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Atrial Fibrillation Support

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Information on Vagus Nerve

CDreamer profile image
8 Replies

Just found this site with some good pointers about how to soothe vagus nerve

theheartysoul.com/6-ways-to...

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CDreamer profile image
CDreamer
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8 Replies
CDreamer profile image
CDreamer

PS - please do ignore the adverts!

doodle68 profile image
doodle68

I have trouble performing diaphragmatic breathing , it feels like trying to pat my head and rub my tummy at the same time. I will have to practice :-) .

I tried to explain to my young trainee GP that I though some of my P-AF was related to my vagus nerve and I got the impression she hadn't a clue what I was talking about .

The start of my progression to more frequent/lengthily/severe episodes of AF began when I had a chest infection and had been coughing a lot. For a period of two weeks almost every meal I swallowed from the first bite (not fluids) made me dizzy/feel faint and caused my pulse to race for a few moments until I stopped eating. It was very scary .

When I saw the young arrhythmia nurse who took my details (on behalf of a cardiologist I have never seen) I explained these events to her and she too ignored them and failed to make any mention of them in my notes.

CDreamer profile image
CDreamer in reply to doodle68

Isn't that just so infuriating! I keep banging on about vagal AF and my EP's only comment was - well if it is vagal it will normally start with Atrial Tachycardia so if you can control your HR that will help, that's why we prescribe HR drugs - (which he knows I cannot take!)

Yes - AND you can improve your vagal tone with a little self observation and monitoring and some training. Resting after eating is the one major thing that has helped me along with breathing exercises - I use a power breather - it has also helped clear mucus so I haven't had the chest infections that I was getting.

I don't know why they don't take more notice or offer advice about simple stuff we can do that we can do ourselves? I have decided I am just most odd in wanting this, most others seem to just take a miracle pill and can't be bothered - which is maybe why......

stix profile image
stix in reply to CDreamer

I don't think they understand that part of it, and as you say they don't seem to want to listen they only interested in stopping it, but as I keep saying to them prevention is better than cure so help me understand the cause.

I have friends with AF that get it and are able to just sit and ride it out, where I go in to panic mode and end up with fast AF of 270+.

I will add that I have stopped drinking tea and coffee and eating late at night plus gone over to Sotolol and only had 2 episodes since June 2016 so massive improvement

Redhead1949 profile image
Redhead1949 in reply to CDreamer

Hope you don't mind me asking, but what is a 'power breather'? Thank you!

CDreamer profile image
CDreamer in reply to Redhead1949

I am not advertising but easier to send a link which will explain. You breath in against resistance - like any weight lifting, resistance builds muscle.

amazon.co.uk/d/Sports-Outdo...

Atheletes use it but also people with MS and muscle weakness, I have not had breathlessness since using it & my sats stay high and it is perfect for improving vagal tone because it trains you to breath in slowly and gradually.

songbird74 profile image
songbird74

thanks for this link - really interesting! Not sure my husband will appreciate the talk more advise though!

secondtry profile image
secondtry

Thanks as always for your valuable contributions.

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