Got pain in Bladder for first time and went twice to hospital admitted me with first time of diverticulitis Iv only treatment 5 data passed blockage went home on oral antibiotics a week later bleeding 3 bout of stomach pain and bloating. Another week a bout of stomach pain belly button level with bloating and vomiting and diarrhoea sh*t hospital send me home. A weeks later pain in bladder again back to hospital again said to have diverticulitis again they didn't want to keep me in but did after fight iv antibiotics but 3 days sent my home again within 2 days pain again in bladder went to two different hospital sent home. It was my general physician for lungs and heart that arranged a special test better that the two CT that showed the diverticulitis he done a test called a label white cell scan that showed the whole colon was inflamed and the bladde was fused to the bowel with and abscess and a significant necrosis between them. My blood test that he arranged showed I have a CRP of 190, high white cells in urine and esr higher that 20. I was placed back into hospital on iv drip and then sent home and kept 9 weeks on oral iv antibiotics before they done high Anterior Resection August 2016.
Overall I have improved but late 2016 one week of water diarrhoea and 2017 3 bouts of waking with stomach pain belly button level although milder than before bloating and vomiting and diarrhoea so in August 2017 an Colonoscopy said to be ok like the other 3 Colonoscopy and Gastroscopy of the past. Since then for last 4 months discomfort after eating where appendix region iand waking with pain in that region one bout of watery diarrhoea and just this week constipation and now pain down where the cut is in the pelvis.
Unsure other than 3 times since 2016 operation have test positive to IgG antibodies against Saccharomyces cerevisiae which shows up in 85% of people with Crohn's Disease.
I try myself I know there is something going on.
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Now 7 months later my left side hurts daily , worse than before surgery . I've had 2 cat scans and the doctors say they see nothing and send me home as if it's all in my mind . The surgeon said I only get 6 weeks off work and a week before my return to work in October 2017 I callled him saying I'm in too much pain to return to work as I lift 30 -40 ponds of product all day long for 12 hour shifts 5 days a weeek
He said 6 weeks is all I get . I hadn't recovered . This is horseshit I have no life anymore . I can't do anything
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I had 3 colon section the first two was a muck up, the third they took out part of small bowel, one way value my cecum and my lower large bowel. The histologic showed I had big roundxsauces of diverticulitis and hard faecal matter as the as bath plugs. They still say I got some more there. Well I have been living in chronic pain since 2013, 5 years and its worse the blocked pain vomiting and they keep doing the old stupid tests that show nothing. My gp told me the truth adhesion s in the joint are the reasons and all specialists telling us was haven't got adhesions are talking BS that o you. They only they can know is by opening you up again then they can fix the adhesions which the pain. I going to just keep on calling the ambulance and make a nuisance of myself till someone helps, this is in humane. Let me your out come.
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I go to different doctor just about a weekly basis but they don't understand me, meaning that I feel like I'm going crazy because the exams,MRI, all the tests they make me do almost all say that I'm ok. So I don't understand why I feel this way and why doesn't anyone understand me. I cry all the time. I can't work like this, I can't barely do anything yet SSI have denied me.
What can do?
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