About Us
Mission
FMDSA
The Fibromuscular Dysplasia Society of America, Inc. was founded on March 11, 2003 and received tax exempt status on October 7, 2003. FMDSA is a Delaware nonprofit corporation which is classified by the IRS as exempt under IRC Section 501(c)(3) and as a “public charity” under IRC Section 509. Donations from individuals and corporations are tax deductible to the extent permitted by law.
FMDSA has become the recognized leader in the support of Fibromuscular Dysplasia (FMD) awareness, education and research. We will continue to achieve our goals by successfully raising money for the purpose of awarding FMD research grants, building awareness programs, and educating the public and medical communities about FMD.
We are a not-for-profit organization and programs like these cannot succeed without your support. Through volunteerism, membership, financial contributions, and event participation, the FMDSA can fulfill our vision and improve the quality of life of those affected by Fibromuscular Dysplasia.
Tax ID: 01-0771966
Beadie Fun Fact
FMD was initially described in 1938 and classified according to angiographic and histopathological findings in the 1960's & 1970's
The Tree as
Our Symbol
Since ancient times and across many cultures, the tree has long been a symbol of many things, including wisdom, protection, strength, inter-connectivity, and life itself. We’ve chosen the tree to represent the Fibromuscular Dysplasia Society of America for these reasons, and because the tree’s branches and roots signify the arteries affected by this disease. The tree’s branches, reaching upward and outward, provide protection and shelter, and represent our mission to help those who’ve been diagnosed with FMD. Trees, strengthened by their continuously spreading roots, symbolize how as we grow together we are stronger and more resilient. As with its growth from a delicate sapling to a giant robust tree, and as its branches and roots grow and spread, the tree symbol represents how we’ve evolved and continue to promote research, education and patient support throughout the years. Together we can achieve much, as we strive to reach for the sky.
“The creation of a thousand forests is in one acorn.”
-Ralph Waldo Emerson
* Please note that our web site does not include any form of advertisement and no external sources of funding, including sites funded by government agencies, pharmaceutical companies or other commercial entities.
Executive Director and Board of Directors
Medical
Advisory Board
Jeffrey W. Olin, DO, FACP, FACC
Board Chairman
Professor of Medicine
Director, Vascular Medicine
Zena and Michael A. Wiener Cardiovascular Institute
Mount Sinai School of Medicine
New York, New York
Heather L. Gornik, MD
Vascular Center at the Harrington Heart and Vascular Institute
UH Cleveland Medical Center
Cleveland, Ohio
Kevin E. Meyers, MD
The Children’s Hospital of Philadelphia and University of Pennsylvania
Philadelphia, Pennsylvania
Warren D. Lo, MD
Associate Professor of Pediatrics,
Associate Professor of Neurology
Nationwide Children’s Hospital
Columbus, Ohio
Santhi K. Ganesh, MD
Division of Cardiovascular Medicine, University of Michigan Health System
James C. Stanley, MD
Alan H. Matsumoto, MD, FACR, FSIR
FAHA Chair and Theodore E. Keats Professor of Radiology
University of Virginia Health System
Michael R. Jaff, DO, FACC, FAH
Bruce Gray, DO
Greenville Hospital System. Greenville
South Carolina
Advisory Council
Kim A. Eagle, MD
Albion Walter Hewlett
Professor of Internal Medicine
Chief of Clinical
Cardiovascular Medicine
Director and Education Lead
Cardiovascular Center
Ann Arbor, Michigan
Robert D. Kubic, MBA
Chief Operating Officer
Honigman Miller Schwartz and Cohn LLP, Detroit, Michigan
James Baranski, CEO
National Stroke Association;
Member of various stroke-focused organizational advisory boards, including the Brain Attack Coalition, National
Forum for Heart Disease and Stroke and the World Stroke Association
Joan M. Legraw, RN, JD, MPH
General Counsel &
Consultant for Ethical &
Regulatory Affairs
Cape Cod Research Institute
Barnstable, Massachusetts
Kay Tanner, JD
Former FMDSA Board Member
Ethics Investigator, Global Ethics & Compliance Office
Dell Technologies
Eileen Grubba
Actress, writer and producer
Former US Ambassador for GE Healthcare’s Get Fit campaign in 2012
Spokesperson for LSI: Families with hereditary cancers, an Advocate for children with rare illnesses and for the inclusion of people with physical challenges in the entertainment industry
Annual
Reports
Our annual reports detail the accomplishments of FMDSA throughout the years, and summarize our financial results as reported in IRS Form 990.
By-Laws
The FMDSA by-laws describe our purpose, structure and how we govern ourselves as an organization.
