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Calgary Silver Linings Foundation (CSLF) is a registered charity that was founded by parents of loved ones who developed eating disorders, mental health specialists and community leaders. Currently, we offer 8-week professionally-facilitated support groups throughout the year, for individuals with eating disorders (18 years and older) and a separate group for parents and loved ones of someone with an eating disorder. CSLF's primary mission is to establish the province's first residential eating disorder treatment centre. Having experienced firsthand the devastation of eating disorders, we are committed to seeing that Albertans navigating these grave mental illnesses are able to access the specialized care that they urgently need right here, at home. To learn more about CSLF, please visit our website, www.silverliningsfoundation.ca
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Black Girls Smile Inc. is a non-profit organization dedicated to promoting positive mental health for young African American females. BGS works to achieve this ...through resource programs, forums, and mentorship initiatives that promote mental health education, awareness, and self-empowerment.
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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 Will To Live® Foundation is a 501(c)(3) public charity that was created in October of 2010 to spread the awareness of teen suicide in our communities. The Will to Live Foundation is dedicated to preventing teen suicide by improving the lives and the ‘Will To Live’ of teenagers everywhere through education about mental health and encouraging them to recognize the love and hope that exists in each other. We achieve this mission by:
RAISING AWARENESS (of teen suicide in our communities)
INCREASING EDUCATION (of mental illnesses like depression & their stigmas)
DELIVERING HOPE (to teens everywhere through our Life Teammates® programs
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International Bipolar Foundation is a not for profit organization whose mission is to improve understanding and treatment of bipolar disorder through research; to promote care and support resources for individuals and caregivers; and to erase stigma through education.
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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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GRIEF WATCH is a publisher and manufacturer of bereavement books and materials used by families and professionals around the country. They are probably most well known for their beloved Tear Soup products which you can check out here: https://griefwatch.com/collections/tear-soup-home. They also create many beautiful ceramics that are the perfect gifts for those who are grieving. From pocket hearts to necklaces to customizable ornaments, they have something for everybody: https://griefwatch.com/collections/ceramics.
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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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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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The Matthew Silverman Memorial Foundation was founded in 2013 in memory of Matthew, who took his own life in January 2006. He was a compassionate and intelligent young man with limitless potential that chose a permanent solution to a temporary problem. Unfortunately, this choice is all too common amongst our youth in today's climate. The rate of suicide among persons 10-24 has increased by 56% between 2007-2017, affecting young adults regardless of race, religion, gender and socio-economical background. Experiencing the hardship that came with the lose of our founder’s son, he was motivated to find meaning and purpose after Matt’s passing. Ron Silverman wanted to reduce the possibility that any family has to go through the pain that he has gone through. With that hope, the birth of the Matthew Silverman Memorial Foundation (MSMF) was formed with the main goal opening the dialogue on mental health between youth, parents and educators.
Our foundation is a nonprofit public charity that strives to backdown the stigmatism that surrounds mental health, primarily focusing on our youth. We provide financial and programmatic support as well as mental health program for teens, young adults, teacher and parents throughout the country. We covered over 99% of the expenses for programming, which can cost up to $10,000.00 per school, per year. Since the inception of our school programming in 2015 we have presented in over 150 institutions and 319 programs in elementary, middle, high schools, colleges and community centers across the United States. We have now reached over 360,000 students, parents and faculty but we need to do more.
Below you will find a list of some of the programs that we offer:
- Parent Training
- Faculty Training
- Student Curriculum
- School Clubs
- Campaigns
- Community Events
- Signs of Suicide Program
- Student Assemblies with speakers that discuss a range of mental health issues (i.e. Anxiety, Depression, Bipolar, OCD ect). The topics are curtailed to whatever you choose
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