What I Value

“ Caritas, Veritas, Fortitudo . . . ” During my childhood, I experienced medical conditions that heightened my awareness of how medicine wa...

Thursday, October 28, 2021

ACR Convergence 2021

Colleagues and experts from around the world have been gathering every year since 1934 to share revolutionary science and discuss timely topics in rheumatology around prevention, diagnosis, and treatment of rheumatic diseases. 

The American College of Rheumatology (ACR) Convergence 2021 is an all-encompassing virtual experience designed for the global rheumatology community. 

The conference takes place November 3-9, with extended programming on November 10. The annual event has become the preeminent scientific event for rheumatology, with over 16,000 attendees in 111 countries.

Following our team's research, examining how the COVID–19 pandemic may be affecting the health and wellness of people with scleroderma, the following poster presentation was created. In highlighting the experience of patients with scleroderma during the COVID-19 pandemic, we are better able to respond in ways that help people stay well.

Pandemic andPatients: Examining Health-Related Behaviors of Patients with SystemicSclerosis During the COVID-19 Pandemic Tuesday, November 9, 2021. Session: Patient Outcomes, Preferences and Attitudes. Nancy Dorr, Ph.D. (The College of Saint Rose), Patricia Fennell, MSW, LCSW-R (Albany Health Management Associates, Inc.), and Lee Shapiro, MD (Steffens Scleroderma Foundation and Albany Medical College).

To learn more about ACR Convergence 2021, please visit https://www.rheumatology.org/Annual-Meeting






by Jennifer Howard













Saturday, October 9, 2021

SHIREY ARCHIE'S "STAND AGAINST RACISM" LEADS TO NEW FILM

Shirey Archie
Shirey Archie

Activist, Shirey Archie, holds a sign that reads, "Stand Against Racism" on the corner of a busy intersection in Albany, NY the first Saturday of every month. Archie receives enthusiastic honks from supporters, choice words from detractors, and an understanding of the reality that is the space in the middle — the silence. "I knew I had to do something. If there is something you are concerned about, there is something you can do about it." Archie's motivation? His teenage son. "As an African American in this society, I have learned how to navigate racism in America. When my son was born, I realized he was going to have to learn the same. I was sad and angry. I decided to do something." 

Creative Action Unlimited is a non-profit organization that creates original theater and films that address current social issues to raise public awareness and to inspire audience members to take action in terms of social change. Director Michael Kennedy invited a group of actors, artists and activists from the Capital region, people who identified as Black or a person of color, to help her create a theater piece around the topics of race and racism. "Working with people of color is amazing," Archie remarked. "I've always worked in spaces, white spaces, where I am the only one. So to work with a group of people who I didn't have to explain about who I was and what I was saying was an amazing event."

Archie: "Stand Against Racism
"The encounters and relationships with other performers were dynamic, we sat in a room, we brainstormed, we created individual monologues, and we collaborated with Ms. Kennedy, who condensed and edited the piece into the version of the play that finally appeared on stage." When asked if the experience of participating in Whitewashed: The Racism Project was freeing, Archie responded, "`Freeing’ is not even the word for it. Just to not be on guard in a space is an amazing feeling."

The play (now turned feature film) is provocative and was repeatedly sold out and well received. It asks the audience to address historical racism but also confront systemic racism, white fragility, and internalized racism. "When I started doing anti-racism work, I had to stop and ask myself, what were my biases? And I had a few. I found that I had to do something about those before I could ask any other person to do something about theirs."

"We are truly a divided people, divided to the point where we won't even take time to talk about the differences anymore. We need to be able to talk across color lines, so that we can solve the problem as a country. Waiting on people to tell us what to do has not worked well. We as individuals, communities and small groups of folks, need to get together, make decisions about what to do and then commit to those actions over time."


We encourage everyone to go see Whitewashed: The Racism Project by Creative Action Unlimited.




Written by Jennifer Howard



Paul Grondahl, Albany Citizen-Times, October 19, 2022
"He held a sign to fight racism. He got racist responses"





Friday, September 10, 2021

Patricia Fennell Appears on "Love Mia Vita" Podcast

Albany Health Management Associates' founder and CEO, Patricia Fennell, joins Femme Pharma's founder and CEO, Gerie DiPiano, and Medical Director, Dr. Deborah Saltman, on the Love Mia Vita podcast.

