The Multiple Sclerosis Association of America (MSAA)
is a comprehensive, not-for-profit, charitable service agency that most specifically helps
people, their friends, their families, and society in general to address the day-to-day
needs of those with MS. It also conceives, builds, and maintains barrier-free housing
complexes open to all disabled people and is involved in programs and research that affect
all with neurological disorders. It is an independent national and organization with
corporate headquarters in Cherry Hill, New Jersey, regional headquarters strategically
placed throughout the United States.MSAA was founded by John Hodson, Sr. and his late
wife, Ruth Hodson, who fought MS for nearly half a century. It was chartered in New Jersey
on June 6, 1970 and has many program, research, and publication facets, many of which date
back to the organizations beginnings. The agency specializes in and has developed an
international reputation for direct one-on-one client services. These take the form of
counseling, by peers and professionals; client meetings; social gatherings, in and outside
MSAA centers; an extensive equipment loan program that distributes wheelchairs, walkers,
canes, crutches, cool suits, scooters and other therapeutic paraphernalia throughout the
world; free MRI testing to quickly and more accurately diagnose MS; a ramp building
program; client-to-client cooperation, including visitation and buddy
programs; family togetherness events that help maintain the bond between MS patients and
families; and various motivational programs that encourage constituents to enjoy life to
the fullest possible extent and to participate as much as possible in the widest of
worlds.
In the 1980s, MSAA embarked with U.S. Department of Housing and Urban Development
(HUD) on an ambitious program of building barrier-free housing for the disabled.
In the 1990s, MSAA pioneered and financed important scientific research into
possible ways of helping people better control and manage MS. These examinations into
alternative therapies include studying cooling, which employs technology developed by the
National Aeronautics and Space Administration (NASA) available to MSAA via an historic,
one-of-a-kind Memorandum of Understanding between MSAA and NASA and which thanks to
portable microclimate apparel lowers a persons core body temperature one degree,
thus warding off fatigue and increasing productivity; experiments involving bee venom
therapy, which will either affirm or debunk the folk notion that bee stings bolster the
human immune system and, therefore, delay the effects of MS; and tests to see whether
electromagnetic fields (EMFs), already proven helpful to people with neurological
diseases, e.g. migraine headaches, are beneficial to those with MS.
Knowing the Difference
MSAA is an independent national and international charity registered with the IRS and
licensed in all jurisdictions in which it operates. It is not affiliated with any other
organization helping those with MS. MSAA is particularly dedicated on delivering direct
service that makes a difference in a constituents day-to-day existence as he or she
fight the disease. It offers broad services while conducting and financing research into
alternative therapies that can enhance the comfort of MS patients and, perhaps, make the
disease more manageable in the future.
Ways to Support MSAA
MSAA cannot do its work alone. It needs a wide spectrum supporters and volunteers to
help it carry out its mission. Donations, whether of cash on in-kind, are always
appreciated. Volunteers have often been the backbone of MSAA, and it is always looking for
sincere, willing, compentent people to help it provide its level of service. Also,
attending or sponsoring special events can be of critical importance. MSAA dedicates
itself to helping others.