Type: Not-For-Profit Foundation
Address: 1275 Mamaroneck Avenue, White Plains, New York 10605, U.S.A.
Telephone: (914) 428-7100
Fax: (914) 428-8203
Web: http://www.modimes.org
Employees: 225
Sales: $181.3 million (1998)
Incorporated: 1938
NAIC: 813212 Voluntary Health Organizations
The March of Dimes is one of the most successful and well-known nonprofit foundations in the United States. It was founded to fight polio, and after the disease was controlled by the invention of a vaccine, the March of Dimes turned its efforts to eradicating birth defects. The foundation funds research, giving grants to hundreds of scientists annually at a cost of more than $20 million. It organizes fundraising events to promote awareness and bring in cash for its programs, and it helps run community services and educational projects. The March of Dimes is responsible for backing major scientific breakthroughs in genetics and prenatal health. The organization has been highly effective in advocating for women's and children's health, for example working through its volunteers to pass legislation guaranteeing women a minimum hospital stay of 48 hours after giving birth to a baby. The March of Dimes also sponsors public awareness campaigns, such as its work in the late 1990s to encourage women of childbearing age to consume folic acid to help prevent birth defects. The roster of esteemed scientists the March of Dimes has supported through grants includes ten winners of the Nobel Prize. Among these laureates are some of the most famous names in medicine, including Linus Pauling, who discovered the relationship between molecular structure and human diseases, and James Watson, the discoverer of the structure of DNA. The March of Dimes is organized into more than 90 local chapters, overseen by a national office.
The March of Dimes began as an organization to combat a baffling and fearsome disease, polio. The sickness caused an inflammation of the spinal cord that could leave its victims unable to move arms, legs, or even lungs. Although isolated outbreaks had been noted since the middle of the 19th century, it was not until 1916 that it became serious enough even to be given a name. The first devastating outbreak of polio in the United States came in the summer of 1916. It began in New York City and spread to neighboring states, striking mainly children. The cause of the outbreak was completely unknown. It began with a few cases in June, and by August almost 9,000 people had come down with the ravaging illness. The epidemic spread, finally covering 26 states, causing 6,000 deaths out of a total of some 27,000 cases. It had lasted approximately six months. Because most of the victims were less than five years old, the disease was called infantile paralysis and given the scientific name poliomyelitis, which means inflammation of the anterior spinal cord.
Most of the victims of the outbreak survived, but many had withered limbs, for which there was no acceptable treatment or therapy. Few facilities existed for the care of such disabled people, and since the cause of the disease was unknown, families who had been visited by it were subject to prejudice that they had brought it on themselves through lack of hygiene. Many outbreaks of polio followed the 1916 epidemic, devastating communities. Though most of polio's victims were young children, it also struck older people. In 1921 Franklin Delano Roosevelt, former Under-Secretary of the Navy, one-time Democratic vice-presidential candidate, and one of the leading lights of the Democratic party, became ill. On August 10 he went to bed fatigued. Two days later, his legs were paralyzed. He had polio, and he never walked unassisted again.
Roosevelt spent the next seven years trying to cure his paralysis. He was a wealthy and influential man, and he used his money on all the available treatments, from massage to stimulation with electrical currents. In 1924 he visited a spa in Georgia called Warm Springs to bathe in its naturally heated waters. Warm Springs was a resort for well-to-do Americans, but Roosevelt's fame attracted other polio victims to the spa, and it soon transformed into a therapeutic center for people trying to recover from paralysis. The waters actually did nothing to cure the paralysis and muscle atrophy, but Roosevelt was able to exercise his other muscles in the warm pools so that he had the strength to support himself on crutches or on someone's arm. He purchased Warm Springs in 1926, spending what was estimated as half his personal fortune to do so. Two years later he ran for governor of New York, and in 1932 he was elected to his first term as president.
