Jump to content
  • Welcome to Celiac.com!

    You have found your celiac tribe! Join us and ask questions in our forum, share your story, and connect with others.




  • Celiac.com Sponsor (A1):



    Celiac.com Sponsor (A1-M):


  • Get Celiac.com Updates:
    Support Our Content
    eNewsletter
    Donate

Has Anyone Had Turbinate Surgery?


munchkinette

Recommended Posts

munchkinette Collaborator

I went to a sleep clinic today. My allergies have gotten insane. I can't breathe. At any rate, they looked into my nose, and the doctor said, "Oh WOW. Your turbinates are totally blocked." I had to look up what these are: Open Original Shared Link

She said they zap them with some kind of microwave or radio wave to bring the swelling down. I've never even heard of this.

Anyone have any experiences?


Celiac.com Sponsor (A8):
Celiac.com Sponsor (A8):



Celiac.com Sponsor (A8-M):



Ursa Major Collaborator

I hope they are not planning on doing something that will cause 'empty nose syndrome', because that would be worse. Open Original Shared Link

It might be better to figure out what causes the allergies, and treat them, rather than messing with your nose. Your stuffy nose is a symptom, not the cause.

When I was 19, I had nose surgery to 'correct' what the doctor claimed was a crooked septum, and that was supposed to have been causing my breathing problems.

The surgery was awful, the recovery worse, and in the end it was all for nothing, because it didn't do ANY good whatsoever!

Live2BWell Enthusiast

I have not had turbinate surgery, but I have serious problems with my turbinates - they are very large and obstructive (as per my ENT.) I am on Vyramist nasal spray, but I tested negative for all allergies so my ENT thinks it's environmental. He also has me on regular saline spray - which helps, and at I have a personal steam inhaler (VICKS) that helps a great deal as well (especially before I go to sleep.) Thing with the steam inhaler is, it doesn't work for me as well unless I have the vapor inhalent pads.

If I were you I'd exhaust other resources before getting the turbinate surgery, but since I don't know what the surgery really entails, I don't know how invasive (or non-invasive) it is.

Good luck with finding your answers :)

Ursa Major Collaborator

Have you tried a neti pot before? It might help, they can be very beneficial.

MauriceReed Newbie

I had mine done and don't regret it. I went to a clinic in Harley Street, London for the work. First up I met one doctor who gave me the once over and to discuss reasons for the op. I.e. I snore rather loudly and also might right nostril was forever closing up, especially when I lay on my right-hand side in bed at night. A quick inspection showed that the turbinates were large and also the septum (wall dividing the nostrils) fattened out towards the top.

The actual operation was very quick. An anasthetic is placed in the nose and shortly afterwards the doctor strips away both with a laser. The whole procedure took about 20 minutes. For about a week or so it feels like you have a bad cold with lots of fluid in the sinuses etc, this is natural.

Now I have no trouble breating at all. I still snore like a road-drill though :rolleyes:

Archived

This topic is now archived and is closed to further replies.


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,017
    • Most Online (within 30 mins)
      7,748

    Sjcucinotta
    Newest Member
    Sjcucinotta
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • sleuth
      He is not just a psychiatrist.  He is also a neuroscientist.  And yes, I have already read those studies.   I agree with benfotiamine.  This is short term while glutened/inflammation occurs.  As I had already mentioned, these symptoms no longer exist when this phase passes.  And yes, I know that celiac is a disease of malnutrition.  We are working with a naturopath.
    • knitty kitty
      Please do more research before you settle on nicotine. Dr. Paul New house is a psychiatrist.  His latest study involves the effect of nicotine patches on Late Life Depression which has reached no long term conclusions about the benefits.   Effects of open-label transdermal nicotine antidepressant augmentation on affective symptoms and executive function in late-life depression https://pubmed.ncbi.nlm.nih.gov/39009312/   I'm approaching the subject from the Microbiologist's point of view which shows nicotine blocks Thiamine B1 uptake and usage:   Chronic Nicotine Exposure In Vivo and In Vitro Inhibits Vitamin B1 (Thiamin) Uptake by Pancreatic Acinar Cells https://pubmed.ncbi.nlm.nih.gov/26633299/   While supplementation with thiamine in the form Benfotiamine can protect from damage done by  nicotine: Benfotiamine attenuates nicotine and uric acid-induced vascular endothelial dysfunction in the rat https://pubmed.ncbi.nlm.nih.gov/18951979/   I suggest you study the beneficial effects of Thiamine (Benfotiamine and TTFD) on the body and mental health done by Dr. Derrick Lonsdale and Dr. Chandler Marrs.  Dr. Lonsdale had studied thiamine over fifty years.   Hiding in Plain Sight: Modern Thiamine Deficiency https://pmc.ncbi.nlm.nih.gov/articles/PMC8533683/ I suggest you read their book Thiamine Deficiency Disease, Dysautonomia, and High Calorie Malnutrition.     Celiac Disease is a disease of malabsorption causing malnutrition.  Thiamine and benfotiamine: Focus on their therapeutic potential https://pmc.ncbi.nlm.nih.gov/articles/PMC10682628/
    • sleuth
      Thanks for your response.  Everything you mentioned he is and has been doing.  Tobacco is not the same as nicotine.  Nicotine, in the form of a patch, does not cause gastrointestinal irritation.  Smoking does. He is not smoking.  Please do your research before stating false information. Dr. Paul Newhouse has been doing research on nicotine the last 40 years at Vanderbilt University Medical Center.  
    • Jmartes71
      Im so frustrated and still getting the run around trying to reprove my celiac disease which my past primary ignored for 25 years.I understand that theres a ray of medical that doctors are limited too but not listening and telling the patient ( me) that im not as sensitive as I think and NOT celiac!Correction Mr white coat its not what I think but for cause and affect and past test that are not sticking in my medical records.I get sick violently with foods consumed, not eating the foods will show Im fabulous. After many blood draws and going through doctors I have the HLA- DQ2 positive which I read in a study that Iran conducted that the severity in celiac is in that gene.Im glutenfree and dealing with related issues which core issue of celiac isn't addressed. My skin, right eye, left leg diagestive issues affected. I have high blood pressure because im in pain.Im waisting my time on trying to reprove that Im celiac which is not a disease I want, but unfortunately have.It  has taken over my life personally and professionally. How do I stop getting medically gaslight and get the help needed to bounce back if I ever do bounce back to normal? I thought I was in good care with " celiac specialist " but in her eyes Im good.Im NOT.Sibo positive, IBS, Chronic Fatigue just to name a few and its all related to what I like to call a ghost disease ( celiac) since doctors don't seem to take it seriously. 
    • trents
      @Martha Mitchell, your reaction to the lens implant with gluten sounds like it could be an allergic reaction rather than a celiac reaction. It is possible for a celiac to be also allergic to gluten as it is a protein component in wheat, barley and rye.
×
×
  • Create New...

Important Information

NOTICE: This site places This site places cookies on your device (Cookie settings). on your device. Continued use is acceptance of our Terms of Use, and Privacy Policy.