Jump to content
  • Welcome to Celiac.com!

    You have found your celiac tribe! Join us and ask questions in our forum, share your story, and connect with others.




  • Celiac.com Sponsor (A1):



    Celiac.com Sponsor (A1-M):


  • Get Celiac.com Updates:
    Support Our Content
    eNewsletter
    Donate

Prednisone for nephrotic syndrome?


Sahil

Recommended Posts

Sahil Newbie

My 3 years old daughter is a celiac which was diagnosed when she was 2 and has been recently diagnosed with nephrotic syndrome. She is on Open Original Shared Link for past one month and there has been no improvement on her protein levels until now. Doctor recommended to go for kidney biopsy.

What should I do?


Celiac.com Sponsor (A8):
Celiac.com Sponsor (A8):



Celiac.com Sponsor (A8-M):



cyclinglady Grand Master
2 hours ago, Sahil said:

My 3 years old daughter is a celiac which was diagnosed when she was 2 and has been recently diagnosed with nephrotic syndrome. She is on Open Original Shared Link for past one month and there has been no improvement on her protein levels until now. Doctor recommended to go for kidney biopsy.

What should I do?

I am sorry your daughter is ill.  I assume she has been gluten free since her celiac disease diagnosis?  Is it possible to get a second opinion from another doctor regarding the kidney biopsy?  

 

 

Sahil Newbie
9 hours ago, cyclinglady said:

I am sorry your daughter is ill.  I assume she has been gluten free since her celiac disease diagnosis?  Is it possible to get a second opinion from another doctor regarding the kidney biopsy?  

I'm not sure at the moment whether I should seek a nephrologist or a gastroenterologist

kareng Grand Master
1 hour ago, Sahil said:
12 hours ago, cyclinglady said:

I am sorry your daughter is ill.  I assume she has been gluten free since her celiac disease diagnosis?  Is it possible to get a second opinion from another doctor regarding the kidney biopsy?  

I'm not sure at the moment whether I should seek a nephrologist or a gastroenterologist

Who diagnosed this?  I would insist on a pediatric kidney specialist!  What doctor is going to do this "kidney biopsy"?  I think you  need to ask more questions.  If you can't do it with the child in the room, bring someone with you to take the child out.  Write down questions.  Maybe bring someone else who is more assertive than you seem to be to help you get actual answers.

Wheatwacked Veteran

Sahil, there is not much more frustrating then to watch our children suffer. It isn't their fault.

"In many kinds of kidney disease, inflammation occurs when immune complexes deposit in kidney. Immune complex is a combination of antigen and antibody and formed when immune system is weak or immunity is poor."

Prednisone treatment for nephrotic syndrome has been researched and proven effective, often the best. If she is not declining, wait on the actual biopsy but a workup by a nephrologist with celiac disease experience would be best and it seems that is your doctors approach. Get her vitamin and minerals levels checked because with celiac disease there are almost certainly nutritional deficiencies that will effect recovery. Do not assume. Especially iodine and vitamin D and, as I just learned Iron.

Biopsy can give important information as to the actual disease process, and may be necessary to  fine tune treatment, but it may not be needed if the treatment works. Biopsy is a rather traumatic procedure for your child.

Open Original Shared LinkPrednisolone is a steroid medicine that will get rid of the protein in the urine and the extra water but it needs to be taken over a long period of time (months)...The use of steroids in children receives a lot of bad press. However, use of prednisolone in nephrotic syndrome provides a lot of benefit, and is unlikely to cause any long-term harm as long as you use the medicine as your doctor has told you to. If you are at all worried, talk to your doctor or pharmacist.

*Oral Prednisone is converted by the liver into prednisolone, so I think a safer choice, and what I believe you say she is on.

nice reads: Open Original Shared Link "Treating Kidney Disease with Steroids" patient information.

                   Open Original Shared Link  Open Original Shared Link

 

 

 

 

 

Wheatwacked Veteran

People get all freaked out when you say you are using Prednisone because it is a steroid and we all know that steroids are bad and are used to cheat in sports, and everyone knows. Wrong.

A prednisone story for perspective.