When the nation's most famous polio victim returned to public office, he left the running of Warm Springs to his law partner, Basil O'Connor. The spa was terribly expensive to keep up, and O'Connor helped Roosevelt transform it into a nonprofit foundation for polio victims. Its new name was the Georgia Warm Springs Foundation. O'Connor began raising money from wealthy patients and their families and used these funds to help other less well-off polio sufferers. Warm Springs was soon joined by a sister foundation, the National Foundation for Infantile Paralysis. After Roosevelt became president, O'Connor used his fame as the key to fundraising. Beginning in 1935, the National Foundation inaugurated a series of fundraising balls in the month of January, pegged to fall near Roosevelt's birthday. In its first year, 6,000 balls were held across the country, and the Foundation raised close to $800,000. The money went both to patient care at Warm Springs and to funding research into the cause and prevention of poliomyelitis.
By 1938, the January balls were in decline, bringing in less and less money each year, and a new kind of promotion was needed. That year the name March of Dimes was coined by the vaudeville entertainer Eddie Cantor, who was a leading fundraiser both for the Democratic party and for the National Foundation's balls. The phrase was a play on the 'March of Time,' a popular series of newsreels. The implication of Cantor's phrase was that even a dime was of use in the fight against polio. Cantor and other entertainment world luminaries stumped for the March of Dimes campaign, urging people to send dimes to the White House. President Roosevelt established the March of Dimes foundation in January of 1938. This name was tagged onto the National Foundation's, effectively revitalizing that organization. The March of Dimes immediately began issuing research grants, giving scholarships to doctors and nurses, and providing equipment for laboratories and hospitals. The nonprofit foundation was desperately needed, because there was little government funding for medical research, no public health insurance, and little private health insurance. The March of Dimes bought iron lungs, crutches, and laboratory equipment as well as trucks to transport it in, so all that was needed could be moved quickly to regions in the midst of an outbreak. National headquarters were in Basil O'Connor's Wall Street law office, and local chapters sprang up across the country. Much fundraising was done by Hollywood stars and other popular idols. Mickey Rooney and Elvis Presley made March of Dimes fundraising appeals, as well as actresses Lucille Ball, Zsa Zsa Gabor, and Helen Hayes, among others. But the local chapters effectively raised money without star power. The March of Dimes called on ordinary people to contribute just a little money. One tactic was to go to movie theaters, stop the film in the middle, turn up the lights, and pass out a collection can. March of Dimes collection cans were placed on store counters, and people filled them with change. Children mailed in dimes on special cards.
Much of the credit for enlisting the middle class into the March of Dimes is attributed to Elaine Whitelaw. A wealthy New York society woman, Whitelaw made her career out of raising money. She first became a fundraiser during the Spanish Civil War, when she raised money for the Loyalists. During World War II, she worked with the National War Fund. In 1943 President Roosevelt appointed Whitelaw to head the national women's committee of the March of Dimes. She moved in high society circles, dining with politicians, writers, and artists. Nevertheless, Whitelaw understood that polio was an issue that touched every ordinary woman with children. She orchestrated the campaigns that had such mass appeal, and she was key to the enormous success of the organization.
Whitelaw arrived at the March of Dimes during World War II, when many men were off in the armed forces. The organization began to concentrate even more on polio as a women's issue, and more women fundraisers came into the foundation. One innovation was the poster child campaign, which began in 1946. The March of Dimes Poster Child was meant to look happy and attractive, though leg braces or some other symptom of disability was evident. These children were far from pathetic, and it was a vision of disability that had not been seen in the United States before. The image of the vibrant, though crippled, child projected hope for recovery and inspired people to give money to the foundation. Another campaign of the 1940s that was enacted all across the country was the porchlight campaign. Local chapters organized marches and told people in the community to turn their porchlights on if they wanted the marchers to stop by and collect.
The March of Dimes put its money into a variety of programs. The foundation set up more than a dozen respirator centers around the country, where doctors, physical therapists, and other health professionals worked with polio patients who had been confined to respirators. They aimed to get the patients back to breathing on their own. As this was not always possible, the March of Dimes also invested in new respirator technology so that some patients could be cared for at home. The foundation also funded rehabilitation centers, for long-term care of polio victims. In addition, the March of Dimes directly funded doctors and scientists working on curing polio. In 1949, the foundation chose Dr. Jonas Salk to lead its research efforts. By 1951, the March of Dimes had spent $1 million to support a number of scientists who finally identified all three types of polio virus. In 1953, Dr. Salk announced that a vaccine for polio was feasible, and the next year the March of Dimes organized and funded the first field trials of the vaccine. A total of 1,830,000 schoolchildren participated in the vaccine trial, and this was called the largest peacetime mobilization of volunteers in the nation's history. The organization had put $9 million toward production of the vaccine, before it was proved safe and effective. If something had gone wrong, that money would have been gambled away. But in 1955, the Salk vaccine was declared effective. Mass inoculation began, and the fear of polio quickly died away.
