Polycystic Kidney Disease (PKD) Support Group
Polycystic kidney disease (PKD) is a progressive, genetic disorder of the kidneys. It occurs in humans and other organisms. PKD is characterised by the presence of multiple cysts (polycystic) in both kidneys. The disease can also damage the liver, pancreas and rarely the heart and brain.
So sorry you have this problem again. Hopefully the antibiotic will start to take effect soon. I was given the same one back in January and I did recover, though nobody actually knows what I had. The augmentin really upset my digestive system, which is just what you need on top of the symptons you already have. Make you you take it with food (diffcult when you have severe nausea). If it doesn't work, you may need a different antibiotic.
Get well soon,
Chewitt
1. Your infection didn't clear up completely whilst in hospital and so it's back.
2. You didn't have a kidney infection and the symptoms were from the cyst bleeds, which can be very painful indeed.
3. You have a new infection.
3. You have new cyst bleeds.
I guess you need to go back to your doctor to check for infection again. Sometimes people neeed to take antibiotics (the right ones) for several weeks to make sure the infection is conquered.
Is it possible that you're over doing things and causing cyst bleeds by something you're doing? I had a terrible time after shovelling snow a few years ago, but also found things like grocery shopping, lifting and carrying any weight at all caused problems. Even wearing shoes with rigid soles which didn't cushion the blow of walking caused me problems with pain which I think was from ruptured cysts. I now avoid any physical stress to my body and choose my footwear carefully.
I completely understand that you are fed up with this. I feel like that at times, too. I narrowly avoided hospital myself back in January and was very relieved. Your GP probably won't know what to do so it might be worth calling your renal consultant for advice.
Let us know how things go.
Take care,
Chewitt
I'm am currently seeing a rheumatologist as they think I have sjogrens which is an autoimmune condition. I know that this can also effect the kidneys but not sure how or if that may be an issue, my rheumatologist and nephrologist are at different hospitals in different areas, I think I need to move care so they are at the same hospital so I can have some joined up care.
Temperature has been ok this week, just painful kidneys, I am just considering changing my nephrologist so it is the same hospital where I end up being admitted too in the hope the treatment may be a bit more catered to my illness rather than general medics