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My Life with Achalasia

A little bit about me – I am a 38 year old married male with 2 young children living in a little place called Northern Ireland. I have up until now lead an active lifestyle playing Rugby for most of my adult life but now eventually hung the boots up so my fitness is going and I am putting on a bit of weight. (still not in bad shape though ha)

Looking back I can only ever remember that whatever I had to eat seemed to stick in my throat but up until October 2007 I actually thought that this was normal and how everybody felt when they ate. However if I had a good drink with my meals they seemed to go down ok and I had no real problems. (Occasionally I did suffer from bad bouts of painful heartburn/indigestion but that was about it and other than that I seemed to be in general good health)

Then in October 2007 my life started to change forever. I started to notice that all food/liquids were sticking after I had consumed them. So much so that I would take on the appearance of a character from a sci-fi movie in that I felt my eyes water and bulge out of my head and I would contort and move about just to get the food down and get a bit of relief. However you do have to eat so this would happen quite a few times daily. At this time I started to get recurrent and painful heart burn. I went to my local GP and explained my symptoms and I was told the heartburn may have inflamed my oesophagus casing a slight stricture hence my difficulty in swallowing. I was prescribed a course of Lansoprasol.

I started the medication and my heartburn disappeared but the problem in swallowing continued, so in Late November I returned to the GP and was told to double up my dose of Lansoprasol.

CONDITION UPDATE: - In December 2007 my condition got worse. I now found myself not only struggling with eating every meal but I started to wake numerous times in bed during the night with coughing fits. During the coughing I would bring up food particles into my mouth. The coughing got so bad that I had to move out of the bed I shared with my wife and into the spare room so at least she could get some sleep.

In January 2008 I again returned to my GP and explained the latest conditions and I asked him if I could be referred to a specialist. Luckily for me I have private Health care so my GP gave me the name of a Consultant and a letter of introduction.

I got an appointment with a Specialist in February 2008 and explained my symptoms and felt that something extremely sinister was happening in my body with visions of cancer becoming more evident. This was because I had tried to self diagnose myself on the internet typing in ‘difficulty when swallowing’ and everything seemed to indicate I had cancer. The Specialist tried to dispel any fears of cancer and he said the best route would be a series of tests starting with an endoscope examination of my esophagus.

CONDITION UPDATE: - By now I found that if I coughed hard enough my mouth would fill with ‘Gloop’ – this is my self made medical term for what I can only describe as a thick sticky substance made from my own body’s saliva and mucus taking the appearance of a clear gunge. On occasions I found myself in public and taking a coughing fit resulting in the gloop making an appearance - now on a good day with not to many people around I could just spit it out discretely but on a bad day when people were about I had to swallow it again. ‘Gloop’ also started to make regular visits when I was in bed trying to sleep.

In March 2008 I got a date for my endoscope examination. I arrived at the clinic and was brought to a theatre room where I met with my Consultant. He explained the examination procedure and I was asked if I wanted a full general anaesthetic or a local throat anaesthetic. I choose the local so was fully awake during the procedure (an option I would still choose). The anaesthetic tasted of rotten bananas a taste I actually liked reminding me of a strong shot of spirits you would get on a night out. A few minutes later and my throat went numb making swallowing even worse but not in a way you can’t handle. The endoscope was inserted into my throat and I felt it move down my oesophagus and into my stomach. There was actually no pain involved in the procedure just a slight uncomfortable feeling when the endoscope pushes air into the cavities so the consultant can see about. 2 minutes later it was all over and I looked at the Consultant with worry asking him did I have cancer. He told me he could see no evidence of cancer but that my oesophagus was grossly dilated with a large amount of food debris indicating I might have a problem with my lower oesophageal sphincter muscle. He said he had a good idea of what my problem was but further tests would be needed to confirm his suspicions.

At this point and based on what I was told I again checked the internet and this is when I first became aware of the condition ‘Achalasia’.

