leadership
Medical Liaison
Dr. Stephen Kinsman, a Pediatric Neurologist, is the Dyspraxia Foundation USA’s first Medical Liaison. He has extensive experience helping children with Dyspraxia and has a newly diagnosed grandson. He will be engaged in our mission to raise awareness, especially in the medical community.
Stephen L. Kinsman, M.D.
Medical Liaison
Bachelor of Arts at Columbia College and MD at SUNY at Buffalo in Buffalo New York.
Practiced Pediatric Neurology in many settings, including running a few divisions, participating in many research projects, and National Leadership and Advocacy with The Spina Bifida Association of America (SBAA). Now a Physician Case Reviewer for Magellan Healthcare. Has been interested in Developmental Coordination Disorder (DCD) and Dyspraxia for over 20 years.
Active as a husband, father and step-father, grandfather, and “down the block” son-in-law, to his wife’s aging parents (one of whom has a neurologic illness and disability).
Grandson was diagnosed with DCD and Dyspraxia and his daughter’s research for knowledge, resources and support led their family to Dyspraxia USA.
leadership
Medical Liaison
Dr. Stephen Kinsman, a Pediatric Neurologist, is the Dyspraxia Foundation USA’s first Medical Liaison. He has extensive experience helping children with Dyspraxia and has a newly diagnosed grandson. He will be engaged in our mission to raise awareness, especially in the medical community.
Stephen L. Kinsman, M.D.
Medical Liaison
Bachelor of Arts at Columbia College and MD at SUNY at Buffalo in Buffalo New York
Practiced Pediatric Neurology in many settings, including running a few divisions, participating in many research projects, and National Leadership and Advocacy with The Spina Bifida Association of America (SBAA). Now a Physician Case Reviewer for Magellan Healthcare. Has been interested in Developmental Coordination Disorder (DCD) and Dyspraxia for over 20 years.
Active as a husband, father and step-father, grandfather, and “down the block” son-in-law, to his wife’s aging parents (one of whom has a neurologic illness and disability).
Grandson was diagnosed with DCD and Dyspraxia and his daughter’s research for knowledge, resources and support led their family to Dyspraxia USA.
Board of Directors
Each member of the Board of Directors shares the common goal of bringing Dyspraxia Awareness to the United States and beyond. They have all been impacted by Dyspraxia and hope to offer support and services to others.
Warren Fried
Executive Director, President, Founder, Chief Advocate
University College Chichester, West Sussex, England.
Warren spends countless hours helping to bridge the realities of DCD and Dyspraxia with the appropriate therapeutic needs and supports.
Warren has spent the last 20 years helping families, adults, medical, governmental, and the media grasp the complexities of 1 in 10 individuals.
In 2026 Warren sees a greater understanding, support and acceptance for not just children but adults who are entering the workforce with a poorly recognized disorder.
15 years married with 10 year old twins.
Because 1 in 10 matters.
Allison Berger
Secretary & Co-Chair
James Madison University, BA, Georgia Institute of Technology, MBA.
Marketing Strategy Consultant serving clients from start – ups and nonprofits to Fortune 100 brands.
I have two daughters, on e diagnosed early on with dyspraxia. I have learned an incredible amount about dyspraxia and brain development in general and find it all fascinating. I am grateful for this opportunity with Dyspraxia Foundation USA to combine my personal and professional passions.
I have found that there is less knowledge and understanding of dyspraxia in the US than other western countries. It is important to increase awareness so that we can better diagnose, remediate and accommodate this growing population. I was fortunate to be able to dedicate a significant amount of time and resources early on to support my child and want to help other caregivers navigate their paths.
Robin Troutman
Treasurer & Co-Chair
Master’s in Nonprofit Management from the University of Central Florida, and a Bachelor of Arts in Political Science from Binghamton University. She is also a Certified Meeting Planner, a testament to her expertise in event planning and logistics.
Robin Troutman is a strategic leader with a passion for driving organizational growth, fostering meaningful partnerships, and creating impactful programs that serve communities at large. With over two decades of experience across various sectors, Robin Troutman’s career is marked by a deep commitment to nonprofit leadership, advocacy, and the development of inclusive, impactful programs. Her strategic vision, operational expertise, and ability to build strong relationships have made her a trusted leader in every organization she has served.
