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Nov 20–22, 2026 | Online
What happens when a psychedelic protocol or study ends? This global virtual gathering unites patients, families, clinicians, researchers, and organizations across the field to examine emerging risks, unmet needs, and how lived experience can shape safer, more responsive care.
Standard $79 · Student $29 · Scholarships available
Meet the 50+ contributors and moderators shaping this year’s working summit
Join 9 live roundtables + 3 daily synthesis panels + open attendee discussions
Learn more about this year’s unique programming theme and why it matters now
Watch Robin Carhart-Harris, PhD in conversation with Pedram Dara, exploring questions shaping psychedelic research beyond the protocol.
Register free and you’ll receive:
✓ Immediate access to the full conversation
✓ Selected most-watched content from the 2025 summit
✓ Early access to additional pre-summit content and updates
Recorded live on October 27, 2026. Register free to watch the conversation on demand.
Our inaugural Psychedelic Lived Experiences Summit reached more than 3,000 attendees from 74 countries.
In November 2025, we brought together more than 60 patients, clinicians, and researchers across 54 in-depth interviews and 12 live panels to explore the benefits, limitations, and real-world complexities of psychedelic treatment. By uniting lived experience with scientific and clinical perspectives, the summit created the foundation we're building on in 2026.
DAYS
SPEAKERS
ATTENDEES
"The greatest resource we have for making progress in healthcare is the lived experience of those who are affected." – Dr. Lisa Sanders
Psychedelic treatments are often framed as breakthroughs, but real-world outcomes are far more complex, ranging from profound benefit to little change to lasting harm.
Clinical trials capture important measures, but lived experience reveals what those measures can miss: delayed risks, unexpected benefits and difficulties, everyday functioning, meaning, and the gap between protocol design and real life.
Yet as psychedelic research, care, and regulation evolve, the people who actually undergo these treatments still have too little influence over the decisions shaping them.
This is not a conference about patients. It is built and led by them, bringing lived experience into direct dialogue with research, practice, and ethical oversight to ask better questions, expose blind spots, and improve the decisions shaping psychedelic care.
2026 summit theme
Psychedelic treatment does not end when the session or study does. Benefits, risks, and destabilization can emerge long after formal follow-up ends, often beyond what research and care systems capture. In 2026, we focus on that gap: what happens next, what gets missed, and what better support, oversight, and accountability should look like.
3 days · 12 live roundtables & panels · 50+ contributors
Meaningful progress cannot come from one group talking to itself. The 2026 summit is designed to bring different forms of expertise into the same room. Different perspectives will not always agree. That is precisely why they need to meet.
Patients and trial participants
People with diverse experiences of psychedelic clinical trials, treatments, and their longer-term consequences.
Family members and caregivers
Spouses, friends, colleagues, and other family members or caregivers of patients and trial participants.
Therapists, physicians, and nurses
Practitioners supporting screening, preparation, treatment, integration, recovery, and longer-term care.
Researchers and trial teams
Professionals designing studies, measuring outcomes, managing safety, and generating the field's evidence.
Ethics, policy, and advocacy
Those examining accountability, participant protection, access, regulation, and systemic change.
Organizations and field builders
Groups developing the infrastructure, communities, standards, and services surrounding psychedelic care.
This summit is independently produced, with no grants, corporate funding, or pharma sponsorship. It is organized by people with firsthand experience of psychedelic clinical trials and treatments, creating space for lived experience to help set the agenda.
Join live and get on-demand access to every session, so you can watch, revisit, and learn on your own time.
$79 USD
Full live and on-demand access to the 2026 summit, plus the complete 2025 summit archive, workshop recording, resources, and community spaces.
✓ Live access to all 2026 sessions
✓ 9 roundtables + 3 synthesis panels
✓ Recordings of all 2026 sessions
✓ Complete 2025 summit archive
✓ 6 months of on-demand access
Pre-summit rate: $79 USD through Nov 19
Regular rate: $119 USD from Nov 20
From $149 USD
Go beyond attending by helping make the summit possible for others while supporting the independent, lived experience work behind the summit.
