Skip to content

Here We Go Egan

Living Life to the Fullest with a Chronically Ill Child

  • Here We Go Egan
  • Blog
  • About
  • Contact

Author: Courtney Egan

Genesis 2:4-25 – Adam and Eve
Posted on January 11, 2022

Genesis 2:4-25 – Adam and Eve

Water Gives Life In Genesis 2:5-6 we see that, until water sprung forth, there could be no life. The Bible tells us that Christ is the living water. If we learn of him and follow the gospel, we will never thirst again. How great is God! He can, and does, provide all that we need. … Continue reading Genesis 2:4-25 – Adam and Eve

Genesis 1-2:3 – The Creation
Posted on January 3, 2022January 4, 2022

Genesis 1-2:3 – The Creation

God is the focus of the Bible The first 4 words of the Bible point to its purpose. The purpose of the Bible is to teach us about God. So, from the first words, we start to learn about God and His creation. As we learn more about Him, we can exercise more faith and … Continue reading Genesis 1-2:3 – The Creation

New Year, Old Testament
Posted on December 30, 2021January 4, 2022

New Year, Old Testament

This year, our church is studying the Old Testament in Sunday School. I am excited to really dive deep into it and learn new things this year. I have not always been a diligent scripture reader. I have gone through different periods with my scripture study (as I am sure you have too). I have … Continue reading New Year, Old Testament

Take It One Step at a Time
Posted on October 18, 2020October 18, 2020

Take It One Step at a Time

Life with Cystic Fibrosis means daily medication and treatments to prevent lung damage and other prescriptions to treat existing symptoms. Going into our daughter’s first clinic appointment, I was worried that I would be overwhelmed by all of the information and instructions for care that I received. Less than a week after our daughter was … Continue reading Take It One Step at a Time

Posted on October 5, 2020October 5, 2020

Our NICU Journey (Part 2)

If you haven’t read my other post about our NICU experience, click here to read it first. We left off with my daughter’s admission to the NICU in a larger hospital downtown. After we left that day, they did another Enema to try and dislodge her bowel blockage. The first night away from her, I … Continue reading Our NICU Journey (Part 2)

Our NICU Journey (Part 1)
Posted on September 27, 2020September 27, 2020

Our NICU Journey (Part 1)

I promised to tell you more about our daughter’s experience in the NICU in my last post. I will do my best to relate the whole story to you, but my memory is terrible lately. Taking care of two under 3 takes a lot of brainpower! I remember when the doctor came in to tell … Continue reading Our NICU Journey (Part 1)

Trust Your Gut
Posted on September 21, 2020September 13, 2020

Trust Your Gut

After our daughter was born, I was on high alert. Because she has Cystic Fibrosis, there was a high likelihood that she would have a bowel blockage. So, I was looking for any clue that she may have a meconium ileus. I struggled to breastfeed her the whole first night after she was born. I … Continue reading Trust Your Gut

Our Daughter’s Arrival
Posted on September 14, 2020September 11, 2020

Our Daughter’s Arrival

Every mom tries to imagine their baby’s arrival. For 40 weeks, we think about what our baby will look like, what our labor will be like, and when our little one will arrive. The waiting feels like an eternity when you are pregnant. When I was pregnant with my daughter, I felt like this eternity … Continue reading Our Daughter’s Arrival

Let the Preparation Begin
Posted on September 11, 2020

Let the Preparation Begin

Remember how I said I need to prepare for everything? Well, that was magnified with our daughter’s diagnosis. After receiving confirmation that she does indeed have Cystic fibrosis, I went on the hunt for all the information I could find. I wanted scientific information, I tried to find moms of children with CF, and I … Continue reading Let the Preparation Begin

It is Okay to Grieve
Posted on September 10, 2020September 20, 2020

It is Okay to Grieve

When I first heard that our daughter might have Cystic Fibrosis, I was crushed. I knew in my heart that she did have CF before the amniocentesis confirmed it. I did not know how to feel. I never imagined I would have a child with any chronic health condition. I figured I would have at … Continue reading It is Okay to Grieve

Posts navigation

Page 1 Page 2 Next page

Menu

  • Here We Go Egan
  • Blog
  • About
  • Contact
Blog at WordPress.com.
Here We Go Egan
Blog at WordPress.com.
  • Follow Following
    • Here We Go Egan
    • Already have a WordPress.com account? Log in now.
    • Here We Go Egan
    • Customize
    • Follow Following
    • Sign up
    • Log in
    • Report this content
    • View site in Reader
    • Manage subscriptions
    • Collapse this bar
 

Loading Comments...