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Active life with POTS?
Does anyone else lead a very active lifestyle while being very symptomatic with POTS? I'm pretty new to this while thing, and very close to being dxed by my EP, who's solution has essentially been to stop my level of activity because I'm now to sick to keep going with it, and will hurt myself if I continue. Thing is, I'm a dance minor in college, and at the moment that's not exactly an option for me. I have a tendency to push through my symptoms, and literally the only thing that will stop me is if I'm about to pass out.
At the moment my symptoms are mostly cardiac in nature, and seem to me to be more reflective of IST than POTS. I'm wondering, is it possible to have IST (or other arrhythmias) and POTS at the same time? In my tilt table my blood pressure didn't drop as expected in the head up position, but my heart rate did sky rocket, and generally increase when I was up. I also had a very marked sensitivity to the isoproterenol. For my stress test, I made it to stage 4, but overshot my high target heart rate by 20% (went to 190), and my blood pressure didn't go up after stage 2 (in fact the systolic dropped a few times) before I suddenly got very dizzy, lost my breath completely and nearly passed out. I got very flushed, but didn't break a sweat before the last few minutes. For an hour after my heart rate was 110-135 at rest, and I was very lightheaded, dizzy, shakey, nauseated, and started coughing and wheezing a little. for another hour after that it went down into the 70's, but would jump back to the 120's with the slightest movement (shifting in my chair, adjusting my jacket), standing sent it to 135, along with the dizziness, weakness, all the usual fun- which is how they sent me home, saying I was back to my "normal". It seems to me that I have some level of symptoms nearly all the time, but they're the most exaggerated when I'm active. As a dancer, this is obviously somewhat of an issue. But it seems that my EPs are telling me that the best way to resolve my symptoms would be to stop dancing, this is POTS, there is no cure, I have to give in to it and manage my life the best I can. I'm currently on 25mg toprol, .1mg florinef, and 75mg topamax, which manage things a little bit, but on bad days everything breaks through like I'm taking nothing at all. To make matters more complex, my bp is all over the place at rest (sometimes too high, sometimes too low), but if I take more than 12.5mg of toprol at a time, it sends my bp and heart rate crashing. I'm also intolerant of any kind of ace inhibitor, and my docs are (understandably) paranoid about giving me anything that will raise my blood pressure, although at this point it doesn't seem like it's gone all that high.
My question is, is it possible to lead an active, athletic lifestyle with POTS? Or does it have to go into remission before you can fully resume activity on that level? I suppose what I miss most is feeling GOOD while dancing... I know there was a time when I did. I can still make myself do the motions, my heart is still in it, I just feel like death while I'm doing it. My symptoms are also spilling over into my every day life too, and starting to get in the way of my everyday activities. Before I started testing my doctors didn't believe me when I said how far I forced myself once I started feeling symptomatic. They do now, but their only answer is stop dancing. There has to be another solution. Athletes with POTS, are there any out there?
Another random question: Why to electrophysiologists end up handling POTS patients so often? I know tachycardia is an EP issue, but POTS in general is a dysautonomia issue. Does it simply depend on the patient's worst symptoms or the doctor near them that can handle their case the best?
Thank you in advance!
At the moment my symptoms are mostly cardiac in nature, and seem to me to be more reflective of IST than POTS. I'm wondering, is it possible to have IST (or other arrhythmias) and POTS at the same time? In my tilt table my blood pressure didn't drop as expected in the head up position, but my heart rate did sky rocket, and generally increase when I was up. I also had a very marked sensitivity to the isoproterenol. For my stress test, I made it to stage 4, but overshot my high target heart rate by 20% (went to 190), and my blood pressure didn't go up after stage 2 (in fact the systolic dropped a few times) before I suddenly got very dizzy, lost my breath completely and nearly passed out. I got very flushed, but didn't break a sweat before the last few minutes. For an hour after my heart rate was 110-135 at rest, and I was very lightheaded, dizzy, shakey, nauseated, and started coughing and wheezing a little. for another hour after that it went down into the 70's, but would jump back to the 120's with the slightest movement (shifting in my chair, adjusting my jacket), standing sent it to 135, along with the dizziness, weakness, all the usual fun- which is how they sent me home, saying I was back to my "normal". It seems to me that I have some level of symptoms nearly all the time, but they're the most exaggerated when I'm active. As a dancer, this is obviously somewhat of an issue. But it seems that my EPs are telling me that the best way to resolve my symptoms would be to stop dancing, this is POTS, there is no cure, I have to give in to it and manage my life the best I can. I'm currently on 25mg toprol, .1mg florinef, and 75mg topamax, which manage things a little bit, but on bad days everything breaks through like I'm taking nothing at all. To make matters more complex, my bp is all over the place at rest (sometimes too high, sometimes too low), but if I take more than 12.5mg of toprol at a time, it sends my bp and heart rate crashing. I'm also intolerant of any kind of ace inhibitor, and my docs are (understandably) paranoid about giving me anything that will raise my blood pressure, although at this point it doesn't seem like it's gone all that high.