Robin’s commitment to professional growth and community service is evident in her active participation in several organizations. She serves on the Boards of Trustees/Directors at Brain Injury Services and Dyspraxia Foundation, USA and holds leadership roles in the MPI Potomac Chapter, where she has been recognized for her contributions to government and advocacy efforts. Robin is also a founding member of the Profound Disability Network, furthering her dedication to advocating for individuals with disabilities.
Robin lives in Alexandria, Virginia with her husband, 2 boys, and 2 dogs.
As she continues to contribute to the broader disability and human rights community, Robin remains dedicated to creating positive change and empowering others to achieve their fullest potential.
Mitchell I. Fried
Board Member
University of Florida with a B.A. Psychology and J.D.
Admitted to practice law in Florida and New York.
Married for 47 years with two boys.
To help those with the condition understand why they may have limitations which are no fault of their own, and that the limitations may be overcome.
Alex Molden
Board Member
College graduate (Bachelor of Science) Univ. of Oregon
Author (The Ultimate Playbook for High Achievement), International Speaker, Personal Development Coach, Consultant, and Podcast Host (The Shark Effect).
Former NFL Defensive back (’96–’04). Married. Proud father of 8.
Our son was misdiagnosed with so many different syndromes…we couldn’t get a straight answer. It was very unsettling. When we found out that his diagnosis had a name it calmed our nerves and helped us navigate the struggles that were ahead of us. It’s not that scary…but being in the unknown is.
Brianne Burger
Board Member
Bachelor’s degree in Communication Studies from California State University, Northridge, a master’s degree in Administration and Supervision from Gallaudet University, and a master’s certificate in Media Management from Emerson College.
Brianne Burger served as the Director/Liaison for the Special Institutions inside the US Department of Education (ED), Office of Special Education and Rehabilitation Services (OSERS) where she supported four institutions: the American Printing House for the Blind, Gallaudet University, Helen Keller National Center for the Deaf-Blind, and the National Technical Institute for the Deaf. She represented ED on the Federal Communications Commission’s (FCC) Disability Advisory Committee for three terms. Brianne also served a detail to the U.S. Department of Transportation (DOT) Office of the Secretary of Transportation in 2022 where she supported the development of the Disability Policy Priorities and helped launch the campaign, #AccessibleAirTravel, to raise awareness about the right of air travelers with disabilities to safe, dignified, and accessible air travel. Prior to ED/OSERS, Brianne served as the National Disability Emphasis Program Manager (DEPM), Selective Placement Program Manager (SPPC), and the Reasonable Accommodations Manager (RAM) for the Natural Resources Conservation Service (NRCS) at the US Department of Agriculture (USDA). Brianne was also co-founder and 2- term President of an employee resource group. Brianne’s first federal position was with the Administration for Intellectual and Developmental Disabilities (AIDD) at the US Department of Health and Human Services (HHS), where she supported the administration of the National Network of University Centers for Excellence in Developmental Disabilities Education, Research, and Service (UCEDD); the National Training Initiative on the Consortium to Enhance Postsecondary Education for Individuals with Developmental Disabilities; and the Protection & Advocacy services for people with disabilities. Before joining federal service, Brianne managed several federal grants to create new accommodations, education methods, and trainings for people with a variety of disabilities through the National Institute on Disability and Rehabilitation Research (NIDRR), National Science Foundation (NSF), and the Department of Education. Brianne also worked with state vocational rehabilitation agencies in Massachusetts, DC, Maryland, and Virginia.
Brianne has more than 25 years of experience in vocational services on employment and education for people with disabilities. Her in-depth knowledge of public policy with disabilities led to her appointment as the Americans with Disabilities Act Access Coordinator for the 2004 Democratic National Convention, the 2010 VSA International Arts and Disability Festival, and as Vice Chair of the WMATA Accessibility Advisory Council.
Brianne advocated and persisted for the successful draft and passage of the Bill to Establish the DC Office for the Deaf, Deafblind, and Hard of Hearing; furthering ensuring the DC Office was funded in the DC Government’s Budget. Brianne has served as the Vice Chair of the WMATA Accessibility Advisory Council and is a member of the New Leaders Council. Most recently, Brianne supported the passage of the Open Captioned Movie Showings Bill, making Washington DC the third state and second city in the USA to mandate open captions in movies shown in movie theaters.
