Summary (paraphrased)
C-SPAN recorded the opening panel of the MAHA Institute's Mental Health and Overmedicalization Summit in Washington, DC (May 2026), where four young adults described harms they attribute to psychiatric drugs taken from childhood or adolescence. Cooper Davis of the Inner Compass Initiative, which organised the panel, said the group is not against medication but for fully informed choice, and that the administration and HHS agencies had consulted it on mental health reform over the past year. Rep. Glenn Grothman (R-WI) said psychiatric drug use had doubled in 20 years without matching education or regulation, blamed the pharmaceutical industry's influence in Congress, referred to the House Oversight forum he had just chaired, and said he hoped to introduce legislation within five or six weeks. The moderator, drug safety advocate Kim Witczak, said her husband died by suicide five weeks after being prescribed an antidepressant for insomnia some 22 years earlier, and that she had campaigned for the boxed suicide warnings.
The post-SSRI sexual dysfunction account came from Lauren Friedman, 23, who said she developed PSSD after taking sertraline in 2022. Describing it as an injury to the nervous system rather than low libido, she reported lasting genital numbness, loss of orgasm, and a loss of libido that came on suddenly, together with emotional blunting severe enough that, years later, she says she cannot feel love for her family and friends or pleasure in music. She said sexual side effects affect 50 to 70% of people taking SSRIs; that persistence after stopping is not on US labels; and that a 2018 citizen petition asking the FDA to add it went unanswered (the library has the petition as LIT-020, and its unresolved status in LIT-076). She also said that Eli Lilly knew of permanent sexual and emotional effects and withheld them, that sexual medicine specialists are finding genital fibrosis in people who took SSRIs, that PSSD may be reversible with intervention, and that some people with PSSD have died by suicide: these are her claims, not assessed here. She said her psychiatrist told her afterwards that he knew of PSSD but thought it rare and had not mentioned it, and she called for recognition of the condition, research funding, and written informed consent before psychiatric prescribing, pointing to efforts in Tennessee.
Two panelists described withdrawal. Danielle Gansky, 30, said she was medicated at 7 after a school-prompted ADHD evaluation and was on stimulants, antidepressants, benzodiazepines, mood stabilisers and antipsychotics before 10. At 23 her doctor tapered her SSRI over six weeks, following standard guidance; she described a severe neurological reaction that did not resolve when the drug was reinstated, years of disability, and a current hyperbolic taper in reductions of under 1% at a time. Cameron LaBarre, 35, said he has taken SSRIs for about 26 years, since a diagnosis of anxiety, OCD and Tourette's at 9 (paroxetine for two decades, later escitalopram). He said no one discussed an end point, that attempts to stop as a teenager and in college brought severe panic that was read as relapse, and that a video by the psychiatrist Mark Horowitz led him to see it as withdrawal; he has been tapering for three years and now attributes years of numbness and indifference to the drug. Nick Taber argued that psychiatric labels recast children's reactions to difficult family and school environments as brain disorders, citing a CDC estimate that about 21% of children have a psychiatric diagnosis.
In questions, a urologist in the audience said SSRIs had been promoted to urologists at low doses for premature ejaculation 15 to 20 years earlier, which he took as a sign their sexual effects were known. Asked what government should do, panelists called for boxed warnings on persistent sexual effects and withdrawal, federal evidence-based tapering guidance, written informed consent and research funding.
Key points (paraphrased)
- 00:00:08Cooper Davis (Inner Compass Initiative) opens: the group argues for informed choice rather than against medication, says about 65 million Americans take a psychiatric drug, and that HHS agencies have consulted it; he frames patients' accounts as evidence.
- Rep. Glenn Grothman (R-WI): psychiatric drug use has doubled in 20 years; blames industry influence in Congress; has just chaired a House Oversight forum on the subject; expects to introduce legislation within five or six weeks.
- 00:07:51Moderator Kim Witczak: her husband died by suicide five weeks after an antidepressant prescribed for insomnia, about 22 years ago; she campaigned for the boxed suicide warnings.
- Danielle Gansky: medicated from age 7 after a school-prompted ADHD evaluation; a six-week doctor-directed SSRI taper at 23 was followed by a severe, prolonged reaction that persisted after reinstatement; now on a hyperbolic taper after seven years of protracted withdrawal.
- Cameron LaBarre: about 26 years on SSRIs since age 9; earlier attempts to stop were treated as relapse; recognised withdrawal through Mark Horowitz's work; tapering for three years, now on about 7.5 mg escitalopram.
- Lauren Friedman (PSSD): onset after sertraline in 2022; genital numbness, anorgasmia, sudden loss of libido and emotional blunting persisting for years; persistence is not on US labels; the 2018 FDA citizen petition is unanswered (LIT-020, LIT-076).
- Lauren Friedman's further claims, not assessed here: that Eli Lilly knew of and withheld permanent effects; that specialists find genital fibrosis after SSRIs; that PSSD may be reversible with intervention (compare LIT-026, LIT-040); that people with PSSD have died by suicide.