I got my further test date early August 2008 and this was for an oesophageal manometry and 24 hour PH level test. The entire procedure was conducted by a trained nurse who I must say was very good at explaining the procedure and again a local anaesthetic (the rotten banana one) was used this time it was sprayed into the back of my nose. (Be prepared it is as if someone just punched you on the nose). Again any pain only lasts seconds so it is not something you can’t handle. The procedure involved a thin wire being fed through the nose down the oesophagus into the top of the stomach. It is done to measure the muscle strength of the oesophagus when you swallow. My results were bad showing no muscle strength at all and my lower sphincter was so tight the nurse couldn’t manage to get the mamometry wire passed it. She off the record informed me it looked as if I had ‘Achalasia’

CONDITION UPDATE: - Since my endoscope procedure until the date of the manometry test my condition had got a lot worse. I could feel any food now that I ate sticking in the oesophagus queueing up and not passing into the stomach at all. As well as the ‘gloop’ appearances I now found my entire meals coming up I had lost over 20lbs in weight (all without any form of training). I was getting little or no sleep at all so was walking around like a zombie most days feeling terrible and dreading meal times. Because of the constant tiredness you become lethargic and everything seems to be a chore so depression starts to kick in and you automatically enter the why me feeling sorry for yourself mood.

In mid September 2008 my Consultant received my tests results and I met with him for my official diagnosis so I now had ‘Achalasia’. The Consultant was a specialist in Laparoscopic Surgery and he told me although my condition will never be cured it can be treated to greatly improve my lifestyle by Hellers Myotomy with Fundoplication and it would be his advice to go straight to surgery. To be really honest if the consultant had said he could do the op immediately I would have got up on his office table there and then but a date for the 18th of November 2008 was made.

CONDITION UPDATE: - from the last consultation up until my Operation date my condition deteriorated drastically losing now I had lost 28 Lbs in weight. I actually after every meal would go to the toilet and make myself cough dislodging any food in my oesophagus which on looking at it was a cross between Achalasia and bulimia.

OPERATION: - I was admitted to the Hospital the day before my surgery where I was spoken to by the anaesthetist and he briefed me about the entire procedure. Samples of my blood were taken for testing etc and I was settled down with some medication to try and calm my nerves. I did try to sleep but must admit this was a very difficult thing to do. My Operation was scheduled for 11:00 am on the 18th so not only was I in the Hospital overnight but I had most of the morning to wait as well. This time was hard and a lot goes through the mind I guess fear of the unknown as I had no form of surgical procedure in my life up until this point.

09:00am: - I was given medication again to settle my nerves

11:00am: -Nobody has came to collect me getting worried

11:20am: -They came in through the door and started to wheel my bed out of the room. Something inside me actually said “get of the bed and run” but I couldn’t move (It wouldn’t have been a pretty sight anyway as my backside was hanging out of the gown they had given me to wear). I looked at the theatre staff in full theatre uniform pushing the trolley this time not through bulging eyes but eye’s the size of dinner plates. I tried to make small talk as I’m pushed along the corridor towards the lifts. The Staff can see my panic and try to make small talk back to me. Then out of the lift and straight into the Operating room.

Once in through the door I see the anaesthetist who spoke with me the night before. He has a really calming influence and then behind him I see my Consultant who stops what he is doing and comes over with a smile. He chats about what is going to happen whilst the anaesthetist puts a line into my arm. No pain so far just nerves. The anaesthetist then starts talking and I say to him I suppose I will wake up later and the operation will be over he tells me yes I will know nothing about the operation at all. It seems surreal but I was probably chatting away for a good 10 minutes up to that point but this is all I remember. The anaesthetist then said you will start to feel a bit wosey in a second or two and I felt a really nice warm rushing feeling travelling up my arm and then my lights went out.

1:30pm: - I wake up confused in the Recovery ward and immediately feel a searing indigestion like pain. The staff immediately noticed my distress and within 10 seconds my pain has gone as they have given me pain relief. I then sleep mostly until 5:30 pm in the recovery ward until I am taken back up into my room again.

5:35pm: - I come round a bit when I am back in my own room and on waking I must admit I was not in any real pain just what I would describe as a mild discomfort. I looked at my stomach area which had 5 small and very neat stab wounds held together by a total of 12 staples. I probably smiled at this point because the operation was over and I had come out the other side without a great deal of pain. Due to the anaesthetic I drifted in and out of sleep for the remainder of that day and woke early the next. The Nursing Staff did constantly check on my progress throughout this time and I was given paracetamol and Voltorol for pain relief. I was also put on an entire food and liquid fast for a period of 24 hours.

