Send us a textWhat if you had to live with a rare, life-altering medical condition? Ruth Makena Mugaa, an advocate of the High Court of Kenya and founder of the Gigantomastia Foundation, faced gigantomastia and founded an organization to connect people to treatment of the rare condition. Join us as Ruth shares her personal journey and more about gigantomastia.Facebook: Ruth Makena Mugaa, Gigantomastia FoundationTwitter: Gigantomastia FoundationSupport the showFollow the show on:Twitter: @RootofscipodInstagram: @Rootofscipod YouTube: The Root Of The Science PodcastFacebook: The Root of The Science Podcast LinkedIn: The Root Of The Science PodcastWebsite

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“What did the council decide on item 42?” — answered with the speaker and the moment.

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