❤EMILY'S NEBRASKA LITTLE GIANT DAY COMING SOON!!!❤

We have our newest red "LOVE" shirts available for purchase @ $20 for locals ($25 if shipped) that the Gretna Middle School Art Club designed and we had for her 5K this year.

Wristbands are 1 for $3 or 2 for $5

People may wear them on either Friday, Feb 10 to work, school, etc in honor of Emily or on the actual day of Saturday, Feb 11, so I will leave it up to you all as to the day you would like to choose.

We would love for you all to post pictures with the hashtag #give10#emilyslittlegiantday via twitter, IG and FB wearing these for Emily.
Twitter @littlegiants14
FB @believeinemily & @believeinlittlegiants
IG @littlegiantemily

ORDERS: Msg me📲402-658-9624/jeek01@gmail.com

*proceeds go for medical research for #SIOD

100 Day Campaign

We are launching a campaign for the Little Giants Foundation on behalf of Emily Koesters, #1of5inUSA with #SIOD.  IF 10,000 people could give even $10 in 100 days we will reach our goalof $100,000 to help provide medical research to prolong these extraordinary Little Giants' lives! #give10 #believeinemily

                                  *If you are unable to give 10 then share and tag a friend!

Our Little Giant Emily Hospitalized

Please click here to follow Emily's medical journey past, present and future.

This link is also available to the far right with other sites of interest.
Thank you for following.
BELIEVE

Wishes Do Come True!

Please watch these video links and see the magic of Christmas at work!

My Christmas Wish

Wish Granted!

Our gratitude to It Works Global!  I am so proud to be a part of such a giving company!

BELIEVE-
Erin Koesters

Author unknown There is no footprint too small to leave an imprint on this world.

It is with a heavy heart I let you all know that this month's featured Little Giant, Jace Williams passed away last night.  In speaking with his mother, Courtney she had told me he had pneumonia in both lungs yesterday and trouble breathing.  Jace was awaiting his kidney transplant and could not fight anymore.  

I told Courtney we will keep fighting for her little giant angel and those that passed before him.  Like I have said since this diagnosis first reared it's head at our Emily, "we are fighting against time".  We cannot and will not take it for granted as we know and have seen and invested in these families and their children.  

Our sincere condolences to Jace's entire family and I will update in regards to his memorial as I have word.

And to all of our friends and family, please wrap your arms of strength around Courtney and her family and show your love for them here in the comments, on our FB page @believeinlittlegiants, or to Courtney Marie Nichols on FB.

BELIEVE-

Jace Williams is our November Featured Little Giant!

Jace Williams is a five year old boy who loves star wars, play doh, singing songs, reading, cars, and Casper the movie!  He was born on August 25, 2011 and was diagnosed at the age of four in May of 2015.

Jace is on dialysis and awaiting his kidney transplant pretty soon. His mom, Courtney and I have become friends through LGF and FB and we actually got to meet along with our two SIOD kiddos one day at Children's Hospital in Omaha recently!  He lives currently in Juniata, Nebraska and his family members include Kendra Nichols, Mark Nichols, Laurie Nichols, Connor Williams, J.j. Williams, Nancie Jones, Greg Jones, Julie Jones.

Courtney shared a fond memory with me of the time Jace go to meet NASCAR drive Jimmie Johnson this past summer!

Paizlee Davenport-September's Featured Little Giant

You all may recall that Paizlee's big brother, Kruz was our July featured Little Giant- read on to see why his little sister is our featured September Little Giant. (Copied from their website written by their mom and my friend, Jessica.)

 "Paizlee was also confirmed to have the same gene path as Kruz, making her "number 6" documented case in the USA on Aug 22, 2016. She also has Schimke's. Possibly making her one of the youngest every diagnosed. Devestation wasnt even the word we felt. Both of our babies are 2 out of 6 cases of an extremely dangerous rare disease right here in Muscle Shoals, AL. We will FIGHT!!!

We will be joining a research team to raise awareness and the funds."