EIN 22-1912812

Multiple Sclerosis Association of America (MSAA)

IRS 501(c) type
501(c)(3)
Num. employees
35
Year formed
1970
Most recent tax filings
2023-06-01
NTEE code, primary
Description
The Multiple Sclerosis Association of America (MSAA) is a leading resource for the entire MS community, improving lives today through vital services and support. MSAA is a national, nonprofit organization founded in 1970.
Total revenues
$8,263,229
2023
Total expenses
$8,371,784
2023
Total assets
$8,324,074
2023
Num. employees
35
2023

Program areas at MSAA

1- patient services: msaa's mri access program provides assistance for ms patients or individuals who have a suspected ms diagnosis or who have an ms diagnosis and need mri scans for the purpose of providing a diagnosis or tracking progression. Msaa's mri, cooling and equipment program serves individuals whose income is below 300% of the federal poverty guidelines and are otherwise unable to afford mri's, cooling vests and safety equipment items. During fy23, msaa approved more than 1,000 eligible individuals for mri scans with a value in excess of $518,000. (continue in schedule o)msaa's equipment distribution program helps individuals with ms obtain equipment items that they need in order to best manage their ms. msaa's cooling program provides cooling apparel that helps to alleviate heat sensitivity issues for ms patients throughout the country. During fy23 msaa delivered nearly 2,200 pieces of safety, mobility, and cooling products to individuals affected by ms with a value in excess of $263,000. During fy21 msaa expanded the hours of its national toll-free helpline and made several revisions to our core signature services in response to the coronavirus pandemic and its impact on the ms community. (msaa's extended helpline hours continued throughout fy22 and have remained in fy23.) All three programs now offer online applications which can be found on mymsaa.org. Program applications are also available as pdf downloads in both english and spanish from the website. Throughout the fiscal year, msaa hosted well-attended virtual educational programs to address vital topics to the ms community including webinars on health disparities among the african american and hispanic american populations, ms research, nutrition, and wellness, as well as other important topics.
Msaa received the following awards during fy23: apex award for excellence for the winter/spring 2022 edition of the motivator magazine featuring the cover story, the therapeutic value of the arts; silver digital health award for msaa's covid-19 vaccines and ms video series; merit digital health award for msaa's ultimate ms treatment guide; merit digital health award for msaa's art showcase. In addition, there were 413,000 cumulative views of msaa's 140 on-demand video programs, 61,000+ total cumulative downloads of msaa's mobile app, my ms manager, 4,200 total downloads of episodes of msaa's podcast and more than 8,300 cumulative members of my msaa community, msaa's online peer to peer forum.
2- public education, information & referral: the msaa's national educational programs deliver high-quality, informative programming to ms patients, care partners and healthcare professionals nationwide. These programs cover a variety of topics all aimed at improving health outcomes for ms patients. Msaa partners with a national network of healthcare professionals to present programs of scientific and educational value. These in-person and virtual educational programs cover a wide breadth of topics, ranging from advances in disease research and symptom management, to nutrition and wellness activities as well as programs tailored to men/women living with ms and programs curated for underserved populations. (continue in schedule o) msaa also regularly offers virtual and digital-programming focused on scientific updates in disease management and best practices in treatment protocol for health care professionals that treat those living with ms, such as neurologists and nurses. In 2019, msaa also convened the ms african-american advisory board, and a hispanic/latinx advisory board comprised of ms healthcare professionals, patients and care partners, to develop a five year plan of initiatives to serve the african-american and hispanic/latinx ms patient communities. Additionally, msaa convened a series of round table discussions with leading ms neurologists and payers to explore how the healthcare system could better serve the ms community and identify common interests. The findings from both of these initiatives are being developed as white papers and will be broadly disseminated within the ms community.through publications, videos, podcasts, the Association's website, a helpline, and educational programs, the Association provides the ms community and the general public with vital information about the disease, the management of symptoms and breakthroughs in research. The Association publishes a national magazine the motivator distributed biannually with a circulation of approximately 95,000. The magazine is also available as a digital edition. Individual client needs are met through the Association's national toll-free helpline. Our trained social workers responded to more than 19,000 client inquiries in fy23 and provided these clients with contacts to appropriate services throughout the nation. Msaa's website had more than 680,000 sessions during the year ended june 30, 2023. The Association offers a mobile phone application to assist its clients in monitoring, tracking and managing their ms as well as sharinge data with their physician. The Association employs various digital tactics to communicate with its constituents. The Association is active on 6 different social media platforms. The Association also hosts a blog, offers an online peer-to-peer community and answers questions through its ms questions email option and website chat feature. The Association received a google grant valued at $130,000 in fy'23. This allowed the Association to promote the organization's programs and services via keywords through google's search engine in an effort to assist individuals searching for information online related to ms.
In 2022, msaa released the ultimate ms treatment guide, a first of its kind reference tool that aides those living with ms, their loved ones, and community neurologists in better understanding the wide array of disease modifying therapies available to the ms community. The ultimate ms treatment guide is fully interactive and allows users to filter available therapy options by type of ms, how it's taken, and by date approved by the fda. The ultimate ms treatment guide also includes in-depth testimonials from leading ms specialists and patient advocates on each of its pages, as well as a comparison tool, allowing a user to directly compare up to three ms therapies at one time.

