Hi everyone I am from Uruguay, tiny country in South America. So first I want to apologize for my English. My father has been in dialysis for 16 years (HD). I’m 35 and I have to be honest and say that I, subconsciously, thought it would be tough but not impossible.
I’m very close to my father and my mother and we help each other out in anyway possible. We are positive and happy.
He has been through many surgeries for new AVF (4 at least). He’s 63 years old now and he seems to be exhausted. He always does his best to “hide” anything from his disease not to cause worries. I know that thank God kidneys are different from any other organ. We love those machines that are people’s kidneys!
However, he’s now overwhelmed with all the details that come with this treatment. Legal actions to receive Renvela (things are different here), paying more than we can in order for meds, treatments, equipment, food, etc.
Last October he seemed to have a sprained ankle. We went to emergency 3 times and they had the diagnosis: sprained ankle. Only one of the traumatologists was concerned with an infection and run some tests. One value shouted infection and still since white cells weren’t high. A month went by and he was told that he had to go to the hospital because he needed transfusions. His red cells were too low and they had to find out the cause. On October 13 test started with no answers. Two days later the nephrologist came to his room and said no more tests, he had an infection from a bacterium which was in the blood. It is staphylococcus epidermis, thank God it seems to be sensible to some antibiotics. He started receiving Vancomycin a month ago and tests showed that it was in the prosthesis. So surgery to demolish the AVF and to place a catheter in his neck.
December 13 and he was sent home with the same treatment (plus Rifampicin that’s taken orally). The center is giving him the vancomycin every time he has dialysis.
Sorry for the long explanation but we’re not showing any worries (dad, mom and I) and we are really nervous about it. I’m afraid to be able to do something for him and not realizing, or for thinking it’s even less serious than what I think it is. I’m not a doctor, but here we either learn something or we are not listened to.
I know that infection has to be completely healed in order to think about the next step specially when they have told us many times that this was the last fistula.
I know I am thinking out loud and I am sorry for doing this but I cannot help thinking about wether to insist on the donation or if he would see that as a negative thing he would be more worried about.
I love him and I want to do anything to help him as he does every day since I was born!
Thanks and sorry again!