Showing All Expert Resources
Our mission is to end online and offline bullying in schools, workplaces, and faith communities. The Tyler Clementi Foundation was founded by the Clementi family to prevent bullying through inclusion and the assertion of dignity and acceptance as a way to honor the memory of Tyler: a son, a brother, and a friend. Through programs such as #Day1, which provides free downloadable toolkits customized for different communities, the foundation encourages leadership to create safe spaces where individuals move from being bystanders to Upstanders who embrace diversity.
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Since 1980, the ACPA has offered peer support and education in pain management skills to people with pain, family and friends, and health care professionals.
The information and tools on our site can help you to better understand your pain and work more effectively with your health care team toward a higher quality of life.
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Mental Health & Addiction Association of Oregon (MHAAO) promotes self-directed recovery and wellness for all individuals with mental health and addiction issues, whom we refer to as peers. We provide community-based and on-call peer support services, weekly peer support for peer support groups, and a virtual 80-hour Peer Wellness Specialist training offered live several times throughout the year.
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Facing Disability is a web resource with more than 1,000 videos drawn from interviews of people with spinal cord injuries, their families, caregivers and experts.
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The Mental Health Foundation of West Michigan is the go-to source for mental health awareness and education. Our mission is to create communities that have good mental health by inspiring people to recognize, understand, accept, and take action.
Our leading program:
be nice. is a mental health education program for schools, businesses, faith congregations, and communities. The be nice. Action Plan to notice, invite, challenge and empower is proven to change, improve, and save lives. Learn more by Taking the Pledge on www.benice.org.
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Hand to Hold’s vision is to enable a network of families to offer support, comfort and understanding to one another, and to provide them with knowledge, information and resources to reduce the impact of a NICU stay and ensure the best outcome for their children and family by:
Empowering parents to advocate for their children
Facilitating peer support and encouraging individual, couple and family counseling when needed
Educating parents about the challenges their babies might face and preparing them to meet those needs
Sharing support and resources to help comfort families following a terminal diagnosis or loss of a baby
Working with healthcare professionals, hospital systems and specialists to ensure families thrive during and after a NICU stay
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Cancer Hope Network provides free one-on-one emotional support to adult cancer patients and their loved ones. Each of CHN’s 400+ volunteers is at least one year post-treatment or successfully undergoing maintenance therapies. They have faced more than 80 cancer types and speak 15 languages. Our volunteers offer support from diagnosis, through treatment and into recovery. Cancer Hope Network serves cancer patients in the United States and Canada.
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Baby’s Breath is Canada’s only national organization focused on sudden unexpected infant & childhood deaths, including SIDS, SUDC and stillbirth. Baby’s Breath provides support for families faced with the traffic loss of an infant or young child. They advocate for the needs of these families, as well as for the need for more research into the causes of these deaths. They educate the public on how to reduce their infant’s exposure to risks. The death of an infant is a devastating event not only for the parents, but for the entire family. Siblings, grandparents, aunts, uncles, cousins and friends are all affected by the sudden death of a baby. Baby’s Breath believes no one should endure the grief of such loss alone. They are there to help.
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Babies affected with Turner Syndrome require a lifetime of specialized care beyond the pediatric setting. Obstacles often impede an early diagnosis for girls to receive critical health screenings and timely, life-altering, interventions. The Foundation’s advocacy efforts identify these gaps and give voice to leaders who can make a difference. The vision to improve the understanding of TS and to render support for women and children living with TS is made possible by advancing communications and inspiring relevant interest in this women’s health issue. Legislative advocacy, education, and research are cornerstone to improved outcomes. For more information about Turner Syndrome, please visit https://turnersyndromefoundation.org/welcome/ or call 1-800-594-4585.
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The National Widowers’ Organization educates the public about the special needs of men who have lost their spouse or life partner. We do this by promoting the development of support groups for men to manage their grief and adjust to a new life and by advocating for research into mens unique needs to deal with grief and spousal loss.
Our vision is to make appropriate groups available nationwide to all widowers that seek support.
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