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Our Group organises 3000+ Global Conferenceseries Events every year across USA, Europe & Asia with support from 1000 more scientific societies and Publishes 700+ Open Access Journals which contains over 50000 eminent personalities, reputed scientists as editorial board members.



The Fibro muscular Dysplasia Society of America, Inc. was founded on March 11, 2003 and received tax exempt status on October 7, 2003. FMDSA is a Delaware non-profit 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.

Our vision is to become the recognized leader in the support of Fibro muscular Dysplasia (FMD) awareness, education and research. We will achieve our goal 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 voluntary, not-for-profit organization and programs like these cannot succeed without your support. Through volunteerism, membership, financial contributions, and event participation, the FMDSA can fulfil our vision and improve the quality of life of those affected by Fibro muscular Dysplasia. Registration and a welcome reception will be held the evening of Friday, May 13th at the Wyndham Hotel from 5-7pm. After the welcome reception we try to arrange a dinner at a local restaurant for anyone who would like to attend, your meal is at your expense. These details will be emailed to attendees as we receive them. Every year we have a packed restaurant with an average of 60 people attending. Saturday morning, May 14th. Registration will be open during breakfast between 7:30-8:30am on the 2nd floor of the hotel in the Palace Ballroom. A light breakfast and lunch are included in your registration fee.

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