Volunteer grant writer
3 people are interested
The Great Lakes Region is seeking passionate volunteers to be part of our team.
A key position we are looking to fill is a grant writer position. Responsibilities below:
Responsible for researching both local and national grant opportunities.
Prepare grant proposals for HDSA programs in draft and final form that make a compelling need for financial support and address organizational funding priorities.
And while COVID-19 disrupts everyone"s lives. Huntington's Disease contiues to disrupt the lives of so many families near and dear to us. They rely on the education, care and advocacy services our organization provides. And for that reason our organization needs to apply for grants because many of our local events are being cancelled.
We are grateful for the creativity of all are volunteers - all of which will help us through this difficult time.
Through it all Family Is Everything and the HD Family will get through this together.
We are all aware that the next few months are going to be challenging for nonprofits. COVID-19 will not stop our mission of supporting HD Families.
No additional volunteer opportunities at this time.
About Huntington's Disease Society of America
PO Box 56172, Chicago, IL 60656, US
The Society is a National, voluntary health organization dedicated to improving the lives of people with Huntington's Disease and their families.
To promote and support research and medical efforts to eradicate Huntington's Disease.
To assist people and families affected by Huntington's Disease to cope with the problems presented by the disease.
To educate the public and health professionals about Huntington's disease.
Woody Guthrie was a storyteller who used music to tell his stories. In 1967, Woody Guthrie, lost his battle with HD. He was just 55 years old. During the more than 15 years that the disease affected him, he struggled to continue to communicate his conviction that every man, woman and child has within them the power to make a difference.
Soon after his death, his widow Marjorie vowed to do something about this silent killer. Dynamic and compelling, Marjorie Guthrie convinced then President Jimmy Carter to form a Presidential Commission to study neurological diseases, including HD. In 1983, HDSA Coalition for the Cure investigator, Jim Gusella, found the very first marker for the disease and, after a ten year search that involved collaboration among the top HD researchers worldwide, the gene was located on the short arm of chromosome 4.
Since that time, research has progressed rapidly and, in 2004, HDSA formed a pipeline for drug discovery that begins in the laboratory with basic science (HDSA Grants & Fellows program and the prestigious HDSA Coalition for the Cure) progresses to applied/transitional research (HDSA partner CHDI) and then moves to patient's bedside in the form of human clinical trials that test the most promising compounds often at HDSA Centers of Excellence. Today the question our families ask is not "if" there will be a treatment or cure, but "when."
In the area of care, HDSA has created a national network of resources and referrals that are unmatched by any other HD organization. HDSA Centers of Excellence provide medical and social services to those affected by HD and their families while a toll free helpline and extensive national web site (www.hdsa.org) help to provide access to services. HDSA chapters, affiliates, regions, social workers, and support groups work in tandem with the Centers of Excellence to increase awareness about HD and raise funds for research, education and family services.
We'll work with your schedule.
This is a Virtual Opportunity, with no fixed address.
March 18, 2020
- Grant Writing / Research
- Orientation or Training
- At your convenience