Hi there, as the title really, hoping to find someone or some people with experience of TOF/OA/peptic strictures in infants. My daughter initially had a stricture of the oesophagus at around 6 months although had been poorly for 6+ weeks before this. We are having a hell of a time getting a diagnosis, we are now 2.5 yrs since the initial stricture. Her symptoms do fit any of the above Any thoughts, advice or experience would be very much greatly appreciated. [wine][wine][brew][thanks][thanks]