Kidney failure symptoms include weakness, diarrhea, and unusual bleeding, which can lead to complications that worsen kidney disease or cause kidney failure. Dehydration can decrease blood flow to the kidneys, causing sudden or acute kidney injury (AKI). A study found that 1 out of 10 adults hospitalized for diarrhea develop AKI. Patients with chronic kidney disease (CKD) commonly experience gastrointestinal symptoms such as dysgeusia, anorexia, dyspepsia, hiccups, nausea, and vomiting. GI hemorrhage occurs more frequently in CKD patients, and lower GI tract symptoms include constipation and diarrhea. Symptoms may include hemorrhage, fever, weakness and fatigue, fatigue, rash, diarrhea or bloody diarrhea, poor appetite, severe vomiting, and weight loss.
Diarrhea can cause complications that can worsen kidney disease or cause kidney failure. Acute kidney injury symptoms include feeling sick or being sick, diarrhea, dehydration, peeing less than usual, confusion, and drowsiness. Patients with end-stage kidney disease (ESKD) most commonly complain of gastrointestinal symptoms, such as diarrhea. Acute kidney injury is common and consequential among patients hospitalized for diarrheal illness, with CKD and hypertension being the most susceptible.
| Article | Description | Site |
|---|---|---|
| Kidney Failure Symptoms | The following symptoms may be observed: The following symptoms may also manifest:1. Hemorrhage (unusual bleeding)2. Fever3. Weakness and fatigue4. Rash5. Diarrhea or bloody diarrhea6. Poor appetite7. Severe vomiting | stanfordhealthcare.org |
| Symptoms of Acute Kidney Failure | The symptoms of acute kidney failure include hemorrhage, fever, weakness, fatigue, rash, diarrhea (either diarrhea or bloody diarrhea), poor appetite, and severe vomiting. | stanfordhealthcare.org |
| End-Stage Renal Disease – Symptoms and Causes | Diarrhea is defined as the involuntary passage of stool on a frequent and regular basis. Individuals afflicted with renal disease frequently present with gastric distress, manifesting as diarrhea and emesis. Weight Loss: A considerable number of patients present with an unidentified reduction in body weight. | www.texaskidneycare.com |
📹 What are the Symptoms of Chronic Kidney Disease and Kidney Failure? | The Cooking Doc®
Do you have family history of kidney disease and want to know the signs and symptoms? Perhaps you have risk factors like high …
Is diarrhea caused by kidney infection?
Kidney infections are always caused by a pathogen in your organs. The beginning of a kidney infection may produce back pain, fever, chills, fatigue, loss of appetite, nausea, vomiting, and diarrhea.
END IMAGETAG Your kidneys are a pair of organs located in the middle of your back, just below your ribs. Their primary function is to filter waste from your blood into your bladder for elimination. Kidney infections are caused by pathogens — like certain kinds of bacteria — in one or both of these organs.
How do you know if you have a kidney infection ? Symptoms tend to set in suddenly — over just hours or days.
What is the first indication of kidney failure?
If your kidneys aren’t working properly, you may notice one or more of the following signs: Extreme tiredness (fatigue). Nausea and vomiting. Confusion or trouble concentrating.
What is kidney failure?. Kidney failure (renal failure) means one or both of your kidneys no longer function well on their own. Kidney failure is sometimes temporary and develops quickly (acute). Other times it’s a chronic (long-term) condition that slowly gets worse.
Kidney failure is the most severe stage of kidney disease. It’s fatal without treatment. If you have kidney failure, you may survive a few days or weeks without treatment.
What do the kidneys do?. Your kidneys are bean-shaped organs about the size of your fist. They sit under your ribcage, toward your back. Most people have two working kidneys, but you can live well with only one kidney as long as it’s working correctly.
Is diarrhea common in dialysis patients?
Background: Diarrhea is one of the symptoms occasionally seen in patients initiating hemodialysis. When they have diarrhea, they need several additional cares for defecation during the hemodialysis sessions and for infection control at dialysis facilities. Methods: We retrospectively examined the prevalence and the characteristics of the patients with diarrhea initiating hemodialysis. Data were collected from medical records. Results: Of 243 patients who initiated hemodialysis therapy, 46 patients (19%) had diarrhea. The age, gender, and etiology of end-stage renal disease did not differ between the patients with diarrhea and those without diarrhea. Body weight in the patients with diarrhea was lighter than those without diarrhea. The prevalence of concomitant diseases, such as cardiovascular diseases, malignancies, and diabetes, was not different between the groups, whereas the patients with diarrhea were complicated more frequently with infectious diseases. Antibiotics and steroids had been used more frequently in the patients with diarrhea (59% and 26%, respectively) than those without diarrhea (10% and 10%, respectively). Inflammatory markers, such as white blood cell numbers, C-reactive protein levels, and body temperature, were significantly higher in the patients with diarrhea. Serum levels of total protein, albumin, and creatinine were significantly lower in the patients with diarrhea, while urea nitrogen levels did not differ between the groups. Conclusion: Results of the present study showed, for the first time, that 19% of the patients initiating hemodialysis had diarrhea and suggest that incident hemodialysis patients with infectious diseases and those under treatment with antibiotics and/or steroids are high-risk for diarrhea.
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- Uremia
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Can diarrhea be a symptom of kidney failure?
- Swelling: The most common symptom is swelling in the hands and feet of kidney disease patients because the body retains water, which causes swelling.
- Urination: The quantity of urine becomes less over time. It goes from normal quantity to very low or not enough urine.
- Shortness of Breath: Kidney patients usually have trouble catching their breath due to excessive fluid buildup near the lungs.
- Rashes: Patients have persistent itching and rashes because of imbalanced chemical elements in their bodies.
- Fatigue: Patients usually feel tired and generally ill. Their immune system also becomes weak.
- Chest Pain: When the fluid is not removed and builds up near the heart lining, a patient might start experiencing chest pain.
- Hypertension: High blood pressure is another symptom of kidney disease. At times it is difficult to control.
- Headaches: Another common symptom is a headache that people easily neglect and do not take seriously.
- Difficulty in Sleeping: A patient may have trouble sleeping due to excessive water in the body and fluid buildup near the lungs or heart.
- Diarrhea: Kidney patients usually have an upset stomach causing diarrhea and vomiting.
- Weight Loss: Many patients experience unexplained weight loss while suffering from this illness.
- Bruising: Kidney patients may bruise very easily anywhere in the body, even from a simple scratch.
Other symptoms include bone pain, confusion, decreased mental sharpness, nosebleed, bad breath, and excessive thirst.
What Are the Major Causes of ESRD?. In kidney disease, the nephrons are destroyed, which are the tiny filters on each kidney that help clean the blood and separate waste materials from it. The damaged nephrons do not clean blood properly, causing severe organ damage and eventually ESRD. As reported by many patients, the major causes of kidney disease are diabetes and high blood pressure.
What are the warning signs of renal failure?
Depending on how severe it is, loss of kidney function can cause:Nausea. Vomiting. Loss of appetite. Fatigue and weakness. Sleep problems. Urinating more or less. Decreased mental sharpness. Muscle cramps.