Who funds Multiple Sclerosis Association of America (MSAA)

Grants from foundations and other nonprofits
GrantmakerDescriptionAmount
The Cameron and Jane Baird FoundationServices for People With Multiple Sclerosis$85,000
Fidelity Investments Charitable Gift FundFor Grant Recipient's Exempt Purposes$45,320
American Online Giving FoundationGeneral Support$36,714
...and 54 more grants received totalling $348,790

Personnel at MSAA

NameTitleCompensation
Gina R MurdochPresident and Chief Executive Officer$297,133
Andrea GriffinVice President of Communications and Marketing$146,390
Rebecca MooneyVice President of Development$149,643
Kyle PinionVice President of Mission Delivery$114,400
Jennifer SchwartzChairperson$0
...and 16 more key personnel

Financials for MSAA

RevenuesFYE 06/2023
Total grants, contributions, etc.$8,039,357
Program services$104,564
Investment income and dividends$141,631
Tax-exempt bond proceeds$0
Royalty revenue$0
Net rental income$0
Net gain from sale of non-inventory assets$-77,598
Net income from fundraising events$-8,986
Net income from gaming activities$0
Net income from sales of inventory$0
Miscellaneous revenues$64,261
Total revenues$8,263,229

Form 990s for MSAA

Fiscal year endingDate received by IRSFormPDF link
2023-062023-11-11990View PDF
2022-062023-03-14990View PDF
2022-062022-11-11990View PDF
2021-062021-11-15990View PDF
2020-062021-02-22990View PDF
...and 10 more Form 990s
Data update history
August 25, 2024
Received grants
Identified 8 new grant, including a grant for $85,000 from The Cameron and Jane Baird Foundation
May 18, 2024
Received grants
Identified 1 new grant, including a grant for $7,500 from Tides Foundation
January 2, 2024
Posted financials
Added Form 990 for fiscal year 2023
January 2, 2024
Received grants
Identified 10 new grant, including a grant for $31,030 from America's Charities (AC)
December 25, 2023
Used new vendors
Identified 3 new vendors, including , , and
Nonprofit Types
Grantmaking organizationsDisease research fundraisersBusiness and community development organizationsHeadquarter / parent organizationsCharities
Issues
HealthEducationDiseases and disordersCommunity improvementBusiness and industry
Characteristics
Conducts researchFundraising eventsNational levelCommunity engagement / volunteeringGala fundraisersFundraising races, competitions, and tournamentsTax deductible donationsAccepts online donations
General information
Address
375 Kings Hwy North
Cherry Hill, NJ 08034
Metro area
Philadelphia-Camden-Wilmington, PA-NJ-DE-MD
County
Camden County, NJ
Website URL
mymsaa.org/ 
Phone
(800) 532-7667
Facebook page
msassociation 
Twitter profile
@msassociation 
IRS details
EIN
22-1912812
Fiscal year end
June
Taxreturn type
Form 990
Year formed
1970
Eligible to receive tax-deductible contributions (Pub 78)
Yes
Categorization
NTEE code, primary
S41: Promotion of Business
NAICS code, primary
813212: Health and Disease Research Fundraising Organizations
Parent/child status
Independent
California AB-488 details
AB 488 status
May Operate or Solicit for Charitable Purposes
Charity Registration status
Current
FTB status revoked
Not revoked
AG Registration Number
075273
FTB Entity ID
2563621
AB 488 data last updated ("as-of") date
2024-11-06
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