Hemorrhoids :: Still Pain - 5 Days Post HALO (Haemorrhoidal Artery Ligation Operation)
Jan 3, 2016
had the above operation done 5 days ago,i would be very grateful if anyone who has had the same operation would be able to advise me as how long the pain and discomfort will last as i am getting like a contraction type pain in my anas area and when braking wind it is very painful.Going to the toilet for a poo is not normal as i was a one a day person.I Am hoping this will all settle down with time.
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I had op 17 days ago and feel today like I can finally see the light! After suffering the agony, bleeding (continually wearing san towels) and life changing effects they bring you i finally decided to have the op. I have had a terrible 17 days 2 visits to docs and 2 to hospital. part of the prob was caused by managing pain relief, allergic to anti-inflammatories, Tramadol gave me a panic attack and made me vomit, been on 60mg codeine 4 X per day and have been more or less sleeping in the bath. Saw surgeon day 15 who told me the op had worked and delay in recovery was because i couldn't take anti-inflam. He offered me morphine for the terrible pain which I declined. Had 6 hours sleep longest since op (only been cat napping due to pain) so cut down on codeine all positive today. Then I went the loo and felt a lump come out like my old piles (only 1 use to have quite a few), now stressing that I have had a prolapse. The surgeon warned me I would have flaps of skin left but this feels more hard and shiny sorry to be graphic!! Just wondered if anyone else had experienced this and whether it would go down again, I have never been able to push them up as some people mention.
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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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I just was wondering who has suffered the same and it's actually got better!? I suffer no pain ok maybe a slight ache if my testicle is squeezed/squashed but it's very hard to touch, I'm 10 days in post op and it's pretty much been ok had swelling that's gone down, I'm just concerned about the hardness of my testicle and the cause!? I'm seeing my GP in the morning and gonna book an ultrasound to check over my jewels.
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I have just had 3 hemorrhoids worked on by THD surgery. This was done Thursday (and Saturday). I am on 2 sachets a day of movicol to soften stools but have not passed anything yet. I am eating fruit and little bit of other stuff such as digestive biscuits a little bit of bread etc. is there anything else I can do to help? When is pushing straining? I tried to go earlier and worryingly passed a jelly like lump of something?
The pain is manageable with occasional paracetamol or ibuprofen.
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I had my THD op 12 days ago. The usual pain and discomfort but no blood until today. Today however I went to the loo and passed enough to make the pan red without straining too much. 4 hours later I passed more with a lump of non poo material in it. Would this be a tied off roid? Bleeding stopped very quickly and no pain. Any ideas?
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I'm a 25 y.o male and have been suffering with stage 2-3 hemorrhoids for two years following a long term stomach infection. For many months local GP's telling me nothing was wrong and to leave it alone. It was only after kicking up a huge fuss did they finally refer me to a surgeon who confirmed I had 3 malteaser sized hems in my rectum. They were treated by banding twice in the course of 4 months to no avail, and eventually I was offered HALO in April this year.
The HALO helped stop bleeding and reduced swelling/pain, but not enough that it no longer affects my life. And the itching - OH MY GOD THE ITCHING!! Also since the procedure I have been experiencing pinching of the nerves which cause sharp stabbing pains. About 90% of the symptoms are coming from the larger of the 3 hems on one side.
I had a follow up with the surgeon last month to discuss surgical removal as the constant itching and pain are still unbearable, but he has refused ANY further treatment on the grounds that it's too soon after my last op and also that it may cause further nerve damage.
While I trust that he is giving me his best advice, I cannot continue to live like this and was thinking about booking further treatment privately. I'm afraid to have a hemorrhoidectomy especially after what he's said, but I was considering going back to less invasive treatments such as banding or sclerotherapy now that the hemorrhoids are smaller.
I would be very grateful for any advice or personal experience you guys could pass on to me as I don't know what to do, I just know I can't "learn to live with it" as the doctors keep telling me.
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In May 2015 I suffered a small heart attack according to my consultant, it was a bank holiday, i was told that there was no consultant until the following week
Over the weekend I was monitored and on the Tuesday went down to laboratory to investigate the causes. They found that the LAD was 90 % blocked and the RCA and LMS were moderate , 3 stents were fitted and I was given medication to control the Colestral , the cardiologist told me I have a good heart and to push every thing to the back of my mind and don't let it control me
I found as time went by month on month that I was still
Getting niggles and angina pain , the angina pain I found difficult and still do find in hard to differentiate , I may now understand as I was taking far to much GTN X 6 instead of one per year. I find I can walk for
Miles and go to the gym with no issues , but what s confusing me when i have been decorating over 3 months period bending low and reaching high to paint gives me angina pain and it's harder to breath , then my heart rate drops from average of 62 to 43 .
