Aa
What helps?!
I have had a horrible flare up of my POTS and have hardly left my house in a month because it has been so bad. I feel like I start to see some improvement but then it just gets horrible again. What do you do when you have a flare up to help get back to "normal" POTS symptoms?
Sorry for the mix-up! Confused you with someone else who PMed me this week with a similar flare-up!! Is there something with the snowstorms that is throwing everyone off balance or what? Oy! At any rate ... sorry, again, here's my response to you ...
Just from what you said, from your currently elevated rather than dropped pressures, it sounds possibly like H-POTS? Is that kind of where you tend to be (rather than the PD form)? For clarification, here's an article from Dr. Grubb that describes the two:
http://circ.ahajournals.org/cgi/content/full/117/21/2814
Have you ever been on Clonidine in the past? And if so, did that work for you at all? It might be something to ask your doctor about.
I also wanted to clarify a bit about your symptoms. I think what you're describing in terms of blood pooling in your head region (nose/ears) may be flushing rather than blood pooling. Blood pools according to gravity, and only in regions with large vascular beds or veins (the "abdominal bed" or "splanchnic bed" is full of vessels, the walls of which can expand allowing a large volume of blood to accumulate in the abdomen; likewise, blood frequently is known to pool in the "dependent limbs," typically the feet and lower legs where vessels likewise swell and accommodate an overly large volume of blood rather than circulating it back to the heart). I can explain this in greater detail if you'd like, but in a nutshell, you wouldn't see blood pooling "up," particularly in an organ that doesn't have heavy vasculature like the ear (which is comprised mainly of cartilage with a thin layer of tissue over that).
Flushing, on the other hand, can cause bright redness in the facial and upper trunk region (as well as the feeling of heat), and is a common symptom of dysautonomia. If you would like to see pictures of flushing, you can search online or click through to my MedHelp profile and browse my user pics (I've posted a few pics on there). I also have pics of the discoloration (sometimes called acrocyanosis) in my legs on there also if you want to see what that looks like. Click my username in blue at the top of this post to get to my profile page. Here are web links (to pictures) as well:
Flushing Pics-
http://topics.dirwell.com/health/5-common-causes-and-cures-for-facial-flushing.html
Acrocyanosis (Note that diff docs use diff terms for same discoloration) Pics-
http://www.ipej.org/0602/raj.htm
http://www.nymc.edu/fhp/centers/syncope/POTS.htm
I've never heard of getting blisters from anything related to dysautonomia, certainly not from blood pooling. The only thing I can think of is if you are having peripheral neuropathy and getting blisters from a pair of shoes or something unknowingly because you're not realizing the sensation due to the neuropathy. I would see your general practice physician about those as soon as possible to try to identify the cause, and see if it warrants a referral to a neuromuscular specialist for a workup to rule out neuropathy. Your GP may find some other cause instead, maybe something dermatological; I'm not sure. It's always wise to err on the side of caution, though, considering how many "issues" can go hand-in-hand with autonomic disorders. Ugh, right?
I'm sorry to hear about the panic attacks. Has your doctor suggested a medication specifically for that? I highly recommend you check out the threads on our forum here where we've been discussing Clonazepam and Anxiety (I think if you look for those words in the topics, you'll have no problem finding them on the main Dysautonomia page, but if you do let me know). Quite a few of us have taken some type of anxiolytic, mainly forms of benzodiazepines, which can help to "calm" the central nervous system "oversensitization" that can occur with dysautonomia (especially forms with overactive sympathetic nervous system as in POTS). This is something you might also want to ask your doctor about, or you may want to ask for a referral to a counselor. But it's important to remember that there's a gray line between where the physiological symptoms of dysautonomia are and any "emotional/mental" symptoms of an anxiety disorder may be and that any counselor you see should be made aware of this, hopefully by a letter explaining your condition in brief from your doc. Reading the links from those other threads I mentioned should help clarify this.
Okay, it's WAY too late for me now. Let me know if you have more questions.
-Heiferly.
Just from what you said, from your currently elevated rather than dropped pressures, it sounds possibly like H-POTS? Is that kind of where you tend to be (rather than the PD form)? For clarification, here's an article from Dr. Grubb that describes the two:
http://circ.ahajournals.org/cgi/content/full/117/21/2814
Have you ever been on Clonidine in the past? And if so, did that work for you at all? It might be something to ask your doctor about.