  • FemmePharma

    FemmePharma
    FemmePharma has been reinventing women's health care for over 20 years. Their mission
    — your wellness. Starting as a pharmaceutical research and development company, this team has become a partner for women over 40 who want to feel their best. With pharmaceutical-grade ingredients, strict product manufacturing (GMP) standards, and a commitment to personal service, their mission is to provide women with relief from the symptoms of menopause through products they can have confidence in. FemmePharma solutions are created by women, for women, and are the highest quality available without a prescription.

  • Love Mia Vita Podcast

    Love Mia Vita Podcast
    The Love Mia Vita podcast is hosted by Gerie DiPiano, founder and CEO of FemmePharma, and Dr. Deborah Saltman, Medical Director. They want to educate women and help them improve their health and happiness.

    ‘Love Mia Vita’ means ‘Love My Life’ and that is exactly what they encourage you to do. Ms DiPiano and Dr. Saltman interview experts in all aspects of women’s health to investigate the misunderstood, sometimes even undiscussed, aspects of life. They engage in lively conversation of tips (and myths), sexuality, feminism, and everything else that is part of womanhood. (Listen*)


  • Patricia Fennell & The Fennell Four Phase Model

    Patricia Fennell, CEO of Albany Health Management Associates, will discuss the Fennell Four Phase Model as it pertains to chronic illness and women's health. This model has been thoroughly developed over several decades through clinical encounters, patient testimonies, and empirical research. The model explicitly captures the changing experience of patients over time in all domains of their lives — their physical, psychological, and social-interactive worlds. 

    Topics addressed within the podcast include: Ms. Fennell's background and the reason for developing the FFPM, each phase within the model, how patients progress within the phases, and how practitioners and loved ones can help.
  • Tune Into The Podcast

Tune into the Love Mia Vita podcast on or after, Monday, September 27, 2021 via Spotify, Apple Podcasts or your preferred streaming platform.

* The Podcast is now available from both Apple and Spotify Podcast platforms. It will appear on the Love Mia Vita platform soon. 







Written by Jennifer Howard 










Wednesday, May 5, 2021

COVID: The Sequel

Mass vaccination and adjusted social behavior may finally get the pandemic under control. Then the medical world will have to turn its attention to the next chapter — millions of people suffering from long-haul COVID

As the pandemic took hold in the United States in March 2020, Caroline, a healthy, athletic woman in her late 20s, began to feel unwell. There was no COVID-19 test to be had at that point, but she called her clinicians to describe mild to moderate symptoms such as fever, respiratory difficulty, gastro-intestinal irritation, and loss of taste and smell — which came and went, and not all at the same time.

Caroline’s clinicians diagnosed her remotely as having COVID.

The fever, the teeth chattering, and the gastro symptoms went away — but not the fatigue, the body pains, or the neurocognitive symptoms, including sleep disturbance. Ten days later, 20 days later, a month later, she still hadn’t fully recovered.

Finally, eight months or so after the onset, Caroline had a COVID test, but it was negative, and an antibody test showed no antibodies. And without a positive test or antibodies in her system, she has found it difficult to find someone to treat or manage her condition. Most clinicians tell her that her persistent symptoms might or might not be COVID. And some say things like, “I have no idea what to tell you,” or “Are you sure this isn’t stress?”

Dan, in his late 30s, is a care provider for diagnosed COVID patients and their families. For a while, he continued to test negative, but began having symptoms about eight months ago. He was never hospitalized, and never had a positive test, without which the clinician who was seeing him would not diagnose him, in spite of all of the clinical indicators.

Dan still suffers from many long-term symptoms; his new clinician is helping him put together a team of specialists to develop and manage his treatment.

Caroline and Dan appear to suffer from what has come to be known as “long-haul COVID,” in which some manifestations of their illness just don’t go away, with symptoms sometimes mimicking those of other types of chronic illness.

