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Reactive Hypoglycemia
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<blockquote data-quote="SarahTee" data-source="post: 2348726" data-attributes="member: 518070"><p>G'day folks,</p><p></p><p>I just wanted to drop back in briefly with an update. I ended up purchasing a basic blood sugar monitor, and was able to establish that my readings were in the normal range, despite my persistant feeling of fatigue that "felt like" low blood sugar.</p><p></p><p>Well, my condition isn't sorted out yet, but I have made important progress by discovering that it is caused by low blood volume.</p><p></p><p>As my symptoms seemed to point towards dysautonomia, and had a lot in common with POTS symptoms apart from the tachycardia, I had been working my way through POTS interventions (with the approval of my GP). Finally I hit the jackpot when a salt and water bolus (drinking a large-ish amount of water and taking in salt over a short period) resolved my symptoms. The effect of a salt and water bolus is to raise your blood volume, so now at least we know what the problem is.</p><p></p><p>It's not all plain sailing yet. I am having trouble working out the right dose, and I still need to have investigations to see what is causing the dysautonomia symptoms. I may end up taking medication, or using a different intervention. I do feel hopeful that the culprit has finally been identified; now to persevere with treating it.</p><p></p><p>I just thought I would post this here in case it was of interest to anyone else, and I also wanted to thank everone here who read my posts and kindly offered support and information.</p><p></p><p>Thank you!</p><p>Sarah</p></blockquote><p></p>
[QUOTE="SarahTee, post: 2348726, member: 518070"] G'day folks, I just wanted to drop back in briefly with an update. I ended up purchasing a basic blood sugar monitor, and was able to establish that my readings were in the normal range, despite my persistant feeling of fatigue that "felt like" low blood sugar. Well, my condition isn't sorted out yet, but I have made important progress by discovering that it is caused by low blood volume. As my symptoms seemed to point towards dysautonomia, and had a lot in common with POTS symptoms apart from the tachycardia, I had been working my way through POTS interventions (with the approval of my GP). Finally I hit the jackpot when a salt and water bolus (drinking a large-ish amount of water and taking in salt over a short period) resolved my symptoms. The effect of a salt and water bolus is to raise your blood volume, so now at least we know what the problem is. It's not all plain sailing yet. I am having trouble working out the right dose, and I still need to have investigations to see what is causing the dysautonomia symptoms. I may end up taking medication, or using a different intervention. I do feel hopeful that the culprit has finally been identified; now to persevere with treating it. I just thought I would post this here in case it was of interest to anyone else, and I also wanted to thank everone here who read my posts and kindly offered support and information. Thank you! Sarah [/QUOTE]
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