Nicholas Mastroianni Raises Funds for the Muscular Dystrophy Association

Nicholas Mastroianni Raises Funds for the Muscular Dystrophy Association

March 26, 2012


Nicholas Mastroianni helps raise money to help children with Muscular Dystrophy attend summer camp.


Florida Regional Center executive, Nicholas Mastroianni, recently helped raise money to send children affected with Muscular Dystrophy to a specialized summer camp.  The goal of the program was to give children with muscular dystrophy conditions, the same summer camp experience and opportunity as unaffected children.  Nicholas Mastroianni was able raise over $3,000, which will allow up to 3 children to participate in the summer camp.  Children affected by MD are often restricted to wheelchairs, as the inherited disorder involves muscle weakness and loss of muscle tissue.  The camp allows the children access to camp activities, such as swimming, ATV rides, and arts and crafts, with the assistance of properly trained camp personnel and volunteers.    Nicholas Mastroianni saw this as a worthy cause to donate his efforts to as the MDA is working to eradicate the disease through the employment of over 330 research projects around the world.  In the interim, they also strive to make life better for those affected with the disease through support programs, medical equipment programs, free flu shots, and MDA summer camps for youngsters.


About Florida Regional Center


Located in a dynamic tropical destination famed for its business and its beaches, the Florida Regional Center provides worthwhile opportunities for foreign investors and their families to obtain permanent U.S. residency through the EB-5 Visa Program. Just as Florida offers the ideal climate for business and pleasure, the Florida Regional Center provides the perfect opportunity for international investors and their families to obtain green cards by investing in exciting Florida Regional Center projects.


For more information about the Florida Regional Center visit:


About Muscular Dystrophy Association:


Muscular Dystrophy Association or MDA is the nonprofit health agency dedicated to curing muscular dystrophy, ALS and related diseases by funding worldwide research. The Association also provides comprehensive health care and support services, advocacy and education. MDA combats neuromuscular diseases through programs of worldwide research, comprehensive medical and support services, and far-reaching professional and public health education. With national headquarters in Tucson, MDA has more than 200 offices across the country, sponsors some 200 hospital-affiliated clinics and supports more than 330 research projects around the world.


MDA supports more research on neuromuscular diseases than any other private-sector organization in the world. MDA scientists are in the forefront of gene therapy research and have uncovered the genetic defects responsible for several forms of muscular dystrophy, Charcot- The Association’s comprehensive services program includes diagnostic and follow-up medical consultations, flu shots, support groups, MDA summer camps for youngsters, a medical equipment program, assistance with equipment repairs and resource referral. Through its national advocacy program, MDA works to make life better for people with muscular dystrophy and related muscle diseases by providing representation in matters of public policy and research advancement, nationally and internationally.


For more information on Muscular Dystrophy and the MDA please visit