Achalasia

Posted , 21 users are following.

who has Achalasia ? and pains do you get.

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  • Posted

    hello.

    i have achalasia and had open myotomy 3 years ago and 2 months prev to that i had the balloon dilation which obviusly only worked for a short time.

    i have found this site because to this day i still get really bad pains and i mean bad to the point where i have to sip water which limits the pain till it goes. the pains can last for any where to a minute or two up to a few hours and god help if i dont have anything to drink immediatly im in agony.

    i still cant really find anything on the internet about pains after the operation so thought i'd reply to your experience in the hope that others will share thiers to, i was starting to think that maybe it was caused by something else but the doctor just said its to do with spasms due to the achalasia. not very helpful.

    • Posted

      Hi

      I just wanted to ask you if you have found out anymore about the chest pains you get? my doctor also said it was spasms,

      sipping water does help.

      The pains are so severe and sometimes feels like the pain travels do you get this?

       

    • Posted

      Hey, I was diagnosed about 10 years ago when my achalasia was really bad I had horrendous pains, my doctor prescribed me an angina spray and it worked wonders! Have a word with your doctor and see what they say!
  • Posted

    My son was surgically treated for achalasia in March and has recently started to get pains. Again the GP was no help....any ideas what this might be?
    • Posted

      It's spasms caused by the throat and they can be horrendous! For years I was told it was heart burn and/or panic attacks but finally got to a specialist and he confirmed that it was spasms caused by the achalasia - prescribed me a GTN spray (usually used for angina) and it worked wonders!

      Get in touch with your doctor and ask about getting your son one (or a few - I used to have one everywhere just incase)

      Hope this helps!

    • Posted

      Thank you for replying so quick, I will go see my gp and see if i can get this.

      thank you

  • Posted

    i had big op in 1990 when i was 19 worked pretty well have to eat with a big glass of water as food still sticks but not like before hand nothing stayed down. the pains that we get go away if you eat a banana i allways have one to hand because nothing else gets rid of it?
  • Posted

    hello,

    i was diagnosed with achalsia feb 07. It came on quite quickly and got progressively worse. I've had one balloon dilation, which worked very well for the first six months. It has now started to get worse and my Dr's are considering a heilers myotomy. I want to avoid this as long as possible. As long as i can keep some food down i'm happy.

    I suffer from lots of pain, and it's nice to hear that i'm not the only one. I thought it was just me. I to can experience it for a few mintues- to few hours. I take water with me everywhere as it's the only thing that seems to alleviate the pain. I also use a hot water bottle/wheat bag (when indoors!!), and place it betwen my shoulder blades. It's like a muscle is in spasm, but no one knows why!!. Am glad to hear it's not me going crazy

  • Posted

    Hi,I was diagnosed with achalasia in 2003 having suffered to the point of weighing a mere 5stone 10 so ill but gp telling me it was imagination and stress after giving birth to my third child , I had dilation and so far so good ,however I am suffering agony at the moment and also have the need to take water out with me everywhere I go, Ithought it was just me who suffered like this,you cant imagine the agony unless

    you have experienced it can you? Hope you feel better soon x x

  • Posted

    I was diagnosed of achalasia in 2002 at 17, first noticed symptoms of hiccups every time I ate at 15. Eventually got my diagnosis and had two dialations, both unsuccessful, and had the hellers op in 2004. I do still suffer from the chest pains. I didn't know what it was and as a consequence sometimes suffer panic attacks too. Attacks last a few mins to a few hours. I can go months without pain and then have lots of attacks all at once. Doctors told me they didn't know what caused the pain, it was most likely spasms of the throat or food decomposing in my throat. Ice cold water and deep breaths are the only relief.
  • Posted

    I get extreme stabbing pains between the shoulders , and sometimes in the stomach . They wake me up in the middle of the night and can last from 15 mins to 3 hours !!!! :shock:I used to just try to jog through them but that became increasingly difficult ! :cry: I now use gaviscon double strength which has helped . smile
  • Posted

    Ive been perscribed Tramadol for my chest pains and also an angina spray. The tramadol helps but it makes me so sleepy i have to spend the rest of the day in my bed.
  • Posted

    I have been suffereing with chest pains for about 10 years and only this week have had a diagnosis! I have always carried water round with me to drink at first sign but on honeymoon I was out and aboutn and I had no water and had horrendous pain. It went eventually but I thought I was having some sort of heart attack. I sat down on the pavement and sent my husband to buy water!
  • Posted

    warning: tramadol is classed as a narcotic in america. it is highly addictive and theres a good site called emilys post at tramadol withdrawal if you have been prescribed it.this site saved me....

    my story..

    IM AN ACHALASIA SUFFERER.

    I was diagnosed after my third child 3 years ago. I had the hellers myotomy op with fundoplication, September 2008.. i have suffered chronic pain ever since, 24/7. i was prescribed TRAMADOL in hospital and decided in jan 2009 to stop it as id stopped the df118 and pain settled a bit so thought i could stop cold turkey.WRONG.IT WAS HELL..

    During the four months on it.i couldnt drive, work, as pain was really bad. I thought i was just recovering from operation and that something had gone wrong, although consultants and g.p. was no help to me at all.

    I stopped the Tram.. and ended up in casualty as pain was excrutiating, but instantly i felt a cloud had lifted so new they hadnt been good for me. Anyway i read about tram,came across the website and realised I was hooked on them. doctors dont believe they are addictive..I know different. I restarted then and began a long weaning process, the hell was worse coming off them and i suffered for another two months.

    They escalate the pain so you need more and then your hooked..We are limited to our presciption doses in england, but americans etc are on whopping doses.

    I had that to deal with as well as the achalasia. My swallowing improved but the pain continued, across my chest and diaphragm.It was made worse by driving, cycling and didnt relate it to swallowing.

    I got a second consultant opinion but they are baffled.

    Where im at now...my pain has settled again. I stopped paracetamol and ibuprofen 6 weeks ago..Ive been taken them every day since the op. I have had to start drinking a lot of water again and have recently vomited for the first time since my op. im back to where i was before the op, with pain.

    my consultant wants to do a dilation. I think not, couldnt go through any more.

    This operation has blighted my life for the past 16 months, made worse by tramadol and the ignorance of doctors.Without that drug .I think, in fact i know my recovery would have been quicker and so differnt..Be very careful.

  • Posted

    i had heller's myotomy around 16/17 years ago and my life has improved enormously since. I do still get pains, sometimes trapped air, sometimes reflux and very occasionally the muscle spasm. Sometimes it's difficult to tell which is causing the pain. I used to drink water to stop the spasms or eat a small piece of chocolate. Now the thing that works best is alcohol (spirits), nothing too gassy with it, and now I manage very well because of it. It must relax the muscles quickly as it seems to work very fast. Not ideal for many I'm sure, but another option.

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