Inflammatory Bowel Disease - Ulceration Of The Ileo-caecal Valve
Apr 10, 2014
GI Consultant has sent to my GP copied to me:
This patient had had a SeHCAT test as well as colonoscopy. The SeHCAT test is reassuringly normal showing no evidence of bile salt malabsorption. At colonoscopy there was ulceration of the ileo-caecal valve. I understand the terminal ileum and colonic mucosa appeared normal. Ileo-caecal valve biopsies shoe benign ulcer with focal cryptitis. There is no granulomata or other features diagnostic of inflammatory bowel disease. Other colonic biopsy show mild nonspecific chronic inflammation.
This taken together with his symptoms and the raised faecal calprotectin is highly suggestive of Inflammatory Bowel Disease.
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I am a 24 year old who works a 12 hour rotating shift pattern (including night shifts). For the past 6 months or maybe more o have had upper left abdominal pain (cramping/aching) and more recently lower pain (sometimes across lower, sometimes left and sometimes a specific place on the lower right). I put it down to IBS due to shift work. My partner convinced me to see the GP as I have a family history of IBD. Oh and my bowel movements vary from constipated (less than once a week) to lose (not diarrhoea and multiple times per day)
Had stool tests and blood tests. I expected them not to find anything to be honest and just did it to please my boyfriend and put his mind at rest.
Doctor phoned and said that "the stool test shows signs of inflammation indicative of inflammatory bowel disease". I couldn't really ask more questions because of where I was. Phoned in for blood results and told by reception that they were fine.
I have been referred to the gastroenterologist and have an appointment in 2 weeks.
I am tired all the time and find it really difficult to get out of bed, frequently have naps at work but put that down to shift working.
I don't want to take any laxatives because I never know when it will change between constipation and loose stools and when I'm working, I often can't get to the toilet.
I often have joint pain but I also have a knee injury and some hyper mobile joints.
I am so confused as to what is going on and hate not being in control of my body. I know I only have mild symptoms, I feel so alone (shift work doesn't lend itself to meeting people regularly).
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My 27 year old son began exhibiting symptoms of inflammatory bowel disease about 2 months ago. He had severe stomach pain and his food wouldn't digest for several days. A CAT scan showed an inflamed ileum. He went to a gastroenterologist who ran more tests and put him on prednisone. The inflammation went away and at the last followup visit the gastro dr. decided not to label my son with IBD yet unless the symptoms come back. My son noticed that, since his problem began 2 months ago, he no longer sweats. Early on, he would get dizzy and light headed at work (it was September and still warm)but he wasn't and still isn't sweating at all. He goes to the gym for a workout and 1/2 hour later his face is bright red and his head feels hot and prickly, but not one little drop of dampness happens anywhere on his body. Since both the inflammatory bowel/digestive problem and the anhidrosis started at the same time, I wonder if they are related, and if so, what disease does he have? He is beyond frustrated at this point because his digestive problems aren't gone completely, and he has days where he's exhausted waking up after a good night's sleep, and has minimal energy a lot of the time.
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I stopped smoking 6 months ago and to be honest feel worse for it. Currently i am suffering from
UC and mouth ulcers. I have never suffered with mouth ulcers before and my bowel has been painful since stopping smoking. What i need to figure out is this: is it worth taking up smoking again or do i need to put up with abdominal pain, bloody diarrhoea, mucus and faecal incontinence and always
having to use pads. I am only 55 and feel like i am 85. I am beginning to think smoking is the lesser of the two evils!! Have read on many forums how people give up smoking and then suffer the indignities of UC. Is there any medical evidence on UC and stopping smoking? If not, why not?
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I have been having bleeding from my back passage, fatigue and tiredness for weeks and finally got to the doctor today. She told me that I had IBD and that she would arrange for an urgent referral for a colonoscopy (2 weeks). She also said that I should come back if the symptoms got worse in the mean time. I am anxious that I maybe underplayed the symptoms slightly. every time I go to the toilet (5 or 6 times per day) it is bright red and seems not to be getting better. Should I go back or is it fine to wait two weeks?
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How likely is it to get pregnant after being diagnosed and treated for PID (pelvic inflammatory disease)? Keep in mind I've only had one child in over19 years with no other pregnancies!