What is kidney disease? An expert explains. Learn more from kidney doctor Andrew Bentall, M. D.
I’m Dr. Andrew Bentall, a kidney doctor at Mayo Clinic. I look after patients with kidney disease, either in the early stages, or with more advanced kidney disease considering dialysis and transplantation as treatment options. In this video, we’ll cover the basics of chronic kidney disease. What is it? Who gets it? The symptoms, diagnosis and treatment. Whether you are looking for answers for yourself or for someone you love, we’re here to give you the best information available.
Chronic kidney disease is a disease characterized by progressive damage and loss of function in the kidneys. It’s estimated that chronic kidney disease affects about one in seven American adults. And most of those don’t know they have it. Before we get into the disease itself, let’s talk a little bit about the kidneys and what they do. Our kidneys play many important roles keeping our bodies in balance. They remove waste and toxins, excess water from the bloodstream, which is carried out of the body in urine. They helped to make hormones to produce red blood cells, and they turn vitamin D into its active form, so it’s usable in the body.
Can kidney or liver failure cause diarrhea?
If you have acute liver failure, you may have symptoms such as: Diarrhea.
What is acute liver failure?. Acute liver failure is a rare condition. It happens when your liver suddenly starts to not work. This often happens right after an overdose of medicine or poisoning. Chronic liver failure happens over a long stretch of time.
What causes acute liver failure?. Taking too much acetaminophen causes most cases of acute liver failure. Acetaminophen is a painkiller found in many over-the-counter and prescription medicines. Certain diseases can also cause acute liver failure, such as hepatitis and Wilson disease. In some cases, the cause for liver failure is unknown.
Who is at risk for acute liver failure?. You are at risk for acute liver failure if you:
Does high urea cause diarrhea?
Methods: This study was carried out in Manipal Teaching Hospital, Pokhara, Nepal over duration of one year. The aims were to find out the association of renal function and electrolyte disturbances with type of diarrhea, severity of dehydration and their relation to outcome. All children more than one month and less than 15 years with acute diarrhea were included in the study. Data were entered and analyzed by SPSS version 19. Statistical analysis applied was Chi-square test. A p-value of Results: Acute watery diarrhea was the commonest type of diarrhea in children. Dehydration was associated more with Acute Watery Diarrhea than with Invasive Diarrhea. Renal function and electrolyte abnormalities were seen more in Acute Watery Diarrhea with increasing levels of blood urea, serum creatinine and abnormal levels of serum sodium seen with increased severity of dehydration.
Conclusions: Abnormalities in renal function and electrolytes correlated significantly with severity of dehydration. The outcome of patients correlated with severity of dehydration with mortality occurring in 18. 1% of patients with Severe dehydration, 0. 8% of Some dehydration with no mortality in the No dehydration group.
Keywords: Acute diarrhea; children; dehydration; electrolytes; renal function..
What is the best indicator of renal failure?
Creatinine is a common measure of kidney function, produced at a constant rate by the body depending on muscle mass. It is used to monitor the progression of renal disease and is usually suspected when serum creatinine is greater than the upper limit of the “normal” interval. Creatinine values may alter due to factors such as muscle function, composition, activity, diet, and health status. Elevated creatinine values are seen in patients with kidney dysfunction, such as muscular dystrophy paralysis, anemia, leukemia, and hyperthyroidism.
Urea is a major nitrogenous end product of protein and amino acid catabolism, produced by the liver and distributed throughout intracellular and extracellular fluid. The most frequently determined clinical indices for estimating renal function depend upon the concentration of urea in the serum. Urea clearance is a poor indicator of glomerular filtration rate as its overproduction rate depends on several non-renal factors, including diet and urea cycle enzymes. Increased blood urea nitrogen (BUN) is associated with kidney disease or failure, blockage of the urinary tract by a kidney stone, congestive heart failure, dehydration, fever, shock, and bleeding in the digestive tract. High BUN levels can sometimes occur during late pregnancy or result from eating large amounts of protein-rich foods.
Cystatin C, a non-glycosylated low molecular weight protein, has been proposed as a marker of glomerular filtration rate. It is produced by all nucleated cells at a constant rate and is freely filtrated by the glomeruli and completely catabolized in the proximal tubules. The concentration of serum Cystatin C is mainly determined by glomerular filtration, making it an endogenous marker of glomerular filtration rate.
In a meta analysis study, Cystatin C was found to be superior to serum creatinine as a marker of glomerular filtration rate. It has been found to be an effective marker for glomerular filtration rate in patients with cirrhosis following liver transplantation, more useful for detecting early renal impairment in both type 1 and type 2 diabetic patients, and associated with mild kidney dysfunction with increased risk for cardiovascular events, peripheral arterial disease, and heart failure.
Does uremia cause diarrhea?
Clinical signs of GI complications or uremia may include anorexia, nausea, vomiting, abdominal pain, diarrhea, and GI bleeding.
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How to stop diarrhea in kidney patients?
Medications for diarrhea Imodium A-D, Kaopectate, Pepto Bismol Imodium A-D is considered safe for people with kidney disease if used for no more than 48 hours.
What are the gastrointestinal symptoms of renal failure?
Introduction. Patients with chronic kidney disease (CKD) frequently experience upper gastrointestinal (GI) symptoms including dysgeusia, anorexia, hiccups, stomatitis, nausea, vomiting, and gastroparesis. Constipation and diarrhea represent the main lower GI tract symptoms associated with CKD.
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📹 Kidney Failure Symptoms: 10 Signs Most People Will Miss!
Today we are discussing kidney failure symptoms, the signs of chronic kidney disease (CKD). Many of my patients whom I …
I was diagnosed 6 months ago when routine blood work showed GFR of 30. After saw nephrologist we determined it was likely caused by an NSAID I was taking. I went for the visit with a lot of anxiety and depression and left the office hopeful. He switched some of my meds to more kidney-friendly and gave me something to focus on—daily BP and daily weight. Over the next 6 months I lowered my sodium intake. at that point my GFR rose to 45 and my BP returned to normal without medication! I’m thrilled, but there is still more I can change to help lower the pressure on my kidneys. The thing is, its easy to panic at all the changes after you are diagnosed. Start slowly with something you think you can manage. Face up to the fact that you grew up with a set of food habits, but you can change those habits. A little success makes the next step easier. Its a journey. Good lick on all your journeys!