✓ Everything included in Standard
✓ Private gathering in Denver (2027)
✓ Helps fund full scholarship passes
✓ Supports free peer support circles
✓ 12 months of on-demand access
Choose your contribution amount and support student and scholarship passes.
$29 USD
Full live and on-demand access to the 2026 summit for currently enrolled students, plus the complete 2025 summit archive.
✓ Live access to all 2026 sessions
✓ 9 roundtables + 3 synthesis panels
✓ Recordings of all 2026 sessions
✓ Complete 2025 summit archive
✓ 6 months of on-demand access
For current students. Institutional email preferred. Valid student status required.
Purchasing for others or need multiple passes? Group discounts and registration are available. Contact us →
Made possible in part through Supporter Pass contributions, scholarship passes provide full summit access for people who would otherwise be unable to attend due to cost. Applications are free and priority will be given to people facing financial barriers, including those from the Global South and other underrepresented regions.
Applications close Nov 4 (11:59 PM ET) · Decisions by Nov 6
Less presentation. More structured collaboration.
Each day features three facilitated 90-minute working roundtables, each bringing together five contributors plus a moderator across lived experience, clinical practice, research, policy, advocacy, and other perspectives. The day concludes with a 60-minute synthesis panel featuring one contributor from each roundtable plus an outside perspective, helping connect themes and priorities across the day. Attendees can contribute through questions and open-discussion periods.
What happens beyond the psychedelic protocol, from real-world outcomes and emerging risks to gaps in measurement, support, oversight, and accountability. Across MDMA, psilocybin, LSD, ketamine, 5-MeO-DMT, and ibogaine, we’ll examine why post-treatment care needs to extend beyond “integration” to include stabilization, safety monitoring, continuity of care, and longer-term support informed by lived experience.
Each of the nine working roundtables is built around a defined question and practical outcome. Together, these outputs will be synthesized into a post-summit paper documenting key findings, gaps, safety signals, research priorities, and areas for future collaboration. The outputs will inform recommendations, guidelines, or other public resources.
Live programming (Nov 20–22, 2026):
Can’t attend live?
Registration includes all 2026 recordings, plus last year’s full archive of 54 interviews and 12 live panels to watch later.
The Psychedelic Lived Experiences Summit runs on November 20–22, 2026.
Live programming: 11:00 AM–6:00 PM ET / 8:00 AM–3:00 PM PT / 5:00 PM–12:00 AM CET
The Zoom room will remain open during breaks for attendee discussion and reflection. Contributors may also join when available.
Roundtables are multidisciplinary. Session titles set the theme. Contributors span perspectives, not always matched by specialty.
Nov 20: Roundtable #1 (90 min)
11 AM ET / 8 AM PT / 17:00 CET
What minimum support should be available when structured psychedelic treatment or a clinical trial ends, particularly during periods of ongoing change or vulnerability?
Contributors: Rosalind Watts, PhD, Chantelle Thomas, PhD, Pedram Dara, Allison Feduccia, PhD, Caroline Lilley
Moderator: Melanie Dignam, RSW
Nov 20: Break #1 (30 min)
12:30 PM ET / 9:30 AM PT / 18:30 CET
Nov 20: Roundtable #2 (90 min)
1 PM ET / 10 AM PT / 19:00 CET
How do culture, race, identity, socioeconomic resources, geography, disability, and other factors shape psychedelic treatment experiences, risks, outcomes, and access to support?
Contributors: Leor Roseman, PhD, Kimberly King, Franklin King, MD, Jana Sladkova, PhD, Joshua White
Moderator: Scarlet Masius
Nov 20: Break #2 (30 min)
2:30 PM ET / 11:30 AM PT / 20:30 CET
Nov 20: Roundtable #3 (90 min)
3 PM ET / 12 PM PT / 21:00 CET
What warning signs and difficult outcomes may emerge after psychedelic treatment, and how should they be recognized, documented, escalated, and responded to?
