Contact Us & Share Your Story

Your experience matters. Help us build the evidence base for medication safety reform.

Please note: As a small team, we're unable to answer individual medical questions — but our FAQ and Resources pages have detailed guidance on tapering clinics, support communities, and treatment options.

Share Your Story

Tell us about your experience with medication-induced harm. Your anonymity is protected unless you choose otherwise.

We use this to follow up with you, never to contact publicly.
Please describe your experience, symptoms, and how it affected your life. Please try to keep the word count to below 1,500 words. Thank you for sharing.

General Inquiry

What Happens Next

Thank you for sharing your experience — it matters. Your story should be available on our website within 5–7 days.

For Researchers

Are you conducting research on medication-induced adverse effects? We welcome peer-reviewed studies and citations. Submit your work through the research inquiry form above, and we can feature your findings on our Research page.

For Journalists

Media inquiries are welcome. We can connect you with patients and clinical experts (with permission) to tell this story with the authority it deserves. Select "Media Inquiry" in the form above.

Stay Informed

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Why Sharing Your Story Matters

Throughout medical history, patient voices have driven regulatory change. The FDA's withdrawal of vioxx in 2004 came not from internal data, but from accumulated patient reports and independent research. The FDA's Black Box warnings on psychiatric medications came only after decades of patient advocacy. The recognition of protracted benzodiazepine withdrawal syndrome exists because patients refused to accept dismissal and demanded recognition of their reality.

The FDA's Adverse Event Reporting System (FAERS) depends on voluntary reporting from healthcare providers and patients. Yet many prescribers lack awareness of medication-induced harms or are biased against reporting them. Patient submissions are critical. When hundreds or thousands of people report the same pattern of harm—PSSD after SSRIs, cognitive decline after benzodiazepines, neuropathy after fluoroquinolones—that collective testimony builds an irrefutable case for regulatory action and medical accountability.

Your story is not just data. It is evidence. It documents the gap between what pharmaceutical companies claimed and what actually happens to real people. It challenges a medical system that has minimized your experience and demands recognition of your reality. Collectively, your stories build the case for reform: better informed consent, more rigorous monitoring of adverse events, genuine accountability when harm occurs, and an end to the systematic dismissal of patient voices.

Your Privacy is Protected

Personal information submitted through this form is treated with strict confidentiality. Stories are only published with your explicit written permission, and only in anonymized form unless you consent otherwise. We do not sell, share, or distribute your information to third parties. Your email address is used only for follow-up communication regarding your submission.