Every year, the child foundation has a conference whereby we, as parents of children with an interstitial lung disease, can meet the leading doctors in the field to learn about new advances in research. It's also an opportunity to meet with other families who face similar challenges. This year the conference is in Denver Colorado-the "birthplace" of nehi. Lucas and I plan to attend but could use a little financial assistance. We would be eternally grateful to all that can help....even if a mere couple dollars is all you can afford. Thank you from the bottom of our hearts.
http://www.child-foundation.com/