ChookityPop
Senior Member
- Messages
- 564
I have made this connection and it happens when I burn either my lower back and buttocks muscles og my upper back/coat hanger pain severly. I burn these muscles regularly but if I really really over do it they severe burns out and when that happens my dysautonomia/POTS symptoms worsen.
Upper back
I have burnt out my upper back muscles to the point I woke up with drop in blood pressure when I went to the bathroom at night and almost fainted. Had to lay down and couldnt go anywhere the first night and had to sleep on the floor. The next two nights I managed to get to the bed.
Lower back
This happened 3 weeks ago. I sat and stood WAY to much. I cant sit in chairs etc as I have to lay/reclined in my bed on top of a perfect constructed duvet and pillow construction not to burn out my stomach muscles.
But a family member visited and I hadnt seen him in over two years and I ended up sitting and standing up until it was too late, I often dont get any real heads up before its too late. I have this thing where Im at the doctors office waiting for my turn I sit in a chair and suddenly I need to stand up and walk since my lower back and stomach burns out if I continue to sit. So I have found this weird balance of managing my symptoms.
So now I overdid it and felt it right away. The super inflamed feeling that runs through the whole body, brainfog, trouble breathing feeling of I dont get enough oxygen etc. So after this my dysautonomia/POTS symptoms worsened. I got dizzy when standing up, fatigue and very brainfoggy. I dont have dizziness, brainfog or that bad fatigue regularly. I have pretty decent energy levels. But this still persists now going on 3 weeks Im not that dizzy but it happens on and off but Im very fatigued and still quite brainfoged. Though all these symptoms comes and goes in ways in a way.
When my muscles burns out I feel terrible. Thats my trigger to feeling worse and PEM. My symptoms do resemble myastenhia gravis and LEMS but I have negative EMG and NCS though I have not had any repetitive stimulation test.
Anyone else?
Upper back
I have burnt out my upper back muscles to the point I woke up with drop in blood pressure when I went to the bathroom at night and almost fainted. Had to lay down and couldnt go anywhere the first night and had to sleep on the floor. The next two nights I managed to get to the bed.
Lower back
This happened 3 weeks ago. I sat and stood WAY to much. I cant sit in chairs etc as I have to lay/reclined in my bed on top of a perfect constructed duvet and pillow construction not to burn out my stomach muscles.
But a family member visited and I hadnt seen him in over two years and I ended up sitting and standing up until it was too late, I often dont get any real heads up before its too late. I have this thing where Im at the doctors office waiting for my turn I sit in a chair and suddenly I need to stand up and walk since my lower back and stomach burns out if I continue to sit. So I have found this weird balance of managing my symptoms.
So now I overdid it and felt it right away. The super inflamed feeling that runs through the whole body, brainfog, trouble breathing feeling of I dont get enough oxygen etc. So after this my dysautonomia/POTS symptoms worsened. I got dizzy when standing up, fatigue and very brainfoggy. I dont have dizziness, brainfog or that bad fatigue regularly. I have pretty decent energy levels. But this still persists now going on 3 weeks Im not that dizzy but it happens on and off but Im very fatigued and still quite brainfoged. Though all these symptoms comes and goes in ways in a way.
When my muscles burns out I feel terrible. Thats my trigger to feeling worse and PEM. My symptoms do resemble myastenhia gravis and LEMS but I have negative EMG and NCS though I have not had any repetitive stimulation test.
Anyone else?