I was wondering what kinds of outreach everyone has done
I was wondering what kinds of outreach everyone has done for peanut allergies? What do you find to be the most effective and/or fun? Do you do letter writing to legislators about restaurant and school policies? Have you held fundraisers for awareness and research? I want to get involved in enacting change to make life easier with a peanut allergy, but I want to see what the best way to go about doing that would be!
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