The POTS is just after surgery as far as I know.. but who knows. It was diagnosed at Mayo in May... and the PCOS was diganosed many years ago... but the majority of the tests I have only had once, not many times... so I don't have a progression to chart... so the results from the tests seem to do just fine and I don't need to chart them again--it would just be repetitive. I have had two nerve conduction studies... and have had bloodwork done often. The bloodwork would be good to chart, but I can't understand what I am reading to transfer it to a chart... so I haven't done that. That seems to be the only chart that would be helpful in my case, since it's the only thing that is done regularly... but I just can't seem to figure it out. It is helpful for those who can, though! It's a wonderful tool.. I just can't seem to wrap my mind around things enough to take advantage of it.
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♥ "Hope is more than a word; it's a state of being. It's a firm belief God will come through. Life brings rain... hope turns every drop into the power to bloom like never before." -Holley Gerth ♥
My name is Sarah and I am 25 years old. I have a lot of chronic health problems. Peripheral neuropathy and POTS (postural orthostatic tachycardia syndrome) keep me bedridden the majority of the time. I also struggle with degenerative disc disease, disc desiccation, spondylolisthesis, arthritis, polycystic ovarian syndrome (PCOS) with insulin resistance, allergies, sound sensitivities, and other health problems.