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 developed a cough when I was in college - it got worse quickly. I noticed that it was worst when I was studying Algebra - no kidding! In Algebra class, I started coughing convulsively until I got muscle cramps in my abdomen - I had to step out so the other students could hear the professor. My algebra book was brand new ... I figured out that micro-particles from the ink were floating into the air as I read, it was printed in soy ink, I'm allergic to soy beans. I started wiping each page with a slightly humid cloth before I read it to keep the particles down. I coughed less, I muddled through that class and escaped with a B. Peggy
Those are my exact conditions, I was on gabapentin for a bit had improvement but had side effects ; so went on Lyrica last 2 months. Its helped make it more manageable but first bit of food triggers it for 1-2 hours. Lyrica causing me to gain +15 pounds in 8 weeks so going to get off and try something else I hope. I have been suffering since I had bronchitis in Feb 2019. Cough was chronic before the drugs but just maintainable now but no cure and side effects from drugs not helping
Hi @jaygats, Welcome to Connect. I ran across this blog that seems like it might be helpful.
Laryngeal Sensory Neuropathy How to Diagnose & Treat and its Relation to LPR
-- https://www.wipeoutreflux.com/laryngeal-sensory-neuropathy/
Did your doctor diagnose you with Laryngeal Sensory Neuropathy?
I tried putting hot sauce on my first bite of food, and it does coat the area and gives it a numbing effect. I read in another blog about capsaicin spray. Not sure it wouldn’t aggravate reflux symptoms.
I tried the pepper capsule supplements at each meal. Most of the time the “heartburn” sensation got eliminated. I eat spicy foods too which I think help.
I have had a chronic cough for 30 years. I have been told I have LSN. I have tried EVERYTHING including Botox injections, amitriptyline, two complete workups at National Jewish Hospital in Denver, CO. I have allergies that are managed with over the counter antihistamine. I am on a small dose of omeprazole. I have tried speech therapy. Nothing so far has worked. I have read through the post and was curious about the voice therapy using a Kazoo? Any other suggestions would be helpful. Thank you
Your symptoms exactly mirror mine. Ohio State doctor started me on Tramadol and Lyrica which gave me 80% relief but I still cannot sing without coughing and when become stressed the coughing increases......not fun. I have been diagnosed with Laryngeal Sensory Neuropathy.
Pleased to discover this site and Connect
I have larynx sensory neuropathy and here I have found others who suffer the same condition. The greatest frustrations I have experienced with the Australian medical system to date are a. that doctors don't listen to me and b. give me so little information. I also have Mac lung disease and the blogs/groups for this have been of enormous benefit to me over the past 4+ years.
@joanna48 Welcome to Mayo Clinic Connect! I found that exactly what you pointed out, is a major reason this site is comfortable. While we each have our own journey with health issues and concerns, others are here to help us along! There is no "one-size-fits-all" and listening to others can give us hope. The website for Mayo Clinic itself offers so much information. https://www.mayoclinic.org
Here is the discussion group for lung health https://connect.mayoclinic.org/group/lung-conditions/
One for neuropathy https://connect.mayoclinic.org/group/neuropathy/
And one for ear/nose/throat https://connect.mayoclinic.org/group/ear-nose-throat-conditions/
Please feel free to wander through the different conversations and join in!
Ginger
@joanna48 Welcome to Mayo Clinic Connect, a place to give and get support.
We are happy you found Connect too.
You'll notice I moved your question to an existing discussion on larynx sensory neuropathy. I did this so you could connect with members like @avmcbellar @arlinebringhurst @tkubby @kimduncan1211 in a central location.
You may wish to scroll through the previous posts in search of information and connection.
May I ask how you are managing larynx sensory neuropathy and MAC lung disease?