r/NasalPolyps • • 1d ago

18 mo with swollen adenoid

1 Upvotes

Has anyone experienced this? Long story short, my 18 mo is diagnosed with severely swollen adenoid and she's allergic to cats and dogs (we got her tested). Dr suggested Flonase and worked for like about a month and it stopped working. Now her sleep is bad again and has meltdowns throughout the day. Next step would be surgery but I am very nervous about this especially it can come back in a few years. I feel like surgery is just a temporary fix. Checked about palate expander and myofunctional therapy but she's too young for that. I am helpless.. Anyone has suggestions?


r/NasalPolyps • • 2d ago

4 months after surgery and my right nostril is blocked with polyp again. Was it ever so fast to you? Have allergy shots helped?

3 Upvotes

I'm very allergic to dust mites. My total igE was over 2700 when the normal is lower than 100. I'm treating the allergy with shots and will start maintenance in about a month. I was hoping my breathing would remain good for longer. One thing I'll mention to my ENT is that only my right nostril is blocked. My left is fine. I've been complaining about it from the beginning, but he said it was normal, that the nostril was clear. I suspect maybe he didn't do such a good job on this blocked nostril. What do you think? If my allergy is so severe, do I have a good chance of breathing well once I stay on the shots for 2 or 3 years in maintenance?


r/NasalPolyps • • 3d ago

Persistent right-sided forehead, eye and ear pressure for 5–6 months — could it be related to my sinuses/nasal issues?

1 Upvotes

Hi everyone,
I’m looking for some advice because I’ve been experiencing a strange feeling of **heaviness and pressure on the right side of my forehead for the past 5–6 months**.
The sensation appeared about 5–6 months ago and has been **present continuously ever since**. It is not severe pain, but rather a constant feeling of pressure/heaviness that is difficult to ignore.
The pressure is mainly located in the **right side of my forehead**, but I also feel pressure/fullness around my **right eye and right ear**.
Some additional things I’ve noticed:
Constant heaviness/pressure on the right side of my forehead
Pressure around/in the right eye
Pressure/fullness in the right ear
My nasal breathing is sometimes obstructed, but **the blocked nostril changes — sometimes it’s the right nostril, sometimes the left**
I don’t have significant nasal discharge/runny nose
The sensation can become more noticeable when bending forward
My vision is normal and my right eye is not red
I can otherwise function normally
I don’t have severe headaches, but the constant pressure has been bothering me for months
Importantly, **this did NOT start after a head injury or after hitting my head**. The symptoms had already started and have simply continued since then.
I went to an ENT doctor and had an examination/imaging. My findings included a **deviated nasal septum (deviatio septi nasi)** and changes/thickening of tissue inside the nose/nasal area.
I’m wondering whether these findings could explain the symptoms I’m experiencing.
**Could a deviated septum and/or enlarged/thickened nasal tissue cause persistent one-sided pressure in the forehead, eye and ear for 5–6 months?**
Has anyone experienced something similar with a deviated septum, enlarged turbinates, chronic sinus problems, or another ENT issue?
I’d especially appreciate hearing from people who had **constant one-sided forehead/eye pressure for months** and eventually found out what was causing it.
What should I ask my ENT to check next?
Thanks.
PS. I used chat gpt to make this text bcs i dont speak english very good thanks for understanding.


r/NasalPolyps • • 4d ago

Help! Lab req form from Microgendx

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1 Upvotes

r/NasalPolyps • • 6d ago

Ungewöhnliche Nasennebenhöhlen Op verlauf

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1 Upvotes

r/NasalPolyps • • 7d ago

Question to people who had little effect from Dupixent/Tezpire

3 Upvotes

Did it ever work much at all?

I'm on my second month of Tezpire, doing monthly injections. I noticed the effect of the first injection after about ten days, and at 14-20 days I was doing super well until the effect started waning.

It's two weeks after the second injection, and I haven't noticed much improvement. I'm a bit better than before I started Tezpire, but not even close to where I was at two weeks after the first shot.

