DermaTalk Skin and Beauty Directory

The Skin Cancer Foundation is the leading skin cancer prevention organization. It comprised of distinguished physicians and laypeople dedicated to reducing the incidence of skin cancer.

This foundation educates the public and the medical profession about skin cancer, its prevention by means of sun protection, and the need for early detection and prompt, effective treatment. It is the only international organization devoted solely to combating the world's most common cancer.

The national Psoriasis Foundation is the largest psoriasis patient advocacy organization in the world. The National psoriasis Foundation is a nonprofit organization which offers extensive programs and services and provides help to more than a million people each year.

Hidradenitis Suppurativa Foundation, Inc. Dedicated to improving the quality of life and quality of care for individuals and families affected by Hidradenitis Suppurativa,also known as acne inversa.

The National Rosacea Society (NRS) is the world's largest organization dedicated to improving the lives of people who suffer from this widespread but poorly understood disorder. Their mission is to raise awareness of rosacea, provide public health information on the disorder, and encourage and support medical research that may lead to improvements in its management, prevention and potential cure.

The National Organization for Rare Disorders is a unique federation of voluntary health organizations dedicated to helping people with rare "orphan" diseases and assisting the organizations that serve them. NORD is committed to the identification, treatment, and cure of rare disorders through programs of education, advocacy, research, and service.

The Ichthyosis Foundation educates, inspires and connects those touched by ichthyosis and related skin disorders through emotional support, information, advocacy and research funding for better treatments and eventual cures.

The Ehlers-Danlos National Foundation is a nonprofit organization with over 2,000 members and over 40 local groups across America. It provides information about Ehlers-Danlos Syndrome and support to people with EDS and related disorders.

IPIF is guided by a Scientific Advisory Council, whose members are acknowledged experts in their fields. IPIF consist of patients, physician, educators, parents, relatives and volunteers who are striving to take a leadership role in supporting research, education and funding with an ultimate aim to ameliorate the burdens of IP. IPIF ia a source of reliable information and support for patients and families in united states and worldwide.

National Council on Aging is a nonprofit service and advocacy organization founded to develop creative solutions that improve the lives of older Americans.

International Hyperhidrosis Society is the only independent organization providing hyperhidrosis and excessive sweating resources, advocacy, support and education worldwide.

The Rosacea Research Foundation is a non-profit organization dedicated to funding novel research on the underlying causes of rosacea, analyzing triggers for rosacea flares, and finding effective treatments that address the root causes of the disorder. The foundation's primary objective is to raise funds for cutting-edge research and human clinical trials.

American Leprosy Missions (ALM) is the oldest and largest Christian organization in the United States devoted to restoring the lives of people affected by leprosy and related conditions worldwide through holistic cure and care.

The American Behcet's Disease Organization Website offers information, support and interative tools to patients, loved-ones and medical professionals about Behcet's Disease. Search for Doctors, chat with others, post your story and more

NOAH is a U.S. based nonprofit, tax-exempt organization that offers information and support to people with albinism, their families and the professionals who work with them.

The Vascular Birthmarks Foundation provides support and resources for children and adults born with hemangiomas, port wine stains, and other vascular birthmarks.

The Nevus Network provides support and understanding to families whose lives have been touched by a large brown birthmark called a congenital nevus, also spelled nævus in Latin

Dystrophic Epidermolysis Bullosa Research Association of America promotes and supports extensive scientific research to achieve a cure for EB.  It assists, supports and guides families in the physical and emotional treatment of individuals with EB through their experienced Nurse/Educator, a national physician referral service, a network of regional support groups and an information filled website.

The Xeroderma Pigmentosum Society is a not-for-profit charitable organization which provides the XP family support and information needed to cope daily with XP.The XP Society offers information, support, advocacy, and protection to the XP family, patient and caregiver while promoting research for a cure.

The Sjögren's Syndrome Foundation is a non-profit organization focused on increasing research, education and awareness for Sjögren's syndrome.

The Ectodermal Dysplasia Society is a charity dedicated to improving the health and wellbeing of people whose lives are affected by Ectodermal Dysplasia (ED).