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Hemophilia Foundation Of Michigan

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

EIN: 381905673 ✦ Ypsilanti, MI ✦ Designated as a 501(c)(3)

Overview

What is Hemophilia Foundation Of Michigan?

The Hemophilia Foundation of Michigan, situated in Ypsilanti, Michigan, is a dedicated nonprofit organization. Its primary mission is to enhance the lives of individuals affected by hemophilia, Von Willebrand disease, and other related bleeding and clotting disorders, including HIV/AIDS and hepatitis. To accomplish this, they provide administrative support and federal pass-through funding to 19 treatment centers that deliver comprehensive care. Their activities extend beyond direct medical services, encompassing community education, prevention, short-term counseling, and referral services, as well as organizing camps and advocating for relevant policies. The foundation also offers programs like short-term counseling, referral, and education to improve overall well-being and quality of life for those affected.


Official website here: www.hfmich.org

Is Hemophilia Foundation Of Michigan legitimate?

Hemophilia Foundation Of Michigan is a legitimate nonprofit organization registered as a 501(c)(3) entity. Hemophilia Foundation Of Michigan 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: $203,056
Professional Fundraising Fees: $0
Other Salaries and Wages: $960,288

For more financial information, click here


Official website here: www.hfmich.org

What is the mission statement of Hemophilia Foundation Of Michigan?

The Hemophilia Foundation of Michigan, in its mission, strives to enhance the quality of life for individuals afflicted by hemophilia, Von Willebrand disease, various coagulation disorders, and related complications such as HIV/AIDS and hepatitis. To achieve this, the foundation offers multiple programs, including community education, prevention, short-term counseling and referral, camps, and advocacy. Its primary goal is to improve the overall wellbeing of those affected by these conditions. Under the Federal Hemophilia Programs, the Hemophilia Foundation of Michigan provides supervision to 19 hemophilia treatment center grantees, ensuring comprehensive care for individuals with hemophilia and other bleeding and clotting disorders. The foundation offers administrative support and federal pass-through funding for these centers. In essence, the Hemophilia Foundation of Michigan is committed to improving the lives of individuals with hemophilia and related disorders, providing essential resources and support services, and advocating for better care and understanding of these conditions.


Official website here: www.hfmich.org

Who is the CEO of Hemophilia Foundation Of Michigan?

Susan Lerch is the President of Hemophilia Foundation Of Michigan.


Official website here: www.hfmich.org

What is the revenue of Hemophilia Foundation Of Michigan?

Hemophilia Foundation Of Michigan's revenue in 2022 was $3,850,387.


Official website here: www.hfmich.org

Who are the executives of Hemophilia Foundation Of Michigan and what are their salaries?

The average compensation at Hemophilia Foundation Of Michigan during 2022 was $68,432. There are 17 employees and 30 volunteers at Hemophilia Foundation Of Michigan.

Here are 12 key members and their salaries:

    Susan Lerch (Executive Di) [Trustee/Director]
  • Compensation: $163,504
  • Related: $0
  • Other: $39,552

    • Gwyn Hulswit (Associate Di)
  • Compensation: $100,683
  • Related: $0
  • Other: $28,250

    • Jim Mohnach (President) [Trustee/Director]
  • Compensation: $0
  • Related: $0
  • Other: $0

    • Elliot Jones (Vice Preside) [Trustee/Director]
  • Compensation: $0
  • Related: $0
  • Other: $0

    • Troy Briggs (Treasurer) [Trustee/Director]
  • Compensation: $0
  • Related: $0
  • Other: $0

    • Patrick Monks (Secretary) [Trustee/Director]
  • Compensation: $0
  • Related: $0
  • Other: $0

    • Kathy Fessler Phd Md (Director)
  • Compensation: $0
  • Related: $0
  • Other: $0

    • Amy Shapiro (Ex Officio) [Trustee/Director]
  • Compensation: $0
  • Related: $0
  • Other: $0

    • Kathleen Donohoe (Director)
  • Compensation: $0
  • Related: $0
  • Other: $0

    • Jason Rogers (Director)
  • Compensation: $0
  • Related: $0
  • Other: $0

    • David Hart (Director)
  • Compensation: $0
  • Related: $0
  • Other: $0

    • Ismael Jaber (Director)
  • Compensation: $0
  • Related: $0
  • Other: $0


  • Official website here: www.hfmich.org

    Where can I find the form 990 for Hemophilia Foundation Of Michigan?

    The Hemophilia Foundation Of Michigan’s most recent form 990 was submitted in 2022 and can be accessed here


    Official website here: www.hfmich.org

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

    Mission Statement of Hemophilia Foundation Of Michigan

    The Hemophilia Foundation of Michigan, abbreviated as HFM, is committed to enhancing the quality of life for individuals affected by hemophilia, Von Willebrand disease, other coagulation disorders, and related complications, such as HIV/AIDS and hepatitis. This nonprofit organization strives to achieve this mission by providing support and resources for those in need.

    One of the ways HFM fulfills its mission is through its involvement in the Federal Hemophilia Programs. The foundation supervises 19 hemophilia treatment center grantees, ensuring these centers deliver comprehensive care to individuals with hemophilia and other bleeding and clotting disorders. HFM offers administrative support and federal pass-through funding to these treatment centers.

    In addition to its work with the Federal Hemophilia Programs, HFM engages in various initiatives to support its mission. These include community education, prevention, short-term counseling and referral, camps, and advocacy. By providing these services, HFM aims to improve the overall well-being of individuals impacted by these conditions, offering them the tools and resources they need to lead fulfilling lives.

    Impact

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




    Saturday, July 20, 2024

    The Hemophilia Foundation of Michigan plays a crucial role in improving the quality of life for individuals affected by hemophilia, Von Willebrand disease, and other coagulation disorders. They provide supervision to 19 hemophilia treatment center grantees under federal programs, offer community education, prevention initiatives, short-term counseling and referrals, camps, and advocacy efforts. Through their work, they ensure that comprehensive care is delivered to those with these conditions, including related complications such as HIV/AIDS and hepatitis.





    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: $20,977
  • Program Service Revenue: $60,583
  • Gross Receipts: $3,865,962

    • Assets and Liabilities:
  • Total Assets: $3,079,008
  • Total Liabilities: $317,383
  • Net Assets: $2,761,625
  • Programs

    Programs are reported by nonprofits in their tax forms and are normally their tax-exempt activities.

    ADVERTISING

    Revenue

    $60,583

    Organization Details

    Founding Year

    1970

    Principal Officer

    Susan Lerch

    Main Address

    1921 WEST MICHIGAN AVENUE, YPSILANTI, MI, 48197

    NTEE Category

    Code: G20 - Disease

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