Blog by a Parent on having a EA/TEF Child

My life keeps flashing before my eyes, with every synchronicity screaming at me from all angles, and it just keeps pouring in. The other day I was contacted by a NICU nurse in charge of finding ways for another NICU nurse to engage with the community and spread awareness about the everyday struggles that NICU babies come across.

She was telling me that she thought I would be a good spokesperson for EA/TEF Awareness, and she is looking for local support groups and websites associated with his defects. Meanwhile, I began sharing Xavier Magnus the Great’s story page in several support groups that I’m in for no good reason except to spread awareness by showing his superpowers off essentially lol.

I was then contacted by a gentleman who runs a blog site on EA/TEF Awareness which is endorsed by some of the most famous surgeons all over the world. He asked if I would be interested in blogging for his website and share my story with the entire world! Now if that isn’t synchronicity right there, then I don’t know what is.

So it looks like I’ll be starting a blog,