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Let’s start with what information you think
helped you the most to manage your child’s food
allergy? Like the “AHA” moment for you.
Where did you find “the
answers” and how do you think it should be
given to parents of newly diagnosed children to make
the process a little bit easier, less stressful?
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Now, what resources did you find or develop that
help you the most to manage your child’s food
allergy?
Where did you find it/them and how and when
do you think it should be given to parents of newly
diagnosed children?
Are there resources that you have been
disappointed with? What are the problems and how
could things have been better?
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What skills do you think you have developed that
help in managing food allergies?
How, when, and where should parents of newly
diagnosed children learn these skills?
Let’s say we want to write the
“essential or most important” things to know
for food preparation at home for children with food
allergies what would you include?
What about the “very most important things
to know” for “crisis” or emergency
management and medication use for an allergic reaction?
What about the most critical “need to
know” information about shopping for foods?
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What problems, for example trouble spots you
experienced and wished you knew about in advance?
Would you warn newly diagnosed families
about?
How would you pass this information
along?
What about tips regarding dealing with health
insurance, schools, ER, doctor’s office?
If you learn that a friend’s child just has
been diagnosed with food allergies, is there anything we
have not talked about that you would warn her/him about?
Is there anything you feel you have not been able to
address yet regarding understanding and managing your
child’s food allergy?
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Have you joined any support group?
What has been your experience? Did it
help?
Have you heard of FAAN?
Is there anything else regarding your experience
managing your child’s food allergy that you think is
important to share with us in our goal to create educational
materials and supportive resources?