Kenneth J. Friedman, PhD
Kenneth J. Friedman, PhD

In fact, more prior investment in chronic illnesses, and a better understanding of how they work, could have helped us to prepare for long-haul COVID, says Ken Friedman, Ph.D., a retired professor of pharmacology and physiology and a longtime researcher of chronic conditions.* Instead, the medical establishment in the United States has been slow to recognize and research chronic illness, and soon will pay the price: dealing with an onslaught of as many as 9 million long-haul COVID cases in the coming years in the United States alone, based on Friedman’s statistical analysis of recorded COVID cases.

Patricia Fennell, MSW, LCSW-R, a researcher and clinician who has been researching and treating chronic illness for more than 30 years, agrees with Friedman’s assessment. “The medical establishment,” she says, “has been slow to recognize the need for specific treatment approaches for the chronically ill, and to integrate them into their medical education curricula. And from what I can already see in requests for treatment of long-haul COVID, we are not prepared for what’s coming.”

So far, Friedman warns, “we have not seen a response proportional to the severity of the crisis that is about to befall us.”

* * * * * *

Friedman, a Brooklyn native, has a combined degree in biology and chemistry from Lawrence College in Appleton, Wisc., and a Ph.D. from the State University of New York at Stony Brook.  He was a NIH Postdoctoral Fellow at UCLA before becoming a Staff Fellow at the National Institutes of Health.  He became an Associate Professor at New Jersey Medical School in Newark.  Friedman had decided he didn’t want to be a medical doctor — “I really didn’t like the sight of blood” — and was more interested in helping people through research.

One day, his desire to help people hit close to home and forever changed the trajectory of his research career.

Someone close to Friedman, an academic standout, had been admitted to a major university. After a few months at college, she became very ill, and explained her symptoms to Friedman. “I said, ‘You have mono. Go to student health services. Mono is very common in college students. They’ll know what to do'.” The student health service misdiagnosed the patient and sent her back to her dorm room.  Eventually, the young patient needed to be rescued from that dorm room.

In the months that followed, the patient tried but was unable to be diagnosed through traditional channels.  Friedman stepped in and persuaded the clinical faculty of his own medical school to examine and diagnose her.  Unfortunately, those physicians too were perplexed and unable to render a diagnosis.

At Friedman’s suggestions, despite not having a confirmed diagnosis, treatments aimed at alleviating symptoms were tried. Eventually, the patient regained sufficient health to, in an extended timeframe, complete college and become employed.  Full health, however, was never fully restored, and eventually the patient became housebound.

“Having a chronic illness,” Friedman says, “is life-changing not only for the patient, but for the family. My initial objective was to cure her. And that was based upon the belief that this was a disease like any other disease,” caused by an infectious agent, “and therefore cured by the removal of that infectious agent.”

“And that belief was based on what was written in the medical literature. But the medical literature was wrong.”

According to Friedman, Long COVID demonstrates that ME/CFS, Chronic Lyme disease, and other chronic, fatiguing illnesses which occur after a significant infection, exhibit similar symptoms and should be classified as belonging to a category of disease which he and colleagues have named PAPIS (Post Active Phase of Infection Syndromes).  He and his colleagues have established an ongoing collection of research articles in the journal Healthcare to promote the publication of research articles on the subject of PAPIS. “Some 90 years after the U.S. Public Health Service first described ME/CFS as a ‘polio-like’ illness, people are beginning to understand what that means!” 

* * * * * *

“For many doctors, the strange symptomology of long-haul Covid calls to mind another mysterious, poorly understood condition: myalgic encephalomyelitis, more familiarly known as chronic fatigue syndrome,” wrote Moises Velasquez-Manoffin in a January 21 New York Times article titled “What If You Never Get Better From COVID-19?”

Velasquez-Manoff went on to point out that “ME/CFS-like syndromes have been linked with infections for more than a century — including, most recently, those caused by the viruses responsible for the SARS and H1N1 pandemics in 2003 and 2009.”

