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

Delayed Growth As A Child


PeggyV

Recommended Posts

PeggyV Apprentice

I wonder if any of you had the same experience. I was very small when I was young. I started high school at 4'9" and 80lb. I am now 5'5. I grew when I turned 16, and also started my period midway through my 16th year. My sister is 3 years younger and was always the same size as me. Could this be the reason I took so long to grow? My mother mentioned this to me a few days ago and I started thinking about it. Just wondered if being Gluten Intolerant could have played into this.


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



Celiac.com Sponsor (A8-M):



Guhlia Rising Star

I'm only 5'3" and that's probably stretching it... I'm the shortest one in my family so I'm assuming that Celiac played a role in my height.

PeggyV Apprentice

I could understand if I stayed small, but I grew, so maybe I was just a "late bloomer" like everyone said.... I used to be 5'6" but now that I am 50, I think I am closer to 5'5". ;)

jacqui Apprentice
I wonder if any of you had the same experience. I was very small when I was young. I started high school at 4'9" and 80lb. I am now 5'5. I grew when I turned 16, and also started my period midway through my 16th year. My sister is 3 years younger and was always the same size as me. Could this be the reason I took so long to grow? My mother mentioned this to me a few days ago and I started thinking about it. Just wondered if being Gluten Intolerant could have played into this.

Yes, it can cause growth delay. My daughter has a double whammy in that she also has Hashimoto's autoimmune disease, which also stunts growth and her bone age is less than 5y/o and she is 61/2. I myself am only 5ft. 1/2in. and have both also! I was always tiny and ate like I had a bottomless pit. My sister just finally got diagnosed with Celiac aftre my nagging and she is 5'2" and we have always been close in size too.

It also causes late onset puberty. I was the same as you 16 y/o when I got it and I had it for a month straight full force!!

I have also been reflecting and goig "Hmm, now it makes sense."

I also had endometriosis...

Good Luck,

Jacqui

wowzer Community Regular

This makes sense to me. I was a late bloomer. I was always the smallest person almost all the way through school. Finally I hit 5 feet when I started high school. I grew until I was 18 and made it to 5'4". My little sister whom was diagnosed at a year, was the same way.

bbuster Explorer

My son is almost 13 and is 4'6". He has always been small, mostly less than 3rd percentile. Over the years he has been to an orthopaedist, urologist, and had growth hormone levels checked many times - and everything always came out normal. I am 5'6" and his dad is about 5'10", and he is barely taller than his sister 3 years younger (many of her classmates are taller than him).

When I learned about 2 years ago that a friend had Celiac, my son's small stature prompted me to have him tested and sure enough, he had it. (He never had any GI symptoms.) It took us several months to get the diet worked out and he finally got negative bloodwork last summer. Since then he has filled out considerably but not grown a lot in height. We are hoping he will have a spurt any time now.

PeggyV Apprentice
My son is almost 13 and is 4'6". He has always been small, mostly less than 3rd percentile. Over the years he has been to an orthopaedist, urologist, and had growth hormone levels checked many times - and everything always came out normal. I am 5'6" and his dad is about 5'10", and he is barely taller than his sister 3 years younger (many of her classmates are taller than him).

When I learned about 2 years ago that a friend had Celiac, my son's small stature prompted me to have him tested and sure enough, he had it. (He never had any GI symptoms.) It took us several months to get the diet worked out and he finally got negative bloodwork last summer. Since then he has filled out considerably but not grown a lot in height. We are hoping he will have a spurt any time now.

I am glad you caught it early. I bet he does grow. Good luck.


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
      131,964
    • Most Online (within 30 mins)
      7,748

    Cbear
    Newest Member
    Cbear
    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

