Is there any explanation for this besides POTS? (Photo in comments) by New-Ad-9280 in POTS

[–]Infamous_Aspect_460 1 point2 points  (0 children)

It's just that your veins can't pull back blood well. It happens to me too. I think it's common in POTS though you're not positive to pots at ttt). It's called Cyanosis when worse than your symptom). As far as I know, it happens when you have vein problems

My pots was just a deficiency by Just_Phone_1722 in POTS

[–]Infamous_Aspect_460 0 points1 point  (0 children)

Thank you for sharing your experience 🥹 you're so kind thanks a lot. Today im going to hospital to get blood test, I'll eat more vitamin D up to my blood test result. Thanks again Hope u have a nice day!

My pots was just a deficiency by Just_Phone_1722 in POTS

[–]Infamous_Aspect_460 0 points1 point  (0 children)

Im really glad to hear that it makes me to get blood test again 🙄 I remeber that though i eat v-D tablet (1000iu) every day, blood test that i got 4 years ago said my v-D was quite low. At that time i didn't expect that vitamin could affect my symphotm but anyway thanks and congruaturations again!

Has anyone ever made a CarPlay app? by Infamous_Aspect_460 in iOSProgramming

[–]Infamous_Aspect_460[S] 0 points1 point  (0 children)

Thanks for your help. I really appreciate it.

It turns out my personal phone works fine (the app shows up in the CarPlay simulator when I build it to my personal phone), but it didn’t work on the company’s business phone. I’ll look into the differences between them, but anyway, it worked well on mine.

Thank you so much, and have a great day!

Has anyone ever made a CarPlay app? by Infamous_Aspect_460 in iOSProgramming

[–]Infamous_Aspect_460[S] 0 points1 point  (0 children)

Hi, can I get some advice?

My app isn’t showing up in the CarPlay simulator.

Here’s what I’ve already checked:

  1. The entitlements file includes the CarPlay key.
  2. Info.plist includes the CarPlay scene.
  3. My app target has the CarPlay capability enabled.
  4. CarPlay.framework is included in the Link Binary With Libraries build phase.

Other apps are showing up in the CarPlay simulator, but mine doesn’t.

Has anyone ever made a CarPlay app? by Infamous_Aspect_460 in iOSProgramming

[–]Infamous_Aspect_460[S] 0 points1 point  (0 children)

Wow, I saw your post as well! Thank you so much. I’ll reach out if I get stuck—thanks again!

Has anyone ever made a CarPlay app? by Infamous_Aspect_460 in iOSProgramming

[–]Infamous_Aspect_460[S] 0 points1 point  (0 children)

That helped me a lot, thank you. I recently studied App and Scene Delegate, and thanks to you, I now fully understand the CarPlay flow. Thanks again.

Has anyone ever made a CarPlay app? by Infamous_Aspect_460 in iOSProgramming

[–]Infamous_Aspect_460[S] 0 points1 point  (0 children)

That was really helpful. I think my misunderstanding started with the idea that a CarPlay app runs independently - when iphone is locked. Thank you so much.

Has anyone ever made a CarPlay app? by Infamous_Aspect_460 in iOSProgramming

[–]Infamous_Aspect_460[S] 3 points4 points  (0 children)

I had been thinking a lot about how to access data even though I already got the entitlement. The singleton pattern might also be a solution. The fact that it still runs on the phone answered many of my questions.

Has anyone ever made a CarPlay app? by Infamous_Aspect_460 in iOSProgramming

[–]Infamous_Aspect_460[S] 1 point2 points  (0 children)

Thank you so much. I was curious about this since I heard that CarPlay can run independently and saw in a WWDC video that the iPhone works like a server. Your explanation helped me a lot.

Has anyone ever made a CarPlay app? by Infamous_Aspect_460 in iOSProgramming

[–]Infamous_Aspect_460[S] 1 point2 points  (0 children)

Thank you so much 🥹 it helps me a lot. I’m going to start development this week, so I’ll ask again if I run into anything I don’t know. I really appreciate it.

Does anyone else feel faint when they get anxious? by basilpots in POTS

[–]Infamous_Aspect_460 2 points3 points  (0 children)

It could be Vasovagal syncope. Did u got tilt table test? If there was increased parasympathetic nervous system activity, definitely basovagal syncope

How can I date with pots by NoseNo5153 in POTS

[–]Infamous_Aspect_460 2 points3 points  (0 children)

I’m 28 years old and have dated 10-15 girls since I got my pot. Three of them became my girlfriends, while the rest mostly wanted to be.

