New Update on Caringbridge on Emily and the foundation.

https://www.caringbridge.org/visit/emilykoesters

Click the link to visit and learn more about Emily's SIOD journey.

Believing in Emily

Please Watch. Please Share. Please Donate. (It is matching funds month😉)
Together We Can Do Something Extraordinary! #BELIEVINGINEMILY #SIOD#LITTLEGIANTS

*Videography by Jessie Addleman ❤- friend & UNL student

https://youtu.be/UrEQwfk7jLw?list=RDMMUrEQwfk7jLw

Giving Tuesday

Today is #GivingTuesday 🎅

Believe in Emily Koesters and our family knows there are many nonprofit organizations to choose from and we hope you are taking time to give to your favorite, which we hope is The Little Giants Foundation❤. See the LGF link called DONATE NOW at the side bar on this page! #believe

Big Things Ahead!

Please go to my personal Facebook page- Erin Koesters and share this video after hearing our big announcement!

October is Dwarfism Awareness Month

Dwarfism Awareness Day is Wednesday October 25th....help spread awareness by wearing Green!

Use the hashtags #believeinemily #dwarfism on Social media with your GREEN selfie on Wednesday, Oct 25!

Emily has a rare type of SED Dwarfism underlying her SIOD disease.  (There are over 200 types of Dwarfism!)

Heavenly Birthday Wishes to our founding Little Giant!

This lil' slugger is the reason Little Giants was originally started and the reason we have some great initial research on #SIOD! ❤ HAPPY heavenly 13th birthday Mitchell Cupps!🎂🎈 We treasure the days we were able to meet you and grateful you brought our families forever together! 😍 Our love to you always Michelle Evans Mitchell & Troy Cupps!

Some insight to SIOD!

Click here for a glimpse into Emily's story with SIOD.