Our primary mission is the dissemination of free, correct and useful information and support for HHD patients and the health care community. We support this website and forum and manage the Yahoo Group, TalkHHD.

To provide information and support to families affected by Hemihypertrophy.

Our mission is to inspire, support and enhance community efforts toward prevention, awareness, education, and treatment of Hepatitis C and promote organ donation. We are committed to working with any organization, agency, or professional individual to develop partnerships resulting in quality programming and good public decision making based on accurate information regarding Hepatitis C. We offer our resources and services freely in a spirit of goodwill and generosity, ever mindful of our purpose

The Hereditary Disease Foundation is a non-profit, basic-science organization dedicated to the cure of genetic disease, with a focus on Huntington disease.

HNF promotes and supports both clinical and primary CMT research. We are also actively committed to increasing awareness of the disease through all available media outlets, including print, radio and television as well as fundraising programs. While our members give a face to CMT, HNF provides a strong, organizational voice to those living with CMT all over the world.

Our mission is to gather and provide information, to promote awareness and research and to offer support to our members.

Our mission is to find a cure for HHT while saving the lives and improving the well-being of individuals and families affected by HHT.

The mission of the Hidradentitis Suppurativa Foundation, Inc. (HSF) is to foster and encourage worldwide research by developing and supporting an interdisciplinary family of scientists and physicians devoted to studying the molecular and cellular basis of Hidradentitis Suppurativa (HS), in order to develop and deliver more effective forms of treatment and preventative measures for those with this common, debilitating, and eminently chronic disease.

Hirschsprung's & Motility Disorders Support Network is an organization of families encouraging families.

Hope for Two...The Pregnant with Cancer Network is an organization dedicated to providing women diagnosed with cancer while pregnant with information, support and hope. We connect women who are pregnant with cancer with other women who have been pregnant with the same type of cancer.

The Foundation's mission is to increase public awareness of Krabbe Disease and other leukodystrophies, as well as to increase the likelihood of early detection and treatment. The Foundationﾒs goal is to fund research efforts to identify new treatments, therapies and a cure for Krabbe Disease.

The New England HDSA office provides education, advocacy, support, and care to people with Huntington's Disease, their families and to professional caregivers in NH, ME, MA, and RI, funds research efforts and provides an extensive education outreach program.

The Hydrocephalus Association provides support, education and advocacy for families, individuals and professionals dealing with the complex issues of hydrocephlaus.

The objective is to increase awareness about the connection between Hypermobility (HMS) and Fibromyalgia (FMS), and their respectively related conditions. In addition, to provide places where people with both of these conditions can meet and exchange information and support, allowing them hopefully to better cope with their illnesses on a daily basis.