Contributors: Christopher Nicholas, PhD, Şerife Tekin, PhD, Ari Polivy, Taylor West, Jagpaul Kaur, PharmD/PhD(c)
Moderator: Jason Luoma, PhD
Nov 20: Break #3 (30 min)
4:30 PM ET / 1:30 PM PT / 22:30 CET
Nov 20: Day 1 Synthesis Panel (60 min)
5 PM ET / 2 PM PT / 23:00 CET
What happens after treatment, who may be underserved, and what can go wrong?
Contributors: Taylor West, Kimberly King, Madison Nobbs, RN, Caroline Lilley
Moderator: Pedram Dara
Nov 21: Roundtable #4 (90 min)
11 AM ET / 8 AM PT / 17:00 CET
What outcomes and follow-up periods are needed to understand whether psychedelic treatment has meaningfully helped—or harmed—someone’s life?
Contributors: Berra Yazar-Klosinski, PhD, Becca Kacanda, MS, Henrik Jungaberle, PhD, Kathy Neustadt, Stephanie Stewart, MD
Moderator: Pedram Dara
Nov 21: Break #1 (30 min)
12:30 PM ET / 9:30 AM PT / 18:30 CET
Nov 21: Roundtable #5 (90 min)
1 PM ET / 10 AM PT / 19:00 CET
What responsibilities should therapists, clinics, researchers, sponsors, and institutions retain when formal treatment or research support ends—especially when problems emerge later?
Contributors: Jesse Gould, Sara Garcia Velazquez, MD, Dave Pounds, Amy Emerson, Steve Allgood
Moderator: Jazz Glastra, MS
Nov 21: Break #2 (30 min)
2:30 PM ET / 11:30 AM PT / 20:30 CET
Nov 21: Roundtable #6 (90 min)
3 PM ET / 12 PM PT / 21:00 CET
What role should families, partners, and other caregivers have before, during, and after psychedelic treatment, and what support do they themselves need, while respecting participant autonomy and privacy?
Contributors: Ismail Ali, JD, Ona Praderas, Jérémie Richard, PhD, Britton Rollins, Amanda Geisinger
Moderator: Sergio Pérez Rosal, MD
Nov 21: Break #3 (30 min)
4:30 PM ET / 1:30 PM PT / 22:30 CET
Nov 21: Day 2 Synthesis Panel (60 min)
5 PM ET / 2 PM PT / 23:00 CET
How do we measure it, who is responsible, and how do support networks fit?
Contributors: Amy Emerson, Jérémie Richard, PhD, Kim Witczak, Becca Kacanda, MS
Moderator: Pedram Dara
Nov 22: Roundtable #7 (90 min)
11 AM ET / 8 AM PT / 17:00 CET
What changes in relationships, work, functioning, identity, meaning, quality of life, and well-being matter when evaluating psychedelic treatment over time?
Contributors: Hanifa Nayo Washington, Heidi Allen, PhD, MSW, Anahita Bassir Nia, MD, Sehrish Sayani, Kerrilee Barrett
Moderator: David Drapkin, LCSW
Nov 22: Break #1 (30 min)
12:30 PM ET / 9:30 AM PT / 18:30 CET
Nov 22: Roundtable #8 (90 min)
1 PM ET / 10 AM PT / 19:00 CET
What mix of clinical, peer, community, and other support is needed after psychedelic treatment, and how should those roles connect across the care pathway?
Contributors: Max Wolff, PhD, Laura Zam, Mourad Wahba, MD, Katie Bourque, Spencer Hawkswell
Moderator: Anne Katrin Schlag, PhD
Nov 22: Break #2 (30 min)
2:30 PM ET / 11:30 AM PT / 20:30 CET
Nov 22: Roundtable #9 (90 min)
3 PM ET / 12 PM PT / 21:00 CET
Where and how should lived experience evidence and lived experience expertise meaningfully influence psychedelic research, clinical practice, safety systems, and policy?
Contributors: Jon Nelson, Wendy Marussich, RN, PMHNP, PhD, Tehseen Noorani, PhD, Bia Labate, PhD, Rogers Masson
Moderator: Chelsea Rose Blake, LMFT
Nov 22: Break #3 (30 min)
4:30 PM ET / 1:30 PM PT / 22:30 CET
Nov 22: Day 3 Synthesis Panel (60 min)
5 PM ET / 2 PM PT / 23:00 CET
What happens over time, how should services respond, and how should lived experience shape decisions?