The March of Dimes campaign to fight polio had been a remarkable victory. The organization had worked on all fronts, responding to the emergency of local outbreaks, funding and arranging long-term care for victims, mobilizing awareness, and paying for the research that led to the vaccine. After 1955, the impetus that had led people to give money to the foundation ebbed away, and the March of Dimes was in something of a quandary. It still had debts owing to its massive spending on the vaccine, but people were not willing to be stopped in the middle of a movie for a disease that could now be easily prevented. In 1958, the organization came up with a new mission. Its work on polio mostly behind it, the March of Dimes turned to another burning issue of infant health: birth defects. At the time, the term birth defects was not in use. Parents of a baby who was born with a debilitating condition were often not given any explanation for what affected their child. The numbers or percentages of babies born with these conditions were not known, and the diseases that affected children at birth were mostly mysteries. The March of Dimes put its volunteer and fundraising organization to work in this new area. The foundation brought together scientists from diverse specialties to work together on birth defects, and as with polio, the March of Dimes had quick and concrete results. In 1961, research the March of Dimes had funded led to the development of the PKU test, which can identify and prevent some forms of mental retardation. In 1968, the organization funded the first successful bone marrow transplant used to correct a birth defect.
But birth defects had many causes, so this issue was not as focused as the fight against polio had been. Eventually, medical researchers identified approximately 3,000 distinct disorders causing birth defects. Some of these were genetic diseases, some were disorders caused by conditions in utero, and others were caused by problems with the birth itself, such as a child being born prematurely. The March of Dimes continued to use many of the techniques it had deployed during its polio campaign to raise funds to combat birth defects. The foundation used celebrities to lead fundraising and appealed to ordinary women with a variety of local events such as marches and store promotions. Elaine Whitelaw still led fundraising for the organization. She used her particular personal panache to launch glamorous events that raised hundreds of thousands of dollars for the charity. One exceedingly successful fundraiser was a fashion show, and another was the Gourmet Gala. The first Gourmet Gala was held in 1976. Hundreds of guests paid regal amounts to the March of Dimes to eat dinners prepared by celebrities and judged by cooking experts. With the money raised, the organization helped make possible many signal advances in the treatment of birth defects. Researchers it funded found in 1973 that alcohol consumption can affect fetal development. The organization also funded the first in utero treatment for a birth defect that year. The foundation had a far-reaching effect on hospital policy when it began working for the development of a regional system of neonatal intensive care units in the mid-1970s.
Education and outreach became a vital part of the March of Dimes agenda once it began work with birth defects, since some conditions turned out to be preventable. Researchers it funded had found that alcohol and drug use by the mother can influence fetal development, and other scientists had made many advances in treating birth defects before the babies were born. March of Dimes-funded doctors had perfected some in utero surgical techniques, and other researchers had discovered ways to diagnose certain birth defects prenatally. Good prenatal care was essential if doctors were to find preventable problems before birth. So in 1982 the foundation launched a public awareness campaign called 'Babies & You,' which brought prenatal education into the workplace. This was followed by several other education campaigns in the 1990s. In 1994, the organization began a program to educate women of childbearing age on the value of taking folic acid supplements, since this can prevent some particular birth defects. That same year, the March of Dimes did something of a follow-up to Babies & You, aimed more succinctly at employers and their pocketbooks. The organization put out a book entitled Healthy Babies, Healthy Business, which detailed to employers the cost to them of poor birth outcomes among their employees' children. It stressed the importance of prenatal care and gave tips to employers on how to make it easier for their workers to obtain the care they needed.