- Nick Taber: psychiatric labelling of children (about 21% diagnosed, per a CDC estimate he cited) treats reactions to family and school environments as disorders.
- Q&A: a urologist says SSRIs were promoted for premature ejaculation 15 to 20 years ago; one panelist recalls being given clonazepam after a single panic attack; the panel's asks are boxed warnings, tapering guidance, written informed consent and research funding.
Claims checked against the library
- “Sexual side effects affect 50-70% of SSRI users” (Lauren Friedman). Reported rates vary widely by study and method; not checked against a specific record.
- “A 2018 citizen petition asking the FDA to label persistent sexual dysfunction was ignored” (Lauren Friedman). LIT-020 (the petition), LIT-076 (still undecided in 2026; a 2024 lawsuit over the delay was dismissed in 2025 on standing).
- “Eli Lilly knew Prozac could cause permanent sexual dysfunction and emotional numbness and withheld it” (Lauren Friedman). No record in the library.
- “PSSD is a nervous system injury, not low libido” (Lauren Friedman). Small studies point to a peripheral-nerve component: corneal confocal microscopy showed peripheral neuropathy in 2 of 3 patients (LIT-040) and nerve damage suggestive of small-fibre neuropathy in Peters' case series (SIDE-002); abnormal quantitative sensory testing (LIT-033); abnormal pudendal evoked potentials in 4 of 16 PFS patients (DISC-013); TRP-channel hypothesis (LIT-026). Against: the Queen Square series found normal pelvic neurophysiology in 8 of 9 PSSD patients and proposes a central mechanism (CUR-003), though its tests don't assess small fibres. No controlled skin-biopsy study yet.
- “PSSD may be reversible with intervention” (Lauren Friedman). Partial improvements only, in single cases or tiny series: laser therapy (LIT-026), electrical stimulation plus shockwave therapy, with central symptoms unchanged (LIT-040).
- “Sexual medicine specialists are finding genital fibrosis after SSRIs” (Lauren Friedman). No record in the library.
- “SSRIs were promoted to urologists at low doses for premature ejaculation” (an audience member (urologist)). CROSS-001 and LIT-026 mention SSRI use for premature ejaculation; promotion to urologists is not documented in the library.
Why it’s in the corpus
On-the-record patient testimony on PSSD and protracted antidepressant withdrawal at a US policy event with a member of Congress and the HHS-linked reform movement, broadcast by C-SPAN. Friedman's account describes the core PSSD picture in the diagnostic criteria (CROSS-002) and case series (CROSS-001): genital anaesthesia (compare LIT-026), anorgasmia, libido loss and emotional blunting persisting after the drug is stopped. Her description of a nervous system injury lines up with the library's small but growing peripheral-nerve evidence: corneal confocal microscopy suggesting small-fibre neuropathy (LIT-040, SIDE-002), abnormal genital sensory testing (LIT-033) and pudendal evoked potentials (DISC-013), and the TRP-channel hypothesis (LIT-026); the Queen Square series (CUR-003) argues instead for a central mechanism, having found normal large-fibre neurophysiology in 8 of 9 patients. The panel documents the policy demands (labelling, tapering guidance, informed consent) and the US regulatory gap the library records in LIT-020 and LIT-076. It is testimony: it shows how the condition is described and argued for in public, not how common it is or what causes it.
Related records
- Peer-reviewed paper
Citizen petition: Sexual side effects of SSRIs and SNRIs
David Healy · International Journal of Risk & Safety in Medicine
This is the published text of a citizen petition asking the US FDA to require boxed warnings and label changes for all SSRI and SNRI products regarding persistent sexual dysfunction after discontinuation. The petition marshals the history of regulatory…
LIT-0202018PSSDLiterature sweep · Oct 2026 - Peer-reviewed paper
Penile anesthesia in Post SSRI Sexual Dysfunction (PSSD) responds to low-power laser irradiation: A case study and hypothesis about the role of transient receptor potential (TRP) ion channels
Marcel D. Waldinger; Ruben S. van Coevorden; Dave H. Schweitzer; Janniko R. Georgiadis · European Journal of Pharmacology
A man who developed penile anesthesia and scrotal hypesthesia on paroxetine, persisting two years after stopping the drug, received 20 sessions of low-power laser irradiation to the glans penis, the nerve branches at the base of the penis and the lower back…
LIT-0262015PSSDLiterature sweep · Oct 2026 - Gray literature
Seven drug regulators, including the EU, UK, and Canada, have warned since 2019 that antidepressant-linked sexual side effects can persist for years after the drug is stopped. The US hasn't.
ScienceBlog (Lab Report column) · scienceblog.com
A 2026 news-analysis piece mapping how seven regulators addressed persistent post-antidepressant sexual dysfunction between 2019 and 2025: the EMA's 2019 PRAC conclusion and label changes, the UK's 2019 label-level implementation, Health Canada's 2021 safety…
LIT-0762026-08PSSDLiterature sweep · Oct 2026
