My experience with a chronic anal fissure

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Hi all

I thought that I would post this as a lot of people appear to be going through the same agony that I was going through for over a year.

Anyway, I was at uni and going through a bad time in my life, whenever I get stressed my guts go into turmoil. As a result I was off uni for a week with severe rectal pain and feeling lower than a snake's belly. I booked an appointment with my GP as I had experienced similar symptoms before.

My GP recognised the symptoms immediately, I thought I had piles, she said I was too young so had a look. The digital examination wasn't fun, in fact she said she had never seen anyway change colour so quickly but it was worth it because I was refered to a colo-rectal surgeon.

I took my sick note back into my tutor and as I was doing a clinical degree, he said straight away that fissures were worsened and sometimes caused by stress. The penny dropped.

As I said I was going through a very very bad time in my life which necessitated me going on antidepressants (Cipralex) for my emotional state. When this was added to wall climbing agony due to fissures I was near breaking point. I remember after one bowel movement almost fainting with the pain, I was lying at the top of the stairs at my mum's house and clawing at the wallpaper with my fingernails - I have had a broken leg and in terms of pain that fissure was far worse, trust me.

I went to see the colo-rectal surgeon a few weeks later, I was terrified, but he was a lovely man, very very considerate. He told me that I had a large fissure that could be helped with an ointment. I told him my background so he talked a bit more openly and said that fissures are an incredibly debilitating condition. He once had a 16 stone rugby player openly weeping on his consulting couch with the pain - I can understand why.

I was prescribed GTN ointment and started using it as directed. I had a slight headache which I could live with, but this was far better than the agony of the fissure and this headache was pretty much gone after the first week. After a week of use the pain from the fissure had also subsided to nothing. After six weeks I went back to the surgeon and I was healed.

I wish that was the end of the story but it isn't, I have probably had four or five bad flare ups since and dozens of other twinges, spasms, bleeds and itches since but I am nowhere near as bad as the first time - I can live with this now. I have seen the surgeon twice since and he has offered surgery but my frame of mind precluded me from that, I was simply terrified.

My GP is very understanding and I can get GTN on prescription whenever I need it. I was prescribed Anoheal by the surgeon as well but this didn't work as well as GTN for me, but I have seen cases in work where this has been incredibly effective.

As I said earlier, I was doing a clinical degree, which I have now passed, so I feel that I am pretty well qualified to offer a bit of advice, so here it is.

1. Go and see your GP. Don't be embarrassed, your doctor has seen dozens of these - they are very very common. If you get fobbed off or feel that you haven't got anywhere, go back and tell him/her that you are not happy and you will go elsewhere i.e. change your GP. Changing your GP hits their bank balance, and as GPs are notoriously greedy, they will do something. Nobody should have to suffer with this.

2. Take something for the pain but NOT codeine. Ibuprofen worked best for me.

3. Drink plenty of fluids and lay off the alcohol while you are healing.

4. Eat lots of fibre and fresh fruit and veg, switch to brown bread and have something like Weetabix for breakfast. This softens stools and makes them easier to pass - less pain and less damage to existing fissures.

5. Use a stool softener, one Movicol sachet daily really really helped me. You can buy these over the counter from your local Pharmacist but tell them what it is for. Alternatively get them on prescription from your GP.

6. Lay off the red meat, there is some science to this as meat increases the residence time in the gut and predisposes to harder stools. This really helped me and I have seen a few accounts here where sufferers also say that.

7. Try to relax, easier said than done, but try simple things like having a hot bath instead of a shower. If anything helps you, no matter how crazy or off the wall it may sound, carry on doing it. Going out for a drive helped me. Staying active also helps constipation and makes you feel better. Don't stay in and stew - stay positive.

8. Stick to the doctor's directions of any drugs you are given. If you are told to apply a cream for 6 weeks into the anus, then make sure it goes into the anus for 6 weeks. And into the anus means into the hole - not nice, but a lot nicer than the agony from an untreated fissure.

Remember you are not alone, these things can be cured. You will feel terrible and you will feel like nobody else understands what you are going through but believe me, these things are very very common.

And if all the above doesn't help there is a simple operation that can be done on a day case basis that has a 95% chance of curing it for good.

If you are reading this you are no doubt feeling horrible but believe me, there is light at the end of the tunnel.

Good luck with your pain in the ass.

