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

Working


Lissa

Recommended Posts

Lissa Apprentice

Hi all,

Since I'm new to the gluten free world (only went gluten free June 6th), alot of my mistakes are found through trial and error and I find myself frequently ill from accidently glutenings. I can control myself with Pepto Bismol, Maalox, and Gravol, but I find it hard to leave the house. However, I have now saddled myself with a new responsibilty. A part time job at my favourite store, Chapters (the Canadian version of Barnes and Noble) and I'm incredibly worried about how my gluten problems and working will work. So my question is,

How do you all deal with it?

Thanks, Lissa


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



Celiac.com Sponsor (A8-M):



melmak5 Contributor

Lissa,

I am confused. Are you asking about working with gluten (as in, you are working within a cafe and will be touching items with gluten) or are you asking how do people deal with possibly needing frequent bathroom breaks?

For the first, I am not sure. I was so sick I had to leave my 2nd job in a bakery and have not been able to go back. (And probably won't with the whole flour-in-the-air problem)

If it is just prepared foods, I would say gloves should work. Gloves and not touching your face, but it is a risk and only you can determine what is best for your body.

For the second...

I was really honest with my boss about what was going on. She knew that I would often have to less than graciously exit a room with haste to make it down the hall to the restroom and it wasn't an issue.

You can ask for a note from your doctor if you feel like its going to be an issue.

Congrats on feeling better and your new job!

StrongerToday Enthusiast

I think it depends on what your responsibilities are. If you're cashiering, it may be hard to suddenly disappear to run to the bathroom. If you're working in another area, then odds are good you can just slip away. I don't make a big deal, sometimes I say "be right back" and just walk out. I've also been known to wear a pager and say "oh, that's my daughter beeping me - be right back" :rolleyes:

I think once you settle into your new routine, both food and work wise, things will settle down for you. Keep checking those labels!!

Guest j_mommy

My work has been great. If I'm sick I can take off, the same when my son is sick. But generally I can get to a toilet fast if I need to. Depends on the day.

You work through it and do what you have too!!!

GFhopeful Rookie

I have been gluten-free for around the same amount of time as you and still have good days and bad days. I had the summer off to recouperate but am really worried about going back to work in a couple of weeks as there is no way I can work how I feel sometimes still. I was so sick and am much better but have bouts and can't imagine being at work when they happen. I don't know what I'm going to do but am interested in the responses you get here. Celiac is so different for everyone but I just don't have the stamina or enough good days to feel like I'm going to be able to work full-time. I guess we have to just listen to our bodies at this stage of the game and not push it too much yet.

loco-ladi Contributor

I guess I am lucky, sort of, when I get on my train I wipe EVERYTHING down with bleach wipes, you have NO idea how some of the other engineers slobber their food!

I also carry my own cooler with all my food either in it or in my "carry on bag" I let my conductor have the little worthless fridge all to themself!

When I get to "the other end of the road" I always wipe down the table and even have begun to carry my own napkins (found the napkin roll sitting on the toaster more than once) I also make sure I heat my meal inside a baggie or completely cover it so I dont get cc in the microwave....

At one spot they gave me my very own cupboard (aint they sweet!) to store my pots, pans dishes and some basic supplies in.

Eriella Explorer

What I do is that I am very honest with my co-workers and bosses. Say that your gut is healing and you are learning where the evil food companies are hiding the gluten in your food. Then be honest, say that if, and when, you mess up, you need to go NOW. Explain celiac to them and that your body freaks out and tries to get rid of the poison as fast as it can.

Everyone has been great once I explained it. I got a whole batch of new co-workers this week and I was starting to explain what celiac was they all stopped me and said "Oh, I know about that. My brother/cousin/best friend has it."

As far as office food goes, either bring your own or offer to go shopping and get naturally gluten-free food for everyone.


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



Celiac.com Sponsor (A8-M):



Lissa Apprentice

This is my first, ever, real job. And these people are super picky about who they hire. And I'm scared that if I tell them about my issues, they're not going to want to rehire me in the spring (I'm a seasonal employee) because it'll qualify me as high maitence. Especially since I'll be working cash and things, and I won't always have someone else there. I guess I'll have to tell them, eventually. But soo many people are incredibly judgemental of the fact that I need bathrooms around me. I just don't want judgment here either.

Thanks for listening...

Ridgewalker Contributor
This is my first, ever, real job. And these people are super picky about who they hire. And I'm scared that if I tell them about my issues, they're not going to want to rehire me in the spring (I'm a seasonal employee) because it'll qualify me as high maitence. Especially since I'll be working cash and things, and I won't always have someone else there. I guess I'll have to tell them, eventually. But soo many people are incredibly judgemental of the fact that I need bathrooms around me. I just don't want judgment here either.

Thanks for listening...

If they don't want to rehire you in the spring, I would say that's their loss, not yours. There are other jobs out there. You want to work for a company that doesn't hold your medical condition against you (which is illegal, by the way.)

sickchick Community Regular

I have not been able to work for 11 years. I for one JUST figured out about a week ago that I have Celiac disease.. I had NO idea... I was reacting to everything and I have the explosive diahrrea and I can literally eat 6 Immodium AT ONCE and it won't even touch it... I am so embarrassed I just stay home.

