Networks
Asbestos exposure causes thousands of cases of pleural mesothelioma in the United States each year, and our mission is to help the families affected by this cancer. Our organization offers free assistance and resources to anyone coping with pleural mesothelioma.
The Plus One Foundation mobilizes resources to inspire hope and enrich the lives of those affected by neurological conditions and educate the community about related issues. According to the World Health Organization (WHO), neurological disorders affect up to one billion people worldwide. They affect people in all countries, regardless of...
The Phelan-McDermid Syndrome Foundation is a non-profit group that offers support for families who are affected by 22q13 Deletion Syndrome/Phelan-McDermid Syndrome. The syndrome, which affects families worldwide, is a rare genetic occurrence and is the result of a damaged or missing protein on the 22nd chromosome. The Phelan-McDermid Syndrome Foundation,...
The PNH Research and Support Foundation is dedicated to funding research to find a cure and new treatments for Paroxysmal Nocturnal Hemoglobinuria, and to helping PNH patients in need with funding for disease-related expenses not covered by insurance.
To connect with POMC Deficiency Disorder= Proopiomelanocortin
Poniard Pharmaceuticals, Inc. is a biopharmaceutical company focused on the development and commercialization of innovative oncology products to impact the lives of people with cancer. We are currently focusing our development efforts on picoplatin, a new generation platinum chemotherapy agent with the potential to become a platform product addressing multiple...
The purpose of this website is to share information about the condition, and to support other families who have children that have been diagnosed with the condition.
PWSA UK is a Charitable Incorporated Organisation (Registered Charity No. 1155846) and the only charity in the UK working with those living with PWS, their families and carers, together with the myriad of professionals from health and social care, residential and education, helping everyone to manage this complex syndrome and...
PWSA (USA) was organized in 1975 to provide support for individuals, families, professionals and organizations and to be a resource for education and information about Prader-Willi syndrome. The organization was first headquartered in Minneapolis, then moved to St. Louis, Missouri, and then found its permanent home in Sarasota, Florida in...
Our mission is to support and represent people affected by primary immunodeficiencies (PIDs) in the UK, working with healthcare professionals and other relevant organisations to improve their care and quality of life.
The primary malignant melanoma of the uterine cervix is rare, usually diagnosed at an advanced stage and with poor prognosis. The diagnosis is made through histological evaluation and confirmed by special staining procedures. Radical surgery has been used and advocated. However in its advanced stages chemotherapy, immunotherapy or radiotherapy can...
Prize4Life is a nonprofit organization dedicated to accelerating the discovery of treatments and cures for ALS (amyotrophic lateral sclerosis, also known as Lou Gehrig’s disease). Our mission is to accelerate the discovery of a treatment and a cure for ALS by using powerful incentives to attract new people and new...