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Hi, I was treated yesterday night with 2 grams of azithromycin for gonorrhea (25 year old female). Didn't have any symptoms, but knew a sexual partner had it. Couldn't take the shot because of a bleeding problem I have. I have pain in my back today. Can this be associated with PID? I was exposed 10 days ago. Going for a follow up in 10 days to make sure the pills worked, should I worry before then? Or give the meds some time to work? I went to the clinic yesterday so I can't run off from work today to ask them.
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I'm 21 and I've been having irregular periods since June 2014; in recent months have had increasingly painful pelvic pain. Went to the GP multiple times in an attempt to figure it out but got nothing. Finally went to the GUM clinic on saturday and was diagnosed with PID, although the cause is as yet unknown. I was told it is likely due to a 'long-standing chlamydia infection'. Thing is, I haven't had sexual contact with anyone since March 2014 and for the year up to that I was in a committed relationship. That guy was the only one I had 'unprotected' sex with (was on pill); everyone else before him I used a condom with. So I had no idea I was even remotely at risk (as stupidly trusted this guy) and I'm now worried that because of this and having no symptoms, that I might've had the infection for a while without knowing and it therefore have a worse effect on my ovaries etc.
I'm really worried as dr was pretty casual about the PID, but from what I've read it's really serious. Did anyone here have chlamydia for a while before PID? Do you know how you got it? And how has PID affected your sex life/fertility since diagnosis? I'm so scared I'm going to find out I'm infertile because someone I trusted did this to me when I was so so careful myself
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Just wondering if anyone else has had LS and Pelvic Inflammatory ? They told me it's not connected. But they couldn't find anything else wrong.
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I was diagnosed with PID last week Monday. The ultrasound scan revealed prominent collection of fluid behind my uterus. I was told to do a HVS/MCS. The result showed scanty growth of Escherichia coli. Before this result came out, I started treatment with ciprofloxacin and metronidazole IV for 4 days with pain killers. Follow up with drugs to complete 10days. I still have sever pain in my legs,lower abdomen and lower back. I had an ovary removed last year August because I had ovarian cyst. Please I need help. It's been 2 weeks plus now in pains. I'm tired of this pain.
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When I was 16 I was forced into having oral sex with someone that I went on a date with. I am now almost 21 years old and have only ever had intercourse or any other sexual encounter with my fiance. For the past years I have had problems with my periods and pain during them, but never thought twice about it. I went to the doctor yesterday for a possible UTI and found out that I may have PID. Though I have yet to be diagnosed with an STD (labs are still out), I am assuming that Chlamydia is the case, given to me from the guy who forced me to have oral with him (seeing as how he probably had many interactions with other girls if he did something like that to me.) I am now TERRIFIED that I have had this disease for almost five years. I am getting married in just 3 weeks and am now afraid that I won't be able to have children... What are the chances of this if I have in fact had this disease for this long?
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I been having pain in my right side of my pelvis some time it will go to the other side and I been having back pain and my periods are missed up it been spiking mouths and they be longer and heavier and i been sicker lately then before.
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From 4 yrs i have been suffering from severe pelvic pain with lots of inflammation in both hips. all blood works come normal but mri does show inflammation. Doctors cannot find what it is, can it be my ovaries or fallopian tubes inflammation or infection which is causing this, plz somebody help. I want to get pregnant but my pain in pelvis which is that worse that I limp many time is not allowing me.
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A little background information about myself: 23 y/o female, diagnosed with PCOS at 19, suffer from multiple UTIs and kidney infections each year.
Starting in about September, intercourse would be incredibly uncomfortable and painful, causing me to cramp severely after and bleed. These symptoms became worse and worse, and I began spotting between my periods. So, after meeting with my GYN in October and her suspecting cervicitis (inflamed cervix), I had an appointment beginning of December for a colposcopy and cervical biopsy. Upon touching my cervix with a q-tip it bled out and was EXTREMELY sore to touch. Waiting on further consultation from the results, but according to my GP: pre cervical cancer cells, uterine lining infection and cervical infection.