Hi Dr. Blake, i am a diabetic and stage 3b kidney patient, so my diet need to watch out for two troubles. I talked my doctor about what to do, he just say “Don’t eat!” I hung on, his next response was “eat sawdust and plywood.” That was a very unproductive meeting. I am trying to figure this out myself and feel overwhelmed. I like keto diet, but isn’t it opposite to my diabetic diet? So, please give me a suggestion as to which diet I should follow. Thank you for your help. Lai Ling
i had a creatinie of 16.1 no swelling no symptoms just gradual weight loss nd loss of apetite towards the end i had intense breathing isssues where i couldn’t lie down even for a sec feeling of being squashed by weight and i had fluid accmulated near my heart i walked to the hospital with a BP at 170 and HB was 4.1 with absolutely no awarness i was immediately diagnosed for ckd stage 5 both the kidneys were normal in size the biopsy wasnt possible so the doc suggest for dialysis it’s been a year since my transplant and yes as you alwyz say every body is different and may not showcase the symptoms thank you for spreading so awarness❤
I had my right kidney removed due to cancer on my left kidney. I had the surgery done in 2010 and my doctor says my kidney has been stable. U have high blood sugar and taking Diovan. I would like to know if taking drinkable aloe vera gel is good or bad for the Kidney. I love your articles. Thanks Domenic
I got it once from drinking excessive amounts of beer with salt. I was informed that it can inflame the kidneys. I had to pee a lot because of that. My reason for an excessive beer with salt was that my then hometown had a problem with water contamination giving me a mouth disease. I also couldn’t stand salt without beer.
I enjoy your articles, but ckd doesn’t get much discussion from doctors. Over the years I have worked with people who had ckd and some who were on dialysis. I had my own wonderous experiences with kidney stones. Yet it was not until I was going through some med notes on a patient portal that I learned that I actually had ckd. Surprise! It took several more years, and another couple of bouts with stones, to learn that one of my kidneys is, for all intents and purposes, not working. Why is ckd not talked about? Is it because the symptoms are so generic and understated (they just don’t make themselves known)? How do you get to know how much you don’t know? You go through pcps and urologists and when ugly starts to hit the fan you hear, maybe it is time to see a nephrologist. What’s with that? It makes it hard to help yourself. (I have a great pcp, and am doing the doc in box thing regarding urologists, finally got referred to a nephrologist, but the process has been confusing and frustrating.)
I just heard I have Chronic 3rd Stage Kidney Disease. New Dr told me it showed since 2021 by GFR ! No other Dr mentioned it. I’ve been exhausted! My skin is very dry with rashes. No nausea. Swelling in hands and shins, ankles. I’m a Covid Long Hauler with viral pneumonia since 11/2020. Not genetic. How do we stop progression? Thanks for article.m
I have had chronic stress since january 2023 and from later march 2024 health anxiety. Since beginning of april I have taken 30mg mitarzapin and later taken 5mg olanzapin for 4 weeks now.. On the 11. of august i got some bloodwork done privately. It showed that my eGFR for both cystatin C and kreatinin were low. My symptoms which is hard to conclude as I take anxiety medication are soreness in legs,, dry eyes and swollen eye lids, Hard time waking up in the morning. (typical side effect of the the medicin i take).. a lot of peeing. I get up every night at 2 o’clock to pee and again at 7 o’ clock in the morning. I do not drink the och coffee in the evening. And i pee before bedtime. I worry because I had probably had a high blood pressure for at least a year,, and especially from late march 2024 to early July were I had severe anxiety and high blood pressure and trouble regulating blood sugar. these things take a toll on the kidneys. Will I be able to regain eGRF rate. ??? My own doctor did not react on my kidney values i got from a private clinic. I think I will get a new test around the 11 of septemeber. A month after the last test to see if my values have changed.
I’m 17 y/o kidney patient I feel. Excessive fatigue Loss of appetate. General weakness I undergo dialysis.twice a week When my doctor first told me that i’m having kidney failure i laughed and said that’s impossable But:) he said to me ” yes i’m tellin the truth” i was totally shocked BUT IT’S OK. MY FAITH IS STRONGER THAN EVERYTHING IN THE WORLD I’LL BE HAPPY FOR EVERY SITUATION IN MY LIFE:) BE SAFE. STAY STRONG.
I had almost all those signs….I was able to fight it on my own…due to the fact I was not allowed to see a doctor because I had no insurance…..every hospital and doctor I saw…was not allowed to help me cause I had no medical insurance…..but I fought it for 3 months in pain….and praying….I started eating garlic…and drinking a tee from a little plant called La Tronadora….3 times a day…..thank God….I still take it 2 times a week…and was able to fight it this past 14 years. I prayed a lot to God to find something to help me…he always answers me….He is my doctor….I Trust in Him.
Hello, As a kidney transplant Patient sometimes I become sick of misinformation on social media regarding what symptoms constitute poor kidney function. As kidney disease can manifest similar symptoms of many other illnesses. Therefore, the only way to check kidney function is to have a blood test to check the electrolytes levels especially creatinine levels, which gives a indication of how the kidney is working as a filter for removing proteins from the blood stream. Equally, I have been so blessed considering my kidney transplant that has lasted almost thirty one years now. Praise God. Martin
I’ve had a history of kidney stones. I’ve had the shock treatment and I’ve also somehow passed them. A few years back I was at work. I had no problem waiting for my brake time. While I was emptying out my bladder. I noticed the color was black like coffer or a Coke. It freaked me out. There was no blood, and there was no pain, stabbing or burning. It seemed to be a one time event. A few months later I went in for an M.R.I of my spine in preparation for another back surgery. My next doctors appointment came up and my orthopedic surgeon talked to me about what his plan was. THEN he said: has anyone talked to you about what was found when you had the MRI done ? I said no. He informed me that there was a large mass on my kidney, probably by the looks of it it’s more than likely cancer. He told me that my double fusion was on hold, even though it was very painful. He said the priority was the mass on the kidney. I went in for the cryonics aka the freeze job. All this was back in 2010. A few weeks back I was with my regular doctor. I mentioned to him that I’ve never had it rechecked for the current status. I got a call from A.R.A and made the appointment. I had the test done. Two weeks ago my doctor called and told me that the cancer was completely gone, no sign of renal cancer. I am cancer free. I proudly ware my orange ribbon hat pin on my hat.
In 2010 I was diagnosed with a 6 cm tumor on my right kidney. My treatment was radical nephrectomy (lab results stage 1 with clean edges, encapulated, and medium aggressive). Suddenly I found myself as a statistic having CKD stage 3, as I recall. Daily I measure and record my BP, watch my sodium intake, and down 2.5 mg enalapril mal. I do annual checkups with my primary physician and nephrologist (sharing my BP data for previous 12 months). He does the standard tests for creatinine and says I am doing very well even improving year to year in small increments because I seem to have additional capacity (I believe those were his most recent comments). I stay active, keep hydrated, and never have swelling. My health is fabulous, even better than before, so I feel very blessed. Oh…prayer and God played into my recovery and life since. I’ve never felt better and my appitite is great. Woohoo!
You may have just have saved my life. I have all but 2 symptoms of kidney failure. I have been a diabetic for 15 years. Suddenly I have new unexplained symptoms. What’s amazing is I was perusal a article and for no reason this article popped in my tv. I was praying about my pain and ask God to show me why my pain has changed. There you were.
