Please support the funding of vital reasearch to treat the seriously debilitating and life threatining disease cystic fibrosis. You may have read about the continuous development on amazing new drugs designed to treat the cellular defects arising from genetic mutations that cause cystic fibrosis. The newest wonder drug on the market promises to benefit 90% of CF patients. Cystic Fibrosis Foundation has been at the forefront of the incredible research that led to these achievements. The fight continues.
Unfortunately, 10% of CF patients have rare and nonsense mutations that do NOT benefit from these amazing new drugs. Turner one of the final 10%. Care about rare, please.
Until it's done!
Family and Friends of Turner Ryan DeMott