Dear Vera, I am so happy watching this videó about your recovery. It is like a nice music hearing your words about this process. I wish you many success on this journey and complete recovery!!!
Vera, I’m suffering from long covid with orthostatic intolerance (diagnosed) and POTS like symptoms (not yet diagnosed). so you’re mentioning having POTS symptoms caught my ear. If you are participating in the comments, do you mind by asking; were you officially diagnosed with POTS via any tests? What type of symptoms did you have? It’s encouraging for somebody with POTS symptoms like me that anybody would get better.
I'm a POTS sufferer too and I'm interested to see if she replies. My POTS was vastly improved with regular osteopathic treatments but 3 bouts of covid sent that all to heck it gave me bad insomnia too, up to 4 days no sleep.. Is your POTS from Covid alone or did you have it before Covid?
@@QuintEssential-sz2wn yes, I had fallen on ice prior, my first appointment my osteopath pointed out that one side of my pelvis was drastically higher than the other. He tilted his plastic office spine deco thing (I don't know what they're called lol) and the misalignments went right up and included the skull..
hi! No, I was not diagnosed with POTS officially. But my heart rate would shoot up if I stood for longer than a minute. I tried using heart rate monitoring, but that made it even worse for me because I was constantly checking the device. As I mentioned in the video, I learned that POTS and other symptoms are just secondary symptoms, the consequences of your autonomic nervous system's imbalance. Once you improve the latter (the imbalance), then the secondary symptoms improve on their own.
@@azigaziroth OK thanks very much for the reply. That’s quite common with these conditions. It’s been three years now for me and I keep adding symptoms rather than getting better, so I’m trying brain retraining
Dear Vera, I am so happy watching this videó about your recovery. It is like a nice music hearing your words about this process. I wish you many success on this journey and complete recovery!!!
Thank you! I'm glad it helped, and I'm also wishing you a complete recovery. We'll get there :)
Vera,
I’m suffering from long covid with orthostatic intolerance (diagnosed) and POTS like symptoms (not yet diagnosed). so you’re mentioning having POTS symptoms caught my ear. If you are participating in the comments, do you mind by asking; were you officially diagnosed with POTS via any tests? What type of symptoms did you have? It’s encouraging for somebody with POTS symptoms like me that anybody would get better.
I'm a POTS sufferer too and I'm interested to see if she replies. My POTS was vastly improved with regular osteopathic treatments but 3 bouts of covid sent that all to heck it gave me bad insomnia too, up to 4 days no sleep..
Is your POTS from Covid alone or did you have it before Covid?
@ my orthostatic intolerance developed from having long Covid. That’s wild that osteopathic treatment has helped your pots
@@QuintEssential-sz2wn yes, I had fallen on ice prior, my first appointment my osteopath pointed out that one side of my pelvis was drastically higher than the other. He tilted his plastic office spine deco thing (I don't know what they're called lol) and the misalignments went right up and included the skull..
hi! No, I was not diagnosed with POTS officially. But my heart rate would shoot up if I stood for longer than a minute. I tried using heart rate monitoring, but that made it even worse for me because I was constantly checking the device. As I mentioned in the video, I learned that POTS and other symptoms are just secondary symptoms, the consequences of your autonomic nervous system's imbalance. Once you improve the latter (the imbalance), then the secondary symptoms improve on their own.
@@azigaziroth OK thanks very much for the reply. That’s quite common with these conditions. It’s been three years now for me and I keep adding symptoms rather than getting better, so I’m trying brain retraining