beenblessed_nana, this website can be confusing for first timers and new users. I would say that more than half of the polls were people simply not understanding how to use the site and getting confused.
I think the OP just wanted some help and reassurance and is probably embarrassed to answer you now. It's always best to play nicely.
Hi there. Still posting, and my kidney function, after almost a dozen years, is still stable. I was never able to return to work, but I had other medical issues. Basically, despite some setbacks over the years, I am a happy camper. I met a great guy and got married between my kidney transplant and my pancreas transplant. By that point I was too old to want to think about kids, but I do know of transplanted women who have had successful pregnancies.
All I can say is keep your head up. You are going to be ok. And if you don't have someone in your life right now, there is every possibility that you will. Best of luck.
I've never seen that before, but just from a language perspective, itmeans that the kidney is producing what it's supposed to, into the bladder. So you are producing normal urine. Double check with the doc if you are worried.
Many of us who have been on dialysis have had problems with cold. Keep in mind, that the dialysis machine cools the patients blood to help prevent clotting. So the patient is cooled from the inside out. Brrrr. And then the machines generate a lot of heat and the nurses need to be kept cool, so the AC is often turned up. Whether this could cause pain, I don't know. I never had pains or cramps, but that could just be me.
I felt better by bringing some warm and cozy blankets with me to dialysis. I looked a bit like I was going camping, but at least I was comfy. Talk to the dr at the center and the nurses. Maybe they can come up with something to help.
I'm so sorry that your aunt isn't doing well. While on dialysis I did see a few elderly folks decide to stop. Have you considered talking to her about giving it a try? She could always decide to not continue if she wants.
That said, there really is no way to tell how long she could last - especially since you don't mention any #s. She oculd pass quickly, if she catches something that makes her ill. Or things could stabilize. There is simply no way to predict. Have you, as family, gone with her to a Dr. appointment?
So sorry. We've been there. The good news is that there is life after dialysis starts. Some people do continue to work. But the transition is hard and requires some mental adjustment. And it also takes some time to get the prescription right. It's just like taking a med, you have to find the right "dosages". Here's hoping things remain stable for a while.
Sorry, I just went on a ramble about peritoneal dialysis and then remembered you talked about a fistula. So I deleted the irrelevant stuff. As for whether or not home hemo is covered, I have no clue as I am Canadian. But had several friends doing it and if you can get it, I would suggest that you go for it. It is considered the next best thing to a transplant. Virtually no dietary restrictions and you feel almost normal. One friend could walk around the block while on in-center hemo and on home hemo he was biking about 20 miles per day. With that said, it's not easy and requires quite a bit of training. But from the sound of it, your husband is a competent individual and should be able to handle it.
You absolutely want to be prepared ahead of time. My plan for PD was to go to a conference on the other side of the continent, come home and have the catheter inserted, and then slide gracefully onto dialysis. Well, my life had other plans. I got double pneumonia and had a small MI wihile at a hotel 3 time zones away from home. I flew home after 2 weeks in hospital with a femoral line. Not fun!
Obviously, I'm an extreme case. And also obviously, I left things too late. Kidneys are unpredictable, as John said. At a GFR of 22, the unfortunate truth is that bad things can happen. What's the worst that can happen if you get it done right away an ddon't need it? Nothing. A friend of mine had his PD catheter put in at what appeared to be roughly the right time. And then things stabilized. And he didn't need it for 6 years. But he had the security of knowing that he was ready at a moments notice. That is what I would want and what I would do if I had a do-over.
Organs don't need to be "detoxed". If you like the taste of cilantro and lemon, then by all means, drink it. It's not like your kidneys get "dirty" and they need to be cleaned and dusted like a nicknack on a shelf. The human body cleans itself.View Thread
It's fairly straightforward, actually. And it's for your friend's safety. Even though "technically" your friend may currently be considered cancer free, it is possible that microscopic cancer cells are still present. Transplant centers require that people with cancer be sure that they are truly cancer free, and that they are not likely to develop cancer again. The immune system battles these tiny cancer cells. If your friend gets a kidney, they will be immunosuppressed. And even in the best case scenarios, they will be at a higher risk for cancer. Right now, shortly after the cancer, getting a kidney and getting the anti-rejection drugs would mean a significantly higher risk of getting cancer again. And more aggressively probably.
Some centers require a 5 year wait to ensure that the former cancer patient doesn't die of cancer shortly after getting a new organ. It's for safety. By waiting a few years, you are making sure that the cancer is truly gone and will not recur.
Hope this helps clear things up for you. And thank you so much for being willing to donate.