Her father Sanekappa did his best and took her to several doctor, but no one could diagnose the problem with Sidamma's health. He was shattered.
Finally a doctor he consulted immediately saw that this was a rare disease and that the girl needed expert opinion. He referred them to Narayana Hrudayalaya, Bangalore. Sidamma was diagnosed with Griscelli's Syndrome. It is a rare, newly discovered immunodeficiency illness. Children will this disease usually do not survive their childhood unless they receive a bone-marrow transplant. For Sidamma, time is running out.
Fortunately, for Sidamma, her little sister is a 100% match and will be donating stem cells to Sidamma. But the family needs Rs 12 lakhs for the procedure. It is a sum that will be impossible for Sanekappa to raise. The family needs your help to raise funds for the little girl's Bone Marrow treatment.