My son used to have Retinitis pigmentosa disease. As it is a genetic disease and there is no cure for this eye disease. People should know how to decrease this at least. When my baby was born, she used to had this problem. She used to see less and sometimes she felt like one eye blind. I and my husband were really anxious about this. We consulted with many doctors. But there was no solution to this. One day, a cousin of mine John visited us, he noticed everything and suggest us to go for stem cell therapy for this. We searched online a lot and had seen a very good review about this. Later, we consulted with few firms and started doing his treatment from this year January. We tried re tinitis pigmentosa treatment for him and now he is doing really well for the last few months.