APFED Conference 2012

The APFED conference is back in San Diego this year!  It's been 3 1/2 years since our last conference and our lives have changed so much since then.   The last time, I was 8 months pregnant with our 3rd child and worried about the likelihood he would have to deal with Eos.  At that point, Kaylin had been on meds for EoE for a year but things were still not right but we had still not removed any foods at all.  We learned so much and realized we were definitely not alone.  Less than a year later, Kaylin had to start removing removing foods and thanks to all the information we got at the conference, we weren't completely overwhelmed.

http://apfed.org/drupal/drupal/annual_conference

Eos on Anderson Cooper

Set your DVR's.  This Thursday, March 22nd an amazing family is on the Anderson Cooper show (daytime show, not CNN) to raise awareness on Eosinophilic Disease.


Here's the info from the AC website.  Check out the link below to view the preview and to find out when it's on in your area.
"What if your child were deathly allergic to food? Anderson speaks with a desperate mom, Cara, whose son, Joshua, suffers from a rare genetic condition that makes even the smell of certain foods potentially fatal. Cara's husband, Brant, and older son, Jacob, join Anderson to discuss how the family copes with this rare condition... and the hope they have for a cure."

http://www.andersoncooper.com/episodes/kathy-bates-the-boy-who-can-not-eat/