Well... I can tell you this much. My husband carries way tooooo much. It is not unusual for them to take off 14 lbs. on the inbetween days of the week and sometimes 18 lbs. after the weekends. I didn't ask how much they took off today. Last night I noticed the fronts of his hands even looked somewhat blown up. I have to think that in order get a dry weight that works best for you, you need to come in at the same weight each time. If you flucuate they'll never figure it out. PS: sometimes when a lot of fluid is taken off he drops his BP (like others I'm sure) and gets dizzy. Why do they put saline in the line to help with this? I can see rehydrating with fluid but saline is essentially salt right? Thanks
I posted earlier on the variance of opinions of some of the health professionals I deal with. One major difference, from my experience, is in how much fluid I should retain, and therefore, what my ideal body weight target should be.I first started on haemodialysis and their objective was to get me as dry as a desert in the middle of a drought.As this was all new to me, I initially accepted that this was how it had to be, - always thirsty, headaches, cramps, blood pressure drops during dialysis etc. After 3 or four weeks I decided that I would be better off carrying more fluid, provided my blood pressure was not adversly affected. Despite their resistance, I managed to get them to raise my body weight by a couple of kilos and the worst of the synptoms disappeared. I had also noticed that my urine output was steadily decreasing from around 900ml daily down to 200 and falling. Because they refused to consider raising my target any further, I developed a couple of strategies to circumvent the system. One of these was to clench the muscles in my ankles when they palpated that area to check for signs of edema. Works a treat. The other was to record my weight as being 2kg less than it actually was. So instead of the 72kg they initially wanted my target to be, I was, unbeknown to them at 76kg and felt so much better. My urine output also began to increase. Everyone was happy.Then I went on to PD. Same hospital, different department and totally different outlook. They encouraged me to carry a little more. I increased my target weight to 78kg. (That's 6 litres more than the haemo people initially wanted me to carry!!.) My urine output increased to 6/800ml per day. That is where it has stayed, with my PD co-ordinator stressing the importance of maintaining that for as long as I possibly can, so as to maintain what little residual kidney function I may still have. Bp is currently a consistent 120/70.Doubtless, that would also go some way to explaining why I feel so well on dialysis, - my kidneys are still doing a little bit of the work.To me this is just a further reminder that there is no "Gold Standard" in renal treatments and that so much depends on the personal views of the professional that I am dealing with at the time.It further reinforces my belief that it behoves us all to question our service providers, make them justify their opinions, (even if that means trading on some toes) and ultimately, makie our own decisions as to the form our treatments will follow.