And according to Fennell, there is growing evidence that COVID-19 already has ignited a public-health crisis that will persist long after vaccinations help us reach “herd immunity” and many of us put our masks away. “We are getting increasing numbers of requests from medical professionals who either have personally suffered COVID with the long-term symptoms themselves, or their family members have,” Fennell says. “We are also getting requests for consultation from physicians who are overwhelmed by the emotional burden of caring for COVID-19 patients. Some of these clinicians are traumatized from the care they are providing, and are suffering long-term after-effects themselves, which is part of the larger, expanding public health issue of COVID-19.”

In addition to SARS and H1N1, Friedman says, there are “post-acute infectious syndromes” associated with many infectious diseases, among them, mononucleosis, Ebola virus disease, and Lyme disease.

But some of the early research into long-haul COVID and its treatment has not taken past research into account. “What they have done,” Friedman says, “is they have ignored the relevant data of other diseases. Why aren’t we looking at these all together?”

Friedman and some other researchers contend that where symptoms of long COVID are similar to those in patients suffering chronic illness in the post-acute phase of any of these diseases, treatments previously developed for those diseases may be effective for long COVID.

“Obviously we want to learn as much as we can about each new infectious disease,” Friedman says, “but in the meantime, treatments have been developed for symptoms which are similar across the spectrum. Why not apply what we already know, and consider how the diseases may be similar?”

“Diseases tend to be viewed as silos,” he continues, “as unique symptoms that have to be treated as no other disease is treated. The treatment is only effective for that one disease and does not apply to any others. That is not true.”

“The body does not care what the infective agent is.”

He offers the analogy that the body has a finite playbook of responses for infection, and it will employ those responses to the best of its ability to overcome the infection.

But, Friedman says, in long-haul COVID — as in ME/CFS — the body’s response is “overblown.”

“The plays in the playbook are not perfect. And some of those plays can do damage. Where medicine comes in, is that sometimes the physician can control the plays in the playbook so that they do not do damage.”

The failure to apply models of care previously developed for ME/CFS, Friedman suggests, is a symptom of a more grave issue: The medical establishment still does not fully recognize chronic illness “as a serious medical condition worthy of treatment. I think that most chronic illnesses are not given as serious a consideration as are acute illnesses.”

With acute illness, he continues, “you go to a physician and describe your symptoms, your physician develops a theory of what is wrong with you. … And once the underlying cause is found, the physician will know how to treat it. But for these chronic illnesses that don’t have a ‘tell,’ it becomes much more difficult to diagnose, and much more difficult to treat. So that’s why these conditions are not treated.”

And the U.S. government, he adds, “was very narrow in its approach to dealing with the pandemic. They put all of their eggs in one basket and focused on developing a vaccine, and avoided development of a treatment.”

“The CDC already has a model of care in place that would work for long-haul COVID, and that model of care is the model they developed for ME/CFS. The question is, ‘Why they would not implement that model of care now?’ ”

“If they would fully implement that model, both the ME/CFS patients and the long-haul COVID patients would be receiving care right now.”

“Going back 30 years,” says Fennell, “I, among others, have developed treatment approaches for long-term chronic illness. They are there. They should be adapted and used.”

Instead, Friedman fears, most people are not aware of or prepared for the “dim picture” that awaits us down the road, with between 3 and 9 million people suffering from long-haul COVID, according to his statistical model.

“That’s a lot of people.”

Potentially making matters worse, 3–9 million long-haulers is a projection based on the number of people who had been diagnosed with COVID as of a few weeks ago. But two current trends do not bode well: (1) the refusal of a significant number of persons in the United States to be vaccinated, and (2) the ongoing failure by the FDA to approve any treatment of COVID in its early stages. If these trends continue, then the number of long-haulers is likely to exceed the estimate.  

“The prognosis in terms of disability, and the number of people requiring social and financial support, is going to be very large in comparison to other diseases,” says Friedman. “And that should be a concern.”



* Effective April 26, 2021, Kenneth Friedman has received an academic appointment as adjunct associate professor, Department of Medicine, School of Osteopathic Medicine, Rowan University, Stratford, N.J.  



