My Experience - 7 Weeks After Nhs Halo And Haemorrhoidectomy

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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 schlerotherapy 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 tteatment - 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 exision 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, espceially 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 thatsome 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 teh starts 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, Codrydamol, 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.

If, and I hope they don't, recur then I would happily go down the same route again. I hope this story helps others.

Mr Relieved of Surrey

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  • Posted

    Hello everyone!

    I haven't been on here for ages, you probably thought that I was better!! No such luck!! It's now 8 months

    since I had my op... And I am still having problems!!

    It seems my sphincter muscle was damaged in my first op, something my surgeon failed to inform me about

    until fairly recently. I still have to go to the hospital regularly, I can not manage without laxatives. Every now

    and again I try to come off them but everything goes into painful spasm and I get constipated.

    I wish to god I'd never ever had this op. I still have a BM 2-3 times a day and I have to leg it to the loo as

    quickly as I can, I still get sore and suffer a lot of pain. Nothing I eat makes any difference. I've tried every

    combination of food known to man.

    I am going abroad in July !!! How that will turn out, heaven only knows. I think the best thing for me to do is

    not eat at all. I am back at work now, I eat at 5.30 am, enough time to go to the loo, then I just drink during

    the day until I get home at 5pm. I can then eat and go to the loo without having to worry.

    It's not ideal but the thought of having a sphincterectomy and having to wear a colostomy bag for the rest of my life horrifies me... And apparently, that's my next option!!

    They don't tell you any of this when you sign up for the op do they??

    It's the most painful and horrific op and I urge anyone thinking of having it done to change their mind.

  • Posted

    Hi Shaz,

    So sorry to hear what's been happening with you, I really feel for you, I think you have been very unlucky and I think it's shocking that your surgeon has left you in the dark about your situation for such a long time. I think you have been treated unfairly by your medical team. Have you considered speaking to PALS? Your hospital should have a representative, usually in the lobby area. They may be able to get you some help.

    I really do think that most surgeries are very routine. I also think that the advice notes and comments from doctors do not really come close to explaining just how painful this op is. I have recovered, I am still worried about getting constipated and during my monthly cycle I have terrible pain (turns out I might have endometriosis, I have a fibroid and when I had my scan the lady said it's probably the same fibroid from when I had my thermal ablasion so it didn't get rid of it, great! sad I might have to have a hysterectomy.)

    Just remember you are not alone, always here to listen. Stay strong, stay positive, take each day as it comes and keep persevering. I will be praying for you x

  • Posted

    Sorry to hear about your pain people, especially Shaz, I'd say don't have the full sphincterectomy until you are completely sure that nothing else could help and there truly aren't any other oprions left Shaz. I'm convinced you haven't got much patience left after so long and so much pain, but please don't rush this unless you are absolutely sure nothing else and no more time could help.

    I'm almost 3 months after my operation, I'm still suffering but I hope it is just a very slow process of healing and nothing more serious.

    2 weeks ago I've had my post-operative review and the surgeon was surprised to see me still in pain. He performed a digital examination, that was extremely painful and he was so cold blooded, (I guess that's essential for any surgeon).

    He said that most likely the wound needs more time to heal and he prescribed glyceryl trinitrate 0.4 ointment to use for 6 weeks. This should help my sphincter relax and improve healing. Since using the cream I have fewer spasms and, I believe, a slight improvement overall. Well, I hope it is improvement and not just my wishful thinking. There is no way I could tell if this sense of improvement is due to the ointment or it is just natural healing that happens by itself, or just an illusion caused by my expectation of the cream to work.

    I still have bleeding after BM but only stains on tissue (on wiping) and I haven't seen it on the poo itself lately. I still have pain during BM but afterwards the pain has somewhat reduced, I believe/hope.

    I do struggle with keeping stools soft, as always in my life, and this is such a challenge at this times.

    I'm off the Movicol/Laxido because I've used it for over 2 months, it served me well but I'm concerned about using it long term, and the label says it shouldn't be used for longer than 2 weeks.

    I'm now back on lactulose, 30-40 ml a day... It is not as effective as Laxido, but I think it's a less scary option for long term use.

