Sara Cahoon reads a book while using a nebulizer Friday morning at her Meridian home. Cahoo, 28, has had cystic fibrosis and uses the treatment up to three times a day. Lawmakers are deciding whether to keep a very small program that pays medical bills for patients with cystic fibrosis. Many patients use the program to pay for multiple prescriptions that each cost around $1,400 monthly. The medicines have been key in turning the lung disease from a childhood death sentence to a chronic condition in which patients live well into their 30s, with life expectancies rising all the time. (AP Photo/Idaho Statesman,Chris Butler)
Frum Helen Back on March 18 at 12:53 p.m.
I certainly hope that someone in Boise realizes what cutting this program will do. Very sad if they do. It seems totally immoral to me. And how scarry for the affected families this must be.
lew2nl on March 18 at 2:16 p.m.
Having a niece who passed away with Cystic Fibrosis at age14 and my husband having a nephew who just passed away in Moscow at age 27, I feel that it is an injustice to take away medical bill payments for people inflicted with this horrible disease.