I had regular bloods taken and was ta... - Fibromyalgia Acti...

Fibromyalgia Action UK

59,988 members67,154 posts

I had regular bloods taken and was taken aback when out of the blue was told I have chronic kidney disease stage 3.

nanatre profile image
11 Replies

This came out of the blue, I wasnt told I had been through stages 1 and 2.

Anyone else?

Written by
nanatre profile image
nanatre
To view profiles and participate in discussions please or .
11 Replies
rosehip profile image
rosehip

yes i was toldthis 3 years ago but had a recant test and it came back normal xxx

nanatre profile image
nanatre

WOw! really? How can this happen? I was told that It could never get better? I have to go for another round of bloods etc tomorrow. Will have a word with my doc. Thanks for that hun xx

nadine1974 profile image
nadine1974

is it something the docs have missed in the past? surely you had symptoms? i have little faith in doctors !!

hugs xx

rosylyn profile image
rosylyn

i also have got stage 3 kidney disease mine was due to taking ibuprofen which made my kidneys bleed.so cant take them anymore. [:))]

rosehip profile image
rosehip

i dont no what stage it was but when they told me it scared me . but honest it is now fine xx

nanatre profile image
nanatre

I have no idea Nadine. As I said, it was routine bloods as I had been put on the cholestrol drug, though my cholestrol is 3.4. My toes were going numb and purple almost black at the end of a day. I went to see my doc, she sent me to a vascular surgeon saying I would need this op where they will go in through my groin. So off I go to the hospital dreading what he would say. He did this test down my leg down to my toes, then said my arteries are brilliant, its the little vessels that supply the blood to my toes that have blocked, then said I needed to go on the cholestrol pill. These can damage the liver so my doc said I needed a test 4 weeks after starting the pill. 2 days after the bloods were taken she called me in, and hit me with the chronic kidney disease. I had no symptoms at all. I asked her what I could do to help myself she said dont get stressed, and lose weight.

kraftyk8 profile image
kraftyk8

Hi Nanatre,

Don't be scared, it's not as bad as it sounds here is a link that explains everything about it quite well and you need to discuss with your GP whether the cause is an underlying condition.

patient.co.uk/health/Chroni...

and you can slow it right down and maybe even improve it, buy stopping any anti-inflammatory meds you may be taking, like Ibuprofen (Nurofen) and Diclofenac (Voltarol), as well as helping your kidneys with diet and drinking plenty of fluids. Here is a link to a free recipe book to start you off.

kidneyresearchuk.org/health...

I've had it for about 10 years and my kidneys have been showing as normal in my blood results for the last 3. Against my better judgement, I have let my GP put me back on Ibuprofen and I have to admit the results have been fantastic, it has knocked off all my OA pain.

I've insisted that my bloods are done 3 monthly to make sure that if there is any change in the results I can sort it out quickly.

I hope that helps a bit

happy hugs, kate :)

thinking of you. are you being reffered to a renal specialist or something?

my gp tests my liver function but i don;t think she tests my kidneys. i will talk to her about this x

nanatre profile image
nanatre

Hiya Kate. Thank you so much, I havent been offered anything like that information. Its like, yep you got it, now go live with it. I had an apointment today my BP Is nice and low, doc was pleased/

Hiya Happe, nope, I just have to be monitored. Have to go in for bloods/urine and BP checks.

Well at least I havent got any worse, thats a positive.

Thank you xx

webby profile image
webby

please do not worry they gps dont routinely tell people as it can be reversible because of meds u take its always good to have regular bloods just tom keep eye on yourself they suggets annually it sound worse that you think

1881ellie profile image
1881ellie

Iam devastated to be told this.meant to be naproxen and furosimide that damage mine.I've had scans and bloods done and no cure,I missed stage 1 and 2,3 has only been picked up as I changed doctors.

Not what you're looking for?

You may also like...

I have had Fibromyalgia for 19 years and have many of the symptoms

. I also have a degenerative disease in my spine. So you can imagine what sort of pain I am in. I...
mollieo profile image

Got taken off high rate mobility and high rate care had it taken off me last year that’s a year before it ran out I have appealed and with

I’m disgusted how they can do this to me as I’m very sick mentally and physically I don’t know what...
Manda688 profile image

Hi all, I,ve noticed that many of you have other conditions as well as fibro. When I was diagnosed the rheumy said that this was usually the

Case, I,m healthy apart from depression which was well controlled with medication. So, I,m...
wildwoman profile image

Fibro and hypothyroid disease I have symptoms of fibro and hypo T. On the Thyroid u.k. site they have polls trying to gather info.

My question is does Fibro Action conduct polls from bloggers, and if so could they possbly do one...
siskin profile image

Hi I have had FMS for 9 years and I was wondering if anyone else has the following symptoms? Or do I need to speak to my GP again.

When I have a flare up and I am eg walking the dog (which isn't far) walking up stairs I find it...
Riles-17 profile image