I also wanted to clarify a bit about your symptoms. I think what you're describing in terms of blood pooling in your head region (nose/ears) may be flushing rather than blood pooling. Blood pools according to gravity, and only in regions with large vascular beds or veins (the "abdominal bed" or "splanchnic bed" is full of vessels, the walls of which can expand allowing a large volume of blood to accumulate in the abdomen; likewise, blood frequently is known to pool in the "dependent limbs," typically the feet and lower legs where vessels likewise swell and accommodate an overly large volume of blood rather than circulating it back to the heart). I can explain this in greater detail if you'd like, but in a nutshell, you wouldn't see blood pooling "up," particularly in an organ that doesn't have heavy vasculature like the ear (which is comprised mainly of cartilage with a thin layer of tissue over that).
Flushing, on the other hand, can cause bright redness in the facial and upper trunk region (as well as the feeling of heat), and is a common symptom of dysautonomia. If you would like to see pictures of flushing, you can search online or click through to my MedHelp profile and browse my user pics (I've posted a few pics on there). I also have pics of the discoloration (sometimes called acrocyanosis) in my legs on there also if you want to see what that looks like. Click my username in blue at the top of this post to get to my profile page. Here are web links (to pictures) as well:
Flushing Pics-
http://topics.dirwell.com/health/5-common-causes-and-cures-for-facial-flushing.html
Acrocyanosis (Note that diff docs use diff terms for same discoloration) Pics-
http://www.ipej.org/0602/raj.htm
http://www.nymc.edu/fhp/centers/syncope/POTS.htm
I've never heard of getting blisters from anything related to dysautonomia, certainly not from blood pooling. The only thing I can think of is if you are having peripheral neuropathy and getting blisters from a pair of shoes or something unknowingly because you're not realizing the sensation due to the neuropathy. I would see your general practice physician about those as soon as possible to try to identify the cause, and see if it warrants a referral to a neuromuscular specialist for a workup to rule out neuropathy. Your GP may find some other cause instead, maybe something dermatological; I'm not sure. It's always wise to err on the side of caution, though, considering how many "issues" can go hand-in-hand with autonomic disorders. Ugh, right?
I'm sorry to hear about the panic attacks. Has your doctor suggested a medication specifically for that? I highly recommend you check out the threads on our forum here where we've been discussing Clonazepam and Anxiety (I think if you look for those words in the topics, you'll have no problem finding them on the main Dysautonomia page, but if you do let me know). Quite a few of us have taken some type of anxiolytic, mainly forms of benzodiazepines, which can help to "calm" the central nervous system "oversensitization" that can occur with dysautonomia (especially forms with overactive sympathetic nervous system as in POTS). This is something you might also want to ask your doctor about, or you may want to ask for a referral to a counselor. But it's important to remember that there's a gray line between where the physiological symptoms of dysautonomia are and any "emotional/mental" symptoms of an anxiety disorder may be and that any counselor you see should be made aware of this, hopefully by a letter explaining your condition in brief from your doc. Reading the links from those other threads I mentioned should help clarify this.
Okay, it's WAY too late for me now. Let me know if you have more questions.
-Heiferly.
Shari,
Ummm, no, I'm not exactly a POTS patient but that was my diagnosis at first ... now mostly my docs are just calling it Dysautonomia ... it's complicated, lol. Basically I sort of bleed outside of the edges of what one would "normally" see in a POTS case, so it's tending away from that. Not important to your stuff at any rate. No, I didn't start this forum ... I suppose MedHelp did, technically. One of the other co-CLs (Community Leaders) here (there are three of us in Dysautonomia ... we're the ones with purple flowers by our names ... you can find CLs in the various patient communities) was the first here in Dysautonomia: Halbashes. You may see her pop in and out now and then; she's a bit busy now because she just got her port (a type of semi-permanent IV line) put in for her IV treatments and is recuperating from that surgery and getting accustomed to her IV pump and all that.
