Finding Your People with Megan Pearson, PCOS Awareness.

Ignite Your PowHER

This week's episode is with Megan Pearson, executive director and founder of PCOS Association. Also the founder of PCOS CON, a virtual event that highlights speakers with an expertise in PCOS.
Most importantly, she is extremely dedicated to fighting for women with PCOS. While working on increasing the reach of PCOS Awareness Association and those it supports, Megan has written the foreword for the Amazon Bestselling book “PCOS Diet for the Newly Diagnosed”, she was awarded Seattle’s Be Bold Be You, Woman of the Year award for her community engagement and advocacy of Polycystic Ovarian Syndrome, she has been featured in and has written numerous articles and publications worldwide, including ones published in Marie Claire, Women’s Health, NY Times and LA Times and has planned, organized and hosted several first-time events in the name of PCOS.
In this episode we chat about:

• Megan's personal PCOS story and how she was frustrated with the doctors that were suppose to help her find an answer.
• How difficult it is to get a diagnosis and support from family.
• What is PCOS awareness association?
• How PCOS awareness association help women struggling to get answers on how to heal their body.
• Advice for what women with PCOS should do.

Thank you so much for tuning in to this episode. I’m beyond honored that you’re here and would be grateful if you could take 2 minutes to leave me a 5-star review in iTunes or on your podcast app, this way together we can inspire, connect and educate even more women.

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Here is Megan's info.
PCOS Awareness Association (@pcosaa) • Instagram photos and videos
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Jennifer Roelands, MD (@wellwoman.md) • Instagram photos and videos

#pcos #pcosaa #polycysticovariansyndrome

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