Thanks so much for taking the time to reply. I’m so overrun by disabilities (EDS for one) and it’s been so emotionally and psychologically traumatic (of course, not to mention physically) for me that I almost always feel as though I don’t know my head from my behind. Dreadful! I’m so needy and under-educated about the complexities and dumbfounding magnitude of my rapidly declining health that I would not have imagined that I could possibly have made a diff to anyone else.
Hey, we all make a difference to each other, we’re a family (LOL! could be in more ways than one!). We’re all travelling down the same path, some are in front of us and some are behind us but there’s one thing for sure, we’ve all felt that level of despair you reach when your health is rapidly declining and even those in the medical fraternity who do have the decency to listen, don’t have any answers. I’m hoping all that is about to change. So, in the meantime, I send you a BIG HUG, hang on in there.
Head & Neck Injury (June 2002); Mild Concussion; Post Concussion Syndrome; Postural Orthostatic Tachycardia Syndrome (POTS); Peripheral Vestibular Dysfunction; Mild Radiculopathy & Small Fibre Neuropathy (right leg & foot resp.); Partially Empty Sella (Oct 2002) Fully Blown Empty Sella (Oct 2004); Whiplash Associated Disorder (WAD); Cranio-cervical Instability (CCI) with Posterior Gliding (PG) & Cranial Settling (CS); Retroflexed Odontoid; Stretched/Elongated Brainstem; Vitamin D deficiency; Ehlers Danlos (EDS) type 111; and now Osteoarthritis!