Scarring Alopecia Foundation

Cicatricial Alopecia Research Foundation (CARF) is the world's only voice for people with Cicatricial Alopecia Scarring Alopecia Foundation (SAF) is a nonprofit public charity organization and the world's only v The mission of the Scarring Alopecia Foundation (SAF) is to provide education and patient support, raise public awareness, and advance and promote research.

• County/Street/Civic/Multi-Arts Fairs and Festivals

• 3863.

The Grishkot Foundation

PROMOTE AND ASSIST IN THE PRODUCTION OF ACTIVITIES THAT ENCOURAGE A GENERAL PUBLIC INTEREST AND EDUCATION IN THE SCIENCES OF AVIATION, AEROSPACE AND PROFESSIONAL NURSING AND RELATED HEALTHCARE FIELDS AND TO PROVIDE COLLEGE SCHOLARSHIPS FOR RESIDENTS OF WARREN, WASHINGTON AND SARATOGA COUNTIES.

• Private Independent Foundations

• 3864.

Sean N Parker Foundation

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• Patient Services�Entertainment, Recreation

• 3865.

9474 Foundation

Consider it Pure Joy. James 124 9474 Foundation Being used by God to bring joy in the midst of trials.

• Cancer Research

• 3866.

Team Twinspirational

Team TWINspirational Team TWINspirational 1 215 8588982 Wex27re going to strike out the silent killer.

• Safety Education

• 3867.

With Angels Foundation Inc

WAF is a Charitable Organization. We focus on assisting families who have lost their children.

• Fund Raising and/or Fund Distribution

• 3868.

Womens Fund of Santa Barbara

The Women's Fund is an independent, tax-exempt non-profit.

• Public Foundations

• 3869.

Foundation for a Better Puerto Rico Inc

Our Work Health Education Community Partnerships Disaster Preparedness and Response Environment Economic Development We hope that Culebras experience in becoming a sustainable community with the highest quality of life will become a model that others will want to replicate in Puerto Rico and the Caribbean.

• Alliance/Advocacy Organizations

• 3870.

BELOVEDS A NANIA FOUNDATION INC

BELOvEDS, A Nania Foundation Inc. is a recognized 501(c)(3) non-profit organization committed to raising awareness of, and research funding for, Vascular Ehlers-Danlos Syndrome (vEDS).