My mother was Diagnosed with total renal kidney failure and lived 31 yrs with dialysis it wasn’t easy for her in the beginning but she managed later on to keep her labs in top tier health doctors use to say she was a walking miracle here in our city God called her home 07/13/20 😢❤ she’s with me everyday. Rest easy my Queen 🫅🏾
My sister had all these symptoms, including back pain, severe hair loss and extreme weight loss, for over a year. She had been under the care of a primary and endocrinologist, and began seeing specialists. NOBODY diagnosed her with kidney disease. By the time she landed in the ER, she was almost dead, and the toxicity had done permanent damage. The ironic thing? Her veterinarian told her, “If you’d brought your cat in here with those symptoms, the first thing I would have done was run a kidney blood panel.” Sis is now on dialysis, waiting for a transplant that will probably never happen. Even when you’re pro-active, our medical community can drop the ball…repeatedly.
I’ve been on dialysis for 3 years and it’s saved my life. I recently have been diagnosed with diastolic heart failure do to a lung deficiency and at times I do retain a lot of fluid. I am a single mother of three it is very important remain as healthy and functional as possible. All is well and all will be well in the name of Jesus. Thank you for this article!
You hit it on the nail I’m a kidney failure. I found out about four years ago and I had no idea how my doctor gave me a routine blood test and told me he could tell by my numbers that something wasn’t right with my kidneys so he referred me to a kidney specialist and he’s a great doctor and he told me everything that you’re telling me and I experienced every symptom I’m on dialysis I’ve been on it for 3 1/2. years, there are so many people that don’t know it was a shock What are experiencing new no urination? And I was on the transplant list, but my last exam showed that I cannot get a new kidney so I’m on dialysis some days I have it hard and we get trained me and my husband to do dialysis at home so don’t give up
My husband was diagnosed with CKD in September of 2021. It just came out of nowhere. We were not educated in the symptoms. He has a few you mentioned. He is a diabetic and has HBP as well. He was given metaformin (sorry if I misspelled it) for his diabetes. Aside from being untreated for his diabetes and HBP we believe this RX did play a huge role in his CKD. How I wish this wasn’t happening to him. He’s in his early 40’s and currently on dialysis. I pray for a miracle and that his health gets better. I want to have my husband for a every long time. Praying for all who have lost a loved one or are going through this and their families. 💔❤️🩹
I wish I had seen this articles years ago. I have been in failure for years. I was in the care if a doc that was crappy. I told him many of my problems, but he blew the off. I have better care now, and want to say,,, Thank you for putting this article out. I am sure it has already saved lives. Listen to her all.. this is a big deal. Find out now before it’s to late.
I had Hypercalcimia and had kidney failure! I didn’t have a clue my kidneys were failing, I had never had kidney problems at all. My urine looked fine and no pain but I couldn’t get my bp down and I was so thirsty it was unbelievable! My former husband could hardly wake me before he left for work that’s when I went to the er and they put me in ICU because my calcium was the highest they had ever seen in a living person! So I’m here to say all symptoms are not the same! God bless all of you struggling with kidney problems and other health problems!!!
I lost the love of my life he had been in acute kidney failure for approximately 18 months. He ignored a lot of the signs we went to bed one night and he went into complete cardiac arrest. I did everything I could to get his heart started again, but I know that the symptoms that you were describing here or how I lost him in June 2022 he lost his appetite. He was falling more frequently other family members were attributing that to his alcoholism, and that he was hiding being drunk he was not drinking not to the excess that he used to do but I’m sure his years of abuse had led him to kidney failure. Thank you for posting this.
I had renal failure I fully committed to the renal diet The key is to portion the intake of food and fluids. That’s what I did in 3 months my kidneys came back my creatinine level was like 13.0 or more 0% kidney function I pray for all going through this 🙏 I believe in you You got this Stay strong Be positive Stay healthy Stay active Don’t let this control your life
I wish I would have paid attention to the symptoms of my kidney problems – instead, I waited until I had a long list of symptoms and could no longer function. I ended up spending a week in the ICU. Early detection is key to slowing the progression of kidney issues. Today I feel much better and live a much healthier lifestyle while working closely with my Nephrologist and renal dietitian.
My mom had many of these symptoms the last year of her life. She was monitored by her doctors but to be honest some thought it was for other reasons but I believe it was from kidney failure. She had tremors and shakes that no one could explain. It makes me deeply sad to think that it was her kidneys. She lived a long life and her organs gave out but I at least have a better understanding of the numerous symptoms of kidney failure. Thank you Dr. Frita for this content.
Incredible! Dr. Frita the Lord put you in my recs and I felt compelled to watch a couple of your vids just before my kidneys stopped working and I ended up in ICU last month. Drs thought I may have had lupus in addition to kidney failure. A nephrologist threatened dialysis, but thank God for restoring my kidney function and for blocking the lupus diagnosis. The 11 days in hospital helped me get used to the renal diet. I’ve struggled for years with drinking enough water, but the Lord is helping me with that too. Thank you for all you do and for the difference you’ve made in my life.🙏🏼
I was at a friend’s house and passed out went to emergency and diagnosised with stage 3 kidney disease I started drinking alkaline water and I had to stop eating nuts ketchup mustard mayonnaise and all the other things bread rice anything White and my kidneys rejuvenated their self so I’ve been kidney disease free sense 2016
As a CKD patient myself, i know what it feels like you’re about to give up because of this endless pain. I have gone through a lot emotional distress but with proper thinking, i was able to overcome it, now living a happy life despite still being under dialysis, and learning much more about this illness.
I had a swollen ankle and fatigue. Couldn’t climb stirs without palpitating. I went to the ER and was diagnosed acute heart failure due to unattended HBP. My BP was 198/120 at the time. Thank God after some medications I am now down to 138/74 and that has significantly improved my heart function. At the time my heart function was 30%. My last MRI on my heart now came out to improved to 45%. I’m hoping it gets better next time I go for test.
I was surprised and disturbed to find out just last year that I had kidney disease and had it for some time. I found out from my new doctor that a previous doctor had indicated it in my medical records but failed to make me aware. I immediately researched what I could do to limit the damage and support positive function. Ten years ago I had crippling plantar fasciitis and took two naproxin daily for over a year. Now I found how destructive that was. Not only was I a 12-year diabetic, but I had been prescribed the antibiotic Doxycycline for Rosacea every other day for 8-9 years and none of my doctors ever mentioned it could damage my kidneys. I immediately terminated it and no longer take naproxen.. I’m 73 and ADHD – so always keeping busy and forgetting to drink enough water throughout my life resulted in long term dehydration and undoubtedly also damaged my kidneys . Now I fill two 32oz jugs and try to drink them daily along with some raw cranberry juice. Hope this will help someone else.
Thank you for saying Lupus bcoz I just reversed diabetes type 2 due to 41kg weight loss from the second month of diagnosis til June 2022. The pharmacy said I had diabetes (I didn’t know until I had a diabetic shock and septic shock my sugar level was 29!!!!!!!!) I was unconscious. Now I’m going through kidney failure at the age of 33! 🤦🏼♀️ I lost 41kg sooooooo quick without even trying no exercise, sweat or anything but not eating for weeks and week and weeks on end
Wow I have stage 4 kidney disease. I have the following symptoms that you mentioned. Diabetes for 27 years, high blood pressure for 20 years, COPD for 4 years, and started having tremors last year. I am fatigued a lot and don’t sleep well. But I can get around and ride my pedal assist bike when weather permits. So even with my problems I feel really blessed. Thank you for your wonderful information. I will check out your diet next.
