Rare Olive Org Inc
Our mission is to push forward the scientific understanding and treatment options for a rare neurodevelopmental disorder. We hope to connect with other families impacted by this disease and ultimately find a cure.
ICO
920771031
Web
Sign in to see organisation website
Address
Kensington
Home - Rare Olive JollyFest tickets are on sale now. Parents fighting to cure LNPK In June 2022 Olive was diagnosed with an ultrarare brain disease caused by a single gene mutation in LNPK Lunapark. She was the first known case in the United States and 1 of 5 in the world. As of 2023 there are 21 known cases and 2 children have passed away from this disease.
From Social media
News about from their social media (Facebook and X).
Data about organisation
Kensington
Organisations from Rare Olive Org Inc
1. KENSINGTON UNITED METHODIST CHURCH
The United Methodist Church is a worldwide connection of close to 10 million members in over 100 countries including Africa, Asia, Europe and the United States.
2. American Childhood Cancer Organization
Founded in 1970, ACCO is the oldest and largest grassroots childhood cancer organization in the U.
Building Community, Neighbor to Neighbor.
4. NATIONAL ASSOCIATION FOR CHILDREN OF ADDICTION
Using our network of the most respected experts in the field, NACoA provides solutions to address these impacts effectively.
Similar organisations
Similar organisations to Rare Olive Org Inc based on mission, location, activites.
Familial Dysautonomia (FD) Foundation, Inc.
Providing treatment & research for Familial Dysautonomia, a rare genetic disorder.
Canavan Research Foundation, Inc.
The Canavan Research Foundation is dedicated to eradicating genetic brain diseases, including Canavan, Alzheimer's, Parkinson's, and MS.
THE CLINIC FOR SPECIAL CHILDREN INC
A nonprofit comprehensive medical practice focused on treating & researching rare genetic disorders.
The mission of the Smith-Magenis Syndrome Research Foundation is to advance scientific research leading to innovative treatment options for people living with SMS.
Similar Organisations Worldwide
Organisations in the world similar to Rare Olive Org Inc.
The Lowe Syndrome Trust is the only charity for the disease in the UK and is extremely small and voluntary.
Genetic Cures For Kids Inc (au)
Please help save Tallulah Moon and all kids living with SPG56.
The Luminesce Alliance is a world-leading paediatric research co-operative, established to harness the strengths of its partner organisations to unlock future prevention, treatments and ultimately, cures, for childhood illnesses.
Interesting nearby
Interesting organisations close by to residence of Rare Olive Org Inc
The Lancaster Cleft Palate Clinic is a not-for-profit organization dedicated to improving the quality of life of infants, children, and adults through comprehensive coordinated treatment of craniofacial conditions.
THE CLINIC FOR SPECIAL CHILDREN INC
A nonprofit comprehensive medical practice focused on treating & researching rare genetic disorders.
The Snyder-Robinson Foundation is a tax-exempt organization formed to advance medical and scientific.
Join us and make a difference for the future!
Sign Up
Please fill in your information. Everything is free, we might contact you with updates (but cancel any time!)
Sign in with Google