told by the nurse that called.I not having any heart pains.I exercise 5 to 7 days a week.walk and lift weights.
I have a rare condition called hereditary angioedema. Many physicians may not know about it unless they have had a patient with it, or unless they are in a certain specialty that deals with it. It is swelling not caused by histamine, but bradykinen problems. It is a strange, traveling edema that usually starts on the left side of my face, then goes down slowly through the throat and GI tract.
When I worked as an RN in a small hospital in St. Helena, CA, of which that is the hospital name, I was unfairly discriminated against when I went to the ER for throat swelling. I was hoping one of the good doctors would be on call, but I got Dr. Mishkin instead. Yes, I will use his name.
Because I have had this condition since I was six years old, I was trying to explain the history and the fact that my mother also had it. I know as an RN, most doctors want to know the history of a patient. This one, however, said it was exacerbation of asthma, but I was only wheezing when the fluid got to the trachael area of my throat. I was not wheezing when it started, two hours before I came to the ER, or after the fluid passed down past the larygeal area.
It is no longer possible. No such thing as a good doctor. They are too quick to make conclusions, and base those conclusions on poor practices, word of mouth by other doctors. Seeing another physician changes nothing. Modern technology makes it impossible to be free of cover-ups by medical professionals, bad medicine, or poor interpretations.
I lost everything many years ago, and continue to fight against PTSD. No point in it anymore. Looking for a means to an end so that I do not end up in the hospital: helpless, vulnerable, and at their mercy. Never going to happen to me again.
As for your situation now: I would consider paying out of pocket to a doctor outside of Medicare. Check map on my website for ideal clinics. You definitely need a doctor who you can have a healing relationship with!
I was denied hysterectomy for thirteen years just because I look like I am not quite all there. By the time I was granted hysterectomy, it was nearly too late. Even so, my gynaecologist said I could not have surgery without parental consent in spite of being 36
All doctors are not the issue. A particular age is. here is something to be said for different generations of healthcare students being taught different things by the state. All doctors are brainwashed though.
Sorry to hear that. I wish you the best and hope things can turn for the better for you. I have been through hell to but I am ready to file suit. Doctors in my own family are saying do it and I understand how hard it is to get through medical school but this is unacceptable.
Dear Wible.
I no Iron in 2012 and all blood levels were very low.
Vitamin D. very low. Then in 2013 I bowel and bladder
repair using the mesh. That surgery did turn out well
and I had to have to cut the mesh. so I could pee.
it left me a bowel dysfunction, where know I have hard
stool that gets stuck. I feel I being profiled. there is
a lot more to this Issues. I could write a book. DRS. Think I am crazy. how do I fine out if this is true. please. thank you mary.
My doctor and his staff, upon making multiple admissions to the doctor and his staff about my gender identity (having felt significant pressure to identify as a woman in order to have my concerns validated), refused to use she/her pronouns or even treat me as such (which I assume is based on my rather androgynous dress).
Disgruntled and feeling completely disempowered as a trans person, my doctor (and his staff) not only repeatedly misgendered me, but also used my lack of presentation in feminine clothing as a piece of evidence with which to patient profile me as drug addled after a mildly contentious dispute, wherein I questioned their authority as a dental official, the dispute was about the crown that was originally doctored and I was asking if that situation could be remedied.
We never intended to harm anyone. We came to medical school just wanting to help people. Sadly, we were dehumanized in our training and abused. This is a cycle of abuse that patients need to understand: -burnout-is-physician-abuse/
I am in a situation now my health is being neglected. I recently got my disability because I have such severe neuropathy I fall, I want feel my feet and I will just fall. These are not even the only medical problems I have. But I had a doctor for near 20 years had me on strong pain meds for the problems. 60mg oxy. I had a good job and Insurance. Then I lost my job and I fought for 3 years to pay for my Insurance under cobra. And then lost out my unemployment stopped. Well In the meantime I was loosing everything my trailer my car got repossessed. And had to move into a hotel well both my daughters were living with me and we had to have an apartment type suite so I had to have a boarder to share expenses so I let a friend of mines daughter also live with us she was 29 just like my married daughter and my youngest was almost 18. Well one of them or there friends stole a zanax RX from me and even though I was going to prosecute my own family, I had police report and turned it over to the FBI not only did the doctor cut me off and also did not take me seriously neither did the FBI. So I have been through hell even getting my disibility. Thank god I did. But the doctor that helped me was 90 years old and retired. He referred me to the pain clinic at this county clinic that is for less fortunate and I was treated kindly at first he retired and within 6 months I was discharged out of the clinic. Mine is a long story and this is only a short portion of it. But I am starting to think I am crazy and need to see psychiatric help. And this is very serious and true. Thanks for Listening Donna in Birmingham
The current status of our medical system is a heart beat away from negligence. People will die either by their own hands or by a system that is set up to judge them before treating them. Currently there are 100 million chronic pain patients in the US. These patients are having medication denied, restricted, and are being told to take OTC meds that are as dangerous as the medications that the CDC/DEA are asking Doctors to restrict. Furthermore, alternative medicine to treat chronic pain often is not covered by insurance. For example physical therapy for my plan is $40 a visit, and capped at 5 visits a year yet the CDC would rather me do PT than have a prescription of Vicodin to maintain my quality of life. Physical Therapy for an incurable disease that I am restricted to just 5 visits a year. It is like the CDC did not even think about the repercussions of their own guidelines. That forcing people off medication that they did well on, with no history of abuse, would likely send people to meets with drug dealers willing to prescribe Heroine. Congrats to the CDC they just made drug dealers a lot richer. THis is often the problem with prohibition type laws and guidelines. Those guidelines were also full of misleading and false data. It ends up pulling the cart before the horse. Less than 5 percent of chronic pain patients abuse their meds. So who are these guidelines targeting? They will have the exact opposite result because most people abusing opiates are not buying them legally anyway. That is the most frustrating thing about this. Also Doctors should be angry- as we are moving away from patient centered care.
Yep. My son is severely disable with Ankylosing Spondilitis. I knew he had the same thing I had when he buckled over while dining in a restaurant. I had no idea it was hereditary. When I was in teens I was informed by a GP that if I ever stopped moving I would be in a wheelchair within a few years. Physiotherapy and dance kept the worst at bay for me, but since the cancer surgery (the chest tube was left in for nine weeks) I have some serious issues. No one will listen. They refuse to believe me.
It is true that your medical records follow you from doctor to doctor. There can be erroneous information in the records that should be amended. It is a good idea to read your own med records every once in a while just to make sure things are presented correctly. As in any human interaction, there can be miscommunication, misinterpretation . . .
Thank you for your lovely blog and fresh ides for being a physician. My dad was a solo practitioner and kept his home phone number in the book. He got calls emergency every Xmas morning and dutifully went off to the hospital.
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