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

How To Handle Family


GFreeMO

Recommended Posts

GFreeMO Proficient

I just got off of the phone with my Mom. She is really mad at me b/c I told her that my husband and I don't feel comfortable going to her house for Thanksgiving if she is going to be making everything. (I said this in a very nice way) I have offered to make the stuffing with Udi bread and offered to make Gluten-Free pumpkin pies and bring Gluten-Free rolls. I don't expect them to cater to my celiac at all thats why I offered to either not go or to make Gluten-Free things that everyone can enjoy. She said that no one is going to want "my gluten free crap" because it tastes horrible.

I don't know what to do. I am not trying to be a pain or trying to cause friction but I am a very very sensitive celiac and if I eat any, I am sick for over a month. Starts with the d for a week then migraines, that joint pain so bad that I have to crawl and drag myself around then I get horrible DH on my knees.

I offered to bring all my own food. She got mad at that too. I don't know what to do! She said she would keep the store bought rolls away from my food and make the stuffing ahead of time but she would be baking it together in separate pans. I am worried about the butter and worried about CC from the flour on the counters even if the stuffing is made the day before. I have gotten sick over there before from a dish rag that wiped up flour and then was used to wipe off the table. They don't understand CC.

Help!


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



Celiac.com Sponsor (A8-M):



kareng Grand Master

Anyone else in your family that will be there that you can explain cc to and will have your back? Not your Hub (he is an interloper) but someone related to your mom.

I would just bring all your own food in your own containers and keep an eye on it the whole time. You don't want someone to be "helpful" and plate it for you if they don't understand cc. If hub can eat the regular food, let him.

If this is still going to cause a huge fuss or fight, say home and have a nice quite day. You or Hub could also get really sick with the flu on Wed. ;)

T.H. Community Regular

So sorry this is an issue. I've run into this with my mother in law and my son's allergy to milk (which is, thank god, very mild and not anaphylactic). I offered make/bring some dairy free dishes for him, she's mad. I offered to just bring his food, she's mad. for the first visit after we discovered the allergy, when she was adamant that she wanted to make his food and it would be dairy free, I made the mistake of believing her, and my son got sick.

We never did that again. When everybody was diagnosed with celiac, I didn't even bother to ask. I just brought our own food.

The thing to remember, in my honest opinion, is that it's not our job to make our mothers (or *cough* in-law) act like reasonable people. They got to take on that job by being an adult. It's also not our job to help our mothers keep their temper because they're finding a way to feel offended that we want to stay healthy.

It is our job to do what's right for us and our families and our bodies. Your bringing your own food harms no one, in fact it actually makes less work for your mom! Your mom's plan to make food food prepared there, on the other hand, will hurt you - you sound pretty certain of that, and it sounds like you have reason. So honestly, it's a no brainer. Bring your own food.

And yeah, the fall out of that will suck. I know it did with my mother in law. But the fact that your mother is ignorant about this, or doesn't believe you, or whatever her issue is - that doesn't mean you should have to sacrifice your health and safety for her. I wish there was a way that you could get through to her, but she doesn't sound too receptive to more talking...she already knows all about celiac disease, right? Or, well...I'm assuming that's what she thinks, anyway. ;)

Hopefully, someone will have some good ideas here. I'm kind of out of anything to say. :(

bonnie blue Explorer

I agree with Shauna, you have to do what is best for you. Don't risk your health for anyone, I know I won't. Bring your own food, and enjoy the day, no one wants to be sick during the holidays, I hope everthing works out for you. ;)

GFreeMO Proficient

Thank you all so much. I am going to bring my own food. I love this forum. Everyone is so supportive. It's so nice to talk with others that get it!

YoloGx Rookie

just be careful that she won't be making last minute pies that day....the dust in the air can be killing.

The turkey too needs to be vetted. Baked in an oven that has had pies etc.? Bought with natural flavors shot into it?? avoid avoid I am afraid.

If it were me I would just have my own non gluten turkey day at home with friends who are supportive rather than just not trying like her. This is supposed to be a relaxed day in Thanksgiving... Eventually your extended family will get it if they want to have you over for events like this. Or not. But at least you will be a lot happier and healthier.

Bea

Takala Enthusiast

Your health trumps their feelings.

Bring all the food you intend to consume yourself. It would be easier to make yourself a plate of it up and pack it in a large cooler, along with your desert serving and some snacks. If you are feeling magnanimous, you can also bring some gluten free things for the glutenoids to eat, like a gluten pie, rolls, etc, but don't leave them out without taking your serving first - I guarantee people will cross contaminate them almost instantly. You will also want to bring a roll of those adjustable sized paper towels that you can tear off a piece and lay it down anywhere as a buffer, then toss in the trash, if you will be having to use their kitchen for anything.

Don't let them bully you into getting sick and ruining your holidays. They can either cope and adapt to your bringing your own food, or they can spend the time by themselves. It is one thing to just not understand the whole cross contamination issue, and I can give most people a pass on that, but if they are actively not wanting to learn and are acting out right hostile to the idea that you will eat safe food that you provide yourself, they need to be guided that this sort of behavior is not acceptable.


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



Celiac.com Sponsor (A8-M):



Skylark Collaborator

You have to tell your mom how much you love her and want to spend the holiday with her (assuming this is indeed the case), and that you will be bringing your own food. You can be very kind and compassionate while still refusing to take "no" for an answer. Setting boundaries never goes over well, but the only way to establish them is to stick to your guns though all her expert attempts to push your buttons. (And she's a-pushing. I can tell from your post.) Your health has to come first if you get that sick from traces of gluten. Skip Thanksgiving with her entirely if that's what it takes to make her realize that you are serious about bringing your food on holidays and hope Christmas goes better.

TPT Explorer

I haven't been diagnosed yet, so I haven't come across this yet. Though I think my family will be supportive. Not to excuse it, but I wonder if it's a generational thing? Meaning, allergies and food intolerances weren't as prevalent or at least as recognized years ago? I wonder if the older generation thinks it's all bunk?

It's still hard to believe your own mom won't be supportive of your health. I hope you don't ever get sick, but if you do, make sure she's around to clean up after you. :unsure:

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,949
    • Most Online (within 30 mins)
      7,748

    Stephanie94
    Newest Member
    Stephanie94
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Who's Online (See full list)

  • Upcoming Events

  • Posts

    • 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
    • DebJ14
×
×
  • 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.