Being a dialysis patient means you have to learn to compromise. Often, this means giving up certain activities and foods, hobbies and pastimes, as well as, in my case, working for a living.Of all the things I've had 'taken away' by this condition, I have to admit that I miss sex the most. I did try viagra, but it wasn't very useful, to tell the truth. I spoke to the doctor and he said he could up the dosage. I have yet to try it.(The stronger dosage, that is.) Mainly because I can't afford it right now, but also because of my experience with it before.It's hard enough being so useless, but being unable to please my wife is really playing on my mind, deeply. I also spoke to the doc about the possibility of getting testosterone injections. He said they could test me for a testosterone lack, but he didn't think injections would be the answer, for me.What's a guy to do?Useless near Seattle.
Right now I really miss swimming and sun bathing.
For me, what I missed most during the nine years I was on dialysis was my sense of being in control of my own life, since every other day was destroyed by the need to devote about 7 hours to renal therapy, counting the time to get to the dialysis center and back, and to wait around to be put on and taken off. Together with the constant exhaustion, it made me feel that my life was some sort of bizarre nightmare filled with punishments, rather than what it had always been before, which was a creative endeavor to shape my own plans and realize my goals.
But i miss the sound of a press and the smell of ink.
I know we could still go on a vacation, but what if I get sick, what if I hit the organ lotto, what if..., what if..., what if.... I feel like I'm serving a prison sentence and I have no idea when or if it will end.