I started using the alaxo 6" stent on July 1 and want to give a 1 month update. My advice would be take your time and insert it slowly and carefully. I had one bad experience where it was too low in the throat when I expanded it and it was not pleasant... So I just started putting it as far back as I could but I don't think it was the correct sinus and because it wasn't in the throat it was pushing against the roof of my mouth and was pretty uncomfortable. So for the past couple of weeks I put it in at night, laying down, watching tv and just relaxing. I can't stand in the mirror and put it in (it would take too long) and you can feel it internally anyway, because you can't see it by looking in the mirror. Anyway, I tried different angles/directions until I could tell it was in the right location. For me, I have better luck on the right side and angled more toward my nose (rather than cheekbone.) When I find the right position, I can just push it in a little at a time and it goes right into the throat.
Because of the bad experience, I was afraid to put it into the throat, but it was positioned correctly twice this week and I didn't have any pain because it was opening up the palate by being inserted further and not pushing against the soft tissue (when it wasn't positioned further enough in the throat.)
Just know that if you start to deploy it and you feel like gagging or choking, all you have to do is pull it out a little bit and you won't even feel it.
I have used the CPAP machine with the stent 3x this week. The last two times were the best location of the stent in the throat and I got excellent O2 levels that I monitor with a Wellue Ring. Last night my 02 levels were above 93% for 63% of the night; Two nights ago, it was above 93% for 76% of the night. There was one night I didn't use the stent but CPAP machine only; that night my 02 levels were above 93% for 68% of the night BUT vibratory snore events were more than doubled that night.
Anyway, I'm finally getting the hang of this stent and it's not as scary as it was in the beginning. Once I get consistent results I'll compare it to the 5 weeks of data I tracked prior to the stent. I'm also noticing pulse rates above 60 are far less with the stent then with CPAP only which I interpret as your heart not having to work as hard to keep O2 levels up.
I think this screenshot shows what would have been a palatal prolapse breathing pattern but with the stent, it appears that it isn't completely collapsed.
That's all for now. Good luck to all who are trying this. Don't give up.