About

Living with PMOS: Understanding my body one day at a time.

Hi, my name is Mikayla, I am 21 years old and was diagnosed with PMOS at 15 years old. This Blog will be about the reality and struggles that surround Polyendocrine Metabolic Ovarian Syndrome. By reading this blog, I hope that people become more familiar with this syndrome and hopefully those with it are able to feel more seen.

I am still learning how to support my hormones and completely understand my body. If you are navigating this syndrome as well, you are not alone. This space is for you just as it is for me.

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CONTACT

  • @Mikayla-wilks.bsky.social via Bluesky
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