Fierce Georgia On My Mind

Hi friends

Many of you know our story, but for those who don't, I'll try to write the short version.

Georgia was born in January of 2017, and at a month old was diagnosed with a rare form of Edwards' Syndrome. We were told 90% of children pass by age one & that she would be a vegetable.

We told them we didn't believe it. She was born little, but fierce.

For years now, Georgia has conquered so much. She has fought hard to change the perception that Edwards' Syndrome is Incompatible with life. She has learned to walk with a walker and goes to school. As her parents, we can genuinely say, this little girl is going places.

After several attempts to receive better care for our daughter, we have decided to leave our home state and travel to Cincinnati Children's Hospital for a second opinion. We travel there as often as needed.

We also receive intensives to help her get stronger from all over the country.

This child was meant to change the world and we are hoping you will help us prove that. Help us as Georgia's parents as we try to find a team of doctors willing to treat the symptoms, not the diagnosis.

Thank you.