Hemorrhoids (stage 3) :: Does Hemorrhoidectomy Worth It?
Sep 19, 2013
Hi! I'm going to preface this post with some background information: I'm 19 and I've been suffering with constipation for my entire life (my parents have videos of me straining to have a BM when I was still in pampers). It wasn't until last year that I was diagnosed with constipation by delayed colonic transit and put on Miralax to help move my BM's.
Unfortunately, because this diagnosis came so late, I've been straining to have BM's for the past 19 years, changes in lifestyle (diet, exercise, fiber supplement, etc.) all for naught. This straining led to hemorrhoids, which brings me to this forum. I've been dealing with hemorrhoids since elementary school, and when I have a flare up, I'm practically debilitated from the pain– my last flare-up kept me awake for 3 days straight and gave me multiple migraines. The flare-ups happen once every few months, but can last up to a week.
I wanted to know if anyone on here has had a hemorrhoidectomy, and what their experience with the procedure was like. I'm figuring that my hemorrhoids are AT LEAST a stage 3, and the surgery looks like the most permanent option. Also, if anyone has constipation by delayed colonic transit and as a result have developed hemorrhoids: how have you dealt with it? What has worked for you?
I see a lot of the post-op for a hemorrhoidectomy has to do with the intake of fiber, but too much fiber can actually make me MORE constipated. :(
Any thoughts, opinions, or personal experiences would be a LIFESAVER. Thanks for listening to my rambles!
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41 year old male. Had piles on and off since I was 15 (damn exam stress). Last year things got worse, explosive toilet sessions, blood everywhere... Decided to go see my GP, it was a new doctor, heard my symptoms and immediately referred me to a hospital. A few months later, saw the conflating (nice chap) and advised to go for the chop.
was due to have a pre-op on 22nd Feb but they had a cancellation so moved my procedure to 11th!
is there anything I can do to prepare myself in the remaining few days?
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I am 34 yrs old, and have grade 3 prolapsed hemorrhoids. I am having my op on wed, I have heard the recovery is long and painful, I have 3 children my youngest being 2, and thought after a couple of weeks I would be ok!
I need to know everything pls, as my husband works full time, how long is it b4 I will be able to do things, school run etc?
I also have a pacemaker which has to be turned off or set differently, i'm not sure as I haven't really been told much. when I went for my pre op yesterday I had a list of a questions that the nurse cud not answer, and told me to ask the surgeon on the morning of my op. I would like to know b4 I even go into hospital.
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I had a hemorrhoidectomy on 3/12 and I just had my follow up appointment. My doctor didn't even look to see if I was healing properly. He asked about pain and discomfort then offered to write another prescription to get me through even though I told him I stop taking the prescribed pain pills and moved to over the counter Tylenol after a BM. Let me rewind, this was my first case of external hemorrhoids which occurred during a LUPUS flare. On top of me having LUPUS, my first case of hemorrhoids were thrombus. Anyway back to the concern at hand. I still see what appears to me as two hemorrhoids, one red, and constantly bleeding and the other itching like crazy. I'm not sure what I can do for the discomfort due to one of the hemorrhoids appearing to be open, I'm afraid to put any type of medication on them due to the fear of pain returning. This surgery was my first surgery, I've never had kids, so the pain I experience during these last three weeks had me on the verge go asking God to take me now. I'm not sure if I should be concerned and schedule another appointment with the doctor and request him to take a look or if this is the normal healing process.
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I am two weeks post surgery and I have a lump where the surgery site was and the stitches. This was external hemorrhoid surgery. I would like to know if this is common and how long does it take to go away? ?
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I had my op 2 days ago and at first I thought that the pain was bearable,what I didn't know was that it hadn't even begun!
I have suffered with painful piles for many many years, I had them injected which eased them for a while the doctor at the hospital told me it was necessary for me to have surgery.
I prepared myself as best as I could by getting healthy. I ate a healthy diet and walked for an hour a day as well as working a 40 hour week.
But nothing prepares you for this. I have been in terrible pain all night, I passed my first motion in the early hours and the pain was so severe I was sick everywhere at the same time, which put a further strain on my bum. The pain since has been so intense that I don't know what to do with myself. I laid in the bath for half an hour which gave some relief but once out the pain was back.
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I had a Hemorrhoidectomy in October of 2012 and I did have some complications with it. It is now 3 years later and things have gotten a little worse. Over time I have developed some internal scar tissue at the site of the wound (this was confirmed today by a Colorectal Surgeon) which has resulted in me having a hard time defecating and constant constipation. The outside of my anal opening is a little irritated as well and he gave me a topical cream for it. However, he told me not to worry about the scar tissue....that I wouldn't have never known it was there until he told me. However, I knew something was wrong because of the narrow stools. So I'm not trying to determine if their are any OTC creams i can use internally to smooth out or get rid of the scar tissue. I remember reading somewhere awhile back about non surgical treatments for scar tissue due to Hemorrhoidectomy surgery but I can't remember where.