    If my situation doesn't improve significantly in a month time, I'll go back to the hospital to investigate further. Needless to say, I really hope I won't have to.

    That's all from me for now, best wishes to you all ladies and gents reading this, wishing you all a good recovery.

  • Posted

    I had a haemorrhoidectomy 5 days ago. It's been helpful to read about your experiences. Thank you for sharing them and I'm very sorry for your pain and stress, particularly those who have had long term complications. 

    I'm a 37 year old male, married and without children. I live in Australia, but this is the most active forum on this topic I've run across so hope you don't mind an Aussie pitching in.

    My procedure in hospital was ok. I was lucky in the sense that my surgeon is widely regarded as excellent and his bedside manner is outstanding. I had a lot of confidence in him going into the procedure.

    I must admit, I still felt a bit anxious though -- this was the first operation I have had so everything was pretty new to me and the implications of this kind of procedure going badly were not lost on me. Also every person I had talked to commented on how painful haemorrhoidectomy is.

    After admission early in the morning I had an enema, they took some blood and I was wheeled into theatre. I remember the first few moments and the oxygen mask going on. I then woke up in recovery. I had a catheter in, and I was not in too much pain that I can remember. 

    I was wheeled back to my room after < 1 hr. i tried to eat a bit for lunch, but threw up due to the medications. that evening the pain started to pick up, and the nurses started giving my paracetamol and oxycodone. that controlled the pain reasonably well. the surgeon checked in with me that evening and indicated that the procedure had gone well, but he had needed to remove a lot of prolapsed tissue and there had been an annal fissure to repair as well. 

    the first night in hospital was ok, but my catheter must have worked its way into a strange position and would not drain at all unless i was standing and would become quite uncomfortable. that made the first night interesting and not particularly restful. the pain would spike now and then, but was manageable with the medication.

    i had been taking movicol which had made my stomach quite uncomfortable and by day two i was thinking about my first bm. they removed the catheter and i walked around the ward a few times to try to help get things moving. that evening i had my first small bm. it was painful as advertised, but i had expected worse. i did not throw up, pass out, or scream, but i did sweat, pant and may have whimpered a bit. 

    having illustrated that i could poo, they released me from hospital on the morning of day 3. i was happy to go home with my little wifey, but i developed a deep hatred for speed bumps on the way.

    recovery at home has been ok. the pain is definitely still there, and particularly pronounced during and after bm's. because of the movicol i am pooing 3 times a day usually associated with bleeding and my stomach is unsettled most of the time. i try to anticipate and take strong pain killers before bm's and sit in the bath afterwards, which helps a bit. could be worse. 

    i have experienced a small amount of uncontrolled leakage between bm's and although it's been very minimal (and i think is improving?) this is my greatest stress because i know in a few cases it is a longer term issue after haemorrhoidectomy. 

    anyway, that is my experience so far. all the best to the rest of you and thanks again for sharing your experiences.