This document is available to the public.
Beadie FMD Fun Fact:
For patients with suspected renal artery FMD, CTA is the initial imaging modality of choice
Milestones Highlights
Please click to see larger images and more information.
2003 FMDSA MILESTONES
FMDSA is Incorporated, March 11, 2003, and gains Public Charity status, October 2003. Our founders: Rich and Susan Gould and Marie Yeh.
Continue Reading →2003 FMDSA MILESTONES
FMDSA is Incorporated, March 11, 2003, and gains Public Charity status, October 2003. Our founders: Rich and Susan Gould and Marie Yeh.
- January 2003 – Richard and Susan Gould began work to build a nonprofit organization to fund research, build awareness, and provide accurate educational materials to patients, medical practitioners, and the general public.
- March 11, 2003 – The FMDSA was officially incorporated in the State of Delaware. The original incorporators were Richard and Susan Gould and Marie Yeh. The three incorporators brought a wealth of experience to the organization.
- October - FMDSA receives interim “public charity” status.
- December - We officially open our doors for business. Our first website is piloted and we begin asking for donations.
2004 FMDSA MILESTONES
First Medical Advisory Board: Susan Begelman MD, Jeffrey Olin DO
Continue Reading →2004 FMDSA MILESTONES
First Medical Advisory Board: Susan Begelman MD, Jeffrey Olin DO
- First Annual Meeting held and FMDSA officially elects Board of Directors.
- Medical Advisory Board established with first two physicians, Susan Begelman, MD and Jeffrey W. Olin, DO
- Website launched and certified by Health on the Net Foundation.
- First fundraising event – Pedal for Progress
2005 FMDSA MILESTONES
Accepted as Associate Member of NORD (The National Organization of Rare Diseases)
Continue Reading →2005 FMDSA MILESTONES
Accepted as Associate Member of NORD (The National Organization of Rare Diseases)
- Accepted as Associate Member of the National Organization for Rare Disorders
- Medical Advisory Board expanded to include Kevin Meyers, MD and Nazli McDonnell. MD. PhD.
- Launched Grassroots Awareness Program (GAP)
- Launched Physician Education Program
- Attended three conferences including two National Stroke Association meetings and American Society of Nephrology meeting.
- Launched FMD Bracelet Program
- Pam Mace invited to first radio interview on FMD
2006 FMDSA MILESTONES
FMDSA Spreads Awareness, stories in several major medical publications help to educate.
Continue Reading →2006 FMDSA MILESTONES
FMDSA Spreads Awareness, stories in several major medical publications help to educate.
- First TV interview reaches over 1 million viewers.
- Dr. Jeffrey Olin invited to speak at the Cleveland Clinic Grand Rounds on FMD.
- Pam Mace elected as new Chairperson for FMDSA.
- First major awareness articles published in major medical journals (Stroke Smart, Kidney Beginnings, and Partners in Health.
- Attended conferences sponsored by the European Society of Human Genetics, the National Stroke Association, the American Neurology Association, the American Society of Nephrology, and the National Organization for Rare Disorders.
- Website grows to over 1,000 unique visitors per month
2007 FMDSA MILESTONES
The FMD Registry is officially created with partnership from the University of Michigan.
Continue Reading →2007 FMDSA MILESTONES
The FMD Registry is officially created with partnership from the University of Michigan.
- American Stroke officially recognizes FMD as cause of stroke.
- FMDSA moves from founders’ home into dedicated office space in Rocky River, OH.
- Work begins on International Patient Registry with the University of Michigan.
- Medical advisory board expands to six with additions of Philip Gorelick, MD, MPH and Warren Lo, MD.
- Patient Stories section added to website.
- FMD makes the cover of Stroke Connection, Renal Life and Cath Lab Digest, as well as being featured in a separate article in Cath Lab Digest.
- Participated in a Women’s Talk Show interview in North Carolina.
- CN8 News TV Interview.
- Website grows to over 3,000 unique visitors per month.
- Participated in Grand Rounds at hospital in Massachusetts, Minnesota and North Carolina.
- Membership increased by greater than 250 members.
2008 FMDSA MILESTONES
First Annual Conference, Westlake, Ohio
- Development completed on International Patient Registry, in cooperation with the University of Michigan.
- Attended first vascular conference (The Society of Vascular Medicine) as well as the American College of Cardiology and American Heart Association.
- First member conference / annual meeting in Westlake, OH. Meeting was attended by nearly 100 patients and family members.
- “Keeping in Circulation” the official publication of the Vascular Disease Foundation featured Fibromuscular Dysplasia in their summer 2008 newsletter.
