Jump to content
This site uses cookies. Continued use is acceptance of our Terms of Use and Privacy Policy. More Info... ×
  • 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

Please Help! Concerned About Potential Of Celiac.


BKnight561

Recommended Posts

BKnight561 Rookie

Hi Everyone....I'm really hoping I can get some help here, and hoping I don't come across like a hypo-chondriac.

The past few years have been medically very difficult. I'm a woman, in my thirties, in the military and a mother of two. Three years ago, I went to the ER for a horrific migraine. In true military fashion they strapped me down and gave me a spinal tap (came out clear) and only then did they run a blood test. I was yelled at for being "malnurished." I didn't understand...I eat all the time and take vitamins.

Fast foward a few years, on and off sick, exhausted (I figured I was working too much), headaches, anemic, hair loss, dermatitis, constant reflux. The reflux was so bad, the acid was eating away my vocal cords. I live on Zantac and Nexium now. I was mute for three months. After six months of wrong diagnoses, I was sent to a civilian specialist in Philly. A surgeon. Brilliant man who I consider responsible for keeping me speaking after three reconstructive surgeries. He SWORE I had signs of hypothyroidism. Three tests - all negative. He was baffled. Then, my molar broke. I've had one cavity my entire life....and now my teeth are breaking.

Then, last night, I saw a news program talking about this strange thing called Celiac Disease - for which hypothryroidism symptoms are often confused. They started listing the symptoms. I pulled out my med record (yes - all 6" of it from just the past few years - I have it all here) and started looking at my recent blood panels and tests.

I'm anemic, Vit K, Vit D and Alkaline Phosphate deficient. Not just a little - MARKEDLY. Like, minimum of 10-15 points below the low baseline numbers on all of them. Low cholesteral and very low triglicerides (with **** next to them).

My teeth are literally breaking, losing my hair, dermatitis, and severe reflux has damaged my esophagus and permanently damaged my vocal cords (three surgeries to keep me speaking over the past year). Blurred vision, constantly sick, fatigued, and diarrhea and/or painful constipation with a ton of gas. Oh, and I didn't hit puberty until I was 16. I'm petite - literally 4" shorter than my shortest female family members. Both brothers are over 6' tall. My father died of Diabetes complications. My children have eczema (from me?).

Causal? Maybe not...I guess my question is this: Am I rightly concerned?? Or am I losing my mind? Please help!!


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



Celiac.com Sponsor (A8-M):



rosetapper23 Explorer

I think you've found the answer you've been seeking! Your medical records read just like ours. Now, if you get tested, ask for a FULL CELIAC PANEL. They may not even know what that is, so they will have to find out. If, however, the blood tests come out negative, fear not. Simply go on a very strict gluten-free diet to find out whether or not you're able to resolve your physical issues that way. You see, celiac can cause your symptoms, but so can gluten sensitivity (which cannot be tested for). I strongly suspect that once you remove gluten from your diet, you'll begin to see improvements in your health. It may take a while for certain issues to resolve, such as the breaking teeth and nutritional deficiencies because it takes a while for the lining of the small intestine to heal. However, your digestive complaints may start resolving sooner. For many of us, while some symptoms diminished quite a bit, it took 18-24 months to fully feel well again.

I'm sorry that your health had to suffer so severely before you discovered what is wrong. Shame on your doctors for not suspecting something as common as celiac disease. Unfortunately, when they were in medical school, they were taught that celiac is very rare and is usually outgrown. This information is patently false, and the AMA has been trying to correct that misinformation during the past five years. Your doctors probably didn't get that memo. They need to be educated so that they understand that they should ALWAYS test for celiac when nutritional deficiencies or digestive complaints don't resolve. However, again, if you test negative for celiac, please consider following a gluten-free diet.

Lastly, and this is important: You are not allowed to serve in the military with celiac disease. If you wish to continue serving our country, you may wish to simply follow a gluten-free diet and let things lie. Your skin condition might be Dermatitis Herpetiformis (DH), which will resolve once you stop eating gluten (and iodine for a while, too). I know a man who remained in the military for years even though he suffered terribly from DH. He told me that his doctor understood that he had to have celiac in order to have DH, but he didn't include that in his diagnosis so that my friend could remain in the Air Force. My friend was treated with Dapsone for the DH and put up with the other symptoms until he retired from the Air Force. If you end up in a situation where only military food is available, you can always say that you have a gluten allergy or that you're gluten sensitive--just don't say that you think you have celiac.

Take care....and I feel very strongly that you're about to regain your health.

shadowicewolf Proficient

who says you aren't allowed to serve? I'm sure she could work on base and whatnot, as long as she isn't sent into deployment. Lying about it won't help much either because its to my understanding that military personnel go through medical examinations every so often.

