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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/PKrQV Rarely Discussed Podcast 🎙️ →Rarely Discussed: https://beacons.ai/rarelydiscussed FOLLOW Rarely Discussed: →YouTube: https://shorturl.at/mtuwO →Instagram: https://shorturl.at/xGHPT →Tik Tok: https://shorturl.at/qEGQZ MEET Nicole Castellano: →Nicole's Story: https://t.ly/IsGK7 →Facebook: https://shorturl.at/krQZ8 →Instagram: https://www.instagram.com/nicowildkat... MEET Andrew McManamon: →Andrew's Story: https://t.ly/01JLz →Facebook: https://t.ly/kHuvX →Instagram: https://t.ly/Htuwg →Tik Tok: https://t.ly/eK1bP American Porphyria Foundation: →Website: https://porphyriafoundation.org/ →Instagram: https://rb.gy/osvb08 →Facebook Group: https://rb.gy/217o99 →YouTube Channel: https://rb.gy/9s0kcm #porphyria #rarelydiscussed #meganparrish __________ This podcast is supported by Recordati Rare Diseases. Recordati has no control or influence over the content mentioned in this podcast.