Parenting a child with a chronic disease has unique challenges. When the disease is rare, like hereditary angioedema (HAE), these challenges may be compounded.
Typically, hereditary angioedema symptoms don't tend to appear in youngsters until puberty; however, that isn't always the case. If you or your spouse have hereditary angioedema but aren't sure if your child has HAE, it's a good idea to have your child tested.
If you know your child has hereditary angioedema, be an advocate for him or her. Learn everything you can about hereditary angioedema, as well as any HAE treatment prescribed for your child. Discuss all available HAE therapeutic treatment options with your child's treating physician.
Make sure that anyone involved in your child's care - teachers, school health employees, coaches, camp counselors, etc. - has information about HAE. For example, you can direct people to this site, HAE Hope, for information, or print out information about hereditary angioedema for them.
It's especially important that your child's caregivers know how to handle an HAE emergency if you are not there. Supply them with a printout of emergency information, including contact numbers.
If you're traveling, make sure you know where the nearest medical assistance is located in case of an HAE attack.
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