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

Pediatric Use Of Miralax


seezee

Recommended Posts

seezee Explorer

Hi - Just thought I'd point out that the NY Times and other papers have had some articles recently about the pediatric use of Miralax. When my daughter was first diagnosed with celiac she had to use large quantities for cleanouts. We had some weird side effects and switched to other things.

Open Original Shared Link


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



Celiac.com Sponsor (A8-M):



Momto2girls Rookie

I saw this, too. We are using LOTS of miralax. Can I ask you if your daughter had a lot of constipation with Celiac? My daughter gets constipated to the point of impaction and having diarrhea and it is so frustrating!

Mizzo Enthusiast

I saw this, too. We are using LOTS of miralax. Can I ask you if your daughter had a lot of constipation with Celiac? My daughter gets constipated to the point of impaction and having diarrhea and it is so frustrating!

My DD had impactions with a stretched colon and we used this for over a year and occasionally had to do Pepto Bismal on weekends for extra clean outs. Going gluten-free changed it pretty quickly. We stopped using it almost immediately. With no problems except the normal CC issue's

Mom2J112903 Newbie

My son, even on an elemental diet thru a g-tube, has to have 3 doses a DAY to keep things moving freely. His colon is MASSIVELY enlarged and we really have NO idea why or HOW it got as large as it did. We are on the path of "do whatever it takes to save the colon" right now.

Momto2girls Rookie

My DD had impactions with a stretched colon and we used this for over a year and occasionally had to do Pepto Bismal on weekends for extra clean outs. Going gluten-free changed it pretty quickly. We stopped using it almost immediately. With no problems except the normal CC issue's

Oh wow -- that's amazing! We are having the same thing - impactions with diarrhea around -- we are on miralax AND 2 senna laxatives a day -- and now we're on sulfasalazine, too, for GI inflammation. And even still she's impacted again within 2 weeks of a clean out -- so we have to do 6 capfuls of miralax for 2 days in a row in order to clean her out again. SO excited to hear that you were able to stop using it almost immediately!! Did you get a Celiac diagnosis or did you just decide to give it a try? I am VERY curious to hear about how this all came together for you! I am getting motivated to actually try this!

Momto2girls Rookie

My son, even on an elemental diet thru a g-tube, has to have 3 doses a DAY to keep things moving freely. His colon is MASSIVELY enlarged and we really have NO idea why or HOW it got as large as it did. We are on the path of "do whatever it takes to save the colon" right now.

Oh gosh, I am so sorry to hear that! I sure hope you can find an answer. Is it Celiac? Crohn's? Both? My DD has inflammation of the ileum and left colon but apparently it doesn't look like Crohn's?

Mom2J112903 Newbie

Oh gosh, I am so sorry to hear that! I sure hope you can find an answer. Is it Celiac? Crohn's? Both? My DD has inflammation of the ileum and left colon but apparently it doesn't look like Crohn's?

Celiac, Megacolon most likely due to an IBD but thanks to the size and shape the colon is in we can't get the proper biopsies taken. He is treated as an IBS case though. We have Dysphagia, GERD, Delayed Gastric Emptying, Celiac, and Megacolon not to mention chronic constipation. So his entire GI system just has awesome :insert sarcasm: motility.

What is really mind boggling is that he had his first colonoscopy when he was just under 3yrs of age, which showed a "normal" colon. His last one was done approx 2 months before his 8th birthday and that is when we found out about his "colon the size of Alaska".


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



Celiac.com Sponsor (A8-M):



MTsky Newbie

So those of you who have kids with celiac who had constipation, how long after going gluten free did it take for them to be normal? And did you just stop using miralax? At what point? My son was blood test positive, but biopsy negative. We took him off of gluten immediately after the biopsy, 4 weeks ago. In those 4 weeks he has gained 2 lbs and one inch. I am still giving him the miralax daily, but I am really hoping that his constipation will resolve being gluten free.

seezee Explorer

I saw this, too. We are using LOTS of miralax. Can I ask you if your daughter had a lot of constipation with Celiac? My daughter gets constipated to the point of impaction and having diarrhea and it is so frustrating!

