Greentext

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This is a place to share greentexts and witness the confounding life of Anon. If you're new to the Greentext community, think of it as a sort of zoo with Anon as the main attraction.

Be warned:

Anon is often crazy.
Anon is often depressed.
Anon frequently shares thoughts that are immature, offensive, or incomprehensible.

If you find yourself getting angry (or god forbid, agreeing) with something Anon has said, you might be doing it wrong.

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Early_To_Risa@sh.itjust.works

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Anon is a test subject (sh.itjust.works)

submitted 4 months ago by Early_To_Risa@sh.itjust.works to c/greentext@sh.itjust.works

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[–] Mycatiskai@lemmy.ca 1 points 1 month ago (1 children)

To anyone not aware of sleep apnea it wouldn't seem like there was anything wrong with my sleep. I don't snore, I just don't breathe continuously when unconscious.

It took about 2 years to fully recover mentally from decades of this shitty sleep. I only found out from visiting my parents and my mom saw me not breathing while I was asleep on the couch. I've also had 6 sleep studies in 11 years to try and figure out why it is happening but it is idiopathic.

I can't remember what people on Reddit with UARS found to be the best treatment but the biggest step always seemed to be getting a doctor to diagnose it properly instead of just signing it off at regular sleep apnea. I hope you find a treatment that helps. The brain can bounce back, so don't give up hope that you can get your mind back.

[–] BugleFingers@lemmy.world 1 points 1 month ago

Thanks, I am trying to stay hopeful. My next step needs to be an ENT and probably to fix a collapsed nasal cavity. I worked with a neurologist for 3 years (where the sleep studies came from) but they ended up leaving state for persona matters. I live in the USA so I have to go through insurance which doesn't really recognize UARS. Though I did scratch my way into diagnosis of apnea (sleep study recorded just above the 5% oxygen drop required by insurance) they refused to let me test with a CPAP. It was the only diagnosis my neurologist could use to get insurance to help, still, they won't really do much for me.

Hopefully soon I can sit in one place without the threat of falling asleep. Or wake up feeling rested and not my eyes burning feeling like I was hit by a brick lmao. Sleep issues are no joke and you're right to tell people to make sure people get it properly handled ASAP