My question is, is it possible to lead an active, athletic lifestyle with POTS? Or does it have to go into remission before you can fully resume activity on that level? I suppose what I miss most is feeling GOOD while dancing... I know there was a time when I did. I can still make myself do the motions, my heart is still in it, I just feel like death while I'm doing it. My symptoms are also spilling over into my every day life too, and starting to get in the way of my everyday activities. Before I started testing my doctors didn't believe me when I said how far I forced myself once I started feeling symptomatic. They do now, but their only answer is stop dancing. There has to be another solution. Athletes with POTS, are there any out there?
Another random question: Why to electrophysiologists end up handling POTS patients so often? I know tachycardia is an EP issue, but POTS in general is a dysautonomia issue. Does it simply depend on the patient's worst symptoms or the doctor near them that can handle their case the best?
Thank you in advance!
I was extremely active before all this happened, and am now barely able to function. However, there are some things I wish I'd known when this started that would have helped keep what I had. Karinosa is right. Get a heart rate monitor and find the level where your symptoms start going crazy. Then do whatever you can below that level. Over time, you may be able to bump that heart rate up. See if your college or local hospital has a good PT program. They should be able to help you come up with activities that keep your HR in the right range without setting off symptoms. You probably will find that some days you can do a lot and other days almost anything will set it off. Also, see if you can add in more strength training to your routine. This is a good way to keep yourself fit without raising your HR, and some people find that the more muscle they have, the less they get symptoms from POTS.
You may have to take a break from dance for a while, because of all the position changes. I've been doing yoga since I was 8, and have really had to modify it to continue. Anything where my head drops forward, back, or side-to-side will set off dizziness. Anything where I change upper body position quickly will cause me to pass out. Some positions I can get away with by not dropping my head. Some I just have to move slowly so my body has time to adjust. Some days I have to lie down immediately between each position to give my body time to adjust.
I really hope you are able to get this under control and get back to dancing. It's so hard to give up something that makes you feel so good!
You may have to take a break from dance for a while, because of all the position changes. I've been doing yoga since I was 8, and have really had to modify it to continue. Anything where my head drops forward, back, or side-to-side will set off dizziness. Anything where I change upper body position quickly will cause me to pass out. Some positions I can get away with by not dropping my head. Some I just have to move slowly so my body has time to adjust. Some days I have to lie down immediately between each position to give my body time to adjust.
I really hope you are able to get this under control and get back to dancing. It's so hard to give up something that makes you feel so good!
I'm no athlete nor consider mysef in the best of shape, but I do agree with what supineallthetime says that yes we are basically operating like athletes most of the time by how our bodies are responding.
With that said I can tell you what has worked for me, I wanted to get back into circuit training twice a week and my weekly yoga that I used to do before P.O.T.S hit me, this a side from my daily duties of home and my 3 children, well I started this September and I forget who suggested it in this site but I bought myself a heart rate monitor to wear while working out, I figured out that if my heart rate went to 160bpm then I would get the chest pains, dizzines, etc and would feel quite sick afterwards, so I set it to beep at 155bpm and there are days that I can hardly do anything without the constant beep and days that it harldy beeps at all!
As soon as I slow down the workout my heart rate drops and I can continue until it beeps again, I don't know if this would help you but at least it is one way to get around completely dropping your dance. You will just have to figure out what your number is before you feel sick.
The last two weeks I have been unable to work out at all as I have been just way too tired and not feeling right but I have now accepted that some weeks I'll be able to do more than others.
Good luck and let us know how you do!
Karin
With that said I can tell you what has worked for me, I wanted to get back into circuit training twice a week and my weekly yoga that I used to do before P.O.T.S hit me, this a side from my daily duties of home and my 3 children, well I started this September and I forget who suggested it in this site but I bought myself a heart rate monitor to wear while working out, I figured out that if my heart rate went to 160bpm then I would get the chest pains, dizzines, etc and would feel quite sick afterwards, so I set it to beep at 155bpm and there are days that I can hardly do anything without the constant beep and days that it harldy beeps at all!
