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Category Archives: Pregnancy / Kids
Hi, My boyfriend used to do dialysis but has not in two years or taken medicine and has told me he can’t have kids because of that, but I am pretty sure I’m pregnant. Is it possible?
Men with chronic kidney disease (CKD) can father children. Men commonly have low sperm counts, but can still father children.
My son, now 5 years old was diagnosed with Hydronephrosis in both kidneys before birth. He was monitored for 2 years and was released of urology and nephrologist but the past few weeks he’s showed high blood pressure, very metallic smelling hair and breath. He has been wetting his bed at night and cannot seem to stop sweating and drinking excessive water. Should I get a lab work up?
I suggest that you consult with your son’s pediatrician for an examination. Laboratory testing may be needed but a good examination by his pediatrician will be important to make sure the proper tests are performed. For more information on children’s … Continue reading →
My daughter has been on dialysis for nearly 17 years with several different complications. She is 35. We never thought she could get pregnant. That seems the possibility now. I can’t find any data on that for her time in ESRD. I’m in shock. What are her chances of survival? The baby’s?
The chances of successful pregnancy for a patient on chronic hemodialysis treatments is very poor. Successful pregnancy has been reported but dialysis treatments must be increased. Dialysis treatment times may have to be increased to more the 30 hours per … Continue reading →
Hi Doctor, My partner was diagnosed 5 years ago, at the age of 26, with a rare Kidney disease called mesangial capillary glomerulonephritis. He has been on steroid treatment and also cholesterol, blood pressure and other pills. He has suffered with many side effects including depression, mood swings, frequency of urination, dizziness, blurred vision and most recently the beginnings of osteoporosis. I have heard of Chinese Medicine Osmotherapy and read about some studies on www.ncbi.nlm.nih.gov and it seems very effective in treating patients with IgA nephropathy. I was wondering if you think this might work for my partner too? and whether it could be used in conjunction with his current medications? My second question is how likely do you think it would be for us to pass this disease down to a child? Thank you for any help you might give us… I worry about our future family and hope that someone will find a cure soon.
Mesangiocapillary glomerulonephritis (MCGN) is an uncommon kidney disease. There are many different forms of MCGN that have been described. Chinese medical osmotherapy is of no benefit in any kidney disease that I am aware. I cannot comment on whether you … Continue reading →
Hello sir. I am from India. I am kidney transplant patient 3.5 yrs completed. But my pressure is always high like 150/100. I am taking antihypertensive medicine from beginning after transplant. Creatinine is 1.5. Can I marry now? and can after marriage can take issue?
Kidney transplant patients may be married at any time and have children. As your transplanted kidney appears to be stable for more than 3 years, it should be safe to consider having children. It is necessary that you discuss marriage … Continue reading →
I am an adult nephrologist and have never used Rituximab (Rituxan) in children. I suggest that you consult with a pediatric nephrologist. For more information on Children’s health click here:
Hello, My 9 year old son recently had an renal ultrasound to look for kidney stones, etc. We don’t follow up with the nephrologist for over a month, and I’m curious about ultrasound report. The nurse told me on the phone that he didn’t have kidney stones, and this is what the report actually says: 1. Mild right pelviectasis in the prone position only (7 mm). 2. Otherwise normal sonographic appearance of the kidneys. No definite calcifications are seen. In the prone position only, there is mild right pelviectasis (SFU grade 1 bordering on 2) with AP diameter of the pelvis measuring 7 mm. I assume the pelviectasis isn’t serious since the nurse didn’t bring it up on the phone, but never having heard the term before, I tried to research it. The only references I can find refer to fetal pelviectasis, and I can’t find anything about this condition in a 9 year old child. I’m also curious about it only being seen in the prone position. Does this point to the possibility of some sort of blockage, or is it likely just a physiological finding? Is it unusual in a child his age?
Pelviectasis (also called pelvocaliectasis) merely means a separation of the collecting system or pelvis of the kidney detected by the ultrasound device. It does not suggest any disease, unless there are symptoms or signs of blockage and none are described. … Continue reading →
My son is 2.5 years old and we are in Romania. I am American and my husband is British. My son is being treated here for Nephrotic Syndrome but we would like to take him to England or America for further treatment. Do you have advice about traveling by plane. Perhaps you need to know more about his condition but if you have general advice it would still be helpful.
Traveling by airplane should not pose a risk to anyone with nephrotic syndrome. The long travel time in an airplane with inactivity could result in blood clots in the legs. Forming blood clots in the legs of patients with chronic … Continue reading →
I originally posted a question on 1/17/17 about my 9 year old son. I don’t see a way to respond to the reply, but have some more information that might be helpful to others looking for information on the same thing. At his doctor’s request, I was able to scrape some off to take in to the lab, and the stone analysis came back as 65% calcium oxalate dihydrate and 35% carbonate apatite. Additionally, a 24 hour urine test indicated a calcium/creatinine ratio of 245 (normal 30-20-) and an elevated creatinine level of .81 (normal 0.11-0.68). The doctor said for him to follow a low oxalate diet and follow-up with a pediatric nephrologist, which we will. Is it important to find the cause of the high creatinine and calcium rather than just treat the symptom? I remembered that my aunt (would be his great-aunt) died from nephritis at age 7, but don’t know if that would be considered a genetic risk for him that far removed.
I am unable to make any specific diagnosis based on the information that you present. It is best if you see a pediatric nephrologist and have further testing. It is possible that he has a genetic kidney stone disease but … Continue reading →
For the past year, my 9 year old daughter has been getting regular immoglobulin treatments (Gammumex)which are responsible for a miraculous improvement in her mobility, since she has Chronic Inflammatory Demyelating Polyneuropathy. For almost a year she got the treatments at 2 week intervals and more recently at three week intervals. These IVIG treatments, necessary as they are, are hard on the liver and kidneys, but do you know just how toxic these IVIG treatments can be to a child’s kidneys over time? Have you heard of this type of treatment ever damaging the kidneys? She doesn’t get an especially high dose, just average, and her neurologist says any irregular reading on the kidney and liver test we took should be disregarded because that’s just due to the IVIG’s. But because this is a rare disease, most of the frequency/dose of the treatment still involves guesswork and experimentation, so I remain watchful for signs of stress on her body. In the last several months she is getting bladder infections now and then that she didn’t get before. So far they just go away with cranberry juice. Then in the last 6-7 weeks I usually have to push her to eat because she frequently gets stomach pain. She was never a big eater to begin with so I worry about her getting enough protein and losing alot of weight again, which she did when she was initially misdiagnosed, wasn’t getting these treatments, and lost most of her mobility. What scares me most is that I read everywhere about how there are no symptoms of kidney disease until it’s advanced. So should I be proactive/concerned, then? If you say yes, my next step would be to show the readings we have to pediatric kidney doctor in our hospital system, to see if a more detailed kidney/liver test should be taken The test the neurologist ordered wasn’t, I was told, but that’s because her neurologist is unconcerned. The reason I feel the need to check with a third party at times is because he was the one who misdiagnosed her, so I had to go to another doctor and then go back and convince him to give her these IVIG treatments, which I think saved her life.
I would recommend blood and urine testing for kidney disease at least every three months to monitor kidney function. This should include a serum creatinine and an estimated glomerular filtration rate (eGFR). Urine testing should be for blood, protein and … Continue reading →