At any rate, get the full celiac panel done as well as the genetic test. Celiac is a genetic disease and it could potentially affect your children as well.

rosetapper23 Explorer

Shadowicewolf,

Please don't shoot the messenger--I'm just trying to make the poster aware of a possible battle she may face. Who says she can't be in the military with celiac? The military! Anyone with celiac is NOT allowed to enter the military (and being the mother of a 25-year-old son, I'm comforted that he cannot be drafted if the draft is reinstated). It could be that she will be met with understanding, but she needs to be made aware of the legal fight she may have on her hands. In the future, once the military understands how many people actually have celiac, it may change its rules on celiac, since it is merely a problem of feeding us that stands in the way of our serving our country. All they would have to do is ensure that the military food be made available gluten free. I believe that Israel ended up doing this (or is considering doing so) so that young people with celiac could still serve.

BKnight561 Rookie

I really appreciate your advice. Since celiac disease is considered an auto-immune disease, it will trigger what we call a MEB (Medical Eval Board) and most likely lead to discharge. :-( I'm ok with that....I'd rather be healthy. There are no rumors of that changing any time soon, especially with all the cuts they're making. I'm already on shore-duty, so that doesn't make a difference either.

I go in on Thursday, and I'm going to request that full panel. You mentioned eating iodine...funny. The dermatologist told me to avoid SHRIMP. Said it's probably flaring up the dermatitis..?? I told her I eat it because I'm anemic. She wants me placed on iron--shots. I need this panel done before they start treating more symptoms inappropriately. Thank you again.

My next question is this, then...let's say I DO come back positive for celiac via blood screen, what's the next step in the process, and how do you recommend I prepare?

rosetapper23 Explorer

Regarding the iodine, many of us with DH need to eliminate it for a while because it seems to exacerbate the condition. Because iodine has been found to exacerbate a number of dermatological conditions, it's common for dermatologists to recommend avoiding it. As for your iron anemic, using iron shots is the old-fashioned way to deal with it. Nowadays, doctors prescribe intravenous iron infusions. Your doctors are probably unaware of this option, so you might have to educate them about it. You'll only need to get the infusions once a week for four weeks. After that, if your numbers fall again, you'll need to through the four-week infusion cycle again. If you have celiac and a gluten-free diet helps you recover from anemia, you can then discontinue the infusions.

Regardless of how your blood tests turn out, you should try to follow a gluten-free diet afterward. There's a great thread here on the Forum entitled either Celiac 101 or Gluten-free 101 (sorry--I can't recall). Someone will jump in shortly, I'm sure, to help you find the correct thread. Generally, though, when you begin a gluten-free diet, it's best to stick with natural foods (meats, dairy, vegetables, fruits, nuts, rice, etc.). This way, your chance of cross-contamination goes way down. Also, if you attempt to eat the gluten-free versions of your favorite foods right away, you may react to the special grains and/or gums that are used and may think that the gluten-free diet isn't helping you. After a few months of eating just natural foods, you can begin to explore gluten-free alternatives....and there are some very good ones out there. Just read some of the postings on this Forum--you'll get lots of great advice!

Also, you should begin addressing your other nutritional deficiencies as soon as possible. For your Vitamin D deficiency, you'll need to take Country Life Natural Vitamin D. The reason for this is that you also need to take Vitamin A at the same time (your cells have two A receptors for every D receptor), and it also contains medium-chain triglycerides to help you absorb both Vitamins D and A. I actually was taking 50,000 iu's of Vitamin D daily for a year--and I couldn't overcome my Vitamin D deficiency. However, when I attended a celiac conference last June in Seattle, one of the presenters discussed how taking Country Life Natural Vitamin D can help celiacs overcome their Vitamin D deficiency--and after only a few months, my Vitamin D level was extremely healthy (and I only take 400 iu's a day!).

You're heading in the right direction....now go and get healthy!

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,188
    • Most Online (within 30 mins)
      7,748

    Leeila
    Newest Member
    Leeila
    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

