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People Not Taking You Seriously


LePandaRouge

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LePandaRouge Rookie

How do you deal with family members and friends who don't take you seriously?

I discovered I have celiac disease and went gluten free 6 months ago. The problem is I've been living abroad for several years so my family has not witnessed my symptoms. All these years I hid from them that I suffered from fibromyalgia and chronic fatigue as well as constant GI symptoms and mental health issues, etc...

And so I'm visiting them this summer and they seem to think going gluten free has only been a diet choice, nothing dangerous. I tried telling them about the symptoms I was getting. Also, my mother has suffered the same symptoms all her life and suffers from cerebellar ataxia and has had difficulty walking for a few years as a result of gluten. I tried explaining this to them and that if I carried on eating gluten, I'd end up like this too. But it's like their face goes blank and they stop listening at this point.

So I feel like I constantly have to defend myself. They especially don't understand why I'm being careful with cross contamination and get annoyed each time I say I can't eat something.

For example, I was making gluten free pasta at my aunt's house the other day and she wanted me to use her colander. I said I'd rather not as they use it for wheat pasta all the time. But she was arguing that it's fine and that it's washed very well. I still said no, but she wouldn't let go.

Or another example of annoying conversations we have is:

Aunt: "can you eat doughnuts?"

Me: "No, unless they are gluten free"

Aunt: "I have some doughnuts in the fridge, can you eat those?"

Me: "Most likely not as doughnuts are generally made from wheat flour unless you took them in the gluten free section, but no one buys baked goods in the gluten free section unless they're looking for gluten free specifically"

Aunt: "You never know, maybe I grabbed gluten free doughnuts without realising, let's have a look"

- So Aunt gets up, walks to the fridge and brings me the doughnuts -

Me: "No seriously, they will be made of wheat. You don't go to gluten free bakeries or shop in the gluten free section unless you are gluten free. It's not something you just stumble on accidently. There are not enough gluten free products on the market for that to happen, unfortunately."

Aunt: "You don't know that. You don't know until you read the ingredients."

- Aunt hands me the doughnuts -

Aunt: "Go on, check the ingredients"

Me: "Fine"

Me: "First ingredient - wheat flour"

Aunt: "ah"

Aunt: "But I have biscuits too, can you eat those?"

Me: "No, biscuits are made of gluten too"

Aunt: "But maybe these are made with gluten free flour"

Me: "No, as I said, baked goods on the market are very rarely gluten free"

Aunt: "Why don't you just look at the ingredients before dismissing them?"

Me: "Because I know they contain gluten! These things are made with wheat flour!"

- Aunt gets up and gets the biscuits and makes me read the ingredients -

Me: "Made with WHEAT FLOUR"

Aunt: "Ah, well what about these other biscuits?"

Me: "As I said, baked goods are generally a no..."

*Sighs*

And so on.... And it gets tiring for me... and them...

And the problem is, they raise the gluten issue in every conversation. And when I respond they always seem tired and bored of me talking about gluten. Well then why don't they just let me eat what I want and stop questing and interfering. :rolleyes:

Is anyone in the same situation? How do you deal with that? :rolleyes:

(rant over)


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  • Replies 52
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Kay DH Apprentice

It gets frustrating. It is why sometimes the best family is people you aren't related to. It takes a long time to adjust to being gluten-free. I started last fall after symptoms kicked in following the flu. It has taken me some time to adjust and for gluten-free to be automatic. Yes, I sometimes have issues with friends. I took almost all my own food while camping with friends last week. With any of their gluten-free food I made sure I was "first in line." Even with that my "brother" asked if I wanted a second helping of the (gluten-free) BBQ, and I said, "no, there is always the risk of cc." He said there was no cc, and we went back and forth until I said someone was eating the non-gluten-free potato chip crumbs and they could have... There are so many sitcoms. seems like Celiac would be a good one. It is important to be anal retentive when it comes to gluten. Even 6 months later my friends ask if coconuts are gluten-free, etc. But they are learning, and more importantly, they sometimes make gluten-free allowances just for me. A friend made me a gluten-free birthday cake last night and kept all the ingredients for me to look at first. With all the frustrations, I find it best to step back and remember all of the things to be grateful for, the friends that invite me to gatherings and accept that I will bring my own food, the acceptance of my limitations, and that chocolate is gluten-free. Your family has lack of knowledge about gluten intolerance and where the nasty molecule lurks, but they also may be in denial and this can take a long time to dissipate. Could there also be a bit of "yanking your chain" to get a reaction from you?