9 months on and I've been back in twice with false alarms getting pain
Last month 26/2 was getting checked out for AF as I had a erratic heartbeat, they were concerned and explained the how the Atrial chamber when pulsing transfer the blood to ventricles and if my heart is missing beats the worry is its retaining blood and this may clot and lead to strokes . However after the investigation they did no do
Anything but gave me two options I was quite shocked 1 CABG or try another stent
I've been out of work now for a 3 months as work on contracts so really need to be back in work, however I gave my wishes to try another stent as the LAD is starting to Narrow before the point of insertion , previously I was informed arteries take a life time to get blocked how can this happen in 9 months with careful food planning and medication being taken, since the blast hospital
Visit I have changed medication on atorvastatin to simvastatin. There was no mention when I came out of theatre about my erratic heartbeat but found it was slightly worse than before the procedure ....
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I had a haemorrhoidectomy about 4 years ago with a very painful recovery and problem now back so going for the Halo/THD procedure very soon.
Has anyone had this done and how was the recovery from it?
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Has this happened to anyone else. I had my op 18 months ago and they have returned with a vengeance !!
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I had a halo procedure for piles 5 weeks ago and treatment for a prolapsed pile how long does the bleeding last with bowel movement I'm still having discharge and spot bleeding afterwards
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I am a 49-year old male and had stage 3 piles for about 5 years. They never really caused me any pain or suffering per se but were an inconvenience. I had been to my GP ages ago to make sure it wasn't anything serious. Towards the end of 2009 I decided to see what options I might have for sorting them out as I figured I wouldn't want them to get worse and despite being fit and healthy and eating well, they had not gone away of my own accord.
I went to my GP and she did a digital exam and said they were very small - didn't seem like it to me - she said she could refer me if I wanted but I declined. A few weeks later I figured I was copping out and returned to get a referral. I went to see a consultant locally who got me to come back for banding. This was very easy and though it was a bit uncomfortable I was optimistic that it would sort it all out. It didn't - even though it seemed like it would work it in fact made no difference whatsoever. I returned to him and he said he would try the sclerotherapy and another banding as they were quite big and the portable banding machine wasn't up to it. Again nothing really changed.
I read all these forums and was in two minds like so many others whether to pursue it any more. After all I was not in pain per se and clearly some people have really awful experiences, sometimes made worse by the treatment - I knew I certainly didn't want anything slicing off! I read up what I could about HALO but it seemed to be mainly sales pitch. I decided to see the consultant again and ask him about it. He said he didn't know anything about it but his next step would be banding under GA and he was confident that would do it.
For one reason or another I wasn't convinced and so I called the HALO people and found out where there was locally that did it. They also told me how much it would cost privately (?3k+) but that with a referral I could probably get it on the NHS. A few weeks later I had a session with a consultant who explained the whole thing - also diagnosing a polyp as well as piles - which would never have responded to banding so I was glad to have taken the 2nd opinion. Anyway he put me on the waiting list for a polyp excision and possible HALO.
Time came around in about 6 weeks and I went into hospital for the first time in my life to have day surgery. I was apprehensive but quite positive. The whole experience was very reassuring - the staff were great and I felt very cared for and the surgeon was friendly and explained things. I signed on the dotted line, had my pre-med and felt the curtains close
Woke up feeling fine about 30 mins later. The surgeon explained to my surprise and a bit of shock that they had had to cut a large pile off so I might have a longer recovery time than expected (he had said at least 2 weeks for HALO and up to 10 for pilectomy). That concerned me a bit, especially when the nurse brought my meds to take home - 3 types of opioid painkiller, 2 types of laxative and some antibiotics. I got the impression they were trying to tell me something. I stayed about 2 hours to satisfy them I'd had a wee, eaten and drunk some fluids etc and got my wife to pick me up.
Felt pretty OK generally even with after effects of the GA - ate and drank lightly and feared the first pooh which came 2 days after the op. Uncomfortable certainly but not especially painful. The absolute best thing after each BM was a nice warm shower spray for a few minutes which really soothed the bruised feeling. This got better over the next 7 to 10 days. I work from home so was fortunate that I didn't need to take time off per se after the first day getting my head clearer but I wouldn't have wanted to have to commute or be away from home.
There were some bad bits but not what I would have expected. The worst bit by far, and it was _horrible_ was the antibiotic (metronidazole)- I had to take it for 5 days and didn't realise what a nasty drug it is (check it out on ****)- around day 3 I was finding alternate nights of complete insomnia, nausea, sweating and a really depressing state of mind feeling like I would never get better. I googled all the meds and realised it was the AB and that these were fairly common side-effects. If I had had a longer run of them I would have asked to change but I figured I would see them out. It was awful and I did have another day off cos I just felt so damn bad from them. My advice here - don't just take what is given to you and not check it out - be aware of what has been prescribed (in fairness they did say that some of the meds could give nausea, constipation etc but I didn't expect this one to be so heavy).
