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Low Pressure Systems


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Just wondering if anyone else is bothered by low pressure systems? We have a storm coming in AGAIN, and I can really feel it, as I always do. I get more short of breath, more fatigued, and just over all feel worse. This has been going in since moving to Colorado, where I generaly feel worse anyway. Also does elevation affect your POTS? When taking a trip, we had to go over a mtn pass, and it was all I could do not to pass out, and my chest felt like it was going to explode. This has happened every time we have traveled to higher elevations in the past few yrs. Any thoughts?

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I have problems and flares with any barometric pressure change. So each time the weather changes I flare...that of course could be daily. I happen to do a bit better in low pressure but I think that is related to my migraines. I just need to find a place where it is 60 degrees, sunny, and has a soft occassional breeze 365 days a year. :-)

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Have the same issues...shortness of breath, more pain, migraines, overall fatigue/weakness etc are much worse with pressure changes. Altitude also affects a lot of people. We're at 5700'. I don't notice altitude so much as humidity and weather changes in general though.


Here's a link to another thread where we discussed this in the past- if you want more input as well

http://forums.dinet.org/index.php?/topic/14802-linking-barometric-pressure-and-how-we-feel/

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I get terrible POTS - the worst when there is a storm coming in.

I actually read this when I first got POTS and honestly thought it was very doubtful.

But over time I did indeed notice a definate pattern to the point where if I have a sudden bad day I check the weather forecast and sure enough a high is moving to a large low with a storm quite often. makes February over here a pain in the butt.

Even weirder though is that sometimes it gives me bad Ank Spond so to me it could be immune-activation for some reason.

Other potential possibilities are ofcourse histamines or serotonin (as both are postulated to increase before and after a storm hence storm migraines).

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My son has the same problems. However what I have noticed this year so far is that sometimes his symptoms do not flare as bad with the weather changes. Just wondering if this has anything to do with how his body is adjsting to the POTS.

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Katybug- I think you're right that it's well accepted with regards to migraines. I have not however had any success with having it acknowledged in relationship to POTS symptoms by any of the specialists I've seen. Ironic, given that those very same specialists do acknowledge the connection between the migraines and the POTS.

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I'm thinking that affects our blood flow and the effects of vasoconstriction vs. vasodilation. If there is more pressure there is greater external pressure on our veins too - like instant compression ---only it would cover our entire body. That could give more headaches and it could also contribute to more POTS symptoms.

Chaos, I have real problems when I try to go back to CO where the family is at 7,000 feet. The difference between 5,000 and 7,000 is huge for me. I have to sleep with oxygen there. I can feel the difference when riding in a car between the altitudes - even subtle differences affect me.

Issie

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Issie, so many times I've felt like I needed oxygen, but Drs I've seen so far don't. ( Going to Mayo in March)I live in Co, and you can't hardly travel anyplace that you don't reach elevation above 5000. How do you qualify? For the last 6 months or so, I have had more trouble with my lung, than ever before.

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Chaos...you're probably right but my migraines are so bad and so intertwined with my POTS symptoms that I think my docs don't differentiate where one begins and the other ends too much anymore. Plus my neuro specializes in dysautonomia and headaches. He is a firm believer that migraines are very closely linked with dysautonomia but just doesn't know what the link is.

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Issie, so many times I've felt like I needed oxygen, but Drs I've seen so far don't. ( Going to Mayo in March)I live in Co, and you can't hardly travel anyplace that you don't reach elevation above 5000. How do you qualify? For the last 6 months or so, I have had more trouble with my lung, than ever before.

I had to do an oxygen study when I was at altitude and see what my O2 was while trying to sleep. Most docs will order this and some places do it for free - but, insurance will pay for it. If your O2 drops below 90 they usually will let you have some oxygen at night. I started out renting a concentrator - but, found that if your insurance doesn't let you outright buy one - it may be better with your co-pay amounts to just purchase your own. You have to have a script to purchase one and I got a script and have my own concentrator. I take it with me when I go to higher altiutudes and sometimes even use it when down lower if my O2 drops out on me.

Issie

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I had real problems when I was at altitude last fall in California. We went to Yosemite and I didn't have any severe issues, but we went to King's Canyon & Sequoia and I felt like I was on my death bed. The altitude there ranged from 4,000 to 6,500 feet. I had tremors, felt short of breath and was almost in a state of stupor as I felt like I was slurring my words. My symptoms got better (back to my normal crappy feeling) once we descended to around 2,000 feet. Not sure why I didn't feel as bad in Yosemite as we were at altitudes of close to 10,000 feet.

I have felt bad with low barometric pressure, but haven't yet determined whether there is a true pattern for me.

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i Live in Colorado also and that storm around the 19th really hit me also. I have noticed that it's the dropping of the barometric pressure that is the trigger and usually it is steep, long drops that trigger thenworst symptoms. Once the pressure levels out, even if it is much lower, my symptoms usually abate a bit. I know here in Colorado sometimes it's just a beautiful sunny a very nice day and I'll feel like crap I wonder why until I check the barometric pressure. Or sometimes I wake up the next day and a big storm has moved in and then I realize why I felt so bad the day before.

any of you colorado folks have a local doc who understands Dysautonomia and keeps up with the research?

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Voner, I'm in western Colo, and I hate Drs here. It finally took a Dr coming from Denver to the western slope, for me to get any real help. She is the one who gave me a referral to Mayo Az. Her exact words to me though were, " I really can't help you with this problem, but we'll get you someplace that can." So still no one here in town. UGH!!

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