Non-Anxiety "Panic Attacks" with POTS?
I'm 27 years old, and 2 months ago (coincident with just before I had an upper endoscopy), I started experiencing symptoms of lightheadedness, dizziness, heart racing and pounding out of my chest, blurry vision, etc. I had a til table test done earlier this month that was positive for probable POTS. However, coincident with these symptoms, I also began experiencing what I would call non-anxiety "panic attacks." At times when I wake up in the middle of the night, my heart will start racing and a sense of panic floods my body. My veins feel as if they go white cold with electric charge, and I feel 'trapped' inside my body, oftentimes shaking. My brain will also often feel like it's being pulled into another dimension. It's a horrific sensation that can take 20 min to pass (I typically have to take a Xanax to get through it). There were also days when as soon as I would wake up in the morning I would instantly be filled with a sensation of panic with a racing heart. My body feels like it's constantly on the edge of fight-or-flight, but it feels entirely physiological rather than psychological (I've been meeting with a psychologist for months and had been doing really well with my anxiety, I never experienced panic attacks before). Has anyone else with POTS experienced these issues? I'm getting better dealing with my issues of lightheadedness during the days, but now I'm terrified to go to sleep at night.
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Try “Heart salt”. - it is mostly Potassium chloride, less Sodium chloride
@azurite You describe exactly what I've been experiencing exactly how I've been experiencing it, almost as if I wrote it myself. I had these "attacks" happen once every few months beginning in 2020 and now they are occurring more frequently with 4 in the last two weeks. Were you able to find something that helps? I hope you have.
Sorry for my ignorance but what is POTS?
Very sorry to hear of your experience & suffering. Very often physicians (especially when diagnosing unusual symptoms with no immediately recognisable aetiology; there's a recent controversial paper published by a team headed by a diagnostic physician from Johns Hopkins documenting the incidence of misdiagnosis by American physicians, particularly emergency-room physicians) refer patients to mental-health care providers when they do not succeed in formulating a biologically-based diagnosis. Curious whether you have had a prior COVID-19 infection (whether asymptomatic, mild or severe)?
I have this exact problem and was diagnosed with pots at Hopkins in 2020. I spent over a month inpatient. Yes, I have these and I have wanted to end my life over these in so scared of going to
Sleep. I developed one of the worst pots cases hiokins has seen. These nocturnal attacks happen around 4am when my cortisol levels are high. My first “panic attack” was in recovery from surgery for partial thyroidectomy 12/2019. I started pots immediately and it’s been 3 1/2 yrs. I still have these and hope they go away.
Yes, I have felt the same thing, and I am still waiting to be tested for POTS, but from everything I've read, I likely have it. I have hypermobility EDS and MCAS as well, which tend to run alongside POTS. I have emotional anxiety, but the physical panic attacks are never caused by emotional anxiety for me. When I hit 27, I started having the physiological panic attacks. No one believes me when I told them I wasn't thinking about anything or doing anything anxiety inducing when they would occur, and like you said, they would jolt me awake and often occurred first thing in the morning. They also sometimes happened during the day when I was doing nothing or mundane things that would not have given me a reason to feel psychological anxiety. I still get them and most of the time if I lay down for a while they go away after an hour or so, but sometimes I have to take hydroxyzine, which makes me sleep anyway. I wish you luck in finding out what helps for you!
Does anyone have random rashes/tingling /burning associated with POTS?
I’m so sorry to hear that you are experiencing this. I’ve been having the exact same thing happening almost every night, about an hour or so after I fall asleep. I’ve been explaining it to everyone as similar to panic attacks but a lot more intense. I hate that you can relate, but glad I saw your post as it helps me make sense of things a little. If you’ve found anything at all that has helped with this, please let me know. I hope you are doing well
A family member has POTS but is getting better by following a POTS protocol involving diet and exercise. Don't know the particulars except that protocols are discussed on line.
Hi! I also was diagnosed with POTS and had these “nocturnal panic attacks” for a span of about two months before diagnosis. I had the tilt table test done which was positive for POTS and once my cardiologist started me on a beta blocker (metoprolol) the late night attacks started becoming less and less frequent and now I haven’t had one in about a month! From my understanding, a beta blocker is usually the first form a treatment for POTS, maybe you should ask your doctor about it!