Advocacy in Georgia
The Lupus Foundation of America is the only national force devoted to solving the mystery of lupus, one of the world’s cruelest, most unpredictable and devastating diseases. Lupus strikes without warning and can have effects that last a lifetime. There is no known cause or cure of lupus, but there is hope.
Are you interested in participating in a Congressional district meeting this August? With such passionate, dedicated advocates like you involved, we are going to make an enormous impact around the Georgia next month.
- Attend a general Lupus Advocacy Teleconference. Confirm by taking a post-teleconference quiz
- Attend a teleconference specific to your elected officials
- Follow-up with the chapter:
- Once your meeting is scheduled, please submit the date and time of your meeting.
- Following the meeting, submit a follow-up survey.
REGISTRATION IS CLOSED. You are still encouraged to sign up to be a lupus activist.
What does a Lupus Activist do? A lupus activist engages in educating their federal, state, and locally elected officials about the cruel mystery of lupus. Whether through a letter, email, phone call, or face-to-face meetings with elected officials, lupus activists are the vital voice on legislation and policies issues impacting people with lupus and their families. An activist’s voice makes a difference.
Who can be a Lupus Activist? Anyone who cares about lupus! You don't have to be an expert in government affairs to share your knowledge and story about lupus.
Lupus Advocacy Milestones
Advocacy Chair Kim Schofield is Elected to Represent District 60 in Georgia
Congratulations to our Advocacy Chair Kim Schofield. As the newly elected State Representative for Georgia District 60, Representative Schofield will continue to fight tirelessly for the interests of Georgians including expanding medicaid and affordable healthcare for all.
Georgia Council on Lupus Education and Awareness (GCLEA)
The Georgia Council on Lupus Education and Awareness (GCLEA) was established by the Georgia General Assembly and Governor Nathan Deal in 2014 to improve the lives of Georgia residents who live with lupus by improving public education and awareness, improving access to resources for patients and family members, obtaining information that will inform current and future public health efforts, and increasing appropriate diagnosis of lupus by non-rheumatologists.
The GCLEA aspires to:
- Develop resources and programs that will improve the level of education and awareness concerning lupus for health care providers and the general public,
- Develop resources and programs for communities that lack access to specialized lupus health care providers, based upon the incidence and prevalence of lupus in the State of Georgia and
- Develop programs that encourage professional development and specialization in the diagnosis of lupus and the care, management and treatment of people with lupus
The GCLEA was established by Senate Bill 352 in 2014, as a result of seven years of the Georgia Chapter’s advocacy efforts. Click here to visit their website.
Lupus Community, including Advocacy Co-Chair Chris Reed, Shares Views with FDA at Historic Patient-Focused Drug Development Meeting
Septmember 29, 2017 - Top decision makers at the U.S. Food and Drug Administration (FDA) heard from over 550 people impacted by lupus this week at an unprecedented in-person meeting and live webcast about what it’s really like to live with the disease and what they need most from new treatments.
Three organizations – the Lupus and Allied Diseases Association, , the Lupus Foundation of America, and the Lupus Research Alliance – organized the meeting as part of the FDA’s externally-led Patient-Focused Drug Development (PFDD) Initiative. The PFDD was created by the FDA to allow regulators to better understand the perspectives of people with diseases such as lupus so they can better assess the risks and benefits of drugs under review.
To learn more about this historic meeting, click here.