Contributors: Berra Yazar-Klosinski, PhD, Tehseen Noorani, PhD, Anahita Bassir Nia, MD, Laura Zam
Moderator: Pedram Dara
Nov 20–22, 2026 | Online
This summit is 100% independent, with no grants, corporate funding, or pharma sponsorship. It is organized by people with firsthand experience as patients and clinical trial participants, putting lived experience at the center of the agenda. That independence is what makes the summit different, and why your support matters.
Can’t attend live? Get all 2026 recordings plus last year’s 54 interviews and 12 panels.
Start with free access to the pre-summit conversation with Robin Carhart-Harris, PhD, hosted by Pedram Dara and recorded live on October 27, plus selected most-watched content from the Psychedelic Lived Experiences Summit 2025.
Bringing together lived experience, clinical practice, research, policy, and advocacy to examine what happens beyond the protocol.
Founder and director of Psychedelic Lived Experiences, MDMA-assisted therapy clinical trial participant, peer support facilitator, researcher
Psychedelic facilitator designing equitable pathways for psychedelic therapy within public healthcare systems, co-director at PMHA Alliance
Lawyer, psychedelic policy leader, and co-executive director of MAPS, advancing drug policy reform and psychedelic policy implementation
Clinical psychologist, founder of ACER Integration, and former clinical lead for the Imperial College London’s psilocybin for depression clinical trials
Senior lecturer and psychedelic researcher at the University of Exeter’s EPIC, founder of Ripples, dedicated to peacebuilding
MDMA therapy clinical trial participant and caregiver to her husband after post-trial destabilization, award-winning author and resilience speaker
Psychologist, researcher, and clinician-scientist in psychotherapy at Humboldt-Universität zu Berlin, Germany
Phase 3 MDMA-assisted therapy for PTSD clinical trial participant (active arm), art therapist, peer support facilitator
U.S. veteran, founder and president of Heroic Hearts Project, a nonprofit supporting psychedelic therapy access for military veterans
Former Chief Scientific Officer at Resilient Pharmaceuticals (formerly Lykos/MAPS PBC), biologist, biotech leader, founder and CEO at Yazar Lab
Lawyer, psychedelic researcher, coach, peer support advocate, founder and executive director of Fireside Project
Phase 3 MDMA-assisted therapy for PTSD trial participant, advocate for trauma-informed healing, integration, and responsible storytelling
Researcher, founder and CEO of the MIND Foundation, head of development at OVID Clinic in Berlin, Germany
Addiction psychiatrist and assistant professor at Yale School of Medicine researching psychedelics, substance use disorders, PTSD and neurobiology
MDMA-assisted psychotherapy for alcohol use disorder trial participant, trauma and recovery speaker and coach, creator of Design For Life
Senior manager of mental health equity and external partnerships for the national office of the Depression and Bipolar Support Alliance (DBSA)
Lived Experience Council member at One Mind, director of lived experience at Motif Neurotech, co-founder at Otherside, mental health advocate
Professor of social work at Columbia University, health policy researcher, developer of psychedelic-assisted therapy training for social workers
Psychiatrist, psychedelic researcher, director of training at MGH’s Center for the Neuroscience of Psychedelics, Harvard Medical School faculty
Anthropologist, educator, author, speaker, activist, co-founder and executive director of the Chacruna Institute
CEO of TheraPsil, passionate advocate for legal, medical, and clinical access to psychedelic therapy for Canadians
Clinical psychologist and researcher dedicated to post-protocol safety, therapist training, and trauma-focused and ethical psychedelic care
Clinical psychologist, psychedelic scientist, and associate professor at the University of Wisconsin studying MDMA and psychedelics for addiction
Patient with lived experience of group ketamine-assisted psychotherapy and SPRAVATO® (esketamine) treatment for depression
Psychiatrist leading mood disorders research clinic in Newcastle, England, psychedelic trial principal investigator, lecturer, advisor, and educator
Former and founding CEO of Resilient Pharmaceuticals (Lykos/MAPS PBC), strategic advisor ensuring patient access to psychedelic therapies
U.S. Army veteran, MDMA-assisted psychotherapy for PTSD clinical trial participant, music producer, founder and CEO of PsySonics
