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Monday, October 24, 2022
The Effects of the Use of Patient-Accessible Electronic Health Record Portals on Cancer Survivors’ Health Outcomes: Cross-sectional Survey Study
Thursday, October 20, 2022
The Federal Telehealth Extension and Evaluation Act: What You Need to Know |
- U.S. Senator Catherine Cortez Masto
On February 7, 2022, Senators Catherine Cortez Masto (D-NV) and Todd Young (R-IN) introduced the Telemedicine Extension and Evaluation Act, important bipartisan legislation to ensure predictable patient access to telehealth following the end of the public health emergency, allow more time to gather data around virtual care utilization and efficacy, and avoid a sudden drop-off in access to care (known as the telehealth cliff).
Key Takeaways for the Telehealth Industry
Here are the key takeaways on how the new legislation may affect the telehealth industry.
1. General Extension of Medicare Payment for Telehealth Services
Under the CARES Act, Congress gave CMS authority to waive certain limitations on Medicare coverage and payment for telehealth services furnished to Medicare beneficiaries, clearing the way for Medicare beneficiaries to receive care in their homes. If passed into law, the Telehealth Extension and Evaluation Act would extend certain Medicare telehealth payment waivers on originating site and geographic location limitations, expand the list of permissible telehealth providers, and broaden the availably of audio-only telehealth services for Medicare beneficiaries for two years after the public health emergency ends. Read our prior coverage here and here.----
Prior to 2020, there was a reticence to adopting telehealth. Although technology had outpaced the use of telehealth there was also a reluctance on the part of physicians to utilize this resource. Reimbursement regulations were also restrictive preventing patients and physicians from utilizing telehealth.
COVID 19 changed that. The emergency CARES ACT provided for the use of telehealth and required reimbursement by CMS and private insurers.
The telehealth provision of the ACT is set to expire on December 31, 2022. A bill is now in progress to extend this benefit for one or two years or make it permanent.
Sunday, October 16, 2022
Everything They Don’t Tell You About Taking Care of Aging Parents | by Adeline Dimond | Oct, 2022 | Medium
Get ready to fight, and don’t expect people to understand.
Yes, this is likely illegal. But large financial institutions know that in order to be held accountable for failing to honor POA documents, the attorney-in-fact would need to sue them. Otherwise, there are no consequences for them at all. But suing a financial institution takes money and grit, which they are betting that the attorney-in-fact does not have.
Review the POA language very carefully.
In my case, my father’s POA documents listed my mother as his attorney-in-fact in the first instance, and me as a successor POA if my mother was “unable or unwilling to act.” My mother’s POA was the same, listing my father as the first POA. Financial institutions seized on this, asking me to “prove” that my parents were “unwilling or unable to act” on each other’s behalf.
Open a bank account with your parents.
I could have avoided all the above POA pitfalls if I simply were a signatory to my parent's bank accounts. Of course, not everyone has the type of relationship with their parents that allows for this; I definitely didn’t. But if you can swing this, being able to immediately access their funds at a moment’s notice is worth the uncomfortable conversations this might require. Parents hate giving up control. I don't know why they would want to maintain control when they are dying or dead. Some parents cannot get over "I know what is best for you."
Go ahead and get the passwords to your parents’ accounts, and pretend to be them.
Eventually, in some cases, after it became clear that the financial institutions were going to block access to my parents’ accounts despite the perfectly executed POA documents, before spending my energy drafting more scary letters, I just got my parents’ passwords (and the answers to the security questions), logged on to their accounts, and pretended to be them.
I was warned by one financial institution that “they don’t allow this,” but I just didn’t care anymore. I have my parents’ authorization to access their accounts, and that’s enough for me.
