blueroses79

Thanks! I hope it goes away! I'm taking 2.5mg twice a day right now. It's not actually lowering my heart rate that much, though.

Does ivabradine make anyone else dizzy? I recently started ivabradine for POTS (diagnosed via ANSAR). It does seem to help me with my heart rate a little; I feel calmer. But I'm having a significant increase in orthostatic dizziness. When I stand up, the blood rushes down and I get dizzy, and my ears pop. It lasts throughout the day instead of just happening in the mornings. Has anyone else had this side effect? It's frustrating, since there are only so many options for a person with POTS and high blood pressure. And beta blockers give me chest pains and overheating. It could be my imagination, and this is just a side effect of warmer weather, but I noticed it when the weather was still cool.

I have hyper POTS (or at least POTS with high-ish resting BP, drops a bit when I stand), and have been advised to use compression stockings, and of course to increase fluids. I also have varicose veins, and have been advised to wear them that too. I haven't had a blood volume test, so I don't know if that's my issue, but I definitely have pooling (can see it), so I wear the stockings when I can. The stockings help, though I admit I don't always wear them in the summer (when I need them most!). I suspect in my case the high HR and BP are compensatory mechanisms for blood pooling, and possibly low blood volume, so preventing the pooling can only help. My BP is also not that high, though.

Did you mean me, or OP? In my case, fluid loading doesn't seem to be lowering my BP. The orthostatic drops I get when I feel dizzy are to fairly normal BPs, and it's otherwise highish (systolic in the 140s). Does tend to go even higher (160s-170s) when supine, which is usually when I feel best. I suspect cutting caffeine would give me a lower baseline BP, but lead to even more orthostatic dizziness and syncope (the latter has mostly disappeared since my BP became high). It's a balancing act. I haven't had blood volume testing. Just ANSAR and HUTT (results, POTS and NCS, respectively). Will ask about it.

This is my situation, too, and I have no idea what to do for it. My BP is moderately high most of the time, but drops when I stand to a normal BP, and I get dizzy. I feel worst when my BP is lowest. I drink fluids constantly and it doesn't seem to do anything. Currently on ivabradine, which also doesn't seem to do anything. I have a history of syncope, again associated with low BP (since my BP has risen as an adult, I faint less, but if anything lowers it, that's back on the table again). Ugh. But to reply to the original question, I've been advised NOT to add sodium to my fluids/diet because of the potential BP increase. I have had low potassium before, so that's fine to add.

Bumping an old post here. But did you ever find out why this was happening? It seems to be happening to me too. Feeling feverish with no fever has always been a part of my dysautonomia but it's increased by at least 80% since I started propranolol. Exactly the opposite of what I wanted and expected to happen. My veins have been hurting more also. (I have varicose veins, so that can happen, but not normally, you know?) I guess I'm going to have to ask my cardiologist for a different drug. It's weird because I'm not a very "allergic" person, at least for my family. Occasionally I get hives for no clear reason. And a few months ago I got random burning mouth with a single hive. But no shock reactions ever. I guess I should look into MCAS. (It would fit. I am also hypermobile.)

I have hyper POTS too! (Suspected, anyway.) Lots of sympathetic nervous system symptoms. That's why my doctor was eager to try it; she's been worried about my high BP for years. My diastolic is often around 90, and systolic usually in the prehypertension or outright hypertension range (often high while lying down, sometimes when I stand). Does propranolol not affect your sleep at all? Do you avoid taking it at night?

My awesome GP did some research and agreed to treat me for POTS (yay!!), and I started propranolol 20mg 3/day. The first pill was fine; I didn't really notice any effects aside from a normal (lower) HR when I tested it. On the whole I felt a little better. Zero dizziness. (But dizziness for me is largely a seasonal and occasional symptom at this point; sleep deprivation and humidity..) I took a second one before bed, and couldn't sleep despite being very tired. When I did fall asleep, I woke up from a dream into presyncope that lasted a few minutes (2-3 cycles of nausea, the sound flooding into my ears, sweating--all while lying down). It makes sense that a med that lowers HR and BP would be most likely to induce syncope when someone's HR and BP are the lowest--when they're asleep; but the only other time I've had either syncope or presyncope lying down I had a high fever. Has anyone else experienced anything like this? Or does it mean my nervous system is extra weird? This morning I was scared to take more of it (especially on around 3 hrs of sleep!), but having chest pain, so I cut one in half and took 10mg. Feeling a bit better.

Thanks! That's super encouraging!!

Thanks so much!

Hi everyone, I seem to have POTS with high BP (prehypertension range consistently), and no one will touch it since Florinef would raise my BP. My last Dr. suggested I see Dr. Grubb, go to Mayo or Vanderbilt (in that order, I think). Toledo is closer to me than the other places. But I would have to wait to see Dr. Grubb for nearly a year, and the symptoms of sympathetic overactivity are pretty distressing. I could see Dr. Grubb's nurse (Beverly) sooner. Has anyone with hyper POTS seen Dr. Grubb's nurse? Is that a good route??

I have what's most likely hyper-POTS (sometimes orthostatic hypertension, sometimes hypo, always standing tachycardia), and have been on Spiro for a couple years for my skin. Recently I dropped it because I thought my insurance was expiring, and my tachycardia got much worse. Weirdly it doesn't seem to lower my BP much. It's always in the same (slightly too high) range. It certainly doesn't make me feel worse. One reason might be that spiro increases potassium, and I have low potassium. But it hasn't cured me, either. I still have temperature dysregulation hot spells, standing tachycardia, and BP spikes and dips. But my baseline HR seems lower on it, which is good.

I have, but it probably wasn't the right time of day; they were normal. That happens to me too, but it's much more pronounced if I haven't had enough sleep. This is an interesting idea, though! I take Spironolactone (for acne), and have noticed it makes me feel better in the morning. Without it I tend to wake up with a headache. Spiro increases cortisol levels. I still get very lightheaded in the Summer, though. And sleep deprivation nausea is still bad.

Nope. I'd love to have one, though. If it looks likely I'll ask my neuro about having one.

It tends to go away as the day goes on, I think. By evening I'll still be out of it, but less nauseous.