As to how I know however much I know, I read peer reviewed medical journal articles and medical textbooks out the yin-yang! :-p My educational background provided a firm basis in the "hard sciences" at two top-notch universities, so I guess I was well prepared to suddenly fall terribly ill at the age of 27 and go into early retirement. So this is my hobby? I volunteer here helping other patients access the info and support they need. I hope I occasionally succeed. :-D
On to YOU! Yes, in my travails through studying random medical stuff, I have heard of CAH, actually. Don't worry about the fludrocortisone, some people tolerate it and some don't and there are lots of other treatments out there. The Midodrine may take a bit to see if it works for you, especially if you're starting with a small dose and your doc wants to play with the dose a bit to see if that can get to a good point for you; also, if you get side effects from that, one thing to note is that for most patients those will go away pretty quickly (about a week or two I think once you get to a given dose) so my advice is give it a chance even if you get something "weird" like the goosebumps from it unless it really REALLY drives you nuts. Because Midodrine is one of the biggest helps for the biggest number of dysauto sufferers that I've seen (both anecdotally speaking and looking at the studies to back it up), and anecdotally speaking, some of the times it fails for people it seems like a part of it is not giving it a long enough shot or not "muscling" through side effects for at least a week or two to see if they go away. I hope that doesn't sound awful. I just think, personally, in the grand scheme of things that if something can improve your quality of life FOREVER, one crummy week or two is worth it. At least to me, your mileage may vary, don't kill me if you suffer through a week of goosebumps for nothing, LOL.
If I haven't said this somewhere you've seen it already, do check out our list of treatments in our health pages (link in the top corner of the page by the little yellow icon ... it says "Health Pages" ... we share with all the other Neurology people so just look for Dysautonomia related topics in the list ... there's a link in there of Dysautonomia Treatments that talks about different meds and such ... not all are appropriate for POTS in particular but you can see that there's a lot out there so don't lose hope if your first efforts at trial and error with meds aren't successful). Whoa, holy run-on sentences, Batman!! Sorry, I said I wasn't at my peak performance today, and I meant it!!!
Moving on ... Cardiologists can make AWESOME POTS docs, particularly EP cardiologists. That is, electrophysiologist-cardiologists. Sometimes, they're better than neurologists for POTS in particular, because it has such a cardiovascular symptomology. You may be able to ask your family doc for a referral to an EP-cardio, or call the hospital and ask for the number of one.
No, you definitely don't need to wait for comprehensive testing before starting treatment, though it's always a bonus the more testing you can get. As for getting IVs as a treatment, getting them as a *routine* treatment is tricky. Getting them as a pick-me-up "emergency" treatment is ... well ... routine. I know, that sounds strange, but hear me out. If you are in the midst of a flare-up, you can VERY likely go to your emergency room and get IV fluids as treatment, especially if you have low blood pressure or tell them you had low blood pressures at home (if you don't have a BP cuff at home, go get one PRONTO. your insurance may even pay for it with a Rx from your doc) over the past few days and are having a flare up of symptoms. They will treat you for "orthostatic hypotension" or "dehydration" with IV saline. A *good* emergency room will keep the fluids running until you are can walk a lap around the emergency department without feeling lightheaded (i.e. until you feel about as good as you did before the flare) AND your standing BP is within the normal range when they take your orthostatic pressures. There are a lot of not-so-good emergency rooms, though, so here is my advice. When you're in a flare, call or go to your primary care doc or cardiologist FIRST and get sent from there to the emergency department (at least the first few times). They can call ahead and send orders for your care, which are to include that your orthostatic pressures are to be taken every L or 2L (my cardiologist said every 2L last time for me, but I take a LOT of fluids to tank up, 1L may be more appropriate for you) to gauge where you are and decide whether to hang/pump another 1L (or 2L) and also that you need to be able to ambulate before they release you. If you need a lot of fluids, be prepared for a longer stay; the first bag or two (or maybe 3?) can be run fast, but if you're going to be going home with 7 L of IV saline on board, they're going to be running it by pump after the first bit goes in for safety's sake so that the bulk of it goes in S-L-O-W. Eventually, your local hospital may get used to your "routine" and be able to look you up in the computer and know what to do with you and you can bypass the call/trip to your doc and just go straight there and tell them you need tanked up for a flare.
In the meantime, if you can identify anything that may be causing the flare, that's good too. My culprits are mainly heat, stress (emotional or physical like surgeries), infections (viral or bacterial), and having done too much physical activity (but I had FUN at the new year's party, right?!) ... so pretty much everything but sleeping. :-p Okay, it's late and my brain is definitely fried. If I think of more, I'll let you know. Go ahead and feel free to hit me with more questions.
