Overview
What is The Joe Martin Als Foundation?
The Joe Martin ALS Foundation, located in Charlotte, North Carolina, is a nonprofit organization dedicated to supporting individuals and families affected by Amyotrophic Lateral Sclerosis (ALS), also known as Lou Gehrig's disease. Their primary mission involves providing homecare aides to assist patients with daily living activities, offering exercise sessions to improve their health, offering respite care to give family members a break, training family members and patients to use assistive devices, loaning such devices to patients, providing transportation, and helping with travel planning and other tasks. The Foundation's significant contribution is delivering these services at no cost, catering to around 16 families per week, totaling approximately 4,992 hours of respite care annually.
Official website here: www.joemartinalsfoundation.org
Is The Joe Martin Als Foundation legitimate?
The Joe Martin Als Foundation is a legitimate nonprofit organization registered as a 501(c)(3) entity. The Joe Martin Als 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: $100,000
Professional Fundraising Fees: $0
Other Salaries and Wages: $184,874
For more financial information, click here
Official website here: www.joemartinalsfoundation.org
What is the mission statement of The Joe Martin Als Foundation?
The Joe Martin ALS Foundation's mission is centered around supporting individuals diagnosed with Amyotrophic Lateral Sclerosis (ALS), often referred to as Lou Gehrig's disease, and their families. The organization provides various services to aid these individuals in their daily lives. This includes supplying homecare aides to assist with activities such as getting in and out of bed, eating, showering, and dressing. Exercise sessions are also offered to improve blood circulation, reduce swelling, and prevent complications. Respite care is provided to allow family members to attend to their own needs. The Foundation trains family members and ALS patients to use equipment and devices for communication, loans assistive devices, offers transportation, and assists with travel planning. These services are offered without charge to the recipients.
Official website here: www.joemartinalsfoundation.org
Who is the CEO of The Joe Martin Als Foundation?
Neil Cottrell is the President of The Joe Martin Als Foundation.
Official website here: www.joemartinalsfoundation.org
What is the revenue of The Joe Martin Als Foundation?
The Joe Martin Als Foundation's revenue in 2022 was $451,741.
Official website here: www.joemartinalsfoundation.org
Who are the executives of The Joe Martin Als Foundation and what are their salaries?
The average compensation at The Joe Martin Als Foundation during 2022 was $35,609. There are 8 employees and 150 volunteers at The Joe Martin Als Foundation.
Here are 7 key members and their salaries:
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Official website here: www.joemartinalsfoundation.org
Where can I find the form 990 for The Joe Martin Als Foundation?
The Joe Martin Als Foundation's most recent form 990 was submitted in 2022 and can be accessed here.
Official website here: www.joemartinalsfoundation.org
Learn more at the official website: www.joemartinalsfoundation.org
Mission Statement of The Joe Martin Als Foundation
The Joe Martin ALS Foundation is dedicated to serving individuals and families affected by Amyotrophic Lateral Sclerosis (ALS), also known as Lou Gehrig's disease. Their mission is threefold. Firstly, they provide homecare aides to assist ALS patients with their daily living activities, such as getting in and out of bed, eating, showering, and dressing. Secondly, the Foundation offers exercise sessions designed to improve blood circulation, reduce swelling, prevent contracture, and maintain bone density. This is crucial in managing the symptoms of ALS. Thirdly, they offer respite care, providing family members with the opportunity to attend to their own needs, ensuring they can continue to support their loved ones while also taking care of themselves.
Beyond these direct services, The Joe Martin ALS Foundation also provides training for family members and patients on how to use various equipment and devices that can help ALS patients communicate more effectively. They also loan out assistive devices to patients in need. Transportation services are offered to help ALS patients move around, and the Foundation aids patients and their families with travel planning and other activities that become challenging due to the disease. In essence, The Joe Martin ALS Foundation is committed to improving the quality of life for individuals and families affected by ALS, providing them with the support and resources they need to navigate this challenging journey.
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Impact
October, 2024
The Joe Martin ALS Foundation significantly enhances the quality of life for individuals living with Amyotrophic Lateral Sclerosis (ALS) and their families. By offering essential services such as homecare aides, the foundation assists ALS patients with daily living activities, ensuring they can maintain some independence and comfort in their homes.
One of the standout contributions is the provision of respite care, which offers family members a crucial break from caregiving duties. Over the course of a year, the foundation serves around 16 families each week, providing approximately 4,992 hours of respite care at no cost. This allows caregivers to focus on their own well-being while knowing that their loved ones are receiving professional support.
In addition, the foundation conducts exercise sessions aimed at improving blood circulation and preventing complications related to immobility, thereby promoting better health outcomes for patients. They also offer training for family members on how to use assistive devices, loan necessary equipment, and provide transportation, making life easier for ALS patients and their families.
Through these multiple avenues of support, the Joe Martin ALS Foundation plays a vital role in alleviating the burdens associated with ALS, ultimately fostering a more supportive and compassionate environment for affected individuals and their families.
This information is meant to be a general summary of The Joe Martin Als 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: $26,840
- Program Service Revenue: $12,450
- Gross Receipts: $462,361
Assets and Liabilities:
- Total Assets: $852,397
- Total Liabilities: $3,858
- Net Assets: $848,539
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Programs
Programs are reported by nonprofits in their tax forms and are normally their tax-exempt activities.
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Revenue
$12,450
Organization Details
Founding Year
2007
Phone
(704) 332-1929Principal Officer
Neil Cottrell
Main Address
100 N Tryon Street 3420, Charlotte, NC, 28202
NTEE Category
Code: G12 - Disease
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