Skylark Collaborator

I don't have much help as far as dealing with family. We all have allergies and are used to reading labels and whatnot.

The thing that struck me about your story is that your mother needs celiac tests. You know celiac can cause cerebellar ataxia, right? If it's at all possible you need to drag your mother to the doctor and get her tested for anti-gliadin IgA. She may not come up positive on the other tests because they're for gut damage.

Good luck staying healthy during your visit and I'm sorry you're having to go through this.

cassP Contributor

yes! you need to drag your mother to get tested.... im "THIS CLOSE" to dragging my dad in ..

i COMPLETELy understand- in addition to family- its everybody else too.... looking at u like you're looney- oh i totally am there with ya

Kay DH Apprentice

Good point regarding the ataxia. If your mother hasn't been tested for Celiac then it is important to do so. There are a great many symptoms that can be associated with gluten intolerance, and finding a doctor familiar with Celiac (not an easy task) can help to sort all of these out. I have a niece with lots of GI problems that is gluten-free, but she won't have the Celiac tests because of the real fear that she won't be able to get insurance for a preexisting condition if it comes out positive :rolleyes: . I have a sister with lots of GI issues as well, but her's aren't severe or obvious, and she won't go gluten-free or get tested. I sent her a lot of gluten-free pastas for her birthday and she said she would save them for when I or her daughter visit. Family. Celiac just offers one more layer of frustration.

  • 2 months later...
shellyinskiatook Newbie

That is soooo annoying. I've started saying something like...I will never be able to eat anything that you cook for me, ever. I will take care of my food, so please don't offer me any. I do not like to call attention to myself so please don't ask me about it.

I've had food issues my entire life. There are always going to be people who don't believe you and that's unfortunate. I've had very close friends accuse me of "making up my food allergies to get attention." Really? Yeah, everybody wants this kind of attention, right? I'm no longer friends with those people.

I've been allergic to citrus since I was a child. My sister sent me a box of grapefruit for Christmas a few years ago. I mean, what the hell? I had to get my neighbor to get the box off of my porch. I've discovered that some people will never get it because they really don't want to. Stay strong and just SAY NO!! *even if they don't want to hear it :)

  • 2 weeks later...
aLayla Newbie

I found it was educating to go with my Mom through Wikipedia articles together (both for ADD or celiac or whatever..) And translate stuff or show her pictures of vilii and explain briefly.. so she understands the mechanisms and the symptoms..

I was gluten-free before and it kinda drove them crazy (even if I cooked my own food, just leaving the extra dishes around was 'soo annoying' ugh)

Celiac has been in the papers in the last few years too, and some acquainatnces have been officially diagnosed, so that helps too..

If there were no articles in your country, consider translating some stuff, especially signs/consequences etc. Some really good tips on this forum too :)

Also, remember old people can have trouble remembering stuff.. They just want you to have a good time.. Sometimes they can't eat cookies due to health reasons and want you to 'enjoy' for them!! (They may also equate cookies=love! :))

Educating, inspiration, or just changing the topic can help?

I've sometimes said that I have a 'pre-diabetic' condition too, my blood sugar can go haywire after sweets and I try to stay away.. They know about diabetes (though some of the diabetic relatives still eat and bake cookies and such!!) at least it helps them relate more easily...


