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String of Pearls was created to provide a nurturing and safe place for families as they navigate the path following a fatal prenatal diagnosis that will result in the death of their baby prior to, or shortly after birth. The path between grief and hope is a difficult place to walk; our desire is to provide guidance, compassion and practical suggestions as plans to honor the life of pre-born babies are crafted. Each life has a story worth telling, and we are here for support as stories are lovingly written.
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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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The Missouri Eating Disorders Association’s mission is to bring hope, compassion and understanding to the fight against eating disorders. We are committed to providing education, resources and advocacy that will change the conversation around eating disorders. We strive to bring understanding and support to those treating or affected by this terrible and serious disease.
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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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Seasons Centre for Grieving Children is a charitable organization serving Simcoe County. We opened our doors in 1995 and have been serving our community with their grief and bereavement since. We offer a variety of no cost peer to peer support groups for children, teens, young adults and their caregivers grieving the death, or life threatening illness of an immediate family member. Participants are supported through the grief process by trained volunteer grief facilitators and program staff in a safe, non-judgmental, home like atmosphere.
Our programs are unique and are designed to provide children with the opportunity to express their feelings in appropriate ways. We discuss and identify coping strategies and how we can replace the negative strategies with positive ones. Several of our participants have expressed that Seasons Centre is the only place where they feel comfortable, understood, and not alone when talking about and expressing their grief. There are no fees for our services. Children are able to attend programs regardless of their family’s financial situation.
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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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The Alliance for Eating Disorders Awareness ("The Alliance") is a nonprofit* organization dedicated to providing programs and activities aimed at outreach, education, and early intervention for all eating disorders. Founded in October 2000, The Alliance has worked tirelessly to raise awareness, eliminate secrecy and stigma, promote access to care and support for those susceptible to, currently struggling with, and recovered from eating disorders. The Alliance creates a bridge for those needing and seeking help by connecting people with resources and information to assist them in their recovery.
The Alliance offers educational workshops and presentations, free support groups for those struggling and for their loved ones, advocacy for eating disorders and mental health legislation, national toll-free phone help line, and referrals, support and mentoring services. All services offered by The Alliance are free-of-charge, therefore, making it accessible to everyone. Since its inception in October 2000, The Alliance has offered presentations on eating disorders, positive body image, and self-esteem to more than 250,000 individuals throughout Florida and nationwide.
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The Louisiana Foundation Against Sexual Assault (LaFASA) is a 501(c) nonprofit organization that supports survivors of sexual assault. The mission of LaFASA is to empower survivors through trauma-informed services, engage advocates, and change system norms to end sexual violence. LaFASA is the coalition agency that serves 11 sexual assault crisis centers in Louisiana through education, professional training, technical assistance, and community engagement resulting in safer, healthier, stronger, and better-informed communities throughout the state. LaFASA also provides counseling, advocacy, and legal services directly to survivors in Louisiana. LaFASA envisions a world free of all forms of oppression that enable rape culture and sexual violence.
The only person to blame for sexual assault is the perpetrator. Call our helpline for free, confidential support, 24/7 at 888-995-7273. For more information, visit our website at www.lafasa.org.
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On September 2, 2005 we received a phone call saying in essence, our daughter Cammy‘s heart was not beating, and she was on her way to Erlanger hospital by way of ambulance. While we huddled with close friends and family in prayer, we were given the devastating news that she was gone.
How does something like this happen to a vibrant 26 year old young woman? How do you reconcile just two days prior taking a long walk with someone who expressed her dreams for the future who appeared healthy and happy. Well, I can only state that eating disorders are deadly.
She suffered from all three of the eating disorders (defined in the Diagnostic and Statistical Manual for Mental Disorders #4). She had binge eating disorder in high school, where she ate in excess in private. During her freshmen year in college she turned to bulimia to rid herself of her excess high school weight. She could eat large amounts of food and then purge by way of vomiting. She was also pairing her bulimia with anorexia which can often be the case. This behavior took its toll when in her junior year of college she went into cardiac arrest, and we almost lost her for the first time. We learned when you purge you rid yourself of essential electrolytes that control the beating of the heart and thus causing it to shut down.
We sent her for treatment to Arizona to save her life, and to hopefully help her overcome her E.D. When she left after almost three months we thought she had it beaten. Unfortunately, there were additional life threatening instances that followed. Eating Disorders seemed to control her in such a way that nothing seemed to help. After many years of therapy and finding the true love of her life we thought she was finally on the road to recovery. This proved not to be the case. We are not sure to this day what exactly caused her final cardiac failure, but for sure it was a result of her eating disorders.
To honor her memory Ashley Yates (her closest friend) and I (Jan Robinson, Cammy’s Mother) founded the Mary Cameron Robinson (MCR) Foundation for the prevention and treatment of eating disorders. It would have been so helpful to me had there been a source like this when Cammy was struggling. There is so much to learn about this disease and the earlier it is treated the better the chance of survival. Denying it will not cause it to go away. We must educate ourselves to be aware of the behaviors and to intervene as soon as possible. This is absolutely crucial. Cammy would be so proud to know her death was not in vain and she lives on with this foundation.
MCR’S Mission Statement
The mission of the MCR Foundation is to provide resources for people who are affected by eating disorders in the Greater Chattanooga Tri-State area. The Foundation is committed to a holistic approach encompassing physical, emotional, spiritual, and social well being.
MCR will do this by:
• Providing education and multi-media resources
• Promoting awareness and developing prevention strategies
• Providing support systems
• Conducting research for community needs
• Promoting a healthy lifestyle and a appropriate self image
• Serve as a resource for referrals for counseling and treatment
MCR’S Vision
The MCR Foundation will be a comprehensive non-profit center in the Chattanooga Tri-State area for education concerning prevention early diagnosis and treatment of individuals and families affected by eating disorders, focusing on healing the mind, body, and spirit.
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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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