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I'm curious about others who have had this experience after the procedure. Mine seems to be getting worse everyday. I'm on day 9 post surgery. I've had a very difficult time going to the restroom when on the toilet, generally I just sit there for a couple of minutes hoping for something (I'm afraid to strain so I don't push at all). It seems to only happen when I'm not on the toilet, and it has been happening almost every hour at this point.
And I'm barely eating, I've lost 20 pounds over these 9 days (I'm a big man, but not obese). What I have eaten has been strictly fiber rich foods. And I'm also taking fiber, along with lortabs for the pain and milk of magnesia at night to counteract the pain killers.
There is no warning though, I simply lose control of my bowels and can't stop it until it wants to stop. If anyone else has experienced this please reply to this. I'd like to know when it stopped. I desperately want to get out of my house but cannot until this ends.
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I'd like to post my experience with these awful, awful hemorrhoids. Let me give you all some background first....so I have a habit of bringing my phone in the bathroom and reading articles, checking emails, social networks, whether, bank accounts, credit cards, bills, but the point is my BMs generally took a few minutes but sat on the toilet far too long, anywhere from 15-30 minutes and maybe longer. I saw having BMs as a perfect break point in my super busy life to get updates on emails and such. DO NOT DO THAT, please God do not make the same mistake as me.
So this behavior has been going on for quite some time and a week or so ago is when it all went downhill. Now I always shower after BMs if I'm home, so I started noticing these bulges in my anal area during my showers. They just went away and they didn't really hurt or anything and my initial thought was, "huh...hmmm that's weird". But other than that, I totally ignored it.
I didn't even really know what hemorrhoids were. So then one Friday night a few days ago I had a BM. Hopped in the shower (as I was home) and noticed another bulge in my anus and initially I was like, "huh, what is this weird thing". Towards the end of the shower I noticed that this time it didn't go away. At this point all I was thinking was, what the f***....so I began googling and soon educated myself on hemorrhoids and made the self diagnosis that I now had a thrombosed hemorrhoid. I immediately called my family doc and Monday afternoon I had it checked out. He confirmed my self diagnosis and referred me to a specialist whose literal job is to look at hemorrhoids. By the way, that weekend while waiting for my appointment was awfully painful, I had a hard time playing with my dog, making love and BMs were the absolute worst. Anyway, my family doc said that the specialist would probably make an incision, drain the dreadful roid and then I'd be fine....WRONG.
So I called the specialist (over 25 years of hemorrhoid experience) and scheduled an appointment later the same day (Monday). I went in optimistic, however, after the specialist checked it he said, "Chris, this is a pretty big thrombosed hemorrhoid, and I'm going to have to remove it. You also have a rather large internal hemorrhoid that needs to be removed as well, I can't just drain it at this level". By the way, it was about the size of a decent grape tomato. So surgery was scheduled for the next day (Tuesday) , a hemorrhoidectomy.
This being my first surgery ever, I was scared out of my mind. I watched the medical procedure on some college website which only worsened my anxiety (please don't do that). The surgery went well and I felt perfectly fine in the recovery room (the drugs hadn't worn off yet). However, the pain started to present itself after a few hours being at home. I tried to have a BM that night but nothing but blood came out, no pain though. After my BM attempt I made a warm bath and sat in it for maybe 30 mins, which really relieved the pain. So this brings me to today, this morning (Wednesday).
I'm currently sitting in another warm bath and the pain is minimal in the water. I have a difficult time walking around as I can't stand up straight. So far the pain has been tolerable and overall not as awful as some other posts suggest. I still haven't had a BM since the surgery about 14 hours ago. Honestly, I'm terrified too. I'll try to keep updating this with comments as I progress through recovery.
I have the idea that when I attempt to have my first BM, it will be in a warm sitz bath. I'll clean it out then hop in the tub, as I heard having a BM in the water is much less painful, gross but I think it will be effective and absolutely worth it. Just remember to stay as clean as possible. This is my first forum post ever so bare with me as I attempt to update. Thanks for reading and wish me luck.
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I had my hemorrhoidectomy and they also removed my right ovary in the same operation on 30 March 2016.
It is now 3 April 2016 so it has been 4 days since my op. I had no pain the first 2 days and then the local anesthetic wore off!
Now it is excruciatingly painful. I have found that bathing in a little lukewarm water with 2 hands of salt for 15 minutes help a lot.
And for constipation you can go to your local pharmacy and buy an enima ask them for one that you can drink!
