TRUST YOUR GUT.

Jenny McGibbon is a freelance graphic designer from Scotland. She created a chronic illness platform, This Thing They Call Recovery to reach others within the community. Jenny offers realism, support, humour and comfort to the thousands of people all over the globe suffering with a chronic condition. Here we talked about everything from managing her […]

Jasmine was diagnosed with Crohn’s disease at 10 years old. Here she discusses the impact of living with an illness that is considered invisible.

Angelina was diagnosed with Crohn’s disease aged 12 and had her ileostomy formed aged 13 after 11 months of unsuccessful treatment. Due to her own struggles with her stoma and finding stoma-friendly clothing, she founded Aura Clothing; a fashion brand that creates custom clothing for those with an ostomy. I interviewed her about her experiences […]

Kate was diagnosed with Crohn’s disease aged 14. She fought a long 3 years while her doctors eliminated medical treatment after medical treatment, searching for one that would stop her body from attacking itself. There is no cure for Crohn’s and Kate was told the best case scenario was long-term remission, where she would have […]

Amy is a nurse on a General Surgery/Digestive Diseases ward in Brighton, U.K. I interviewed her about her experience as a nurse, looking after patients and how social media has helped her understand her patients. 

While I’ve got a very good medical team now, it hasn’t been an easy ride to find the care I have at the moment. 

So there I was in the hospital so excited that I was going to finally meet my baby. As a first-time mother I was so excited but also very anxious… Will she be ok? Will I be enough? Will we be best friends? These thoughts consumed me whilst being induced. Sure, the thought of giving […]

Abi was diagnosed with Ulcerative Colitis after a long battle with her medical team to find out what was wrong. Read her story here.

Sophie Medlin is a Consultant Dietitian and Director of CityDietitians. She specialises in helping people with colorectal disorders and surgery. I interviewed her about the amazing things she’s doing on social media and pick her brain on how to help those with a gut condition and/or surgery. 

Two years ago, Michaela was diagnosed with Familial Adenomatous Polyposis (FAP); a rare and hereditary bowel disease. She bravely talks about her surgery, continuous fight with the disease & what it means for her future. Here is her incredible story.