Coming Soon
Dr. Yasser Salem
Medical Advisor & Board Member
Dr. Salem earned his Doctor of Philosophy (PhD) from the University of Central Arkansas, Conway, Arkansas, in 2004. He completed his Master (MS) degree from Cairo University in 1997. He earned his Bachelor of Science (BS) degree in physical therapy from Cairo University in 1992. Dr Salem completed a Fellowship in Higher Education and Leadership, American Board of Physical Therapy Residency and Fellowship Education (ABPTRFE) – American Physical Therapy Association (APTA) in 2018.
Dr. Salem has a distinguished record of leadership in research, teaching, and service, which will enhance our mission to prepare the next generation of physical therapy professionals.
As a scholar and prolific researcher, Dr. Salem, has authored over 60 peer-reviewed publications, contributed to scientific books and book chapters, and delivered over 400 peer-reviewed presentations at conferences worldwide. His contributions as first author on many of these works reflect his thought leadership and commitment to advancing physical therapy practice and education. His research has garnered multiple grants and accolades, including the Lucy Blair Service Award from APTA in 2022 and the Outstanding Physical Therapy Researcher Award from the Texas Physical Therapy Association in 2016.
Dr. Salem remains engaged in professional service and leadership, having held influential roles within the American Physical Therapy Association Academies and Chapters, (APTA), Commission on Accreditation in Physical Therapy Education (CAPTE), American Board of Physical Therapy Residency and Fellowship Education (ABPTRFE), and World Physiotherapy. He also lends his expertise to the scholarly community as a co-editor, associate editor, and editorial board member for several prominent journals, while regularly reviewing national and international scientific publications and conferences.
Coming Soon
Dyspraxia is one of the developmental disorders that is frequently underrecognized or misunderstood, resulting in delayed intervention, and missed opportunities for early support.
As an educator, researcher, and clinician working with children with developmental disorders and individuals with disability, I am committed to advancing research, service, and evidence-based practice to support these children, their families, and the professionals who care for them.
Tiffani Perry
Grant Writer / Fundraiser & Board Member
The University of Tennessee at Chattanooga
Director of Marketing and Communications for the Memphis In May International Festival. The largest cultural and civic festival in the state of Tennessee.
25+ year Marketing and Communications professional with a love for family, traveling, sports, and gardening. Wife and mother of one brilliant student athlete basketball player.
Dyspraxia matters to me because a few years ago, it became a part of my son’s everyday life and has shaped who he is becoming. Being his mom has taught me patience, empathy, and the importance of advocating for him, so he has the understanding, support, and opportunities he deserves and continues to EARN day after day. His journey with dyspraxia inspires me to raise awareness and help create a world where children like my son are recognized for their strengths, not defined by their struggles. I see the extra effort it takes for him to do things others may find easy, and I admire his determination, resilience, and courage in facing those challenges head-on. I have been amazed at what repetition and consistency has done to help my sone overcome challenges associated with dyspraxia. It is important to educate parents on the condition and what challenges are associated with it so that we feel our children are being supported.
Daniel P. Malloy
Director of Public Policy | Board Member
B.A. in Political Science and Sociology, Boston College. Juris Doctor, Boston College Law School. Recipient of six honorary degrees recognizing leadership in public service and education
Dannel P. Malloy has devoted more than two decades to public service and executive leadership across government and higher education. Since 2019, he has served as Chancellor of the University of Maine System, leading Maine’s public universities through a period of historic collaboration, enrollment growth, and systems reform. Under his leadership, the System became the first statewide public higher education enterprise in the nation to unify its institutional accreditations under the New England Commission on Higher Education, strengthening access, accountability, and shared resources.
Prior to his work in higher education, Malloy served two consecutive terms as Governor of Connecticut and spent 14 years as Mayor of Stamford, Connecticut. His career also includes service as a prosecutor, practicing attorney, and educator. As governor, he championed major reforms in education, criminal justice, and human rights, including the repeal of the death penalty and national leadership on refugee resettlement. In recognition of his principled leadership, he received the 2016 John F. Kennedy Profile in Courage Award.
