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

1 Year Gluten Free And Still Not Gaining Weight


Genna'smom

Recommended Posts

Genna'smom Apprentice

Hi my almost 3 yr old has been gluten free since May 08 and she is still not gaining weight and she is on a feeding tube. I am concerned for her and no one has been able to find anything else wrong with her. She was diagnosed when she had not been eating anything for a month or more and ended up in the hospital for 1 month trying to figure out what was going on......

I try so hard to keep any gluten out of her diet and she is eating small amounts of food and gets pediasure in her feeding tube at night.....

Any adivce or if anyone has been in similar situation please let me know. She goes back to the GI dr this friday and I have lots of questions for her...


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



Celiac.com Sponsor (A8-M):



Pattymom Newbie

We just finished out first year gluten free in Feb., and saw only minimal weight gain. My dd isnow 4.5 years. That said, I had her also off dairy for the last 3 months and saw a slight improvement in the growth, though still not much weight. She's also had and endocrinology workup, and we just had a endo/colonoscopylast month to look for other things and found nothing new, though, thankfully ruled out Crohn's Disease, which my brother has. Seems like the million dollar work up for tiny, and we are no closer to understanding why this child jsut doesn't gain, b/c it's not like we aren't' trying. No calorie we can get her to eat is a wasted calorie. I also started giving her extra zinc supplements in the last month, and it is since then that the height growth seems to hit.

I have no ideas or explanations, just that someone else is in that same frustrating place of trying everything and not finding answers. I try to focus on that we ruled out many awful diseases and know what she doesn't have, and just keep hoping for everythign else to remain normal. I would really like to have her summer clothes this year not be 24 months size like the last 2 years!

patty

debmom Newbie

Are the rest of the people in your family gluten free also? If not, she may be getting gluten from other sources other than what you are feeding her. I'm sure you know that cross contamination can cause a lot of problems. We were surprised to find that once we had all gone gluten free, we had lots of problems with even the tiniest bit of gluten, or even from the gluten escaping from an old bag of flour when we still had items in the house containing gluten. Once we eliminated all gluten in our food, we started seeing much more rapid improvement in my daughter and the rest of us who were gluten intolerant. My husband, though, does bring gluten items into the house on occasion, such as beer or pizza, and we do see problems. When he drinks beer, we now make him take the bottle out to the recycling after he washes it out, and he no longer asks our daughter to empty the recycling. But it took her showing him the eczema she had all over her arms to convince him that the little he did bring into the house could cause her problems.

I hope you get some good answers when you see the doctor tomorrow. It took us 7 months of hospitalizations to find some answers for my daughter, and that was after several serious misdiagnoses. My heart goes out to you-- it is so difficult tracking down what is hurting your child. But you will find it.

mellajane Explorer
Hi my almost 3 yr old has been gluten free since May 08 and she is still not gaining weight and she is on a feeding tube. I am concerned for her and no one has been able to find anything else wrong with her. She was diagnosed when she had not been eating anything for a month or more and ended up in the hospital for 1 month trying to figure out what was going on......

I try so hard to keep any gluten out of her diet and she is eating small amounts of food and gets pediasure in her feeding tube at night.....

Any adivce or if anyone has been in similar situation please let me know. She goes back to the GI dr this friday and I have lots of questions for her...

after being gluten free for almost two years I still had not gained any weight. Has she been tested for gastroperisis. I was diagnosed later and its been almost 5 years now in the last year i have just now started to put on weight. I am 32 and was diagnosed when i was around 25. I was sick since i was little. Not being diagnosed correctly for years damaged my small intestines thats where the gastroperisis comes in. Do research on the internet see if it hits home... Good luck

Genna'smom Apprentice
after being gluten free for almost two years I still had not gained any weight. Has she been tested for gastroperisis. I was diagnosed later and its been almost 5 years now in the last year i have just now started to put on weight. I am 32 and was diagnosed when i was around 25. I was sick since i was little. Not being diagnosed correctly for years damaged my small intestines thats where the gastroperisis comes in. Do research on the internet see if it hits home... Good luck

Thanks - she does have delayed gastric emptying....... the drs seem to think this is no big deal and she will grow out of it..... I want to push for more but do not know what else to do.....

Pattymom Newbie

Did you already rule out Cystic Fibosis and the other metabolic disorders? I know our GI I said the next place to look was pancreatic issues and or renal related concerns, though my dd doesn't have any symptoms of that. It's so hard to keep testing and testing when none of it seems to leads to anything but hassle and expense, and stress on the kids.

