Voluntary Health Associations & Medical Disciplines
Joe Martin Als Foundation
CHARLOTTE, NC
Total revenue
$521K
Total expenses
$475K
Net assets
$1.0M
Grants received
$679K
91 grants
EIN
260163120
Tax year
2024
Mission
The purpose of the Foundation is to provide service to individuals living with Amyotrophic Lateral Sclerosis ALS, also called Lou Gehrig's disease, and their families by providing homecare aides who will i assist ALS patients with daily living activities such as getting in and out of bed, eating, showering and dressing for the day ii provide exercise sessions designed to improve blood circulation, reduce swelling, prevent contracture, blood clots and the loss of bone density iii respite care to provide family members of ALS patients the opportunity to attend to their own needs iv train family members and ALS patients to use various equipment and devices designed to enable ALS patients to communicate v loan assistive devices to ALS patients vi provide transportation for ALS patients vii provide ALS patients and their families assistance with travel planning and other activities that become much more difficult when a family member has ALS. The Foundation provides these services without c
Programs
4 programs
Therapy Sessions - Poor blood circulation, kidney stones, edema, and contracture are just a few of the problems associated with paralysis. The progression of ALS leads to paralysis, but range of motion ROM, standing sessions, and exercise can prevent these problems and help maintain mobility for as long as possible. These therapies are provided in the patient's home. The average number therapy sessions per week for the year were 34, at one hour per session. Therefore, approximately 1,768 hours of therapy was provided at no cost to ALS patients.
Other Program Services/Joe's Camp
Education Services - The Joe Martin ALS Foundation provides ALS caregiver education and training. We promote safe methods and techniques to keep both the person with ALS and their caregiver safe. We also raise ALS awareness and educate the public about Lou Gehrig's disease and advocate to improve quality of life for families fighting ALS.
Client Transportation - Many of the Foundation's clients do not own wheelchair accessible transportation. The Foundation owns and maintains a wheelchair accessible van to transport ALS patients to doctor appointments, ALS clinic days, to high school graduations, family reunions, and trips to get out of the house. The van was used for 70 of these events for an average of 13 miles per event. Employee hours, gas, and maintenance are included in the cost of this service at no charge to the ALS patients.
Financials
FY 2024
Revenue
Expenses
People
10 listed
Neil Cottrell
President
$100K
40 hrs/wk
Sandra Bobbitt
Chairman
—
5 hrs/wk
Pat Martin
Director
—
5 hrs/wk
Jennifer Yoxtheimer
Director
—
5 hrs/wk
Claudia Ramirez Tate
Director
—
5 hrs/wk
Theresa Kletch
Treasurer
—
5 hrs/wk
Sara Slone
Director
—
5 hrs/wk
Robbie Howell
Director
—
5 hrs/wk
Aaron Putnam
Director
—
5 hrs/wk
Greg Burson
Director
—
5 hrs/wk
Grants received
Showing 91 of 91
Funded by
$679K from 29 funders · 91 grants · 2017–2024
$252K · 1 grant · 2020
$74K · 5 grants · 2019–2023
$73K · 6 grants · 2017–2024
$57K · 4 grants · 2020–2024
$45K · 2 grants · 2023–2024
$40K · 3 grants · 2021–2023
$40K · 4 grants · 2020–2023
$26K · 3 grants · 2021–2023