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

4yr Old Boy, Autism, Nosebleeds, Soy, Wheat Allergies.


mikepattonsgirl

Recommended Posts

mikepattonsgirl Newbie

Ohhh please help me!!!!

I am starting to freak out/lose hope!

Firstly, I'm really not like crying or anything like that, just a drama queen I guess :)

My lil one...I don't know what to do at this point! He's been wheat free for about 2 years, not 100%, but he hasn't had wheat in about a year. Then a year ago we realized he was allergic to Soy. He's had almost daily bloody noses since a year old, which the dr brushed off as nothing, now I've determined it means he's eaten something he's allergic too. I watch him like a hawk. All he is eating right now is banana's, and lays potato chips, he's autistic so getting him to eat fruits is like fate worse then death....

Today we got some rice krispies which I read he can eat, and has in the past, and gave him his rice milk with it.

Okay, now, here's the tricky part. Ohhhh I really hope you all have some input!!! So, we got Red Robin for take out, we don't go out to eat because it's just not fair to Caleb, and we don't let him have mcdonalds fries of course, but I didn't think it would hurt him to give him french fries from red robin, and literally within 10 minutes his nose started bleeding ssoooo bad. I don't know if it's from fries, rice krispies or what. I mean, it bled a few days ago, that day I didn't feed him anything different, I don't know if he's eating stuff when i'm not looking, but he's really good about that. It's sad, he'll pick up an oreo at someone else's house and sit and smell it, like he knows he can't eat it. Poor lil guy :(

Anyway, oh yeah!

During the day he's totally fine, then at night he's SOOOO congested, just sounds like a ton of phlegm, and he coughs and coughs, and last night he was coughing then he gagged and vomited and couldn't breathe, and I turned him over and was doing everything I could. I just don't get it...I don't know if these are all coincedences, or if he's eaten something, or if there's something worse...We did just change climates, moved from Utah to washington, which we did last year, we spend time down there and here.

I don't think I left anything out, of course I will take him to an allergenist tomorrow, or asap, but does anyone else have anything like this?

Thanks in advance..

Kelly :)


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



Celiac.com Sponsor (A8-M):



Fiddle-Faddle Community Regular

Oh, you've got it tough!

I'm not familiar with Red Robin, but I'm somewhat familiar with autism (one of my kids has Asperger's), and I'm learning about celiac/wheat allergy/gluten intolerance. Stay with this board--the people here probably know more than any of the doctors, I'm not kidding.

Okay. If it's gluten your little guy has a problem with, then Rice Krispies are a definite no-no--they contain barley malt, which tastes great, but contains gluten. Many autistic kids have problems with gluten and casein. Look up Lisa Lewis (Special Diets for Special Kids--fantastic book) if you haven't already, or check this site out: Open Original Shared Link. I would not trust amy husband to leave "forbidden" food alone, let alone a 4-year-old. If he can't eat it, don't bring it in the house, at least for now!

You also need to be very, very careful how many vaccines you give your little guy, and which ones. For example, the flu shot contains thimerosal, which is 50% ethyl mercury, which is definitely linked with autism no matter what the pharmaceutical giants say. The MMR may also be involved. It IS possible to obtain a measles-only vaccine, wait a year, obtain a mumps-only vaccine, wait a year, and obtain a rubella-only vaccine. While my child didn't react to the MMR that I could tell, I have talked to way too many moms whose kids DID react terribly--and then developed full-blown autism. (My sister-in-law's sister-in-law actually has video from the day before and the day after, and it looks like two totally different children.)

If he's having trouble breathing just at night, could whatever you wash the sheets in be an allergy source? Fabric softener, maybe? Or could he be allergic to down pillows? (Or conversely, polyester pillows?) If you just moved, could paint fumes, new flooring or carpeting, or vinyl shades be emitting something he's allergic to? Or were there animals in the house before?

Any possiblity he picks his nose, and that might be causeing the nosebleeds, or at least exacerbates the situation?

Do you mind if I ask how severely autistic your little guy is? Is Washington good with early intervention services?

Good luck--let us know how things are going, okay?

Girl Ninja Newbie

I don't have any experience with autism, but I am a pro at feeding picky kids. He should be able to have Fruity Pebbles or Cocoa Pebbles from Post. I know they're gluten free, but you'll have to check for soy.

If it was the fries it would be hard to pinpoint the problem. Their fryer could have been contaminated with anything.

Good luck to you guys.

mommida Enthusiast

I just wanted to add to the other posts. My son used to vomit phlegm before he went on a gluten free diet. I have heard others say gluten ingestion has caused them to have severe congestion, wheezing and asthma.

It sounds like you are looking for a gluten free, casein free, and soy free diet. (You can find links to this diet and autism here at celiac.com, I think it is under other or misc connections.)