At the same time, March of Dimes funded research that led to impressive results. In 1985, research sponsored by the organization led to a new method to treat respiratory distress syndrome in infants. Four years later, a doctor funded by the foundation performed the first in utero surgery to repair a diaphragmatic hernia in an unborn child. In addition, scientists backed by the March of Dimes made a number of significant advances in the 1990s in identifying the genes responsible for particular syndromes.
The March of Dimes was also influential in getting legislation passed in the 1990s that benefited mothers and children. In 1996, the organization's volunteers were very visible in the fight to get the Mothers' and Newborns' Health Protection Act passed. This legislation guaranteed mothers a minimum hospital stay of 48 hours after delivery, ending the practice of some hospitals and insurers to send new mothers home as soon after the birth as possible. The next year, the organization was again influential in getting the State Children's Health Insurance Program passed. This legislation ensured health insurance coverage for an estimated five million children. In 1998, March of Dimes volunteer workers helped bring about the Birth Defects Prevention Act, which established a national network for monitoring birth defects.
By 1998, the March of Dimes was composed of more than 90 local chapters, with approximately three million volunteers contributing to its work. Its revenue had grown to more than $181 million. A total of 75 percent of this went to its programs, with the remainder spent on fundraising costs, management, and general expenses. The March of Dimes set aside money that year for a six-year research program. It planned to invest more than $11 million over the six years in research into methods to deliver healthy genes to patients needing gene therapy. The organization planned to spend another $3.8 million over the same period on research into the causes of premature birth. The March of Dimes also launched a new, massive public health campaign beginning in 1998 and expected to last three years. This was a $10 million effort to get the word out about the benefits of folic acid. The foundation had been working on this since the mid-1990s, and the latest campaign was an intensification of that effort. The foundation also gave out $20.5 million in grants in 1998, awarded to 300 scientists. With a lot of vital work left to do, the March of Dimes seemed to be thriving as the century came to a close, expanding its revenue and attracting a growing number of volunteers.
Further Reading
Carey, Joseph, 'New Insight into Genes: Now the Payoff,' U.S. News & World Report, August 6, 1984, p. 57.
Clune, Ray, 'A Stroke of Generosity,' Daily News Record, October 12, 1995, p. 4.
'Coke Campaign Involves March of Dimes, Coleco,' Wall Street Journal, August 24, 1984, p. 14.
'March of Dimes Still Leading the Fight for Healthy Babies After 50 Years,' American Baby, May 1988, pp. 16-19.
Noble, Barbara Presley, 'A Guide to Lower Health Care Costs,' New York Times, January 4, 1994, p. F25.
O'Neill, Molly, 'Elaine Whitelaw, 77, March of Dimes Backer, Dies,' New York Times, December 17, 1992, p. B22.
------, 'Learning To Turn Dimes into Millions,' New York Times, October 17, 1990, pp. C1, C7.
Seavey, Nina Gilden, Jane S. Smith, and Paul Wagner, A Paralyzing Fear: The Triumph Over Polio in America, New York: TV Books, 1998.
— A. Woodward
President Franklin D. Roosevelt established the March of Dimes in January 1938 to save America's youth from polio. The agency was officially known as the National Foundation for Infantile Paralysis. Roosevelt, a polio survivor, created the partnership between scientists and volunteers to conquer poliomyelitis.
Eddie Cantor, a comedian and entertainer, coined the phrase "March of Dimes." It reflected the first grass-roots fundraising campaign he started when he asked Americans to send dimes to the president.
The first president of the March of Dimes, Basil O'Connor, directed the foundation's early activities, including providing the first iron lung to assist polio victims in 1941. A year later Dr. Jonas Salk began leading research on the poliovirus. In 1953, Salk confirmed that a killed-virus vaccine for polio could stop the epidemic. In 1954, the foundation ran field trials of the Salk vaccine on 1,830,000 schoolchildren. The vaccine was declared safe the next year.
Virginia Apgar, an anesthesiologist and creator of the "Apgar Score" for newborns, was president of the foundation from 1959 to 1973. The foundation established the Salk Institute for Biological Studies in La Jolla, California in 1960. In 1962, the government licensed an oral polio vaccine developed by Dr. Albert Sabin with March of Dimes funding.
