Can I please find out how I would go about get some of the information that you may have on P.O.T.S and fibromyalgia with out having a Facebook page please.
Absolutely, please email us at connect@activehealthclinic.com.au and let us know what support/resources you're looking for and we can find some more videos and resources for you.
This is not correct for people living with EDS and HSD. You are only referring to the population of ME/CFS. People with Dysautonomia and EDS and HSD have very identifiable triggers such as ligament laxity as muscles are both affected by weak CT in addition to having to work extra hard to compensate for ligament laxity, OI, OH, Inadequate blood flow also means low O2 to the cells and impaired perfusion leads to failure of the M’s to function adequately, not to mention MCAS, Medication, Sleep aponea and hyperarousal, Hormonal dysfunction, Autoimmune dysfunction and Anemia. What you have covered is ME/CFS, not the other more complex conditions. This doesn't cover any of the complexities of the multisystem issues.
Thanks for your comment, we absolutely agree, if we dive into this concept further, there is so much context that could be covered that you've mentioned. We do have quite a few longer videos that tend to cover this rather than this short one, but we do appreciate your feedback.