    bob 1="" hr.="" i="" tried="" to="" eat="" a="" bit="" for="" lunch,="" but="" threw="" up="" due="" to="" the="" medications.="" that="" evening="" the="" pain="" started="" to="" pick="" up,="" and="" the="" nurses="" started="" giving="" my="" paracetamol="" and="" oxycodone.="" that="" controlled="" the="" pain="" reasonably="" well.="" the="" surgeon="" checked="" in="" with="" me="" that="" evening="" and="" indicated="" that="" the="" procedure="" had="" gone="" well,="" but="" he="" had="" needed="" to="" remove="" a="" lot="" of="" prolapsed="" tissue="" and="" there="" had="" been="" an="" annal="" fissure="" to="" repair="" as="" well. ="" the="" first="" night="" in="" hospital="" was="" ok,="" but="" my="" catheter="" must="" have="" worked="" its="" way="" into="" a="" strange="" position="" and="" would="" not="" drain="" at="" all="" unless="" i="" was="" standing="" and="" would="" become="" quite="" uncomfortable.="" that="" made="" the="" first="" night="" interesting="" and="" not="" particularly="" restful.="" the="" pain="" would="" spike="" now="" and="" then,="" but="" was="" manageable="" with="" the="" medication.="" i="" had="" been="" taking="" movicol="" which="" had="" made="" my="" stomach="" quite="" uncomfortable="" and="" by="" day="" two="" i="" was="" thinking="" about="" my="" first="" bm.="" they="" removed="" the="" catheter="" and="" i="" walked="" around="" the="" ward="" a="" few="" times="" to="" try="" to="" help="" get="" things="" moving.="" that="" evening="" i="" had="" my="" first="" small="" bm.="" it="" was="" painful="" as="" advertised,="" but="" i="" had="" expected="" worse.="" i="" did="" not="" throw="" up,="" pass="" out,="" or="" scream,="" but="" i="" did="" sweat,="" pant="" and="" may="" have="" whimpered="" a="" bit. ="" having="" illustrated="" that="" i="" could="" poo,="" they="" released="" me="" from="" hospital="" on="" the="" morning="" of="" day="" 3.="" i="" was="" happy="" to="" go="" home="" with="" my="" little="" wifey,="" but="" i="" developed="" a="" deep="" hatred="" for="" speed="" bumps="" on="" the="" way.="" recovery="" at="" home="" has="" been="" ok.="" the="" pain="" is="" definitely="" still="" there,="" and="" particularly="" pronounced="" during="" and="" after="" bm's.="" because="" of="" the="" movicol="" i="" am="" pooing="" 3="" times="" a="" day="" usually="" associated="" with="" bleeding="" and="" my="" stomach="" is="" unsettled="" most="" of="" the="" time.="" i="" try="" to="" anticipate="" and="" take="" strong="" pain="" killers="" before="" bm's="" and="" sit="" in="" the="" bath="" afterwards,="" which="" helps="" a="" bit.="" could="" be="" worse. ="" i="" have="" experienced="" a="" small="" amount="" of="" uncontrolled="" leakage="" between="" bm's="" and="" although="" it's="" been="" very="" minimal="" (and="" i="" think="" is="" improving?)="" this="" is="" my="" greatest="" stress="" because="" i="" know="" in="" a="" few="" cases="" it="" is="" a="" longer="" term="" issue="" after="" haemorrhoidectomy. ="" anyway,="" that="" is="" my="" experience="" so="" far.="" all="" the="" best="" to="" the="" rest="" of="" you="" and="" thanks="" again="" for="" sharing="" your="" experiences.="">

    the first night in hospital was ok, but my catheter must have worked its way into a strange position and would not drain at all unless i was standing and would become quite uncomfortable. that made the first night interesting and not particularly restful. the pain would spike now and then, but was manageable with the medication.

    i had been taking movicol which had made my stomach quite uncomfortable and by day two i was thinking about my first bm. they removed the catheter and i walked around the ward a few times to try to help get things moving. that evening i had my first small bm. it was painful as advertised, but i had expected worse. i did not throw up, pass out, or scream, but i did sweat, pant and may have whimpered a bit. 

    having illustrated that i could poo, they released me from hospital on the morning of day 3. i was happy to go home with my little wifey, but i developed a deep hatred for speed bumps on the way.

    recovery at home has been ok. the pain is definitely still there, and particularly pronounced during and after bm's. because of the movicol i am pooing 3 times a day usually associated with bleeding and my stomach is unsettled most of the time. i try to anticipate and take strong pain killers before bm's and sit in the bath afterwards, which helps a bit. could be worse. 

    i have experienced a small amount of uncontrolled leakage between bm's and although it's been very minimal (and i think is improving?) this is my greatest stress because i know in a few cases it is a longer term issue after haemorrhoidectomy. 

    anyway, that is my experience so far. all the best to the rest of you and thanks again for sharing your experiences.

    bob>

    • Posted

      Hi Bob, your experience sounds positive so far. It’s good to hear that somewhere in the world the health care system works and you can trust your surgeon.

