Evanston Hospital’s Annual ISCU Picnic
The Annual ISCU picnic is coming up at the end of June! I’m thrilled to be a part of this event, and know that the families who come back to reunite with their nurses & doctors always look forward to it. if you’re a graduate of the ISCU and you’d like to register your child, please follow the link – it’s free to attend. Come join us!
By now you have hopefully heard or read our story / the story of Delilah, the inspiration behind the Tangerine Owl Project. We’re happy to share her story with you, but moreso, we want to hear your stories. We invite any of you who have experienced time in the NICU to share with us. Near and far, the good, the bad, the ugly, and everything in between.
Are you there now with a preemie? Did you get to take your precious one home having “graduated” from the NICU? Are you still battling with the loss of a dear little angel? Struggling to find the right diagnosis? Maybe you’re on day 542 of your child’s NICU stay – it’s old school by now, but you have a story –
There is so much that can happen, so quickly and so turbulently, so please share, and know that you are not alone going through this.
Tangerine Owl Project Founder Stacey Porter, and husband Schoeller Porter at the walk.
I was honored to speak this past Sunday at the Pre-eclampsia Foundation’s Chicago Promise Walk. We couldn’t have asked for a better day to enjoy Busse Woods & to make an impact in awareness for the foundation. Sharing my story was somewhat difficult with the flood of memories that returned as I was speaking, but I also knew that I was in a place where a great deal of the audience had a similar experience, if not worse, battling Preeclampsia.
Teams of walkers/runners and their families and friends hit the course because they were survivors, or in honor of those they had lost. It was there that it sunk in that this condition effects so many people… Many silently battle or find out too late that they have it, and it strikes without rhyme or reason. My story is just one story, and I am so proud to be a survivor. I will look forward to working with the Preeclampsia Foundation to spread awareness so that others will recognize the signs and we will continue to support the families whose lives have been effected by this puzzling, chaotic condition. (For more info on the condition, please go here: www.preeclampsia.org)