E
elizabeth__
Guest
Hello everyone!
Thought I would introduce myself to the board (shall try and do so with limited moaning!).
I'm 19, currently a biomed student and have recently been given a half hearted diagnosis of Crohns disease whilst at University. Now back home for the Summer, I'm trying to get this confirmed with a specialist here in London but NHS referral is not in my favour with my appointment not until the end of July.
I've only had a flexible sigmoidoscopy which did show some inflammation but apparently not to the extent which would cause the symptoms I've had (typical passing of blood and mucus, diarrhea for months, constant "need to go" - upwards of 10 times a day, cramping pains etc). My consultant said that he believed the problem to be higher up in the bowl suggesting Crohns, but then my health insurance money ran out so back home to London I came.
Towards the end of Uni semester things got pretty bad, being shattered almost all the time as well as not wanting to go out – as would just be standing in the queue for the bathroom all night, doesn’t really conform to University protocol! Sharing a bathroom with 20 other girls was not pleasant at all, especially trekking to it a hundred times a night, does anybody else find themselves hunting for a disabled toilet where you can just sit with a pillow for hours!
I’m on asacol 6 times a day which only seems to deal with lowering the frequency of trips to the loo but not any of the other symptoms. I’m struggling with the side effects – feeling extremely nauseous and headachey after taking it but should perhaps give it a little longer to see if this subsides. Colifoam did absolutely nothing – apart from thoroughly amuse my boyfriend who felt that he should watch the administration…
Look forward to sharing even more delicious details with you all!
Lizzie xx
Thought I would introduce myself to the board (shall try and do so with limited moaning!).
I'm 19, currently a biomed student and have recently been given a half hearted diagnosis of Crohns disease whilst at University. Now back home for the Summer, I'm trying to get this confirmed with a specialist here in London but NHS referral is not in my favour with my appointment not until the end of July.
I've only had a flexible sigmoidoscopy which did show some inflammation but apparently not to the extent which would cause the symptoms I've had (typical passing of blood and mucus, diarrhea for months, constant "need to go" - upwards of 10 times a day, cramping pains etc). My consultant said that he believed the problem to be higher up in the bowl suggesting Crohns, but then my health insurance money ran out so back home to London I came.
Towards the end of Uni semester things got pretty bad, being shattered almost all the time as well as not wanting to go out – as would just be standing in the queue for the bathroom all night, doesn’t really conform to University protocol! Sharing a bathroom with 20 other girls was not pleasant at all, especially trekking to it a hundred times a night, does anybody else find themselves hunting for a disabled toilet where you can just sit with a pillow for hours!
I’m on asacol 6 times a day which only seems to deal with lowering the frequency of trips to the loo but not any of the other symptoms. I’m struggling with the side effects – feeling extremely nauseous and headachey after taking it but should perhaps give it a little longer to see if this subsides. Colifoam did absolutely nothing – apart from thoroughly amuse my boyfriend who felt that he should watch the administration…
Look forward to sharing even more delicious details with you all!
Lizzie xx