Hi everyone,
I'm looking for a bit of advice please as I'm feeling a bit in the dark and confused, and figured this might be the best place to come!
I had a colonoscopy yesterday after months of horrible symptoms such as pain, diarrhoea, weight loss, fatigue and joint pain. They diagnosed me with ileitis yesterday as well as noting inflammation and extremely enlarged Peyers nodules, and took 6 biopsies that I will get the results of in a few weeks. Am I right in thinking that ileitis is one of the 5 types of crohns? And do the enlarged nodules which are an immune response also point to crohns?
Feel a bit in the dark as they printed me a report which diagnosed ileitis and then said my gp will see me in 4 ish weeks when they get the biopsies back.
Can anyone offer insight or advice please?
Thanks
A x
I'm looking for a bit of advice please as I'm feeling a bit in the dark and confused, and figured this might be the best place to come!
I had a colonoscopy yesterday after months of horrible symptoms such as pain, diarrhoea, weight loss, fatigue and joint pain. They diagnosed me with ileitis yesterday as well as noting inflammation and extremely enlarged Peyers nodules, and took 6 biopsies that I will get the results of in a few weeks. Am I right in thinking that ileitis is one of the 5 types of crohns? And do the enlarged nodules which are an immune response also point to crohns?
Feel a bit in the dark as they printed me a report which diagnosed ileitis and then said my gp will see me in 4 ish weeks when they get the biopsies back.
Can anyone offer insight or advice please?
Thanks
A x