I will be thrilled if I can work again and leave my house without toilet paranoia :lol:

be well and good good luck with you job and your boss :)

lovelove

sickchick

blueeyedmanda Community Regular

I am actually holding down my job now, better than I did when I was still figuring out what was causing me to be so sick. Things are good now since I am in an office setting so if you miss a day a work it is not as big of a deal, when I worked at my previous job, they needed someone to be there when there was a call off. Hopefully all will go well for you.

kali-mist Apprentice

I work in an office and I've been working here for about a year and a half. I had just started working here when I first was having health problems. I was throwing up at least once a week and would have to go home. Finally my boss said that if I wanted to go home I would have to get a doctors note. That was the start to finding out I have Celiac. It took about a year to get the final diagnosis and in the meantime I was sick all the time. My boss was not understanding at all, and kept asking me why I was sick all the time. When I finally found out the reason and told him he still wasn't very understanding. So far this year I have missed 4 days from work for doctors appointments or because I was sick. Everytime I miss a day my boss asks me why I'm so sick all the time and tells me that I'm all out of sick days. I remind him I have Celiac and if I eat something with gluten I will get sick. There are a lot of days when I throw up or have diarrhea or just feel really run down and would like to go home but I know I will get harrassed if I do so I just stick it out. I wish I had a more understanding boss but I guess we can't all be so lucky. The hardest part about work is lunch time. I hate leftovers and the obvious sandwich or soup is not an option anymore. I've been going to Wendy's everyday for like 6 months and getting baked potatoes or salad, but I'm starting to get sick of it.

blueeyedmanda Community Regular
I work in an office and I've been working here for about a year and a half. I had just started working here when I first was having health problems. I was throwing up at least once a week and would have to go home. Finally my boss said that if I wanted to go home I would have to get a doctors note. That was the start to finding out I have Celiac. It took about a year to get the final diagnosis and in the meantime I was sick all the time. My boss was not understanding at all, and kept asking me why I was sick all the time. When I finally found out the reason and told him he still wasn't very understanding. So far this year I have missed 4 days from work for doctors appointments or because I was sick. Everytime I miss a day my boss asks me why I'm so sick all the time and tells me that I'm all out of sick days. I remind him I have Celiac and if I eat something with gluten I will get sick. There are a lot of days when I throw up or have diarrhea or just feel really run down and would like to go home but I know I will get harrassed if I do so I just stick it out. I wish I had a more understanding boss but I guess we can't all be so lucky. The hardest part about work is lunch time. I hate leftovers and the obvious sandwich or soup is not an option anymore. I've been going to Wendy's everyday for like 6 months and getting baked potatoes or salad, but I'm starting to get sick of it.

Wait you missed 4 days and it is already the end of August. I say that is pretty decent. I know healthy people who have missed more days this year than you. I wish you had an easier time with you boss. Can you look into getting an FMLA or something until you get things more under control?

kali-mist Apprentice
Wait you missed 4 days and it is already the end of August. I say that is pretty decent. I know healthy people who have missed more days this year than you. I wish you had an easier time with you boss. Can you look into getting an FMLA or something until you get things more under control?

At the risk of sounding stupid...what's an FMLA?

sickchick Community Regular

Open Original Shared Link :)

I am temporarily on SSI (I am bi-polar too)

I am certified in Reiki though and plan on starting a business when I am able to work again.

Hope that link helped I had never heard of it either~

sickchick

blueeyedmanda Community Regular

FMLA is the Federal Medical Leave Act. It a law which protects people who have to take off work due to an illness, accident, or other reason. I ended up getting one when i was in the process of getting diagnosed for celiac, I was missing alot of work due to being sick. My supervisor was the one who helped me get it and understand it. You need to get the paperwork filled out by your doctor.

kali-mist Apprentice
FMLA is the Federal Medical Leave Act. It a law which protects people who have to take off work due to an illness, accident, or other reason. I ended up getting one when i was in the process of getting diagnosed for celiac, I was missing alot of work due to being sick. My supervisor was the one who helped me get it and understand it. You need to get the paperwork filled out by your doctor.

I live in Canada so it would be different here. I would have to go on EI (Employment Insurance) and take a sick leave. You can only take a maximum of 15 weeks and you only receive 55% of your wage, which is not enough for me to pay the bills. Mostly work is not a problem for me, I just don't appreciate when I'm sick and I get the third degree on why I'm sick all the time. I must have told my boss 3 times it's because I have Celiac. I don't like feeling guilty about calling in sick when I'm having a rough day.

GFhopeful Rookie

it's tough i know. i have pretty understanding boss and coworkers and i still feel guilty but i also realize that i need to take care of myself or i could end up back in the hospital and that is good for no one. maybe you could start looking for a new job or different source of income while you keep this job - but it's a hard situation when your health is not great to get a new job. i hope you feel better soon and try not to take your boss personally as he/she obviously has never been in your shoes so doesn't really understand.

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
      131,957
    • Most Online (within 30 mins)
      7,748

    Dogdad21
    Newest Member
    Dogdad21
    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.