We were beyond excited when we found out we were pregnant with Eliana. Early on we found out Eliana had fluid in her head and neck, but we were hopeful this would resolve on its own as time went on. Unfortunately, with more testing it was determined that she had Turner's Syndrome (one of her X chromosomes was missing) and the fluid had spread throughout her body restricting her organs from developing. Her chances of survival were slim to none. We were faced with a decision no parent ever wants to make, and ultimately chose to end her suffering at 24 weeks. We made this decision out of love and selflessness given all her complications and struggles she would face. 
The SLF was a huge help after losing Eliana and I am forever grateful to them.