      I’ve never seen the surgeon who performed my operation (I only spoke to another one in the team at the post-op. review). My experience was a total chaos, with an overbooked day where I had to wait from morning till 5 pm – with no food or water allowed before op. then with stressed and confused nurses wheeling me around on isles towards the theatre. Once in the theatre something didn’t go to plan because one of the nurses kept saying: “this is unacceptable… this is unacceptable” - just what you don’t want to hear before you’re put to sleep and are about to be operated sad

      When I woke up after the operation I wanted to ask questions about the procedure, there was nobody to answer apart from a clueless nurse who was terribly bad at making up answers in an attempt to keep me happy. I hot a signed report before leaving – it must have been the most rudimentary medical report ever written –my daily BM notes are far more comprehensive that that!

      I’m now exactly 3 months after, fighting with a complication of some kind – I don’t know what exactly, and the surgeon who saw me recently was reluctant to talk about it but he promised to investigate it in a month time if necessary.

      So, Bob, if you ever hear rumours about NHS in the UK not working very well, you can safely believe it. I know about countless negative experiences (mine and people who I know) with the NHS in the UK.

      I’ll stop with this now cons it doesn’t make me feel terribly good...

      Wishing you, and everyone else, a good and safe recovery.

    • Posted

      "This is not acceptable" over and over really is the last thing you want to hear before going under! Brilliant.

      I must admit they were more organized the day of my op and my surgeon came to see me every morning and once in the afternoon as well when I was in hospital.

      In Australia you have a choice whether to pay for private medical insurance. I'm no expert, but based on my limited experience if you do opt for private you have access to considerably better services and doctors. 

      My life these past few days is almost comically centred around the timing and quality of BM's. It does make you reflect on the phenomenal difference something small we take for granted for years can make to our health and quality of life. If I get back to full health after this if nothing else I'll certainly try to be a bit more grateful and a bit more empathetic.

      Anyway I certainly hope that you don't have any sort of complication that will require more serious medical intervention mate. Have things continued to improve a bit since you've been using the cream?

      Bob

    • Posted

      Cheers Bob, yes I believe I can notice an improvement in the last week or so, but that might be because my stools have been softer and easier to pass. The cream might help, I certainly hope so, but there is no way I can verify the healing effect of the cream. My improvement can be a result of many factors (better stool balance, or just the natural course of healing). The only thing I can tell certainly about the positive effects of the cream is that it does relax my sphincter muscle. This means fewer anal spasms, which are such a nuisance. Because of all these I’m inclined to believe that it is worth the pain of applying the cream twice daily, despite the headache that it causes (literally) as a side-effect. I’ve read that this cream is also prescribed for chronic anal fissure, so yes - I’m feeling positive about using it.  

      You’ve mentioned private health care – I know, but unfortunately I couldn’t afford that.

      My life too has been, and still is, centred on the timing and quality of BMs – this is the challenge. Indeed people take a healthy anus for granted, as they take for granted their healthy heart, or stomach and so on.

      However the upsetting difference is, while most people are aware that stomach or kidneys are important, they don’t think in the same way about their anus. The anus is seen as a fairly useless orifice that just allows the dirt to get out...

      Few people know that the anus is a complex set of muscles, nerves and layers that are finely tuned to perform numerous essential contractions daily. When the anus suffers, the impact on life can be profound and debilitating.

      It is definitely unfair that people underestimate so much this part of the body which is a social taboo (at least here in the UK it is, for sure) and it’s used as a swear word when people want to insult each other.

      I’ve learnt two things from this experience so far: firstly it’s been an insight in human pain; any pain that I ever had before was mild in comparison. And secondly, I’ve decided to never use it for swearing again, or to think of it in a derogatory way, as most people do. The anus certainly deserves more respect.  

      Hope your healing goes smoothly!

       

    • Posted

      Brilliant news that you've noticed an improvement Alex. I really hope it continues on a positive trajectory for you.

      The last couple of days have been better for me as well. BM's are still pretty uncomfortable and I'm still bleeding a bit, but I haven't needed the stronger pain killers much at all. I've been able to drive for a short time and get some things done outside the house. Tomorrow I'm going to try to walk a km or 2 as a symbolic effort to start exercising again. Planning to go back to work on Monday.