I hope you get some answers or ideas.

Patty

Genna'smom Apprentice
Did you already rule out Cystic Fibosis and the other metabolic disorders? I know our GI I said the next place to look was pancreatic issues and or renal related concerns, though my dd doesn't have any symptoms of that. It's so hard to keep testing and testing when none of it seems to leads to anything but hassle and expense, and stress on the kids.

I hope you get some answers or ideas.

Patty

Patty - she has had so many tests, CF sweat test, MRI of the brain for tumors, 3 endoscopies, swallow study as she gags all the time, blood work, food allergy tests, delayed stomach emptying test - you are right it is so hard but as a parent and as my OT said it is so hard when you do not have any kind of official diagnosis........... how much does your daughter weigh and how tall is she - what was she at 3...... My GI is also very laid back and I have to push for things but not sure where to go to anymore and his answer will be to increase her feeding tube feeds - YUCK I hate that as I feel it is not a solution just a band aide to cover up what is really wrong with her...... thanks for all your support and ideas...

Bonnie


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



Celiac.com Sponsor (A8-M):



shayesmom Rookie
Patty - she has had so many tests, CF sweat test, MRI of the brain for tumors, 3 endoscopies, swallow study as she gags all the time, blood work, food allergy tests, delayed stomach emptying test - you are right it is so hard but as a parent and as my OT said it is so hard when you do not have any kind of official diagnosis........... how much does your daughter weigh and how tall is she - what was she at 3...... My GI is also very laid back and I have to push for things but not sure where to go to anymore and his answer will be to increase her feeding tube feeds - YUCK I hate that as I feel it is not a solution just a band aide to cover up what is really wrong with her...... thanks for all your support and ideas...

Bonnie

My daughter had a lot of similar issues and I also have met other parents who went through the same. As controversial as this may sound, I would recommend finding a homeopath or a naturopath for a second opinion. Preferably one with an MD (a little harder to find, but worth it).

My daughter tested negative to allergens like soy on regular allergy tests. Our homeopath did a different kind of allergy test and found that soy, food colorings, artificial coloring and certain preservatives were a major issue for her. Sure enough, once we removed those foods, the weight started climbing and all of our "weird" symptoms disappeared.

Gluten, dairy and eggs were also major problems and only dairy and egg came up "slightly" positive on standard tests. Meanwhile, the simple fact is, those foods are major problems for her.

We went the pediasure route with little success for a very short amount of time. We saw major results with an extended elimination diet with weight gain tripling when compared to Pediasure and other weight gain measures the GI and pedi suggested.

Another parent I know also did an extended elimination diet in conjunction with a mostly raw food diet. Her dd's (both with multiple, undiagnosed/undetected food allergies) both thrived once she implemented this. Weight gain started immediately with all other random symptoms disappearing.

A common theme between our kids is they react to miniscule amounts of their "allergens". Trace exposures completely stunt growth and so both of our households need to be completely free of the offending items. It amazes me that dd barely gains weight during the school year....except when on Winter Break and during Summer Break....probably because the trace exposures are completely removed.

Good luck in finding answers with your child. And keep perservering. The answers will eventually come. It's just that sometimes, they don't come with an official, "medical" explanation.

Pattymom Newbie

how much does your daughter weigh and how tall is she - what was she at 3......

My dd is 29 lb at 4.9 years. She is 38.5 inches tall. At 3, I believe she was almost 24 lbs, 35 inches. At her 2 year old check up she was 23 lbs, most of the gain and growth has occurred in the past 9-10 months, since she turned 4 and we have been stricter with the dairy free. It almost doesn't seem so bad here, she is doing a little growth and gain--I do follow her around with cups of chocolate soy milk. I do understand how important it is to find out what is going on, and frustrating to not get answers.

Patty

Genna'smom Apprentice

Patty

Thanks - she is 26 lbs which puts her under the 10th percentile as compared to her heright which is 37"..... WE did talk about looking for a natural way of helping her and we just might do that. We also talked about taking her to a better hospital but just do not want to put her through all these tests again. Her GI dr gets me so frustrated - I asked if we should be a gluten free household and maybe take her off dairy and see and he said nooooooooo. Thanks again for your advice...

Also she has really bad behaviors and does not sleep good at night....

