“I have not had to go back,” Megan said. “I have my lifetime membership, but I have not had to go back since then. My skin has been absolutely clear. My aunt is an esthetician, and she’s in shock at how much the hyperpigmentation just went away.”
Megan took it upon herself to help others navigate her path by founding the PCOS Awareness Association in 2012. What started as a social media movement to bring awareness to the condition turned into a non-profit organization.
It’s not easy working a full-time job in addition to helping run the PCOSAA, but Megan always sees signs of her purpose with the organization. One event she attended in New Orleans comes to mind.
“One day I’m sitting at the booth, tired and cranky,” she said. “My friends always say, ‘If it doesn’t glitter and doesn’t shine, it’s not Megan.’ I looked across the crowd and saw this girl who saw the glitter teal and PCOS sign, and she bee-lined it to my booth. She said ‘Are you Megan?!’ She said she has followed my journey since I first started posting about PCOS. She ran off and had her whole family at the booth. They said I had helped her so much in her path with PCOS and asked to pray with me. That’s when I knew I had to keep doing this.”