4 people are interested
4 people are interested
The partnerships coordinator will contribute to the growth and sustainability of the Turner Syndrome Foundation, a New Jersey based nonprofit established in 2009. To learn more about the mission and the people we serve, please visit: https://turnersyndromefoundation.org/who-we-are/mission/. You can be a part of the history we are making to improve women's health.
The applicant should possess interest in the area of development with an eye on creating new relationships and partnerships. The position will entail good communications, phone, email, letter writing and possibly meeting with potential funders. If you are a people person and influence, we want to speak with you!
Complete the online application. https://turnersyndromefoundation.org/volunteer_take_action/talent-application/
TSF offers a COVID safe workplace and possible virtual opportunities.
About Turner Syndrome Foundation
1 Bethany Road, Building 1, Suite 5, Hazlet, NJ 07730, US
Turner Syndrome affects 1 in 2,000 females. We can help! The goal of the Turner Syndrome Foundation is to support research initiatives and develop educational programs that will increase professional awareness and enhance medical care of those affected by Turner Syndrome. Early diagnosis and comprehensive treatments over the lifespan will lead to a brighter and healthier future for all young girls and women with Turner Syndrome.
Turner syndrome is a random mutation of chromosomes that occurs spontaneously at the time of conception and affects females. There is an absence of all or part of the second X chromosomes in some or all of the cells in the body. As an advocacy organization, our vision is to increase awareness, education and research for this complex disorder. Statistics show that Turner Syndrome takes the lives of 97% or more female fetuses. Our goal is to provide the 1-3% of survivors, who account to 1 in 2,000 females) with a chance at living a full and productive life while gaining additional knowledge and therapies for improvements. If a child does not exhibit classic TS characteristics, but is short and falling below the curve on the growth chart, has delayed pubertal development, presents verbally gifted, or expresses academic or social challenges, she may have TS. Diagnosis is confirmed with a Karyotype blood test. An endocrinologist will monitor the patient, screen for other conditions and provide specialized medical care, and treatments. Early interventions can promote a positive self-esteem and improved prognosis.
1-3% of Turner Syndrome babies will survive birth
10-20% of all miscarriages are babies lost to Turner Syndrome
For every 2,000 females, one will be affected by Turner Syndrome
This is a Virtual Opportunity with no fixed address.
July 31, 2021
- Sales Coaching & Training
- Customer Acquisition
- Relationship Building
- Verbal / Written Communication
- 10+ hours per week for 3-4 month commitment
- Apply here: https://turnersyndromefoundation.org/volunteer_take_action/talent-application/