2 YEARS OLD KIANA NEED OUR HELP
Kiana, an 18-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.
She was acting normal in every way until she was 9 months old. Her parents noticed she was gradually losing her strength. After undergoing various tests, Kiana was diagnosed with SMA type II. SMA is a rare genetic disease that impairs the control of muscle movements and if not treated in time will impact muscles used for breathing and swallowing which will ultimately lead to death.
There are attempts around the world to find a reliable cure for this devastating disease. Biogen’s Spinraza (Nusinersen) is the only available drug in the market for SMA (with FDA approval in late 2016) and unfortunately it is a very expensive treatment (750,000 USD for a full-year treatment). This is far beyond what Kiana’s family can afford, yet they are desperately looking for help so that they may save Kiana’s life before it is too late.
Kiana’s parents will never stop fighting to save their precious daughter’s life. We cannot just sit and watch her struggle to survive. Kiana deserves to be cured and given an opportunity to experience the beauty of life.
Together we can confirm that borders do not stop humanity. Help Kiana see more days with her loving parents. Do not let Kiana and her parents struggle alone; every dollar counts! Please donate and invite family and friends to this fundraising campaign. Inviting just a hand full of friends will make a huge impact. Kiana is my relative and it is truly heartbreaking watching this baby girl suffer from this cruel disease, but I have hope that together we can save her life!