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Emergency Preparedness for Families with Special Needs

Categories: General, Natural Disasters, Preparedness, Response

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By Georgina Peacock

When Hurricane Katrina hit, Julie thought she was ready.  She always had an emergency kit prepared because her son Zac needs medical supplies and equipment to keep him happy and healthy. Zac has spina bifida, a major birth defect of the spine; hydrocephalus, which means he has extra fluid in and around the brain; and, a number of food and drug allergies. He has sensitivities to changes in temperature and barometric pressure. Therefore, she always made sure they had a week’s worth of supplies and medicine ready when it was time to evacuate. “There is a very delicate medical balance,” she said.  “When he has an issue, the dominos tend to fall quickly.”

As communities around the Gulf braced for Katrina, Julie’s family left New Orleans for Baton Rouge with their one week reserve of Zac’s medical supplies including catheters, feeding tubes, and special medications. But like most families facing the devastation of this hurricane, they ended up being gone for much longer.  “It was a very challenging time for so many people, but especially for families of children with special health care needs, like ours,” said Julie. “Zac is a unique guy who needs a lot of support.” 

Zac posing in his wheel chair for his baseball team photo“Now, we always keep a one month supply of Zac’s supplies in our emergency kit,” she said. “It’s critical. It’s life and death for us.” Her insurance pays for this stockpile of emergency supplies. She also keeps a document of Zac’s daily needs and medical history in print and electronic format.  This vital document includes:

  • Daily plan of care
  • How to use his medical equipment
  • Recipe for formula
  • Catheterization schedule
  • Allergy information: food and medication allergies, type of reaction, and what to do if he has a reaction
  • Surgeries
  • Diagnoses by body system
  • List of his doctors with contact information
  • Equipment providers
  • Pharmacist
  • Medications and supplies including stock numbers and basic descriptions of products for comparable substitutions
  • Allergy information
  • Insurance information
  • Case manager for his Medicaid waiver
  • Since he is over 18 – legal documentation of  “continuing tutorship” which allows parents to make medical decisions for him.
  • Biographical sketch including his likes/dislikes; hobbies/interests; and triggers-things that will disturb him.

Julie urges families with children who have special needs to know what emergencies are likely in their area. For Julie’s family, they know the areas that flood and prepare for hurricanes and tornados. Also they live in an area that is home to many chemical factories and a nuclear plant, so they prepare for plant explosions, nuclear reactor accidents, and fires.  “Preparing and planning can give you peace of mind,” she said. “Get a kit. Make a plan. Be informed. It applies to everyone, especially to those of us who care for children with special needs.”

Children with Special Healthcare Needs in Emergencies

Children with special healthcare needs may be more vulnerable during an emergency.  They may have difficulty moving from one location to another, urgent or persistent medical needs, difficulty communicating or have trouble with transitioning to different situations. A disaster can present all these difficulties at once. Knowing what to do can help maintain calm in your family and keep them safe.

Please visit the following sites for more resources:

Leave a Comment

Does someone in your family have unique needs? How do you prepare? How have you addressed these needs during an emergency? Share your experiences and tips below.

Georgina Peacock, MD, MPH is a medical officer and developmental-behavioral pediatrician with the Prevention Research Branch in the Centers for Disease Control and Prevention’s National Center on Birth Defects and Developmental Disabilities.  Follow her on Twitter @DrPeacockCDC!

Public Comments

Comments listed below are posted by individuals not associated with CDC, unless otherwise stated. These comments do not represent the official views of CDC, and CDC does not guarantee that any information posted by individuals on this blog is correct, and disclaims any liability for any loss or damage resulting from reliance on any such information. Read more about our comment policy ».

  1. July 2, 2013 at 3:11 pm ET  -   Karen Scallan

    THANK YOU JULIE for participating in providing this important info to CDC and families in Louisiana and across the US! I know Julie well and she’s a great resource. So proud to see our families out there advocating and educating!!!

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  2. July 3, 2013 at 9:29 am ET  -   Byron Breedlove

    This is a very thought-provoking post, and it makes me realize we are not as prepared for an emergeny as I thought. My daugher also has spina bifida but not as many allergies and sensitivities as Zac.

    The complexity of this medical documentation again underscores why electronic health records would really be helpful, too.

    And I would not have thought readily about having a biographical sketch. That is also key as children with special needs may not always make their needs and likes known.

    Link to this comment

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