Dear Doc – I had 8 of the 10 symptoms you mentioned along with pain in the lower back over the past almost one year. Recently, I began to do foot reflexology 2 or 3 times a week and at this time, I have almost no symptoms. Urine has cleared up from a deep orange/brown to mostly normal and clear/slight yellow. Please look up foot reflexology on YouTube and get a book on it so you can really help your patients. I wish you health and success and an open and clear mind.
Itching!!! See tip at end of comment…My mother died of kidney failure and she had unexplained itching for years. When she was in Hospice in the last week, our nurse told her to take a Tums and it stopped the itching almost immediately. It balances out the electrolytes in some way. Wish we had known this years earlier….
Thanks for your excellent article. I was having joint discomfort and pedal edema. I went to my primary care MD and she did test and found out my sodium level was high. She suggested to stop drinking carbonated beverages and read food labels to restrict my sodium. I stopped drinking carbonated drinking and my joint discomfort discomfort was reduced by 90%. I now seek low sodium or no added salt foods. My edema has almost completely disappeared.
In 2005 I had literally all of these signs. I thought I had diabetes but every test came back negative. I guess as time went by everything went back to normal. I never at any point thought it could be something to do with my kidneys. Today I still drink lots of water and urinate frequently even at night but that’s just about all the sign I have.
I have type 2 diabetes, and just found out from my doctor that my kidneys were getting weaker and warned me to change my diet or suffer having to go to dialysis. This instantly scared me and so i had to change my eating habits drastically.For those of you that are new to diabetes,take it very serious,as there are many factors that can cause your diabetes to spiral downward.
I started peeing blood, Doctor said I was ok and no blood in my pee, next day same again peeing blood (looked like a bucket of red paint in the toilet pan) got to a&e went to the toilet it was like peeing jelly then couldn’t pee at all, receptionist got me taken straight in to get a pipe in me, that was a relief. Ended up as kidney cancer, had it removed been very lucky and 5 years all clear 👍😀
Thanks so so much for this article. Sadly my sister Beatrice had all these symptoms as at late November 2020. She collapsed in the house and when she was rushed to hospital, after ruling out covid-19, they noticed that her kidneys were not functioning. They did dialysis three times but she did not improve. She had blood clots in her brain that were drained. She was also diagnosed as diabetic. Everything was diagnosed all at once. She also had HBP – High Blood Pressure. Sadly she lost the battle and died after three weeks two days shy of her 59th birthday. I am still devastated.
I was diagnosed with stage 4 kidney disease over a year ago and neither my primary care physician nor my nephrologist seem to be taking this as seriously as I am. I have not seen my kidney doctor in a year, he said I did not need to come back before then. I have been given no information about what I need to be looking for as far as symptoms getting worse, no one has talked to me about how mush fluids I should be drinking and what kind of diet I should be following. My family history is that I lost my father to Kidney failure along with my uncle and my grandfather all on my father’s side of the family. There could be more that I don’t know about but I think that is enough to make me concerned
A larger problem is that almost all of those symtoms can be attributed to other factors. Allergies can interfere with just about everything. Stress can cause a lot of those symptoms. Sometimes these articles can do more damage than good. Start by looking at your general health and lifestyle/diet. Go from there.
Dr. Frita, you hit every nail on the head. My mom just recently passed away, as of matter of fact today makes exactly two months ago my number #1 fan passed away. She had all of these symptoms and signs. None of the doctors mentioned kidney disease, they put the blame on COVID-19 more so than renal failure. She started out with fluid on the lungs. On three different occasions my mom was put in the hospital to drain fluid from her lungs. She started being encoherent, she thought the family was putting things in her food. She wouldn’t eat, it was just so, so, so hard to see my mom suffer like she did. In just a matter of months my mom went from being a vibrant, outgoing, laughing woman to just sickly all the time. 🚬 didn’t help either with the type 2 Diabetes, hypertension, heart failure, having anemia either. I miss my mom so much and I will always ❤️ her. I just wish she would have listened to me. She was only 63 yrs. Old. She died 13 days before my 42nd birthday. When you loose your mom it’s a different kinda hurt. Your information is very, very, very valuable. Don’t take life for granted. Do what you have to do to live and live life to the fullest. To all that reads this, trust it’s very real and GOD bless you all. Take care of yourself and most of all ❤️ yourselves, please see your doctor ASAP. God bless you, Dr. Frita. Thanks, for informing the masses.😘😘. One thing I did not mention Dr. Frita she started eating Argo starch as well. I was told it has something to do with the anemia as well.
My mom had lupus most of her life and lived to 76. In the last couple of years her kidneys failed and she went on dialysis. When my dad went into the hospital I learned how to do peritoneal dialysis because the alternative was wrecking her body. In the end having kidney failure saved her as she had a stroke and was given one painful year spent in the hospital to live due to bleeding in her heart. I sat down with her and we both decided to end dialysis and she went into hospice, fell asleep on the first night, and never woke up. She died 3 days later pain free which seems to be rare these days. It seems strange that something which is so bad ended up giving her a peaceful death in the end.
How I found out that I had chronic kidney failure was when I had my blood drawn at a regular doctor’s appointment. I was totally shocked when I received this news. My doctor told me I had PKD aka Polycystic Kidney Disease. Another form of kidney disease where cysts take over both of my kidneys and grow like crazy. I’m currently on dialysis. I go on Mon, Wed and Fridays at 4 hour each treatment. I suffered from all of the symptoms. My worst symptoms are the insomnia followed by fatigue. My appetite has increased since starting dialysis. I’m probably the biggest I’ve ever been in my 56 yrs of living. Before all of this I was a exercise fanatic. I did aerobics, lifted some weights and really watched what I ate. However, that’s OK. I’d much rather be alive and overweight than the alternative. I thank God for each day that I’m given on this earth 🌎. I’m on a transplant list here in Wisconsin. I pray that one day soon…that the Lord blesses me with the perfect matching kidney. Otherwise, I’ll just continue to receive my dialysis treatments. Thank you and stay blessed and safe through these trying times.
My wife who is a chronic alcohol abuser has fatigue issues and the itchy skin symptoms and back pain. I figure it’s either a liver issue or kidney issue due to all the alcohol she consumes. I’ve brought up this many times and she says she’s fine. But hasn’t been to a Dr in over 7 years now FYI she’s only 44 years young. This is just what I’ve witnessed god knows what else is bothering her that she doesn’t tell me. It’s sad been together for 20 years now and her alcohol has gotten so bad that it’s cost us our marriage. She has requested a divorce cause she isn’t happy anymore. I know a lot of negative comments will come in now since the divorce part has been raised like why do you care she wants a divorce. Well I’m a human being that cares about others and it’s sad to sit back and watch someone basically kill themselves slowly. Thank you very much for your article it was very informative.
