Are my breathing problems and Hiatus Hernia related?

Posted , 22 users are following.

I was diagnosed with an Hiatus Hernia eight years ago and take 40mg of Omeprazole twice a day. Last February I started having problems as in gulping when talking and feeling as if I was going to run out of breath whilst talking. This progressed to the feeling (and it's every breath) of not being able to fully breathe in or out. The doctors spent months telling me it was anxiety. I had my heart checked as I have SVT and also saw a Respiratory Consultant who after doing test said it was down to being 'de-conditioned. After he said that I joined Slimming World and have a Personal Trainer at the gym three times a week and am now over three stone lighter! I went through a period last year of having to sleep sat up as it was even harder to breathe. I've been able to sleep back on two pillows for months and then this week I had a bad night again. Last August I woke up and wasn't breathing. Have been checked for Sleep Apnea. The Clinic said could be due to Hernia-consultant says no way. Have had this sixteen months and counting. Does anyone have the same symptoms? Thanks.

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  • Posted

    The brathing problem when you have hiatal hérnia is because of the stomach, when goes up, keep pressing tour diaphragm keeping him from expanding properly. Also the hiatal hernia irritates the vagus nerve, wich passes through the stomach and can make you Dizzy and give you a lot of other symptons. Just search for that and you find about It. There are vídeos in YouTube too about that.

    • Posted

      I thought my breathing problems might have been caused by the hernia, but according to the Consultant, my hernia is far too small to be causing a problem.  I remember reading about the vagus nerve a few years ago.  I'm going to have another read of it.

  • Posted

    I don’t care what these drs say if they have never had a hiatal hernia they can’t say if it would bother some people’s breathing I just had surgery in March and it took 5 years and several dr to figure out what I had and I had the paraesophageal hernia where the intire stomach slipped in to my chest the only way to get relief was to push my back into a wall when they found my hernia it was 8 in wide and when the surgeon did his test that’s when he said the hole stomach was in my chest ....most dr will never no what it feels like unless they have 1 and I wouldn’t wish that on my worst enemy...the chiropractor is the 1 who did it to me he didn’t no I had a hernia and neither did I but the size of mine was so large so when he pushed on my back I felt it happen but I didn’t no what had happen till I had all my test done 
  • Posted

    I've read through all these posts and can relate to most of them. I am considering surgery after dealing with similar symptoms for 17 months now. I have found some relief on my own, so I will share my story in case it can help anyone else. I'm 37 and living in Los Angeles, so my doctor experiences might be very different. In March 2017, I woke in the middle of the night with shortness of breath and pain that felt like an elephant was on my chest. I literally could not inhale without excruciating pain. It passed gradually, but this continued to happen at least once monthly. I was in and out of the Emergency Room each time - dismissed as having "reactive airway disease." My insurance was bad, so I could not see specialists without a referral...and my doctor took months and months to write any referrals. Aside from the night breathing episodes, I was dealing with other symptoms (tight feeling when swallowing, congestion, raspy voice) - everything indicating LPR. I got to a GI Dr. for endoscopy finally (the anesthesia also did not with for me) & I was diagnosed with a small hiatal hernia (I was never told the size). I was given high doses of PPIs and inhalers to help my breathing. The inhalers helped initially with my breathing, but then they stopped working altogether and I kept ending up back in the ER for breathing treatments - even though I never had wheezing or asthma (just a tight feeling with pain and the sensation of being unable to take a full breath). I took the PPIs but saw zero improvement so I came off them. I started trying to find my own answers since the doctor were not helping. I did a strict diet (I was already underweight when I started the diet, so that was not the cause of my problems). The diet is a high PH diet that can be found online for LPR by searching: "LPR anti-reflux diet voice dr. Koufman." The diet is very strict and I didn't eat for 5 hours before sleep. I also slept sitting up completely at a 90 degree angle for over 9 months. These things helped, but it still wasn't perfect and I still ended up with horrific chest pain episodes that I could not link to any one thing. Those episodes always occurred between 2-3am...which is when our antihistamine production is the lowest and when people usually die in the middle of the night from asthma attacks. On my own I requested a referral to an allergist who did a lot of testing and found nothing...but she gave me Singular, which is an antihistamine known to help with night asthma. I have not had my severe breathing episodes since (2 months)...but I still have shortness of breath all the time, especially if I have a big meal or eat the wrong foods. My diet is VERY strict now and I feel depressed about it (no wheat, no soy, no dairy, and no feeds with a PH below 5.5). I finally have an appointment for lung function testing with a pulmonologist next week (I had to change my insurance to get that scheduled). I am quite certain he will say that my lungs are fine. I feel pretty certain that my HH is causing all of this. I see a chiropractor regularly to manually release my diaphragm and attempt to push my HH back into place. Sometimes it seems to help, not always. Deep diaphragmatic breathing also helps sometimes, not always. Changing sleep positions sometimes helps. Alkaline water has also helped a lot. I read so much about how gaseous pepsin particles from the stomach are refluxed into our lungs with HH, contributing to our breathing problems (I would cough up congestion from my lungs for hours each morning even after sleeping upright all night). It is the pepsin combined with the acid that creates a problem (this eats our healthy tissue). Pepsin cannot survive in a PH above 8. So drinking good quality alkaline water (PH above 8) helped my breathing and stuffiness...I gargled it too and steamed it to breath into my lungs. Now it seems like my symptoms are consistently bad shortness of breath and belching, about 1 week before my menstral cycle... The only thing I can think of is that some hormones cause muscles to relax...perhaps my HH is worse then (if that's even possible?). I know this is similar to how women have heartburn while pregnant due to hormone changes. I still have the pain in the middle of my upper back too - consistent with reflux. Overall I am much better, but I still want to be able to breath normally. Deep diaphragmatic breathing does seem to help along with side sleeping (it's always worse on my back). I would love to get Linx, but I am not a good candidate since my HH is small - but I will request a CT to look at it more closely based on the comments here. Thank you all for some encouragement.

    • Posted

      Every thing your writing I have went through my was 5 yrs with any dr that could figure it out till I found a gastroenterologist I couldn’t breath I couldn’t eat sleep and I also went to a chiropractor what happen with that is when he pushed on the middle of my back my hernia slipped up into my chest I had what you call a paraesophageal hernia I would lose my breath when I would talk I also did the diet the med everything the first scope I had they didn’t even tell me I had a hernia but the thing that made it worse was the chiropractor he didn’t mean it by all means but if your going to have the surgery make she it isn’t just a surgeon it should be a gastroenterologist that has done thousands of these types of surgery it’s not an easy surgery but it was well worth it ....when you have the scope don’t they can tell you the size of it mine was 8 in wide and with it so large when the chiropractor pushes on the back the force can push it in to your chest it was the worse thing I have ever went through because your mind tell you it’s your breathing it isn’t your stomach may have been pushed into your chest the pressure it unreal 
    • Posted

      That's frightening about your chiro experience. I agree though, this could make my problem worse. I saw a new Dr today who seemed thorough. More labs next week with ENT and pulmonology. I am very skeptical of most doctors by this point (getting no where for the last 17 months). I don't want a surgery that might not help. Has anyone heard of Stretta? This might be another HH repair option for me.

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