Cure LBSL is a registered non-profit organization dedicated to raising awareness and funds for research into LBSL, a progressive and very rare genetic disorder that affects the brain and spinal cord; most often developing in children, affecting their ability to walk, then even to stand and coordinate fine and gross motor skills. The organization connects families, advocates for research, and provides resources for those affected by this condition.
2013
46-2829156
$535.1 thousand
Join our annual event to raise awareness and funds for LBSL.
Offering information and support for patients and families impacted by LBSL.
Funding and advocating for crucial research into LBSL.
Raised Over $3.5 million for Research
Significant funding gathered for research efforts
2017 Rare Impact Award Winner
Recognition for outstanding contributions to rare disease advocacy
Host First-Ever International LBSL Patient Conference
First global event gathering patients and families affected by LBSL
Created Network of Families and Scientists Across Six Continents
Established a global support network connecting affected families and researchers
Overall Score
47
32
/100
Program Expense Ratio
94.95%
20
/20
Program Revenue Growth
0.00%
2
/20
Leverage Ratio
0
2
/20
Working Capital Ratio
0.4054
6
/20
Fundraising Efficiency
0
2
/20
Fiscal Year:2022
Source:Source: Self-reported by organization
Category | Amount | Percentage |
---|---|---|
Contributions, Gifts, and Grants | 1.41M | 100.00% |
Program Services | 0 | 0.00% |
Investment Income | 1 | 0.00% |
Sales of Non-Inventory Assets | 0 | 0.00% |
Other Notable Sources | 0 | 0.00% |
Total Revenue | 1.41M | 100.00% |
Health Associations
Geriatric PhysiciansHealth Associations
Geriatric PhysiciansHealth Associations
Geriatric PhysiciansHealth Associations
Geriatric PhysiciansHealth Associations
Geriatric Physicians