Hey everyone! I haven’t followed up since my last post about my CPAP experience. I have been reading your posts though and continually hope you all find answers.
If you remember, using a CPAP increased my apnea events significantly and left me sleep deprived to the point I couldn’t even walk. I did do a sleep study at a sleep center. It was supposed to be a split night, 1/2 without the CPAP and 1/2 with. I never even met the criteria to need one, so I quit the CPAP entirely.
The great news is my legs recovered fully. It took some time though. It shows how incredibly important sleep is!!
However my body is an attention seeker and I caught a cold and then entirely lost my voice. Everything was so tight from the roof of my mouth going down my throat it seemed paralyzed.
After lots of scans and tests, nothing could be found. I finally saw an ENT last week who used a camera and found thick callouses on my voice box! He said it’s from coughing so hard. Now I’m not supposed to talk or whisper for six weeks to let them heal.
it’s already been 30 days with no voice. It’s very isolating to not speak. But at least the ent said my nerves are fine so it’s not MS related. Every ER Dr wants to find a MS connection so it’s tricky.