Chancellor Malloy is married to his wife, Cathy, whom he met while they were students at Boston College. They have three sons. Throughout his career, he has remained deeply committed to public service, education, and policies that expand opportunity and dignity for individuals and families.
Dannel Malloy’s commitment to learning and developmental differences is deeply personal. As a child, he struggled with significant learning challenges that affected reading, writing, and academic performance—at a time when such differences were often misunderstood or overlooked. His mother became his strongest advocate, insisting that educators recognize his ability rather than define him by his challenges, and reinforcing both high expectations and perseverance.
With her support and a handful of teachers, he developed strategies that allowed him to succeed in environments not designed for students who learn differently. He graduated magna cum laude from Boston College with a double major in political science and sociology, earned his law degree, and was the first non-visually impaired person to take the bar exam orally—passing on his first attempt—demonstrating that achievement is possible when individuals are given appropriate pathways to demonstrate their knowledge and skills.
These experiences shaped his lifelong focus on education policy, equity, and access. Throughout his career in public service and higher education leadership, he has emphasized early identification, individualized supports, and institutional flexibility so that learning and motor-planning differences do not become barriers to opportunity.
His service on the Dyspraxia USA Board reflects a conviction that personal potential should never be constrained by systems that fail to accommodate difference. As the Board’s liaison for public policy, he brings both lived experience and policy leadership to advancing awareness, advocacy, and inclusive practices that help individuals with dyspraxia and related conditions thrive in education, the workplace, and their communities.
Board of Directors
Each member of the Board of Directors shares the common goal of bringing Dyspraxia Awareness to the United States and beyond. They have all been impacted by Dyspraxia and hope to offer support and services to others.
Warren Fried
Executive Director, President, Founder, Chief Advocate
University College Chichester, West Sussex, England
Chief Advocate Dyspraxia USA / Entertainment with Jeremy Kareken
Married over 11 years and has 6 year old twins who also live with Dyspraxia
Because 1 in 10 matters.
Jessica Applegate
Treasurer
BA, UNC Greensboro. Currently completing MBA at UNC Wilmington.
Executive Director for The North Carolina Association for the Gifted and Talented.
Homeschooling mother of five children; runner and exercise enthusiast.
For almost eighteen years I have watched one professional after another ignore a very early recognition of what an occupational therapist called developmental coordination delay. Most attempts to receive help ended with someone telling us that they could see something was “off ” about my oldest son, but they couldn’t diagnose it. For those of us who rely on help from insurance to cover medical costs, no diagnosis equals no treatment. Because of this, he missed out on important opportunities to receive the proper support and care, and it has impacted him socially, cognitively, emotionally, and in every other part of his life. I often wonder how different his life might be had our medical system been willing and able to have him diagnosed and treated. Ignoring Dyspraxia will not make it go away. Individuals with Dyspraxia need and deserve to have appropriate and early recognition, and support throughout their lives to help them reach their full potential.
Allison Berger
Secretary
James Madison University, BA, Georgia Institute of Technology, MBA.
Marketing Strategy Consultant serving clients from start – ups and nonprofits to Fortune 100 brands.
I have two daughters, on e diagnosed early on with dyspraxia. I have learned an incredible amount about dyspraxia and brain development in general and find it all fascinating. I am grateful for this opportunity with Dyspraxia Foundation USA to combine my personal and professional passions.
I have found that there is less knowledge and understanding of dyspraxia in the US than other western countries. It is important to increase awareness so that we can better diagnose, remediate and accommodate this growing population. I was fortunate to be able to dedicate a significant amount of time and resources early on to support my child and want to help other caregivers navigate their paths.
Bob Delaney
Director of Organizational Development
St Mary’s College of California: MA Leadership – Traumatic Stress. NJ City University – Bachelor Science Criminology.
Well known author. PTS Advocate. Supporting Military. Honors President Obama (2010). NBA Hall of Fame: Human Spirit Award. Recognized via TAPS. Special advisor Southeastern Conference and NBA Cares Ambassador. Awarded highest honor: National Collegiate Athletic Association.
Passionate leader 30 plus years in sports. One of the most dedicated referees in the history of the NBA. Former State Trooper. Has appeared in many forms of media.
Because each citizen matters.
