Finding out more about crohns...
In 2006, aged 13, my Dr discovered i was anemic and after having stomach pains for as long as i can remember, i was diagnosed with crohns/UC after a barium follow through. At this time i was going through a bad flare up and was in hospital for a week. My weight dropped from 8 stone to 4 stone which was the main cause of concern to my Dr. I also had terrible stomach pains and bloody bowel movements every 5 or 10 minutes including through the night and also lost alot of my hair (is this a common symptom?). I dont know much about IBD as i was diagnosed at a young age and as it is common in my family (my brother, gran, aunt and cousins on both my mum and dads side have it) so i was never there when it was explained to my parents in detail for the first time, so i only know what i have found on wiki and around the internet. Now that im getting older im more interested in researching it. Hence me coming across this forum
I didn't have a colonoscopy at the time as my consultant thought it would irritate my bowel more and after taking galfer (iron supplement) and 16 weeks on pred i was in remission complete with the moon face, lots of weight gain and stretch marks to show for it. Anyways the consultant thought it was better not to disturb anything again and let it be.
In early 2010 after 4 years of remission (taking a maintenance dose of 2g pentasa daily) and only having mild stomach pains occasionally, i started having diarrhea 4 or 5 times a day and losing weight and bad pains again. Since then I have managed to maintain my weight but have very regular diarrhea and on and off moderately bad stomach pain. During my period the pain/diarrhea becomes very bad and i have absolutely no energy, all i want to do is sleep (i could easily sleep for 15 or 16 hours only getting up for toilet breaks) and can barely being myself to walk down the stairs in the morning.
In june 2010, sept 2010m jan 2011 and recently I have felt really unwell and finally managed to get an appointment with my consultant a few weeks ago and had blood taken showing i was very low on iron so now i am on galfer again and my normal 2g of pentasa and mefenamic acid to help reduce period pain and flow during that time of the month. Also getting my first colonoscopy in july which will be interesting to see whats really going on. I also feel dizzy and at time nauseous but im guessing this is a side effect of the medication.
Anyways sorry about the big essay got slightly carried away and it felt therapeutic just to be able to write stuff down, get my head sorted a bit. The point of all this is everytime ive had a flare up it is caused by stress. My dad died in 2005 - first recognized flare up a couple of months later in 2006. June 2010 was during public exams i was taking and i havent felt well at all since then and bad very sick in september (start of term) and January during my a levels and now i have exams next week and have started feeling terrible again going to the toilet 7 or 8 times a day. I no that i dont have as severe a case of IBD as some people on here, when not on my period i can get through the day with paracetamol atleast get the school day over with and deal with the pain in the short term for an hour or so then i can go home to my bed to comfort me lol. (how often do people on here need to take painkillers, is it usual for it to be daily?)
The thing that most worries me is urgency and accidents (not sure how acceptable it is to talk about this on here :$ but if its not ok here then where else will it be??)
Even when im not in much pain i have urgent bowel movements with only a couple of seconds warning so accidents are inevitably really. If i am in a routine (ie at school going to the bathroom before each class) i have always been able to manage at school and so far away from home atleast but my IBD has got progressively worse since last year and with 2 stressful months of exams ahead i dont no how to best manage these symptoms. I have arranged with the school and exam board to be able to leave the exam hall urgently through an exam if needed and a seat beside the door so i can leave discreetly and have extra time if i need a long toilet break but i wont be able to do an exam having to leave every 10 mins for the toilet and in pain all the time in between, worrying more about getting to the toilet than completing the exam.
Im here looking for any tips on how to manage through stressful times which are only made more stressful by knowing the stress will make me more sick.. and the cycle continues until im taking every painkiller i can find in the shop and staying as close to the bathroom as possible. Has anyone else been in a similar situation with exams or can anyone offer any advise just to settle my mind slightly?
Thanks for reading, sorry about how long it is. The only food i have found that affects me is apples which cause really bed stomach pain for me. I have not had any blood in my bowel movements since 2006 that i have noticed. When im remission should you be symptom free? or is it possible to be?