My daughter had stool retention that was diagnosed via xray. (Basically that means her colon was filled with old hard poop) we worked with the pediatric GI dept. at childrens hospital and it took around a year to resolve. We had multiple visits and xrays and cleanouts. It's hard to say when it started because she was diagnosed with celiac at the end of 4th grade (now in 7th). That year her teacher mentioned at our parent teacher conference in Feb. that he was annoyed because she seemed to need the toilet too often and he was restricting her bathroom use. This was before we figured out about the celiac around April, so that probably made it worse. She is a super well behaved kid and if her teacher wasn't letting her use the toilet as often as she needed...

In fifth grade a few months into the gluten-free diet, she had severe stomach pains and GI took xrays that showed dd was full of stool. I don't know if ours was especially bad but it did require multiple clean outs with massive amounts of miralax and other icky stuff. After the last one my dd complained of having trouble concentrating and feeling weird after something like a whole bottle of the stuff. Luckily that one did the trick otherwise the next step would have been to have her do a cleanout in the hospital that involves putting a tube down her nose through her stomach and literally flushing with water. yuck. I had no idea that this could be such a serious problem and always worry when I see things that make it sound like the kid is being bad by holding it in on purpose. I think it takes the colon a long time to heal once it's been stretched and I recommend working with a pediatric GI specialist. The digestive system is fairly complex and I really just don't believe that kids especially little ones are misbehaving by holding in poop deliberately -- I think there is an underlying medical issue that needs to be addressed.

We never used miralax again after daughter complained of other side effects.

These are two more articles:

Open Original Shared Link

Open Original Shared Link

Momto2girls Rookie

My daughter had stool retention that was diagnosed via xray. (Basically that means her colon was filled with old hard poop) we worked with the pediatric GI dept. at childrens hospital and it took around a year to resolve. We had multiple visits and xrays and cleanouts. It's hard to say when it started because she was diagnosed with celiac at the end of 4th grade (now in 7th). That year her teacher mentioned at our parent teacher conference in Feb. that he was annoyed because she seemed to need the toilet too often and he was restricting her bathroom use. This was before we figured out about the celiac around April, so that probably made it worse. She is a super well behaved kid and if her teacher wasn't letting her use the toilet as often as she needed...

In fifth grade a few months into the gluten-free diet, she had severe stomach pains and GI took xrays that showed dd was full of stool. I don't know if ours was especially bad but it did require multiple clean outs with massive amounts of miralax and other icky stuff. After the last one my dd complained of having trouble concentrating and feeling weird after something like a whole bottle of the stuff. Luckily that one did the trick otherwise the next step would have been to have her do a cleanout in the hospital that involves putting a tube down her nose through her stomach and literally flushing with water. yuck. I had no idea that this could be such a serious problem and always worry when I see things that make it sound like the kid is being bad by holding it in on purpose. I think it takes the colon a long time to heal once it's been stretched and I recommend working with a pediatric GI specialist. The digestive system is fairly complex and I really just don't believe that kids especially little ones are misbehaving by holding in poop deliberately -- I think there is an underlying medical issue that needs to be addressed.

We never used miralax again after daughter complained of other side effects.

Oh wow -- good to know. We are working with a ped GI but we are still having issues. In fact, I am pretty sure we are going to have to get another x-ray today. Luckily we haven't let the problem go for long without a cleanout, but it does take 6 capfuls of miralax a day for 2 days to get her cleaned out and we end up doing this every 2 weeks. This is with a maintenance dose of miralax AND 2 senna laxatives a day. And now she is also on sulfasalazine for the inflammation they found on her recent scope. And even with all of that she is backed up again. So we are taking out gluten today and praying it'll make a difference. I am so frustrated!!

Momto2girls Rookie

So those of you who have kids with celiac who had constipation, how long after going gluten free did it take for them to be normal? And did you just stop using miralax? At what point? My son was blood test positive, but biopsy negative. We took him off of gluten immediately after the biopsy, 4 weeks ago. In those 4 weeks he has gained 2 lbs and one inch. I am still giving him the miralax daily, but I am really hoping that his constipation will resolve being gluten free.

I am wondering the same. How much miralax is he taking? And has he had any constipation since going gluten-free? Could you try going down on the dose for a few days and see what happens?

sarah.allgood1019 Newbie

OMG! I am so glad I found this thread! My son just got his paperwork for celiac testing, but he is full of poop and the doc gave him miralax and insisted there was no way to overdose on it. Also said to just continue the dosing. Agh....

Any safer ways to do a cleanout?