Tuesday, October 11, 2022
APIC urges members to disregard new CDC masking guidelines
Long COVID Experts: U.S. Government Needs to Do More | Time
Long COVID Experts and Advocates Say the Government Is Ignoring 'the Greatest Mass-Disabling Event in Human History'
Sunday, October 9, 2022
Prosopagnosia (face blindness) Do you suffer from this? Brad Pitt has it
People who are diagnosed with prosopagnosia often fall into one of two categories: either they are born with it or they acquire it.
Prosopagnosia is not related to memory problems, vision loss, or learning disabilities, but it's sometimes associated with other developmental disorders, such as autism spectrum disorder, Turner syndrome, and Williams syndrome. However, estimations reveal that as many as one in every 50 people may struggle with some lifetime form of the disorder, and experts hypothesize that it may run in families.
According to Blum, research “suggests that congenital, or lifelong, prosopagnosia is less prevalent.”
According to Andrey Stojic, director of general neurology at the Cleveland Clinic, children born with the illness “don’t seem to have any visible structural abnormality” in the brain.
Notably, doctors don’t fully understand what causes congenital prosopagnosia because there aren’t any obvious brain lesions in persons who have it.
In contrast, people who develop prosopagnosia later in life may have brain abnormalities brought on by a trauma or head injury.
According to Bonakdarpour, individuals can also develop prosopagnosia while dealing with Alzheimer’s illness or following a stroke.
What therapies are available for prosopagnosia?
Borna Bonakdarpour, MD
Assistant Professor of Neurology (Behavioral Neurology
Prosopagnosia is now untreatable, according to Bonakdarpour. The problem can be treated, though.
People who have the syndrome frequently attempt to distinguish between people by focusing on physical characteristics like hair color, gait, or voice.
Usually, a set of tests that measure a person’s memory and face recognition help neurologists make the diagnosis.
As doctors frequently take care to ensure that a patient’s face blindness is not an indication of a more extensive degenerative neurological disorder, Blum adds, “it can be a drawn-out process.”
It’s noteworthy that many people with the illness, like Pitt, won’t get an official diagnosis.
Many of the difficulties he’s discussing and the issues he has are not unusual for people to go through them, according to Stojic.
He continued, “It may be relatively crippling for folks. “Others find it difficult to comprehend,”
Thursday, October 6, 2022
Worldwide Directory of Pregnancy Help
Listening to Black Californians: How the Health Care System Undermines Their Pursuit of Good Health - California Health Care Foundation
California, home to the most culturally diverse population in the country and the fifth-largest Black population of any state, has a major opportunity to be a leader in health equity. But glaring racial and ethnic inequities pervade its health care system, from insufficient access to worse health outcomes to excess mortality.
Black residents have the shortest life expectancy (75 years) at birth of any racial/ethnic group, six years shorter than the state average. Black Californians have the highest death rates from breast, cervical, colorectal, lung, and prostate cancers. Black birthing people experience the highest rates of prenatal and postpartum depression, preterm births, low birthweight births, and pregnancy-related mortality. And Black infants have the highest mortality rates.
As part of its commitment to ending health inequities, CHCF commissioned Listening to Black Californians, a three-phase qualitative and quantitative study to understand the health and health care experiences of Black Californians. The research is being conducted by EVITARUS, a Black-owned public opinion research firm in Los Angeles. An advisory group composed of academics, policymakers, providers, and community advocates is guiding the study.
This report describes the results of Phase I of the Listening to Black Californians study. In this phase, EVITARUS conducted individual, hour-long interviews with 100 Black Californians from June to August 2021 to understand their views on health and well-being, their perceptions of discrimination and bias in the health care system, and their views on what a quality health care system looks like. Each story provided unique insights. Still, taken as a whole, the stories revealed many similarities in how Black Californians view health and how they experience health care.
Key findings include:
- Respondents held a holistic view of health and prioritized it in their everyday lives.
- Experiences with racism in health care were widespread and negatively impacted participants’ health.
- Participants envisioned high-quality health care as patient-centered and proactive.
The complete report is available under Document Downloads.
In Their Own Words: Black Californians on Racism and Health Care — Executive Summary (PDF)