I watched a video by this young woman today and it made me angry.
She was bravely sharing what it’s like living with POTS — Postural Orthostatic Tachycardia Syndrome.
To be told by a doctor, “There’s nothing you can do… just wear compression socks, drink water, don’t climb high ladders or swim alone” — WTAF?!
Of course I did a quick investigation – my mission is to help humanity thrive, remember? I immediately wanted to know: Can I help?
This condition affects so many — often young women — leaving them exhausted, dizzy, foggy and dismissed.
Turns out… YES, I absolutely can help.
Cellular-level support and nervous system regulation can help address the underlying issues:
- Oxidative stress
- Mitochondrial dysfunction
- Autonomic nervous system overload
- Connective tissue instability
I work with a cellular activation system designed to gently switch the body’s healing processes back on AND as a Spinal Flow Practitioner, I also support deep nervous system regulation — where so much of the dysfunction starts.
If you or someone you love is living with this, please reach out.
There are tools – I can help you find a Spinal Flow Practitioner and the cellular-level support is global.
There IS hope.
#POTSawareness #Dysautonomia #HopeIsReal #CellularHealth #YouAreNotAlone #WomenDeserveBetter