Bonnie

Pattymom Newbie

We got the same reaction from our first GI and endo when I suggested going off dairy, as if I suggested locking her in a closet. the firts G did guilt me into ptting her back on Dairy, she had only been off for 2 months. As soon as I did it, her eczema came back and weight gain and growth stopped again. not to mention the tantrums and whining. We went off again,in the next 3 months she grew an inch--when her previous rate was an inch a year. she does better off dairy. We did switch GI, and it was worth it, even with the waiting. He didn't repeat most of the tests, though he did scope her--they were great at the hospital, she was in my arms until she was asleep, and in them again before she was awake--and they carefully explianed stuff to her stuffed animal and Maggie check out her animal using the stethoscope, cuff, even the mask before it was her turn.

He also supported me taking her off dairy--said it's perfectly healthy not to have it as long as she gets calcium somewhere. Not sure what you woud tube feed without dairy, but there must be soy or elemental formulas. I had foster kids with feeding aversions and tubes 15 years ago, it was tricky stuff. I'm sure you've tried it all, but just in case, we had on Speech Therapist who had use frozen things--started with ice cubes to crunch, but switched to frozen chocolate pediasure pops--LOL< had forgotten those stuggles, I don't envy you.

Patty

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,983
    • Most Online (within 30 mins)
      7,748

    CRae
    Newest Member
    CRae
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Mari
      There is much helpful 'truth' posted on this forum. Truths about Celiac Disease are based on scientific research and people's experience. Celiac disease is inherited. There are 2 main Celiac 'genes' but they are variations of one gene called HLa - DQ What is inherited when a person inherits one or both of the DQ2 or the DQ8 is a predisposition to develop celiac disease after exposure to a environmental trigger. These 2 versions of the DQ gene are useful in diagnosing  celiac disease but there are about 25 other genes that are known to influence celiac disease so this food intolerance is a multigenic autoimmune disease. So with so many genes involved and each person inheriting a different array of these other genes one person's symptoms may be different than another's symptoms.  so many of these other genes.  I don't think that much research on these other genes as yet. So first I wrote something that seem to tie together celiac disease and migraines.  Then you posted that you had migraines and since you went gluten free they only come back when you are glutened. Then Scott showed an article that reported no connection between migraines and celiac disease, Then Trents wrote that it was possible that celiacs had more migraines  and some believed there was a causal effect. You are each telling the truth as you know it or experienced it.   
    • tiffanygosci
      Another annoying thing about trying to figure this Celiac life out is reading all of the labels and considering every choice. I shop at Aldi every week and have been for years. I was just officially diagnosed Celiac a couple weeks ago this October after my endoscopy. I've been encouraged by my local Aldi in that they have a lot of gluten free products and clearly labeled foods. I usually buy Milagro corn tortillas because they are cheap and are certified. However, I bought a package of Aldi's Pueblo Lindo Yellow Corn Tortillas without looking too closely (I was assuming they were fine... assuming never gets us anywhere good lol) it doesn't list any wheat products and doesn't say it was processed in a facility with wheat. It has a label that it's lactose free (hello, what?? When has dairy ever been in a tortilla?) Just, ugh. If they can add that label then why can't they just say something is gluten free or not? I did eat some of the tortillas and didn't notice any symptoms but I'm just not sure if it's safe. So I'll probably have to let my family eat them and stick with Milagro. There is way too much uncertainty with this but I guess you just have to stick with the clearly labeled products? I am still learning!
    • tiffanygosci
      Thank you all for sharing your experiences! And I am very thankful for that Thanksgiving article, Scott! I will look into it more as I plan my little dinner to bring with on the Holiday I'm also glad a lot of research has been done for Celiac. There's still a lot to learn and discover. And everyone has different symptoms. For me, I get a bad headache right away after eating gluten. Reoccurring migraines and visual disturbances were actually what got my PCP to order a Celiac Panel. I'm glad he did! I feel like when the inflammation hits my body it targets my head, gut, and lower back. I'm still figuring things out but that's what I've noticed after eating gluten! I have been eating gluten-free for almost two months now and haven't had such severe symptoms. I ate a couple accidents along the way but I'm doing a lot better
    • trents
      @Mari, did you read that second article that Scott linked? It is the most recently date one. "Researchers comparing rates of headaches, including migraines, among celiac patients and a healthy control group showed that celiac subjects experienced higher rates of headaches than control subjects, with the greatest rates of migraines found in celiac women.  Additionally, celiacs had higher rates of migraine than control subjects, especially in women. In fact, four out of five women with celiac disease suffered from migraines, and without aura nearly three-quarters of the time."
    • Mari
      As far as I know and I have made severalonline searches, celiac disease disease has not been recognized as a cause of migraines or any eye problems. What I wrote must have been confusing.
×
×
  • 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.