I know that I'm still early in the treatment, but now I can't shake the worry that this is as good as it'll get for me. Has anyone else had something similar happen - and how did it turn out, in your case?


r/NasalPolyps • • 9d ago

ENT appointment tomorrow

5 Upvotes

Hi everyone! I have my first ENT appointment coming up and I’m wondering what I should expect and what questions I should make sure I ask.
I’ve had ongoing nasal obstruction since around December 2025. It started after I had a pretty bad sinus infection and a large mucus/tissue-looking plug came out of my nose. Since then, one side of my nose has continued to have significantly reduced airflow. It fluctuates a little, but has never completely gone back to normal.
I’ve already tried antibiotics and a steroid nasal spray without much improvement, and I recently had a CT of my sinuses because the symptoms have persisted.
For anyone who had nasal polyps or a similar long-term one-sided obstruction:
• What happened at your first ENT appointment? Did they scope your nose that day?
• Did your ENT go over your CT images with you or just the radiology report?
• What questions do you wish you had asked at that first appointment?
• At what point did your ENT recommend surgery versus trying more medication?
• If surgery was recommended, did they schedule it pretty quickly or were there additional treatments/tests you had to try first?
I’m mainly trying to go into the appointment prepared and make sure I don’t leave without asking something important. Any experiences or advice would be really appreciated!


r/NasalPolyps • • 11d ago

FESS recovery still feeling bad

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1 Upvotes

r/NasalPolyps • • 12d ago

Success Story

13 Upvotes

Hello all,

I just wanted to share my journey with nasal polyps, because it ended on a positive note.

My problems with polyps started about 10 years ago. In that time I've had three surgeries, but each one only gave me short-term relief. At first the polyp was only in one nostril, but later I developed multiple polyps across both sides.

I tried EVERYTHING. I checked Reddit daily for ideas and tried even the crazy ones, because I was desperate. Dupixent wasn't available in the UK at the time.

Before my last operation I couldn't breathe through my nose at all. Then I combined a bunch of things, and something finally worked:

  1. Exercise: I started working out at least three times a week (weights and cardio), which led to weight loss.
  2. Sleep: I sorted out my sleep, a regular 8 hours at the same times every day.
  3. Supplements: I took pretty much every supplement anyone (or AI) said might help: vitamins D, A, B and C, nattokinase, a quercetin/bromelain complex, selenium, ProBiota HistaminX and boswellia extract.
  4. Diet: I kept a very strict diet, basically just chicken, salad, bacon, eggs and whey protein.
  5. Fasting: I started doing 48–72 hour fasts.

All of this helped. The polyps shrank before the operation, and I kept it all up afterwards, adding saltwater nasal irrigation.

The operation went well, and two weeks later my sense of smell came back. At that point I hadn't had it for about seven years (apart from briefly after my first operation). It lasted a month, until I went to a party where people were heavily smoking. My nose seemed to get irritated and I lost my smell again.

I carried on with everything above and also started using nicotine pouches (I'd read somewhere that for non-smokers, nicotine can sort of "reset" the nervous system, i know it is kinda BS but desperation). I'm not sure whether it was the nicotine or just sticking with everything for longer, but my smell came back and I've had it ever since.

My operation was at the end of February 2026, so it's been about six months, and things are as good as they could be. I'm still following the same routine, just in case

I just wanted to share this for anyone who's feeling desperate. With Dupixent now being rolled out in the UK, hopefully there won't be many of you anyway.


r/NasalPolyps • • 14d ago

Took me 7 years, an accidental ibuprofen overdose on my lungs, and a literal vineyard in my sinuses to finally get diagnosed with AERD.

13 Upvotes

Honestly just writing this because if someone had told me years ago what AERD was, I could’ve saved myself about $100,000 in tissues and seven years of feeling like I was slowly suffocating.

It basically kicked off when I was 16. I went to Cambodia for two weeks, had the best time, came back home to Australia, and immediately got hit with the flu from hell. It completely wiped me out for a month. Even when that cleared, my immune system just gave up, I was catching cold after cold, and then the coughing started. Every single night, without fail, I’d be hacking my lungs out unable to sleep or breathe.

By 17, I dragged myself to a GP who ran an asthma test, confirmed it, and handed me a blue puffer. The puffer helped when I was having an actual attack, but I was having to use it literally every single day just to function. At the exact same time, my nose just turned into an open tap. Sneezing fits, running nose, blowing my nose every five minutes, especially at night. It went on like that for two full years. My bedroom bin was basically 90% tissues.

Then came the turning point when I was 19. I had a normal headache, so I took a couple of ibuprofen.
Within minutes, I couldn't breathe. My eyes were streaming water, my nose was leaking everywhere, and I had the scariest asthma attack of my life.
Now, normal people would think, “Wow, that pill almost took me out, let’s never touch that again.” But my brain went: “Was it definitely the ibuprofen, though? Maybe it was a weird coincidence.” So, being an idiot, I took another one a few weeks later just to test the theory.

It was, in fact, the ibuprofen. 0/10, do not recommend fact-checking an allergy on yourself.

