Overview
What is Lymphedema Advocacy Group Lag?
The Lymphedema Advocacy Group Lag is a nonprofit organization that focuses on raising awareness and providing support for lymphedema. They achieve this through an online advocacy platform, which is utilized by approximately 4000 individuals annually. This digital platform serves as a platform for advocacy and fosters a sense of community around the cause. The organization also incurs expenses associated with travel to Washington D.C., accommodations, meals, transportation, and banquet events in order to further their mission. Ultimately, their objective is to enhance the lives of those impacted by lymphedema.
Official website here: www.lymphedematreatmentact.org
What do the Facebook reviews say about Lymphedema Advocacy Group Lag?
100% of 37 reviewers on Facebook recommend the Lymphedema Advocacy Group. Here's a summary of their testimonials:
Many individuals express their appreciation for the organization’s resources and support regarding lymphedema treatment. Users highlight the nonprofit's commitment to educating and advocating for those affected by this condition, making it a valuable resource for individuals seeking guidance.
Overall, the sentiment is overwhelmingly positive, with users feeling empowered and supported by the information provided. The group appears to effectively deliver on its mission to enhance awareness and access to treatment for lymphedema patients.
This AI summary has been generated from reviews found on Facebook.
Is Lymphedema Advocacy Group Lag legitimate?
Lymphedema Advocacy Group Lag is a legitimate nonprofit organization registered as a 501(c)(4) entity. Lymphedema Advocacy Group Lag submitted a form 990EZ, 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.
Official website here: www.lymphedematreatmentact.org
What is the mission statement of Lymphedema Advocacy Group Lag?
The Lymphedema Advocacy Group advocates for its cause primarily through an online tool, which is utilized by around 4000 individuals annually. This tool aims to raise awareness and garner support for lymphedema. Beyond this digital platform, the organization also incurs expenses related to travel, accommodations, meals, transportation, and banquet events in Washington D.C. The ultimate goal of Lymphedema Advocacy Group is to enhance the lives of those affected by this condition.
Official website here: www.lymphedematreatmentact.org
Who is the CEO of Lymphedema Advocacy Group Lag?
Heather Ferguson is the Executive Director of Lymphedema Advocacy Group Lag.
Official website here: www.lymphedematreatmentact.org
What is the revenue of Lymphedema Advocacy Group Lag?
Lymphedema Advocacy Group Lag's revenue in 2023 was $73,808.
Official website here: www.lymphedematreatmentact.org
Who are the executives of Lymphedema Advocacy Group Lag and what are their salaries?
Here are 20 key members and their salaries:
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Official website here: www.lymphedematreatmentact.org
Where can I find the form 990EZ for Lymphedema Advocacy Group Lag?
Lymphedema Advocacy Group Lag's most recent form 990EZ was submitted in 2023 and can be accessed here.
Official website here: www.lymphedematreatmentact.org
Learn more at the official website: www.lymphedematreatmentact.org
Mission Statement of Lymphedema Advocacy Group Lag
Lymphedema Advocacy Group Lag, a nonprofit organization, fosters its mission primarily through an online advocacy tool. This tool is utilized by approximately 4000 individuals annually, serving as a platform to amplify awareness and garner support for lymphedema. The group's primary objective is to enhance the lives of others affected by this condition. Beyond this digital platform, Lymphedema Advocacy Group Lag incurs expenses related to travel, accommodations, meals, transportation, and banquet events in Washington D.C., all in pursuit of their mission.
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Impact
October, 2024
Lymphedema Advocacy Group Lag significantly impacts the awareness and support for lymphedema, reaching approximately 4,000 individuals each year through its online advocacy tool. This initiative fosters a greater understanding of the condition and helps those affected find resources and community support. By organizing advocacy efforts and facilitating travel for key events in Washington, DC, the group amplifies its voice in policy discussions, pushing for better recognition and resources for individuals living with lymphedema. This commitment ultimately improves the quality of life for many, emphasizing both awareness and action.
This information is meant to be a general summary of Lymphedema Advocacy Group Lag. 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 2023.
- Gross Receipts: $73,808
Assets and Liabilities:
- Total Assets: $222,747
- Total Liabilities: $0
- Net Assets: $222,747
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Organization Details
Phone
(703) 587-7825Principal Officer
Heather Ferguson
Main Address
6031 Hanna Ct, Charlotte, NC, 28212
NTEE Category
Code: G30 - Disease
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