Overview
What is The Mpn Research Foundation?
The Mpn Research Foundation, situated in Chicago, Illinois, is a dedicated nonprofit organization that channels its resources into investigating Polycythemia Vera, Primary Myelofibrosis, and Essential Thrombocythemia, commonly referred to as MPNs. Their primary mission is to foster, finance, and support groundbreaking research aimed at uncovering the causes, developing effective treatments, and potentially discovering a cure for these conditions. The foundation actively encourages collaboration within the scientific community to expedite MPN research progress. With a team of eight dedicated individuals, they are committed to making significant strides in the field of MPN research.
Official website here: www.mpnresearchfoundation.org
What are the reviews and ratings of this charity?
Charity Navigator Rating: 100%
The MPN Research Foundation has received an exemplary Four-Star out of Four Star rating from Charity Navigator, reflecting its strong performance in accountability and finance. The foundation boasts a perfect score in financial management and transparency, with independent board members and comprehensive policies in place, which ensures that funds are utilized efficiently. Such high ratings in program expense and fundraising efficiency indicate that the organization is dedicated to maximizing the impact of its resources.
User feedback highlights the foundation as a vital resource for individuals affected by myeloproliferative neoplasms (MPNs). Reviewers praise its comprehensive website, which provides valuable information and support for patients. The foundation not only focuses on patient advocacy but also actively funds research in this specialized area, demonstrating a commitment to both education and advancements in treatment.
While user reviews are overwhelmingly positive, they primarily reflect individual experiences rather than a broad spectrum of stakeholder insights. As such, potential supporters may want to consider a range of perspectives when evaluating the foundation's overall impact and community engagement. Nonetheless, the MPN Research Foundation stands out for its dedication to service and effective use of donations.
This AI summary has been generated from information found on Charity Navigator and Great Nonprofits.
What do the Facebook reviews say about The Mpn Research Foundation?
100% of reviewers on Facebook recommend The MPN Research Foundation. Here is a summary of their reviews:
Many users express their appreciation for the foundation's efforts in raising awareness about myelofibrosis and other rare blood disorders. The organization is praised for providing valuable information that helps individuals better understand these conditions. There's a strong sentiment of hope among the reviewers as they rally behind the foundation’s goal of finding a cure.
Overall, supporters feel empowered by the foundation's mission and recognize its significant contributions to research and education in the field of myeloproliferative neoplasms. Their unwavering positivity reflects a community committed to finding solutions and supporting one another.
This AI summary has been generated from reviews found on Facebook.
Is The Mpn Research Foundation legitimate?
The Mpn Research Foundation is a legitimate nonprofit organization registered as a 501(c)(3) entity. The Mpn Research 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.
Heare are some key statistics you may want to consider:
Executive Compensation: $209,184
Professional Fundraising Fees: $0
Other Salaries and Wages: $763,321
For more financial information, click here
Official website here: www.mpnresearchfoundation.org
What is the mission statement of The Mpn Research Foundation?
The Mpn Research Foundation's primary mission is to actively promote, finance, and support groundbreaking and effective research aimed at uncovering the causes, treatments, and potentially, a cure for Essential Thrombocythemia (ET), Polycythemia Verra (PV), and Myelofibrosis (MF). The organization's funds are allocated towards research in these specific blood disorders, and it also encourages collaboration within the scientific community to expedite MPN research.
Official website here: www.mpnresearchfoundation.org
Who is the CEO of The Mpn Research Foundation?
Barbara Van Husen is the President of The Mpn Research Foundation. The CEO's salary of The Mpn Research Foundation is $209,184 and their total compensation is $209,184.
Official website here: www.mpnresearchfoundation.org
What is the revenue of The Mpn Research Foundation?
The Mpn Research Foundation's revenue in 2022 was $3,895,930.
Official website here: www.mpnresearchfoundation.org
Who are the executives of The Mpn Research Foundation and what are their salaries?
The average compensation at The Mpn Research Foundation during 2022 was $121,563. There are 8 employees and 14 volunteers at The Mpn Research Foundation.
Here are 15 key members and their salaries (The Mpn Research Foundation's CEO's salary is $209,184 and their total compensation is $209,184):
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Official website here: www.mpnresearchfoundation.org
Where can I find the form 990 for The Mpn Research Foundation?
The Mpn Research Foundation's most recent form 990 was submitted in 2022 and can be accessed here.
Official website here: www.mpnresearchfoundation.org
Learn more at the official website: www.mpnresearchfoundation.org
Mission Statement of The Mpn Research Foundation
The MPN Research Foundation, in its mission, is committed to advocating, financing, and backing research aimed at understanding the root causes, developing effective treatments, and potentially finding a cure for Essential Thrombocythemia (ET), Polycythemia Vera (PV), and Myelofibrosis (MF). This nonprofit organization's primary objective is to promote and support the most cutting-edge and successful research in these areas. Furthermore, The MPN Research Foundation encourages collaboration within the scientific community to accelerate the progress of MPN research. By funding research, this foundation plays a significant role in advancing our understanding of these diseases and bringing us closer to finding effective treatments and potential cures for individuals affected by ET, PV, and MF.
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Impact
October, 2024
The MPN Research Foundation significantly advances the understanding and treatment of myeloproliferative neoplasms (MPNs), specifically Polycythemia Vera (PV), Primary Myelofibrosis (MF), and Essential Thrombocythemia (ET). By funding innovative research initiatives, the foundation catalyzes the discovery of new treatment options and potential cures.
Through its commitment to promoting collaboration within the scientific community, the foundation fosters a cooperative environment that accelerates MPN research. This collaboration not only enhances the quality of research but also unites various experts, leading to more comprehensive studies and findings.
The foundation's focus on innovative research projects addresses the urgent need for advancements in understanding the underlying causes of these diseases, which ultimately benefits patients by paving the way for improved treatments and therapies. The impact of its work is felt across the medical and patient communities, driving hope and progress in the fight against these life-altering conditions.
This information is meant to be a general summary of The Mpn Research Foundation. Please take the time to review official sources before making any decisions based upon the content provided here.
Financials
This financial information is from Propublica.
Other financial information:
This information is from the most recently submitted tax form from this organization, which was in 2022.
- Investment Income: $150,712
- Gross Receipts: $3,895,930
Assets and Liabilities:
- Total Assets: $8,745,848
- Total Liabilities: $2,074,615
- Net Assets: $6,671,233
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Organization Details
Founding Year
1999
Phone
(312) 683-7228Principal Officer
Barbara Van Husen
Main Address
180 N MICHIGAN AVENUE 1870, CHICAGO, IL, 60601
NTEE Category
Code: H50 - Medical research
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