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
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)
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
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
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
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
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
The Results are In
We waited for what seemed like forever for results. My blood work came back and showed that I am a carrier for cystic fibrosis. So, my husband needed to get his blood drawn to see if he was a carrier. That meant another two-week wait. His results finally came back and confirmed my gut feeling: … Continue reading The Results are In
We Got Surprising News at Our 20-week Ultrasound
I had my son a little more than a year after we got married. Having a baby changed our lives in a lot of ways. We learned how to care for that sweet little boy, and he quickly had our hearts. When we found out we were expecting our second, I assumed pregnancy and birth … Continue reading We Got Surprising News at Our 20-week Ultrasound
First Comes Love. . .
I come from a religious culture where marriage and family are very important. Most of my friends were married before they finished college. I, on the other hand, finished school and served a full-time mission for my church before getting married. My husband (N) and I have talked about how we had both almost given … Continue reading First Comes Love. . .
Follow My Blog
Get new content delivered directly to your inbox.