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DownWithGluten Explorer

It is extremely frustrating. I don't have it nearly as bad as you (OP)...but yet even the occasional callous comment like "Well I'd assume someone on your diet would know what you could or could not eat" (at a fair)...when of course it's like...not unless I see the ingredients of EVERY food, and even THEN there could be contamination, hidden gluten, etc ad infinitum. It's not like I'm doing it to be paranoid or finicky. I'm doing it because every thing I eat has a potential bomb lodged inside it that will go off in my instestines if ingested. So, heck yeah I'm careful and always air on the side of caution. I'm sure there ARE things I could eat that are gluten free, but unless I KNOW, or it is labelled gluten-free, or I have checked the brand, or it's just a plain carrot...etc...I'm not gonna eat it. sorry. but people do seem to get annoyed occasionally, like the fact I'm not eating gluten is an inconvenience to THEM so how...even when it does not affect what they eat at all. It's like...why does it matter, then? Just let me be lol. I'm not complaining and don't stand around whining about what I can't eat to everyone all the time...so just leave me alone and believe me when I say I don't want to eat something because it might make me sick.

So kudos to you for having way more patience than I would with your aunt.

GlutenFreeManna Rising Star

Since you posted this a few months ago, I'm just curious, did it get any better? That's a very strange conversation with your aunt. My thoughts were either she is illiterate and unable to read the ingredients herself or she is just trying to annoy you. Some people that think this disease is fake will go to great lengths to tempt you to eat gluten. Then again I have heard of people thinking white bread is made of rice so I would not be completely surprised if she is just that ignorant of what is in her food. If they are not being annoying on purpose I would try to educate them. It sounds like your mom needs testing. I hope you can convince her someday to get it before she is completely diasbaled by the gluten ataxia.

coffeetime Explorer

I think sometimes that if a reaction to gluten was similar to peanuts and the need for epi-pens (I know it's NOT an allergy but an autoimmune response) people would take it more seriously. When I read the conversation with the aunt I immediately thought of my dad who at 85 is always offering me food (often gluten laden), I think it stems more from lack of knowledge and understanding about how many products have gluten--think how hard it is for us just navigating the grocery store. Food is equivalent to love for many people and I would bet for your aunt it may be the same. I find in these situations, it's easier to say thank you but I'm so full from lunch, breakfast, etc and remember she loves you. We have to find a way to live safely in the food world around us, if we are lucky enough to have family members who are knowledgeable and willing to accommodate that is wonderful, but I don't think we should ever assume that family and friends are out to trip us up.

K-Dawg Explorer

I have also had that sort of conversation....I remember my dad getting into it with me and saying something like "the label says MAY contain gluten, not that the product DOES contain gluten" and he was suggesting that I should give it a go! lol. I finally said, "Dad, I'll pass. I'm happy with my lettuce wraps right now"

In the end I appreciate that he just doesn't get it. I mean, there is some sort of huge block for him. He is a smart guy, but this 'gluten free thing' just doesn't jive with him for whatever reason. No big deal. I simply REFUSE to engage in any conversation with him on it. If I am at his house, I bring my own food, cutlery, dishware, microwavable container, etc and if he asks "would you like this or that...do you think it contains gluten" i don't even bother trying to educate him. I just say "no thanks, Dad. I'm good"

At the end of the day, he is not going to ever appreciate the nature of celiac disease and that is okay. I know he loves me and now that I've given up trying to educate him, there's no more of those idiotic stress-filled conversations. phew.

KDawg

  • 2 weeks later...
Cypressmyst Explorer

Hahahaha! Replace "Aunt" with "Mom" and you just glimpsed my life. <_<

Thank you, my husband and I laughed out loud reading that. Very "Whos on First." :P

I am currently dealing with this as well. And I'm pissed because I've averaged 8 hours a day worth of in depth research into Gluten for the past 6 months. I think at this point I know a little something about the issue. :rolleyes: So when people act like idiots it is very hard not to take it as disrespectful of my intelligence...as if I don't know what I'm doing.