My last black lab was on prednisone from nine months old until he died at nine and a half years old of degenerative myelopathy complications. He had congenital hip dysplasia.  We found it on x-ray when he was nine months old. He lived a normal life, mostly an indoor guy. When he was x-rayed at nine, to find why his rear toes were dragging the vet found that his hips had no arthritic deterioration compared to his puppy films. It seems the prednisone had protected him. Almost every other dog I have had prior to Riley, most living to 13, ended up on prednisone because of arthritic damage.

Do not discount your doctors treatment plan because of social pressure or scary stories. It might be the best choice.

Posterboy Mentor
On 1/28/2018 at 10:00 PM, Sahil said:

My 3 years old daughter is a celiac which was diagnosed when she was 2 and has been recently diagnosed with nephrotic syndrome. She is on Open Original Shared Link for past one month and there has been no improvement on her protein levels until now. Doctor recommended to go for kidney biopsy.

What should I do?

Sahil,

Let first say this is not medical advice.

But I have done a lot of nutrition research and often research other topics as they come up.

But you should look into taking a good B-Complex preferably 3/day (each meal) or 2/day if that is not convenient. Most B-Vitamins/complexes can be taken on a cycle of 6 to 12 months with only positive benefits unless there is MTHFR gene defect for Folic Acid etc.

Both B-1 and B-3 have been shown to help kidney issues.

Open Original Shared Link

entilted from 2008 "Thiamine 'reverses kidney damage'" in those who have type 2 diabetes research shows.

I can confirm this research I have TD2 and had creatine in my kidneys at the time I began supplementing with Thiamine (B1) and have not had Creatine or Albumin issues since taking a cycle of B-1.

A B-1 deficiency is an oft forgotten disease today known as Beri Beri.

Also here is the B-3 research.  Again a B-3 deficiency is an oft forgotten disease today known as Pellagra.

from the kidneyabc website.

Open Original Shared Link

quoting

1. Vitamin b3 can slow down the progression of PKD

"The medical research has proven that vitamin b3 has the effects in inhibiting the activity of SIRT1, which affects the formation and growth of cysts. Besides, vitamin b3 may decrease the rate of infants who are at risk of experiencing PKD."

it did not say reverse but slow the progression.  The B-3 is working when she begins burping if she does not now. This will take 3 months time to notice any descernable signs Niacin/Niacinamide is working.

So this is not some magical cure . .  but any help it can provide I think I would be interested in exploring.

Ask your pharmacy if the Niacinamide form or the flushing Niacin form is best.  Being 3 she might not understand how the Niacin flush is helping her by opening her capillaries letting more blood flow into her kidneys.

I usually recommend to my friend the non-flushing Niacinamide form but Niacin (flushes over2 days usually for 30 minutes after a meal) might be better in this case due to the vasodialtion effect of Niacin. 

I honestly dont' know which form is best or if it matters.  Again ask your Pharmacist/Doctor.

This may be true for B-1 as well.  It could take 3 to 6 months before her kidney function improves if this helps.  So be patient with this approach.  there are various forms of B-1 too.  Benfortiamine is the fat soluble form where thiamine is the water soluble form.  Again ask your Pharmacist/Doctor which is best.

And B-Vitamins are known/have been shown to help Celiac's on a gluten free diet.

https://www.celiac.com/articles/21783/1/B-Vitamins-Beneficial-for-Celiacs-on-Gluten-Free-Diet/Page1.html

Sahil I hope this is helpful.

AGain this not a magical cure but research shows B-Vitamins helps celiac's and that B-1 and B-3 specifically have shown to slow and even help/reverse kidney issues in those who take it aggressively for a cycle (especially in TD2) patients and there is no reason it might not help those who are having Kidney issues for other reasons.

I do know taking thiamine helped my creatine and Albumin levels.

I was taking it for my creatine levels due to my TD2 but my Albumin levels got better too!

Though my blood sugar is not super elevated these days . . . it is not under control either. . . but my Creatine and Albumin levels are normal.

Only a Vitamin explains the difference.

Again I hope this is helpful.

********* and again this is not medical advice just things I have learned from studying nutrition and form taking B-Vitamins that helped me with some of my TD2 complications.

