• Alliance/Advocacy Organizations

• 1306.

Dyspraxia USA NFP

Dyspraxia Foundation USA is the first organization in the United States dedicated to raising awareness about Dyspraxia Dyspraxia Foundation USA is a non-profit with the mission to raise awareness and advocate for individ This neurological disorder often affects motor skills but very few know what it is or how it affects kids and adults.

Marcus Foundation Inc

The Marcus Niziak Childhood Brain Tumor Fund is a public foundation established in the memory of Mark S.

THE JOE NIEKRO FOUNDATION

The Niekro Foundation is committed to supporting patients and aiding in the research, treatment and awareness of brain aneurysms, AVMs & hemorrhagic strokes.

• Cancer

• 1309.

Stop3Org Inc

TO PROVIDE CAREGIVERS AND PATIENTS OF BRAIN CANCER SUPPORT AS WELL AS FUND PROJECTS WHOSE PURPOSE IS TO DEFEAT BRAIN CANCER.

• Nonmonetary Support N.E.C.*

• 1310.

Ncmic Foundation Inc

Search this site OUR COMMITMENT To Fund Chiropractic Research Education Get Involved Our mission is to invest in the advanced education of chiropractic research experts and to fund ongoing research projects that demonstrate the cost effectiveness safety and cost efficiency of chiropractic and alternative healthcare.

• Fund Raising and/or Fund Distribution

• 1311.

Brooklyn Project Foundation

TO FINANCIALLY SUPPORT RESEARCH PROGRAMS FOR PEDIATRIC CANCER PATIENTS.

• Biological, Life Science Research (includes Marine Biology, Physiology, Biochemistry, Genetics, Biotechnology, etc.)

• 1312.

Invincible Wellbeing Inc

Along with our academic partners, our mission is to investigate and treat the phylogenetic roots of pain.

• Human Service Organizations

• 1313.

Institute of Health Beyond Earth Inc

Institute of Health Beyond Earth Inc IHBE is a 501c3 organization.

• Alliance/Advocacy Organizations

• 1314.

Ctx Alliance NFP

Providing education, support, advocacy, and promoting research for CTX patients, their families, and medical professionals who treat and study this rare disease Providing education, support, advocacy, and promoting research for CTX patients, their families, and medical professionals who treat and study this rare disease.