Trust me it is much better than to put a tube up your sore bum!!! The doctor can also prescribe a numbing ointment that helps a lot!!
Goodluck to all my buds out there!!! I know how it feels!!!
One question i have is it normal to still have the swollen loose skin on the outside of your anus?
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Three months post stapled hemorrhoidectomy. Still experiencing terrible pain throughout rectum and butt cheeks. Feels like someone crushed glass, poured alcohol on it, then smeared it inside me. Symptoms indicate prolapse as well, but surgeon has examined multiple times and says that is not the problem. No hemorrhoids present and surgery has healed normally. He does not know what to do though. I did have similar pain for many years before the surgery, but more like sand paper was rubbing against my skin and rectum and only half as painful. Anyone else with this experience?
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I'Ve had hemorrhoids my whole life, i'm 35 and overweight and not active. I sit for hours on the toilet and usually only eat meat. I have fast tracked surgery and am now terrified to get it done. My piles have since become a normal part of my life, but every once in awhile ill have flare ups when i eat something i KNOW my bowels don't like, like pork fat or beef fat or if foods were cooked or defrosted improperly, like rotting meat etc. AFter every flarup i usually go through what i ate and i can pinpoint what it is by buying what it is and trying to only eat that product for the day to see how my bowels react. My question is that should I get this surgery done to remove my internal and external piles? I have heard that people lose the ability to control it and my own parents have both had hemorrhoidectomies, and my father has had leakage ever since that surgery. Needless to say hemorrhoids run in my family. I want to be able to eat whatever foods and enjoy my life. I hate having to live in fear of food and how it totally screws my life up for work and play. I just want to live a normal life like all the normal people who eat whatever they want and don't get hemorrhoids. I realise that even when I get the surgery I still cannot eat anything that will cause my bowels to flare up because it will just cause more "new" hemorrhoids to flare up? Proper diet, exercise etc will make sure that I never get them again, but should I get the surgery done? I have had rubber banding done and I had a real bad flareup after it so I booked surgery instead of spending a year of rubber banding my anus. My uncle told my mom that he had the rubber banding done and still had to have surgery because they can come back after the rubber banding! My doctor said that it could take more than 1 surgery to remove them all and I'm terrified at having to have one surgery let alone 2? I'm at a place right now in my life where I can cope and live with it, and live with the flare ups, but i keep wondering that if there is hope i can live a normal life without hemorrhoids, should i take that chance? Please I need help from fellow sufferers of this affliction, or medical professionals. I tried to talk to my surgeon and he wants to continue rubberbanding and then discuss surgery. I then went to see him again to talk about surgery and that I had heard that they can come back even after banding and that I want them removed and never to come back again, and he then said that he can do the surgery and scheduled my hemoroidectomy in 2 weeks. Should i just continue with RBL(rubber band ligation) although painful flareups for two weeks happen afterwards? Should I just keep my surgery appointment and get them cutout and then deal with whatever consequences? Im scared reading about people getting fistula's or puss and bleeding and other complications from surgery which turn their lives into a living hell. living with hemoroids seems much better than having your *** swell up so huge and be constantly painful and having to have more surgeries or procedures to cut and drain the puss from absess's or fistula's that are a result of surgery.
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Just want to inform people of my experience taking the Cerazette pill.
I had happily been taking the Microgynon for a few years when I forgot to get my prescription one month and ended up not going back on it. I went to the doctor as I felt so much better for coming off the Microgynon, I had lost weight and just felt happier within myself.
I saw the doctor and spoke about all my options, I am dead set against the implant and the injection, I thought I'd prefer to go on a pill again.. I was prescribed the Cerazette and thought nothing more about it.
I went to see the doctor about an on-going knee complaint, a few days prior to my appointment I noticed I had a lump to my left shin, I showed the nurse the lump, she reassured me it was nothing and it would go away. I wasn't 100% convinced.
Around two weeks later, my knee still being sore, the lump had only got bigger and I now had a swollen ankle, I went back to see a doctor, I saw a locum doctor who was concerned about the lump on my leg and queried "?osteosarcoma". I asked the doctor at the time if my swollen ankle could have been caused by the pill but she said no, it would be "lateral". The next day I went for an urgent x ray on my shin, the lump was painful. I waited four days for my results and went back to the doctor, this time I saw a different Locum doctor- My results showed no signs of a sarcoma, that day I was sent for blood tests and an urgent ultrasound was requested.. In the meantime, I found a second lump on my other leg, just under my knee, it was also painful. Five days later, my blood results came back and I was hopeful to get answers about my ankle. Blood tests were fine, not even my inflammatory pointers were up, the doctor was pleased but also confused as to what it could be. I was told I would referred to a specialist consultant and I was still awaiting an appointment for my "urgent" ultrasound.. Three weeks later and I have only just had said ultrasound. The radiographer said he was confident that I do not have cancer, which is brilliant news. I may still be referred to a specialist as they are still unsure as to what is wrong with my ankle, however, my mum has been doing lots of research and considering I am only 21 and on no other current medication other than the Cerazette, we could not think of anything else that may be causing these problems. On Thursday, I took it upon myself to stop taking the Cerazette, it is now Tuesday and my ankle has gone down considerably, the lumps on my legs have also reduced.