The day after Surgery: - I woke early again with discomfort not pain and was able to get out of bed and get up on my feet. I went to the bathroom and washed myself then back into bed. My Consultant and Anaesthetist both came to see me at separate times and they informed me of their findings during the operation. I was told that on endoscope examination they found a huge amount of old and decaying food around the lower muscle that was starting to adhere to my oesophagus wall. So not only was my lower muscle tight and nearly closed but the food was causing an obstruction as well. They removed the food and cleaned the area. The Hellers Myotomy and fundoplication went exactly as the Consultant planned and overall they were extremely pleased with how it all went.

At 1:30pm that day I was allowed lunch (30ml of water) and I drank it all down and couldn’t believe it when I felt the cold of the water passing the lower muscle and into my stomach. On the hour up until 5:00pm I was allowed 30ml of water and then this increased to 60ml up until 9:00pm when I was allowed an unrestricted amount of liquid.

I then had a full glass of water followed by several cups of tea and all flowed into the stomach without any problems.

The next morning I was allowed a bowl of Rice Crispi’s to eat for breakfast followed at lunch with scrambled egg and an omelette for dinner. All the food passed with only a sip of water. I cannot express this feeling of being able to eat again it is like I have been given a second chance at life.

All in all I spent a total of 4 days in Hospital and have walked out the door a new man. I was even able to walk to nearby shops on my own and buy chocolates for the nursing staff and when my wife collected me we went shopping and I had a cup of coffee whilst out. Again I was in discomfort but absolutely no pain when walking about.

So now the aftermath.

It has only been 6 days since my operation and my Consultant has even told me to start food experimentation and I have had Toast and ham sandwiches (wow bread that I haven’t had for about 5 or 6 months) but I have mostly been very good taking sloppy foods but everything so far has sailed down into my stomach. I do however think mentally that this is too good to be true and I am waiting for the old feeling to come back again but I am just thankful for what I have now and will just live for the moment. I haven’t coughed at night at all and have had full sleep which is another wonderful feeling.

I am not so stupid as to think that I have been cured as we all know there is no cure for achalasia but what I can say is that I have been helped to a degree that will change my life completely. I don’t know how long this will last for and I am aware it can come back again but on the other hand it might well just last me a lifetime. I am also all too aware that my swallowing will never be that of a normal person but please let me tell you that at the minute it’s not too far of it and being honest it is the best I have swallowed in my entire life.

I cannot stress enough to anyone out there who has this condition and who is frightened, depressed, and suffering that whilst there is no cure there is excellent treatment available to help elevate the symptoms so that you can get back to a normal life. My Consultant informed me that the best treatment for me and my particular case was the Laparoscopic Surgery and I can say so far it is turning my life around completely. I can promise you if you are trying to make your mind up about this form of treatment that there is little pain involved more discomfort than anything else and it is probably less discomfort that you are feeling without being treated.

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  • Posted

    I does not look like there has been any activity on this blog for more than a year. I am hoping some of the original bloggers will update us on their current health state post surgery. I find comfort in knowing I am not alone, all of the symptoms are exactly mine. Weight loss, can't eat, throw up phlegm by the hands full. Throw up in the night (I belched a lot too, and hic ups). Trouble swallowing, pressure in chest. Making myself throw up (had an idea what bulimia is like) My doctor blew me off for 2 years telling me it was acid reflux. Changing my diet and taking medication did NOTHING to relieve any pain or allow me to eat. I finally went to Facebook and asked for help! Within two hours a sympathetic contact knew a specialist and I was in within 2 hours. Next day I had a series of tests (barium swallow, endoscope with stretch, motility test and a visit to a surgeon . Now I am on a wait list for POEM surgery. It scares me that this disorder is somewhat rare, so doctors don't get a lot of experience. I am concerned about the success of the surgery and possibility of having to have it redone in a few years (I am reading others have). Also, cancer is a big concern for me. I hate that I have gone much longer than needed without dealing with this. I am so frustrated today. Anybody positive out there? I am 55
  • Posted

    Just got this message through my e-mail. I thought I would take the time to put your mind at ease. I am now almost 23 years old and had my operation in the middle of April 2012. My surgeon was an absolute gem of a man and let me choose the date of my operation as I had it while being at University. Luckily, the way the operation is performed, you are left with very little pain. The only pain I had was the cuts to my stomach where the machinery used in the operation was put in place.

