This Fellowship takes on a key challenge: the reality that professionals are not well prepared to deal with or talk about death, dying, and grieving families, especially during an era of COVID-19. The Fellowship allows participants to learn, confront, and discuss the legal, medical, social, cultural, familial, and spiritual aspects of death and dying within a multi-disciplinary group in a low-pressure environment. The sessions include opportunities to practice conversation skills, facilitated conversations, and virtual site visits.

The home for the 2019 Salk Health Activist Fellowship.

We are going to use this platform to be able to communicate effectively, collaborate, and build each other up for this fellowship. Activism starts here. Let us learn and use each other's strengths to the best of our ability. 

Together, we can change the world. 

Achieve the Triple Aim of healthcare quality improvement by providing patients with the information  on their care plans but encouraging them to ask “why?” In regards to physician orders. Additionally, encourage providers to be smarter with the care plans created for their patients by thinking more critically about what they are ordering.  

I dream of a world where assault by providers in birth doesn't occur, and every procedure is done with genuinely informed consent. Until that time people are suffering at the hands of providers who are physically assaulting them, not asking for consent, mocking, and terrorizing laboring people. When people find the courage to speak out, they are silenced and told to be grateful for having birthed a child. The trauma and PTSD they suffer carries into their lives long past that one day. We must acknowledge that assault during birth is sexual assault and that no means no when it is said to anyone anywhere even in a hospital, even if you are in labor. Providers must be held accountable, but they won't be until as a country we can say medical sexual assault and be taken seriously

In an attempt to de-stigmatize drug use and promote access to care, an intiative to educate on the benefits of harm reduction methods, with an emphasis on access to syringe exchange programs, will be implemented. Using testimonials, infographics, and other promotional materials, myths and misconceptions of needle exchanges will be debunked. In addition, participants will be encourage to write their representatives to 1. decriminalize syringes, and 2. promote the legalization of needle exchanges statewide for Pennsylvania.

Patients who lack the basic access to Food Transportation and Housing are at greatest risk for being isolated from the healthcare system. Efforts underway to improve and remove that barrier are needed to ensure long term patient improvement.

Connect 4 Care calls on heathcare leaders to adopt one system-wide electronic health record (EHR) platform within thier healthcare system in order to alleviate burnout among healthcare professionals and improve patient outcomes.  

The home for the 2018 Salk Health Activist Fellowship.

We are going to use this platform to be able to communicate effectively, collaborate, and build each other up for this fellowship. Activism starts here. Let us learn and use each other's strengths to the best of our ability. 

Together, we can change the world. 

"On Drugs" is a podcast where people will talk about everything related to drugs. Their experience with drugs, addiction, treatment, benefits, harms, research, drug policy, and anything else we can think of it in the future.

The goal of this podcast is to de-stigmatize this topic, to expose those who know nothing about the topic, and to put a human face and human voice to the stories we all hear about drugs.

Before we can tackle the question of what our relationship with drugs should be, we need to bring it out of the shadows, to see it for what it is, and to talk about it, openly and honestly.

There is only one problem that has affected every person who has ever lived on Earth, and it is the last one any of us ever face.

Americans have a unique problem with death: it's not simply that we don't know how to talk about it, it's that we largely refuse to talk about it at all or engage with the concepts and realities of our only truly unifying experience.  Healthcare providers feel they are failing if they even consider the topic of end of life conversations.  Popular culture debases our understanding of death by portraying it in every conceivable way other than the one in which we actually experience it. Only through preparation, understanding, and normalization can we improve end of life and the grieving and bereavement process of those we leave behind.

A popular modern author wrote: If you have ever lost a loved one, then you know exactly how it feels.  And if you have not, then you cannot possibly imagine it.

If loss is so universal, why do we not make it a priority to better prepare ourselves to face it?

That is the goal of this Action Group: to face the problem of illiteracy on the topics of death, grief, and bereavement with supportive materials that can be distributed or shared by anybody, in any forum, at any stage of life or in any setting of healthcare.

The vision of this group is to realize the implementation of medical marijuana as a viable therapeutic option. Although legislation has enacted its use in Pennsylvania for a select number of disease states, a number of barriers to implementation exist before comprehensive medical marijuana therapy can become a reality.

This action group hopes to learn from local leaders in medical marijuana policy reform, anticipate these barriers to impelementation, and combine resources to address the root causes that might affect the greatest downstream change. 

Last, this action group hopes to investigate research showing the influence of comprehensive marijuana policy on opioid abuse and overdose in pilot states across the country. Synthesis and analysis of this research may illuminate the role of medical marijuana as an alternative to opiate therapy in the management of long term pain. We hope to investigate this with both precision and urgency and present our findings to experts in pain management.

* To move from "diversity education" to inclusivity training.

* To empower entry-level clinicians in training, by giving them the tools they need to practice more inclusively across the lifespan of their careers: from classroom, to clinic, to educator.

* To empower educators to deliver high-quality inclusivity education and training, despite deficits in knowlede, background or self-efficacy.

We are going to use this platform to be able to communicate effectively, collaborate, and build each other up for this fellowship. Activism satrts here, let us learn and use each other's strengths to the best of our ability. 

We are here to help, and are open to any and all questions that you may possess. If we don't know the answer, we will do our best to find someone who does. Together, we can change the world. 

When patients are selecting a surgeon to perform a procedure it would be helpful for the patient to know the surgeon's personal history of complications when performing similar surgeries so that the patient could select the "best" surgeon.

Care coordination mistakes are costly... and not just in terms of financial expenses. Some of the most common care coordination mistakes are also major culprits for death and exacerbated patient health problems. U.S. News & World Reportindicates, “Medical errors are [the] third leading cause of death in the U.S. 10 percent of U.S. deaths are due to preventable medical mistakes" such as: Documentation errors  Communication Disconnects Lack of Coordination Neglecting Follow-ups Delays