Another fun event my team and I hosted in honor of child life month was a teddy bear clinic. This event is usually a great hit with the patients and families.
We started off by giving each “doctor” their patients chart. Here we included some information on the “top 10 reasons to call your child life specialist” as well as information on the different stations at the event.
These are all of our “bear-y” sick patients. We contacted our marketing department and they had many bears with our hospital’s logo that they were happy to donate to us!
This first station is where our “doctors” would gown up and get ready to treat their patients. This was a very popular station and it was so adorable to see kids proudly walking around looking like doctors.
The next station was triage followed by the IV station. We had a CCLS at each of these stations helping guide the “doctors” as they cared for their patient. Here is where we were able to sneak in our education & address misconceptions.
Here’s a closer look at our triage station and IV station.
Finally, the patients were able to do an x-ray by dipping our demo bear into white paint and smudging it on black paper. This was a very fun and creative way to incorporate medical art into our teddy war clinic.
Some other activities we had at the clinic were a photo booth station with props and a table with markers, crayons, and construction paper for the “doctors” to write a get well soon card to a patient in the hospital. We also included band-aids and gauze at this station to continue to promote medical art. Needless to say our clinic was a big success and all of our teddy bears were cured. Thanks, doctors!
I first learned about the child life profession when one of my child development professors my junior year of college very briefly mentioned it during one of his lectures. I jotted down “child life specialist” on the corner of my notebook and googled it when I got home. As soon as I looked it up, I knew this was it! I read every single word written on the entire child life council website but I still wanted more! I wanted to know what a typical day looked like for a CLS, I wanted to see pictures of their workspace, I wanted as much information as I could get to feel confident in my decision to pursue this career. I didn’t find what I was looking for that day so I started adventures in child life in hopes of providing others with what I was looking for at the start of my adventure.
It’s no secret that becoming a certified child life specialist is a lot of work! And how can you be sure that you’re ready to do all that it takes to become a child life specialist when you’ve never even seen what the job entails first hand? I get a lot of e-mails from people interested in the field asking me how they can be sure child life is for them before they dive in. I often asked myself this question too during the early stages of my adventure. I realized that child life was for me by truly understanding what the job entailed and see the magic first hand during my time volunteering, my practicum, my internship, and even during as a professional. This brings me to my favorite find of the month:
John Hopkins All Children’s Hospital in St. Petersburg, Florida will be hosting a seminar for those interested in learning more about the child life profession. This seminar will include a panel discussion with child life staff, information about education options & certification requirements, a hospital tour, and exposure to therapeutic activities. There are two seminars left this year – one will take place on July 27th and the other on November 16th. Space is limited to 25 participants per seminar so make sure and register online ASAP!
To see the flyer for the event, click here https://www.hopkinsallchildrens.org/getmedia/792ad66a-178e-43b5-9116-8ccb6f983e9c/DayInTheLife
Working on a respiratory unit I often have patients that have been diagnosed with Cystic Fibrosis (CF). This is a population I never worked with at my previous position in the pediatric emergency room so I had a lot of learning to do coming into my new position. May is CF awareness month so I thought I’d share some of the amazing resources I have found to help educate and support our CF patients.
With a quick google search, I was able to find (free!) resources via the cystic fibrosis foundation web page. I requested a couple of items, one of which is my ultimate favorite: a coloring/story book about a little panda with CF name Huxi! I was also sent booklets for parents/caregivers, booklets for teens, and a big “ultimate guide to CF” binder, stress balls, and luggage tags. I am so thankful for all of these resources and how they will help my patients (and myself) learn more about CF.
To see where I found these resources, follow the link below:
One of my wonderful readers recently e-mailed me this infographic for me to post & spread the word about special education then & now. This is a topic that is near and dear to my heart as my mother owns and operates her own group home for people with disabilities and my best friends brother has down syndrome – we are actually hosting a holiday party for him & his friends later this month! Understanding the needs for people with disabilities is a big part of child life & many other careers that focus on working with children. It’s great to see from this inforgraphic how far we’ve come and how important it is that we continue to move forward in being able to provide our special needs community with the best resources available.
Thanks for sharing, Lauren!
It’s a rainy afternoon here in Miami today, perfect for cuddling up with a good book!
I’m a nut when it comes to geography/culture/travel so these paper dolls really caught my attention.