Pregnancy & Porphyria: Living Life With Porphyria - Rarely Discussed hosts Nicole Castellano and Andrew McManamon had the opportunity to sit down with the one and only Megan Parrish, who has been a big advocate for herself during her Porphyria journey as well as the American Porphyria Foundation. Megan discusses living with Porphyria, what she's learned along the way as well as her pregnancy journey too. Stay tuned!
Meet Megan Parrish→Megan's Story: https://shorturl.at/PKrQVRarely Discussed Podcast 🎙️→Rarely Discussed: https://beacons.ai/rarelydiscussedFOLLOW Rarely Discussed:→YouTube: https://shorturl.at/mtuwO→Instagram: https://shorturl.at/xGHPT→Tik Tok: https://shorturl.at/qEGQZMEET Nicole Castellano:→Nicole's Story: https://t.ly/IsGK7→Facebook: https://shorturl.at/krQZ8→Instagram: https://www.instagram.com/nicowildkat/?hl=enMEET Andrew McManamon:→Andrew's Story: https://t.ly/01JLz→Facebook: https://t.ly/kHuvX→Instagram: https://t.ly/Htuwg→Tik Tok: https://t.ly/eK1bPAmerican Porphyria Foundation:→Website: https://porphyriafoundation.org/→Instagram: https://rb.gy/osvb08→Facebook Group: https://rb.gy/217o99→YouTube Channel: https://rb.gy/9s0kcm__________This podcast is supported by Recordati Rare Diseases. Recordati has no control or influence over the content mentioned in this podcast.
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