L.

Tony'sMom Rookie

Hello Kelly.

I'm sorry to hear that your son isn't feeling so well. I have son with autism and years ago I tried the gluten-free/CF diet. I didn't do a good job at it and gave up after seeing no benefit. I'm now going to try again since I have another son who has celiac. Give Gluten-free Casein-free.com a look- they should have some good resources about the diet there. I second the Special Diets for Special Kids book- it's great.

As for the congestion- my son with celiac gets horribly congested when he gets glutened. He also has a million other allergies that make it bad. Has your son been evalutated for Asthma? That was the only clue that we had that Tony had asthma- a night time cough that never went away.

I hope you can get this all figured out soon and that your son feels better.

Good luck!

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. - asaT replied to Scott Adams's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      48

      Supplements for those Diagnosed with Celiac Disease

    2. - asaT replied to Scott Adams's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      48

      Supplements for those Diagnosed with Celiac Disease

    3. - nanny marley replied to hjayne19's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      20

      Insomnia help

    4. - David Blake commented on Scott Adams's article in Product Labeling Regulations
      1

      FDA Moves to Improve Gluten Labeling—What It Means for People With Celiac Disease

    5. - nanny marley replied to wellthatsfun's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      4

      nothing has changed

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

    • Total Members
      133,343
    • Most Online (within 30 mins)
      7,748

    emoryprose
    Newest Member
    emoryprose
    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

    • asaT
      plant sources of calcium, such as spinach, have calcium bound to oxalates, which is not good. best source of calcium is unfortunately dairy, do you tolerate dairy? fermented dairy like kefir is good and or a little hard cheese. i do eat dairy, i can only take so much dietary restriction and gluten is hard enough! but i guess some people do have bad reactions to it, so different for everyone.  
    • asaT
      i take b12, folate, b2, b6, glycine, Nac, zinc, vk2 mk4, magnesium, coq10, pqq, tmg, creatine, omega 3, molybdnem (sp) and just started vit d. quite a list i know.  I have high homocysteine (last checked it was 19, but is always high and i finally decided to do something about it) and very low vitamin d, 10. have been opposed to this supp in the past, but going to try it at 5k units a day. having a pth test on friday, which is suspect will be high. my homocysteine has come down to around 9 with 3 weeks of these supplements and expect it to go down further. i also started on estrogen/progesterone. I have osteoporosis too, so that is why the hormones.  anyway, i think all celiacs should have homocysteine checked and treated if needed (easy enough with b vit, tmg). homocysteine very bad thing to be high for a whole host of reasons. all the bad ones, heart attack , stroke, alzi, cancer..... one of the most annoying things about celiacs (and there are so many!) is the weight gain. i guess i stayed thin all those years being undiagnosed because i was under absorbing everything including calories. going gluten-free and the weight gain has been terrible, 30#, but i'm sure a lot more went into that (hip replacement - and years of hip pain leading to inactivity when i was previously very active, probably all related to celiacs, menopause) yada yada. i seemed to lose appetite control, like there was low glp, or leptin or whatever all those hormones are that tell you that you are full and to stop eating. my appetite is immense and i'm never full. i guess decades or more ( i think i have had celiacs since at least my teens - was hospitalized for abdominal pain and diarrhea for which spastic colon was eventually diagnosed and had many episodes of diarrhea/abdominal pain through my 20's. but that symptom seemed to go away and i related it to dairy much more so than gluten. Also my growth was stunted, i'm the only shorty in my family. anyway, decades of malabsorption and maldigestion led to constant hunger, at least thats my theory. then when i started absorbing normally, wham!! FAT!!!    
    • nanny marley
      Great advise there I agree with the aniexty part, and the aura migraine has I suffer both, I've also read some great books that have helped I'm going too look the one you mentioned up too thankyou for that, I find a camomile tea just a small one and a gentle wind down before bed has helped me too, I suffer from restless leg syndrome and nerve pain hence I don't always sleep well at the best of times , racing mind catches up I have decorated my whole house in one night in my mind before 🤣 diet changes mindset really help , although I have to say it never just disappears, I find once I came to terms with who I am I managed a lot better  , a misconception is for many to change , that means to heal but that's not always the case , understanding and finding your coping mechanisms are vital tools , it's more productive to find that because there is no failure then no pressure to become something else , it's ok to be sad it's ok to not sleep , it's ok to worry , just try to see it has a journey not a task 🤗
    • nanny marley
      I agree there I've tryed this myself to prove I can't eat gluten or lactose and it sets me back for about a month till I have to go back to being very strict to settle again 
    • trents
      You may also need to supplement with B12 as this vitamin is also involved in iron assimilation and is often deficient in long-term undiagnosed celiac disease.
×
×
  • 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.