Louisiana Hemophilia Foundation

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

EIN: 510207472 ✦ Baton rouge, LA ✦ Designated as a 501(c)(3)

Overview

What is Louisiana Hemophilia Foundation?

The Louisiana Hemophilia Foundation is a nonprofit organization situated in Baton Rouge, Louisiana. Their mission is to enhance the lives of individuals affected by inherited bleeding disorders. They achieve this through various programs, including hosting approximately 20 educational events annually, facilitating access to medical care by addressing obstacles that hinder patients from receiving proper treatment, organizing summer camps for children, providing support service resources and connections when needed, and offering patient assistance programs such as MediAlert services and general aid. Additionally, they advocate for the cause and promote research to further improve the quality of life for those affected by inherited bleeding disorders.


Is Louisiana Hemophilia Foundation legitimate?

Louisiana Hemophilia Foundation is a legitimate nonprofit organization registered as a 501(c)(3) entity. Louisiana Hemophilia 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: $0
Professional Fundraising Fees: $0
Other Salaries and Wages: $115,495

For more financial information, click here


What is the mission statement of Louisiana Hemophilia Foundation?
Who is the CEO of Louisiana Hemophilia Foundation?
What is the revenue of Louisiana Hemophilia Foundation?
Who are the executives of Louisiana Hemophilia Foundation and what are their salaries?
Where can I find the form 990 for Louisiana Hemophilia Foundation?

Mission Statement of Louisiana Hemophilia Foundation

The Louisiana Hemophilia Foundation is committed to enhancing the lives of individuals affected by inherited bleeding disorders. Through its mission, the organization aims to achieve this by offering education, advocacy, access to care support services, and promoting research. This mission is essential in improving the quality of life for these individuals, ensuring they have the necessary resources and support to navigate their conditions.

To bring this mission to fruition, the Louisiana Hemophilia Foundation implements various programs. One such program involves providing ongoing education through approximately 20 educational events held throughout the year. This educational initiative enables individuals affected by inherited bleeding disorders to gain valuable insights and knowledge, empowering them to manage their conditions more effectively.

Another key aspect of the Louisiana Hemophilia Foundation's mission is facilitating access to medical care for these individuals. This is achieved by addressing and removing obstacles that may prevent patients from obtaining necessary medical attention. The foundation also offers support services and resources when needed, connecting individuals with the assistance they require.

Furthermore, the Louisiana Hemophilia Foundation provides patient assistance programs, including MediAlert services and general assistance when required. These programs offer crucial support to individuals affected by inherited bleeding disorders, helping them to manage their conditions and improve their overall quality of life.

In addition to its core programs, the Louisiana Hemophilia Foundation is also involved in advocacy efforts. Its advocacy work focuses on promoting policies and initiatives that support individuals affected by inherited bleeding disorders. By advocating for their rights and needs, the foundation strives to ensure that these individuals have the resources and support they require to live fulfilling lives.

Impact

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




Wednesday, July 24, 2024

The Louisiana Hemophilia Foundation is significantly impacting the lives of individuals affected by inherited bleeding disorders by providing crucial support services, education, advocacy, access to care, and research opportunities. Through approximately 20 educational events held throughout the year, the organization ensures ongoing education for individuals and families facing these challenges. They also work to remove obstacles that prevent patients from accessing necessary medical care, provide support services and resources, and offer patient assistance programs, including medical alert services and general assistance when needed. Additionally, the foundation provides access to summer camp for children affected by bleeding disorders, further enhancing their quality of life. Through their comprehensive and multifaceted approach, the Louisiana Hemophilia Foundation is making a tangible difference in the lives of those impacted by these conditions.





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: $19
  • Program Service Revenue: $215,518
  • Gross Receipts: $511,517

    • Assets and Liabilities:
  • Total Assets: $82,972
  • Total Liabilities: $24,480
  • Net Assets: $58,492
  • Programs

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

    RETREAT REVENUE

    Revenue

    $78,067

    ANNUAL MEETING

    Revenue

    $73,500

    SUMMER CAMP

    Revenue

    $23,312

    FAMILY DAY REVENUE

    Revenue

    $20,639

    COMMUNITY GATHERING

    Revenue

    $20,000

    Organization Details

    Founding Year

    1976

    Principal Officer

    Ashley Castello

    Main Address

    3084 WEST FORK DR A, BATON ROUGE, LA, 70816

    NTEE Category

    Code: G50 - Disease

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