The other downside was the laxative - I should have had clearer instructions. You definitely want to make sure you have soft stools etc and are acutely aware that what you eat has to come out the other end - soups, bran flakes, porridge etc are great for this. However if you just take teh laxatives as prescribed - and you are not already constipated (I am always regular)- then they will just play havoc and have you very windy (which also seems to come from the GA gases) and farting all the time with a sore anus is quite painful/uncomfortable in itself (esp if you're not too sure what might be coming down the pipes!) It kept me awake a bit.
What I should have thought with the meds from the start is - take them /if/ needed (except see below)
So I had been prescribed metronidazole as mentioned - I took that for the 5 days. I had 3 painkillers - Tramadol which I didn't bother taking, Co Dydramol, I took a couple but then didn't bother (and my wife used them all up on migraines!) and Diclofenac - this last one I should have taken all the time but didn't. It is an anti-inflammatory and because I didn't bother with it I think I put myself back a couple days with a very sore and inflamed bottom - so this one I would say take as a matter of course (and I didn't have any side effects). For laxatives I had lactulose syrup and ispagel husks - both are palatable enough but as above I realised after a coupe of days that I probably didn't need them.
All told I was not incapacitated at all. It took a good week to not be too worried about the next BM. After that it just was a process of it getting better every day. The main thing was that the prolapsing piles/polyp were gone and that was a great relief. Had a check up last week and I would say I now feel 100% down there and no concerns at all.
I am very pleased I went ahead with it - I had overcome embarrassment about it ages ago and plain speaking is all that is needed - my reticence had been around being "operated" on but that all went very smoothly. I know there are some horror stories on here where people say that the op is worse than the piles but I am sure that complications are in the minority and I would not hesitate in recommending anyone suffering and holding back, check out a good consultant and have it all sorted out. I was glad I had it sorted out when I was fit and in good shape - I think that plays a big part in making the op run smoothly and the caring for oneself that much easier. If was old, infirm or very overweight I think it would be harder. Weight wise I had lost nearly 3 stone over the last 18 months and again I think that helped keep recuperation short.
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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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Anybody else had severe pain in wrist and new bruising 11 days post op. no issues with movement of hand or scar. Just this horrible pain when i put any pressure on my wrist.
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I had a haemorrhoidectomy and a staple procedure along with a fisher repaired and I'm now on week 5 and not feeling good
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My husband was referred to a specialist to undergo ligation for internal hemorrhoids using the CRH O'Regan System. They told him they will need to rule out colon cancer before the ligation procedure. He is 39 and has dealt with hemorrhoids since his 20s, no familial history of colon cancer, no anemia or other red flags that he is at risk for cancer. I am more concerned about the colonoscopy than the ligation. Do all physicians require that testing?
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After having sporadic bright red blood in my poop last year, I went to the doctor in late Oct/early Nov. They took a look inside, saw I had a hemorrhoid. I took some vasculera for a couple weeks, started taking fiber daily, drinking water, etc. But every 2-3 months since, the bleeding returns (usually after I've had a stretch where I went 24+ hours without pooping). There is the occasional mild burning back there, but nothing severe. At what point is the rubber band ligation recommended?
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All of you who have suffered from post tubal ligation syndrome and have had a tubal reversal : Have the side effects of the tubal ligation gone?
I have suffered from post tubal ligation syndrome for many years and I am thinking to have a reversal, but I want to know if it really helps.
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I had my third baby 2/15/11 and my bilateral tubal ligation 2/16/11. No complications after the laparoscopic surgery. Breastfed and formula fed together from the beginning, pumping from about 4 weeks to 6 weeks until I went back to work and supply diminished. Bled after birth until 5 weeks, when I had my post natal appointment. Started first period after that around 3 weeks later (baby was 8 weeks). It was 'normal' for me - lasted about 6 days, had cramps before and the first 2 days. All normal for me. I know my normal cycle because I had not been on BC for about 8-9 months before becoming pregnant and was very regular until the month before I got pregnant. So anyway, had my second period beginning may 6 and lasting til may 11. Again, all very normal for me. My husband and I had regular intercourse probably about every other day during the time I was not bleeding, with only the tubal ligation as birth control. 17 days after I stopped my second period, on may 23, I began spotting. It was very light, and I thought it was sex-related. It varied from brownish to light red to slight pinkish. The next day the same. The third day I needed a tampon, but only a light one. After that for a few days I bled more heavily, but not as heavy as the start of a normal period -- about how I normally would towards the second 1/2 of my regular periods. On most days during this I would go several hours with no bleeding and think it was all over. I went all last night with only a pantyliner which was ahem,not needed by the time I woke up this morning. However, I got to work and around 9am it started, very very light again. This is day 11.
Any ideas? Please no hijacking here, I am looking for some help.
I've called my GYN and left a msg for the MA or nurse to call me about it but that was yesterday morning and I've not yet heard back. . .
To mention, this long 11 days has had NO cramping whatsoever.
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Yesterday I had rubber band ligation and all went well but as at 3am I went to the bathroom and after test that I am in pain and uncomfortable and taken 600 and ibuprofen and still the same and I feel I still have the muscle outside ! What can I do, .
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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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