In 1958 the March of Dimes initiated its first efforts to save babies from birth defects. Subsequently, the foundation funded research on the in-utero treatment of birth defects, prenatal diagnosis of sickle cell anemia, spina bi-fida, and Marfan and Fragile X syndromes. In 1994 it began its successful folic acid campaign, which promoted the B vitamin to women of childbearing age for the prevention of birth defects of the brain and spinal cord called neural tube defects.
The March of Dimes has helped pass several national acts: the Mothers and Newborns' Health Protection Act (1996), the State Children's Health Insurance Program (S-CHIP) (1997), and the Birth Defects Prevention Act (1998). It also worked to enact the Children's Health Act of 2000. Nearly 3 million Americans volunteer with the March of Dimes.
Bibliography
Gould, Tony. A Summer Plague: Polio and its Survivors. New Haven, Conn.: Yale University Press, 1995.
Sills, David L. The Volunteers, Means and Ends in a National Organization. Glencoe, Ill.: Free Press, 1957. Reprint, New York: Arno Press, 1980.
Smith, Jane S. Patenting the Sun: Polio and the Salk Vaccine. New York: William Morrow and Company, Inc., 1990.
| March Of Dimes | |
|---|---|
| Formation | January 3, 1938 |
| Headquarters | White Plains, New York, U.S. |
| President | Jennifer L. Howse |
| Website | marchofdimes.com |
The March of Dimes Foundation is a United States nonprofit organization that works to improve the health of mothers and babies.[1] It was originally founded by then-President Franklin D. Roosevelt in 1938 to combat polio.
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Contents
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The March of Dimes is a not-for-profit organization with 501(c)(3) tax-exempt status. The mission of the March of Dimes is to improve the health of babies by preventing birth defects, premature birth and infant mortality.[2] The foundation is headquartered in White Plains, NY and has 51 chapters across the U.S., including the District of Columbia and Puerto Rico. The March of Dimes provides mothers, pregnant women and women of childbearing age with educational resources on baby health, pregnancy, preconception and new motherhood, as well as supplying information and support to families affected by prematurity, birth defects, or other infant health problems.[3]
The organization began as the National Foundation for Infantile Paralysis. The name "March of Dimes"—coined in the late 1930s by vaudeville star Eddie Cantor as a play on the contemporary newsreel series "The March of Time"—was originally used for the foundation's annual fundraising event and gradually became synonymous with that of the organization.[4] It was officially adopted as the organization’s name in 1976, when it became known as the March of Dimes Birth Defects Foundation. In 2007, the name became the March of Dimes Foundation.[5]
The group was founded by President Franklin D. Roosevelt on January 3, 1938, as a response to U.S. epidemics of polio, a condition that can leave people crippled. Roosevelt was himself diagnosed with polio in 1921, and it left him unable to move his legs. The foundation was an alliance between scientists and volunteers, with volunteers raising money to support research and education efforts.[5] Basil O’Connor, an attorney and close associate of Roosevelt, helped establish the foundation. He became its president in 1938, a position he held for more than three decades. His first task was to create a network of local chapters that could raise money and deliver aid; more than 3,100 county chapters were established during his tenure.[5] From 1938 through the approval of the Salk vaccine in 1955, the foundation spent $233 million on polio patient care, which led to more than 80 percent of U.S. polio patients' receiving significant[clarification needed] foundation aid.[6][verification needed]
With its original goal of eliminating polio accomplished, the March of Dimes faced a choice: to either disband or dedicate its resources to a new mission. Basil O’Connor, president of the March of Dimes at the time, directed his staff to identify strengths and weaknesses of the organization and reformulate its mission.[5] In 1958, the NFIP shortened its name to the National Foundation (NF) and launched its "Expanded Program" against birth defects, arthritis, and virus diseases, seeking to become a "flexible force" in the field of public health. In the mid-1960s, the organization focused its efforts on the prevention of birth defects and infant mortality, which became its mission thereafter.[7][8] At this time, the cause of birth defects was unknown; only the effects were visible. In 1976, the organization changed its name to the March of Dimes Birth Defects Foundation.[5] In 2005, reducing the toll of premature birth was added as a mission objective.
