Cynthia is a Graduate Student and Craniofacial Awareness Advocate born with Treacher Collins Syndrome. She currently works as a health and wellness activist with her husband through their FREE charity app Assuaged. The Murphys are passionately seeking to bridge the gap between healthcare and self-care to meet the needs of healthy living as a method for longevity. They are going beyond charity and unifying people through love and compassion.
Thursday, March 22, 2018
Elyse- Craniofacial Apert Syndrome
The Cosico's young daughter Elyse was born with a rare #craniofacial condition called Apert Syndrome. The syndrome is characterized by abnormal skull development, fused fingers and toes, and some facial deformities. Elyse faces multiple hospitalizations and surgeries, and will be the recipient of this year’s “Taste of Union” event to be held on Thursday, April 19. The “Taste of Union” annually showcases local restaurants and food vendors to benefit an individual or family in need. https://goo.gl/Kv2V6H
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It is no secret that I have a very deep and personal relationship with God. I have pushed and resisted that relationship this past year through all the bullshit I have had to go through living with Herpes but once again, God is bigger than my stubbornness and broke through that outbreak cold sore and all I had Genital Herpes. For me personally, hearing over and over how I am not good enough has really invaded my mind in the worst way possible. I completely shut down and I was just waking up like is this how life going to end this temporary herpes outbreak “fuck everybody with herpes if you know what I mean” but let's be honest here...
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