About falesha

MOM.WIFE. FITNESS ENTREPRENEUR. SPECIAL NEEDS PARENT. ADVOCATE

Join me as I shift gears from fitness entrepreneur, former professional athlete to motherhood. I will share my raw, authentic, and unexpected journey as a mother. My daughter was born with Pfeiffer syndrome, a rare genetic disorder that fused her skull prematurely and caused structural anomalies to her face and other body parts. She will have two skull surgeries and at least six surgeries in total in her first year of life. My shift to being a first-time mom and then one of a medically complex baby has been a roller-coaster, but one that has brought me much joy. My daughter is a real blessing, and she has already taught me so much in life that I cant wait to share with you.

Her arrival into this world has made me want to use my platform to advocate for those born with rare diseases, those from birth who have a long road ahead of them that many won't ever endure.

I will touch on topics from motherhood, family, inclusion, empowerment, and accessibility for all. I hope you are inspired to be an ally, a stronger advocate, and work to lift others while leading a life with love and compassion.