Afraid to sleep. Most episodes happen at night. What can I do?
Hi. New here. Was diagnosed with paroxysmal Afib in March and was hospitalized in ICU. Now realize first episode was probably in Sept. They happened about once every three months but now more than once a month. I live afraid. Not sleeping at all since most episodes happen at night. Last night had one and pulse was 208. Drove to er parking lot and took the Flecanaide pill In the Pocket for the first time. It cardioverted me after about an hour. Came home and have been up all night. Afraid to sleep and it happening again but no sleep triggers episodes so it’s worse. I don’t know what to do. I had taken a Xanax .25 during the day yesterday because I felt anxious and had lots of PVC/PAC so I figured it was going to be a bad night. I hadn’t slept in about 3 days. And that’s exactly what happened. The Xanax did nothing though which was strange. PVCs/PACs continued , was extremely nervous and afraid and went into Afib. Can someone recommend what I can do? I need to sleep but afraid to close my eyes and sleep. Actually afraid all day. This has changed my life and I am nothing of who I used to be. I don’t know how to live like this. Thank you for any answers you can provide.
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Update
Early this morning I had Afib. I thought I was doing good. I’m on carveldilo. I’ve had Eliquis induced stomach problems for 5 months and the Afib has really kicked in (Eliquis is bad for me)
My Afib nearly always comes around 1-2am with a gas bubble. But not this time no gas bubble but I did gently introduce a few new foods back into my restricted diet..
Since the heart rate was seldom over 110, I decided to try things.
Lymphatic massage and tapping would keep the Hrt under 75.
But it wouldn’t convert. Cold water didn’t work. Tried the bath room, no luck.
Warm chamomile tea with the hot cup sitting on my chest felt amazing, with an HRt of 60-70, but wouldn’t convert. Got a warm pack with a slight chest massage felt amazing too, didn’t convert. It’s been 1 hour and 45 minutes so far.
Then…even though I had no chest bubble, I took Pepcid. Guess what 10-15 minutes later I converted and went back to sleep. This morning when I awoke the first thing I did was 5 big burps.
Why won’t the Dr’s listen ?? Let’s fix the stomach or the vagus nerve. No they’d rather an ablation that they said would be a 50 -80% chance of working? Or more drugs. At least with acupuncture I’m way more chill about this.
Thanks for your insight on sleep apnea and CPAP machine. I definitely agree with you and will look into purchasing one. Do you know if Medicare covers these machines?
Either way, I will get one and start using it asap. That way, it will not only help my heart somewhat, but it will also prevent my wife from having to worry about me whether I am breathing or not during the night.
Thanks again.
This comment is wisdom! Please listen to it and than talk to your DR! 🙂
I live in Canada and have no connection or knowledge about health care in the USA....sorry. I would guess that, with a formal diagnosis from a qualified MD, you should have 'some' help getting a CPAP machine.
Have you been tested for sleep apnea. My heart was beating so fast at night that it woke me. I am now on a CPAP machine and my heart is not having to react to apnea episodes.
Has anyone had any experience with Aspire - as alternative to CPAP. I have mild-moderate sleep apnea which I have chosen largely to ignore; I get a little relief from sleeping with elevated head/shoulders from my raised mattress but find a CPAP claustrophobic. I am concerned, tho, if ignoring it is bad for my heart health. Since my ablation about 1&1/2 yr ago I have been AFIB-free but still concerned about general heart health