MTsky Newbie

I am wondering the same. How much miralax is he taking? And has he had any constipation since going gluten-free? Could you try going down on the dose for a few days and see what happens?

He is currently just taking 1/3 capful daily. I haven't tried weaning him off of it or stopping it yet. I am leery of stopping it because when he has missed more than a dose or two in the past, he starts vomiting, and then he finally poops and all is well. I am thinking of maybe weaning down a bit and seeing how he does.

Momto2girls Rookie

OMG! I am so glad I found this thread! My son just got his paperwork for celiac testing, but he is full of poop and the doc gave him miralax and insisted there was no way to overdose on it. Also said to just continue the dosing. Agh....

Any safer ways to do a cleanout?

Nope -- it is the best way to do a clean out -- we've done it several times, and it looks like we're impacted again and will be facing another clean out. But we've been on miralax for close to 2 years and now I want to get to the bottom of the problem so that we can get this all straightened out, and get off of it! It is so frustrating!

Mom2J112903 Newbie

OMG! I am so glad I found this thread! My son just got his paperwork for celiac testing, but he is full of poop and the doc gave him miralax and insisted there was no way to overdose on it. Also said to just continue the dosing. Agh....

Any safer ways to do a cleanout?

Miralax is the safest and least invasive. We have had to do hospital clean outs, which are NO fun. We did one cap full of Miralax in 8ounces of CLEAR liquid with NO solid food during waking hours until we saw "Mt Dew" colored stool. No more than 48hrs though and for my son, that was never enough.

Mom-of-Two Contributor

To the poster with kiddo who had pos blood test but neg biopsy- did your GI doc suggest going gluten-free or you decided to take that route due to symptoms? I am ticked that my GI is telling us our 7 year old does not have celiac, even though I have it and she has elevated tTG testing at 78.20. I am getting an opinion of another pediatric GI that has a speciality in kids celiac. Hoping for a full panel done through him, and better info. This other guy is trying to tell me she is a false positive!

sarah.allgood1019 Newbie

Wth?? False positive? Yeah that's nonsense!

MTsky Newbie

To the poster with kiddo who had pos blood test but neg biopsy- did your GI doc suggest going gluten-free or you decided to take that route due to symptoms? I am ticked that my GI is telling us our 7 year old does not have celiac, even though I have it and she has elevated tTG testing at 78.20. I am getting an opinion of another pediatric GI that has a speciality in kids celiac. Hoping for a full panel done through him, and better info. This other guy is trying to tell me she is a false positive!

No our GI did not tell us to go gluten free. She told us that he was fine and needed no special diet. I decided to try him gluten free on my own. If it makes a difference, his tTG was only a "weak positive". He did NOT get the full celiac panel done. Just the tTg and IGA. I tried to fight our ped on that one and he felt it was unnecessary to run the additional tests. I didn't push it because we had the biopsy scheduled and I figured that was more important. I am beyond frustrated by it now that his biopsy is negative and he is showing so much improvement being gluten free!

  • 2 weeks later...
CeliacMom2012 Newbie

My son was on very large doses of this and it never helped. We have change to a liquid med but it helps very little. We have been on the gluten-free diet since Feb 2012 and still have constipation issues.

Mom2J112903 Newbie

My son was on very large doses of this and it never helped. We have change to a liquid med but it helps very little. We have been on the gluten-free diet since Feb 2012 and still have constipation issues.

Have they done other GI testing? Have they thought about gut rest meaning an elemental formula whether by mouth or by tube? My son has a dysfunctional GI system and the elemental diet is the ONLY thing helping him. If they have not done a colonoscopy, that is where I would start.

MelanieS Newbie

What a great article. My daughter is almost 2.5 and is on a full capful of Miralax daily for the last 2 months when she had to be hospitalized due to impaction. She has not been diagnosed with Celiacs yet but her last few scopes have shown indicators. Her Celiac panel was drawn on Wednesday. Regardless of the results, we will be going gluten-free and I'm really hoping that it will help wih her stool issues and also with gaining weight (she has been diagnosed as Failure to Thrive).

Archived

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

  • Get Celiac.com Updates:
    Support Celiac.com:
    Join eNewsletter
    Donate

  • Celiac.com Sponsor (A17):
    Celiac.com Sponsor (A17):





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - knitty kitty replied to xxnonamexx's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      47

      My journey is it gluten or fiber?

