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Living at University with IBD

Living at University with IBD can be very daunting, especially if you're very used to living at home with your parents, near your doctors...

Accepting you need help.

So, I haven't really been posting on my blog in a few months, and I have been questioning whether to talk about why. I have always been...

Learning to grieve your old self

Autoimmune Diseases like IBD can have a debilitating impact on the way you live. I have spent the past 6 months learning to adapt and...

Toxic Positivity

People always ask me how I manage to stay so positive throughout my battle with Crohn's, I find the answer very complicated to word. I am...

The Gracie Effect

For those of you who don't know who Gracie Keeping is, she’s one of my closest friends and biggest inspirations. I met her almost 3 years...

Body Positivity and Weight Fluctuation

I have always been a massive advocate of body positivity and have preached self love for many years, but when I started to notice Crohn's...

My Diagnosis Story

On the 27th of December 2020 I was diagnosed with Crohn’s Disease, a form of Inflammatory Bowel Disease. It is an autoimmune condition...

My Feeding Tube Experience

Many IBD fighters have to have a feeding tube at some point in their lives, often this is because Crohn's is active in the oesophagus, or...

Introduction to my Crohn's Blog

My name is Lucy Harman and I have an incurable autoimmune disease called Crohn’s. What’s Crohn's you ask? Well, to put it scientifically...

 
Cute Notebooks

Contact Me!

Feel free to pop me an email or a DM on Instagram.
I am happy to answer any questions or just have a chat if you want.
Instagram: @my.crohns.and.me