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Support Miles for Migraine

ACT Now:
The Advocacy Connection Team

We are thrilled to offer you participation in this initiative for fellows and people affected by migraine and  other headache diseases. This series is designed to  educate and train Migraine & Headache Fellows along with two-to- three patient and/ or caregivers, to incorporate and encourage Advocacy in every Migraine & Headache  Disorder Treatment Plan.

What’s Involved:

We require you and your fellow partner to attend a 1.5 hour/month Zoom lecture. Sessions will be held alternating Tuesday and Thursday evenings at 8pm ET. Participation in a private Facebook group is encouraged.

Program Details

Learning Objectives: 

  • Learners will understand what stigma is and how it operates in the headache  community
  • Learners will be exposed to the different models of advocacy and how they have  operated in other disease states
  • Learners will be aware of the current state of headache advocacy in the areas of  policy and regulation
  • Learners will be aware of the current state of headache advocacy relating to  work and educational accommodations
  • Learners will discuss strategies to change the narrative in a way that is beneficial  to patients and headache medicine
  • Learners will discuss how to bring advocacy into the patient’s care plan

Learning Outcomes:

  • Increase numbers of provider advocates
  • Increase numbers of patient advocates
  • Advocates will be trained in speaking, writing, and political skills so that they can  effectively community their message
  • Advocates will be empowered with the knowledge, community, and resources to  take on a role in an advocacy movement
  • Advocates will be educated in the current state of advocacy for headache  medicine and patients
  • Advocates will develop creative strategies to identify and address gaps in the  current advocacy movement

Content Exposure:

  • Stigma
  • Policy and Regulation
  • Lessons learned from advocacy in other disease states
  • Advocacy with payers
  •  International advocacy, and interacting with businesses
  • Advocacy as part of the treatment plan
  • Advocacy in schools and education
  • Support groups
  • Landscape of the patient movement
  • How to tell your story
  • How to make an advocacy plan
  • Using social media in advocacy

Schedule 

Day Date Time ModalityFacilitator Facilitator
Tues 1/12 8:00 PM EST Stigma Bill Young and Joanna Kempner
Thurs 2/11 8:00 PM EST Lessons Learned from Advocacy in Other Disease States Rachel Kahn Best
Tues 3/9 8:00 PM EST Advocacy as Part of the Treatment Plan Karissa Arca and Amaal Starling
Thurs 4/8 8:00 PM EST Advocacy with Payers Lindsay Videnieks
Tues 5/11 8:00 PM EST Advocacy for Underserved Populations Sheila Thorne
Thurs 6/10 8:00 PM EST How to Make an Advocacy Plan Dave Watson

Past Session Resources

After a session is complete, resources such as video, articles, PDFs or links will be collected here for disribution.

Joanna's Book: Not Tonight: Migraine and the Politics of Gender and Health

Kempner/ Young Publication: The Stigma of Migraine

Parikh/Young Publication: Migraine Stigma in Society

Presenters

Karissa Arca

Dr. Karissa Arca, MD

Dr. Arca is currently the Headache Fellow at Mayo Clinic in Arizona. She received her medical degree from Loma Linda University and went on to complete a Transitional Year residency and Neurology residency at Mayo Clinic in Arizona. During her final year of residency she was awarded the Manfred D. Muenter Award for Excellence in Clinical Neurology.

Dr. Arca is an active member of the American Academy of Neurology and the American Headache Society. She has received multiple scholarships to attend AHS meetings as well as multiple poster presentations and an oral presentation. Most recently, she was awarded the Frontiers in Headache Research scholarship award by the AHS which will be presented in the upcoming Scottsdale meeting.

Dr. Arca has multiple peer-reviewed publications and abstracts in the field of Headache Medicine. She has a special interest in the cross-section of  autonomic disorders and headache as well as CSF dynamics. She currently serves as a board member for Miles for Migraine.

 

Rachel Best

Rachel Kahn Best

Rachel Best is an Assistant Professor of Sociology at the University of Michigan. Her book, Common Enemies: Disease Campaigns in America, argues that when Americans come together to fight social problems, they focus their largest efforts on diseases. Fighting one disease at a time has unintended consequences for health policy. Her current research uses computational methods to explore the relationship between disease stigma, advocacy, and policy outcomes.

Joanna Kempner

Dr. Joanna Kempner, PhD

Joanna Kempner is an Associate Professor of Sociology at Rutgers University where she studies science, medicine, and inequality. Her work on health and justice, stigma in medicine, and the political suppression of science attempts to give a voice to those we rarely hear from. Her writing addresses the lack of effective treatments for pain, gender, race and stigma, and the extraordinary lengths that people will go to in order to find relief. She is the author of the award-winning book, Not Tonight: Migraine and the Politics of Gender and Health (Chicago), and is currently writing about cluster headache patient-led efforts to bring psychedelics back to medicine. Her research can also be read in a wide-range of academic and popular publications, including Science, PLoS Medicine, Social Science & Medicine, and Migraine.com.

