Showing All Expert Resources
My Sister's House, serving the Lowcountry community for 40 years, is a local expert in Domestic Violence survival. Domestic violence can affect any individual regardless of race, gender, sexual orientation or any other defining characteristic. At MSH we serve victims from all walks of life and make our services available throughout the Lowcountry free of charge. If you or someone you know is in an abusive situation or looking for resources, please call our 24-hour hotline at 1-843-744-3242 or 1-800-273-HOPE. We offer individual therapy, group counseling, emergency shelter and more.
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Women Against Abuse, Inc. is the leading domestic violence service provider in Philadelphia. We serve an average of nearly 12,000 people each year through emergency safe havens and transitional housing, legal representation, community-based supportive services, trauma-informed behavioral health therapy, hotline counseling, community education, advocacy, and technical assistance.
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Support. Research. Hope.
The mission Cure SMA Canada Society is:
To fund the best possible Canadian research in search of a treatment or cure for Spinal Muscular Atrophy.
To support Canadian families and individuals affected by Spinal Muscular Atrophy in every province and territory.
To work closely with CURE SMA (USA) and the Scientific Advisory Board in our selection of recipients of research and trial grant monies.
To offer and supply information to any Canadian requesting it.
To support Canadian families and individuals affected by SMA as newly diagnosed, during the affected person’s lifetime and the family after an affected person passes.
To offer support for activities that bring families and individuals together mutually benefitting all that are involved. (example: the annual SMA conference, SMA Family Camp, Parent’s retreat)
To support individuals with their fundraising activities benefitting Cure SMA Canada.
To supply members with newsletters for the purpose of information, connecting and communication.
To connect families to each other through various methods including our website, social media, through our national office, our newsletter and group activities.
To help families realize they are not alone with the diagnoses of SMA. That Cure SMA Canada is here for them and will support them in any capacity we can. We understand, because we too are affected by SMA or are parents of children born with Spinal Muscular Atrophy.
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Created and supported by The Moyer Foundation, Camp Mariposa is a national addiction prevention and mentoring program for youth impacted by substance abuse in their families. Children ages 9-12 attend transformational weekend camps multiple times a year, always free of charge. Additional education and mentoring activities are offered to campers, teens, and their families throughout the year giving youth the knowledge, coping skills and confidence to prevent them from developing an addiction of their own. Led by mental health professionals and trained volunteers, Camp Mariposa provides a safe, fun and supportive environment critical to help break the cycle of family addiction across 12 locations nationwide.
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Men's Health Network (MHN) is a national non-profit organization whose mission is to reach men, boys, and their families where they live, work, play, and pray with health awareness and disease prevention messages and tools, screening programs, educational materials, advocacy opportunities, and patient navigation.
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Brighter Days Grief Center is a nonprofit organization serving grieving families in the state of Minnesota. They provide free grief support resources, services and programs to adults, young adults, teenagers and children who are grieving the death or terminal diagnosis of a beloved family member. Through their many partnerships and gracious donors, they tailor compassionate resources for each family member including access to grief and trauma support, legal and financial guidance, peer-based connections and youth/family events and workshops. Their signature program, Embrace-A-Family, provides financial assistance for basic necessities, academic support and psycho social care. Additionally, they work with schools, churches and community organizations to ensure grieving children and families receive compassionate and appropriate support in all settings. To learn more, visit their website at www.brighterdaysgriefcenter.org
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The Young Carers Program of Hospice Toronto is a GTA based program supporting children and youth 5-18 who are in a caregiving role for a family member living with a chronic or life-threatening illness, a disability, a mental illness or addiction, or a language barrier.
The Young Carers Program offers programs, workshops and special events throughout Toronto to support Young Carers. The therapeutic and recreational programs offer Young Carers opportunities to foster resilience, build skills, connect to peers and just have fun! Programs include, but are not limited to, cooking workshops, sports programs, camp, expressive arts, games, day trips, homework help, leadership workshops, medical education, and so much more!
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HeadsUpGuys is a resource for supporting men in their fight against depression by providing tips, tools, information about professional services, and stories of success.
Our team of clinicians, researchers, and mental health advocates bring together their expertise and personal experiences to provide you with this unique resource, HeadsUpGuys.
HeadsUpGuys was developed through the generous support of the Movember Foundation and is based at The University of British Columbia (UBC), Canada.
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The Missouri Eating Disorders Council, in collaboration with appropriate organizations and stakeholders, in addition to the Departments of Mental Health, Health and Senior Services, Elementary and Secondary Education and Higher Education, will lead the development of eating disorders education, awareness and research initiatives throughout the state, and promote increased access to treatments supported by clinical practice guidelines (i.e., considering the relevant scientific literature, as well as the potential harms and benefits of treatment for each case).1-3
The Council will focus on children, adolescents, and adults with anorexia nervosa (AN), bulimia nervosa (BN), binge eating disorder (BED), atypical AN, sub threshold BN, sub threshold BED, and avoidant/restrictive food intake disorder (ARFID). These are the major diagnostic categories included in DSM-5.4 It will include the sub threshold diagnoses (atypical AN, sub threshold BN, sub threshold BED) because patients with these disorders demonstrate levels of distress and/or impairment similar to full-syndrome AN, BN, and BED.5
Eating disorder awareness, detection, prevention, treatment and recovery is of paramount importance and must start early. Early intervention is linked to better treatment outcomes, but requires enhanced awareness and screening.6 The Council will focus on helping professionals to recognize individuals with eating disorders and individuals at high risk for developing an eating disorder (e.g., those with high weight/shape concerns or low levels of compensatory behaviors).7-8 The Council will advocate for increased access to care for this population, as well as promote early intervention and prevention programs and recovery supports.
The absence of adequate coverage for treatment is a critical barrier to access to care for the patient.9 The high costs of medical complications, disability, and loss of life are significant health concerns.10-12 The Council will advocate for third party reimbursement for eating disorders, including coverage through private and public insurance plans.
The Council will work with identified partners, including state departments, to develop an eating disorders awareness program that targets patients with eating disorders as well as non-patient community members. This program will be designed to communicate that eating disorders are serious illnesses that require complete treatment, and to foster recognition of eating disorder symptoms and support for seeking treatment. The objectives of the awareness program are to educate Missouri citizens on the true and serious nature of the disease, dispel myths on who is affected, drive early intervention and encourage appropriate treatment for those suffering or those at risk.
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The BC Council for Families is a non-profit organization that develops programs, workshops resources and services to support diverse families and advocates for public policy change to improve the lives of families throughout BC.
The Council offers training for family service professionals to assist families in increasing their confidence and preventing problems before they start with the following programs: Nobody's Perfect Parenting, My Tween and Me, Parent-Child Mother Goose, Alliance of Professionals Serving Young Parents, Home Visitor Initiative and Fathering workshops.
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