- Cleveland Clinic announces first ever FMD Clinic. FMD patients will have access to multiple specialists to manage their disease. Other institutions show intent to follow suit.
- Medical advisory board expands to include Heather Gornik, MD.
- Cheryl Bailey was successful in getting an article published in Atlantic County Women. The article, "Fibromuscular Disease Awareness", was a two month run publication in all of Atlantic, Cape May and Cumberland Counties in NJ.
2009 FMDSA MILESTONES
WSJ - Front page story about Fibromuscular Dysplasia.
- FMDSA hires first full time employee. Pam Mace appointed as Executive Director.
- International Patient Registry, in cooperation with the University of Michigan moves into production and starts gathering data.
- First National Awareness Opportunities. Front page article in the Wall Street Journal (June 2009) and TV coverage on Mystery Diagnosis on Discovery Health Channel (first aired September 2009).
- First FMD Public Service Announcement created.
- Article in Kidney Beginnings (May 2009)
- Continued to attend medical conferences to educate face-to-face including the International Stroke Conference (San Diego, February)
- Cleveland Clinic holds live web chat for patients in February and November.
- University of Illinois begins FMD Medical Clinic.
- 2nd Annual Conference well attended at the Wyndham Hotel in Cleveland.
- School Nurse News Article (September).
- Rare Disease day interview Monica Robins and Pam Mace (Cleveland-February)
- Craines Business Magazine- Cleveland.
- Grand Rounds- University of Michigan (June)
- Doctors Channel FMD Video series with Dr Heather Gornik
- Stroke Awareness Month- presented at three professional education seminars.
2010 FMDSA MILESTONES
Dr Olin Reach MD interview, professor of cardiology and director of vascular medicine at Mount Sinai Hospital.
Continue Reading →2010 FMDSA MILESTONES
Dr Olin Reach MD interview, professor of cardiology and director of vascular medicine at Mount Sinai Hospital.
- Click here to view "Dr Olin Reach MD interview"
- The US FMD Registry has 268 patients enrolled (spring) and 6 centers participating, with more to be added
2011 FMDSA MILESTONES
- VIVA 50K donation to FMDSA
- Dr. Kevin Barrett and FMD patient/Board Member Lisa Foster shared Lisa’s story with Fox News in Florida
- Dr. Olin and FMD patient Jodi Roth shared Jodi’s story in a video clip with Fox New York
2012 FMDSA MILESTONES
The United States Patient Registry for FMD: “Results in the first 447 patients”
Continue Reading →2012 FMDSA MILESTONES
The United States Patient Registry for FMD: “Results in the first 447 patients”
Click here to view "The United States Patient Registry for FMD: Results in the first 447 patients"
The United States Registry for Fibromuscular Dysplasia publishes: “Results in the first 447 patients”
- Pam invited to speak at the European Society of Hypertension meeting in London
- FMDSA President Bradley Daar DDS produced and aired a 30 minute segment of an interview with Connecticut State Rep. Pamela Sawyer
- . FMD patient/former FMDSA President Cheryl Bailey recorded a 90 second video on FMD that ran every day for one week on the Health Update show on NBC40 (South Jersey’s local NBC Affiliate)
- A Patient Page on Fibromuscular Dysplasia is published in the AHA’s journal “Circulation”. Thanks to Dr. Olin, Dr. Gornik, Pam Mace, and Stacey Ploskey for writing this article.
2013 FMDSA MILESTONES
FMDSA named an official charity of the Union Home Mortgage Cleveland Marathon.
Continue Reading →2013 FMDSA MILESTONES
- FMDSA named an official charity of the Union Home Mortgage Cleveland Marathon.
- To help fund the US Registry for FMD, the FMDSA creates “The FMDSA Circle of Friends”, a group of committed benefactors of the FMD Registry
- The FMDSA celebrates its 10 Year Anniversary
2014 ( 1st ) FMDSA MILESTONES
1st International Fibromuscular Dysplasia Research Network Symposium - May, 2014
Continue Reading →2014 ( 1st ) FMDSA MILESTONES
- 1st International Fibromuscular Dysplasia Research Network Symposium - May, 2014
- Multiple articles published from the US Registry for FMD
Click here to view "1st International Fibromuscular Dysplasia Research Network Symposium"
2015 FMDSA MILESTONES
- First Belgian meeting for Fibromuscular Dysplasia, held in Brussels, Belgium. Organized by P. Vanderbilts Niepen and A. Persu.
