Your Journey Starts Here.
Your Journey Starts Here.
Learn more about the creators of Spica Life, our journey, and our passion to increase knowledge and awareness.
Read our Advocate Spotlight, featured by the International Hip Dysplasia Institute.
The feeling is similar to when you left the hospital for the first time with your newborn. What do you do with him? How do you care for her? Is there something you forgot to get? Find your answers here.
Our "How To" videos cover various spica cast topics, demonstrating for you the best methods we have found. From diapering and bathing to just getting out of the house, this is your starting point.
Every new spica parent has tons of questions. Many of those questions are the same. Here you can find answers to some of the most common spica cast questions.
Here you can read the story, week by week, of our daughter's 18 weeks in a spica cast. Experience the highs and lows of our journey, and gain insight into what spica life is like.
Some of the baby gear you already have will still work with a spica cast. Some of it will not. This is a list of items that we found to be incredibly helpful and necessary during our spica journey that can make your life easier.
You need support. Your family and friends will be key, but odds are they have not lived the spica life. There is a strong community of other spica parents out there that want to help and answer your questions.
The fastest and most helpful community we have found is through the DDH - Hip Dysplasia - Children Facing Surgery or Spica Casts Group on Facebook. This thriving community of spica parents can answer questions more specific to your situation, offer encouragement, or simply share with you in your experiences common to spica life. Request the group Admins to become part of this private group.
There are many awesome examples of blogs written by current and former spica parents, telling their stories and experiences. These are a great resource for unique tips, tricks, and insight. Here are some of our favorites:
2. Baseballs, Butterflies, & Blessings
3. Donna Jayne
There are several other great resources we have found that provide info on hip dysplasia and spica casts. Here are some of the best we have found:
1. International Hip Dysplasia Institute
3. DDH UK
4. Cast Life, by Natalie Trice
4. 101 Things to Do With a Child in a Spica Cast, by IvyRose Spica Chairs
The stories in this blog will uplift your spirits, give you advice, and help you keep the end of your spica journey in sight. Our goal is to create an archive of knowledge from parents who have lived the spica life. If you have experienced a spica journey, please join us by clicking the link below to share your story, and allow it to be an encouragement to others!
“Your child will surprise you and just when you think you couldn't love them anymore, you do. It still amazes me that my baby taught ME so many life lessons during her time in the spica cast.”
“Take it one day at a time and everything else will fall into place! Kids are amazing and the way they adapt is incredible! It was joyous to watch how proud of herself she was when she learned to do new things in the cast like crawl, climb stairs, and even stand. The hardest part was constantly keeping Kacey entertained! We did lots of reading over and over again which ended up really increasing her vocabulary!”
Have you endured a spica journey? Do you have tips, tricks, and encouragement to share with new spica parents out there? Let your story encourage others! Here you can submit your spica baby's story, along with your thoughts and advice, to be featured in our blog and on Instagram!
“Nothing will prepare you for the shock after the initial treatment. There are times I felt like a robot. Sleep deprivation, emotions are all apart of it…Brooklyn has made us better parents and blessed to be apart of this wonderful community.”