I’ve just come through a partial-Nephrectamy and knew some things were not right. I saw signs which were not good and pestered my doctor to go further than just monitor symptoms. 8 months later after an ultrasound & 2 CT scans, they found a pole tumour which has been removed successfully. You have-to look after one self.
I was in the hospital a number of times with stroke and heart disease and other problems from the time I was in my early 50’s, but not until a year ago was I diagnosed with kidney disease. I was shocked. Stage 4. I was terrified to picture myself on dialysis in the future (I’m 69 years old now), but I’m following the lifestyle changes I was told to do and hoping I can avoid stage 5. I see a kidney doctor regularly now.
Doctors seem to miss these symptoms too. I took my grandmother to the doctor 3 months ago and they didn’t test her kidneys. I took her to a different doctor for a second opinion. They phoned today with her blood results to say she is at end stage kidney failure and at 91 years old there is nothing they can do. It’s functioning at 15%. I never thought these symptoms of hers would be kidney failure. Please check with your doctor if you have these symptoms before it’s too late.
I was recently diagnosed with Stage 3 kidney failure. It’s taken 5 years of intermittent symptoms for them to finally figure it out. I kept seeing things on the test results that for some reason, the doctors seemed to think not important enough to talk about, even when I asked about the findings. Things like Prediabetes, why I was consistently showing as slightly anemic, the elevated blood pressure with no change to my medication. Couldn’t they see the high blood pressure meds were not working well enough and needed to be adjusted? My leg swelling was first diagnosed as cellulitis. Since then, my episodes of lower leg swelling have increased in severity and duration. And the most recent episode lasted 45 days before the swelling subsided. Of the 10 symptoms in your article, I have or had 7 of them. And the doctor who pointed to the kidneys as the major issue turned out to be my cardiologist. Well he’s only half right. The high blood pressure falls into his area of expertise. I knew untreated high blood pressure could cause kidney damage. But I was under the impression that my blood pressure was being treated and managed within the acceptable range that would prevent kidney damage. Especially since there were no changes being made to my blood pressure medication. My suggestion, if something doesn’t seem right with your care of test results and you have questions, ask the questions to your doctor and don’t let anyone gloss over your questions like they are not important. If you have a question, it’s important, otherwise you wouldn’t ask.
I got diagnosed 2 weekends ago. I literally went in for a hysteroscopy and they found that my adrenal glands were not working and that I had a kidney disease. I was diagnosed with Endometriosis 4 years prior, and I related my symptoms to that. But I am grateful I got diagnosed and can manage and continue to live a normal life without too much damage having being done. Such a blessing ❤️
The problem with these symptoms is that they are generic symptoms that can mean several different things. I have several of them but it’s because i am a diabetic, not from kidney disease. You can have several of them if all you have is a UTI. Most doctors just treat symptoms and RARELY check for kidney issues.
Hey there blessings to you and your family! I battle all but two of these symptoms you mention! I am not a diabetic nor do I have high blood pressure! I had swelling in my ankle and legs but was told it was water retention! I’ve been fighting with my doctors to help me find the root cause but to no avail! My health began to decline 3yrs ago from h pylori but since been eradicated! The h pylori damaged the lining of my stomach called ulcer and since then I’ve been having issues after another! I went back to the doctor because of these ongoing problems but every test came back negative! I know there’s an infection somewhere in my right side because I can smell it but they say I dont have one! Lord knows if it has reached my kidney’s or other organs I would be devastated! This is an emergency with no one to help me find out where it’s coming from! Thank you for sharing your wisdom and knowledge on this matter! I pray it helps me and many others who have been misdiagnosed! God BLESS you my sister ❤🤗🙏😇 new friend btw!👍
I had at least 5 of the symptoms,lost 2 stone,Doctor I went to asked me if I was on diet,been going to this clinic 35 years,went to another Doctor did blood test next day rang me I need to see you,so went,had to go to Hospital for emergency procedure,had stents put in,1 Kidney no longer works,the other at 29%
Last June I had renal failure with severe sepsis. I was dying and a healthcare professional, that I told all my symptoms to, told me not to worry, I did. I called my doctors, told the receptionist my symptoms and the doctor called me back, told me to get to hospital immediately. Now after three operations I am under control. Thank you NHS.
I’m 26 and have never had kidney failure till my recent encounter that I knew of but anyways. I was a pill popper addicted to opiates so I never knew my being sick had something more to it till I had 2 seizures and was told my kidneys were working at 6% my creatinine levels were at 9.23 so when I woke up from sedation I was told I had pneumonia too. It was wild but thankfully things have taken a turn for the better and I started and was taken off dialysis at the hospital during that stay I was there 3 weeks but my kidneys started to turn around on their own thank god. Thank you for your insight.
When my husband was diagnosed with end stage kidney failure we were in total shock. He is dietetic with high blood pressure but was never given this information, when we rushed him to the ER, he had every symptom but we just didn’t know. So thank you. I think doctors should really stress this to diabetic patients.
Hello Dr. Frita, I’m so happy I came across you very informative website. I have a dear friend, who has two of the symptoms you mentioned in this article. They are: itchy skin and trimmers. She has already had blood work done; which came back normal. What specific test Should her doctor order, to find out if she is actually experiencing kidney failure or not?
This is a very interesting article. I was just telling my daughter that I think I may have kidney issues but I may also be paranoid because of a fear I had. When I was pregnant with her, I developed a kidney infection and it was a horrible and traumatic experience. My daughter is now over 30 years old and I am still scared. I am at an increase because of diabetes II. I am working to better myself and definitely drinking water. Thanks for the info.
Very informative. My last test showed GFR 51 and Creatine 1.37. Will be discussing with my PCP in a few weeks. I’ve been having itching mainly on my back and upper arms for several years. an occasional swelling of my feet and lower legs and have gotten to where no food sounds good. I eat only to survive. I miss the days when I looked forward to a good steak.
I just noticed and viewed this article again and will be checking with my doctor after viewing this article again since I do have some of the things you mentioned in your article and want to be checked out. I thank you for sharing this information and make sure that I am okay since I am retired and living alone and want to live as long as possible.
I found out that I have Stage 2 Kidney Disease by reviewing my lab results. My PCP never notified me. When I contacted my PCP to inquire why she never notified me, she stated that Stage 2 isn’t serious and that there isn’t any need to worry until it progresses to Stage 3. I was gobsmacked. I have a family history of Kidney Disease. I grew up being well versed in Kidney Disease. Reason being, both of my parents had and died from renal failure, which my PCP was well aware of and is documented in my medical records. I stated to her, well isn’t the goal to keep the Kidney Disease from progressing? She didn’t even respond. In addition, the reason why I started making inquires is due to the fact that I had a severe adverse reaction to a prescribed medication from another doctor. From my research of this medication, I found out that a patient with Kidney Disease should not be prescribed this medication. Since my PCP never informed me that I had Kidney Disease, I could not disclose this information to my other doctor. The pain and suffering that I endured from that adverse reaction was preventable. Needless to say, I am still furious. P.S. I received this treatment from the VA.
