Als Association Louisiana-Mississippi Ch

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

EIN: 201742120 ✦ Baton rouge, LA ✦ Designated as a 501(c)(3)

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Overview

What is Als Association Louisiana-Mississippi Ch?

The Als Association Louisiana-Mississippi Chapter is a nonprofit organization situated in Baton Rouge, Louisiana. Their primary mission is to combat Lou Gehrig's disease, also known as ALS, by engaging in global research and advocacy efforts nationwide. They strive to empower individuals diagnosed with ALS to lead fulfilling lives. The core of their operations includes conducting in-home assessments for individuals with ALS, providing resources, and serving as advocates. They also offer a durable medical equipment and assistive technology loan closet, support group meetings, respite care for caregivers, a multi-disciplinary clinic, and transportation services to attend the clinic. With a team of nine dedicated individuals, the Als Association Louisiana-Mississippi Chapter provides comprehensive care to individuals living with ALS and their families.


Official website here: www.alsalams.org

Is Als Association Louisiana-Mississippi Ch legitimate?

Als Association Louisiana-Mississippi Ch is a legitimate nonprofit organization registered as a 501(c)(3) entity. Als Association Louisiana-Mississippi Ch 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: $0

For more financial information, click here


Official website here: www.alsalams.org

What is the mission statement of Als Association Louisiana-Mississippi Ch?

The Als Association Louisiana-Mississippi Chapter is committed to leading the fight against ALS, also known as Lou Gehrig's disease. Their mission is twofold: to drive global research aimed at treating and ultimately curing ALS, and to advocate nationwide for those affected by the disease. Furthermore, they strive to empower individuals with ALS to live fuller lives. Their activities include providing care services, such as in-home assessments, resource advocacy, and access to durable medical equipment. They also offer support groups, respite care for caregivers, and a multidisciplinary clinic. Additionally, they have a transportation program to facilitate access to medical care.


Official website here: www.alsalams.org

Who is the CEO of Als Association Louisiana-Mississippi Ch?

Greg Mitchell is the Cfo of Als Association Louisiana-Mississippi Ch.


Official website here: www.alsalams.org

What is the revenue of Als Association Louisiana-Mississippi Ch?

Als Association Louisiana-Mississippi Ch's revenue in 2021 was $3,700.


Official website here: www.alsalams.org

Who are the executives of Als Association Louisiana-Mississippi Ch and what are their salaries?

There are 9 employees and 53 volunteers at Als Association Louisiana-Mississippi Ch.


There is 1 key member and their salary:


Greg Mitchell (Cfo)
  • Compensation: $0
  • Related: $0
  • Other: $0


Official website here: www.alsalams.org

Where can I find the form 990 for Als Association Louisiana-Mississippi Ch?

Als Association Louisiana-Mississippi Ch's most recent form 990 was submitted in 2021 and can be accessed here.


Official website here: www.alsalams.org

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

Mission Statement of Als Association Louisiana-Mississippi Ch

The Als Association Louisiana-Mississippi Chapter is committed to leading the fight against Amyotrophic Lateral Sclerosis (ALS), also known as Lou Gehrig's disease. Their mission is multifaceted, focusing on both research and advocacy to treat and cure ALS, while simultaneously empowering individuals living with the condition to lead fuller lives.

Through global research, this nonprofit organization is dedicated to uncovering new treatments and potential cures for ALS. By collaborating on a national level, they aim to advance the understanding of this debilitating disease and bring hope to those affected by it.

In addition to their research efforts, the Als Association Louisiana-Mississippi Chapter is also deeply involved in advocacy. They strive to influence policies and legislation at both the state and national levels, with the goal of improving the lives of those with ALS and increasing awareness of the disease. By advocating for their cause, they aim to create a more supportive environment for individuals with ALS and their families.

In essence, the Als Association Louisiana-Mississippi Chapter is a beacon of hope for those affected by ALS. They are not only fighting for a cure but also working to improve the quality of life for individuals living with the disease, empowering them to lead fuller lives. Their mission is a testament to their commitment to making a difference in the lives of those affected by ALS.

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Impact




October, 2024

The Als Association Louisiana-Mississippi Chapter significantly impacts the lives of individuals affected by ALS (Amyotrophic Lateral Sclerosis) and their families. Through a comprehensive Care Services Program, they provide personalized in-home assessments to understand the unique needs of people with ALS and support their families. By acting as advocates, they navigate available resources to ensure patients receive the necessary assistance.

Their services include a durable medical equipment and assistive technology loan closet, enabling access to essential tools for daily living. Support group meetings foster community among those affected and their caregivers, offering emotional support and shared experiences. The chapter also provides respite care, relieving caregivers from their demanding roles while ensuring that their loved ones are well cared for.

A notable aspect of their work is the multidisciplinary clinic at Our Lady of Lourdes Regional Medical Center in Lafayette, which offers specialized care under one roof. Additionally, the transportation program eases access to this clinic, ensuring that individuals with ALS can receive timely medical attention.

Through advocacy and support initiatives, this chapter not only contributes to the fight against ALS but also empowers individuals to lead fuller lives despite their diagnosis.




This information is meant to be a general summary of Als Association Louisiana-Mississippi Ch. 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.

Revenue
$375,322 (2021)
Expenses
$491,642 (2021)
Efficiency

Other financial information:

This information is from the most recently submitted tax form from this organization, which was in 2021.

  • Gross Receipts: $3,700

Assets and Liabilities:

  • Total Assets: $0
  • Total Liabilities: $0
  • Net Assets: $0

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Organization Details

Founding Year

2005

Principal Officer

Greg Mitchell

Main Address

14241 Coursey Blvd A12374, BATON ROUGE, LA, 70817

NTEE Category

Code: G50 - Disease

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