Thanks for taking the time to visit my JustGiving page.
Firstly! Thank you to everyone who contributed last year. We raised £675.000. That's enough to fund 4 days of research with funds still left over to contribute elsewhere.
As I'm sure a lot of you know, I suffer from a disease called Crohn's Disease which is a form of Inflammatory Bowel Disease. IBD affects over 300,000 people in the UK, children & adults. There is no known cure for IBD yet. Contributions big or small will make all the difference. Research is a crucial part to finding a cure. The more we know about IBD the better chance we have to improve diagnosis and treatments, fund research into finding a cure, and raise awareness of these invisible diseases.
This year I am taking part in the 10K walk around Bristol with my super cool dad, my loving partner Ben, superstar James L & his wonderful parents Jackie & Graham. If you wish to support us any contributions big or small are extremely appreciated.
I was diagnosed when I was 16. My first symptoms of Crohn's disease were multiple ulcers around my mouth and down my throat. I thought they would naturally just go away but more kept appearing each day. I was no longer able to eat or drink. I lost my appetite almost instantly and it became really painful to talk or swallow. Later on I started getting intense stomach cramps and I was extremely tired all the time. I would only do half a day at school or I would end up sleeping in the nurses office. I figured that eating caused the pain, so I stopped eating, but then drinking caused pain too so I stopped drinking. Although I wasn't eating or drinking I was still going to the bathroom and my toilet trips increased rapidly. I started passing a lot of blood at this point. Something that sticks out in my mind was when I couldn't move from my bed or talk because I was too exhausted just from walking to the bathroom and my dad said we're going to the doctor's. I didn't move or say anything so he picked me up and put me in the car. After that I was in hospital for over 2 weeks. I was on IV fluids pretty much the whole time and they put me on IV steroids to try and control the inflammation. They also had to try & get me to eat which I didn't co-operate with. I was going to have modulen but I refused because it gave me cramps and I was going to have an NG tube which my dad was against. So they decided to put me on a liquid diet. I drank nothing but supplement milkshakes.
Fast forward to now. I've been in an ongoing flare for way over a year now, I went back to a liquid diet for 6 weeks, was on a 24 week course of prednisolone, dropped to 6.5 stone, and this had an effect on my mental health. Recently, I've started Methotrexate, have iron infusions, am up to 8 stone, self inject adaludimab and have lots and lots of blood tests.
Crohn's disease and Ulcerative colitis are debilitating diseases. We are easily misunderstood because our symptoms are hidden. So here's a big walk to raise awareness for everyone who suffers with these diseases.
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