Resource and Groups online. Information on self-help groups, therapy, and referrals to professionals. Meetings led by members with professionals as sponsors. Newsletter and group development guidelines.
ANAD is a donation-based recovery community. We believe eating disorder support should be affordable and accessible to all. To continue offering our services for free, we rely on
Read moreA resource for patients, health professionals, and the public who are seeking information on the oral health of special care patients.
Read moreProvides services to families who have adopted and reside in the state of Kansas, have an APA in place, or have a kinship placement. Opportunities for resources, education and support specifically tailored for families who have been shaped by adoption and guardianship.
Read moreSADD fosters a sense of belonging and promotes resiliency, leadership, and advocacy skills so that young people make positive life decisions that will carry them throughout life. Initiatives include: NHTSA Programs, Drowsy Driving, Physical and Emotional Abuse, Suicide and Self Harm, Depression and Anxiety, Emotional Abuse and Violence Prevention, Drugs, Tobacco. Newsletter, group development
Read moreAddresses needs and concerns of veterans and their families. Leadership and advocacy in areas that have an impact on veterans, emphasis on Agent Orange related problems and post-traumatic stress disorder. Monthly newsletter and group development.
Read moreABCD provides free, personalized information and one-to-one support to people affected by breast cancer – patients, families and friends.
Can get emotional support, and matched to a mentor, Get support form – After Breast Cancer Diagnosis by visiting their website at: abcdbreastcancersupport.org
Read morePromotes welfare of people with phobias and related anxiety disorders. For consumers, health care professionals, and other concerned individuals. National membership directory, self-help group directory, ADAA reporter, and newsletter. Online chat.
Read moreTo improve the quality of life for individuals with CFC Syndrome and their families through family support, research, and education.
Read moreFellowship sharing experience, hope and strength with each other, using a 12-step program, in order to gain better emotional health. Correspondence program for those who cannot attend meetings. Chapter development guidelines.
Read moreInformation, Education, Research, Resources, and Advocacy for those with different types of ectodermal dysplasias and their families. Connection to other families like yours.
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