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Kiana, a 20-month old baby girl and relative of mine, has been diagnosed with a rare disease called SMA (Spinal Muscular Atrophy) type 2, which is a terminal, degenerative disease, that takes away a child's ability to walk, stand, sit, eat, breathe, and even swallow. A new medication, SPINRAZA, can not only stop the disease, but can restore previous degeneration. Unfortunately, Spinraza is VERY expensive, costing $750,000 USD! Without Spinraza Kiana will die. It is imperative that we raise funds immediately in order to save Kiana's life. We are so grateful for your support! You are literally saving Kiana's life. Kiana was born in January of 2017 in a rural area of Khatam in Yazd province, Iran. She was acting normal in every way until she was 9 months old.