I have now been on 2 rounds of different antibiotics with no improvement, I believe I am getting worse. Ever since the biopsy, I have bled EVERY DAY FOR SEVEN WEEKS! I have a fever that comes and goes, chills, nausea, constant pelvic pain and am extremely tired all the time.
I have been researching (bad idea I know) what could be causing all these symptoms and am thinking PID or uterine fibroids? Any advice out there?!
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I'm scheduled to get one of these , a mechanical one in about five weeks time , and seeing I know little about this surgery and the after effects, I'm trying to find out as much as I can through the internet.
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I have recently been diagnosed with an thoracic aortic aneurysm and a badly damaged left ventricular valve. The aneurysm is 5.9cm and on the arch at the top of my heart. It was found by accident when I had a ct scan for difficulty swallowing then further tests followed which found that the 'murmur' I was diagnosed with 7 years ago had deteriorated so badly the left ventricular valve would have to be replaced with a mechanical one. At the moment I am waiting for a final visit with the surgeon before being given a date for the op. The thing is I feel perfectly fine, I have no pain, no shortness of breath, have as much energy as always and in fact feel fit as a fiddle. I am 58 and have kept as upbeat as possible about all this, but my family are distraught with worry about the 10 - 15% chance that I won't make it through the surgery (national statistics) and the possibility of stroke or paralysis. My dad had an aortic aneurysm (unknown to him) and it ruptured, he survived the surgery but died 3 months later having never left the hospital. This was only 4 years ago and my mum is now sick with worry, literally, about me. I am worried that I will never get back to how I am now, that I will become reliant on family and friends. Its usually me who helps the family with the children and my mum. I live alone but have family close by and my ex husband (who is my best friend) has been a great support. My family, bless them, are fussing around and not letting me do anything and I know I would be the same if I were in their shoes but I feel like an invalid although I should be grateful for their concern. I am feeling so confused, I refuse to cry about this and I am holding myself so tightly together but seeing my families tears is breaking me up. I am putting my 'healthy self' up for a life threatening, painful operation. Has anyone else been in a similar position and could give a few words of encouragement?
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My 12 yr old son is experiencing no BM after 4 days of switching him to this GFDF diet ... Before he was IBS .... Not sure what to do
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removed large bowel due to years of suffering from pain and constipation
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Hope right forum at end of post its about ibs. So few years ago started having ruq pain, Dr said lung xray clear ultrasound small liver cyst, alt slightly elevated, no doubt drinking, thinks stress, went on, bowel movements from normal, loose, some days 3-5 times, some days none, but never more than a day or two constipated, Er visit a few months ago for stomach virus, full blood panel because of history normal, abdomen palpation normal. Pain persist on daily basis more last two ribs both sides front and back doesn't seem deep, lots of bowel sounds and gas, worse in evening, worse sitting, better standing or laying down.Got nervous went to walk in clinic, nurse practitioner(I'm in USA) said probably cirrhosis with my history, gi appointment in 3 weeks, paniced and went to Er next day, Dr said no way cirrhosis, this muscular or ibs, his blood work said normal alt 52, good to him, but walk in NP said alt 55 elevated.no other symptoms, no jaundice, no blood anywhere, gassy, occasional bloating and the pains in front sides and back come and go. Have a lot anxiety issues. Lots of intestinal noise and bowel movements, losing my mind. any Thoughts. Ibs?
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I have had IBS for 20 years, and have been treating it with fiber therapy pretty successfully. In the last few months, i've had some odd bowel movements. the first one i noticed was long and thin and tough, like an elastic. i thought tapeworm, but my stool tested negative for worms. i can't explain it, but after wiping and checking it flings itself off the toilet paper a fair distance. I'm afraid to ask my doctor because he scoffed at me when i told him that i thought i had worms. i had a colonoscopy for my 50th birthday in august and everything checked out. Any idea as to what's happening?
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I got my results back from the needle biopsy and primary Doctor didn't know what it meant and said I had to go to a Endocrinology specialist so I wanted to see if anyone knows what it means the results were:
FNA-Lt Upper Pole Thyroid Nodule, 1 Thinprep slide, 1 Cell Block:
-Non-Diagnostic
-Thin Prep and cell block are hypocellular and consists of occasional tiny groups of follicular cells, colloid and mixed inflammatory cells.
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