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

Very Sick Teenager


michelle4boys

Recommended Posts

michelle4boys Newbie

I really need some help :unsure: I have a 15 year old that has been very sick for 3 months now. I wont even go into the FULL story because it would be just WAY too much reading. Basically.... he has been diagnosed with TONS of different allergies. In the course of 3 months he has been prescribed 13 (i think) different medications. The latest med is Zantac. Zantac was prescribed for the vomitting and pains he has been having on and off. He can vomit several times a week. He complains of stomach pains - sharp and dull, stomach cramping - sometimes severe. (He has not lost any weight)

We found out he had a wheat allergy thru the allergist. He was also just tested for molds. One that he is allergic to is Candida. No one ever told us to do anything about the Candida. We started him on a wheat free diet (not gluten free) a few weeks ago. I have not noticed any significant change in the way he feels. He still complains and still vomits a couple times a week. I discussed at our last visit the possiblity of Celiac. The doctor dismissed this - saying "Most Celiac's have diareaha". Is this true? Instead of walking out of the office with any answer - we walked out with yet another prescription and a "well maybe he is developing ulcers". @@

I dont even know what to do at this point in time other than to change to a more aggressive doctor. I guess my question would be... does it sound AT ALL like Celiac? I'm just at a loss. I'm at the end of my rope with watching my child get sick and dont know what to do. ANY information or advice would be GREATLY appreciated!!


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



Celiac.com Sponsor (A8-M):



chrissy Collaborator

no---not all celiacs have diahreah (SP?) can you ask the doctor to just humor you and run the test? one of my twins was nauseated for 3 months and now that ashe is gluten free, her nauses has improved.

christine

michelle4boys Newbie

what tests would I ask for?

key Contributor

I am sorry your son is so sick. He definitely should be tested for celiac. They don't have to have diarhea. ARe you seeing a pediatric Gastroenterologist? If you are, then you need to find another one and if you aren't you need to find one.

I hope you find the answer soon.

Does he having any gas or bloating with this?

Hope you get some answers. Obviously though it is time to find a new doctor.

Monica

michelle4boys Newbie

No he is only seeing our family practice doctor. She only wants him to see an allergist. I think its time to move on....

jerseyangel Proficient

I would also suggest you have him tested for Celiac. I am 49, but had nausea as my main symptom from the time I was in my 20's. Because nausea and dizziness were my main symptoms, I was misdiagnosed for many years. The D did not begin to be a problem until about 10 years ago--and did not get severe until 2 years ago. You need to ask for the complete Celiac blood panel. Moving on from the allergist is a good idea for this. A gastroenterologist with Celiac experience would be the best person to talk to.

michelle4boys Newbie

Well - I took your advice. I was under the impression I needed a referal to see any specialist. This is new insurance we have. I called my insurance company and NO referal needed!!! I will call in for a gastro.... specialist tomorrow! Thank you very much! I know it sounds like such a 'minor' thing but I already feel this is a huge step forward in finding out what is wrong. And here I was trying to get a referal that was refused by the family practitioner @@ So, believe it or not - you've all helped me so much already! Any step forward is a good step! Thank You!


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



Celiac.com Sponsor (A8-M):



celiac3270 Collaborator

Diarrhea is not necessary for a celiac diagnosis by any means--there are over 212 symptoms and diarrhea is not even the most common of them! Definitely get him tested.

jerseyangel Proficient

Michelle--It's not minor at all! So happy you got the go-ahead from the ins. co. Good luck--and let us know how he does :)

Merika Contributor

Diahrea is not always there. It could swing all the way to constipation. Or bowel movements could be perfectly fine. Mine were always fine and it took me 12 YEARS and an accidental diagnosis to find out about celiac. I wish you and your son luck in feeling better.

Merika :)

marciab Enthusiast

My daughter just turned 18 and has severe environmental and food allergies. I worry about her too. Her body, esp her face, swells on a regular basis. She takes Zyrtec daily and uses a rescue inhaler as needed. We are going to her doctors for asthma meds today. They prescribed Zantac too, but her stomach issues come and go, so she refuses to take it every day. Did they tell you that Zantac has an antihistamine in it ?

I completely agree with the rest about having him tested for celiac. But meanwhile, your son should start paying more attention to which foods he is eating and what the results are. Be sure he keeps a journal. The elimination diet would be the fasted way to see if he has food allergies, but he has to be eating wheat, rye, barley and oats for the celiac tests to be accurate. My daughter has concluded that she is allergic to bananas, coconut and pineapple. Bananas make her mouth tingle. She loves Reeses and is in denial about peanuts.

I'm planning on having my daughter tested for celiac the next time they draw blood on her. I heard about that woman who's body swelled up from celiac. My daughter sees what I eat and really wants no part of it. This should be fun !!!!!!!!!!!!!

Good luck and Hang in there ... It's tough being a Mom... Marcia

Ashley Enthusiast

I would absolutely recommend having him tested for Celiac. I had no Diarrhea whatsoever. The symptoms are different with each individual. With some cases, some lose significant amounts weight (which happened to myself...eighty pounds :wacko: ) and others have none. Hope your Son makes way to feeling much better!

Rachel--24 Collaborator

Hi,

I never had diarreah either. Don't let the doctor tell you that w/out diarreah you cant have celiac...its not true. My doctor said the same thing...they are just misinformed.

pixiegirl Enthusiast

I have tons of food allergies as well and similar symptoms, pain, gas, all sorts of GI symptoms. You might want to talk to the GI doctor about having your son take Gastrocrom... its a mast cell inhibitor... (which are allergy related) its got virtually no side effects, you mix a few drops with a glass of water before you eat and it mitigates the allergic response to food. As far as drugs go, its very low on the scale of being bad for you. It is the only thing that has worked for me with my food allergies, I'm feeling almost totally normal right now. The only bad thing about it is: it has to be take before every meal and bedtime and it takes about 2 weeks to really work.

However even if he takes it for the short term it would give his system some time to heal up. I really suggest you ask your doctor about it and do some Google research, its help me tons and I believe there are others on this list that have taken it and I am on a few other lists for GI disorders and it seems its helped tons of people. Again very low on side effects (I've had none at all, other then feeling great).

Just an idea!

Susan

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,856
    • Most Online (within 30 mins)
      7,748

    Sonya Haskin
    Newest Member
    Sonya Haskin
    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

    • Jillian83
      He is. Which makes everything even more difficult. I’m not a believer in “staying for the kids” but I have nowhere to go and it’s not just me, it’s me plus my babies. We live in a beautiful place, lots of land in the country and me and the kids love the place we’ve called home for their entire lives. But Im seeing that he’ll never change, that my kids deserve a happy healthy Momma, and that staying in this as is will be the early death of me. Then I look at the scars covering my entire body…this disease and the chronic stress I’ve been enduring for years that tell me I’m no longer beautiful and no one will ever look at me with interest again. I try self care, try to give myself grace so I can just start loving myself enough to gain strength but the slightest sparkle in my eye and skip in my step attracts his wrath and it all comes crashing ten fold. Life is just absolutely railing me from every single direction leaving me wanting to wave that white flag bc I don’t feel like there’s much hope no matter what happens. 
    • 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 .
×
×
  • 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.