As soon as I slow down the workout my heart rate drops and I can continue until it beeps again, I don't know if this would help you but at least it is one way to get around completely dropping your dance. You will just have to figure out what your number is before you feel sick.
The last two weeks I have been unable to work out at all as I have been just way too tired and not feeling right but I have now accepted that some weeks I'll be able to do more than others.
Good luck and let us know how you do!
Karin
I'm not really sure about the issue of pushing through symptoms. My impression is that there is a virtual consensus that maintaining the most activity you can, short of triggering aggravation of symptoms, is a recommended overall strategy. I've read that extended rest is generally not beneficial and my personal experiments with that have resulted in very bad setbacks to my abilities (rather than any restorative effect). Modest rest is a necessary part of a cycle of activity, so it cannot be neglected, of course.
I can completely relate to pushing through things, and sadly I know what you mean about not enjoying activities even if you still manage to do them. I have only sparse memory of exercising and feeling good while doing it any time recently.
Some people recommend riding a balance between doing enough and avoiding any sort of "overdoing it". I tend to not be good at that discipline! Luckily I have only been bitten by overdoing it a few times and usually get away with it... others are not so lucky and suffer major setback and symptom increase if they push too hard. It is going to take some experimenting and keen observation on your part to know what works for you. Certainly seek all the advice you can from docs, but their insight will likely be limited and problematic so you're going to have to become a self-taught expert.
I guess the key is assessing how much, if at all, pushing hard through symptoms is biting back at you. Some of us can end up practically in the hospital after too much exertion. It sounds like you are spared from that. I personally think that a "remission" of POTS is basically required to return to that "feeling good while exerting" state... the hard thing to answer is whether pushing through symptoms is getting you closer or farther from a remission or healing up. I guess it's going to vary from person to person and you'll need to experiment. I think we tend to get hit by random setbacks too, so even if you are doing everything right there will be hurdles.
I've rambled a bit without saying much, but I do have one specific observation! I find that the state I am in *while exercising* greatly effects the post-exertion result. I believe this applies to healthy exercisers too. So make sure you're in solid hydrated state and such, prior to exercise... and perhaps make it a minimal day if you're not for whatever reason. Athleticism is often about "pushing limits" so it is complicated to have a condition that counters that.
My general attitude is that no matter what activity we are doing, we're basically operating like athletes most of the time... our heart rates, exhaustion, and strength-of-will necessary certainly indicate that!
I can completely relate to pushing through things, and sadly I know what you mean about not enjoying activities even if you still manage to do them. I have only sparse memory of exercising and feeling good while doing it any time recently.
Some people recommend riding a balance between doing enough and avoiding any sort of "overdoing it". I tend to not be good at that discipline! Luckily I have only been bitten by overdoing it a few times and usually get away with it... others are not so lucky and suffer major setback and symptom increase if they push too hard. It is going to take some experimenting and keen observation on your part to know what works for you. Certainly seek all the advice you can from docs, but their insight will likely be limited and problematic so you're going to have to become a self-taught expert.
I guess the key is assessing how much, if at all, pushing hard through symptoms is biting back at you. Some of us can end up practically in the hospital after too much exertion. It sounds like you are spared from that. I personally think that a "remission" of POTS is basically required to return to that "feeling good while exerting" state... the hard thing to answer is whether pushing through symptoms is getting you closer or farther from a remission or healing up. I guess it's going to vary from person to person and you'll need to experiment. I think we tend to get hit by random setbacks too, so even if you are doing everything right there will be hurdles.
I've rambled a bit without saying much, but I do have one specific observation! I find that the state I am in *while exercising* greatly effects the post-exertion result. I believe this applies to healthy exercisers too. So make sure you're in solid hydrated state and such, prior to exercise... and perhaps make it a minimal day if you're not for whatever reason. Athleticism is often about "pushing limits" so it is complicated to have a condition that counters that.
My general attitude is that no matter what activity we are doing, we're basically operating like athletes most of the time... our heart rates, exhaustion, and strength-of-will necessary certainly indicate that!
RA,
Hopefully someone will be able to answer your question. I'm very new to this, just diagnosed with dysutnomia (if they're correct), and just starting treatment with propranolol.
My opinion, and that's all it is, is that everyone will react differently. Some will see their life return to almost normal, and others will not.
Over the last 4 couple of years, I've gone from working 70 to 90 hrs per week, kick-boxing and yoga nearly every day, weight-lifting, etc., to barely being able to work 4 hours per day (and that was more tiring than a 90 hr work week)... So, I guess time will tell, whether anything works for me, or whether or not things go through cycles.
Hopefully, some one will answer your questions soon.
Take care.
Mar
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