PSSD Network Podcast
A podcast that features discussions with individuals who suffer from Post-SSRI Sexual Dysfunction (PSSD), their loved ones, and medical professionals. The podcast delves into the experiences of living with, coping with, and managing PSSD, shedding light on the challenges and strategies associated with this condition. Through candid conversations, the podcast aims to provide valuable insights into the emotional, psychological, and physical aspects of PSSD, while fostering a supportive and informative space for those affected by it. Get in touch on contact@pssdnetwork.org or pssdnetwork.org.
Listen on:
Episodes
Monday Aug 28, 2023
Monday Aug 28, 2023
Bryn, Simon, and Roy discuss their realization of the enduring impact of PSSD over time.
Learn more about PSSD at pssdnetwork.org.
Monday Aug 28, 2023
Monday Aug 28, 2023
In this podcast episode, Rosie, Sean, Carlton, and Emily share their experiences with Post-SSRI Sexual Dysfunction (PSSD), a condition where individuals face persistent sexual side effects and other side effects after taking or discontinuing certain antidepressants. Rosie introduces the discussion by highlighting the lack of open conversations about PSSD and the importance of raising awareness. The group comprises individuals from different parts of the world, all in their twenties, who found each other online due to their shared struggles with PSSD. Each member recounts their unique journey.
Carlton was prescribed nortriptyline for IBS, which led to PSSD after discontinuation. Emily experienced genital numbness and emotional changes shortly after tapering off Lexapro. Rosie took Fluvoxamine and later Escitalopram, both of which triggered immediate genital numbness and emotional blunting. Sean's PSSD emerged after Celexa intake, causing genital numbness and emotional disconnection.
They discuss how PSSD has significantly impacted their lives, hindering emotional connections, relationships, and personal development. The group agrees that the loss of sexual function and emotional range has taken a toll on their overall well-being. Throughout the conversation, they emphasize the need for increased awareness and research on PSSD, sharing personal stories to shed light on this often-overlooked condition.
Despite the challenges they face, they remain determined to advocate for recognition and support for those suffering from PSSD. To learn more about PSSD, visit pssdnetwork.org.