Facial Pain - Empty Nose Syndrome
Looking to discuss coping mechanisms/treatment options for atypical facial pain/empty nose syndrome - mine is a result of sinus surgery
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I was diagnosed with possible empty nose syndrome, please, please please, I need help for the condition worsens with severe dryness burning stinging in ears throat chest , can’t breath fully because it causes unbearable inhuman symptoms. Dizziness and lethargy, inflammation non stop, thickening of mucosa is also present . I beg, for the sake of my daughter and family, help me . Thank you sooo much !
I also have information in left ear more than right, and besides the surgery I had left occipital nerve blocks and PRP in same places . A doctor with a compassionate heart might be able to help. Where there is a will there is a way . Thank you !
Hi, @marinelastef - the severe dryness, burning, stinging in your ears, throat and chest, plus difficulty breathing, dizziness and lethargy sound very challenging. I've moved your posts here so that you can connect with others who have been there.
Hoping others like @nrd1 @healthiswealth1 @joannemaisey @ashleyhall @jrsigurl will return to this discussion and share what has helped them with their potential or confirmed empty nose syndrome. @lioness @jenniferhunter and @sirgalahad also may have some input.
Is there anything you've found so far that brings any relief to these symptoms, marinelastef? Are you planning to get another opinion from another physician on your condition?
Thank you for the help Lisa !! I got to a point where nothing really helps, except a body temperature shower once in a while , and my left turbine is constantly burning, inflamed, stinging, swollen and sensitive to cold wind air conditioning, dust smell, you name it . I feel my respiratory system weak, stiff and compromised a lot . If anyone has any suggestions I’ll be very thankful !
Hi. Have you seen a doctor who specifically assesses empty nose syndrome? Have you been seen by your original surgeon? Have you had these symptoms progressively over the past from your surgery or sudden onset? I have had similar symptoms that I am trying to currently get addressed 1.5 years post surgery.
I think they are referring to Stanford University, California. There is a doctor who is familiar with ENS there.
you sound like you have ens. caused by removal of too much turbinate tissue; can occur during septoplasty. You have all the symptoms - go to facebook ENS support group (the main group). Will meet others and get advice from them. Most doctors won't recognize ENS. There are a few here and there that do.
Anyone in this group have any new tips or advice for the pain portion or dryness?
You might want to check out the following website: http://buteykoclinic.com/ for your breathing. It offered some help for me. Also: https://youtu.be/FtMLN9i9cdE. Above all keep your nose moisturized with saline spray or Ayr saline gel. Nasal rinses also help. By the way, how can a doctor do this to us? Surely they know the functions of the nasal turbinates. Unbelievable. P.S. I apply the saline gel to inside of my nose at night with a Q-tip. It helps. Good luck...Jim s
@drumline7860 -would you mind sharing your experience or type of surgery?
I’ve tried many things. Can not figure out if it’s ENS or not. The name of the syndrome is misleading as it should be post surgical nasal dysfunction. ENTs have given me mixed follow up assessments/consultations.