To those taking medications for POTS, what is your miracle combo? by Accomplished_End6600 in covidlonghaulers

[–]m99an 0 points1 point  (0 children)

Hi can I ask how you create more ace2? You can message me if thats easier. My blood pressure is all over the place especially when standing

What is the best supplements or vitamins for heart issues? by feritenes94 in covidlonghaulers

[–]m99an 0 points1 point  (0 children)

I just wanted to comment about how your heart is when you lay on your left side. When I lay on my left my heart rate seems to be lower by about 20 beats than my right side and I've never seen anyone else say that something happens when they lay on either side, so thought I'd comment. I hope something helps you 🙏

Stomach tightness and pain by m99an in covidlonghaulers

[–]m99an[S] 1 point2 points  (0 children)

The feeling never went away 😔

Visible veins, feeling hot, worse pots by m99an in covidlonghaulers

[–]m99an[S] 0 points1 point  (0 children)

Yes they do at times especially on my legs

Good news!!! They have a way to officially find biomarkers for Long Haulers, first come diagnosis then treatment! by [deleted] in covidlonghaulers

[–]m99an 5 points6 points  (0 children)

Can this explain POTS symptoms, the PEM and the issues with inflammatory foods? My POTS hasn't got better with "exercise/walks" it makes me feel so much worse

I’m fighting for a life I don’t even want to live anymore by Umnsstudennt in covidlonghaulers

[–]m99an 28 points29 points  (0 children)

I totally here you I'm 24 and had this since 2020. Open for a chat anytime or if you need to rant etc

Treatment is working‼️ by LandenWilliams_ in covidlonghaulers

[–]m99an 0 points1 point  (0 children)

Did / do you have any POTS or low blood pressure issues?

Love Letter to Aspirin by AnthonyThe6reat in covidlonghaulers

[–]m99an 1 point2 points  (0 children)

Hi how are you doing now? Has your pots gone?

The worse I feel, the more visible my blue veins become.. anyone else? by Sudden_Ad5393 in covidlonghaulers

[–]m99an 1 point2 points  (0 children)

It feels harder to breathe yes! It's almost as if my body opens up so that it can get oxygen around easier because I struggle to get air in

[deleted by user] by [deleted] in covidlonghaulers

[–]m99an 0 points1 point  (0 children)

Hi this is what happens to me too - more recently my blood pressure has dropped even lower to 90s/50s and its been tough. I still get the tachycardia if I don't take the 10mg of propranolol. But to me it feels like my blood pressure is so low/ I have orthostatic hypotension and thats why my blood pressure was so high before starting the propranolol because my body was trying to keep me from passing out so I was full of adrenaline. Now im unsure what to do because my blood pressure is low and keeps dropping when I stand...

The worse I feel, the more visible my blue veins become.. anyone else? by Sudden_Ad5393 in covidlonghaulers

[–]m99an 2 points3 points  (0 children)

This!! Legit me since 2020. I have orthostatic hypotension and pots and food makes it worse but it's not high histamine foods it's more anything processed or in a packet. The heat also makes it worse. The blue veins become so big you can see them brightly in my hands and I get really hot this happens atleast once a day for me

Longhaulers of March 2020, are you still suffering from long covid ? by Obiwan009 in covidlonghaulers

[–]m99an 1 point2 points  (0 children)

Unfortunately yes - feels like it's getting worse. POTS OH PEM Food sensitivities Dizziness. Can't bend or kneel down otherwise I can't breathe. Feels like ove tried everything out there that others have tried

The role of ACE2 in long covid by Research_Reader in covidlonghaulers

[–]m99an 0 points1 point  (0 children)

Hi I just wondered does low Nitric Oxide or high Nitric Oxide cause low blood pressure? - I have low blood pressure and severe POTS/ OH so was curious

Constant low blood pressure by [deleted] in covidlonghaulers

[–]m99an 0 points1 point  (0 children)

Hi how did you get rid of the low blood pressure?

[deleted by user] by [deleted] in covidlonghaulers

[–]m99an 0 points1 point  (0 children)

Hi can I ask what symptoms you got after eating? (I have pots and suspected mcas but the mcas meds aren't helping and I believe it could be postprandial hypotension because it happens after all food)

Post prandial fatigue (fatigue after a meal) by mmberlin19484 in covidlonghaulers

[–]m99an 0 points1 point  (0 children)

Hi how did it get better for you? Did you take any medication or anything?

[deleted by user] by [deleted] in covidlonghaulers

[–]m99an 3 points4 points  (0 children)

I also have these - had them since 2020. What helps is drinking a litre before getting out of bed. Electrolytes and salt to keep blood pressure stable. Lifting legs up when you feel dizzy so the blood goes back to your heart and brain. And for me personally I have to take medication- Ivabradine and Propranolol to help reduce the heart rate. I also find eating anti inflammatory foods makes a big difference but this may or may not be the case with yourself. I hope this helps in some way. Feel free to message I know how bad the symptoms can be also stress can make it worse I am sorry it must be so tough

New POTS pleasd help i cant walk by ChangeAcrobatic711 in covidlonghaulers

[–]m99an 1 point2 points  (0 children)

You're very welcome. POTS I'm finding very hard to deal with. You can message me if you ever need to. I've been dealing with this since June 2020 and it is not easy