- Rare Disease Report released their “Top 10 Interviews of 2015” and our Dr. Olin’s interview on FMD made the list
- The FMDSA received recognition for being a Top Rated Nonprofit from Great Nonprofits and also Best Nonprofit Organization in Rocky River
- In November, at the AHA (American Heart Association) sessions in Orlando, Florida, fibromuscular dysplasia was recognized with a session dedicated to FMD titled: “Fibromuscular Dysplasia and Related Conditions: What the Cardiovascular Community Needs to Know.”
2016 FMDSA MILESTONES
House Bill 434 passes in Ohio, designating May as Fibromuscular Dysplasia Awareness Month
Continue Reading →2016 FMDSA MILESTONES
- House Bill 434 passes in Ohio, designating May as Fibromuscular Dysplasia Awareness Month
- New York Times features fibromuscular dysplasia as their disease of the week
- “Rare” diseases: Motivated patients make the difference
2017 FMDSA MILESTONES ( 2nd )
The 2nd International FMD Research Network and SCAD Symposium - May 2017, Cleveland.
Continue Reading →2017 FMDSA MILESTONES ( 2nd )
- The 2nd International FMD Research Network and SCAD Symposium - May 2017, Cleveland.
Link to video: https://www.youtube.com/watch?v=4otZEgIfApM The US Registry for FMD has over 1600 participants
The FMDSA Inspire support group has 2,078 members
2018 FMDSA MILESTONES
1st Belgian International Meeting on Fibromuscular Dysplasia (2015 was National, this year was International)
Continue Reading →2018 FMDSA MILESTONES
- Click here to view "The International Symposium Revisiting Fibromuscular Dysplasia & Related Vascular Disease"
- October 15 was an amazing day of advocacy in Washington, DC. Pam Mace was an invited speaker at the NORD Conference
2019 FMDSA MILESTONES
First International Consensus on the Diagnosis and Management of Fibromuscular Dysplasia - January, 2019
Continue Reading →2019 FMDSA MILESTONES
- The First International Consensus on the Diagnosis and Management of Fibromuscular Dysplasia
- The FMDSA moves to a new (larger) office space
Click here to view "First International Consensus on the Diagnosis and Management of Fibromuscular Dysplasia"
2020 FMDSA MILESTONES
FMDSA is honored to be the recipient of the Global Gene’s “Champion of Hope” Award
Continue Reading →2020 FMDSA MILESTONES
- FMDSA is honoured to be the recipient of the Global Genes “Champion of Hope” award
- November zoom Webinar with Dr. Jeff Olin. “What We’ve Learned in the Last 10 Years”
2021 FMDSA MILESTONES
The United States Registry for Fibromuscular Dysplasia exceeds 3,100 patients
Continue Reading →2021 FMDSA MILESTONES
The United States Registry for Fibromuscular Dysplasia exceeds 3,100 patients
* First “Virtual” International FMDSA Annual Conference, December 4th
Sept 2021 Social Media Numbers
- Facebook page likes 6200
- Instagram followers 994
- Twitter followers 1968
- Inspire members 4824
Awards
The Founders Award is awarded to an individual or institution, who has taken extraordinary measures to advance awareness, research, or treatment of Fibromuscular Dysplasia.
We wish to express our sincere gratitude to our Founders Award recipients for their outstanding achievements in promoting research and awareness of Fibromuscular Dysplasia.
- Pamela Mace, RN
- Nazli McDonnell, MD, PhD - NIA
- Jeffrey Olin, DO, FACP, FACC -
Mt Sinai, New York
Cleveland Clinic Heart and Vascular Institute
- Heather Gornik, MD
- Jerry Bartholomew, MD, FSVM
University of Michigan
- Kim A. Eagle, MD
- James B. Froehlich, MD, MPH
- Eva Kline-Rogers, RN, MS
Children's Hospital of Philadelphia
- Kevin Meyers, MD
- Susan Begelman, MD, FSVM
- James Stanley, MD - University of Michigan
Santhi Ganesh, MD - University of Michigan
Jackie Saw, MD - Vancouver General Hospital, Canada
Pr Pierre-François Plouin - Hospital European G Pompidore, Paris France
FMDSA Lifetime Achievement Award
Pamela Mace, RN
- Dr Nabilia Bouatia-Naji - Paris, France
- Dr Alexandre Persu - Belgium
- Dr Xavier Jeunemaite - Paris France
- Dr Jason Kovacic
- Dr Andrzej and colleagues of the Institute of Cardiology in Poland
- Dr. Esther Kim, Atrium Health North Carolina
Past members that have served with distinction and made a significant contribution to FMDSA's success.
- Susan and Rich GouldFounders
- Marie YehFounder
- Robert KubicVolunteer / Professional Advisory Council
Beadie FMD Fun Fact:
For patients with suspected renal artery FMD, CTA is the initial imaging modality of choice