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The Chromosome 18 Registry & Research Society is a lay advocacy organization composed primarily of the parents of individuals with a chromosome 18 abnormality. We consist of three separate organizations located in the United States, Australia, and Europe, all with a common mission: to help people with chromosome 18 abnormalities overcome the obstacles they face so they may lead happy, healthy, and productive lives.

Transforming the lives of orphans and destitute in Kenya, with care & schooling, nurturing their integrity & responsibility so that they lead prosperous lives.

The Lupus Foundation of America is dedicated to improving the quality of life for all people affected by lupus through programs of education, advocacy, support, and research. The Utah Chapter supports people with lupus and their families throughout the intermountain west.

The International FoxG1 Foundation’s Mission is to raise awareness and educate others about this rare genetic condition, to facilitate relationships within the FOXG1 community, and to raise funds to directly benefit families impacted by FOXG1.

To enhance the quality of living for those facing the final phases of life and to support those who love them.

Part of an international organization called L'Arche founded in 1964, L'Arche Atlanta was founded in 2012 and seeks to build community around the gifts of people with developmental disabilities and to sensitize the wider public to the gifts and contributions of people with disabilities.

The mission of the national NF Network is to find treatments and a cure for neurofibromatosis by promoting scientific research, improving clinical care, providing outreach through education and awareness, while offering hope and support to those affected by NF.

Aarogya Seva is an international, humanitarian micro-volunteering organization estd in 2014 that is dedicating to providing quality healthcare services to affected communities worldwide. Our Vision To instill the spirit of seva in doctors and the medical fraternity To provide a structured platform for medical and non-medical professionals, to volunteer their time and skills, and strengthen the healthcare system. Our Objective Build a global network of medical and non-medical volunteers Provide meaningful volunteering opportunities in the health space Create models within the healthcare ecosystem that will demonstrate and showcase the effects of an organized network

Cerebral Palsy of North Jersey is dedicated to enhancing the lives of people with disabilities and other special needs by supporting personal growth, independence and participation in the community.

The Mission of Chestnut Hill Benevolent Association is to provide a healing refuge and services that minister to the needs of mankind with Christian Science nursing.

Our mission is o insure that no child or individual around the globe goes untreated. We want to make sure that every parent knows that they are not alone in this struggle, and has the support they need at criticial times. Also that newborn screening is efficient and never misses a child's diagnosis ever again across the globe. If anybody is affected by Tyrosinemia Type 1,2 or 3 we are here for them 100%

The APS Foundation of America, Inc. is the only United States nonprofit health agency dedicated to bringing national awareness to Antiphospholipid Syndrome (APS), the major cause of multiple miscarriages, thrombosis, young strokes and heart attacks. We are a volunteer run, community based 501(c)3 non-profit Public Charity organization and is dedicated to fostering and facilitating joint efforts in the areas of education, support, public awareness, research and patient services. The APSFA's Medical Advisory Team includes nationally & internationally recognized experts on Antiphospholipid Syndrome. Our URL is apsfa.org