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» LymeNet Flash » Questions and Discussion » Medical Questions » How do you exercise with POTS or tachycardia?

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Author Topic: How do you exercise with POTS or tachycardia?
CD57
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I need to get back into exercising/swimming but even climbing stairs has me out of breath. I am woken at night with tachycardia also, when lying flat. I am not on regular meds for any of this but do have an RX for a beta blocker, which I am trying to avoid. I take salt and electrolytes.

How do you exercise with this incredibly annoying problem?

Posts: 3528 | From US | Registered: Apr 2007  |  IP: Logged | Report this post to a Moderator
WPinVA
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Can you manage five reps of arm curls with very light weights, like 3 pounds? And then you can work up slowly. Or very slow short walks? That was all I could do, but it's better than nothing.
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Keebler
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Pilates, Yoga, Qi Gong, Tai Chi. Even lying down, some of these can be fashioned to your level.

Are you taking a good kind and enough magnesium? Other minerals, too? Magnesium can calm a racing or out of synch heartbeat.

Hawthorn has some beta blocker properties. It's in the Cardiac thread.

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www.mbschachter.com/importance_of_magnesium_to_human.htm

The Importance of Magnesium to Human Nutrition

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http://flash.lymenet.org/scripts/ultimatebb.cgi?ubb=get_topic;f=1;t=077325;p=0#000000

Topic: To everyone with CARDIAC symptoms please read!

Includes articles & discussion about exercise safety & methods. Adrenal support is also included as that is essential with POTS.
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opus2828
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I take a very low dose atenolol beta blocker - I take it in pediatric liquid so I can control the dose. I take 4.5 mg twice a day and 2 mg at bedtime. I am med sensitive and it seems to help some.

I exercise on a recumbent bike or rowing machine. Everything in supine position if possible. It doesn't always work but it is better than nothing.

I found that taking just 1/2 of a .5 klonopin at night helped adrenaline surges that were causing tachy. I seem to be sensitive to adrenaline.

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CD57
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Interesting Opus. The adrenaline surges can be caused by low adrenal function. Do you support adrenals?

Swimming should be good too then, since it's supine.

I am often woken up by racing heart so it seems my issue may be POTS but something else too, as lying supine can cause this. Thoughts?

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opus2828
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People with POTS can get high adrenaline which can cause tachy while lying flat as well.

I also seem to get it after eating.

My adrenals are not good - my LLMD is doing a saliva test for that.

I think all of the symptoms are from the autonomic nervous system being damaged from lyme and possibly babs as well.

The test for POTS is an increase in heart rate of 30 beats per minute or more when you go from lying to standing.

A lot of times there are blood pressure issues too.

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kisekis
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so i was wondering do people with dysautonomia/POTS supposed to have no tachycardia/palpitation when exercise/do activity/exertion supine?
maybe like lifting themself or something heavy. or push-up/sit-up.

does getting tachy, palp after eating also the symptoms of POTS/dysautonomia?
i read it also related to blood volume? also insulin.

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Summer3
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I am having a VERY tough time with exercise since starting treatment for tachycardia and low BP. Before I could still force it, now I'm completely out of breath and exhausted.

My HR before got up to 180 just walking up a hill and now on a beta blocker it's rare for it to get much higher than the high 70's.

As soon as I'm feeling better I'm going to try reconditioning again. I used to be a runner.

Kisekis, I get a lot of palps after eating and sometimes even faint. I believe that's called postprandial hypotension. It's where the blood pools in your stomach for digestion. The treatment (non-medication based) is to eat small low-carb meals instead of large ones.

CD57, I was VERY against taking the beta blocker, but I have to say that I never realized how many skipped beats and heart irregularities I had until I took it and they stopped. They were a lot more frequent/worse than I realized. I must have gotten used to my heart beating like that. I take metoprolol 25 mg and 12.5 mg per day. It does make me more out of breath though.

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LymeMECFSMCS
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Look up the Vanderbilt (I think) research on astronaut POTS/OI and recumbant bicycle training/recovery. I'm too sick to do it myself, but that's what I would do (astronauts often have POTS/OI).
Posts: 929 | From Massachusetts | Registered: Oct 2007  |  IP: Logged | Report this post to a Moderator
   

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