We created this blog to share the story of our family with our friends and family. Our twins, Asher Dennison and Hudson Taylor, were born on Monday November 29, 2010. They arrived into our family a little premature at 35 weeks and were taken to the Neonatal Intensive Care Unit (NICU). As of the creation of this blog their big brother Zachary (3 1/2 years old) has not been able to meet them as they are still in NICU.

They receive excellent and compassionate care from the doctors, nurses and staff at the hospital. Their reason for being in NICU is due to their premature development state, they need to learn little things like maintaining their temperature and feeding to be able to come home. We were not worried about their condition until Saturday, December 4, when they were 5 days old we received a call that changed everything.This is our ongoing story.

Tuesday, March 22, 2011

Long Overdue Update

Amy’s Posting – I can’t believe it has been so long since we’ve updated the blog. Asher and Hudson are now three months old! Todd has been back at work about six weeks now and I’ve been settling into a routine. Ironically enough, the routine pretty much takes every moment of my day and leaves little time for anything else, even things that I love doing like writing. But, I’ve taken this time to try and enjoy all (well, if not all, at least most!) of these moments that I know are so precious.

I spent the little bit of free time I had in January doing research on neuroblastoma in newborns. One of my neighbors introduced me “via email” to another family in Atlanta that is dealing with a neuroblastoma diagnosis with their son. I can’t explain how helpful this introduction was to us. This new friend has been so supportive and has introduced us to several good web sites with research and information including a listserv for parents of children with neuroblastoma. Todd and I posted an inquiry on the listserv to see if we could be connected with any families with a situation similar to our situation (we’ve since learned that the chance of a newborn being born with neuroblastoma is 24 in 1 million). Following our post, we received several heartfelt emails from families across the country who had similar experiences to ours. Some of the families opted for surgery on their newborn babies while others followed the “wait and watch” approach that our doctor is recommending. For some, that protocol has been successful and for others, the cancer spread. Another mother, not knowing where we lived, emailed me explaining that our situation sounded very familiar to someone else she knew. She sent me a blog link for this family and when I started reading it, their story was exactly like ours (except that their newborn son’s diagnosis was several years ago). As I continued reading their story, I discovered the family lived in Atlanta and that they had seen the same doctors as we had. We’ve been able to connect with each other and she has shown me so much compassion, kindness and support. I still feel amazed at how God works in our lives to provide comfort to us when we need it most. A few other neighbors and friends have also given us some connections and I am hoping to find some time soon to reach out to these families for additional support and advice.

We did ask receive a second opinion from St. Jude’s, and they concurred with Asher’s oncologist’s treatment plan. It was good to have this confirmation. Overall, we are still struggling with our decision about the best path forward for Asher, but are trying not to let the situation define our lives.

I’ve have spent more time going to doctor appointments than I would like to. Since our last post, Asher has had an ultrasound and another appointment with the oncologist. Based on the results of the ultrasound, it appears that the tumor has not grown in size. We were very relieved to hear that news. His next CT Scan will be at the end of March. Following that scan, we have an appointment with a pediatric oncology surgeon to discuss the pros and cons of surgery. We’ve mostly accepted the new reality of our life and feel at peace with the path forward, but we still find it difficult to find strength close to his appointment times. It seems to be the real reminder that we have a child who may have cancer. And, the more I read the stories of children with neuroblastoma, the more I feel led to become an advocate for childhood cancer once again. It saddens me to read the statistics for neuroblastoma such as only 30 percent of children diagnosed survive it. We feel so grateful that even if Asher does have neuroblastoma, the survival rate for a newborn diagnosis is very favorable.

As February approached, Todd returned to work. It was such a blessing to have him home with us for about two months. It was very special to see his bond with Zachary grow even stronger. I also started some small project work for my client. In the beginning, I was afraid of my new responsibility of caring for three children, but in other ways, it felt comforting to get back into a normal routine. I needed this time away from the blog in many ways so we could feel like a normal family again.

As March begins and the weather turns warmer, we are once again spending lots of time outside, with Zachary riding his bike around the neighborhood and me walking the babies. As many of you know, Zachary has always loved spending time outside playing so this very “normal” activity has been very comforting to me.

We are now faced with some other health-related obstacles with Hudson. We are not seeing the rate of growth that we should be experiencing for his age. He’s now up to 8 lbs. During the next several weeks, we will be meeting with some specialists for consultations and test to help identify if there are any other obstacles besides his severe reflux. The doctors feel pretty confident that the reflux is the cause of the slower weight gain. A few weeks ago, we started adding rice cereal to his high calorie formula in hopes of promoting more rapid weight gain. He remains one of the most content and happy babies we’ve seen. The only thing we’ve identified that he dislikes is his bath!

Even with all of the health obstacles, we have a lot of laughter and love in our house. Our hearts melt every time Zachary, Asher or Hudson smiles at us. And, we continue to be amazed at how much Zachary loves his brothers even through all of the chaos we’ve experienced the past several months.

We are also planning a very important event for our family in April, Zachary’s 4th birthday party! To stay with his obsession with anything with wheels, he’s asked Mommy to make him a dump truck birthday cake this year. In years past, he’s had a school bus, train and fire truck birthday cake!

We recently had some professional photos taken of the babies and our family. We will post some of those photos to the blog soon!

We appreciate everyone’s continued prayers and friendship during this time.