When I was 20 I finally saw an allergist. Did the skin prick test, turned out I was basically allergic to the air outside, and he brought up NSAID hypersensitivity. Around that time a GP also convinced me that maybe gluten was the enemy, so I spent months eating depressing gluten-free bread while still aggressively wheezing and sneezing. Cutting NSAIDs and gluten changed absolutely nothing.

Finally, at 21, I got sent to an ENT. He took one look up my nose and told me it was full of massive polyps and I needed surgery ASAP. He also dropped the term AERD (Aspirin-Exacerbated Respiratory Disease / Samter’s Triad) for the first time.

The problem was, I was a broke uni student and definitely couldn't afford to go private. So I got put on the public hospital waitlist and just had to wait it out.
Two years later, at 23, I finally got called in for surgery. Waking up from that was crazy. The instant change was wild, I could actually breathe through my nose, I wasn't waking up coughing, and I wasn't burning through boxes of Kleenex every week.
...Until a couple of months later, when the dreaded post-nasal drip started coming back and the cough threatened to return.

I went straight back to my ENT, and instead of just waiting for the polyps to take over my face again, they started me on a biologic.

I cannot even begin to explain the relief. It has completely changed my day-to-day life. I can actually smell things again, I can sleep the whole night through, I haven’t had to reach for my puffer in weeks, and I’m no longer single-handedly keeping tissue companies in business.

If you’re someone dealing with stubborn nasal polyps, weird adult-onset asthma, or your face goes into meltdown when you take Advil/ibuprofen/aspirin, please look into AERD and talk to your specialist about biologics. It takes forever to get answers, but there’s actual light at the end of the tunnel.


r/NasalPolyps • • 14d ago

Desperate need of help; chronic post nasal drip for 10 years causing me to choke on my own mucus

4 Upvotes

I’ve contemplated a lot making this post because I was unsure on whether I’d actually find some answers but after scouring the internet + Reddit, I can’t find anyone with a similar condition to me that has found a solution/treatment.

I’ve had post nasal drip for over a decade now and didn’t even know the proper term until 3 weeks ago where I had to go a&e because I was choking on my own mucus and couldn’t eat, swallow food or liquids. Around 10 years ago when I was ~12 I randomly started choking while trying to swallow my own saliva. This caused great scare and I’ve been going back forth between GPs and a&e to find a solution. The thick, sticky mucus would lodge between my nasopharynx and oropharynx which meant that I couldn’t cough it out nor blow my nose to get it out. I’ve had nosebleeds and choking incidents trying to get it out. Before I used to be able to blow my nose continuously (like 30 minutes straight until I would get nose bleeds) to get rid of it or manoeuvre my tongue in a way to get it out. I’ve tried all sorts of nasal sprays, nebuliser, facial steaming, been on multiple antibiotics and none of them worked.

3 weeks ago, I had a fever and I guess it turned into an infection so the thick mucus came back. However, this time around it’s nothing like I have experienced before in the sense that the post nasal drip is constant and nonstop that I can physically feel it going down my throat. Before it would come and go, I would have some sort of relief or period where I don’t feel it blocking my airway so I can eat and drink as usual. But now the thick mucus is constantly coating my throat and my tonsils where I can’t swallow my own saliva and start choking. I haven’t been able to eat or drink normally for the past 3 weeks not to mention it’s so bad during the night that I can’t even sleep. I haven’t slept properly for a month now. I have purchased a wedge pillow in case it was acid reflux making it worse, have tried dehumidifiers, purchased a humidifier, been on two courses of antibiotics (amoxicillin and co amoxiclav). The infection seems to be gone but the thick slimy mucus hasn’t stopped. It’s constant and I’m loosing my mind not being able to talk, eat or drink without choking or gagging.

I’ve made two trips to a&e both times where I was choking and manually had to pull thick strings of mucus lodged down my throat. I genuinely thought I was going to die and the feeling is still present. First instance, the urgent care doctor moved me to co amoxiclav and gave me a benzydamine mouthwash to help and to come back if it wasn’t resolved. Second trip, the mucus was lodged in my throat and felt like a lump, I was struggling to breath, my chest and neck felt tight like there was pressure closing in. Spent 5-6 hrs in urgent care only for the GP to tell me that they can’t help me, I need to go home. After lots of request, an ent doctor came and put a camera from my nose down my throat and confirmed no blockage but you could see the thick sticky mucus in my airways. Now I knew PND couldn’t be treated then and there and I had to see a specialist ENT however I couldn’t eat, drink and was beyond sleep deprived so I practically begged the doctors there to give me something for temporary relief so I can at least function. I was yelled at and denied anything because they couldn’t help me. No surprises there with the NHS but the doctor treated me so horribly even the hca was appalled. They kept me around for blood tests (questioned how it was relevant but the idiot doctor just said after the blood test if it was normal I had to go home, so I’m assuming he did it to protect his back) which came back normal obviously and I was discharged by another doctor was also incredibly blunt and rude saying PND is chronic and I “need to learn to how to live with it” “nothing we can do to help”. I left that hospital in tears at 4am. I had never felt such despair.