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  • Posted

    I keep my fingers crossed for you. There was no pain let up for me for 3 months. Now (using all medicines aavail

    able) i hav some pain free hour a day, the majority is spent in moderate to severe but generally tolerable pain. Since the botox injection appears to have caused nerve damage, I was told the pain might never go away. I am now awaiting my appointment in a pain clinicl

  • Posted

    update...

    now back at work. Fissure almost healed. Still have large sentinel pile and skin tag but much better re pain. Pain is down to a duration of one hour after each BM (it was previously 4 hours of intense pain after each BM a few weeks back so a definite improvement!). Also discomfort when sitting for long periods (eg car) but I can live with that. I am not quite there but I feel 2000% better than last month!

    For me the Diltiazem has worked well so far. Side effects include itching and loose muscle tone in the anus so its still deadlyu important to be within 30 seconds of a toilet when I get the urge to go (2-3 times a day)

    My routine for the past 2 months to get to this place has been:

    Get up and have a Laxido sachet in water first thing

    Ibuprofen and paracetamol

    BM normally by 7am

    Immediate hot bath

    apply Diltiazem immediately after

    breakfast of bran flakes or brown toast

    water throughout the day and alternating paracetamol and ibuprofen to the maximum dosage allowed in 24 hour period

    salads, fruit and brown bread sandwiches for lunch/snacks throughout day

    2nd BM normally late morning or just after lunch

    Immediate hot bath after 2nd BM

    Dinner normally pasta or rice dish

    sometimes 3rd BM in evening

    hot bath around 9pm even if no 3rd BM

    2nd application of Diltiazem following 3rd bath

    2nd sachet of Laxido in water just before bed

    It seems to have worked for me so far (fingers crossed)

    Got consultant appointment soon. Hoping to avoid surgery and that will continue to improve

    Being back at work is a real bonus as its given me stuff to do and keep me occupied and the pain is much more manageable now

  • Posted

    Another great thread, with lots of info that the medics don't give. I'm 6 days post botox, and dropping from 8 movicol to four a day, after chatting to lovely people on here. Have been in agony since the op, and have today got a prescription for tramadol and Diltiazem which I hope, in conjunction with the movicol, shouldn't impact too much. I'm interested to try the manuka honey, as I know honey has wound healing properties. Respect to everyone who is living through this nightmare; it's been a huge relief to know I'm not an anomaly! I've lived with extreme anxiety and depression for years, am slowly sorting myself out with CBT, mindfulness and have just started meditating. Dreading my next BM!
  • Posted

    Hi, I'm suffering again and have been back to my doctor and have been referred back to my surgeon. I have been living with this for 14 years now and the last procedure was supposed to be 95% success rate, trust me to be in that 5% :-(. Let's see what my next option is, I want yo go back to work but feel this rules my life too much again at the minute
  • Posted

    Suleika did they explain beforehand that the nerve damage was a risk? It sounds like you have been left worse off im so sorry... I didnt get told that I was being botoxed so couldnt make an informed choice (although I was so desperate that I would have said yes to anything!) They said I was going into theatre for a Sigmoidoscopy which I had along with the addition of surprise botox. I have had a virtually pain free day today but have been horizontal the whole time. I also havent had a bowel movement so these will be the reasons why. Ive taken extra Movicol so will see what delights tomorrow brings. Best wishes.
  • Posted

    I had a perineal abcess to start with and had surgery which left. Me with a fissure,omg the pain is unbearable ,I think abcess has come back off to docs in morning to see if anyone will actually listen to me been of work for 3 months now surely this pain isn't normal xx
  • Posted

    I truly feel with you all as i have been suffering for 20+ years on and off. I realized that m flareups are caused by stress. For the past year i have been doing great, no pain, no forcing, soft stools but since lat week my 2 fissures and my internal hemorrhoids are putting me through hell every morning during BM. Blood is there of course , i literally hear my fissure open up and bloop here comes blood and the push push sessions begin. After seeing so many doctors and gone through sigmoidoscopy, colonoscopy i was told i needed to have a sphincterotomy ( sorry if misspelled) . I didn't want to do any surgeries. I had a blocage that led me to see an emergency doctor to perform manual defecation (NIGHTMARE) ! they put me on morphine, castor oil, manual defecation, ativan, enema. 4 hours later i was ok.. it took me 2 weeks to get better with : Lax-a-day (powder mix) and ducosate sodium 100 mg(stool softener) twice a day. Sitz bath, creams, plenty of water, no alcohol sad and i was ok... until last week it is all back. Now back to taking all the meds and hoping that tomorrow will be a better day sitting on the throne.... PS: dried prunes helped me as well...
  • Posted

    I investigated squatting to do a BM a while ago, as I kept hearing that this is a more natural position, but discovered that more beneficial is having your feet raised so the the thighs are horizontal, or knees slightly higher. I made myself a small wooden plinth, and I have to say that pooing with my feet on it, and a straight back, is generally easier, especially if I breath to expand my tum rather than lungs. I believe that there's a muscle that is relaxed when in this posture that, when sitting 'normally', like slumped forward with elbows on knees, usually pulls tight, making pooing more difficult.