      I was thinking about the most useful thing I could share from my experience for others that are considering or are having a haemorrhoidectomy. In hindsight the best thing we (my wife and I) did to try to tip the odds in our favor for a good outcome was to be quite proactive in our selection of doctor. 

      Although my initial doctor was ok, we reached out to people we knew in the medical community to find the best colorectal surgeon in our city. Nurses in particular really seem to know who the best doctors are and the worst ( more so than other doctors I think?). I figured doctors are no different to people in my industry or any other--there's huge variation in competence level from person to person. With something as potentially life changing as a haemorrhoidectomy I don't think you should leave this to chance and even a good GP will not always know or refer you to the best specialists. It was inconvenient and more expensive for me to switch doctors, but with the benefit of hindsight I definitely think it was worth it.

    • Posted

      That's great if you can be active already and walk, etc, thumbs up Bob!

      I went for a short walk today, it started ok but it got painful before long sad

      The mass and grade of hemorrhoids also determines the severity of the operation and recovery time. I've had grade 4 and a large mass of internal and circumferential external hemorrhoids. Even after my second procedure, I've been told that it wasn't safe to remove all of them, so I'm still left with hemorrhoids that are considerably large and prolapsed.

      I totally agree with your point on surgeon competence levels. For me it was extremely hard to get to any surgeon to operate me. In the UK getting a referral on NHS is difficult to start with, then I had to confront a clueless consultant that I needed surgery in the first place. They kept dismissing me, (as they do) and the first couple of diagnosis were useless - they kept telling me I'm fine - I might need some banding perhaps frown   (it's like they are trained on how to dismiss patients effectively here!). They agreed however to have a proper look by performing a sigmoidoscopy and only at that point the true severity of my hemorrhoids has been acknowledged.

      At every appointment I spoke to a different consultant (don't know why) and eventually they agreed to a THD procedure which I have requested and which treats internal hemorrhoids (but not those below a certain level - nevertheless there was a chance that would have been enough). It wasn't enough, but the operation went fine, and recovery from that - although it took 3 weeks, it was a walk in the park compare with the hemorrhoidectomy, at least in terms of pain.

      I don't know exactly who operated me, and I certainly couldn't choose the surgeon. It was a challenge to get to any surgeon, competent or not.

      Things are much better on the private sector, for sure, but that simply was/is not an option for me.

      I can only hope that I'm heading in the right direction, and that I'll be able to work one day, with a bit of luck... actually, with plenty of luck [neutral]  

      Have a nice and painless walk Bob smile

       

    • Posted

      Well, I managed to walk/shuffle about 750 m and had to take a pain killer and sit in a warm bath when I got home. I'm also actually quite exceptionally tired from the effort of the walk. Unbelievable. My earlier comment about 1-2 km being a "symbolic effort" seems a bit ridiculous now. I'm still going to view this as a win though given that it's the first real physical activity I've undertaken since the op. I just need to adjust my goals a touch.

      You make some excellent points Alex--I know that not everyone will have the same options that were available to us with respect to selecting our surgeon. In fact I was a bit hesitant to share our experience here because of the differing health systems and people's differing financial situations (During most of my 20's this would have been very different for me: I was at uni and as poor as a Bolivian church mouse). On balance though I thought there was a chance our experience might helpful to someone. 

      Maybe I'll modify the lesson from our experience to something more general. Based on our limited experience: understand your options, get independent advice if you can, and to the extent possible don't compromise once you've made an informed decision. In your case it definitely sounds like you are a very informed and proactive patient, which is all you can do. From reading through the different experiences including yours on this thread it does not sound like the UK public health system is very efficient or "patient friendly" at all frankly. That really limits what you can do from the sound of it.

      I feel sure that you will get back to work Alex! You are young and obviously smart and resourceful. I think your odds are very good. You'll not only recover, but be a stronger, wiser and kinder person as a result of this experience.

    • Posted

      Well Bob you're determined, that's for sure. You seem to be doing well at this stage though.

