I have received a number of e-mails from readers wanting to know more about my family’s journey with eosinophilic esophagitis (EE/EoE). Since the questions are usually along the same lines, and since I suspect there are lots more people out there who could benefit from this information, I decided to address some of the questions in a general way via a series of blog posts.
If you'd like to learn more, please check out these posts where I share my family's experience with EE:
Noticing the problem
As always, please consult your physician on the right treatment for you or your child.