Teri Flynn
Sports, Media and Entertainment. Co Board Chair
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Julie Van Bysteren
Head Volunteer
Bachelors of Science in Nursing, Linfield School of Nursing, Portland Oregon 2002. Currently pursuing Masters of Science in Nursing, psychiatric mental health nurse practitioner program at Frontier Nursing University.
Registered Nurse 20 + years, specialized in hospice since 2011. Veteran of United States Marine Corps.
I am a wife and mother of 4 children, grandmother to 3. I live in the beautiful Columbia River Gorge. We have a small off grid homestead where I raise goats, rabbits, chickens and guinea fowl. I also run a Facebook page called All Things Dyspraxia, where I hope to further spread awareness and support parents who are on this dyspraxia journey.
After our youngest son and third child was born in 2004, we saw a constellation of developmental differences that we had not previously encountered. As he got older these differences became more evident, but no one seemed to know what it was or how to help. I finally took him to see a neuropsychologist at Doernbecher Childrens hospital who diagnosed him with Dyspraxia. A few years later, our youngest daughter who was born in 2008, began exhibiting her own set of developmental concerns, we went back to the neuropsychologist who diagnosed her with dyspraxia as well. Since then it has been a struggle to get them the supports they need as awareness in this area is sorely lacking. Many experienced teachers and educational professionals are yet to hear the word, let alone understand its lifetime effects. Partly due to this, we have homeschooled them since 2012. I want more for my children. I want them to be supported, understood and recognized for their unique strengths throughout their lives.
Jeremiah White
Head of Finance. Board Chair
Wake Forest University
Accra Capital Partners (Hedge Fund) White Sport Ventures (Private Equity).
Former US National Team soccer player, four children, one with Dyspraxia
By understanding and addressing Dyspraxia, we can provide targeted support and interventions to help those affected lead fulfilling and productive lives.
Dr. Matt Zakreski
Head of DEI
Wake Forest University (BA in psychology and communication). Widener University (Doctor of Psychology)
Co-founder and Director of Therapy for The Neurodiversity Collective. Professional speaker and trainer.
Professional cartoonist. Father of two Neurodivergent kiddos.
When we increase awareness and knowledge of dyspraxia, we help all people who serve kids to understand more about their specific neurotypes and how to intervene.
Mitchell I. Fried
Board Member
University of Florida with a B.A. Psychology and J.D.
Admitted to practice law in Florida and New York
Married for 47 years with two boys
To help those with the condition understand why they may have limitations which are no fault of their own, and that the limitations may be overcome.
Jeremy Karekan
Board Member
University of Chicago and the Actors Studio Drama School
Currently a playwright living in New York and Baltimore. His play The Lifespan of a Fact ran from 2018–2019 on Broadway and starred Daniel Radcliffe, Bobby Cannavale, and Cherry Jones. Served as producer and researcher for Bravo TV’s Inside the Actors Studio. As an actor he appeared in a number of commercials and two feature films.
Two children
Jeremy is passionate about improving access to education and professional development for all neurodiverse children.
Alex Molden
Board Member
College graduate (Bachelor of Science) Univ. of Oregon
Author (The Ultimate Playbook for High Achievement), International Speaker, Personal Development Coach, Consultant, and Podcast Host (The Shark Effect).
Former NFL Defensive back (’96–’04). Married. Proud father of 8.
Our son was misdiagnosed with so many different syndromes…we couldn’t get a straight answer. It was very unsettling. When we found out that his diagnosis had a name it calmed our nerves and helped us navigate the struggles that were ahead of us. It’s not that scary…but being in the unknown is.
“Never underestimate the valuable and important difference you make in every life you touch for the impact you make today has a powerful rippling effect on every tomorrow.”
Leon Brown
Ambassadors of the Dyspraxia Foundation
These dedicated professionals work to champion people with Dyspraxia and the work of the foundation across the United States.
- Rachel Barcelona
- Theresa Bidwell
- Elissa Fried
- Shanda Husted
- Joe Mancini
- Randy Schmidt
Ambassadors of the Dyspraxia Foundation
These dedicated professionals work to champion people with Dyspraxia and the work of the foundation across the United States.
- Rachel Barcelona
- Theresa Bidwell
- Elissa Fried
- Joe Mancini
- Randy Schmidt