-Heiferly. :-)
Ummm, no, I'm not exactly a POTS patient but that was my diagnosis at first ... now mostly my docs are just calling it Dysautonomia ... it's complicated, lol. Basically I sort of bleed outside of the edges of what one would "normally" see in a POTS case, so it's tending away from that. Not important to your stuff at any rate. No, I didn't start this forum ... I suppose MedHelp did, technically. One of the other co-CLs (Community Leaders) here (there are three of us in Dysautonomia ... we're the ones with purple flowers by our names ... you can find CLs in the various patient communities) was the first here in Dysautonomia: Halbashes. You may see her pop in and out now and then; she's a bit busy now because she just got her port (a type of semi-permanent IV line) put in for her IV treatments and is recuperating from that surgery and getting accustomed to her IV pump and all that.
As to how I know however much I know, I read peer reviewed medical journal articles and medical textbooks out the yin-yang! :-p My educational background provided a firm basis in the "hard sciences" at two top-notch universities, so I guess I was well prepared to suddenly fall terribly ill at the age of 27 and go into early retirement. So this is my hobby? I volunteer here helping other patients access the info and support they need. I hope I occasionally succeed. :-D
On to YOU! Yes, in my travails through studying random medical stuff, I have heard of CAH, actually. Don't worry about the fludrocortisone, some people tolerate it and some don't and there are lots of other treatments out there. The Midodrine may take a bit to see if it works for you, especially if you're starting with a small dose and your doc wants to play with the dose a bit to see if that can get to a good point for you; also, if you get side effects from that, one thing to note is that for most patients those will go away pretty quickly (about a week or two I think once you get to a given dose) so my advice is give it a chance even if you get something "weird" like the goosebumps from it unless it really REALLY drives you nuts. Because Midodrine is one of the biggest helps for the biggest number of dysauto sufferers that I've seen (both anecdotally speaking and looking at the studies to back it up), and anecdotally speaking, some of the times it fails for people it seems like a part of it is not giving it a long enough shot or not "muscling" through side effects for at least a week or two to see if they go away. I hope that doesn't sound awful. I just think, personally, in the grand scheme of things that if something can improve your quality of life FOREVER, one crummy week or two is worth it. At least to me, your mileage may vary, don't kill me if you suffer through a week of goosebumps for nothing, LOL.
If I haven't said this somewhere you've seen it already, do check out our list of treatments in our health pages (link in the top corner of the page by the little yellow icon ... it says "Health Pages" ... we share with all the other Neurology people so just look for Dysautonomia related topics in the list ... there's a link in there of Dysautonomia Treatments that talks about different meds and such ... not all are appropriate for POTS in particular but you can see that there's a lot out there so don't lose hope if your first efforts at trial and error with meds aren't successful). Whoa, holy run-on sentences, Batman!! Sorry, I said I wasn't at my peak performance today, and I meant it!!!
Moving on ... Cardiologists can make AWESOME POTS docs, particularly EP cardiologists. That is, electrophysiologist-cardiologists. Sometimes, they're better than neurologists for POTS in particular, because it has such a cardiovascular symptomology. You may be able to ask your family doc for a referral to an EP-cardio, or call the hospital and ask for the number of one.
No, you definitely don't need to wait for comprehensive testing before starting treatment, though it's always a bonus the more testing you can get. As for getting IVs as a treatment, getting them as a *routine* treatment is tricky. Getting them as a pick-me-up "emergency" treatment is ... well ... routine. I know, that sounds strange, but hear me out. If you are in the midst of a flare-up, you can VERY likely go to your emergency room and get IV fluids as treatment, especially if you have low blood pressure or tell them you had low blood pressures at home (if you don't have a BP cuff at home, go get one PRONTO. your insurance may even pay for it with a Rx from your doc) over the past few days and are having a flare up of symptoms. They will treat you for "orthostatic hypotension" or "dehydration" with IV saline. A *good* emergency room will keep the fluids running until you are can walk a lap around the emergency department without feeling lightheaded (i.e. until you feel about as good as you did before the flare) AND your standing BP is within the normal range when they take your orthostatic pressures. There are a lot of not-so-good emergency rooms, though, so here is my advice. When you're in a flare, call or go to your primary care doc or cardiologist FIRST and get sent from there to the emergency department (at least the first few times). They can call ahead and send orders for your care, which are to include that your orthostatic pressures are to be taken every L or 2L (my cardiologist said every 2L last time for me, but I take a LOT of fluids to tank up, 1L may be more appropriate for you) to gauge where you are and decide whether to hang/pump another 1L (or 2L) and also that you need to be able to ambulate before they release you. If you need a lot of fluids, be prepared for a longer stay; the first bag or two (or maybe 3?) can be run fast, but if you're going to be going home with 7 L of IV saline on board, they're going to be running it by pump after the first bit goes in for safety's sake so that the bulk of it goes in S-L-O-W. Eventually, your local hospital may get used to your "routine" and be able to look you up in the computer and know what to do with you and you can bypass the call/trip to your doc and just go straight there and tell them you need tanked up for a flare.