Amaal Starling

Dr. Amaal J. Starling, M.D.

Dr. Starling is an Assistant Professor of Neurology in the Mayo Clinic College of Medicine. She joined Mayo in 2012 and is  currently a consultant within the Department of Neurology.

Dr. Starling received her M.D. degree from Drexel University College of Medicine in Philadelphia. She completed a Transitional Year residency, a Neurology Residency, and a Headache Fellowship at the Mayo Clinic College of Medicine in Scottsdale, Arizona.

She is an active member of the American Academy of Neurology, the American Headache Society (AHS), the American Medical Association and the American Pain Society. She is the Co-Chair of the American Headache and Migraine Association, Chair of the New Investigator and Trainee special interest section of the AHS, and serves as a member of the AHS Annual Meeting Scientific Committee. She is a perennial speaker at the AHS Annual Meeting in Scottsdale, Arizona. Dr. Starling has been the recipient of numerous awards including the AHS Above and Beyond Award for Service, Manfred D. Muenter Award for Excellence in Clinical Neurology, the American Academy of Neurology Annual Meeting Residency Scholarship, the 2012 Spirit of Mayo Clinic Award, and the Mayo Brothers Distinguished Fellowship Award. Dr. Starling has several peer-reviewed publications and abstracts related to her fields of interest which include migraine, concussion, posttraumatic headache, trigeminal autonomic cephalalgias, secondary headaches, telemedicine and teleconcussion, neurology resident education, and professionalism and clinical ethics.

Sheila Thorne

Sheila Thorne

A native New Yorker and former senior executive in five preeminent health marketing and communications companies, Sheila Thorne has spent more than two decades designing marketing and media campaigns for Fortune 500 companies throughout North America, Latin America and Western Europe with a focus on people of color. A former high school teacher of foreign languages, she teaches and lectures on cultural competency and health disparities at four U.S. universities. She has given over 250 keynote presentations and conducted workshops on cultural competency, anti-bias and diversity in healthcare delivery.  She is published in numerous marketing trade publications and in a variety of consumer health publications. Sheila has received numerous awards for her innovative marketing strategies to reach people of color and her unique ability to build coalitions and galvanize communities of color around health and social justice issues.

Lindsay Lawrence Videnieks

Lindsay Lawrence Videnieks

Lindsay Videnieks is Executive Director of the Headache and Migraine Policy Forum (HMPF), a diverse stakeholder coalition which brings together policy-minded partners that care about patient access. HMPF helped convene the migraine community to prepare comprehensive input during recent ICER reviews of new therapies to treat migraine disease and headache disorders and brings a campaign approach to state level patient access issues.

Ms. Videnieks has more than a decade of experience advising non-profit institutions on strategies to support public policy goals and to secure funding through the federal appropriations process. She previously worked in the office of Congressman John E. Baldacci (D-ME) as well as on his re-election to the U.S. House of Representatives. She provides counsel to voter protection programs nationwide and managed the voter protection Boiler Room operation for the DNC in 2016. Lindsay graduated from the University of Maine at Orono with Bachelor of Arts degrees in Political Science and English and received her law degree from Catholic University. She is admitted to practice law in Maryland where she also lives with her husband and three children.

 

Dr. David Watson

Dr. David Watson, MD

Dr. David Watson is Chair of the WVU Department of Neurology and Director of the WVU Headache Center. His clinical work focuses on patients with headache disorders, and in access to clinical care for under-served populations. He has been active in clinical research focused on new treatment options for headache patients. In addition, Dr. Watson is involved with resident and student education at all levels.

He is very active in patient and professional advocacy, having founded Runnin' for Research, Inc., a charity which raises funds for headache and migraine research, and attending numerous lobbying days in Washington D.C.

He currently is a member of the AMA Opioid Task Force, has served as the Chair of the AAN Grassroots Working Group, currently chairs the American Academy of Neurology Advocacy Engagement Subcommittee and is a member of the Advocacy Committee of the American Academy of Neurology.

He was awarded the Palatucci Advocate of the Year award in 2017 by the American Academy of the Neurology, and the American Headache Society Above and Beyond Award in 2018.

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Dr. William Young, MD, President

Dr. Young is a neurologist at the Jefferson Headache Center. He received his medical degree from Penn State College of Medicine and has been in practice for 30 years. The Jefferson Headache Center is one of a very few academic headache centers in the country. The Center, founded in 1982, specializes in the treatment of patients with all types of headache pain. Dr. Young is the President of the Alliance for Headache Disorders Advocacy. Click for Detailed information pertaining to Dr. Young’s extensive research profile. Click for detailed information pertaining to Dr. Young’s extensive research profile, including research pertaining to migraine and stigma.

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