SnowFoxFairy

228d

hi there! I'm starting my journey learning about POTs while managing my anxiety and depression. Two years ago my high heart rate was misdiagnosed as my anxiety but recently my cardiologist has reassessed it and decided it's likely POTs, I'll be getting a tilt table test to make sure but he didn't think it's necessary. Looking for advice on how to function now that I realize constant weakness and blacking out every time I stand up isn't normal lol

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Top reply
    • imaginaryloaf

      227d

      hey! I'm hopefully being diagnosed by my cardiologist soon too. I was also previously diagnosed with anxiety. it's super frustrating. drinking a lot of water - and I mean a lot - can help significantly as it increases blood volume, which can help with your symptoms. I have inappropriate sinus tachycardia, not POTS (on this app it changes IST to POTS) and I've found that drinking electrolytes has really helped my high heart rate upon standing, so it might help for you too. keeping moving, rather than standing still, has helped me with blood pooling in my hands and feet if you experience that too. good luck on your journey!! I hope you get a diagnosis and recognition soon.

    • superstellar

      227d

      hey! i was diagnosed with POTS last april. every doctor will tell you this, but PLEASE make sure you are drinking a TON of water. it will not alleviate your symptoms but dehydration and POTS do NOT mesh well. in terms of lifestyle changes, i’d recommend buying a few pairs of compression socks and wearing them as often as possible. these move the blood from your legs up to your head so your blood pressure doesn’t go all over the place when you change positions! also, try to increase salt in your diet! i usually carry around pretzels/goldfish or even pickles in my lunch. increased salt in my diet has lessened my symptoms. i would also recommend investing in a shower seat or even just a regular stool. most of my accidents happen during hot showers, because POTS comes with the inability to manage heat, LOL listen to your body!! do not overexert urself or you will be feeling it the next day. sit or lay down when you need to! finally, remember that your POTS is not your fault. for me, i have a lot of guilt regarding not being able to do the things i used to— but it doesn’t make you less of a person, it just makes you chronically ill. you’re still you! i wish you luck on your journey! reach out if you need anything! ❤️

      • SnowFoxFairy

        227d

        @superstellar I'm lucky I've always been a water o holic lol, I feel like I get dehydrated so easily I drink at least 40 ounces a day. Showering has always been a problem for me 😭 I just haven't moved the shower seat into the bathroom cause I've been sharing with roommates and I feel guilty making them move around it. Speaking of guilt, thanks for the reminder that it isn't my fault. It's really tough as I've always worked in very physically active fields and I just can't keep up anymore, I'm frustrated as my entire professional history feels like it's completely useless the worse it gets 😭 thanks for the kind words, its helpful to know I'm not isolated in this

    • imaginaryloaf

      227d

      hey! I'm hopefully being diagnosed by my cardiologist soon too. I was also previously diagnosed with anxiety. it's super frustrating. drinking a lot of water - and I mean a lot - can help significantly as it increases blood volume, which can help with your symptoms. I have inappropriate sinus tachycardia, not POTS (on this app it changes IST to POTS) and I've found that drinking electrolytes has really helped my high heart rate upon standing, so it might help for you too. keeping moving, rather than standing still, has helped me with blood pooling in my hands and feet if you experience that too. good luck on your journey!! I hope you get a diagnosis and recognition soon.

☝ This content is generated by our users and it is not a substitute for professional medical advice. Please consult with your physician before making any medical decision

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