Written by Stephen Leon


© Albany Health Management Associates




Tuesday, March 30, 2021

A Life in Hospice

Deborah Lee talks about the joys, challenges, and rewards of her 30-year career in Hospice: A Memoir of Life Among the Dying


The song playing in Deborah Lee’s head wasn’t just a temporary annoyance, like a tune that gets lodged in your brain after you hear it over the supermarket sound system.

It was a sign that she had found her calling.

The story of “Graciela Hernandez” is such an important milestone in Lee’s 30-year career as a hospice worker that she decided to tell it in the first chapter of her 2020 book Hospice: A Memoir of Life Among the Dying.

The chapter, titled “There’s a Lot They Don’t Teach You in Graduate School,” recounts how Lee, then a relative newcomer to social work, had been assigned to the Hernandez family because they were not feeling a positive connection with the nurse who had been visiting from Lee’s hospice team. Graciela, 15, was dying of cancer; as Lee prepared to ring the doorbell of the Hernandez family on a February day in 1991, she worried that she, too, would fail to connect.

For one thing, she was afraid there might be a cultural barrier with Graciela’s parents, who were Mexican-American. And while the parents were losing their only daughter just as Graciela was coming of age, Lee was eight months pregnant, visibly ready to experience the joy of bringing a new child into the world.

Mr. and Mrs. Hernandez were polite but cool; the girl lay comatose on her bed. Lee stayed by Mrs. Hernandez’s side while she administered a feeding tube, and as Lee sensed a slight warming from the woman, she found herself quietly shifting from an intellectual approach to a more intuitive one. Back at the kitchen table, Lee began to notice a song that was running through her head.

“I was relatively new to hospice, and relatively new to social work,” Lee recalled in a recent interview. “I was not accustomed to trusting my gut in my work. I was still pretty concerned with doing things ‘right’ [here Lee, sitting across from me, raises her fingers in quotation marks] — So when I first started hearing that song in my mind, it was more a distraction than anything else. I didn’t initially perceive it as having any clinical relevance.”

But the song would not go away, and Lee couldn’t ignore it any longer.

“I started to feel like I was supposed to say something about this to the family. And that feeling just kept getting stronger … to the point that it almost felt like screaming in my mind: Say it! Say it! So I did.”

“Never in a million years could I have anticipated what that unleashed.”

Lee told Graciela’s parents about the song in her head — “You Are My Sunshine” — and added that she must sound crazy, but felt for some reason that she needed to share it. As Lee waited for a reaction, first Mrs. Hernandez, then Mr. Hernandez, burst into tears. The song, they explained, was their daughter’s favorite as a young girl. Then Lee burst into tears as well.

Suddenly, the family’s experience with the previous nurse made sense; “the Hernandezes,” Lee wrote in Hospice, “felt that she did not truly understand what they were going through. They needed someone to see past their controlled, critical presentation to the agony within. When I ‘heard’ their daughter’s song — despite the disease, despite the passage of many years — they knew I could hear them.”

“As my hospice work continued,” Lee says, “I came to recognize this experience as what I call a ‘God moment.’ Hospice is full of God moments if you listen for them.”

* * *

Deborah Lee was born in Chicago and raised there until she was 14, when she moved with her mother and stepfather to the Milwaukee area. Her parents had divorced when she was 2, and her father also remarried. Her complicated family life as a youth fed her restlessness as a young woman; in her college years, Lee “wandered around a bit” and attended three of them, “but the piece of paper says Northwestern.”

Next, she fulfilled a dream to move to California, where she lived from 1978 to 1983. “And that was a very significant awakening to the real world,” Lee says. “My California fantasy was that that was where all the hippies lived. And I was going to go out there and be a hippie.”

However, she says, “absolutely nothing that happened in California worked out the way I hoped it would. The whole hippie ship had sailed by that time. In retrospect, it was a good experience. Let’s just say I got a lot out of my system. At the end of five years, I slunk back to Chicago with my tail between my legs.”

Lee returned to her hometown “feeling like I needed to get serious about what I was going to do when I grew up.” She worked for two years as a legal secretary for a divorce attorney in downtown Chicago; she liked her boss and enjoyed the job. But the wheels in her head were turning.