    I've also been experimenting with breathing techniques, and try to do the 7/11, which seems to help with the pain, and is also supposed to have other health benefits.

    To be honest I'd be willing to try anything, from magic beans to chanting smile

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  • Posted

    Thank you Jamie for the reply. I sure will try your recommendations. Also, been trying to do it half standing with legs closed. Yes I know it is strange but it helps to not expand the anus for no reason until the BM is ready. One thing as well that is helping me is the BIDET, it brings water to the wound which make the blood circulate to heal it. Anything to have pain free morning BM. smile
  • Posted

    JamieInPain, did botox work for you? i'm thinking of getting it done. Any suggestions?
    • Posted

      The jury's out at the moment. The aftermath of the op was horrendous, as I went into urinary retention and had to go to A&E with awful pain, a distended abdomen etc. Since then the pain worsened until my GP finally prescribed morphine, diclofenac, omeprazole and of course paracetamol. She also diagnosed me as having proctalgia fugax, which hasn't been mentioned before even though I've described the spasms to a few clinicians previously. It's worstened since the op - at its peak I was spasmsingfrom my knees up! Of course this basically grips the fecently scraped fissure leading to more pain, so more gripping etc etc. I'm on an asthma pump for that and a combination of the pain killers and this seems to have settled things down. With that in mind it's hard to say the botox has made any improvement as (sorry!) my poo is still coming out the width of toothpaste due to spasming. I'm going to contact my consultant (who was on leave, according to his secretary, although I'm guessing his regitrars weren't, and it was one of them who operated on me) after easter and ask for a rethink. Four weeks out and I'm wishing I hadn't had it done, to be honest.

       

  • Posted

    HELLO mcoula,

    before you go for the botox you should enquire about all possible side effects. I had two botox injections within the space of 10 months and have not stopped suffering since. In fact, it was the botox treatment that has brought about my current condition - which is very painful neuralgia. I nearly hit the roof when the hospital offered me a third treatment of this kind and a sphincterotomy. I insisted on 2nd opinion and they found that through the botox injections sphincter nerves were damaged and the damage may be incurable.

    As botox treatment is relatively new (does anybody know how long it has been around?) I am possibly one of the first cases who were injured in the course of the injections. Maybe I just had an incompetent surgeon. i wonder whether anybody else had the same misfortune as I. It would be interesting to exchange experience.

    Currently I am waiting for a discussion of the pain treatment and referral to a pain clinic.

    It is no exaggeration that I have become disabled through the botox because there are days on which I cannot leave the house at all because of the nerve pain, and even on good days I cannot walk more than about 500 metres without getting very sharp pains. They are brought on through the friction through movement.

    Life after botox has been life in hell for me.

    I forgot to mention, the fissures have long since healed. I was treated by a very competent acupuncturist , who however at that time did not know of the additional nerve damage. Still, the pain relief I received while I was seeing him, was also considerable.

    • Posted

      Hey Suleika, I've been thinking about seeking acupuncture for this. Could you tell me how many treatments it took you? I realise that every case in unique but a ball park figure would be useful. My sister in law is an acupuncturist but she lives in Ireland, annoyingly smile
  • Posted

    Suleika, thanks for the heads up dear. I am sorry for the pain you are going through due to botox injections and i truly think that it probably was done by an incompetent dr because it seems that most people are doing well.... i used it on my forehead never down south smile however, i will ask my dr and other ones for their opinion because i can no longer suffer. I must admit that with Lax-a-day (equivalent to Miralax in the usa) has helped me tremendously and also docusate 100 mg twice a day, with lots and lots of steamed zuchini and i eat lots of beet roots. Let us not forget about water. i drink 2 small bottles of water at night before i go to sleep. In your case, i think sphectoronomy is your best bet and make sure the stools are soft. Good luck and thank you for your heads up on botox, i will keep you posted and please do the same.
  • Posted

    Hi I had 2 lots of Botox both helped reduce the pain but not eliminate it. This was about 10 years ago. Since then I have had a sphincterotomy which help loads it did vanish at one point this was 5 years back, but has recently re appeared. Have been re referred back to my surgeon, will let you know how I get on xx

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