    2. - Known1 replied to Jane02's topic in Gluten-Free Foods, Products, Shopping & Medications
      12

      Desperately need a vitamin D supplement. I've reacted to most brands I've tried.

    3. - SilkieFairy replied to catnapt's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      4

      results from 13 day gluten challenge - does this mean I can't have celiac?

    4. - Wheatwacked replied to Scott Adams's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      50

      Supplements for those Diagnosed with Celiac Disease

  • Celiac.com Sponsor (A19):
  • Member Statistics

    • Total Members
      133,361
    • Most Online (within 30 mins)
      7,748

    Xpedit73
    Newest Member
    Xpedit73
    Joined
  • Celiac.com Sponsor (A20):
  • Celiac.com Sponsor (A22):
  • Forum Statistics

    • Total Topics
      121.6k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Upcoming Events

  • Posts

    • knitty kitty
      Try adding some Thiamine Hydrochloride (thiamine HCl) and see if there's any difference.  Thiamine HCl uses special thiamine transporters to get inside cells.  I take it myself.   Tryptophan will help heal the intestines.  Tryptophan is that amino acid in turkey that makes you sleepy after Thanksgiving dinner.  I take mine with magnesium before bedtime.
    • Known1
      I live in the upper mid-west and was just diagnosed with marsh 3c celiac less than a month ago.  As a 51 year old male, I now take a couple of different gluten free vitamins.  I have not noticed any reaction to either of these items.  Both were purchased from Amazon. 1.  Nature Made Multivitamin For Him with No Iron 2.  Gade Nutrition Organic Quercetin with Bromelain Vitamin C and Zinc Between those two, I am ingesting 2000 IU of vitamin D per day. Best of luck, Known1
    • SilkieFairy
      I am doing a gluten challenge right now and I bought vital wheat gluten so I can know exactly how much gluten I am getting. One tablespoon is 7g so 1½ tablespoons of Vital Wheat Gluten per day will get you to 10g You could add it to bean burgers as a binder or add to hot chocolate or apple sauce and stir. 
    • Wheatwacked
      Raising you vitamin D will increase absorption of calcium automatically without supplementation of calcium.  A high PTH can be caused by low D causing poor calcium absorption; not insuffient calcium intake.  With low D your body is not absorbing calcium from your food so it steals it from your bones.  Heart has priority over bone. I've been taking 10,000 IU D3 a day since 2015.  My doctor says to continue. To fix my lactose intolerance, lots of lactobacillus from yogurts, and brine fermented pickles and saurkraut and olives.  We lose much of our ability to make lactase endogenosly with maturity but a healthy colony of lactobacillus in our gut excretes lactase in exchange for room and board. The milk protein in grass fed milk does not bother me. It tastes like the milk I grew up on.  If I drink commercial milk I get heartburn at night. Some experts estimate that 90% of us do not eat Adequite Intake of choline.  Beef and eggs are the principle source. Iodine deficiency is a growing concern.  I take 600 mcg a day of Liquid Iodine.  It and NAC have accelerated my healing all over.  Virtually blind in my right eye after starting antihypertensive medication and vision is slowly coming back.  I had to cut out starches because they drove my glucose up into the 200+ range.  I replaced them with Red Bull for the glucose intake with the vitamins, minerals and Taurine needed to process through the mitochodria Krebs Cycle to create ATP.  Went from A1c 13 down to 7.9.  Work in progress. Also take B1,B2,B3,B5,B6. Liquid Iodine, Phosphatidyl Choline, Q10, Selenium, D and DHEA.     Choline supplemented as phosphatidylcholine decreases fasting and postmethionine-loading plasma homocysteine concentrations in healthy men +    
    • knitty kitty
      @catnapt, Wheat germ has very little gluten in it.  Gluten is  the carbohydrate storage protein, what the flour is made from, the fluffy part.  Just like with beans, there's the baby plant that will germinate  ("germ"-inate) if sprouted, and the bean part is the carbohydrate storage protein.   Wheat germ is the baby plant inside a kernel of wheat, and bran is the protective covering of the kernel.   Little to no gluten there.   Large amounts of lectins are in wheat germ and can cause digestive upsets, but not enough Gluten to provoke antibody production in the small intestines. Luckily you still have time to do a proper gluten challenge (10 grams of gluten per day for a minimum of two weeks) before your next appointment when you can be retested.    
×
×
  • 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.