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

Celiac In The Military


gaingus

Recommended Posts

gaingus Rookie

I am wondering if there are any service members from the U.S. Military that haven't been discharged. I can find many stories of people that have gotten out because of it. I want to know of anyone that has successfully stayed in with it.


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



Celiac.com Sponsor (A8-M):



ravenwoodglass Mentor

There have been a couple that I remember seeing over the years that were able to stay in. You may want to do a board search with the words military and celiac to see if you can find the past posts. If memory served they were well established in their careers at diagnosis and did not have jobs that required them to be in the field living on MREs. A celiac diagnosis as far as I know would prevent you from joining in most cases.

*Daniella* Apprentice

Hi!

I am a diagnosed celiac in the Air Force. I was diagnosed about 7 months ago and went to a medical board to decide my fate. The Air Force decided to keep me in the military however, I am no longer able to deploy to war zones. That doesn't mean I can't deploy at all, it means I have to be more careful about the places they send me. I've been in the AF for 12 years and I know the next 8 will be difficult trying to get the military to understand my needs involving the entire celiac lifestyle. If you have any questions feel free to ask.

psawyer Proficient
Here is a link to a discussion about celiac and military service. It is old, but is probably still relevant.
gaingus Rookie

I can say that this is not easy. Thank you for the help so far. I have been in the Navy for almost fourteen years and I want to finish my 20 and retire. Unfortunately, the biggest issue I am running into, is I am not deployable at all. The Navy went away from actually cooking meals not too long ago. We now get a lot more heat and serve frozen meals. Unfortunately, gluten is used as a long term frozen food preservative. I've been in long enough that I can easily be an instructor, it is just trying to be placed on permanent shore duty. I will try to keep everyone informed through here (I know there are many of us). My gastro doc is going to help preserve my career, it is up to higher ups to make the ultimate decision.

*Daniella* Apprentice

I will keep you in my thoughts because I know exactly how you feel. I will have another medical board in a few months. This is going to be an annual occurance. I will be on pins and needles every year trying to keep my career in tact also. Please keep us informed with your status. Like I said before let me know if you want to chat. I'll give you my military celiac support. :)

gaingus Rookie
I will keep you in my thoughts because I know exactly how you feel. I will have another medical board in a few months. This is going to be an annual occurance. I will be on pins and needles every year trying to keep my career in tact also. Please keep us informed with your status. Like I said before let me know if you want to chat. I'll give you my military celiac support. :)

Good luck on your next board. I am still waiting to hear on when I will have an actual board. I am only on the first period of limited duty (less than 6 months) and about to go on my second (6 months to 1 year). I really don't like the hurry up and wait that we have to go through. I don't know how long I am going to stay in, I don't know if I am going to have to move soon or not. It sucks how unpredictable it is. I will keep you in my thoughts as well. I really appreciate the support. :D


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



Celiac.com Sponsor (A8-M):



  • 1 month later...
Jaime A Newbie
Hi!

I am a diagnosed celiac in the Air Force. I was diagnosed about 7 months ago and went to a medical board to decide my fate. The Air Force decided to keep me in the military however, I am no longer able to deploy to war zones. That doesn't mean I can't deploy at all, it means I have to be more careful about the places they send me. I've been in the AF for 12 years and I know the next 8 will be difficult trying to get the military to understand my needs involving the entire celiac lifestyle. If you have any questions feel free to ask.

Hi Daniella,

I'm going through a similar situation and I'd like to contact you but i'd like to do it through personal email. I've been trying to send you a personal message but it won't allow it to go through. Is there any way that you can contact me? Can you try to send me a message?

  • 5 months later...
gaingus Rookie

Wow, it's been a while since I have updated on this one. For those that have been wondering, I have been cleared "fit for duty". This will get me to the point where I can be medically retired. Good thing is that I am on shore duty and I can control what I eat fairly easily. Sea duty will be an interesting challenge and I will figure it out from there.

  • 1 year later...
jsltrumpet Newbie

I am nervously awaiting my fate as my Med Board in the AF is being evaluated as we speak. I really have NO idea what the final decision will be. How long did it take you guys to find out? This is really hard.

silk Contributor

My husband was in the military when we were married 33 years ago tomorrow. Having only been diagnosed with this 4 years ago, I did not consider how difficult this issue would be for 'our kind :blink:" as he left the service more than 20 years ago. My heart goes out to all of you. I have dined on the lovely MRE's. They are the most delicious, imaginative use of cardboard I have ever tasted! However, I am quite sure that that cardboard was not grown in dedicated, gluten free fields! :lol: It is amazing to me how we can not force someone out of the military for their religious convictions or sexual orientation (I am fine with that and not starting a political discussion here) but that your career could hang in the balance because of a digestive issue. Wow! We can develop night vision glasses but we can't figure out how to feed one in every 133 people who serve our country but can't ingest toxic cardboard? Life is a mystery! God Bless America!

*Daniella* Apprentice

I am nervously awaiting my fate as my Med Board in the AF is being evaluated as we speak. I really have NO idea what the final decision will be. How long did it take you guys to find out? This is really hard.

It only took a few months for my medical board results to come back (I was in the middle of a PCS so it was quicker than normal). If it's taking long time maybe you can contact your medical admin and see what the status is. I know the initial board goes to HQ to determine your fate. In addition to the initial board you will go through an annual board called a RILO to insure your health status hasn't changed. That approval only takes about a month.

  • 6 years later...
Christian alexander Newbie

For the people that been  diagnosed with celiac diseased and med board, when you got out of the army did you get and disability I've been in the army for 6 years and this has been my family's income for the 6 years, so what assistants have you guys been given???

Archived

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

  • Get Celiac.com Updates:
    Support Celiac.com:
    Donate

  • Celiac.com Sponsor (A17):
    Celiac.com Sponsor (A17):





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - Scott Adams replied to Jhona's topic in Introduce Yourself / Share Stuff
      35

      Does anyone here also have Afib

    2. - Jacki Espo replied to CDFAMILY's topic in Related Issues & Disorders
      5

      Covid caused reoccurrence of DH without eating gluten

    3. - Mari replied to tiffanygosci's topic in Coping with Celiac Disease
      1

      New Celiac Mama in My 30s

    4. - Mari replied to Jmartes71's topic in Coping with Celiac Disease
      2

      My only proof


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,956
    • Most Online (within 30 mins)
      7,748

    Crismedin
    Newest Member
    Crismedin
    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.