    • Ginger38
      So I recently had allergy testing for IGE antibodies in response to foods. My test results came back positive to corn, white potatoes, egg whites. Tomatoes, almonds and peanuts to name a few.  I have had obvious reactions to a few of these - particularly tomatoes and corn- both GI issues. I don’t really understand all this allergy versus celiac stuff. If the food allergies are mild do I have to avoid these foods entirely? I don’t know what I will eat if I can’t  have corn based gluten free products 
    • Kris2093u4
      Geography makes a difference.  I'm in the West and Trader Joe's gluten-free bread tastes great and is a better price than most gluten-free breads sold elsewhere in my area.  
    • JForman
      We have four children (7-14 yo), and our 7 year old was diagnosed with NCGS (though all Celiac labs were positive, her scope at 4 years old was negative so docs in the US won't call it celiac). We have started her on a Gluten Free diet after 3 years of major digestive issues and ruling out just about everything under the sun. Our home and kitchen and myself are all gluten-free. But I have not asked my husband/her dad or her other siblings to go completely gluten-free with us. They are at home, but not out of the home. This has led to situations when we are eating out where she has to consistently see others eating things she can't have and she has begun to say "Well, I can't have <fill in the blank>...stupid gluten."  How have you supported your gluten-free kiddos in the mental health space of this journey, especially young ones like her. I know it's hard for me as an adult sometimes to miss out, so I can't imagine being 7 and dealing with it! Any tips or ideas to help with this? 
    • Jane878
      By the time I was 5 I had my first auto0immune disorder, Migraine headaches, with auras to blind me, and vomiting, sensitivity to light and sound. I was 5 years old, and my stepfather would have pizza night, milling his own flour, making thick cheesy gluten pizza, that I would eat and the next day, I would have serious migraines, and my mother & stepfather did nothing about my medical problems. When I was 17 in my first year at college, I was diagnosed with my 2nd known auto-immune disorder, Meniere's disease. I was a elite athlete, a swimmer, and soccer player. And once again my parents didn't think anything of understanding why I had a disorder only older people get. Now after my mother passed from Alzheimer's disease she also suffered with living with gluten. She had a rash for 30 years that nobody could diagnose. She was itchy for 45 years total. My brother had a encapsulated virus explodes in his spleen and when this happened his entire intestines were covered with adhesions, scar tissue and he almost lost his life. He has 5 daughters, and when I finally was diagnosed after being pregnant and my body went into a cytokine storm, I lost my chance to have children, I ended up having Hashimoto's disease, Degenerative Disc disease, and my body started to shut down during my first trimester. I am 6ft tall and got down to 119lbs. My husband and I went to a special immunologist in Terrace, California. They took 17 vials of blood as we flew there for a day and returned home that evening. In 3 weeks, we had the answer, I have Celiac disease. Once this was known, only my father and husband made efforts to change their way of feeding me. At the family cabin, my stepfather & mother were more worried that I would ruin Thanksgiving Dinner. It wasn't until one of my cousins was diagnosed with Celiac disease. They finally looked into getting Gluten Free flour and taking measures to limit "gluten" in meals. He did nothing but ask for me to pay for my own food and wi-fi when I came to the cabin to stay after our house burned down. When he informed my mother, they proceeding to get into a physical fight and she ended up with a black eye. The is just more trauma for me. Sam had no interest in telling the truth about what he wanted. He lied to my mother that he had asked my husband if I could pay for "food" when he asked Geoffrey if I had money to pay for my wi-fi. My mother hates when he spends so much time on the computer so he lied and said I could pay for my own food. I will remind you I weighed 119lbs at this time. (At 6ft) that is a very sick looking person. Neither parent was worried about my weight, they just fought about how cheap my stepfather was. As my mother was diagnosed with Alzheimer's disease in 2014. He had her sign over the will to a trust and added his children. He had no testimonial capacity at the time, so she signed without proper papers. Making this Trust null and void. When I gave my brother my childhood home, my mother stated I would be getting an equal part of inheritance to the house on Race. It currently worth 2.0 million $. I got nothing, and my stepfather has since disowned me b/c of my claim and he knows that my mother would never have left it uneven between my biological brother and myself. She sat me and my husband down, as we lived at the Race Street house and treated and took care of it as our own. My brother took over b/c he was going through a horrific divorce and needed a home so he could get a better custody deal with his soon to be ex-wife who was a Assist DA for Denver. She used the girls against him, and he & I were the primary caregivers. We, Judd and I spent the most time with them pre the divorce. Once Judd moved into the house, he threw all of my mother, grandmother and my family heirlooms out to the Goodwill. Nobody told my mother about this as she was going through cancer treatment and had Alzheimer's disease in her mother and her sister. My stepfather and biological brother took advantage of this matter, as I called a "family council" that my brother just never could make it to at the last moment. All of the furnishing, kitchen ware, everything was in the house my brother just moved into. He had had 2 weddings, I chose to elope b/c my stepfather ruined my brother's first wedding by talking about his relationship with my brother in front of my dad and his entire family, insulting him and having my grandfather leave the ceremony. It was a disaster. My stepfather just plays dumb and blames my father for the slight. I was the only child not to have a wedding. So, my mother and stepfather never had to pay for a thing. My mother had had an agreement with my father he'd pay for college and all medical issues with their kids, myself and Judd. So truly my mother never had to pay for anything big for me in her entire life. I am looking for anyone that has had a similar story, where they grew up in a household that had a baker that regularly milled flour and ate gluten. What happened to you? DId you suffer from different auto-immune diseases b/c of living with a baker using "gluten" Please let me know. I have been looking into legal ways to get my stepfather to give me what my mother had promised, and he erased. Thank you for listening to my story. Jane Donnelly  
    • trents
      Possibly gluten withdrawal. Lot's of info on the internet about it. Somewhat controversial but apparently gluten plugs into the same neuro sensors as opiates do and some people get a similar type withdrawal as they do when quitting opiates. Another issue is that gluten-free facsimile flours are not fortified with vitamins and minerals as is wheat flour (in the U.S. at least) so when the switch is made to gluten-free facsimile foods, especially if a lot of processed gluten-free foods are being used as substitutes, vitamin and mineral deficiencies can result. There is also the possibility that she has picked up a virus or some but that is totally unrelated to going gluten-free.
×
×
  • Create New...