Emily, our daughter and the voice and face of the Little Giants Foundation has an extremely rare, genetic life limiting dwarfism disease called SIOD. ( She is 1 of 5 in the USA, 50 in the world) She is a little person (dwarf) and has a rare form of dwarfism called SED. There are over 200 types of dwarfisms!
This Wednesday, October 25th is World Dwarfism Awareness Day.
Please join us in wearing GREEN in support of dwarfism awareness in honor of our Emily. Also, feel free to take a selfie wearing your GREEN and use the hashtags: #believeinemily #dwarfism and tag me, Erin Koesters on your social media sites.
Thank you-
Together we can make an extraordinary difference!
BELIEVE
October is Dwarfism Awareness Month
