DC had constipation issues since toddler. Been on & off lactulose & movicol. Tested when 4, dairy intolerant but then advised just needed more water.
This episode not had poo for 4 weeks & been off school for 3rd week. Usual lactulose & movicol didn’t work, movicol causing stomach pains. GP prescribed senna but this just increased leakage, up 10 times a night, dc more lethargic, drinking & eating less. Returned to gp (different), prescribed suppository which dc found painful (screamed when I gave it).Then gp prescribed enema. Didn’t work so prescribed another 3 days later, no joy.
When dc woke 4 days later with pain when pee, unable to pee but needed & continuing leakage took to a&e. Urine infection diagnosed, Trimethoprim & Picosulphate prescribed for 3 days. Returned when no poo. Saw different doc who gave us more movicol & told to increase up to 12 sachets. Refused as dc unable to consume enough liquid now, told next step is nagostric tube to give movicol. Agreed combination of lactulose & Picosulphate for 10mg each twice day, but only increasing leakage.
DC finding relief sitting in shower for hour+ and now trying to pull out bits poo. This has enabled dc to eat & drink bit more for energy. Bottom is v sore & struggling with continuing leakage.
GP (different) call yesterday was v difficult, GP agreed to refer to gastroenterologist but admitted issuing letter alone will take days (grrrr).
At wits end, dc & I exhausted. Can someone pls offer advice? I’ve read about sedated removal but never been offered.