In 2006, aged 13, my Dr discovered i was anemic and after having stomach pains for as long as i can remember, i was diagnosed with crohns/UC after a barium follow through. At this time i was going through a bad flare up and was in hospital for a week. My weight dropped from 8 stone to 4 stone which was the main cause of concern to my Dr. I also had terrible stomach pains and bloody bowel movements every 5 or 10 minutes including through the night and also lost alot of my hair (is this a common symptom?). I dont know much about IBD as i was diagnosed at a young age and as it is common in my family (my brother, gran, aunt and cousins on both my mum and dads side have it) so i was never there when it was explained to my parents in detail for the first time, so i only know what i have found on wiki and around the internet. Now that im getting older im more interested in researching it. Hence me coming across this forum
I didn't have a colonoscopy at the time as my consultant thought it would irritate my bowel more and after taking galfer (iron supplement) and 16 weeks on pred i was in remission complete with the moon face, lots of weight gain and stretch marks to show for it. Anyways the consultant thought it was better not to disturb anything again and let it be.
In early 2010 after 4 years of remission (taking a maintenance dose of 2g pentasa daily) and only having mild stomach pains occasionally, i started having diarrhea 4 or 5 times a day and losing weight and bad pains again. Since then I have managed to maintain my weight but have very regular diarrhea and on and off moderately bad stomach pain. During my period the pain/diarrhea becomes very bad and i have absolutely no energy, all i want to do is sleep (i could easily sleep for 15 or 16 hours only getting up for toilet breaks) and can barely being myself to walk down the stairs in the morning.
In june 2010, sept 2010m jan 2011 and recently I have felt really unwell and finally managed to get an appointment with my consultant a few weeks ago and had blood taken showing i was very low on iron so now i am on galfer again and my normal 2g of pentasa and mefenamic acid to help reduce period pain and flow during that time of the month. Also getting my first colonoscopy in july which will be interesting to see whats really going on. I also feel dizzy and at time nauseous but im guessing this is a side effect of the medication.
Anyways sorry about the big essay got slightly carried away and it felt therapeutic just to be able to write stuff down, get my head sorted a bit. The point of all this is everytime ive had a flare up it is caused by stress. My dad died in 2005 - first recognized flare up a couple of months later in 2006. June 2010 was during public exams i was taking and i havent felt well at all since then and bad very sick in september (start of term) and January during my a levels and now i have exams next week and have started feeling terrible again going to the toilet 7 or 8 times a day. I no that i dont have as severe a case of IBD as some people on here, when not on my period i can get through the day with paracetamol atleast get the school day over with and deal with the pain in the short term for an hour or so then i can go home to my bed to comfort me lol. (how often do people on here need to take painkillers, is it usual for it to be daily?)
The thing that most worries me is urgency and accidents (not sure how acceptable it is to talk about this on here :$ but if its not ok here then where else will it be??)
Even when im not in much pain i have urgent bowel movements with only a couple of seconds warning so accidents are inevitably really. If i am in a routine (ie at school going to the bathroom before each class) i have always been able to manage at school and so far away from home atleast but my IBD has got progressively worse since last year and with 2 stressful months of exams ahead i dont no how to best manage these symptoms. I have arranged with the school and exam board to be able to leave the exam hall urgently through an exam if needed and a seat beside the door so i can leave discreetly and have extra time if i need a long toilet break but i wont be able to do an exam having to leave every 10 mins for the toilet and in pain all the time in between, worrying more about getting to the toilet than completing the exam.
Im here looking for any tips on how to manage through stressful times which are only made more stressful by knowing the stress will make me more sick.. and the cycle continues until im taking every painkiller i can find in the shop and staying as close to the bathroom as possible. Has anyone else been in a similar situation with exams or can anyone offer any advise just to settle my mind slightly?
Thanks for reading, sorry about how long it is. The only food i have found that affects me is apples which cause really bed stomach pain for me. I have not had any blood in my bowel movements since 2006 that i have noticed. When im remission should you be symptom free? or is it possible to be?
Last edited: