Words matter. These are the best Patients Quotes from famous people such as Jed Mercurio, Jimmy Fallon, Siddhartha Mukherjee, Tony DiTerlizzi, Bennet Omalu, and they’re great for sharing with your friends.
There’s a classic medical aphorism: ‘Listen to the patient; they’re telling you the diagnosis.’ Actually, a lot of patients are just telling you a lot of rubbish, and you have to stop them and ask the pertinent questions. But, yes, in both drama and medicine, isolated facts can accumulate to create the narrative.
Researches tested a new form of medical marijuana that treats pain but doesn’t get the user high, prompting patients who need medical marijuana to declare, ‘Thank you?’
Good physicians are rarely dispassionate. They agonize and self-doubt over patients.
Now, as Global Ambassador for Starlight Children’s Foundation, which brightens the lives of poorly children, I visit hospitals and tell stories to the young patients. Sometimes I read. Sometimes I draw.
I am a spiritual person. I’m a Catholic. I treat my patients, the dead patients, as live patients. I believe there is life after death. And I talk to my patients. I talk to them, not loudly but quietly in my heart when I look at them. Before I do an autopsy, I must have a visual contact with the face.
Serving people is never a problem for me, because I’ve already served all my patients. Even as a doctor, I also wasn’t purely a doctor.
My deceased patients have taught me over the years to believe in the glass half full, to make good use of the time we have, to be generous – that was their lesson for the Uber-mind, and it was free. ‘Do that,’ they said, ‘and then perhaps death shall have no dominion.’
My job as the doctor is to provide my patients with the information and services they need to make the best decisions for them and their families. Medicine is complex, and every situation is different.
I do mean this – I had the good fortune of being around a number of Alzheimer’s patients in the last three years of my mother’s life. She was in a care facility that was devoted to just people with memory-loss issues. I found those people engaging and generous in ways that I had not imagined.
It was a mutual thing. I made a deal with them: I asked them if they did not bring out the place card of Malachi, I would let them have two minutes with each one of my patients.
As a physician, I would never encroach upon the religious freedoms of my patients.
Encouraging wellness and prevention helps improve quality of life and can lower costs, too. I saw too many patients who had poor health because of their decisions, but too often, all they needed was a doctor to help point them in the right direction.
A democratic medical establishment does not alter people’s bodies to fit regressive social norms; it advocates for patients by demanding the social body get its act together.
What is clear is that stalking can happen to anyone. Doctors are targeted by patients, people in the public eye are watched by obsessed fans, and ex-wives are followed by former husbands.
We will empower patients as well as health professionals. We will disempower the hierarchy and bureaucracy.
The nanofibrillar scaffolds designed to guide the process of cellular repopulation is an important step towards prolonging life and enhancing the quality of life for patients with advanced heart disease with defective valve.
I use music in the operating room to help create a healing environment for patients and staff. There is a reason that certain heart rates are healthy and certain beats of music heal and relax us.
There are two things panic patients hate to do. They hate to take medication – and they hate to go to doctors. They hate to come to grips.
Communication is everything, especially as a doctor, you need to communicate with your patients.
These days the technology can solve our problems and then some. Solutions may not only erase physical or mental deficits but leave patients better off than ‘able-bodied’ folks. The person who has a disability today may have a superability tomorrow.
The fact remains that many of the most creative and innovative hypotheses that are eventually verified by empirical research are born in the consulting room out of practitioners’ work with individual patients.
Everyone is filtering their selfies to make them look perfect. We’re seeing it more and more in my clinic – patients want to look like a photo they’ve tweaked. They show me the picture and say: ‘This is the new me.’ But many times it’s not realistic.
We will hold Planned Parenthood accountable for knowingly endangering their patients by providing illegal abortions at a facility that was not properly licensed nor prepared to handle an emergency.
Let’s lower costs for health care. Let’s put patients in charge of their solutions.
Health care providers can follow guidelines for responsible painkiller prescribing and talk with their patients about the risks and benefits of taking prescription painkillers.
My dad was a physician. As a kid, I remember driving around with him on weekends so he could do his rounds at the hospital and talk to patients. We’d spend time in the car talking about what was going on with them, their stories.
I think legislation needs to put an end to doctors profiting on businesses to which they can funnel patients – that is business, not medicine. If you try to call it medicine, then it is corruption. Without legislation, it will keep happening.
Patients who have suffered appalling medical negligence, abused children ignored by social services, mistreated residents of care homes – they have all been given a voice by the Human Rights Act.
Covid-19-affected patients cannot be orphaned.
The more we know about Lyme, the more we can do to treat patients and educate families to stop the spread of this debilitating disease.
Affordability is critical so that patients have access to medicines. At the same time, it’s also important that we have the kind of incentives that allow us to do the kinds of studies that we need to do to go after these diseases like Alzheimer’s.
With the Lower Drug Costs Now Act, we are taking bold action to level the playing field for American patients and taxpayers. This legislation is one that I am proud to have voted for, and the House can be proud to have passed. It is essential to save the lives of Americans and improve our quality of life.
Doctors and hospitals should be paid for keeping their patients well. Paying them for doing more tests and surgeries creates bad incentives.
We’re really going after truly creating sustainability of a disease-free state, creating a complete system for managing cancer patients for life, so that you can manage from onset of disease all the way through.
When I became ill, I started to experience what my patients had suffered under my care.
There is a social stigma attached to ambulance services, mostly because ambulances in India are often used as hearses for carrying the dead rather than transporting patients. We made presentations to graduating students at various healthcare institutes, trying to debunk this myth.
We have lost close friends and relatives to cancer and Parkinson’s disease, and the level of personal suffering inflicted on patients and their families by these diseases is horrific.
Every single cancer is a genetic disease. Not necessarily inherited from your parents, but it’s genetic changes which cause cancer. So as we sequence the genomes of tumours and compare those to the sequence of patients, we’re getting down to the fundamental basis of each individual person’s cancer.
We can trust our doctors to be professional, to minister equally to their patients without regard to their political or religious beliefs. But we can no longer trust our professors to do the same.
Please, let patients help improve healthcare. Let patients help steer our decisions, strategic and practical. Let patients help define what value in medicine is.
Congress should let HRSA release its guidance and analyze its impact before making changes to the 340B program that would harm safety-net hospitals and our vulnerable patients.
One of the shortcomings of our medical system is that doctors have very little time with their patients.
Once an effective drug is approved to treat a deadly condition, introducing a second drug to treat the same disease can be hard. It’s tough to recruit patients with a debilitating disease for a clinical trial when a proven medicine is already available.
Smartphones can relay patients’ data to hospital computers in a continuous stream. Doctors can alter treatment regimens remotely, instead of making patients come in for a visit.
We can create more affordable coverage options for all Americans and help patients with pre-existing conditions – without forcing any satisfied Americans to lose coverage they like – through high-risk pools and reinsurance options.
Since I do not believe that there should be different recommendations for people living in the Bronx and people living in Manhattan, I am uncomfortable making different recommendations for my patients in Boston and in Haiti.
We’ve seen the benefits of expanded telehealth services during the COVID-19 pandemic and the importance of making sure access to care is available if patients have to stay at home. That value won’t go away when the pandemic ends.
In 15 years, we’ve raised $225 million, sequenced the myeloma genome, and opened 45 trials of 23 drugs – six approved by the FDA – which have doubled the life span of multiple myeloma patients. I’ve taken both Velcade and Revlimid, which we helped develop.