    Before my procedure he explained everything thoroughly and although I was very scared, the staff were lovely to me and the operation was done within 2 hours. It took about 2 weeks after the operation for me to be able to bend down properly and move about without feeling sore. My scars are basically invisible now and I feel great. I can eat almost anything now with ease, hardly any liquid and eating out is so enjoyable now. My only demon is still bread, but with a couple of gulps of liquid I can get it down.

    With regards to chest pains, I still get them occassionally but it is a lot less. It normally happens when I am under a lot of stress and so I still need to carry water with me wherever I go but i accept this as part of the illness. It's safe to say I have definitely gained weight in the past couple of years. I had all the symptoms you had and they are all gone, bar the chest pain sometimes. Which I think is pretty damn good! I am on medication everyday and it works perfectly fine. I rarely get heartburn.

    Although you think this illness is rare, my surgeon told me he has performed this operation on lots of people my age and I shouldn't think I am the only one.

    He is a lovely man and will be happy to speak to you. He was very caring towards me when I was going through my ordeal.

    I hope you are alright. Things will be fine and you will be sorted out. Life is so much better after the operation, trust me!

    Let me know how you get on!

    Louise

  • Posted

    HiPaddie

    I'm still going strong and haven't needed any further intervention since my big op in 2007.. Just annual scopes.all still well. I eat what I like. Bigger meals need water and I stop eating meal when I've had my fill of water.

    Hope this is positive for you

    Good luck with op.

  • Posted

    That sounds promising! Has anyone else had the laparoscopic surgery through the esophagus that they are doing now? Mine is being done in Hamilton Ontario (Canada) . I am on a waiting list. None of the doctors have given me any reason for concern, but as I read this blog, it does not sound as cut and dry as I had originally thought. I know I have gone undiagnosed for 2 1/2 years, but not sure how long before that I may have had achelasia. I know my esophagus has zero function and is 4x it's normal size. I am a vegetarian, so for the most part have not forced tough food down my throat. I am feeling overwhelmed not only with the surgery, the recovery and with the success of the procedure, but afraid this may not offer a permanent fix. Just venting. Thanks
  • Posted

    I replied earlier, but I had left a link to my surgeon's details for you, and it said my reply was pending approval to be posted...

    Anyway... to answer your question I had the laparoscopic surgery through my stomach. It consisted of 5/6 cuts but one of them cannot be seen as it was inside my belly button. It went well and I feel amazing now. After almost 2 years after my surgery, the cuts are practically invisible and you can't notice them. I am able to eat anything I want but bread is still a bit of a demon. I have to drink when eating bread or it just won't go down properly. I was told after my operation that I only have about 20% peristalsis left and now that my sphincter is completely open, I need to make sure I take my medication everyday. My surgeon saw me just last year for a check up and his words were ''if you feel great go and enjoy the rest of you life''. He has no worries about me having further trouble, but I am not sure if that is to do with my age or not.

    I still worry about the future and how it will be the older I get, but so far so good. I'm living normally and eating out all the time. Funnily enough I was out tonight and did not even have to drink a whole drink for my food to go down. That's how well it worked.

    Hopefully you get my other message as it has other details in there.

    Hope you are feeling ok!

    Louise

  • Posted

    Thank you so much Louise & Ellis, I have always been fit and healthy and this has come as such a blow to me, so permanent. I am terrible at drinking the best of times so this will be an adjustment (I know I should drink) I actually think Achalasia could be part of the reason I drink so little, so that may change. Do any of you bloggers experience any problems with food coming back up (at night) since that door now remains open. Also, I don't think acid reflux was ever my problem, but I understand 20% of the people that have this surgery do experience it. Any comments? What is different after the surgery from when before achalasia. And one last concern..... How was the surgery? I am told 24 hours in the hospital and taking it easy for a few weeks after. Is it that easy? Thank you and sorry for all the questions. I am so happy to have found this group!

