I'm frustrated with myself. To be more accurate, my body. I have always struggle with drinking water and I have been dehydrated and sent to the hospital because of it three times already. When I was diagnosed with POTS, I never thought that water would be the golden ticket to functioning. It's not only that I hate water, it's that drinking 64 oz or more in a day has proven to make me nauseous. Putting anything in my stomach makes me nauseated.
So what's the solution? IV hydration therapy. I thought, wow I can't believe I can do it this way! Then after two months of getting stuck with needles twice a week, I realized that I couldn't endure long term. Not just because of nurses missing the vein and having to stick me again or the crazy bruising around every area they poke and not even just the poking itself. It was because long term veins train themselves not to get poked and I would have to get a port.
What is a port you ask? To be honest all I know is that it's a device that gets surgically inserted into your body and it allows you to get fluids from there. Yes I'm chronically ill and I'm used to tests, procedures, and needles but I have never had a surgery as an adult. So I thought I'd try to drink water on my own again. I can't describe the dark yellow color that my urine is right now. And I'm drinking as much as I can endure.
So I'm frustrated. I don't want to do this but I know I have to. I have to take care of my body even if it means doing things I don't like. Until then, I am going to do anything else to ignore the fact that I'm crazy dehydrated. Hopefully until I can set everything up, I won't be hospitalized.