Mission: MDA is leading the fight to free individuals — and the families who love them — from the harm of muscular dystrophy, ALS and related muscle-debilitating diseases that take away physical strength, independence and life. We use our collective strength to help ...
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Our brand purpose defines why MDA exists and the role we play in the world. It briefly explains who we are, what we stand for and our reason for being. This is not a tagline or a slogan; rather, it’s a reflection of what we’re doing together in communities every day to achieve our mission and fulfill our promise to the countless families who are depending on us. This is why we’re here.
At MDA, we are fighting to free individuals — and the families who love them — from the harmful effects of muscle-debilitating diseases so they can live longer and grow stronger.
You can change that.
Together, we can free families from the harm of these devastating diseases so they can live unlimited. Join us to save and improve the lives of the courageous families we serve.
Discover Your Potential.
We are progress.
Together, we help kids and adults live longer and grow stronger.
The Muscular Dystrophy Association (MDA) is the nonprofit health agency dedicated to finding treatments and cures for muscular dystrophy, ALS and related diseases by funding worldwide research. The Association also provides comprehensive health care and support services, advocacy and education.
MDA was created in 1950 by a group of adults with muscular dystrophy, parents of children with muscular dystrophy and a physician-scientist studying the disorder.
MDA is leading the fight to free individuals — and the families who love them — from the harm of muscular dystrophy, ALS and related muscle-debilitating diseases that take away physical strength, independence and life. We use our collective strength to help kids and adults live longer and grow stronger by finding research breakthroughs across diseases; caring for individuals from day one; and empowering families with services and support in hometowns across America.
Learn how you can fund cures, find care or champion the cause at mda.org.
MDA combats neuromuscular diseases through programs of worldwide research, comprehensive medical and community services, and far-reaching professional and public health education. With national headquarters in Chicago, IL. MDA has 120 local offices across the country, sponsors 150 Care Centers across the US. In 2015 there were nearly 50,000 visits to MDA's Care Centers. The Association's programs are funded almost entirely by the voluntary contributions of concerned individuals and cooperating organizations.
Some of MDA's special events and volunteer opportunities include:
Our employees like working at MDA because of our career opportunities, inclusive environment, work-life balance, benefits and culture. By joining our dedicated team, you will experience the gratification of knowing your work impacts the well-being of millions of people — both directly and indirectly — affected by neuromuscular diseases.
Our commitment extends to our employees, and we recognize their need to balance work and personal responsibilities. Some of the comprehensive benefits we offer our employees include:
Founded in 1950, the Muscular Dystrophy Association today is one of the world’s leading nonprofit health organizations, funding research, health care and support services covering more than 43 neuromuscular diseases affecting more than 1 million Americans.
Active in local communities around the country, MDA is dedicated to finding treatments and cures for neuromuscular diseases, and to supporting the individuals and families affected by these diseases.
The majority of diseases under MDA’s umbrella are caused by genetic factors. All result in progressive muscle weakness. Symptoms can range from mild muscle weakness to complete paralysis of all voluntary muscles, including those used for breathing and swallowing. Among these diseases, the age of onset varies from birth to adulthood, and life span after diagnosis can be as short as a year or as long as several decades.
For detailed information about each of the neuromuscular diseases in MDA's program, visit the MDA Disease Directory.
MDA is currently funding more than 150 research projects in 11 countries. Thanks to MDA-funded research:
Health care and support services
MDA’s comprehensive services program helps individuals and their families meet the challenges imposed by chronic, progressive muscle diseases through:
Each year, MDA hosts nearly 75 summer camps across the country. In 2015, more than 3,800 kids received teh best week of the year at no charge to their families by attending this camp. Youngsters ages 6 to 17 attend a free weeklong accessible summer camp session where they get to be “just kids.”
Public and professional health education
Online and in print, MDA offers a vast library of information about research, clinical trials, health care and daily living strategies. MDA also regularly convenes international scientific meetings and conferences for researchers and MDA clinic directors.
MDA represents the needs of the neuromuscular disease community in matters of public policy and research advancement, and facilitates involvement in these areas by the people it serves.
Public awareness programs such as the MDA Art Collection and Personal Achievement Award demonstrate that disability is no barrier to creativity and service.
Designated a “Top-Rated Charity” by the American Institute of Philanthropy, MDA is the first nonprofit to receive a Lifetime Achievement Award from the American Medical Association “for significant and lasting contributions to the health and welfare of humanity.” MDA spends 77 cents of every dollar on its research, services and information programs.
MDA’s programs are supported nationally and in local communities by businesses, associations, organizations, and the care and dedication of countless individual volunteers.
I have been working at Muscular Dystrophy Association full-time (More than 3 years)
There are many many pros, the mission the families the pto, super awesome holiday time of about 2 weeks time off at Christmas and finally the return of 403b match.
The incompetent former employees who worked here, MDA has a great mission and found that many employees were not here for the misson and those folks are gone now, they have hired amazing replacements for those people and finally work is getting done, whats sad is those who feel MDA should hire more but how can they when the horrible past people are out to abuse the Mission, complain about a company that asked they do their jobs or leave and now they want to hurt the families because they were not competent employees, its a really sad situation of self centered staff in some areas. I am thankful my office and team has been great but I have seen so many people that would be better off leaving and never working for another nonprofit who depends on them again. I would say if you arent flexible and you are a horrible person who is selfish and out to hurt others you should not work here, its not for you, maybe used car sales is?
Advice to Management
Please get rid of any remaining employees who are not invested in the mission and causing others to do more work because they can’t give 100% and feel entitled to disparage everyone elses work.
I applied through other source. I interviewed at Muscular Dystrophy Association (New York, NY) in August 2018.
Company interview process bad HR work not proper becouse not informed you proper rules of company an policy are also bad company management bad not informed proper rules of company in hr round technical person not right away question
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