In the meantime, if you can identify anything that may be causing the flare, that's good too. My culprits are mainly heat, stress (emotional or physical like surgeries), infections (viral or bacterial), and having done too much physical activity (but I had FUN at the new year's party, right?!) ... so pretty much everything but sleeping. :-p Okay, it's late and my brain is definitely fried. If I think of more, I'll let you know. Go ahead and feel free to hit me with more questions.
-Heiferly. :-)
I think I saw a PM from you in my inbox, so I'm going to go ahead and answer you by PM and try to hit all of your stuff at once. Sorry for the delay; I'm having my own issues at the same time and I'm trying to deal with all of our crises at once, LOL. Not to downplay your stuff, I mean, the reason I'm on here is because I see several of you folks who need help just as badly as I do right now so I'm trying to do my best to make my rounds. But that's why I'm moving slower than normal. If that makes sense. Sorry. :-p
I read your post about your symptoms and I feel like we have a lot of symptoms in common! I'm having a horrible time with the dizziness and weakness right now. I even made a makeshift toilet for my bedroom so that I don't have to get up and walk all the way to the bathroom. Thankfully I still live with my parents so they help empty the "toilet" if I can't get up and they make food for me. But it is so frustrating to have to depend on people for everything and not to be able to do anything for yourself. I'd had bad dizziness for a while before i got diagnosed with POTS and the Florinef had really helped a lot with that, but my dr. tried to increase my florinef during this flare and I had bad swelling in my feet from it, and hypokalemia symptoms. It seems like everything I do to try to help only makes things worse right now.
Thanks for your response. Sorry I didn't put in more details. I do not have syncope. I get near syncope quite a bit though. My "normal" POTS symptoms are extreme fatigue, weakness, headaches and GI problems. During this flare up, I've had horrible panic attacks that last for hours on end. I have had blood pooling in my feet, hands, nose, and ears. I have blisters on my toes from them getting so hot from the blood pooling in them. I have also had a lot of dizziness. I have been taking zebeta (bisoprolol) and florinef for my symptoms. I also have IST. My sitting bp and hr are usually 110/70 and 80 on the zebeta and when I stand my bp doesn't do anything and my hr goes up to 95 or 100. But even on the zebeta right now, my bp is 125/85 sitting and goes up when standing and my hr is still 80 sitting but around 125 standing. It increases to that almost instantly while standing and doesn't increase any more unless I stand for a long time. For non pharmacological treatment, I exercise daily, eat a lot of salt, drink a lot of water and do respirate (deep breathing). I have just recently gone to a cardio in town who knows about POTS (my main dr. for POTS is electrophysiologist and is about 5 hours away). The cardio I went to told me to take Celexa and changed my beta blocker to Propranolol. I had a hard time even going to see him because I had a horrible panic attack the whole time I was there. Since I've started the Celexa and Propranolol, I have such bad panic attacks, near syncope when standing and dizziness that I haven't been able to get out of bed. I'm supposed to call the cardio monday to let him know how I am doing on the meds. I know that some of those symptoms are supposed to go away in time with the Celexa, but it is frustrating to have things worse than they were before. I have not gone to the ER for this flare. I live in a small town and most of the dr's here do not understand POTS and tend to make things worse. So my main bad symptoms at the moment are the blood pooling, constant panic attacks, and dizziness. It has been so bad, I have bad brain fog when trying to talk to people or do anything too. Sorry this is so long! I'm just hoping someone will have an idea what is wrong and how I can get my body back into balance again!
One more thing...I live alone, but I do have some very supportive friends who will stay overnight if I need, and parents who come on weekends to help me with shopping and other things. I didn't want it to sound like I had no support. I have people who care about me, but it's just really rough when you live alone and this all happens, its scary.
Shari
Shari
Have an Answer?
You are reading content posted in the Autonomic Dysfunction Community
Are there grounds to recommend coffee consumption? Recent studies perk interest.
Salt in food can hurt your heart.
Get answers to your top questions about this common — but scary — symptom
How to know when chest pain may be a sign of something else
A list of national and international resources and hotlines to help connect you to needed health and medical services.
Herpes sores blister, then burst, scab and heal.
