Hello! I’m Louise. Welcome to my blog, Young Crohns, I’m really happy you found your way here.

A little bit about me…

I have Crohn’s Disease, a form of Inflammatory Bowel Disease (IBD). I also have an permanent ileostomy.

I was diagnosed in September 2011 after several months of symptoms that didn’t really make much sense. But if I am really honest, I had been suffering with bowel problems on and off for about a year prior.

I’ve had many hospital admissions; most of them occurring in the first year of my journey with IBD. The rest have been for my surgeries and the period of time in between them during the Summer of 2016.

I tried all of the medication options open to me at the time but chose to have surgery in 2016 to remove a large narrowing in my small bowel. Unfortunately, three months later, I had my colon removed and a stoma created. In March 2019, after almost a year of struggling with my rectal stump, I had it removed and made my stoma permanent; an end ileostomy.

Life since those surgeries has been really great; but not without some post-op complications and challenges throughout recovery,  but my Quality of Life (QoL) has significantly improved.

A little bit about the blog…

I’ve been writing since I was first diagnosed and this blog chronicles my journey with IBD. Even now years later, I am still ‘accepting’ the changing face of my disease but I do try to have a positive outlook on life; to not let the beast control my life and overwhelm me. I hope that this blog tells the truth about everything I struggle with when it comes to a chronic illness and now with having an ostomy.

It also offers blog series on IBD medications, examinations, procedures as well as daily aspects of stoma care.

My writing comes from a place where I challenge the questions around my own health, my condition – what IBD means to me as an individual patient, as well as the disease as a whole – navigating life with a chronic and invisible illness as well as how that has impacted me mentally and sexually.



Some of my blog posts contain medical information but are not intended as medical advise. Any post pertaining to be in this vein will always have a clearly stated disclaimer at the beginning of the post.


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Get in touch

Email – info@youngcrohns.co.uk

Twitter –  sapphire20 (personal) and youngcrohns (blog specific)

Instagram – louisehelenhunt

Facebook – Young Crohns

1 Comment

  1. ellie
    18/03/2015 / 11:28 pm

    I hope you’re doing ok at the moment Louise. Your blog has saved me a little tonight, I’m in a bad place with my Crohn’s and mental well being, but reading your blog was like looking into a mirror, I understand completely and it made me feel less alone. x

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