2026-02-27T04:42:32-08:00 2025-12-31 610567366 CHARLES T MITCHELL CO PLLC 229 W MAIN ST STE 103 FRANKFORT KY 40601 990EZ 2025-01-01 010771966 FIBROMUSCULAR DYSPLASIA SOCIETY OF AMERICA INC FIBR 2168342410 26777 LORAIN RD 311 NORTH OLMSTED OH 44070 KAY TANNER President 2026-02-27 true Greg Miklavcic CPA P00946625 5022277395 2025 2025-03-06 01:10:19Z X X X WWW.FMDSA.ORG X X 158513 X 158506 7 0 0 0 0 158513 50000 65694 5050 3600 37468 161812 -3299 136693 133394 X 137816 134555 137816 134555 1123 1161 136693 133394 FMDSA is a public healthcare related charity working towards better diagnosis and treatments for Fibromuscular Dysplasia (FMD). The organization is engaged in funding and facilitating research, physician education and support, building awareness of FMD within the medical community and patient communities, providing patient support, and in patient education programs. In 2007, FMDSA laid the foundations for the creation of an FMD medical data registry with the goal of increasing understanding of FMD and providing physicians and researchers with a vehicle to capture and analyze characteristics associated with the disease to identify potential markers and commonly used treatment modalities. The Michigan Clinical Outcomes Research and Reporting Program at the University of Michigan is the coordinating center for the registry. Patient enrollment in the FMDSA Registry increased from 4598 patients at the end of 2024 to 5118 patients at the end of 2025. There are 21 actively participating Medical registry sites. New sites in 2025 included The University of Pennsylvania and Virginia Mason Franciscan Health. 134965 Patient support is a large program due to the significant increase in the number of patients diagnosed with FMD annually. The organization continues to grow Volunteer Support Networks with volunteers across the United States and internationally. Patient support also includes social media outreach, including Inspire, Instagram, and Facebook, where thousands of patients participate. The organization is also active on Twitter, allowing patients and physicians to communicate directly. Materials and videos are continuously added to the FMDSA website and YouTube channel, and we offer nearly sixty FMD related videos in multiple languages and work with our international colleagues who offer additional language specific materials. FMDSA continues to host virtual patient meetings for all patients in the US - and worldwide. Patient and family member education services. The organization provides educational support and resources for patients educate their family, friends, and healthcare providers about FMD with written materials and videos. Resources that help communicate the complex medical language and physiological elements of FMD are laid out in easy-to-understand terms and materials include a Public Service Announcement and tailored materials designed to bridge the gaps between patients and physicians. The Program also includes educational work with media outlets, other organizations, journals, speaking engagements, and articles. It is a rare day when we are not contacted by a newly diagnosed patient. We have seen the diagnosis rate grow in direct proportion to our programs. We also participate in events such as the Cleveland & Detroit Marathons, along with other high profile well attended events, to help increase awareness and to raise funds to support our programs. Physician, research specialist, and other healthcare provider education. We educate medical professionals worldwide at meetings such as the International StrokeConference, Hospital led Conferences, Hospital Grand Rounds, and Research Meetings. The awareness, education, and research happening around the world is a direct result of the seeds FMDSA has been planting since 2003. In person meetings. In 2025, the organization participated in in-person meetings, including the American Heart Association Scientific Sessions, the VanSCAD meeting in Vancouver, Canada, the Atrium Health Southeast FMD Patient Symposium, and the Kentucky Neuroscience Expo. The result of this participation is patient representation and awareness of FMD patient perspectives for medical community. It has facilitated improved medical knowledge, the development of critical partnerships and research activity. We maintain a research database on the website which contains medical findings from the FMDSA patient registry, and from other researchers for patients. There are also PowerPoint presentations and videos available for healthcare providers. Registry funding. FMDSA has been the sole source of funding and has been the sole sponsor of the North American FMD Registry since 2008. The first participant's data was entered in January 2009. Patient data is collected and rigorously analyzed to learn more about the disease. Research from the date contained in this registry has contributed to the identification of genetic variants connected to FMD (PHARCTR1, ATP281, LRP1, and LIMA1), and in 2024, a key driver gene called UBR4 was discovered. This was a huge advance. Based on the associated genes, researchers believe that 3-5% of the U.S. population may be afflicted with FMD. When held in person, FMDSA Conferences bring together FMD patients, including those who have had spontaneous coronary dissection (SCAD), caregivers, and medical professionals. These meeting provides an opportunity for patients to meet others also affected. FMDSA also hosts a separate meeting with researchers to discuss updates and current and future research projects. The forum has provided a platform for research projects, including blood draws, saliva collection, and quality-of-life studies. There is no other meeting in the world where patients have the opportunity to participate in research. Most recently, FMDSA has also participated in and coordinated Zoom webinars and, in 2025, the Annual Conference was held as a virtual event, to support broader, national and global participation. One of our most important charters is to educate patients and families about FMD. We offer educational materials, videos, a research section, news and events, and contacts for patients worldwide. The website is a resource for patients, family members, and medical professionals worldwide. FMDSA is the premier resource of FMD information for the layperson and an excellent place for physicians to easily find medical articles and abstracts. The FMDSA website also offers community events for those wanting to get more involved. FMDSA is the recognized leader in FMD support and resources. 134965 KAY TANNER President 5.00 0 ROSIE MIKLAVCIC Secretary 5.00 0 GIAMILA FANTUZZI Director 2.50 0 CATHLIN JAMISON Director 40.00 0 ALLISON GAINES Director 2.50 0 PAM MACE EXECUTIVE DIRECTOR 60.00 0 false false false false false false false 0 0 0 false 0 0 false AL AR AZ CA CO FL HI IN KS KY MA MD MI MN MO NC ND NH NJ NM NY OH OK OR PA RI SC TN UT VA WA WI WV ANITA MEYERS 26777 LORAIN RD NORTH OLMSTED OH 44070 2168342410 false false false false false false false false false false false NONE NONE true X 202598 142236 147938 145428 158406 796606 11428 11428 0 0 0 202598 142236 159366 145428 158406 808034 0 0 808034 22 11 11 7 51 0 22 11 11 7 51 0 0 202620 142247 159377 145428 158413 808085 0.99990 0.99990 0.00010 0.00010 X Grants and Similar Amounts Paid In Excess of $5,000.1 | Donee's Name: MCORRP UNIVERSITY OF MICHIGAN | Donee's Address: 24 FRANK LLOYD WRIGHT DRIVE ANN ARBOR MI 48106 | Cash Amount Given: $50000 Other Expenses.1002 Office Expenses $8394 Other Expenses.1003 Information Technology $8571 Other Expenses.1005 Travel $18788 Other Expenses.1012 Insurance $1715 Total Liabilities.1001 Accounts Payable and Accrued Expenses - Beginning $1123 Accounts Payable and Accrued Expenses - Ending $1161