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ECT Justice is a website dedicated to advocating for individuals who have suffered from Electroconvulsive Therapy (ECT) and their families. ECT, also known as electroshock therapy, is a controversial psychiatric treatment involving the induction of seizures through electrical currents passed through the brain. The site provides information, resources, and support for ECT survivors, and it aims to raise awareness about the potential risks and long-term effects of the treatment. The website's content includes personal stories from ECT survivors, discussions about the medical and legal implications of ECT, and information about the risks and side effects associated with the treatment. It also offers a questionnaire for individuals who believe they have been damaged by ECT, with the goal of gathering data to support advocacy efforts and potentially seek compensation for those affected. The site's founder, Deborah Schwartzkopff, is an ECT survivor herself and has been a vocal advocate for the rights of ECT patients. The website serves as a platform for her and others to share their experiences and work towards greater transparency and accountability in the use of ECT. It's important to note that while ECT has been used in psychiatric treatment for decades and is considered effective in certain cases, it is not without controversy. Critics of ECT argue that it can cause significant and sometimes long-lasting cognitive and memory impairments, and they advocate for more stringent regulations and informed consent processes surrounding its use. The website's emphasis on empowering survivors, gathering data, and advocating for change aligns with the broader movement within mental health care to prioritize patient rights, informed consent, and the recognition of the long-term impact of treatments. By providing a platform for survivors to share their stories and by collecting data on adverse effects, ECT Justice contributes to the ongoing dialogue about the ethical and medical considerations of ECT."

• Advocacy for ECT survivors, Raising awareness about potential risks of ECT, Providing resources and support for those affected by ECT, Gathering data through a questionnaire for individuals who believe they have been damaged by ECT, Emphasis on informed consent and patient rights in mental health care, Platform for sharing personal stories of ECT survivors, Aligning with broader movement in mental health care to prioritize patient rights and recognition of treatment impact, Contributing to ongoing dialogue about ethical and medical considerations of ECT