My cardiomyopathy is genetic so I guess I have had it all my life. That being said its only really impacted my life over the last 5/6 years. Not sure (and don't care) where the 53 years came from.
I am sorry you are going through this and I'm sorry I can't really help much. Just thought I'd mention an article in the paper yesterday saying how the drug Empagliflozin is helping people with kidney issues and it also protects the heart. Are you on this? It's normally only given to people with diabetes. I take it. Just a thought that might be worth mentioning.All the best, Susie.
My report says chronic renal impairment but the doctor says it usually happens in people as they get older. I was concerned because my mother died of renal failure but he said my results were not a worry. I haven't been referred to a renal specialist, though. I just have 6 monthly blood tests.
Good morning curryandchips. No there is no cure for kidney disease. But it's good that you are being referred to a kidney specialist. Who will keep you under observation and try to maintain your present Egfr. With the help of you keeping fit and exercises and eating the right food and then depending on your age. You will be able to go on the kidney transplant waiting list for when your Egfr gets a lot worse. I have a friend who got the call just last Friday morning at 2am to go to hospital. He has had his new kidney and is walking around the ward now. There's a very informative Facebook group. Chronic kidney disease uk. You will get plenty of information from there.Your Blood pressure is also very good. Which helps your kidney function. Good luck and keep in touch. Brian
Sorry to hear your situation. I have dilated cardiomyopathy and my kidneys function are reducing too.
I had some new tablets added and I’ve been taken off warfarin to one of the newer anticoagulation tablets. Even that one was reduced because it was affecting my kidneys. I also have pulmonary hypertension.
I feel these things are part of my reduced life expectancy. I’ve had 20 yrs good run since I went into heart failure. I think because of my weakened heart I can’t expect too much because eventually my other organs will suffer too, which is what is happening. I’m taking so many tablets now daily, I’m being monitored by my GP and cardiologists mainly to check my kidney function.
Just seen this.......A new, first-in-its-class treatment for hypertrophic cardiomyopathy, mavacamten, has been a game-changer for my patients with obstruction.
Obstructive Hypertrophic Cardiomyopathy. I have dilated Cardiomyopathy so I don’t know if it will work the same. I see my heart failure cardiologist in May then my EP a month after, so I will find out how I’m coming along. At the moment they’re trying to improve my kidney function which is dropping.
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