Everything you mentioned pertains to me except #9 my Dr sent me to a Vascular Surgeon for the swelling in my legs and feet maybe poor blood circulation. I used to be diabetic but lost weight and lowered A1C . Now I have had problems with my kidneys over the years. I hope someone sees this and reply’s back before all these Drs let me Die. Thanks so much for your article 💞
Kidney disease runs both on my father and mother’s side both on dialysis both have passed. 2 years ago, my youngest son was involved in an vehicle accident as a passenger he sustained major injuries, I noted everything down (like a nurse) that he was experiencing and 2 days later the attending physician was ready to dismiss him until I explained to the doctor about other areas and complaints my son was having. The doc went and did an MRI of the complained areas and next thing we know the attending walks in with two other doctor’s one surgeon for the knee and the other from Urology. The doctor’s told us both that I needed to put my son on disability ASAP because he has stage 3 kidney disease with renal failure and also sustained a hematoma to the left kidney and that he needed to be put on dialysis my son has refused since then and I can see the drainage in his eyes which hurts me to no end. My son told me that when he had seen a doctor (NP) she told him at two different times within a year that his blood test showed something about his kidneys but that was it so me not knowing at the time and him not understanding went on as if everything was ok. He has become more drained extremely drained and living in a town where a Nephrologist will not see him because they are saying he is going AMA so he only has his PCP, I have noticed that he has become a little wonky when standing and since my only daughter has lupus it seems to have increased dramatically and I have noticed her being more unsteady when standing and seems like they’re both going to fall at any minute.
Your article is great dr. Frita. Thank you. I am now 70. In the past 20 years i did a urinetest every year. My doctor tells me every time all is ok. Can he be wrong or is the urinetest not good enough to identify the kidney problem? The only symptom i could have is the frequency of urination in the evening after i went to bed. But i don’t know what to take as “frequent” in this regard and what the connection is with the amount of fluid i drink a couple of ours before i went to bed. And what about the connection with the possible problem of prostate enlargement?
My PCP failed to notice a Stage 3 renal disease (GFR)on my routine bloodwork. Luckily my wonderful neurologist noticed it and informed me. I was Shocked to say the least. I have HTN and NIDDM and it is my fault for not following a proper diet 🙁 Ty Dr for listing all of these symptoms to educate us and RE-educate myself as nursing school was 41 years ago. God bless you and keep up the wonderful work, with gratitude, a Mom and old grandmother and very old RN 🙂
Thank you, Doctress Frida! I am in New York (City), and am a fan for best health. Your excerpts teach things about the various causes of disease that are taught only by the medical professionals. During the last several years, I drank only water at home, except on some sick days when I would have some Celestial Seasonings peppermint tea or lemon zinger tea.
This was very informative, thank you. I have had lifelong frequent urination and going to the bathroom at night. About a year ago, I was suprisingly diagnosed with Stage 2 CKD. I have many of the symptoms you listed. Ankle swelling-yes that too. My doctor said it is not to worry about unless it doesn’t go down to normal once I get off of my feet. One thing I would like to know, sometimes I get an overwhelming feeling in my body that I have too much salt! My lips will taste like a salt factory and when this happens I notice I feel really crappy, so I will constantly drink water to try to neutralize it. Could this be due to kidney issues? Again, thank you, I’m subscribing now. Have a blessed week.
I have HBP and some of the symptoms mentioned above can also be from your meds according to my PCP. The swelling of your ankles, feet as well. And the bubbly or foamy can also be from how fast the urine strain can be when it hits the water also according to my Dr. I have no idea, but luckily my blood work for my kidney function has been good so far….
1. Fatigue 2. Insomnia 3. Itching skin/elevated phosphorous 4. Frequent urination/esp middle of the night 5. Foamy/bubbly urine (like beer, etc.)–protein in urine 6. Leg or ankle swelling 7. Loss/decrease appetite (elevated toxins) and/or unintentional weight loss 8. Nausea/vomiting 9. Bad taste in mouth/bad breath (metallic taste or ammonia smell of breath) 10. Tremor/shakes (elevated toxins poisonous to nerves) and/or abnormal gait/walk 11. Memory loss 12. No symptoms in early disease**
I was diagnosed with RCC,a tumor down deep in the back of my kidney.My Doctor suggested a Nephrectomy ( since I was young & healthy) hah ! I suffer from congestive heart failure,with 25 % heart function, and have a difibiberator ! So, I told him I was neither,I was in my late 60’s. So nothing,zilch has been done except for a lot of Prayers,the last time I had test done,I was told the the tumor the size of a walnut,was now the size of a penny ! I get chill’s, temor’s, shakes.I can hardly urinate than all of a sudden I can’t stop urinating.My apetite is ok, than I can hardly swollow,and have no desire for food. I don’t know if its my heart,my kidney? I suffer with Fybremyalgia also ! I don’t know what to do,I’m so tired of suffering.
Thank you for this and ALL of your articles! This explains a whole lot of what was going on with my late mother. While helping take care of her, I was under the assumption that her hyperthyroidism was due to 3 myocardial infarctions in the past and hypertension. Her nephrologist and primary care physician never explained any of that to me.
Thank you for your interesting article Ma’am. I am blessed to be under the care of urologists in UK as I have bilateral hydronephrosis associated with a urostomy for myelomeningocele. I have ureteric stents which are changed every 3-4 months. Recently (during the last couple of months or so)I found I was sleeping a lot and I was prescribed different courses of antibiotics. I am about to start my 4th course today. I am still tired, stressed and so on but I was happy that you mentioned tiredness, as, at least now I can feel a little less guilty for my state. Warm regards from UK.
I have had severe leg and ankle swelling off and on for the past 4-5 years. It has put me in the hospital twice a year since it’s onset but no-one could ever give me a definitive answer as to why it was happening. Wasn’t until I got a new primary care physician that really cared about my health that I found out I had kidney disease. I have since been trying to adjust my diet and my lifestyle and hopefully this will somewhat reverse the damage.
Thank you so much Doctor Frita you have been more than helpful ! You have diagnosed what I had suspected for the last few years absolutely perfectly. I have the symptoms of a failing right Kidney, I ticked nearly all of your boxes of concern…98% in fact, you’ve saved me from many severe problems in my later years and potentially a shortened life span. I will now turn my whole life around I will do some research….types of food to eat, drinks which are none toxic how to eliminate Chlorine bleach from my domestic water supply. Life style will surely catch up with everyone at some stage in their lives and for me it is the turning point in mine………right now !
I found out I had FSGS from urinating foam…went through biopsy to determine what type of kidney disease I had. My disease wasn’t from birth. My dad was in the Marines went to Vietnam and was exposed to agent orange. I have two brothers, only one was affected because he was born in 1969. My other brother wasn’t born during the time my father was in the military. We’ve all (Father, One Brother and myself) since received kidney transplants.
