Overview
What is Lowe Syndrome Association?
The Lowe Syndrome Association is a nonprofit organization dedicated to enhancing the lives of individuals with Lowe Syndrome and their families. Their mission encompasses fostering communication, delivering education, and backing research, aiming to help those affected achieve their full potential. The organization's efforts center around community education and supporting research, ultimately contributing to a better quality of life for all involved.
Official website here: www.lowesyndrome.org/
What do the Facebook reviews say about Lowe Syndrome Association?
90% of the 7 reviewers on Facebook recommend the Lowe Syndrome Association. Here is a summary of their reviews:
Many individuals express deep gratitude towards the organization for the support and resources provided, highlighting its role in connecting families with necessary medical professionals. The sense of community fostered through meetings and interactions is also a standout feature, with some users mentioning the meaningful friendships formed as a result of their involvement.
Overall, the testimonials reflect a positive sentiment, with users feeling that the association significantly impacts their lives and those of their loved ones. The dedication and effectiveness of the organization in addressing the needs of families affected by Lowe Syndrome are well appreciated.
This AI summary has been generated from reviews found on Facebook.
Is Lowe Syndrome Association legitimate?
Lowe Syndrome Association is a legitimate nonprofit organization registered as a 501(c)(3) entity. Lowe Syndrome Association 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: $0
Professional Fundraising Fees: $0
Other Salaries and Wages: $10,063
For more financial information, click here
Official website here: www.lowesyndrome.org/
What is the mission statement of Lowe Syndrome Association?
The Lowe Syndrome Association seeks to enhance the lives of individuals affected by Lowe Syndrome and their families. They accomplish this mission through various means, including communication and education, as well as supporting research. Their ultimate goal is to enable those with Lowe Syndrome to achieve their fullest potential. The organization's activities are geared towards improving the overall well-being of affected families, providing them with the necessary resources and knowledge to navigate their challenges.
Official website here: www.lowesyndrome.org/
Who is the CEO of Lowe Syndrome Association?
Jeri Kubicki is the Vice President of Lowe Syndrome Association.
Official website here: www.lowesyndrome.org/
What is the revenue of Lowe Syndrome Association?
Lowe Syndrome Association's revenue in 2022 was $207,028.
Official website here: www.lowesyndrome.org/
Who are the executives of Lowe Syndrome Association and what are their salaries?
The average compensation at Lowe Syndrome Association during 2022 was $10,063. There is 1 employee at Lowe Syndrome Association.
Here are 8 key members and their salaries:
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Official website here: www.lowesyndrome.org/
Where can I find the form 990 for Lowe Syndrome Association?
Lowe Syndrome Association's most recent form 990 was submitted in 2022 and can be accessed here.
Official website here: www.lowesyndrome.org/
Learn more at the official website: www.lowesyndrome.org/
Mission Statement of Lowe Syndrome Association
The Lowe Syndrome Association, a dedicated organization, strives to enhance the lives of individuals affected by Lowe Syndrome and their families. Their mission is accomplished through three primary avenues: communication, education, and the support of research. This approach aims to empower those with Lowe Syndrome and their families, enabling them to reach their full potential. By fostering open dialogue, providing educational resources, and backing research initiatives, the Lowe Syndrome Association is committed to making a significant impact on the lives of those affected by this condition.
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Impact
October, 2024
The Lowe Syndrome Association significantly impacts individuals with Lowe Syndrome and their families by enhancing community awareness and understanding of the condition. Through effective communication and education, they empower families with knowledge that enables better management and support for their loved ones. By advocating for and supporting research initiatives, the association actively contributes to advancements in treatment and care options, aiming to improve the quality of life and help individuals reach their highest potential. Their work fosters a stronger sense of community among families, creating a network of support that plays a crucial role in navigating the challenges posed by Lowe Syndrome.
This information is meant to be a general summary of Lowe Syndrome Association. 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: $1,052
- Program Service Revenue: $16,347
- Gross Receipts: $209,749
Assets and Liabilities:
- Total Assets: $1,102,649
- Total Liabilities: $57
- Net Assets: $1,102,592
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Programs
Programs are reported by nonprofits in their tax forms and are normally their tax-exempt activities.
Conference Fees
Revenue
$16,347
Organization Details
Founding Year
1983
Phone
(910) 622-4455Principal Officer
Jeri Kubicki
Main Address
8190 Beechmont Avenue Ste Suite 111, Cincinnati, OH, 45255
Website
www.lowesyndrome.org/NTEE Category
Code: G20 - Disease
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