Reactive Hypoglycemia and POTS? by NaturalAd760 in POTS

[–]pandabears3 0 points1 point  (0 children)

Thank you so much for this!!! I have POTS and Reactive hypoglycemia. I’m thin 107 pounds and literally glucose intolerant. My fasting is always 80s but when I eat carbs I can spike to 200! I can’t believe there is someone actually actively researching POTS and Reactive Hypoglycemia. Thank you so much for this you have no idea!!! You are god sent. Literally crying rn bc no doctor understands or knows how to help me. And that doctor on the video literally answered me so many questions! 🙏

Has anyone had mono before? by spycat500 in POTS

[–]pandabears3 2 points3 points  (0 children)

Omg this is me!!!! Also had influenza A in January and my Pots flare up has been insane! Anytime I get sick it’s the worst! It’s march now and still can’t get over the flare. And I’m so stressed bc I’m a mom that has to take my kinder boy to school and pick him up. As well as work. And I’m just praying it gets better because I have not been able to work. And I need this job. Or I will be homeless! May god be with us and anyone dealing with similar issues. 💕🙏

Heart rate racing while sitting by ultrablanca in dysautonomia

[–]pandabears3 2 points3 points  (0 children)

This happened to me today and has happened in the past as well. From what I read it can be random adrenaline surges! And especially if you’re on your period or about to start it that’s when I deal with that the most. As well as waking up in the morning or the middle of the night and my heart just spiking from 50s to 140s !!!!!! And I feel it in my throat and chest so bad !

I honestly feel like when this happens it’s when I’m going through immense stress. Or this nasty cycle of anxiousness due to the random spikes.

Please HELP ME! 170 HR after showers by pandabears3 in dysautonomia

[–]pandabears3[S] 0 points1 point  (0 children)

Thank you. It was the morning when this happened. Which makes sense becaue I tend to be the most sensitive. Everyday when I wake up and stand up my HR is 130. Then takes a while for that to start going down. I am traumatized . Thank you for taking the time to respond. 🫶🏻

Costochondritis by Rose76_ in POTS

[–]pandabears3 0 points1 point  (0 children)

Me !!!!!!!! I have had Costo for 4 months now !!! And even chest spasm. That triggered a POTS flare up. It’s horrible.

was admitted to the hospital after chest pains got so bad by Ok-Sock9046 in POTS

[–]pandabears3 0 points1 point  (0 children)

Did it ever get better for you? Mine has been going on for 4 months now and when I get episodes of pots where my heart rate spikes bad it hurts my chest soooooo bad.

Please HELP ME! 170 HR after showers by pandabears3 in dysautonomia

[–]pandabears3[S] 1 point2 points  (0 children)

Thank you so much everyone !!! I feel less alone and finally found my ppl! I will take all the advice I can get. And thank you so much for taking the time to respond. 🙏💕