Don’t every stop being your own advocate!

2 Corinthians (KJV) 1:3,4 3) “Blessed be God, even the Father of our Lord Jesus Christ, the Father of mercies, and the God of all comfort; 

4) who comforteth us in all our tribulation, that we may be able to comfort them which are in any trouble (fellow sufferer), by the comfort wherewith we ourselves are comforted of God.”

2 Timothy 2: 7 “Consider what I say; and the Lord give thee understanding in all things” this included.

Posterboy by the grace of God,


 

 

 

 


Celiac.com Sponsor (A8):
Celiac.com Sponsor (A8):



Celiac.com Sponsor (A8-M):



Archived

This topic is now archived and is closed to further replies.


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,855
    • Most Online (within 30 mins)
      7,748

    Tara M
    Newest Member
    Tara M
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.4k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • trents
    • Jillian83
      Hi, I was recently diagnosed with Celiac and dermatitis herpetiformis after years of suffering without answers. I lost my mind. I lost my job. I lost so much time. I lost Me. Conventional doctors are opulent come near me and the one who did sat across the room, misdiagnosed me, pumped me full of steroids which collapsed my entire hip for 6 months. So without answers I began my holistic journey. Fast forward a couple of years and still struggling with a mysterious whole body itchy, crawling “skin hell”, perfect teeth now deteriorating, thick hair now thinning rapidly and no more than a day or 2 at most relief….An acquaintance opened up a functional medicine practice. Cash only, I found a way. Within a month tests clearly showing my off the charts gluten allergy/sensitivity as well as the depletion of vital nutrients due to leaky gut and intestinal damage. dermatitis herpetiformis was more than likely what I was experiencing with my skin. I was happy. I thought this is easy, eat healthy Whole Foods, follow the diet restrictions and I finally get to heal and feel confident and like myself again very soon! 😔 Supplements are very pricey but I got them and began my healing. Which leads to the other major issue: not working, stay at home Mom of young kids, entirely financially dependent on my man of 7 plus years. He’s never been supportive of anything I’ve ever done or been thru. He controls everything. I’m not given much money ever at a time and when he does leave money it’s only enough to possibly get gas. His excuse is that I’ll spend it on other things. So my “allowance” is inconsistent and has conditions. He withholds money from me as punishment for anything he wants. Since being diagnosed, he’s gained a new control tactic to use as punishment. He now is in control of when I get to eat. He asked for proof of my diagnosis and diet bc he said I made it up just to be able to eat expensive organic foods. Then after I sent him my file from my doctor he then said she wasn’t a real doctor. 😡. I go days upon days starving, sometimes breaking down and eating things I shouldn’t bc I’m so sick then I pay horribly while he gets annoyed and angry bc I’m not keeping up with all the duties I’m supposed to be doing. His abuse turns full on when I’m down and it’s in these desperate times when I need his support and care the most that I’m punished with silence, being starved, ignored, belittled. He will create more of a mess just bc I’m unable to get up and clean so that when I am better, I’m so overwhelmed with chores to catch up that the stress causes me to go right back into a flare from hell and the cycle repeats. I’m punished for being sick. I’m belittled for starving and asking for healthy clean water. I’m purposely left out of his life. He won’t even tell me he’s going to the grocery or to get dinner bc he doesn’t want me to ask him for anything. I have no one. I have nothing. Im not better. My supplements ran out and I desperately need Vitamin D3 and a methylated B complex at the very minimal just to function….he stares at me blankly…no, a slight smirk, no words. He’s happiest when im miserable and I am miserable.  