Swollen ankles and red prickly spots up to my knees were said to be due to UTI medication. Changed to several kinds. Each did the same red swelling thing, but still had UTI, so whole classes of meds were suspect. Last one seems to have worked for the UTI. Ankles itch bad for the last two of 14 days, then stopped when the med stopped. UTI seems to be gone now. Glad of THAT!
Hi Dr. Frita! Love your Podcast and its content and many thanks for your service in the field of Nephrology. Literally out of NO WHERE in 1993 I suddenly became very ill and experienced several of the symptoms you spoke of. I had to be rushed to the hospital and was diagnosed with a Kidney Disease. My story is immense however, yet with a Blessed outcome not only for myself but also how my trials with this illness afforded me the opportunity to help others. I did end up needing a Kidney Transplant which I received from a Living Donor in 2005. I will be “20 YEARS” post transplant in March of 2025! I don’t know if you have periodic guests on your platform to Share their stories but, if you do I would love to. Thank you for continuing to enlighten the African American community and countless others on this devastating illness🌻🙌🏽
My husband had prostate disease that is now under control with medication. When he first had problems, he didn’t really say anything until he could not urinate at all. Eventually, his urine backed up so badly from the obstruction and caused him to go into kidney failure. We really went through some times with that, catheterization, etc. I don’t remember him complaining about much. He’s very tight-lipped and uncommunicative about how he feels sometimes. The thing I noticed the most was that he became very affected mentally. He became very senile. He still is somewhat senile, but he has much improved and the kidney failure did clear up once his prostate problems resolved. So, remember, prostate, and urinary retention problems can also cause kidney failure, but it can resolve.
I actually have a family member that has experience every symptom in addition to excessive diarrhea. They were at stage 3-4 for a while and now at stage 4 more falls have happened, along with UTI’s and the shakes. Swelling of the legs and some swelling even in the face area I’ve observed. Each day is different. Diet and so life choices can play a big factor with CKD.
Thank you for your wonderful information. I am still going on w,my life. Still haven’t had dialysis yet but getting close. GFR 15 I have my Fistula installed. Hopping to get through this summer riding my bike. I have a real good handle on my diabetes. I have a dietician and the Libretto 2 testing system. Running 98% blood glucose. A1C 6.8. At 76 years old I feel very lucky. I hope everyone is as Blessed as me.
Thank you for your informative information. I had a renal ablation in 2015, had a stroke the same day. I recovered from my stroke quite well, I’ve been checked by a urologist every year up to now. Received CT scans w/o contrast each time. Was told that I’m doing fine. However, was prescribed Metformin to help with neuropathy for the past 3 years. After some blood work, was contacted by my physician and told to stop taking the Metformin. Have not had any other diabetic medication until I mention it to my Dr. At a recent appt. Now I’m told that I am being referred to a Nephrologist because my kidney function bn is insufficient. What a bomber. I”ve been telling my doctor about foaming urine, pain under my shoulder blade, etc… just recently, I started having swelling at the ankle. I thought it was from excessive standing. I guess I am doomed. Thanks anyway. I’m trying to eat like renal patient until I can see the Nephrologist and a dietitian. I’ve learned more about CKD by researching on my own than I’ve gotten from my private physician and urologist. Shameful
I cannot express to you, you truly nailed everything. It began in my liver, over enlarged ” fatty liver”, with lesions. Then, blood,, now( how odd the doctors were asking me this, blood in the urine), plus pain on my left side. I honestly feel they were waiting for my whole body system to begin to just fail. Also, hair loss, yellowing of eyes, strange sores on my arms, hands, face. My nails once were thick, break, bruises, this has been going on for awhile. Two weeks ago it took them 1 1/2 hr. To put an Iv in, the nurse knew I was really sick, he had to do this before, I was in the hospital for about a month. Why can’t the doctors hear this? I’ve have CLD, MS, RA, & I truly suffer from some not hearing me. I deeply feel, once organs start fighting, the rest do become so traumatized by this fight. I’ve lost rapid weight, 110, to possibly 90, pushing it. What am I missing to explain to the doctors?
Mine was from Wegener’s Granulomatosis and almost died same with my lungs. The urinating at night mostly and not during the day was a big red flag and my urine was brown later on. I didn’t have too much of the foaming urine. Glumonephritis from blood vessels being destroyed. Doctors just sent me home during my lung biopsy when I was dying and could barely walk and was hemorrhaging from everywhere and my eye was swollen and had facial paralysis. I had lost 55 pounds. This was in Canada! So I went to the ER four days later and an infectious diseases specialist and lung doctor saved my life after ENT and rheumatologist neglected my health for so long and almost let me die. She was getting my lab work sent to her and my sed rate was 120! Just ignored it.
I have all of these symptoms. I have CKD with an eGFR that was at 48 for years. After removing a tumor-filled uterus, cervix, tubes and canal, it has gone up to 78! But the symptoms have worsened. I’ve lost 17% of my body weight in 8 weeks 😮 My back feels like I have been kicked relentlessly. I’ve asked for total honesty from my doctors. I know that it is looking like the surgery wasn’t a success. They just don’t know if the surgery caused it or if they missed that it spread 🤷🏾♀️
2 months ago I was switched from Benazepril (persistent cough)to Amlodipine. I immediately had lower leg swelling. I have now had a vein test, and an artery test. I have a Renal scan coming up this Saturday. I started work on my diet. My potassium is high, My sodium is low, but my Creatinine is very high. I do not have diabetes, and consume very little alcohol. Also started drinking Dandelion tea, and green tea.
Okay I am freaking out. My skin started itching like crazy, started last year. My legs and feet started swelling as well. I started urinating much more as well. I told my doctor and told them that my kidney seemed like maybe it was infected. She checked my urine and blood and said I was fine. I’m getting a second opinion.
I do have insomnia, and itchy skin, and do urinate often, but not the other things you mentioned. I will check with my doctor to see if I have kidney problems, but was told before that I only had high blood pressure which I was prescribed medication for and also taking lose dosage aspirin for problems which older persons have.
thanks so much for this article Dr. i was diagnosed with kidney disease 4 years ago pyelonephritis after some medications i got well but right now i feel tired easily pls Dr what do i need to do im just a housewife and cannot afford Nigerian hospital bills for now. Thanks Also Dr, my husband use to have bad breath, frequently urinating, and sometimes back pain kindly help us Dr, cannot afford to go for a hospital check that was why i decided to check the internet. Thanks so much.
Hello Dr.Frita, am from philippines, from the symptoms you mentioned i have 2 symptoms that i may have kidney case. 1. Fatigue 2. Too much bubble in my urine. Here are the results of my Whole abdomen ultrasound. 1.small left renal cystic 2.moderate pelveocaliectasia right 3. Do CT STONOGRAM Rest of organ are normal. I did the test because had painful experience. I was able to eject the small cristals during urinating. My question is can i go to a nephrologist w/o doing the CT Stonogram coz its too expensive test? Want to have prescribed medicine first. Im also a hypertensive person i have maintenance am 54yrs.old. Your reply is greatly appreciated. Thanks hope you can help me.