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September 2024

The Power of Stories
“The battles we face regarding prescription drug prices is something I know of all too well. I am a mother, a doctor, and a patient diagnosed with type 1 diabetes. Within a year of giving birth to each of my two sons, I received the feared and painful news that both my sons shared my diagnosis. My oldest is now 6, my youngest 3. They have a long lifetime ahead of them that should not be burdened by struggling to afford the very medications needed to save our lives.
 
My diagnosis has become a driving force in my life. It is what drove me to the medical profession, and it’s impacted what jobs I’ve taken due to the insurance benefits offered by employers as not all coverage is equal especially when it comes to diabetes medication. Many of my patients face the same fate as my sons and I. There is not a week that goes by where I don’t find myself and my patients trapped in our frustrations and dismay over the rising, unaffordable costs of insulin. A drug which is estimated to only cost $2 to $4 to produce a vial of, yet we are charged hundreds for— often times even with insurance.
Insulin rationing led to the life of one of my long-time patients being lost. This loss, and the devastation felt around not knowing what was happening, absolutely breaks my heart. Drug prices in the U.S. are inaccessible for many Americans and more and more patients lose access to these life-saving medications everyday.
 
While I cannot bring back my patient, I can fight for his memory, I can fight for my patients who are still here, I can fight for our nations citizens who deserve equitable access to their healthcare and their medications, and I can fight for my sons so that they never have to face the struggles we Americans are facing today. No medications should be rationed, no medications should be unaffordable— especially those that are designed to save and improve the lives of millions.”
 
— Lynne B., Indiana.
 
None of us like being told what to do. However, when we use a story to make a point, it allows individuals to decide for themselves. Stories of challenges, change and progress can motivate people to take action. I know that I’m “speaking to the choir”, so let me offer you this: if there are particular patient narratives that get you fired up due to the injustice of it all, please consider sharing your story on Doctors for America’s Advocacy Story Portal. You can share your stories in written form or upload a video. 
 
Your stories matter, they make a huge difference in changing hearts and minds. Plus, sharing your patient accounts is a great way to advocate for meaningful policy reform at the local, state and federal level. Doing nothing is not an option, so please do something and share your story!
 
In solidarity,
 
Angie Bakke
Executive Director

Our 2025 Copello Fellowship Cohort
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DFA Welcomes a New Team Member
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Meet Sophia Phillips, she is the new program manager for the FDA Task Force where she will work to educate and empower advocates to engage in FDA issues. Prior to joining Doctors for America, Sophia worked at the National Center for Health Research where she served as a resource to Members of Congress and Congressional staff on health policy issues pertaining to the FDA. She was also responsible for tracking and analyzing active legislation and regulatory changes within HHS. 
 
Sophia previously interned at Public Citizen in their Access to Medicines Program, where she was actively engaged in policy surrounding drug pricing and COVID-19 vaccine recipe sharing. She was also a research assistant with PharmedOut, a Georgetown University Medical Center project that works to educate healthcare professionals and the public on pharmaceutical marketing practices and their impact on public health.
 
Sophia received her M.S. in Health and the Public Interest from Georgetown University, where she was trained in health advocacy. She also holds a B.A. in Psychology from the State University of New York at Geneseo. In her free time, Sophia is an avid concert and movie goer!

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