Lupus and Allied Diseases Association

Lupus And Allied Diseases Association

Non Profit Organization Management, P.O. Box 170, Verona, New York, 13478, United States, 1-10 Employees

ladainc.org

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Who is LUPUS AND ALLIED DISEASES ASSOCIATION

The Lupus and Allied Diseases Association, Inc. was founded in 1978 and is a national non-profit organization dedicated to enhancing quality of life for those impacted by lupus and allied...

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  • P.O. Box 170, Verona, New York, 13478, United States Headquarters: P.O. Box 170, Verona, New York, 13478, United States
  • 1978 Date Founded: 1978
  • 1-10 Employees: 1-10
  • dollar-icon Revenue: Under $1 Million
  • tech-icon Active Tech Stack: See technologies

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Employees

Kathleen Arntsen

President & CEO & Patient Advocate

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Frequently Asked Questions Regarding Lupus and Allied Diseases Association

Answer: Lupus and Allied Diseases Association's headquarters are located at P.O. Box 170, Verona, New York, 13478, United States

Answer: Lupus and Allied Diseases Association's official website is https://ladainc.org

Answer: Lupus and Allied Diseases Association's revenue is Under $1 Million

Answer: Lupus and Allied Diseases Association has 1-10 employees

Answer: Lupus and Allied Diseases Association is in Non Profit Organization Management

Answer: Lupus and Allied Diseases Association contact info: Phone number: Website: https://ladainc.org

Answer: The Lupus and Allied Diseases Association, Inc. was founded in 1978 and is a national non-profit organization dedicated to enhancing quality of life for those impacted by lupus and allied diseases and other conditions of unmet need by fostering collaboration among stakeholders and wielding the patient voice as a catalyst to advance innovative advocacy, education, awareness and biomedical research program initiatives that will identify causes, and discover better diagnostics, superior treatments, and cures. As a passion-driven, patient-focused charity led by individuals with lupus and their loved ones, we strive to promote patient-centered care, patient-engaged research, and empowerment programs to ensure that the patient perspective is included and recognized as an equal stakeholder in the healthcare, regulatory and public policy arenas and across the research continuum.

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