Blog

Practical reads, and where each one came from

40 short posts on the parts of life with Crohn’s, colitis, a stoma or an ileoanal pouch that the appointment does not have time for. Each one is a reading of published patient guidance — from the Ileostomy & Internal Pouch Association, the UK charity, and from Dansac — and links to the sources it was read from, so you can check it yourself.

Eating & drinking

What actually changes about food after bowel surgery, and what does not.

Fluids, salt & kidneys

Why hydration works differently without a colon, and what to drink instead.

Movement & recovery

The exercise programmes published for people recovering from abdominal surgery.

Infections & antibiotics

The infections that complicate inflammatory bowel disease, and the drugs used against them.

Symptoms in remission

Why the bowel can still misbehave once the inflammation is treated, and how that is measured.

Tests & monitoring

What the tests measure, what the numbers mean, and why the intervals differ from person to person.

Beyond the bowel

The parts of inflammatory bowel disease that are not bowel symptoms — fatigue, anaemia, and what alters risk.

Living with a pouch

What an ileoanal pouch is, how it is built, and what to expect from it.

Stoma day to day

The practical routines of stoma care, day to day.

Work, travel & confidence

Going back to the rest of your life — work, travel, sport and telling people.

Before you change anything

These posts are readings of published patient information, and every one links to the sources it came from. They are general information, not medical advice, and they cannot account for your own diagnosis, surgery or treatment. Anything you plan to change — what you eat, how you manage your bowel, your medication, your activity, your stoma or pouch care — is a conversation to have with your IBD team or stoma care nurse.