RIVERBEND DOWN SYNDROME ASSOCIATION

The Riverbend Down Syndrome Association is a volunteer-run organization providing support and inform To advocate for the needs of individuals with Down syndrome To offer support, acceptance and encouragement for parents and families of persons with Down syndrome To increase our awareness and knowledge of issues relating to Down syndrome To educate the community about the presence, the potential and the needs to people with Down syndrome To promote inclusive environments for all persons Amplifying the voices of individuals with Down syndrome fosters acceptance promotes inclusion and advocates for their rights inspiring others to support and embrace people of all abilities.

• Services to Promote the Independence of Specific Populations

• 254.

Down Syndrome Information Alliance

DSIA provides support and resources to empower individuals with Down syndrome, their families, and our community.

• Specifically Named Diseases Research

• 255.

PROJECT ALIVE

A Hunter syndrome research and advocacy foundation.

• Educational Services and Schools - Other

• 256.

Womxns Collaborative

Womxn39s Collaborative afabNPO afab assigned female at birth 20251 46 5 426 12 53 3Satoko Fox 2025NPOJWIBA Japanese Women39s Initiative in the Bay Area Click here to donate Your donation will help Wecolla nonprofit volunteering group achieve better community health by providing support groups classes and highquality health educational materials on pregnancy birth postpartum parenting menopause grief and more.

• Specifically Named Diseases

• 257.

YBRP Inc

YBRP is a non-profit organization whose mission is to positively impact the lives of individuals with HNRNPH2 genetic variations.

• Specifically Named Diseases Research

• 258.

Cacp Research Foundation

Our Mission Awareness. Research. Cure.

• Birth Defects, Genetic Diseases

• 259.

Skraban-Deardorff Syndrome Foundation

The Skraban-Deardorff Syndrome Foundation has been formed by parents and medical professionals worldwide to foster relationships and organize resources to benefit individuals with Skraban-Deardorff Syndrome.

• Cultural/Ethnic Awareness

• 260.

May5Foundation

The May5Foundation and founder Dr. Alexia Mays are committed to supporting the communities of sickle cell, grief & loss, thru research ,advocacy &awareness The May5Foundation is centered in the values of dedication to education,community and service WE DO AMAYSING THINGS Programs and Events Support Our Efforts Who We Are More Community Events 2024 Warrior of The Year .

• Services to Promote the Independence of Specific Populations

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1P36 DELETION SUPPORT & AWARENESS

1p36 Deletion Support & Awareness Support, Awareness & Education to improve the lives of individuals affected by 1p36 Deletion Syndrome Support Awareness and Education to improve the lives of individuals affected by 1p36 deletion syndrome If you have a loved one affected by 1p36 deletion syndrome were here to help 1p36 deletion syndrome occurs in approximately 1 in 5000 to 10000 live births and 1p36 Deletion Support Awareness is honored to currently serve hundreds of families affected by this rare genetic disorder.