Clinic operations lead at FlowState Therapy ketamine clinic, art therapy student, ACER Integration facilitator, caregiver and family support advocate
Clinical psychologist, psychedelic researcher, assistant professor at the University of Ottawa School of Psychology
Emmy-winning user experience designer, One Mind Lived Experience Council member, IV ketamine and SPRAVATO® with therapy patient
Social scientist and psychedelic researcher focused on first-person inquiry at the University of Auckland, New Zealand
Clinical research physician, former associate medical director at Resilient Pharmaceuticals (Lykos/MAPS PBC), quality assurance lead at Changemark
Psilocybin-assisted psychotherapy for life-threatening cancer through Canada’s Special Access Program, psychedelic therapy advocate
Global drug safety advocate and speaker, consumer representative on an FDA advisory committee evaluating new drugs and patient safety
Phase 3 MDMA-assisted therapy for PTSD trial participant (placebo then crossover), ibogaine patient, VETS Foundational Healing Grant recipient
Psychiatric nurse practitioner, co-founder of OPENurses, clinician providing TMS and esketamine treatment in outpatient psychiatry
Founder, CEO, and board chair of the National Psychedelics Association, supporting professionals working in psychedelic-assisted care
Executive director of the Healing Advocacy Fund, supporting access to psychedelic therapies through state-regulated programs
Associate professor of philosophy and bioethics at SUNY Upstate Medical University, author of Reclaiming the Self in Psychiatry
Neuropharmacologist, psychedelic researcher and educator, co-founder of Psychedelic Support, scientific advisor to psychedelic nonprofits
Faculty for Yale School of Medicine's Lived Experience Transformational Leadership Academy, former director of operations at Fireside Project
Biotech leader focused on patient strategy at AtaiBeckley, strategy consultant at Amandala Neuro, previously with Johnson & Johnson
Registered nurse specializing in emergency nursing and ketamine-assisted therapy for mental health conditions and chronic pain
Phase 3 MDMA-assisted therapy for PTSD clinical trial participant (placebo only), mental health and psychedelic participant rights advocate
Psychoactive substance for PTSD Phase 2 clinical trial participant (double blinded then open label), mental health counsellor
Pharmacist, psychedelic researcher, educator, and policy advocate for advancing safer, equitable, patient-informed psychedelic care and access
Integrative psychiatrist, psychedelic educator advancing culturally grounded healing, Indigenous reciprocity, and social justice
A special guest will join the Psychedelic Lived Experiences Summit 2026 for a featured appearance. Details coming soon.
Facilitating the summit’s roundtables and helping guide focused, multi-stakeholder dialogue.
Community strategist and consultant, trained psychedelic peer support facilitator, focused on participatory communities, harm reduction, and public education
Emergency medicine physician, anesthesiologist, neuroscientist, and researcher specializing in psychedelic medicine, adjunct professor at the University of Ottawa
Chartered psychologist and head of research at Drug Science, honorary senior fellow at UK's Imperial and King’s, focused on psychedelics, real-world data, ethics, and patient access
Psychotherapist, clinical social worker, psychedelic educator, and harm reduction specialist focused on integration, practitioner education, and mental health care
Executive director of Zendo Project, licensed therapist and psychedelic harm reduction practitioner with extensive experience in peer support and crisis response
Clinical psychologist and psychedelic researcher, principal investigator of an MDMA-assisted therapy trial for social anxiety, and psychotherapy trainer focused on therapeutic change
Integrative psychotherapist specializing in trauma and IFS, with experience across ketamine-assisted therapy, psilocybin clinical trials, and Canada’s Special Access Program
Senior director at BrainFutures, leading U.S. national initiatives on psychedelic therapy access, clinical integration, policy, and mental health system implementation
Hi, I'm Pedram Dara, a former MDMA-assisted therapy clinical trial participant and founder and director of the Psychedelic Lived Experiences, a patient-led initiative strengthening decision-making by bringing lived experience and clinical science together for safer, more ethical psychedelic research, care, and policy.
