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X-ORIGINAL-URL:https://southsidesupport.org/
X-WR-CALNAME:Southside Support
X-WR-CALDESC:Connecting families of children with special needs to valuable resources in our community and also with each other
X-WR-TIMEZONE:America/New_York
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TZID:America/New_York
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TZOFFSETFROM:-0500
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TZNAME:EDT
DTSTART:20260308T030000
RRULE:FREQ=YEARLY;BYMONTH=03;BYDAY=2SU
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DTSTART:20261101T010000
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UID:MEC-f4f6dce2f3a0f9dada0c2b5b66452017@southsidesupport.org
DTSTART;TZID=America/New_York:20210908T000000
DTEND;TZID=America/New_York:20210908T120000
DTSTAMP:20210923T104242Z
CREATED:20210923
LAST-MODIFIED:20210923
PRIORITY:5
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TRANSP:OPAQUE
SUMMARY:NICU Awareness Month
DESCRIPTION:Many of our families have experienced lengthy stays in the NICU after their superhero were born. Here is one mom’s account and experience there. We love our special needs families and we love our community!\nIt is NICU awareness month and it has been on my mind a lot the past few nights. It’s extremely overwhelming feelings even four years later.\nIt was the absolute horror of having my baby taken from my arms to go to the NICU, thinking he would be back soon.\nIt was having to go 12 hours without seeing him because of my blood transfusions.\nIt was getting phone calls about intubations.\nIt was being at the hospital before rounds and not leaving until I knew his night nurse.\nIt was the frantic feeling of coming in the next day and having no idea what new medicine he would be on, where his IV would be, what his ventilator settings would be, what he would look like with the swelling.\nIt was the horrid feeling of not knowing if he would make it through the night.\nIt was the devastating feeling of leaving every day without my baby in my arms.\nIt was pumping in an empty nursery every night so I could provide Easton with some kind of nutrition.\nIt was barely being able to touch him for the first 12 days while he was on the ventilator.\nIt was watching him breathe over the machine and look around, a feeling that we were both helpless.\nBut, we also celebrated every little milestone. We had nurses turn into lifelong friends. I think the hardest part for us, was Easton enduring all of that and us thinking the worst was over, only for him to be dealt a horrible diagnosis. The only positive I can find out of that is that we were already a strong family and it gave us some medical background to carry with us to the future.\nIf I could give anyone one piece of advice it would be to always ask questions, be involved in your child’s care however you can and talk/sing to them even on the ventilator, they can hear you.\nCredits:\nBecca Walker\nEaston’s mom (Hunter Syndrome)\nrnday07@gmail.com\nLink:\nwww.eastonismyhero.org\n
URL:https://southsidesupport.org/event-calendar/nicu-awareness-month/
ATTACH;FMTTYPE=image/jpeg:https://southsidesupport.org/wp-content/uploads/2021/09/NICU-Awareness-Month.jpg
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