Caleb's CDH Story
  • Home
  • About Caleb
  • About Us
  • What is CDH?
  • Our Blog
  • Years
    • 1st Year
    • 2nd Year
    • 3rd Year
    • 4th Year
  • Photo Album
    • Aug. 12 - June 7, 2019
    • Nov 20 - August 11, 2018
    • May 5 - Nov. 19, 2017
    • Sep. 29 - May 4, 2017
    • Feb. 12 - Sep. 29, 2016
    • Oct. 20 - Feb. 11, 2016
    • Jul. 18 - Oct. 19, 2015
    • First Year by Month
    • May 20 - Jul. 17, 2015
    • Mar. 24 - May 19, 2015
    • Feb. 11 - Mar. 23, 2015
    • Jan. 7 - Feb. 10, 2015
    • Dec. 20 - Jan. 6, 2015
    • Nov. 28 - Dec. 19, 2014
    • Nov. 1 - Nov. 27, 2014
    • Oct. 20 - Oct. 31, 2014
    • Sep. 27 - Oct. 19, 2014
    • Sep. 1 - Sep. 26, 2014
    • Aug. 13 - Aug. 31, 2014
    • Caleb's CDH Surgery Day
    • Aug. 1 - Aug. 11, 2014
    • Jul. 19 - Jul. 31, 2014
    • Caleb's Nursery

One Little Boys Legacy is Another Family's Hope

3/21/2016

0 Comments

 
On March 9th, 2016, a story about toddler name Logan Miceli was posted in the Russell Street Report/Lombardi's Way. 

Logan Miceli Played Like a Raven 

Logan was born in 2013 with a congenital heart disease. He survived two open heart surgeries and was thriving until he received another devastating diagnosis.  Sadly, he passed earlier this month after losing his battle to leukemia. His parents have turned their loss into something incredible and founded Logan's Never Be Alone Foundation. This non-profit foundation "aims to provide financial assistance to hospital parents, so that they may comfort their children and be more involved in their everyday medical care."  Through our experience, we personally struggled with the difficult decision to continue to work and satisfy our financial obligation or stay at Caleb's bedside. It was a heartbreaking decision, but returning to work was our only option, which meant Caleb would spend more hours alone in the hospital than with us by his side. Caleb was hospitalized for nearly eleven months. This foundation will help ease the financial suffering of families, so that parents may remain with their sick children at Johns Hopkins Hospital, where Logan, Caleb and many other children from around the world go to seek medical treatment.


Tony Lombardi wrote "I never met Logan but I will never forget him. His story, his smile, his selfless parents, taught me something about life’s simple joys. And through their actions and words they reminded me that such simple joys are all around us. We only need to look for them." He could not have said it any better...

This is an amazing cause and together, I hope we can help fulfill Logan's legacy. If you would like to donate, please CLICK HERE!
Picture
0 Comments



Leave a Reply.

    Archives

    April 2019
    August 2018
    May 2017
    September 2016
    April 2016
    March 2016
    October 2015
    July 2015
    May 2015
    March 2015
    February 2015
    January 2015
    December 2014
    November 2014
    October 2014
    September 2014
    August 2014
    July 2014
    June 2014
    May 2014


    Categories

    All
    1st Birthday
    6th Pregnancy
    Bringing Everyone Up To Speed
    Caleb & Brody Meet
    CDH Reherniation
    CDH Surgery
    Decision Day
    Extubated
    First Week Of Life
    Follow Up Appointment
    G-J Tube
    Homecoming
    Mt. Washington
    Never Be Alone Foundation
    Nitric Oxide
    One Month Old
    PICU
    Retinopathy Of Prematurity (ROP)
    Shunt Surgery
    Tour Of Hopkins NICU
    Tracheostomy
    Visit To CHOP
    Visit To Hopkins
    Visit With Another CDH Family



    eMail Tim & Candice

    Subscribe to Caleb's CDH Story

    Enter your email address:

    Delivered by FeedBurner

Caleb's CDH Story
Tim & Candice Salkeld
calebscdhstory@yahoo.com


Caleb's Visitors Since June 2014
Website by Novair Group