Madeline Cohodes /
Bellevue Hospital Program for Survivors of Torture /
New York, USA /
by Madeline
Madeline Cohodes /
Bellevue Hospital Program for Survivors of Torture /
New York, USA /
by Madeline
Madeline Cohodes /
Bellevue Hospital Program for Survivors of Torture /
New York, USA /
As the summer progresses, I have certainly developed a deeper understanding and appreciation for PSOT. My daily schedule normally consists of waking up at six in the morning to fit in three hours of studying for the MCAT before heading over to Bellevue. The dichotomy between the mundane routine of studying for the test that helps determine medical school acceptance and then the constantly changing environment of the hospital couldn’t be more apparent.
Each day brings new clients, different operational projects, and a revolving door of emotions. On one particularly stressful day, I was ruminating on the pressure of MCAT and trying to focus my attention on finishing a grant with a quickly approaching deadline. It was one of the few times that I’ve brushed against what emotional burnout in the human rights field feels like. Even as an intern who isn’t directly involved in therapeutic contact with patients, reading trauma narratives and compartmentalizing life stories to data points can take its toll.
by Madeline
Madeline Cohodes /
Bellevue Hospital Program for Survivors of Torture /
New York, USA /
It has officially been one year since I began interning at Bellevue PSOT. Throughout this time, I have worked on a variety of operations projects, many of which have been focused on assisting our client base during the COVID-19 pandemic. Coincidentally, as my fellowship began this summer, PSOT was also placed in a new position as our executive director, Dr. Hawthorne Smith, was elected president of the National Consortium of Torture Treatment Providers. This allowed us to work on national-level research projects along with policy and advocacy efforts.
So far, the topic that has interested me the most is the confluence of research and policy/advocacy. In order to effectively promote policy to legislators and community leaders, data on the subject is typically required. Therefore, it takes plenty of conversations to decide what needs to researched and how that can be repurposed as a policy tool. For instance, a current priority is expanding the U.S. government’s definition of torture to include survivors of sexual and gender-based violence, those who suffer torture related to LGBTQI identities, and those who experienced gang-related torture.
Compiling data on the number of of our clients who fit these categories is the first step in the arduous process of convincing the U.S. government to change its policy. However, with this fairly simple structure of obtaining data and using it for advocacy, the individual needs of survivors can be overlooked. Often mentioned is how to transfer information into the hands of survivors so it may be used not only for national platforms but also in local communities.
While change on the federal level can sound more important and impactful when working in large human rights organizations, it seems prudent to think about how the microcosm of each NCTTP clinic can also benefit from this research. For example, having a clear demographic summary of a clinic population could assist directors in reaching out to marginalized groups in their local community that may not be accessing services. Or, it could provide them with the incentive to strengthen ties with community groups of their most-served populations in order to reach anyone that may be hesitant about joining or just unaware of the program. Either way, having a vast array of readily available information can have a variety of benefits.
Research and data collection aren’t typically buzzwords in the human rights field. Yet, my year so far at PSOT has shown me that when used correctly, there are infinite ways to improve not only the program’s operations but also assist individual clients. Whether that’s working on a macro or a micro scale, the intersection of research and policy/advocacy has become a surprisingly critical facet of my daily work at the Program. And as for national-level outreach, we can only keep trying with the confidence that our voices (and data) will be heard.
by Madeline
Madeline Cohodes /
Bellevue Hospital Program for Survivors of Torture /
New York, USA
My name is Madeline Cohodes and I have just finished my third year as a dual-degree BA/MPH student. My undergraduate Gallatin concentration focuses on extrapolating issues found in healthcare to broader societal contexts, and my master’s concentration is in public health policy.
This summer, I will continue my current internship at the Bellevue Program for Survivors of Torture (PSOT), a nonprofit that supports people affected by torture, a human rights violation. Torture can inflict not only physical but psychological and emotional pain, and PSOT works with immigrant and refugee communities to provide medical, social, legal, and mental health services. The program’s medical/mental health components include a multifaceted combination of primary care and referrals to trauma-informed therapists, psychiatrists, and group therapy.
All of these services work to restore and improve our clients’ health. More broadly, the services address issues beyond basic medical assistance, such as how to achieve a stable immigration status, adequate housing, and an overarching sense of safety. Such things are necessary for most people to feel healthy mentally, or at least feel secure enough to focus on their mental health. Furthermore, fiscal stability is necessary in the context of the American healthcare system to gain access to non-emergency care.
PSOT assists in stabilizing these critical needs and providing further assistance with clients’ needs. The work my colleagues and I do at PSOT helps to ensure that the human right to health encompasses all aspects of wellbeing.
As the operations and development intern at PSOT, I will continue this summer to assist clients with scheduling appointments in all of these areas. I will also refer clients to grants that compensate people impacted by COVID-19 and will monitor new clients’ cases so that I can connect them to necessary resources. Additionally, I will assist with grant writing and research projects.