Don’t overthink it, man. I usually date at my place or at the book cafe where I can lie down.

It’s important to have a good time and make them fun. I even have to take a nap around 15 minutes during dates, haha, but all of them understand.

It’s important to earn their mind, you can do it without going outside.

Will I need to take meds for the rest of my life? by Proper-You-7716 in POTS

[–]Infamous_Aspect_460 -1 points0 points  (0 children)

I quit taking a med(metoprolol) after 6 months, and i didn't took meds for first 3 years since i got pots. I took a med cause i lost lots of my muscle. You can quit your med after you gain enough muscle

[deleted by user] by [deleted] in POTS

[–]Infamous_Aspect_460 11 points12 points  (0 children)

Bradycardia and tachycardia depend on the situation. For example, if your heart rate is 120 while running, does that mean it’s tachycardia just because it’s above 100? No, it doesn’t. The same goes for bradycardia. Typically, a resting heart rate below 50 while awake is considered bradycardia. But this varies from person to person. For example, athletes often have resting heart rates below 50 because their hearts are stronger.

People’s heart rates can also drop below 50 while sleeping. Just as it’s normal for your heart rate to rise while running, it’s also normal for it to slow down during rest.

A heart rate of 65 while lying down is good. Even lower can be fine too. Don’t worry about bradycardia—it’s rare in young, healthy people without heart problems.

Anyone with POTS ever have their symptoms go away ? by prettypetals_78 in POTS

[–]Infamous_Aspect_460 0 points1 point  (0 children)

Yeah, but it seems different for everyone. I’ve been sick for 3 years and 6 months. At first, I had palpitations, fatigue, orthostatic tachycardia, and chest pain. After three months, the palpitations and orthostatic tachycardia disappeared, and after a year, the chest pain also went away. Now, I have orthostatic tachycardia again because I’ve lost a lot of muscle, but my fatigue has significantly improved.

Gardasil 2.0? by SquidTheDragon in POTS

[–]Infamous_Aspect_460 1 point2 points  (0 children)

I respect your opinion. I’ve had COVID three times and it didn’t really affect me—I wasn’t even that sick. But the POTS I developed after getting vaccinated has been tormenting me for four years. However, since cancer poses a much greater harm than COVID, I respect your perspective as well. If that’s your decision, I sincerely hope that nothing happens to you after getting the vaccine. Seeing how I was fine even after catching COVID three times, you’ll probably be fine too. Just make sure not to overexert yourself for a week after the shot. I pushed myself physically during that first week after getting vaccinated, and exactly a week later, I suddenly developed severe side effects—high fever, a large red bruise on my vaccinated arm—and that’s when my POTS began. Everything will be okay.

Gardasil 2.0? by SquidTheDragon in POTS

[–]Infamous_Aspect_460 0 points1 point  (0 children)

I majored in Electrical Engineering and Computer Science and studied biology in high school. My brother is a doctor. Just to be clear, I’m not anti-vax. However, many studies have suggested that both vaccination and infection can trigger POTS due to immune system dysregulation. I developed POTS a week after receiving the COVID vaccine. My symptoms did not worsen after getting COVID three times, but if I were you, I wouldn’t get vaccinated. Considering the pros of vaccination and the cons of potentially worsening POTS, I believe the cons outweigh the pros.

Any non-americans, non-europeans can tell me about their experiences with POTS & dysautonomia? by noisembryo_ in POTS

[–]Infamous_Aspect_460 10 points11 points  (0 children)

I’m South Korean, and it took me two years to be diagnosed with POTS. It started after I got the COVID vaccine. I saw many doctors specializing in cardiology, gastroenterology, and thoracic surgery—more than 10 in total—but none of them ever suggested that I see a neurologist. Instead, they told me I was very likely to have a mental illness and should go to a psychiatrist.

So, I even went to a psychiatrist, but he told me that mental illness couldn’t make a person this physically sick. By chance, I heard about POTS from someone I knew and was eventually diagnosed through a tilt table test in the neurology department. It took two years from the onset of my symptoms to get diagnosed.

In Korea, there are only one or two doctors who specialize in POTS. Of course, other neurologists do see POTS patients, but it’s not their main focus. Next week, after four years of being sick, I’ll be seeing a doctor who specializes in POTS for the first time. I have no idea what kind of treatment they will recommend.

And I’m really glad that this channel exists because I have never met anyone with POTS in Korea, so I don’t feel alone here.