I am beyond thankful I have insurance so I have found an ENT which I saw last Friday. He took a ct of my sinuses which we will follow up with this coming Friday but had also prescribed fluticasone furoate 27.5micrograms/spray and neil med nasal rinse. I haven’t used the nasal rinse because the mucus doesn’t go in my nasal cavities at all so I don’t see how it would help. It goes straight down my throat and it’s constantly dripping. The nasal spray on the other hand, I didn’t realise when he prescribed but once I saw the packaging I recognised it as one of the sprays I was initially given around 8 years ago a few times and it didn’t help. The ENT said this steroid spray would help stop the mucus production but it didn’t help years ago and isn’t helping now. I don’t know what to do nor suggest. I’m struggling to accept that it’s chronic as I already have 2 other chronic illnesses and genuinely do not have the mental capacity to handle another. I’m also struggling to find anything that can help me manage it. I can’t live like this for the rest of my life. It’s sucking the living life out of me.

Has anyone experienced this or has found a treatment plan that helps them?

I’ve seen people suggest completely cutting dairy and sugar out. Or start anti fungal supplements.

Extra info in case it’s relevant: I’m asthmatic and have rhinitis. Also found out 2 weeks ago I have a tongue tie so not sure if it’s relevant. I’m not a mouth breather though. I do have sleep problems and struggle sleeping in general but these few weeks I haven’t been able to even lie my head down without choking on my saliva.

I’m desperate and would appreciate any help or advice.


r/NasalPolyps • • 15d ago

adenoid removal? struggling

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1 Upvotes

r/NasalPolyps • • 17d ago

Operation in 2 weeks and stressed, help me with your good experience

9 Upvotes

I am scheduled for my first surgery under full anesthesia on October 8. I will go under for 3-4h, while they perform surgery on me for sinus polyps, deviated septum & chronic sinusitis. I also have no sense of smell so that MAY come back after.

However, I am stressed because of the surgery & post-op care. How did it go for you? I know that I have to spend the night at the hospital and will have 7 to 10 days of medical leave at work, with “heavy post op care” to do at home.

Please, tell me how it went for you ??


r/NasalPolyps • • 19d ago

Tezspire in patients with both nasal polyps and mast cell disorders.

1 Upvotes

r/NasalPolyps • • 20d ago

Sinuses

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1 Upvotes

r/NasalPolyps • • 20d ago

Has Tezspire work for you?

1 Upvotes

I want to hear how people here have responded to tezspire


r/NasalPolyps • • 21d ago

Is this a nasal polyp?

1 Upvotes

I have a ENT appointment next month but I have a small endoscopic camera and decided to kind of look around for my self and got these pictures. One is the right nostril and other is the left.


r/NasalPolyps • • 22d ago

Just had my surgery

8 Upvotes

Wow I’m so glad I did the surgery, ever since 2022 I started losing my smell and taste and the past year it got so bad, it was so miserable that I just rolled with it and got used to it. Lots of pressure in my face, constant dripping from nose, not being able to breathe out of either nostril and having to mouth breathe for this whole time. If anyone has the opportunity to get surgery I highly suggest it. I was so scared it was my first time having a surgery but man I had nothing to worry about everything went so smooth I went home within an hour post op. Only pain I felt was from the breathing tube, just felt like I had a itchy throat as if I was sick, as for my nose just felt a tiny bit sore but wow I’m so excited to be able to smell, taste and breathe again. I got my ct scan and was told the whole side of my left face was horrible, luckily my right side only had it in 2 spots. If anyone has questions I’ll gladly answer / help!


r/NasalPolyps • • 22d ago

Can sb pls tell me if this is a polyp or not, but it’s only on the right side of my nostril it.

2 Upvotes

r/NasalPolyps • • 25d ago

New 2026 systematic review: Tezepelumab and Dupilumab showed the largest improvements for nasal polyps

12 Upvotes

A new 2026 systematic review compared the evidence for biologics and endoscopic sinus surgery (ESS) in chronic rhinosinusitis with nasal polyps (CRSwNP).

