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The Bulimia Anorexia Nervosa Association (BANA) is a not-for-profit, registered charity, community-based organization servicing the Windsor-Essex Region in Southwestern, Ontario. Since 1983, we’ve been committed to the provision of specialized clinical treatment, education and support services for individuals affected directly and indirectly by eating disorders.
As the primary regional source for the prevention and treatment of eating disorders, BANA is a leader in the promotion and acceptance of diverse body shapes and sizes through the adoption of a healthy, balanced lifestyle. Since its inception, BANA has provided services to thousands of individuals of all ages, genders and social/economic backgrounds with an ongoing case load of approximately 300 clients. In addition, we annually organize and host 250 educational health promotion presentations and programs that reach more than 20,000 children and adults.
Services are provided free of charge, without age restrictions and are supported by the Ministry of Health and the Erie St. Clair LHIN. For more information visit www.bana.ca.
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Hope for Two…The Pregnant with Cancer Network offers free support for women diagnosed with cancer while pregnant. We connect women who are currently pregnant with cancer with other women who have experienced a similar cancer diagnosis.Our mission here at Hope for Two is to provide women diagnosed with cancer while pregnant with information, support and hope.
Our Guiding Values:
We serve women in all socioeconomic, ethnic and religious backgrounds world-wide.
Volunteers with a history of cancer while pregnant are the mainstays of our support network.
We strive to remove barriers to women obtaining complete and accurate information about their options for dealing with cancer while pregnant.
We respect and support every woman’s personal decisions without judgment.
If you are looking to request support or become a volunteer support women you can visit our website at http://www.hopefortwo.org/
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The Attention Deficit Disorder Association provides information, resources and networking opportunities to help adults with Attention Deficit Hyperactivity Disorder lead better lives.
We provide hope, empowerment and connections worldwide by bringing together science and the human experience for both adults with ADHD and professionals who serve them.
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Faith’s Lodge supports parents and families coping with the death of medically complex condition of a child in a peaceful environment to reflect on the past, renew strength for the present, and build hope for the future. They help families through their darkest hours by creating a nurturing setting together with other parents who are coping with the same struggles. Set apart from daily life and surrounded by the calming North woods of Wisconsin, families at Faith’s Lodge are supported in an emotionally safe environment. The lodge accommodates up to eight families at a time and operates year-round serving either couples or families on designated dates. After 11 years, Faith’s Lodge is still the only dedicated retreat facility of its kind in the country. Faith’s Lodge has served over 9,000 people from 40 different states. To learn more or to register for a programming weekend, visit www.faithslodge.org.
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PFLAG Canada is a national charitable organization, founded by parents who wished to help themselves and their family members understand and accept their non-heterosexual children. The "coming-out" process can be a critical time for families. When the adjustment period is particularly long or painful, relationships can become permanently damaged, resulting in a lifetime of emotional scars. People cannot always rise above the challenge of accepting themselves or their family member, and the results can be devastating, even fatal. We support these families through today, and give them hope for a better tomorrow.
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Since its founding in 1986, the National Educational Association of Disabled Students (NEADS), has had the mandate to support full access to education and employment for post-secondary students and graduates with disabilities across Canada.
NEADS is a consumer-controlled, cross-disability charitable organization (corporation # 1007761975RR0001). We represent our constituents through specific projects, resources, research, publications and partnerships. NEADS is governed by a national Board of Directors representative of all of the provinces and territories.
Our work as an organization focuses on three core Strategic Program areas:
Student debt reduction
Student experience in class and on campus
Student and graduate employment
The organization functions collaboratively with post-secondary stakeholders, other non-governmental organizations, employers, disability service providers (on college and university campuses) and communities that can improve opportunities in higher education and the labour market for persons with disabilities in Canada. NEADS also provides ongoing expert advice to Employment and Social Development Canada and provincial/territorial governments. We have been a stakeholder group of the Government of Canada's National Advisory Group on Student Financial Assistance -- Chaired by the Director General of the Canada Student Loans Program -- since 1987. Our work includes promoting government programs and services that support higher education for Canadians with disabilities. The Association is a member organization of the Council of Canadians With Disabilities (CCD).
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Mental Health America (MHA) - founded in 1909 - is the nation’s leading community-based nonprofit dedicated to addressing the needs of those living with mental illness and to promoting the overall mental health of all Americans. Our work is driven by our commitment to promote mental health as a critical part of overall wellness, including prevention services for all; early identification and intervention for those at risk; integrated care, services, and supports for those who need it; with recovery as the goal.
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When it comes to dealing with grief, it can be a challenge to find the resources we need to educate ourselves and our loved ones on what is happening and how to best keep going forward.
Having been down this road, we want to give back. We want to reach out to those who are earlier on this road. We cannot make your pain go away, nor can we provide answers for you. What we can do is help you to find the tools that you need to work through your grief journey. Thus was born The Grief Toolbox. The Grief Toolbox is an ambitious project. Its goal is to be an all-encompassing place for grief tools: a singular area where a person can find all the resources they need to help them with that grief that neither time nor money can solve.
We here at the Grief Toolbox understand that needs change as we go from the raw encompassing pain of the first year to the stark reality of the second year, and then to the growth and reinventing ourselves of the middle years to the acceptance and blessing that now coexists with the pain and love that will always be a part of our life.
Grief, in our opinion, falls into two categories: grief that can be solved with time or money, and grief that can not be solved. If you leave your favorite coat on a plane, with time and money you can replace it and the grief will slowly fade. However, with the loss of a loved one - whether a spouse, a parent, a child or a sibling - no time and no amount of money will make this grief go away.
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The Compassionate Friends is a self-help support organization that provides highly personal comfort, hope, and support to every family experiencing the death of a son or a daughter, a brother or a sister, or a grandchild, and helps others better assist the grieving family.
Each chapter, along with the supporting National Office, is committed to helping every bereaved parent, sibling, or grandparent who may walk through our doors or contact us.
TCF has over 600 chapters serving all 50 states plus Washington D.C., Puerto Rico, and Guam, that offer friendship, understanding, and hope to bereaved parents, siblings, grandparents, and other family members during the natural grieving process after a child has died. Around the world more than 30 countries have a Compassionate Friends presence, encircling the globe with support so desperately needed when the worst has happened.
To find a local chapter: www.compassionatefriends.org/find-support/chapters/chapter-locator/
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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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