New Hope for Jonna Simcox

At two years old, my spunky, charismatic little niece, Jonna Polczynski Simcox, was diagnosed with Spinal Muscular Atrophy (SMA).  Jonna has fought the effects of this genetic disease all her life with nothing but her will-power and determination because the medical field had no answers for this rare progressive disease.   Fortunately, the drug Spinraza is giving new hope for SMA patients.  Some recipients have increased muscle strength by 40%. Prayers were answered when Jonna was accepted as a recipient of the new drug.  This answered prayer comes with a very large financial burden on this family.  Now if you know Jonna and Jacob, they would NEVER ask for help although they have helped many because they are both caregivers with very loving hearts.  Please support Jonna and Jacob with your prayers and if you are able or so inclined, your monetary donation (no matter how small), is greatly appreciated.