Rubella, also called German measles, is associated with a disorder called congenital rubella syndrome, which can cause miscarriages and birth defects such as deafness, blindness and mental retardation.[9] Vaccination is an effective preventive measure. On behalf of the March of Dimes, Virginia Apgar testified to the United States Senate in 1969 about the importance of federal funding of a rubella immunization program,[10] and the organization funded[clarification needed] a vaccine, which was licensed in the early 1970s.[11] In 2006, a statement published in Birth Defects Research Part A credited the "remarkable success of the immunization program to eliminate rubella is due to joint efforts by the Centers for Disease Control and Prevention, various state and local health departments, the American Academy of Pediatrics, the American College of Obstetrics and Gynecology, and the March of Dimes".[12]
In 1976, the March of Dimes published a report titled Toward Improving the Outcome of Pregnancy (TIOP), and in 1993 they published Toward Improving the Outcome of Pregnancy: The 90s and Beyond (TIOP II).[13] TIOP "stratified maternal and neonatal care into 3 levels of complexity and recommended referral of high-risk patients to centers with the personnel and resources needed for their degree of risk and severity of illness."[13] TIOP was published when "resources for the most complex care were relatively scarce and concentrated in academic medical centers."[13] TIOP II updated care complexity designations from levels I, II and III to basic, specialty and subspecialty, and the criteria were expanded.[13] In 2001, the March of Dimes introduced a family support program for those with babies in a neonatal intensive care unit (NICU).[14] The program seeks to educate NICU staff to communicate effectively with patients' families.[15][16] The March of Dimes hosted the Symposium on Quality Improvement to Prevent Prematurity in October 2009.[17][18][19] In December 2010, the March of Dimes released TIOP III, subtitled Enhancing Perinatal Health Through Quality, Safety, and Performance Initiatives.
Fetal alcohol syndrome (FAS) is categorized as a group of birth defects ranging from mental retardation to various growth and behavioral problems.[20] The March of Dimes has provided grant funding for FAS research,[21][22] and they supported the National Council on Alcoholism in its push for legislation to bring public attention to the dangers of alcohol use by pregnant women.[verification needed] This led to a 1989 law mandating a warning label about the risk of birth defects that alcoholic beverages still carry today.[23][verification needed][24]
The March of Dimes has campaigned for public education on folic acid,[25] a vitamin which can prevent spina bifida if mothers have enough of it in their body. The March of Dimes has funded polls on folic acid from The Gallup Organization.[26] Analysis of some of the results, said that women aged 18–24 years had the least awareness regarding folic acid consumption or knowledge about when it should be taken.[27] On the issue, the organization partnered with the Grain Foods Foundation, an industry group, in public education efforts.[28][29]
Awareness about preterm birth, which is associated with a variety of negative health outcomes, is an organizational goal. According to an editorial in the May 2004 issue of the Journal of the National Medical Association, the original goals of the campaign were to raise awareness of the problem from 35 percent to at least 60 percent and to decrease the rate of premature births by at least 15 percent (from 11.9 percent to 10.1 percent).[30] In 2008, the Prematurity Campaign was extended by the Board of Trustees until 2020, and global targets were set for prematurity prevention.[31] In 2008, the March of Dimes started its annual Premature Birth Report Card, which grades the nation and each individual state on preterm birth rates.[32]
March of Dimes states on its website that it supports mandated newborn screening of all babies in all states in the U.S. for at least 30 life-threatening conditions for which effective treatment and reliable testing is available to prevent catastrophic consequences to the child.[33][34]
In 2003, the March of Dimes began releasing an annual, state-by-state report card on each state’s adoption of expanded newborn screening recommended by the American College of Medical Genetics. March of Dimes president Jennifer L. Howse, Ph.D. has stated that this program is intended to inform parents of the tests available in their state, enabling those with affected babies to pursue early treatment.[35]
According to a presentation at the 2005 annual meeting of the American Public Health Association, individual, state-based March of Dimes chapters work with governors, state legislators, health departments, health professionals, and parents to improve state newborn screening programs and to make comprehensive newborn screening programs available to every newborn throughout the country.[36]
