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Muscular Dystrophy Family Foundation

Learn about this cause: Is it Legit? Do I like the mission? What is the CEO's salary?

EIN: 351040153 ✦ Carmel, IN ✦ Designated as a 501(c)(3)

Overview

What is Muscular Dystrophy Family Foundation?

The Muscular Dystrophy Family Foundation, based in Carmel, Indiana, is a dedicated nonprofit organization that focuses on improving the lives of individuals with neuromuscular diseases, such as muscular dystrophy. Over the past nine years, they have shown their commitment by purchasing an accessible van annually for a deserving family and providing over $745,000 in adaptive equipment to families in need. Their mission revolves around advocacy, education, and financial assistance, aiming to enhance the quality of life and independence of people with muscular dystrophy, thus empowering their families. In 2022, the Parker, O'Connor, and Winegardner families of Indianapolis were the fortunate recipients of an accessible van through their Give-Away program, with a cost of $107,571.


Official website here: www.mdff.org

Is Muscular Dystrophy Family Foundation legitimate?

Muscular Dystrophy Family Foundation is a legitimate nonprofit organization registered as a 501(c)(3) entity. Muscular Dystrophy Family Foundation submitted a form 990, which is a tax form used by tax-exempt organizations in the U.S., indicating its operational transparency and adherence to regulatory requirements. Donations to this organization are tax deductible.

Here are some key statistics you may want to consider:

Executive Compensation: $72,093
Professional Fundraising Fees: $0
Other Salaries and Wages: $0

For more financial information, click here


Official website here: www.mdff.org

What is the mission statement of Muscular Dystrophy Family Foundation?

The Muscular Dystrophy Family Foundation's mission is to enhance the quality of life and promote independence for individuals with muscular dystrophy and their families. This is achieved through advocacy, education, and financial assistance. Over the past nine years, the foundation has provided at least one accessible van to a family annually and has distributed over $745,000 in adaptive equipment. The organization's primary goal is to empower those affected by muscular dystrophy, offering them the necessary support to live their best lives. The foundation's activities include an annual accessible van giveaway program to assist families in need.


Official website here: www.mdff.org

Who is the CEO of Muscular Dystrophy Family Foundation?

Tim Doyle is the Director of Muscular Dystrophy Family Foundation.


Official website here: www.mdff.org

What is the revenue of Muscular Dystrophy Family Foundation?

Muscular Dystrophy Family Foundation's revenue in 2022 was $469,590.


Official website here: www.mdff.org

Who are the executives of Muscular Dystrophy Family Foundation and what are their salaries?

The average compensation at Muscular Dystrophy Family Foundation during 2022 was $24,031. There are 3 employees and 10 volunteers at Muscular Dystrophy Family Foundation.

Here are 10 key members and their salaries:

    Jim Badger (Director)
  • Compensation: $0
  • Related: $0
  • Other: $0

    • Mindy Cameron (Director)
  • Compensation: $0
  • Related: $0
  • Other: $0

    • Justin Rumer (Director)
  • Compensation: $0
  • Related: $0
  • Other: $0

    • Nikki Hybben (Director)
  • Compensation: $0
  • Related: $0
  • Other: $0

    • Barney Quinn (Director)
  • Compensation: $0
  • Related: $0
  • Other: $0

    • Jacob Buehler (Director)
  • Compensation: $0
  • Related: $0
  • Other: $0

    • Tim Doyle (President)
  • Compensation: $0
  • Related: $0
  • Other: $0

    • Matt Sigler (Vice President)
  • Compensation: $0
  • Related: $0
  • Other: $0

    • David Thyen (Secretary)
  • Compensation: $0
  • Related: $0
  • Other: $0

    • Omar Rosas (Treasurer)
  • Compensation: $0
  • Related: $0
  • Other: $0


  • Official website here: www.mdff.org

    Where can I find the form 990 for Muscular Dystrophy Family Foundation?

    The Muscular Dystrophy Family Foundation’s most recent form 990 was submitted in 2022 and can be accessed here


    Official website here: www.mdff.org

    Learn more at the official website: www.mdff.org

    Mission Statement of Muscular Dystrophy Family Foundation

    The Muscular Dystrophy Family Foundation, a charitable organization, aims to enhance the quality of life and promote independence for individuals diagnosed with muscular dystrophy and their families. Utilizing the power of philanthropy, this foundation implements advocacy, education, and financial assistance initiatives. Their mission is to empower these individuals and their families, providing them with the necessary support to navigate their challenges more effectively.

    Over the past nine years, the Muscular Dystrophy Family Foundation has demonstrated its commitment to this mission by purchasing at least one accessible van annually for a deserving family. In addition, they have distributed over $745,000 worth of adaptive equipment to families in need. These resources have played a significant role in improving the mobility and everyday lives of these individuals, thereby enhancing their overall independence.

    In essence, the Muscular Dystrophy Family Foundation is dedicated to making a tangible difference in the lives of individuals affected by muscular dystrophy. Through their advocacy, education, and financial assistance programs, they empower these individuals and their families to live more fulfilling lives, despite the challenges posed by this condition.

    Impact

    This information is meant to be a general summary of Muscular Dystrophy Family Foundation. Please take the time to review official sources before making any decisions based upon the content provided here.




    Wednesday, July 24, 2024

    The Muscular Dystrophy Family Foundation's impact is significant and direct. They assist individuals with neuromuscular diseases, including muscular dystrophy, by purchasing accessible vans for families in need. Over the past nine years, they have purchased at least one accessible van each year and provided over $745,000 in adaptive equipment to families. Their annual accessible van giveaway program, like the recent one in 2022 for the Parker, O'Connor, and Winegardner families of Indianapolis, Indiana, exemplifies their commitment to increasing the quality of life and independence of people with muscular dystrophy. Their advocacy, education, and financial assistance initiatives empower both individuals with the disease and their families, making a tangible impact on their lives.





    Financials

    This financial information is from Propublica.

    Revenue
    Expenses
    Efficiency

    Other financial information:

    This information is from the most recently submitted tax form from this organization, which was in 2022.

  • Investment Income: $10,661
  • Program Service Revenue: $0
  • Gross Receipts: $557,100

    • Assets and Liabilities:
  • Total Assets: $734,362
  • Total Liabilities: $0
  • Net Assets: $734,362
  • Organization Details

    Founding Year

    1958

    Principal Officer

    Tim Doyle

    Main Address

    PO BOX 776, CARMEL, IN, 46032

    NTEE Category

    Code: G52Z - Disease

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