Weak Sphincter Muscle And Colostomy Reversal
Feb 4, 2012
I have a 38 year old developmentally handicapped son who had emergency abdominal surgery due to Fournier's Gangrene last August which resulted in a temporary transverse colostomy in order to give his rectal area a change to heal. There was infection around his sphincter muscles and that is why the colostomy was done. We are now contemplating have this reversed. The surgeon says that his sphincter muscles are working but not as good as they should and she is afraid she may render him incontinent if she reverses it and he will be unhappy but he cannot be more unhappy than he is right now.His transverse is in a terrible place and we encounter a lot of flange changes as it doesn't stick even with paste, etc. and is bowel is prolapsed which is very upsetting to him. Another option is to move it down lower in his abdomen but we are considering having it reversed and seeing if he can control his muscles. We are believing that we have to try. Are there others out there with the same issue of weak sphincter muscles who have opted for a reversal?.
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I have diarrhoea all the time since having my gallbladder removed 30 years ago, i now have sacral nerve damage which has caused my annal sphincter to weaken so i now suffer from incontinence. I have been told i may need a colostomy, does anyone out there have one or faecal incontinence.
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My mom had emergency surgery that almost cost her her life. She had her bowels rupture into her stomach and she almost died. She went septic and it was really bad and scary. She has a colostomy and it will be reversed in six months. Her surgeon said to see a special doctor that specializes in reversals. She is 71 years old and they said she will make the decision to reverse or just end up keeping it. I know it is major surgery again and your age is a risk factor and your health etc. They also said if she were to decide to reverse it, she would need a colonoscopy done first. It scares me, because we almost lost her once. She is doing well with the colostomy and I actually helped her with it and we did well our first time on our own. I was proud.
The one thing she does do all the time is pull her pants down to check it all the time. Is this something that is normal in the beginning? I will be standing in the room and she has her pants down checking it.
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I am a US citizen living in Costa Rica the last 10 years. I had my second child on Nov. 28th at age 40. It was a difficult birth and the wall between my anus and vagina was torn 10 cm. They had to do emergency surgery to repair the wall and also did a colostomy in order to prevent infections to the repaired wall.
The stoma education provided in a third world country is lacking in every way possible. If it wasn't for the internet I wouldn't have survived the first difficult weeks. Eventually I was able to live a pretty normal life, even with a colostomy bag.
It is six months later, and I am scheduled for my colostomy reversal in two days. I have started a clear liquid diet. What can I expect? Is it a painful recovery? How soon will I have a bowel movement?
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I've had uc from the age of 16, i'm now 52. my life consisted of meds, pain and lots of hospital stays until 3 years ago when i had my stoma fitted. since then i've been able to get on with my life pain and meds free so imagine my shock at my last checkup to be told i need another op....
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I had a 8 day course of these antibiotics and after taking them I have felt 100% worse. I feel weak, muscle pains all over my body, no appetite, back pains, my anxiety has gone really high I have headaches and not able to do day to day things. I'm scared that this isn't going to pass. I have been off the antibiotics nearly 3 weeks and these symptoms are not getting any better. Can anyone help me and tell me when this will pass or start getting better?
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When in bed at night I struggle to turn over or move as I feel so stiff and sore. Once out of bed and moving I am much better. I initially find it hard to become upright after sitting for any length of time. About 2 years ago my daughter noticed my right calf was much smaller than my left one. I cannot raise my self onto my toes on my right leg due to loss of muscle/strength in the affected leg.
I have had blood tests, nerve stimulation tests and a muscle biopsy. My CK level from my blood tests was slightly raised, my nerve study tests were abnormal and my biopsy only showed minimal change.
I now cannot raise my arms above shoulder level to the front and if I walk at a quicker pace my lower back feels like I have no support and I get pain around my lumbar region.
I go spinning 4/5 times a week and cope with this very well. It's as though once I'm warmed up my stiffness diminishes. I am 51 and have only one period every 3/4 months , I have been to the dr's re the menopause but have been told all my blood tests are normal.
i have been referred to a neurosurgeon and neurologist with ? A form of muscular dystrophy but now my muscle biopsy result has not shown the expected result.
i struggle going up and down stairs often. I feel so fed up with my inability to do what I want to do as I have always been an active person. I have put weight on and cannot motivate myself to control my diet.
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Although I try to be as active as possible my muscles are making life for me difficult, as for years they have been wasting, causing pain and tiredness. All other symptoms point to Fibromyalgia, which I believe doesn't cause muscle wasting.....also have Osteoarthritis. My muscle problems started in my mid. 30s.....am now 63 and is much worse. Recent blood tests show normal muscles values....but something must be wrong as my energy level is very low. Has anyone been /going through the same??
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Have a bag fitted after history of DV and UC in sigmoid long story short and much doctors scratching their heads, the op was 5 weeks ago and seeing the follow up tomorrow with the surgeon.
Ok with the bag but had a fistula fitted for mucus and still having the nurse around each day to change the dressing. A bit from the back end also but not much. Has anyone had a similar thing and how long it should take? Is this time normal as the surgeon at the time said it would be around two weeks.
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Colostomy bag keeps coming off because stoma keeps recessing and fecal keeps building up under the sticky pad. What to do?
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Anyone out there had a colostomy for faecal incontinence. Anyone got a colostomy done recently and how are you coping.
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I am in a new relationship with someone who has had Hidradenitis Suppurativa for the past 10 years. Due to the severity of this condition in the past , he was fitted over a year ago with a colostomy bag, the doctor suggest this is a perm bag? if this condition is controlled can this be reversed? ( he is only 27)we no this condition is very hard to control, he has just started a new antibiotic and believes it is starting to work, he also has chemo once a month to try and put this into remission...
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I often find I am changing up to 8 times a day not because the bag is full but because my skin sweating causes the adhesive to break down and the leaks begin. This is worse in hot countries and when travelling as I will need to change to make sure I have an empty bag before queuing up for aircraft etc. I also need to change before driving any distance as the seat belt position can cause leaks. Is there anyone out there with a similar problem
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Has anyone had a colostomy bag fitted through having severe IBS-D?
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My grandmother just had a big surgery through which she had removed her ovaries, uterus and part of her gross intestine. Part of her surgery was colostomy.
I know that she now needs a low-fiber diet but I am not sure what can she eat and what not!
What are the worst regular foods for the right now?
What are the good foods?
What kind of tea should she drink?
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I had total colectomy and ileostomy five weeks ago and even though I do have some help from my ostomy nurse, I’m now left alone to take care of my stoma bag and I immediately ran into one simple question – how often should I change the wafer? I’ve been changing the bag every three days and when I changed it last time I noticed skin underneath the wafer is reddish, so I’m wondering if I’m changing the wafer too rarely, or am I doing something else wrong? I do first put the protective powder, then the wafer then the pouch, but like I said, the skin underneath the wafer is red and maybe I’m supposed to change it more often?
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Has anyone got a colostomy or recently had the op. It is possible this is what i will need in the near future and i am terrified as i swim three times a week at a class. Have fecal incontinence which is making me more and more housebound.
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Had colostomy surgery, etc * see above *
Is it normal to develop I.B.S. after these kinds of surgery. It have been going on for around 4 years now.
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Has anyone had a reversal?
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I had my tube tied a little over 6 years ago and now my husband and I would like to have another child but without a reversal what can we do
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I wanted to know if anyone here had a vasectomy reversal. If so, what was your experience like? I am thinking of getting a reversal. I got a vasectomy as a young man and today regret it deeply.
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