Anyone with CKD can give me answers or advise?
Hello. End of second week of July I got a yeast infection. OTC Montistat 1 day oval. 2 days later felt improvement. Several days later, symptoms of UTI. Waited few days. Called Clinic. Went in for labs. Confirmed. Recommend do another round of OTC treatment. I did. RX prescribed Cefpodoxime 5 days, 2 pills a day. However, before I started RX, suddenly I got these skin sensations: prickly, pins& needles, itchy skin random. Even my eye lids & inside my ears. Last night my breasts were tingling.Comes and goes. I have NO rash. This is been going on for near a month. July 27 started feeling Kidney pain through the night until July 28. Called clinic. Concerned my UTI spread into Kidneys. Advised to go to ER. At ER July 28 all blood/urine tests done.My eGFR was 68. Creatinine 0.95 BUN 13. All in normal range. I asked ER doctor why I was having this skin sensation & he did not know why. Sent home. Went to my clinic for follow up on 07/31blood work & urine. My creatinine rose to 1.05 my BUN rose to 18 & my eGFR lowered to 60. Can I assume this was from the Cefpodoxime? I went back to clinic 08/07 for urinalysis labs ( I asked for another Basic Metabolic Panel, doctor refused. My urine looked good except Hemoglobin. This time, on Aug.7 the word TRACE was there. This is the first time ever this has happened. With my trends all were negative prior. Of course I My Chart my Doctor with concerns. My Doctor's response was this: "As for your urine lab results, trace hemoglobin is not concerning as the microscopy findings did not show any RBCs". As of current, I do not know what my eGFR is, my creatinine or my BUN. I had to remind my doctor since I trend in the 50's for my eGFR we both should "Be concerned" of my trends. She then put in a lab order for a BMP. I guess because my eGFR was "60" I was "Stabilized" but not considering 80% of my eGFR's are in the 50 range. I should point out on June 3rd I had a CT/Contrast at ER. I will regret that for the rest of my life. So here are my questions if anyone wishes to answer, is my skin sensations related to my kidneys? Could I possibly be having adverse affects a little over a month AFTER my CT/Contrast scan? And what could cause my Hemoglobin Urine test to say TRACE. I go in on 09/11 for a BMP after I had to ask for one. Anyone who has thoughts about this would be greatly appreciated. Thank you.
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Good point. That should be tested as well.
Hi Windyshores. Yes, I think this is the test for Lyme's?I will copy/ paste what it said for you too see. I do not know if this is the Western Blot or Elisa.Thank you for your reassurance. I probably seem silly with all this, but gosh, I am dumbfounded with the "why's", and I will admit, I am worried.
BORRELIA BURGDORFERI AB, TOTAL WITH REFLEX TO IMMUNOBLOT
Collected on August 24, 2023 10:42 AM
Lab tests - Blood
Results
Borrelia Burgdorferi AB, Total
View trends
Normal value: Negative
Value
Negative
Your value is Negative Normal value Negative
Absence of detectable Borrelia burgdorferi antibodies. A negative result does not exclude the possibility of Borrelia burgdorferi infection. If early Lyme disease is suspected, a second sample should be collected and tested two to four weeks later. There currently is no test of cure for Lyme disease, and this test should not be ordered for that purpose.
No that is not a Western Blot. Even if you do have a Western Blot there is controversy about how to assess the results. The W. Blot has numbered "bands" and some are Lyme specific antibodies. The CDC wants a certain number to be positive but "Lyme literate" doctors want those that are specific to Lyme regardless of how many. It is complicated! Go to lymenet.org for more info if you would like it.
Just want to say that tai chi and quigong have helped me a lot!
Does anyone know if quercetin for relief of itching caused by histamine intolerance is ok to take with a 55 GFR. I am taking 500mg pill daily which I think is helpful particularly at night. I would like to increase to twice daily to 1g which would be recommended dosage. Concern for affect on kidneys which are stable after being damaged by taking some aleve almost 20 years ago.
@cniebler38 Good question! I looked up quercetin on WebMD and found this information. It is not recommended for use in kidney patients [see under precaution tab, but entire article is worth reading]: https://www.webmd.com/vitamins/ai/ingredientmono-294/quercetin
Histamine intolerance can be an ordeal to work with. Have you figured out what is causing the itching? Environmental, or another medication, perhaps?
Ginger
@sallylynn It normally takes some time for a medication to get to a therapeutic blood level, sometimes several days. I hope you are feeling better today.
I was not able to take Gabapentin at the dose that would work for me, since I have end stage kidney disease.
There has been a lot going on in your life recently. Taking time to take a deep breath, and recentering yourself, not focusing on the discomfort you might be feeling at that moment, may go a long ways in settling your mind and by trickle-down effect, your body. Do you think that is worth a try?
Ginger
Thank you for taking time to look at quercetin. I read it could further damage kidneys at higher dosages which is why I am trying one half dose.
Yes problem with histamine is an ordeal although of the possible related symptoms I have only two major at this time: severe full face breakout controlled by histamine diet and intense whole body itching primarily at night as histamine highest at that time for which quercetin is ranked highest. I do take Zyrtec and claratin daily recommended by an allergist. Of the 3 dermatologists. One allergist, one gastro, and my PCP I have seen none of them have dealt with the 1% of the population who experience histamine intolerance. I will continue to search on line and perhaps find a study on it. Have a Histamine Intolerance Explained book that covers available supplements and a list of most foods high in histamine. Avoiding a wide range of specific foods does control facial breakout which is damaging to the skin and possibly eyes as well as painful.
Good morning Ginger, it is so nice to hear from you. I hope you day is going well.
Yes Ginger, so much has been going on.:( . I am trying to distract myself from the pain.~Last night I slept maybe 4 hours. In my sleep I was awoken with pains on the bottom of my feet accompanied by of course the tingling, pins & needles throughout my body. I am losing much sleep. I am groggy today. I am worried why my ankles ache & my calves ache. Is that even a symptom of neuropathy? I review my labs & doctors notes. The exact date this started was July 26 so now it's a month and it's intensifying. I can't help but wonder if it's more than neuropathy and it's something much worse. The chain of events was first a yeast infection, then a UTI. The only thing out of the ordinary was I took a cranberry supplement on the 26th, and was still using miconazole.About 2 hours after the cranberry, it all started, I was on the internet relaxing & my skin started the pins & needles, prickly and itchy. I am trying so hard to deal with this, I truly am. ~ I have an appt, with my doctor Sept.5. I hope she will agree to get me lined up with a Neurologist, I think they can help pinpoint the cause, I hope. If you could respond if bones aching is a symptom that would be appreciated.
@sallylynn To my knowledge, bones aching is not a symptom of neuropathy.
Ginger