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.


Another Ryan Update


I know, I know, all I do are quick Ryan updates. I swear I’ll have some real content soon.

He’s doing great! He woke up from a super long nap this afternoon in great spirits, totally back to himself, with no fever. He’s eating without spitting up, and so it seems his probable stomach virus has run it’s course. He’s still on the IV, but provided he’s still doing this well tomorrow morning, they will release him! YAY!

I miss him (and Aaron!) so much. Ryan and I cuddled the whole time and Dylan just lit up when he saw his Daddy. He’s in this cute little hospital gown, and his arm is all bandaged up to keep him from eating his IV. He likes to put it in his mouth LOL. I can’t wait until everyone is back home where they belong.

Quick Ryan Update

His fever shot back up last night after going down. But now today it’s not as bad. He’s got an ear infection, which would explain the fever, but not the diarrhea and vomiting last night. So far, all his blood work has come back negative. They’re giving him some pretty powerful antibiotics and also some anti-nausea meds like he gets during chemo. But he’s keeping down Pedialite today and acting more like himself. If all goes well, he might get to come home tomorrow night.

Thank you, everyone- for your thoughts and prayers. They mean the world to us!

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.