“I had two insights during the two years I worked for him,” she says. “The first was that the most enjoyable part of the job for me was listening to his clients pour out their hearts about what they had been through. I encouraged them to get this off their chests with me, because unlike my boss, I wasn’t charging by the hour.”

“The second thing I realized is that I was not going to want to be doing that same job when I was 50.” At that point Lee decided it was time to go to graduate school “and have a career and not just a job.” She applied to Loyola University in Chicago, where she earned a master’s in social work.

The idea of social work had been bubbling under the surface for some time. As a teen, Lee had enjoyed hanging out at a drop-in center staffed by students doing graduate study in social work. Also, “my stepmother was a social worker. And I admired her tremendously. So you put all that together with the fact that I enjoyed listening to my [lawyer] boss’ clients and trying to help and support them.”

There was one more piece to the puzzle, and her therapist helped her figure it out.

“I essentially grew up with four parents,” Lee explains. “They were all good people, but they were not perfect. I was certainly not abused or deprived in any way, but I wasn’t particularly happy.”

After her return from California, she went into therapy for about a year. “Toward the end of that time, I told my therapist that I was planning to go to social work graduate school. He asked me, ‘What is it in yourself that you’re trying to fix?’”

“I came to the realization that I was still trying to sort out the many mixed and conflicting messages I had gotten while growing up. And that was basically it; he gave me the insight that there was something I was trying to figure out by going to graduate school.”

* * *

About a decade into her hospice career, Lee got to thinking that she was having experiences, through her patients, that the average person didn’t have. “And I started writing about them,” she says, “just to process my own thoughts and feelings about them.”

Twenty years later, at the end of her 30-year career in hospice, Lee had about 20 pages’ worth of stories. “When something happened that I felt was worthy of writing down, I wrote it down. But I still was not thinking ‘Oh, I’m going to write a book.’”

After the pandemic hit, and it became apparent that it was going to go on for a while, the now-retired Lee was looking for something constructive to do with her time. And she started thinking seriously about turning those 20 pages of stories into a memoir. But she was unsure which direction to take; some of the stories (like Graciela’s) were interesting case studies, while others were more like educational essays. She could take a pragmatic approach and write an educational book for hospices to buy in quantity and give to families, or she could write more of a memoir.

At that point, Lee enlisted the services of a freelance editor, Elizabeth Judd, for what was called a developmental assessment. “She had done a lot of editing on books related to health care and to spirituality; she was the perfect person to guide me,” Lee says.

“She was a tremendous encouragement to me. She told me that she really enjoyed the excerpts that I sent her, and that it was one of the more gratifying things she had edited recently because she actually felt I was a good writer.”

And Judd nudged her toward memoir: “Write more stories. Write more stories.”

Hospice is a testament to the complex, poignant, rewarding, and often spiritual nature of hospice work. It also is eye-opening for anyone who might wonder why people like Lee do such “depressing” work.

“First of all, it’s not depressing. We, the hospice team, walk in and find some miserably sick person lying in a bed, and there’s lot we can do to make them better. When the family looks at their dying loved one, they see what I call ‘ghosts.’ They see not just the person in front of them at that moment, but all the people that he or she used to be. We, the hospice team, don’t know all those people. … We only know the person who is there now. That gives us a different perspective than what the family has, and a greater degree of objectivity.”

“For me, and probably the majority of hospice workers, there is a strong spiritual component to our work. Hospices themselves are not religious organizations. … But the majority of hospice workers that I have known bring some sort of spiritual perspective with them. They may or may not be religious, but the majority of them are highly spiritual. For me personally, I have a very strong sense that hospice work was my ministry.”

While some theories of human development end with physiological maturity, the psychologist Erik Erikson postulated eight stages of development through life, the last being “ego integrity vs. despair,” in which people attempt to reconcile their life successes and failures. Lee says she used the Eriksonian eighth stage a lot in her work with hospice patients.

“All of us want to think that our lives have some kind of meaning,” Lee says. “And as the hospice patient tells me about himself, I can help them see what some of that meaning might be and I can validate that for them.”