In 2005, only 38 percent of infants were born in states that required screening for 21 or more of 29 core conditions recommended by the American College of Medical Genetics; but by 2009, all 50 states and the District of Columbia required screening for 21 or more of these treatable disorders.[37]
The March of Dimes has lobbied the United States' Congress to support the continuation of the State Children's Health Insurance Program (SCHIP) in 2007 and 2009. SCHIP is a program provides health insurance to 11 million low-income children and pregnant women. March of Dimes partnered with the American Academy of Pediatrics (AAP) and the National Association of Children's Hospitals (NACH) on the issue.[38][39][40]
The March of Dimes published their Global Report on Birth Defects in 2006, which estimated birth defects' global burden.[41]
In 2009, the March of Dimes partnered with the Department of Reproductive Health and Research of the World Health Organization (RHR/WHO) to publish a white paper on the global and regional toll of preterm birth worldwide. This report, which was the first attempt to identify the global scope of premature births and related infant deaths, found that an estimated 13 million infants worldwide are born premature each year and more than one million of them die in their first month of life. Further, premature births account for 9.6 percent of total births and for 28 percent of newborn deaths. The highest rates of premature birth are in Africa, followed by North America (Canada and the United States combined).[42]
Established in 1970, the March for Babies, previously called WalkAmerica,[43] is the largest fundraiser of the year for the March of Dimes, as well as the oldest nationwide charitable walking event.[44] In the decades since, many other organizations have used the "walk-athon" format to help raise money.[45] Funds raised by the event support March of Dimes-sponsored research and other programs to prevent premature birth, birth defects and infant mortality.[46]
According to the March of Dimes, March for Babies is held in more than 900 communities across the nation. Every year, 1 million people—including 20,000 company teams, family teams and national sponsors—participate in the event, which has raised more than $1.8 billion since 1970.[47] The March of Dimes states that seventy-six cents of every dollar raised in March for Babies is spent on research and programs to help prevent premature birth, birth defects and infant mortality.[48]
Once rare in the United States, cases of pertussis (whooping cough) are appearing across the country with greater frequency.[49] To address this issue, the March of Dimes and Sanofi Pasteur launched a national education campaign in 2010 called "Sounds of Pertussis" to raise awareness about the seriousness of pertussis and the need for adult vaccination to prevent infecting babies.[49][50][dead link] NASCAR driver Jeff Gordon is a national spokesperson for the campaign.[51] The campaign recently sponsored a song-writing contest called Sound Off About Pertussis, which was won by Maria Bennett with her original song, "Give Pertussis a Whooping."[52]
In 2007, the March of Dimes, the Johnson & Johnson Pediatric Institute, and the Kentucky Department for Public Health partnered with six Kentucky hospitals to launch “Healthy Babies Are Worth the Wait,” a health promotion and prematurity prevention initiative intended to reduce the rate of preventable preterm births in targeted areas of Kentucky.[53][54] The primary goal of Healthy Babies Are Worth the Wait is a 15 percent reduction in the rate of singleton (one baby) preterm births in these targeted areas.[55]
The March of Dimes Perinatal Data Center includes the PeriStats Web site, which provides free access to U.S., state, county, and city maternal and infant health data.[56]
Animal rights organizations have raised concerns about March of Dimes-funded medical research involving animals.[58] The foundation states it supports the use of non-animal research alternatives wherever possible. March of Dimes grants for research involving animals are awarded only to studies that comply with ethical standards to protect the health and welfare of animals.[59]
The March of Dimes has been described as a bureaucracy that has taken on a life of its own through a classic example of a process called goal displacement. Faced with redundancy after Jonas Salk discovered the polio vaccine, it adopted a new mission, "fighting birth defects", which was recently changed to a vaguer goal of "breakthrough for babies", rather than disbanding.[60][61]
Charity Navigator has given the organization a rating of two stars (out of four), meaning "Meets or nearly meets industry standards but underperforms most charities in its Cause." It also notes that the president Jennifer Howse was paid $633,132 in 2009.[62]
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