Has any here had a child who was diagnosed with PUJ (Pelviureteric junction obstruction)
If so who long did it take from the early diagnosis (MAP3 and scan done) and referral to specialist?
Currently watching ds (age 13) on the sofa in pain for the 23rd time this year just waiting for him to start throwing up. Loosing patience with the waiting game and hate watching my sporty energetic son in pain.