Since 2019, I’ve advocated for patient safety and treatment efficacy, speaking at major forums such as the European Parliament and the FDA, and at leading conferences like Psychedelic Science, ICPR, and International Trauma Conference. My story and insights are featured in news, documentaries, training programs, research projects, and journal publications.
I believe true progress in psychedelic care requires moving beyond hype and fear to embrace the depth, complexity, and wisdom of those who’ve lived it.
"Research leads to meaningful healing when it’s done with people, not just on them. When lived experience informs how studies are designed, conducted, and understood, research becomes more than data generation; it becomes a compass for healthcare transformation." – Pedram Dara
Nov 20–22, 2026 | Online
Join patients, families, clinicians, researchers, advocates, and organizations from around the world to explore what happens when psychedelic treatment ends and real life continues. Together, we’ll examine what we know, what we’re missing, and what safer, more responsive care requires.
Can’t attend live? Get all 2026 recordings plus last year’s 54 interviews and 12 panels.
This summit is independently produced, with no grants, corporate funding, or pharma sponsorship. It is organized by people with firsthand experience of psychedelic clinical trials and treatments, creating space for lived experience to help set the agenda.
Join live and get on-demand access to every session, so you can watch, revisit, and learn on your own time.
$79 USD
Full live and on-demand access to the 2026 summit, plus the complete 2025 summit archive, workshop recording, resources, and community spaces.
✓ Live access to all 2026 sessions
✓ 9 roundtables + 3 synthesis panels
✓ Recordings of all 2026 sessions
✓ Complete 2025 summit archive
✓ 6 months of on-demand access
Pre-summit rate: $79 USD through Nov 19
Regular rate: $119 USD from Nov 20
From $149 USD
Go beyond attending by helping make the summit possible for others while supporting the independent, lived experience work behind the summit.
✓ Everything included in Standard
✓ Private gathering in Denver (2027)
✓ Helps fund full scholarship passes
✓ Supports free peer support circles
✓ 12 months of on-demand access
Choose your contribution amount and support student and scholarship passes.
$29 USD
Full live and on-demand access to the 2026 summit for currently enrolled students, plus the complete 2025 summit archive.
✓ Live access to all 2026 sessions
✓ 9 roundtables + 3 synthesis panels
✓ Recordings of all 2026 sessions
✓ Complete 2025 summit archive
✓ 6 months of on-demand access
For current students. Institutional email preferred. Valid student status required.
Purchasing for others or need multiple passes? Group discounts and registration are available. Contact us →
Made possible in part through Supporter Pass contributions, scholarship passes provide full summit access for people who would otherwise be unable to attend due to cost. Applications are free and priority will be given to people facing financial barriers, including those from the Global South and other underrepresented regions.
Applications close Nov 4 (11:59 PM ET) · Decisions by Nov 6
Every 2026 pass includes access to the complete inaugural summit archive, exploring benefits, challenges, safety, integration, ethics, research gaps, and the complexities of psychedelic treatment.
Share this event with your network and join together in shaping the future of patient-centered psychedelic care.
The Psychedelic Lived Experiences Summit runs November 20–22, 2026. Live programming: 11:00 AM–6:00 PM ET / 8:00 AM–3:00 PM PT / 5:00 PM–12:00 AM CET.
Yes. All 2026 sessions will be recorded. Standard, Student, and Scholarship Pass holders receive 6 months of on-demand access, while Supporter Pass holders receive 12 months.
You’ll receive a confirmation email immediately after purchase. Closer to the summit, we’ll send your access details, schedule reminders, and information about joining the live sessions. After the summit, recordings and the 2025 archive will remain available for the access period included with your pass.
If you’ve checked all your inbox folders (including spam, junk, and promotions) and still don’t see the email, please reach out to us. We’re happy to help! Contact us at contact@psychedeliclivedexperiences.com