“Sometimes they have regrets. I try to help each person sort out those things that they felt good about, and help them come to a place where they can feel that their life overall had a positive effect. Some people, sadly, are truly in despair. There were those few that truly felt they had wasted their lives and messed up their opportunities. And that’s not something you can fix on somebody’s deathbed. What I could give them was the opportunity to be heard and accepted by me, without judgment.”

And then there are the crazy spiritual moments that sometimes accompany the last hours of a person’s life—or maybe even the hours just afterward. These are Lee’s “God moments”: improbable situations that invite us to consider mystical explanations over rational ones. A group of robins gathering in a tree outside a hospital window in the middle of a snowstorm. A red balloon that hovers around an apartment entryway on a windy day, never blowing away, as if waiting for someone inside. An experienced Air Force pilot who dies a few hours before a living pilot engineers a miracle Hudson River landing of his distressed plane, carrying all passengers to safety.

While the paranormal explanations for these stories (especially the one involving “Sully” Sullenberger) can seem farfetched, still, one has to wonder: On that winter day back in 1991, by what passageway did “You Are My Sunshine” enter Deborah Lee’s brain?

The day she “met” Graciela, Lee began to better understand hospice work as her calling, and hospice patients and their families as people whose lives and connections with loved ones can be improved under the empathetic care of hospice workers.

“I learned a tremendous amount, over the course of 30 years, about how different people face their own mortality,” Lee concludes. “And that has been helpful to me in thinking about my own eventual death. I hope that when my own time comes that I can bear up as gracefully as some of the people that I met.”

Hospice: A Memoir of Life Among the Dying, by Deborah Lee, was published on October 5, 2020 by BookLocker of Saint Petersburg, Florida.

See Mensa Bulletin review of Hospice



Written by Stephen Leon

 © Albany Health Management Associates




Wednesday, September 30, 2020

What I Value


“Caritas, Veritas, Fortitudo . . . ”

During my childhood, I experienced medical conditions that heightened my awareness of how medicine was practiced and how society regards people who are ill.

Patricia Fennell

As a young hospice worker, I saw the kind of assessment and care that I believed all people, not just the dying, deserved and required. At the same time, a paradigm shift was happening, from acute to chronic illness and thus an opportunity to reconsider how we care for the chronically afflicted and their loved ones. This paradigm shift continues worldwide.

Decades ago, I saw the epigraph, “Caritas, Veritas, Fortitudo,” carved into a building scheduled for demolition. These words captured for me what is required of those with chronic illness and those who work with them … these words guide us in our work:

  • Caritas means not only “love,” but also compassion.
  • Veritas refers not only to “truth,” but also to authenticity
  • Fortitudo is not simply “strength, but also courage

It is my hope that our work gives professionals and caregivers the help they need to assist patients in achieving “Caritas, Veritas, Fortitudo” and, with them, better, more meaningful lives.


Written by Patricia A. Fennell


© Albany Health Management Associates



Wednesday, September 16, 2020

COVID and Scleroderma: How Are You Really Doing?

Experiences with Scleroderma During the COVID-19 Pandemic

 

A team of researchers* are conducting a study examining how the COVID–19 pandemic may be affecting the health and wellness of people with scleroderma.


COVID-19
Participants with scleroderma are answering questions that involve healthcare during the pandemic – how people are coping with the risk of COVID-19, how people feel about the uncertainty the pandemic can bring to their lives, what health behaviors people are engaging in (both in general and COVID related, and how people are feeling physically and mentally. Volunteers are providing valuable knowledge to health care professionals involved in the care of people with scleroderma.

The more we understand about the experience of people with scleroderma during the COVID-19 pandemic, the better able we are to respond in ways that help people stay well.

 

Direct questions to Patricia Fennell at communications@albanyhealthmanagement.com

 

* Lee Shapiro, MD (Professor of Medicine at Albany Medical College), Patricia Fennell, MSW, LCSW-R (CEO of Albany Health Management Associates), and Nancy Dorr, PhD (Professor of Psychology at the College of Saint Rose)


COVID-19 ("Coronavirus")
Information and recommendations from the Scleroderma Foundation
Medical & Scientific Advisory Board Leadership Committee

(reviewed July 1, 2020)