this is so long and im condensing as much as I can but this situation is so complicated and disgusting. And it’s currently my life. The “IT” girl, the healthy, beautiful, perfect skin, perfect teeth, thick and curly locks for days, creative and talented IT girl….now I won’t even leave this house bc Im ashamed of what this has dont to my body, my skin. Im disgusted. The stress is keeping me from healing and I think he knows that and that’s why he continues to keep me in that state. He doesn’t want me confident or successful. He doesn’t want me healed and healthy bc then how would he put the blame of all his problems on me? This journey has been hell and I’ve been in Hell before. I’ve been killed by an ex, I’ve been raped, robbed, held hostage, abused beyond nightmares but the cruelty I’ve experienced from him bc of this disease is the coldest I’ve ever experienced. I’ve wanted to give up. Starving and in tears, desperate…I found a local food pantry in our small town so I reached out just saying I had Celiac and was on hard times. This woman is blessing me daily with prepared gluten free meals, donations, educational info, people who know this disease and how they manage life and the blessings just keep coming. But it’s overwhelming and I feel like I don’t deserve it at all. He just glared and I know he’s going to sabotage it somehow. I don’t even know what to do anymore. I’m so broken and just want peace and healing. 
    • cristiana
      @Colleen H   I am just curious,  when you were tested for coeliac disease, did the doctors find out if you had any deficiencies? Sometimes muscle pain can be caused by certain deficiencies, for example, magnesium, vitamin D, calcium, and potassium.   Might be worth looking into having some more tests.  Pins and needles can be neuropathy, again caused by deficiencies, such as iron and B12,  which can be reversed if these deficiencies are addressed. In the UK where I live we are usually only tested for iron, B12 and vitamin D deficiencies at diagnosis.   I was very iron anemic and supplementation made a big difference.  B12 was low normal, but in other countries the UK's low normal would be considered a deficiency.  My vitamin D was low normal, and I've been supplementing ever since (when I remember to take it!) My pins and needles definitely started to improve when my known deficiencies were addressed.  My nutritionist also gave me a broad spectrum supplement which really helped, because I suspect I wasn't just deficient in what I mention above but in many other vitamins and minerals.  But a word of warning, don't take iron unless blood tests reveal you actually need it, and if you are taking it your levels must be regularly monitored because too much can make you ill.  (And if you are currently taking iron, that might actually be making your stomach sore - it did mine, so my GP changed my iron supplementation to a gentler form, ferrous gluconate). Lastly, have you been trying to take anything to lessen the pain in your gut?  I get a sore stomach periodically, usually when I've had too much rich food, or when I have had to take an aspirin or certain antibiotics, or after glutening.  When this happens, I take for just a few days a small daily dose of OTC omeprazole.  I also follow a reflux or gastritis diet. There are lots online but the common denominators to these diets is you need to cut out caffeine, alcohol, rich, spicy, acidic food etc and eat small regularly spaced meals.   When I get a sore stomach, I also find it helpful to drink lots of water.  I also find hot water with a few slices of ginger very soothing to sip, or camomile tea.  A wedge pillow at night is good for reflux. Also,  best not to eat a meal 2-3 hours before going to bed. If the stomach pain is getting worse, though, it would be wise to see the doctor again. I hope some of this helps. Cristiana    
    • Me,Sue
      I was diagnosed with coeliac disease a couple of years ago [ish]. I love my food and a variety of food, so it's been hard, as it is with everyone. I try and ensure everything I eat doesn't contain gluten, but occasionally I think something must have got through that has gluten in. Mainly I know because I have to dash to the loo, but recently I have noticed that I feel nauseous after possibly being glutened. I think the thing that I have got better at is knowing what to do when I feel wiped out after a gluten 'episode'. I drink loads of water, and have just started drinking peppermint tea. I also have rehydration powders to drink. I don't feel like eating much, but eventually feel like I need to eat. Gluten free flapjacks, or gluten free cereal, or a small gluten free kids meal are my go to. I am retired, so luckily I can rest, sometimes even going to bed when nothing else works. So I feel that I am getting better at knowing how to try and get back on track. I am also trying to stick to a simpler menu and eat mostly at home so that I can be more confident about what I am eating. THANKS TO THOSE WHO REPLIED ABOUT THE NAUSEA .
    • Francis M
      Thanks. Since the back and forth and promises of review and general stalling went on for more than six months, the credit company will no longer investigate. They have a cutoff of maybe six months.
×
×
  • Create New...

Important Information

NOTICE: This site places This site places cookies on your device (Cookie settings). on your device. Continued use is acceptance of our Terms of Use, and Privacy Policy.