    • Scott Adams
      If black seed oil is working for his Afib, stick to it, but if not, I can say that ablation therapy is no big deal--my mother was out of the procedure in about 1 hour and went home that evening, and had zero negative effects from the treatment. PS - I would recommend that your husband get an Apple watch to monitor his Afib--there is an app and it will take readings 24/7 and give reports on how much of the time he's in it. Actual data like this should be what should guide his treatment.
    • Jacki Espo
      This happened to me as well. What’s weirder is that within a couple hours of taking paxlovid it subsided. I thought maybe I got glutened but after reading your post not so sure. 
    • Mari
      Hi Tiffany. Thank you for writing your dituation and  circumstancesin such detail and so well writte, too. I particularly noticed what you wrote about brain for and feeling like your brain is swelling and I know from my own experiences that's how it feel and your brain really does swell and you get migraines.    Way back when I was in my 20s I read a book by 2 MD allergist and they described their patient who came in complaining that her brain, inside her cranium, was swelling  and it happened when she smelled a certain chemical she used in her home. She kept coming back and insisting her brain actually swelled in her head. The Drs couldn't explain this problem so they, with her permission, performed an operation where they made a small opening through her cranium, exposed her to the chemical then watched as she brain did swell into the opening. The DRs were amazed but then were able to advise her to avoid chemicals that made her brain swell. I remember that because I occasionally had brain fog then but it was not a serious problem. I also realized that I was becoming more sensitive to chemicals I used in my work in medical laboratories. By my mid forties the brain fog and chemicals forced me to leave my  profession and move to a rural area with little pollution. I did not have migraines. I was told a little later that I had a more porous blood brain barrier than other people. Chemicals in the air would go up into my sinused and leak through the blood brain barrier into my brain. We have 2 arteries  in our neck that carry blood with the nutrients and oxygen into the brain. To remove the fluids and used blood from the brain there are only capillaries and no large veins to carry it away so all those fluids ooze out much more slowly than they came in and since the small capillaries can't take care of extra fluid it results in swelling in the face, especially around the eyes. My blood flow into my brain is different from most other people as I have an arterial ischema, adefectiveartery on one side.   I have to go forward about 20 or more years when I learned that I had glaucoma, an eye problem that causes blindness and more years until I learned I had celiac disease.  The eye Dr described my glaucoma as a very slow loss of vision that I wouldn't  notice until had noticeable loss of sight.  I could have my eye pressure checked regularly or it would be best to have the cataracts removed from both eyes. I kept putting off the surgery then just overnight lost most of the vision in my left eye. I thought at the I had been exposed to some chemical and found out a little later the person who livedbehind me was using some chemicals to build kayaks in a shed behind my house. I did not realize the signifance  of this until I started having appointments with a Dr. in a new building. New buildings give me brain fog, loss of balance and other problems I know about this time I experienced visual disturbances very similar to those experienced by people with migraines. I looked further online and read that people with glaucoma can suffer rapid loss of sight if they have silent migraines (no headache). The remedy for migraines is to identify and avoid the triggers. I already know most of my triggers - aromatic chemicals, some cleaning materials, gasoline and exhaust and mold toxins. I am very careful about using cleaning agents using mostly borax and baking powder. Anything that has any fragrance or smell I avoid. There is one brand of dishwashing detergent that I can use and several brands of  scouring powder. I hope you find some of this helpful and useful. I have not seen any evidence that Celiac Disease is involved with migraines or glaucoma. Please come back if you have questions or if what I wrote doesn't make senseto you. We sometimes haveto learn by experience and finding out why we have some problems. Take care.       The report did not mention migraines. 
    • Mari
      Hi Jmartes71 That is so much like my story! You probably know where Laytonville is and that's where I was living just before my 60th birthday when the new Dr. suggested I could have Celiacs. I didn't go on a gluten challange diet before having the Celiac panel blood test drawn. The results came back as equivical as one antibody level was very high but another, tissue transaminasewas normal. Itdid show I was  allergic to cows milk and I think hot peppers. I immediately went gluten free but did not go in for an endoscopy. I found an online lab online that would do the test to show if I had a main celiac gene (enterolab.com). The report came back that I had inherited a main celiac gene, DQ8, from one parent and a D!6 from the other parent. That combination is knows to sym[tons of celiac worse than just inheriting one main celiac gene. With my version of celiac disease I was mostly constipated but after going gluten-free I would have diarrhea the few times I was glutened either by cross contamination or eating some food containing gluten. I have stayed gluten-free for almost 20 years now and knew within a few days that it was right for me although my recovery has been slow.   When I go to see a  medical provide and tell them I have celiacs they don't believe me. The same when I tell them that I carry a main celiac gene, the DQ8. It is only when I tell them that I get diarrhea after eating gluten that they realize that I might have celiac disease. Then they will order th Vitamin B12 and D3 that I need to monitor as my B12 levels can go down very fast if I'm not taking enough of it. Medical providers haven't been much help in my recovery. They are not well trained in this problem. I really hope this helps ypu. Take care.      
    • knitty kitty
×
×
  • 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.