My name is Muhammad Faisal Javaid, my life motive was almost changed by my kids, when my first son was born, and he was diagnosed mild hemophilia. For his tests I literally travelled between Karachi and Lahore several times. But never imagine that much worse part is coming. When my second son Rohaan was born, he was fine but at the fifth day he felt difficulty in breath, his heart beat was very fast and he was pale. We took him for tests and he was diagnosed jaundice, during its treatment we came to know about the fact that he is CHD Child. From that day i searched every possibility for his treatment, I saw people having same difficulties we are facing, but the worst part was many knew nothing about CHD, neither they were aware of basics. I observed there is lack of proper technical support and infrastructure. Limited number of surgeons and cardiologist in our country make it even more difficult to cope with this disease. After receiving negative responses from everywhere, I decided on spot that whether my son will be treated or not I will do something for other parents who are going through same. By that time i came to know about PCHF, by Mr Farhan Ahmed, his kind guidance helped us to think in broad perspective. I searched hard; my son first surgery was done without any support from my homeland, for which my heart still bleeds. I know we have to go from same difficulties which we faced before, and that motivates me to work with PCHF, so we could together pave way to some solution, so no one other can suffer.