PTSD and Medically Complex Kids
/Most people know the definition of Post Traumatic Stress Disorder (PTSD), as it has become an unfortunate, common after-effect of war, terrorism and assault. What many people don’t know is that PTSD can occur in people who have had significant, complex medical issues. This is the case with my daughter, who is eleven. I wanted to share our experiences, because I believe that it’s crucial to understand trauma from a child’s perspective, and to increase awareness of the potential connection between trauma and children with complex or ongoing medical issues.
PTSD
Post-traumatic stress disorder is described by the National Institutes of Health as, “a type of anxiety disorder. It can occur after you’ve seen or experienced a traumatic event that involved the threat of injury or death.” Symptoms of PTSD fall into three main categories:
1. “Reliving” the event, which disturbs day-to-day activity through flashbacks, memories, nightmares and/or strong uncomfortable reactions to situations that remind you of the event.
2. Avoidance – emotional numbing, feeling detached, not being able to remember certain aspects of the traumatic events.
3. Arousal – difficulty concentrating, startling easily and feeling hypervigilant (increased awareness), increased irritability and anger, having trouble falling asleep or staying asleep
Our story:
My daughter lives with a rare, progressive disease. She is eleven years old, and has–at current count–had sixteen major surgeries, over 40 MRIs, too many hospitalizations to keep track of, a ton of poking and prodding, and medical emergencies and situations where she had little or no control. In 2008, when she was six years old, she was diagnosed with Post Traumatic Stress Disorder. The PTSD diagnosis came after a three-month hospitalization (due to significant post-operative spinal surgery complications) and then a type one diabetes diagnosis.
After the several big medical events of 2008, we saw a real change in behavior and temperament, and a significant increase in inattentiveness and anxiety. She was six years old and was having intense angry outbursts, emotional meltdowns, and panic attacks many times a day. We saw these changes in her often during transitions or when something unexpected happened. In addition, she was frequently triggered by strong smells (like chemical smells or the smell of rubbing alcohol), or by loud noises or changes in schedule.
At that point in time, we sought professional help, and saw a licensed clinical social worker, who diagnosed her with PTSD. The therapist recommended treatment with an approach called Trauma-focused Cognitive Behavioral Therapy (TF-CBT). The therapist that diagnosed our daughter provided a foundation for us to be able to understand our daughter’s new mental health needs. But the diagnosis was just the very tip of the iceberg for us, in terms of learning about trauma and how to help our daughter deal with it.
Since the PTSD diagnosis six years ago, we have learned an enormous amount from listening to our daughter, from talking with other parents who have kids with medical PTSD, by doing our own work in counseling, and from connecting with a new therapist. This is an ongoing process that varies from day to day. We are now able to see patterns and predict changes in behavior before it happens, and sometimes we can even head off a trigger before it happens. These days, our daughter can accurately identify her triggers and we have lists (literally lists!) of ways to help her or ways she can help herself get through a difficult time. But on some days, despite all that we know and have learned, and despite all of our ways to help her cope, PTSD still has the upper hand and triggers lurk around every corner. We are all still learning.
Children with Medical PTSD
For children who are medically involved since birth, they may not have the words, understanding or ways to comprehend why all of this medical “stuff” is happening to them, and this may impact how they deal on a day-to-day basis. What has been most challenging for us is knowing that our daughter has medically induced PTSD, and knowing the triggers for her, like being at the hospital, having a change in routine, or pain. However, we still have to subject her to those triggers, because she has several chronic, complex medical diagnoses that must have some level of medical intervention on a regular basis. That’s been a real struggle for us to manage, and painfully upsetting for to bear witness to as her parents, as we continue to make decisions that are traumatic for her.
The silver lining is that with treatment and intervention, and tons of carryover at home, our daughter often functions like a ‘typical’ eleven-year-old. She has friends, is doing well in school and has activities that she loves to do, like drama, writing and reading. She loves animals and is kind and compassionate. Similar to how she has managed the unfair hand that was dealt to her medically, she is finding her voice and becoming a phenomenal advocate for both her medical and emotional needs. Her resilience and spirit are amazing, and that has been a true a blessing to see.
Strategies for Identifying and Coping with PTSD (or what has worked for us – not an all inclusive list)
Some thoughts for parents and providers of kids with complex medical issues:
- Be observant of changes in behavior, attention, mood, sleep or appetite.
- Trust your gut.
- Ask for help from a professional if you see changes in your child.
- Take care of your own emotional needs and figure out your own self-care plan.
- Connect with others who may be going through similar circumstances.
- Be your child’s advocate in medical situations, and situations that may be traumatic, even if it means disagreeing with doctors, nurses or other well-meaning professionals. You know your child best, and by doing speaking up, you are modeling how to advocate to your child.
The following is a list of what has worked for our daughter, or how we help her cope:
- We talk all the time.
- We have discussed PTSD without stigma and have helped her understand it in age-appropriate terms.
- We’ve helped her develop a toolbox for coping, including strategies, activities and ideas on how to help her manage difficult situations.
- We listen to her words to understand what she needs.
- We strive to find ways to give her choices, so she has some control of most situations, and we are upfront about things/situations that we (and she) cannot control.
- We are proponents of medications to decrease PTSD symptoms
- We educate others about medical PTSD.
- We shopped around for the “right” therapist after we did not make the right choice initially. Through trial and error and observation, we figured out that our daughter needed someone low key and super engaged and creative. We learned that she immediately shuts down with people who want to jump right into the medical stuff.
- We take breaks from therapy and from talking about trauma, to just do typical kid stuff.
- We model self-care strategies like rest, stress management, our own therapy meditation, and taking part in activities that provide joy.
These lists are (as we are) works in progress. Thanks for reading
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Thanks for posting this. I have a 4 year old son who was born in Chronic Renal Failure, and had a kidney transplant at the age of 2. He manages, as kids somehow seem to, the ongoing medical interventions, treatments, procedures, tests, and doctors’ visit with miraculous grace and strength, but we know and see stress about it creeping into his interactions and life in other ways. He is bright and articulate, and sometimes, we fall into a trap of confusing verbal comprehension with emotional comprehension. We have connected with a great child therapist, and do our best to comfort and talk him through the hard parts, but it’s BIG, this parenting challenge, and it’s not easy. Your advice is helpful–any resources you can point us to (books, websites) would be much much appreciated! Thanks again.
Hi Celine! Thanks for your message.
One of the biggest challenges we have faced around PTSD and medically complex kids, IS the grievous lack of resources!! We’ve had to make up our own and learn from our daughter and be really selective about providers….One of my long term goals is to develop/partner with others around how to better support kids and families with these challenges.
Stay tuned – and best wishes to you and your family
Kristen
Hi Kristen–
I am happy to do anything I can do to help you in your quest to develop and partner with others around this! There is a real vacuum for so many of the supports that parents and kids who have to negotiate complex medical systems need. I love that this website exists and am happy to have found it, but here in NYC where I live, I have not been able to find a real local network/help. So again, happy to discuss and help in any way that I can!
Thanks,
Celine
Hello,
I am a pain medicine specialist. My problem is that a lot of the kids that I see have had PTSD from Mental Health Professionals. The mere mention of one, sends these kids to breakdown. Anybody, with any suggestions?
Thank you