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Julie Maida has been in abstinence-based recovery since May of 2000, and has worked in the field of addiction since. In 2012, after the birth of her youngest son, she battled a severe bout of postpartum depression, OCD, and agoraphobia; which made it impossible for her to keep up with her 12 step recovery responsibilities.
Julie realized how much recovery support can often depend on regular meeting attendance, and how lonely it can feel without such support. She started thinking about women who, for whatever personal reasons, choose not to attend 12 step meetings or do not practice complete abstinence. She wondered if they felt as lonely in their process as she did at that moment.
In May of 2013, she “came out” about her personal recovery in a post titled I Got Sober Today. The post received an incredible response, and alerted Julie to the need for a supportive, judgment-free community for moms in and contemplating recovery.
Julie believes ALL women deserve to have a supportive and encouraging tribe. She created Sober Mommies to connect women with a diverse, inclusive community and to help moms build their personal recovery tribe.
The members of Sober Mommies understand the unique struggle, guilt and shame often associated where substance use/abuse and motherhood collide. Sober Mommies offers a platform for sharing stories, promoting identification and self-forgiveness, and an opportunity to receive and provide peer-to-peer support and mentorship.
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The Walking Through Grief product line is divided in to two sections. One is a series of single short DVDs with a variety of different focuses. Each DVD is designed to stand-alone and be used by individuals or groups around a specific topic. The second section is a grief program designed to be used in a facilitated environment that includes everything you need to run and facilitate a successful grief support group.
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Girl Power 2 Cure - Rett University is a 501(c)(3) organization chartered to raise funding to support:
1. Rett Syndrome treatment and curative research
2. General family resource and emotional support of children/families affected by Rett Syndrome
3. Educational programs for disabled and non-verbal children suffering from Rett Syndrome and other debilitating neurological conditions (Downs Syndrome, CP, Angelman Syndrome, Autism, etc.) which limit their ability to communicate, read, and write in traditional classroom settings (includes teacher and professional training/seminars for therapists and other specialists targeting services to complex-needs individuals).
Note: Rett Syndrome is a debilitating neurological condition which predominantly affects females, robbing them of the ability to speak, walk, or use their hands. It is caused by a random genetic mutation on the X-chromosome. 1 in 10,000 girls are affected, without regard to race, origin or any other common factor.
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The National Pancreatic Cancer Foundation exists to deliver unwavering support for patients and families fighting pancreatic cancer. NPCF aims to increase awareness for pancreatic cancer and transform the experience of pancreatic cancer by delivering immediate unwavering support to all who seek it. Our primary programs include education, awareness, and financial assistance. Since it's inception in May of 2009, NPCF has helped over 237 families affected by pancreatic cancer with basic living expenses.
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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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The Self-Injury and Recovery Research and Resources(SIRRR) is part of the Cornell Research Program on Self-Injury and Recovery and summarizes our work, and provides links and resources to self injury information. Our work is intended to generate new research and insight into self-injury. We also aim to translate the growing body of knowledge about self-injury into resources and tools useful for
those seeking to better understand, treat, and prevent it.
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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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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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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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OPACC was established in 1995 and supports families of children with cancer throughout Ontario through our in-hospital Parent Liaison program, which provides non-medical, peer-to-peer and virtual support and financial assistance; by establishing local parent support groups in communities throughout the Province; and by advocating on issues of importance to childhood cancer families.
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