It has really made me think, putting all these hormones in our bodies is not good ladies and you really should be careful with what you are taking. I know plenty of girls that take these pills and have no problems what so ever, but there are plenty of other girls, like myself, that have had bad experiences with them and it is really really scary.
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I'm a 25 year old female who has recently moved to Singapore with her partner.
I began attending a specialist in Glasgow in 2010 after minor palpitations that would always disappear on their own or with a forced cough. The longest lasted 10 minutes. They never caused me too much concern and after lots of tests and ECG monitors, which returned nothing, I put it at the back of my mind. My Dr. suggested it was a minor AV Node SVT and that we would just monitor it over time.
Last Sunday morning I woke out of my sleep at 0630 with a severe attack. Nothing would stop it at home. After 15 minutes I made my way to the nearest A&E where I was injected with Adenosine (not pleasent) and was kept under observation for the rest of the day before being sent home being doing that I had SVT. I had no caffeine or alcohol that night and made sure that I rested well.
The following morning I was woke out of my sleep at 0530 (an hour apart - strange) with another severe attack and followed the same process at A&E. Again, I was kept in for observation for the rest of the day before being sent home with Verapamil, to be taken as and when required.
The following day I was tired, extremely anxious and now afraid to be on my own or fall asleep but I had no palpitations. I followed my no caffeine and no alcohol diet hoping for the best but by Wednesday evening, after leaning over, another attack presented itself.
I have an appointment with a specialist here in Singapore on the Thursday the 22nd and it can't come quick enough, this whole thing has flipped my world and has put everything on hold. Even with a supportive partner, not having my family here has been an upsetting experience. My Dr. in the UK has suggested that I have RFA done to cure the condition once and for all. I'm terrified of the risks but don't want to have to take medication for the rest of my life either. My other problem is, do I get RFA done here or back in the UK when i'm home on leave in July? Should I wait or could I be making my condition worse?
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I am crying with pain as I write this had an mri yesterday which revealed prolapsed L3 ,4 and 5 . wet myself and the other as had no feeling in that area , they wanted to do surgery but I discharged myself to be reviewed in 6 weeks , I have a very physical job , I ride and compete horses , is the surgery worth it ?
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I have been taking Amiodarone for 2 months now for cardioversion as I have AF. I have been told that it is unlikely to be successful but that I might as well give it a go. So far I have had no problems at all - I take 200mg daily. I will be on it for a maximum of 4 months so my specialist says that I am unlikely to run into problems which he says are usually connected with much longer term use. My message to others is - please don't be afraid of this medicine - it's at least worth a go in the short term to see if you can tolerate it. The chance of getting rid of AF is just too important not to take it. As I say, so far, I am lucky in being able to tolerate it amongst at least 8 other meds which I take. I was very afraid to start with but now I just see it as "another pill to take".
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I have just been diagnosed with CKD stage 3 (GFR 48) and I can't understand why. I have low blood pressure and don't have diabetes. I am slim fit and healthy and age 52 so not that old. I also have a low white blood count. Can anyone shed some light? My GP does not seem worried, and so nor should I be, but I feel uncomfortable not knowing what has caused this.
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How can I improve my Stage 3 kidney disease, having a G.F.R. of 34?
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I'm 10 weeks pregnant with our first child and I think I've hit the emotional eat everything stage. I can't stop eating I'm like the hungry caterpillar or something, but my husband's in Arizona for work and I'm in Virginia and I just wanted to talk to him so I hop on FB and I see he shared a video about 40 minutes ago so I send him a simple hello message and no response. It just makes me feel like hey pregnant wife should be the first thing you talk to when you get off work considering I'm your wife and pregnant with our baby. I went from so mad that I wanted to punch something to crying am I wrong for feeling this way ?
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I am a 34 year old male who was diagnosed with hemochromatosis only after a liver biopsy because i only have one of the genetic markers. When diagnosed my ferritin was over 5000. Shortly after i was diagnosed with stage 4 cirrhosis of the liver. Is anyone out there in the same boat as me.
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I have recently been diagnosed with Parkinson's disease and am worried and confused. Are there exercises I should do? I am not on medicine but I understand that there are some that should be considered. Which ones are best for the early stage of the disease.
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