      On a different note, yeah, I’m similar to how you were in your 20’s: poor as a Bolivian church mouse - I’ve graduated from uni 2 years ago, I have student debt as graduates have these days, and my hemorrhoids have done a great job in preventing me from working and getting into my industry. I’ve been trying to sort it out ever since. The odds haven’t been much on my side so far in my life, they've been such a puta madre, as the Bolivian mouse would say. However I’m going to learn from your attitude and stay positive…

      I’m glad you’ve posted here Bob, people like you perhaps make us here in the UK think more about our health care. In fact I want the UK forums of all kinds to be flooded with Australians, Canadians, Japanese - or whatever nations have decent health care. I want them to talk to us about health care, and maybe… I don’t know - just maybe we here in the UK will want a better health care more, and I mean want it badly - not just roll eyes - or otherwise it won’t happen. If we just roll our eyes about NHS, in an admirable British manner, then just put up with the misery and move on, as we’re so brilliant at doing it as a nation, this won't do much good.

      Most people seem to expect politicians to sort out things by themselves, which is a little naive me thinks. Politicians never do it by themselves, why would you give a Bolivian rat’s backside about NHS when you can afford the best private care money can buy? It’s the people, collectively, who must put pressure on politicians, be proactive and make some noise... Politicians want to get elected and they pick up on what their voters are interested in. What are we interested in right now? Political parties have started to pitch for elections here, and guess what is at the top of their agenda? Health care? The NHS that is suffering from acute underfunding and chronic mismanagement? Of course that’s not the primary concern! Instead, it’s referendums on the EU, Brussels and EU work migration. These are apparently the nation’s greatest concerns right now. Because, dear friend Bob, it is so much easier to blame others for your mess than it is to blame yourself. It’s just a lot more convenient.

      Very well; a society that doesn’t prioritise health care is doomed to be sick, very sick. Serious improvement on this sector is imperative, and the sooner we make it happen, the better.

      So yeah, it’s good that you’ve posted Bob, we need some inspiration perhaps, we need to think more about our health care here, talk more about it, demand more political atttention, demand more funding, effective services, etc. Because things are in a right mess right now neutral        

       

       

    • Posted

      Well tomorrow's day 12 and I'm going to try to go back to work tomorrow. I have been weening myself off the stronger pain killers because I can't take them at work. The last couple of days have been a bit painful as a result. I will say that constant pain, even though not severe certainly makes you tired and gives you a sort of detached feeling from the world after a few hours.

      I have been managing to walk longer distances (~2 km) and we've been going out for lunch and to seeing friends. The pain and the continuous slow leakage and need for bandages is inconvenient when you're trying to be normal -- we'll see how work goes tomorrow. I'm lucky that it's only office work!

      Hope all is well Alex. How have you been feeling ?

    • Posted

      Day 14. I've been at work 2 consecutive days and things are going well. I've been able to work full days with minimal pain and no real restrictions. I check in with my specialist on Thursday and will ask about starting to exercise seriously again. I've been lucky and feel very confident of a full recovery at this point, so this will be my last post on this forum. Very best of luck to you Alex and everyone else that has undergone this procedure. Stay strong and positive and I wish you the very best of luck.

      Bob

    • Posted

      Thanks Bob, it's great that you're pretty much recovered. Anyone who's looking for encouragement should better read your posts, as your experience has been a lot more successful than that of others. 

      I'm not at the end of the tunnel yet myself, so I'll come back with updates.

      I hope the other posters in here are better too, and if they have any updates - positive or negative - would be good to hear from you all.

      Best of luck to you too Bob, your story is refreshingly positive which is a rare and encouraging thing on medical forums, so thanks for posting.   

       

    • Posted

      Hi Bobsbob

      Hope all is still well with you. I had my op almost 3 weeks ago and wonder if you would mind just answering a couple of questions that are worrying me?

      Did you get a burning/slicing sensation after Bowl movements for a while, mine seem to have lessend off now but i find i am getting a bloated feeling at my rear weighing it down, and because all this was causing either tress or pain i have gone a couple of days of not eating and now find myself very tired,cold and getting stomach cramps which demand an immediate bowl movement.

      Please could you let me know what your diet was 3 weeks after the op. Sorry to have to contact you but it would really help.

      Many many thanks

      Paul 

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