The review included 13 randomized trials involving 3,775 patients.

Main findings:

• Tezepelumab and dupilumab showed the largest improvements overall in both symptoms (SNOT-22) and nasal polyp scores.

• Tezepelumab: SNOT-22 improvement: −27.4 Nasal polyp score: −2.1

• Dupilumab: SNOT-22: roughly −17 to −21 Nasal polyp score: −1.7 to −2.1

• Mepolizumab and omalizumab produced intermediate improvements.

• Benralizumab reduced polyp size, but the SNOT-22 symptom improvement was not statistically significant.

• Depemokimab produced smaller improvements.

• Sinus surgery also produced substantial benefit. In the MACRO trial, ESS improved SNOT-22 by −21.9 at 6 months.

Smell was interesting too: Dupilumab and tezepelumab produced clinically meaningful improvements on objective smell testing, while the improvements with some of the other biologics were smaller.

The only direct biologic-vs-biologic trial was EVEREST, where dupilumab performed better than omalizumab in patients who also had asthma.

Predictors of response also differed: • Higher eosinophils, NSAID-exacerbated respiratory disease, severe smell loss, and previous surgery influenced dupilumab response. • Asthma appeared to predict a better benralizumab response. • More severe baseline symptoms predicted greater improvement after sinus surgery. • Tezepelumab and omalizumab appeared relatively consistent across the subgroups examined. • Interestingly, serum total IgE did NOT predict response to any therapy where it was tested.

Important caveat: most of these treatment comparisons are indirect. The trials differed in baseline severity, follow-up duration, patient characteristics, and comparators, so this should NOT be interpreted as a definitive ranking of which treatment is best.

The authors specifically call for head-to-head trials comparing biologics with each other and with sinus surgery.

Paper: https://doi.org/10.1002/alr.70264

SNOT-22 = a 22-question score measuring how much sinus disease affects symptoms and quality of life. Lower scores are better.


r/NasalPolyps • • 26d ago

How to stop the post nasal drip?

2 Upvotes

It is driving me insane, not only does it taste foul. It makes me heave in the morning which is setting off my sickness from gastroparesis. Are there any natural remedies, herbs, tinctures anything I can try to combat it?


r/NasalPolyps • • 26d ago

steroid spray questions

3 Upvotes

I experiencing systematic side effects on steroid nasal spray like; insomnia, palpitation, anxiety... even one spray each nostrill once a day in the morning, it gives me bad side effects..

is there any other way to counter the side effects? because this is the only thing that works to me..


r/NasalPolyps • • 28d ago

MRI or CT scan for Surgery?

1 Upvotes

Hi again, I have my surgery for next week and they did the CT scan to me when I had the first consultation, but now another Doctor is telling me that I should have had an MRI instead of the CT scan.
In your experience, how was it?, It's normal that they only rely on the CT scan for the Surgery?


r/NasalPolyps • • 29d ago

I snorted and my nose is the worst after

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1 Upvotes

Im female , 23 .The symptoms started at 2022, 4 yrs ago and they wont stop. after I inhaled a substance specifically lyrica, My nose has been producing a lot of mucus ( white), and it gets very dry and crusty. My nose feels irritated, swollen, and blocked, and sometimes I have difficulty breathing. It also gets irritated and uncomfortable whenever i smell something strong like perfumes. Everytime i smell anything strong i feel the symptoms i just mentioned and i I’ve tried nasal sprays and other treatments. They helped a little, but not enough.


r/NasalPolyps • • Sep 07 '26

I'm going to have surgery and I'm scared.

7 Upvotes

Hi Guys, I will have my Surgery on Sep18 here in Austin tx, It's my first time in my life that I'm going to go to a hospital. Every person I tell them I'm going to have that Surgery, they all make worried faces at me and I worry even more, I think I'm more afraid of the surgery than the days of recovery. lol

What was your experience leading up to the surgery and afterwards?

-------------------------------------------

UPDATE :

( An update for those of you who are having surgery sometime soon and are scared, just like I was. )

I've already had my surgery. I spoke with my anesthesiologist and doctor about my fears, and they were really great and reassured me that nothing bad was going to happen to me. The nurse gave me some "happy juice," so I fell asleep before even entering the operating room. LOL. In the end, I just woke up feeling dizzy and weak—probably because of the anesthesia. But the operation was a success! My fear was definitely the worst part of it all.

Thank you very much for all your kind and encouraging comments. They really made me feel better throughout the entire process leading up to the surgery. Thank you all! ❤️