I’ve got all the symptoms count ‘em 1, 2, 3

Aaron spending time with Elora in the NICU

November 17th is Preemie Awareness Day- and you guys know I’ve had several preemies. Before I had an early baby, I very ignorant about the issues that preemies face.  I naively thought once they went home from the NICU, they were just like a full term healthy baby.  Sometimes you get lucky and that’s the case, but unfortunately for many more of these early birds have weaker immune systems and are more susceptible to respiratory issues do to underdeveloped lungs at birth.

I’d never heard of RSV until we had Amelia.  She was born five weeks early, and despite the fact that Lili was also born at the same gestation and was fine, Mia needed medical intervention at birth to breathe.  She spent almost 2 weeks in the NICU taking the steps necessary to wean down to room air before she came home.   Because of this, her fall birth, and the fact she had four older siblings who were cesspools of germs, she received monthly Synagis shots to help protect her from RSV.

RSV (respiratory syncytial virus) symptoms present like the common cold in most full-term babies, and the majority contract it by the age of two with parents and caregivers not even realizing they have it.  But for preemies, their compromised immune and respiratory systems increase their risk for developing much more serious issues.

Looking back, my now 13 year old was hospitalized for several days when he was just a few months old with what the doctors called bronchiolitis, but I’ve since learned that is most commonly caused by RSV.  He was full term, and it was super scary.  I’m so glad that my preemies all received the shots to protect them!

According to the CDC, RSV season typically runs from November to March in most of the U.S., but can vary based on where you live, so check with your child’s pediatrician.  Half a million babies are born early in the US each year- so we really need to spread the word to protect these babies- and that’s why I’m posting about this today, November 17th, World Prematurity Day.

To learn more about RSV, go to RSVProtection.com where you can find great info on prevention, risk factors, and more.

I wrote this review while participating in a blog tour by Mom Central Consulting on behalf of MedImmune and received a promotional item to thank me for taking the time to participate.


Fight for Preemies, 2010.


Today, November 17th, has been dedicated to raise awareness of the crisis of premature birth. The March of Dimes invites bloggers to get involved and spread the word.

Every year, 20 million babies are born too soon. 20 MILLION! This is a topic very close to my heart, as we’ve lost three preemies, and had several more. In 2001, our daughter Raime was stillborn at 23 weeks, and in 2007, our son Connor was stillborn at 24 weeks. In 2006, Elora Jade was born 15 weeks early at 25 weeks and lived a day shy of 9 weeks, all of which was spent in the NICU.   Then there are the twins, who were born at 33 weeks, and spent almost two weeks in the NICU.  Amelia was born at 35 weeks and also spent some time in the NICU for breathing issues.

Hopefully someday soon, more babies like Elora will survive. I know I wish I had been able to know her longer.


Fight for Preemies


Today, November 17th, has been dedicated to raise awareness of the crisis of premature birth. The March of Dimes invites bloggers to get involved and spread the word.

Every year, 20 million babies are born too soon. 20 MILLION! This is a topic very close to my heart, as we’ve lost three preemies. In 2001, our daughter Raime was stillborn at 23 weeks, and in 2007, our son Connor was stillborn at 24 weeks. In 2006, Elora Jade was born 15 weeks early at 25 weeks and lived a day shy of 9 weeks, all of which was spent in the NICU. You can read more about them in my loss blog.

Hopefully someday soon, more babies like Elora will survive. I know I wish I had been able to know her longer.

Homecoming!

Yesterday, we were given three choices with what to do with the boys, because they’re still having a few bradys (where their heartrates go to slow or fast) here and there.
1. Stay in the NICU in Bigger-Than-TaterTown Ville until they stop having them.
2. Transfer to the local hospital where they would stay until they stop having them.
3. Bring them home on monitors today.
We picked #3, so that meant we had to be there all day and half the night- we had to meet with the monitor guy and learn how to use them. Take a CPR course. Watch several videos. Stay X amount of time to show them we could handle the monitors when they go off…
We left the house yesterday at noon and got home from the hospital at 2.
As soon as we’re dressed and ready, we go back today to do all the discharge stuff and bring them home!!!


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Ryan hating the flash

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Dylan, with his Flashdance shoulder

These were the first things I got for the babies before I even knew they were boys I think- and I could only order one from the site & my friend Amity sent me the other- she lives close to a store :)

Update

Dylan & Ryan
Early this afternoon, I got a call from the NICU. The boys’ neonatalogist said that they are not in need of a level 3 NICU like the one they’re in right now, that they are ready to move to the step-down unit. She wanted to know if we’d like them transferred to the local hospital that is 10 minutes away instead of keeping them where they are, which is almost an hour and a half away. So, tomorrow or Wednesday, as soon as two beds are open, our boys will be one step closer to coming home!!