  • Posted

    All my symptoms have compeltely gone. No food regurgitation and no acid coming through my nose at night or anything. It's literally like I'm a completely new person. If I don't take my medication I can get heartburn and my chest pains sometimes but this is rare and only when I'm under stress.

    The surgery was a breeze. Went to sleep within seconds, actually started laughing during the anesthetic and next minute I woke up being asked how I felt. I wasn't even sleepy after it. My surgeon made me eat straight after the operation to make sure I was fine, and I didn't feel a thing. It was like magic! After I had my litres of oxygen after the operation my surgeon gave me permission to go home at night. I was in the hospital for only about 12 hours then home tucked up in bed.

    My cuts were only sore for about a week then they got itchy. My operation was 3 weeks before my 21st birthday and I was worried I wouldn't get to celebrate it, but by the 21st April I was out with my friends drinking and eating and having a great time.

    It really has changed my life and I'm a much happier and calmer person for it. I don't worry nearly as much about things and I enjoy food so much more. Maybe a bit too much.... hence my belly haha!

    I honestly believe you will be fine. Have faith in your surgeon and it will all go well. I think it's rare things can go wrong. It's even got me over my fear of hospitals and operations. After the op you will feel gassy though as they pump you full of air to see inside to get to the sphincter. That subsides in a couple of days. My surgeon said there is no reason why you shouldn't eat straight after and this is also to check there are no leaks in the oesophagus.

    Hope this answers your question

  • Posted

    Thank you so much! My family have to,d me to GET OFF THE INTERNET, but this blog has been so helpful. Thanks again
  • Posted

    Glad I could help! :D
  • Posted

    Hi LouLou/paddie,

    I have had to remove the link and surgeon's details as we do not publish contact details like this. Please use the message service to exchange these links.

    Regards,

    Alan

    Emis Moderator

  • Posted

    I'm interested to know how this guy is doing now in 2016? I recently went through almost exactly what he describes in his story. Almost to a TEE. Difference is I dropped 50lbs And I am a very athletic basketball player. This story helped me a lot in making my decision to get the surgery thanks for sharing, I'm scheduled for Aug 11 2016. I'm very nervous but reading this helped. I just want to be able to live normally again but I'm afraid after this surgery I won't be able to workout and play basketball at the same level I have before my symptoms got bad smh

  • Posted

    Hi Ray - I've recently found out I have suspected Achalasia and I live in Lisburn, I'm 31 with 2 young children and getting quite scared about what seems like it will be a long journey ahead for me. I await the scope and other tests in September to diagnose the Achalasia. Do you mind me asking the surgeons details who operated on you? I go to Lagan valley for my initial testing which I'm not that happy about to be honest.

    Looking forward to hearing from you soon!

    Lynsey Gray X

  • Posted

    Thanks so much for sharing your story. I have an appt coming up to be examined once again before i can go in for my heller myotomy surgery. I went thru alot of mis diagnoses of heart burn, then gerd, etc. But finally achalasia was my diagnosis. Its a horrible thing to live with. I'm so happy to hear your story and the fact that you can live your life again. Congratulations.

  • Posted

    Thank you much for sharing. I have been suffering from this ailment for ten years plus. It isn't constant but seems to happen for months on end in the winter....only today I met my lunch twice!! Just like you the gloop is horrid. I had test et al but I think they didn't know what to look for. They diagnosed reflux!!! I also suffer from rectocele which is a muscle problem the other end, so this does not surprise me- perhaps I can combine both ops together eh ;-) . The coughing is awful and often it is so extreme that I find blood in the gloop. It is frightening and embarrassing-and little known about!! I haven't lost weight as mine tend to be a small portion of my meal. It is really starting to affect me now ( I just turned 41) I have 2 very young children who worry about mummy!

    Thank you again. I think I should seek surgery.

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