I've really been enjoying reading all of the testimonials on here, and seeing people sort through things in the spirit of this forum. Since I know there are lots of fellow problem solvers on here, I figured I'd put this out there and see what theories you all have. Mine are half-baked, mostly. But at this point anything is worth considering, so here we go....
I have had 2 pregnancies in the last 3 years. Both went quite well overall, I had zero medical interventions and delivered at home with a midwife. However, something happens that nobody can really seem to help me with. At about 20 weeks gestation both times, I began to have extremely low blood pressure. Not all day long, just in the mornings. It didn't matter when I woke up or what I did. I tried everything, from eating first thing and drinking salt water before getting up to taking large amounts of b and c vitamins, magnesium, and potassium, high protein, herbs, you name it. Anything that was supposed to support healthy blood pressure and support the adrenals, I tried, and nothing made a dent in it. I was quite literally completely incapacitated for the first half of the day. It would often be 1 or 2 o'clock before my blood pressure stabilized and I could actually function. This was extremely hard, especially the second time around because I felt the dizzy spells were more intense and lasted longer and I also had a toddler to take care of. The only label anyone could offer me was POTS, but along the lines of gestational diabetes because the odd thing was the SECOND I delivered the baby, poof, no more POTS. Also, I really didn't have the other symptoms of POTS, nor did it come and go throughout the day. Once my blood pressure stabilized after a few hours, I was good to go for the rest of the day. No more laying on my side, trying to catch my breath and not faint.
One theory I've revised several times is that this is due to a TBI I had 7 years ago. I suffered whiplash, a serious neck injury, and occular damage. I couldn't drive for several months and did PT as well as therapy to "retrain" my eyes to work together. I've had damage to my peripheral vision and visual sensitivities ever since, as well as other unpleasant things. I've long been interested in fully healing my brain and eyes, but I've been searching for how. It's occured to me that this could play a part in what appears to be an nervous system malfunction that's only symptomatic when I have expanded blood volume.
The other theory has only recently began to form since finding low vA. POTS is not technically an autoimmune disease as I understand it, and I've not seen Grant refer to it at all in his book with the others. However there seems to be enough reason to believe it's in the same genre for me to wonder-- is this just damage to the epithelial tissue of the adrenals? Or the peripheral nervous system? But then why only come out to play during pregnancy (at least, for now.) I have so many questions since finding the vA and autoimmune connection, and wonder am I on the right track but not quite hitting the mark? Or maybe I'm looking in the wrong places entirely. If you've read this far you know as much as I do now, really. This is critical to me though. If I can't get to the root of this, I don't know how many more pregnancies my body can handle, especially if my second one being much harder is any indication of how this "disease" will progress. We want to be happy with as many children as God gives us but I have a hard time accepting that we might have to put a cap on that prematurely because of some mysterious medical event. If you love a good puzzle, give me your best take. Idc if it has nothing to do with my theories, which are as I said are half-baked as it is. I'd just love some fresh eyes on this situation! We'd like to try for a third in the next year or so.
I have had 2 pregnancies in the last 3 years. Both went quite well overall, I had zero medical interventions and delivered at home with a midwife. However, something happens that nobody can really seem to help me with. At about 20 weeks gestation both times, I began to have extremely low blood pressure. Not all day long, just in the mornings. It didn't matter when I woke up or what I did. I tried everything, from eating first thing and drinking salt water before getting up to taking large amounts of b and c vitamins, magnesium, and potassium, high protein, herbs, you name it. Anything that was supposed to support healthy blood pressure and support the adrenals, I tried, and nothing made a dent in it. I was quite literally completely incapacitated for the first half of the day. It would often be 1 or 2 o'clock before my blood pressure stabilized and I could actually function. This was extremely hard, especially the second time around because I felt the dizzy spells were more intense and lasted longer and I also had a toddler to take care of. The only label anyone could offer me was POTS, but along the lines of gestational diabetes because the odd thing was the SECOND I delivered the baby, poof, no more POTS. Also, I really didn't have the other symptoms of POTS, nor did it come and go throughout the day. Once my blood pressure stabilized after a few hours, I was good to go for the rest of the day. No more laying on my side, trying to catch my breath and not faint.
One theory I've revised several times is that this is due to a TBI I had 7 years ago. I suffered whiplash, a serious neck injury, and occular damage. I couldn't drive for several months and did PT as well as therapy to "retrain" my eyes to work together. I've had damage to my peripheral vision and visual sensitivities ever since, as well as other unpleasant things. I've long been interested in fully healing my brain and eyes, but I've been searching for how. It's occured to me that this could play a part in what appears to be an nervous system malfunction that's only symptomatic when I have expanded blood volume.
The other theory has only recently began to form since finding low vA. POTS is not technically an autoimmune disease as I understand it, and I've not seen Grant refer to it at all in his book with the others. However there seems to be enough reason to believe it's in the same genre for me to wonder-- is this just damage to the epithelial tissue of the adrenals? Or the peripheral nervous system? But then why only come out to play during pregnancy (at least, for now.) I have so many questions since finding the vA and autoimmune connection, and wonder am I on the right track but not quite hitting the mark? Or maybe I'm looking in the wrong places entirely. If you've read this far you know as much as I do now, really. This is critical to me though. If I can't get to the root of this, I don't know how many more pregnancies my body can handle, especially if my second one being much harder is any indication of how this "disease" will progress. We want to be happy with as many children as God gives us but I have a hard time accepting that we might have to put a cap on that prematurely because of some mysterious medical event. If you love a good puzzle, give me your best take. Idc if it has nothing to do with my theories, which are as I said are half-baked as it is. I'd just love some fresh eyes on this situation! We'd like to try for a third in the next year or so.
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