Anyone have Laryngeal Sensory Neuropathy?
I am looking to talk with anyone that has been told they have larynx sensory neuropathy. In other words, over active nerves in the larynx.
Interested in more discussions like this? Go to the Ear, Nose & Throat (ENT) Support Group.
I'll def try Fisherman's Friend lozenges, too. I have found that when I'm too hot it triggers cough. When I am rushing it triggers cough. And of course, one can't just sit still all day so I have to really time myself. I've stopped the steroid shots in my neck for now and am off all neuro meds. I am seeing an acupuncturist about once a month hoping that will help. Good luck with all you try.
Hello. I feel your pain. Same thing here for over a decade, worsened during Covid. It’s definitely a quality of life issue. Am seeing an ENT next month who deals with larynx and will see where that goes, followed by allergist because I have bad allergies. Have you seen an allergist? Is it worth taking Gabapentin (side effects?) and Amitriptyline if they don’t really help? Or do they reduce your severe cough somewhat? I think there’s a lot more of us out there. Hoping medical community comes up with a solution.
I’ve used Ricola for years. I can’t be without them. Will look at Fisherman’s too.
I have laryngeal dysphonia (spasmodic dysphonia). Started with the very first covid, self-treated, fungal infection in throat. Saw an ENT who diagnosed it with silent acid reflux and spasms in larynx. Referred me to a ENT/Laryngologist. They told me not to use menthol cough drops but to use Breezer's instead. Also I found that gargling with warm salt water does help to get the phlegm out. I get allergy injections once a month that help too. Now I am getting Botox injections to the throat so I can talk. I feel your pain, it is very troubling and frustrating. Blessings.
I just tried going off the Gabapentin and Amitriptyline to see what would happen. My cough definitely got worse so apparently they are working. I did see an allergist and took allergy shots for 2 years but that didn't help at all. I'm seeing a new ENT now because I have developed severe mucous in my throat which increases my coughing. He recommended a sinus rinse which I hate using but it definitely helps so will continue with that. I'm waiting for a miracle cure. LOL..
A miracle cure! Would love that! I have the chronic throat-clearing and cough due to post nasal drip too. Was looking forward to allergy shots to minimize that. But they didn’t work for you which is so disheartening. If your ENT comes up with something that alleviates the symptoms please let us know!
I have LSN and have for all my life (72 years). It has gotten progressively worse over the years and is very bad by now. Following every possible treatment (including a tonsillectomy) years ago, and test after test (at National Jewish Health (Denver) for seven days straight, it was concluded that I have LSN....an "over sensitive larynx".
At this time, the only POSSIBLE medication for LSN that I have found through research only that does help is called Gefapixant (LYFNUA). Studies showed that it helped 85 % of the patients (subjects in the study).
Unfortunately, it is ONLY available in Japan at this time. Merck Pharmaceuticals did a study on it and the FDA did not approve it (March 2022) due to a side effect of a metallic taste left in some "subjects" mouths. I have been in contact with Merck and two different people there have told me that there are "documents" saying that they will revisit their request. Hopefully, this will happen soon!
My triggers are any odors (good or bad) and cold drafts. I ALWAYS carry a thermos with hot, hot water, and Ricola cough drops. I wear knit scarves a lot. When I go into a store and cough, of course I wear a mask, and I just tell people who give me mean looks, "I'm fine. I have asthma" ....which I do not really have! Lakarol lozenges, (order on Amazon) under my tongue, helps to keep my throat moist. A voice therapist told me to exhale slowly through the nose.
Those are my suggestions. I have researched this for many years (before the doctors or anyone knew what LSN was). Now that the doctors have labeled this, we need to hope that Gefapixant or another medication or procedure will one day be available in other countries.
Perhaps we can all telephone Merck Pharmaceuticals and pressure them to revisit their study in hopes that the FDA will soon approve that medication!
Ronda
Welcome @rondakalan18. You sure have done your research. I see that there may be another potential drug in development by Bellus Health Inc (BLU.TO) called BLU-5937.
Hi
I’ve had LSN for several years and like you I was getting worse whilst going through multiple tests to finally get a diagnosis from a neurologist and respiratory physician. At one stage I was ventilated because of a severe intractable laryngeal spasm.
I take gabapentin which does work to some extent however I’ve got the greatest benefit from CPAP normally used for sleep apnoea. The theory is that it splints the larynx whilst you sleep and over time retrains it.
I also have several
Other neurological conditions being treated by an immunologist, neurologist and ENT and am looking at a complete change of therapies.
I hope you get some relief
Thank you for your reply. I will discuss that with my otolaryngologist.
Ronda