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Is it our responsibility to educate others about CF?
A couple of months ago, in one of my first columns on the site, I wrote about whether or not it’s our responsibility to educate others about CF. I’ve always chosen to be open and transparent about my CF but sometimes that can be a bit overwhelming so I go back and forth.
1. To spread awareness, are you open? Is it your goal to “educate?”
2. What are some of your thoughts on this? Do you feel like awareness is best spread through adults with CF leading the charge?
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