:blink:

I have no advice as I keep on trying to educate whenever possible and completely against the odds (But this is too important not to!).

Anyway, know that you made two people smile today and you do have support here on the forum. :P

cap6 Enthusiast

my Dad is sort of like your aunt. "So, you can't eat that then Sis". "No Dad". "well let's look at this." I can't get upset cause he really cares but at 82 he just doesn't get it. When we visit I take my cooler, scrub a spot in his refrig, take my own pan and cutting board, a sense of humor and love and... pray! He means well and cares and he always takes me out to eat at Outback cause he knows I can eat there!

revenant Enthusiast

Ohh yes it's hard... Right there with you.

My mom keeps threatening to send me to an "eating disorder clinic". She takes me to the emergency room and tries to persuade the doctors that I have an eating disorder because I do not eat gluten and lactose. Because I'm self diagnosed and too late for testing... they seem to be on her side.

Quite a hard place to be put for us! But we'll grow from it. All that matters is that you are feeling well

mushroom Proficient

Ohh yes it's hard... Right there with you.

My mom ...... takes me to the emergency room and tries to persuade the doctors that I have an eating disorder because I do not eat gluten and lactose.

What you need to tell the doctors is if you ate gluten and lactose you would really have an eating disorder - called untreated celiac disease. :P

Salax Contributor

I find it fascinating how people give a crap what you are eating or not eating. Your body, your mouth. You can decide what not to eat and what to put in it. End of discussion, no need for further explanation. Maybe it's just me, but who cares. Really, why are other people so concerned with what other people are eating? I think our society is obsessed with food. Nosey? Maybe. Silly...definitely. :angry:

*gets off soapbox*

:D

Judy3 Contributor

OMG reading these posts made me laugh and cringe at the same time. I'm new to this so 'that gluten thing again' seems to be a topic of conversation with just about everyone I eat with. Last week eating dinner with a friend: "All your having is a salad?", my response "Yes, I like salad". But they have so many good things here at this 'SANDWICH' restaurant" I try to explain for the 100th time that I can't eat the bread to no avail so I outright asked the manager if they had gluten free bread for their lovely sandwiches and she said oh no we don't. End of conversation or so I thought. I get my salad and friend says to me 'you forgot your croutons, I'll get them for you"... heavy sigh and want to escape through the bathroom window!

Another friend via email that I love dearly and we laughed about this later when I called her on it.. I said I tried the gluten free frozen waffles and the texture of them was a little strange once I put the syrup on them they seemed to melt on my plate. Lovely friend replies "You should try the whole wheat one's in the health food section at the store they are really good"... I stop, I reread this again and then I ask her if she's gone mad.... she says why zo I explain to her again that wheat has gluten... she feels dumb and says omg I must have been tired when I wrote that, I know that.. Note to self never eat at her house in case she's tired when she's cooking... LOL (I told her that too)

Trying to keep my sense of humor in tact above all else as I venture into the gluten free world that to others seems to be a dark and evil place! :P It's not so dark and evil so far, it's a wee bit texture challenged but I'll get used to it (I hope)

  • 4 weeks later...
jessicaj Newbie

Since June of 2009 I have been having what I thought were allergic reactions to food. People in my extended family told me it was in my head, even my allergist said I wasn't allergic to red dye after an anaphylactic reaction landed me in the Emergency Room. Since I left him I found a Nurse Practioner who discovered that I was a celiac. I am also allergic to food dyes, potatoes, wheat, shellfish, walnuts, kale and intolerant of almost every grain including rice. My immediate family, husband and two daughters, are not going gluten free and I am sick and tired of being sick and tired. I also have candida issues so I feel like garbage most of the time. Does anyone have any advice on how to manage life with food allergies and intolerances when you live with someone who does not take this seriously and is practically a gluten addict? I have my own pots and pans and some of my own food storage containers. My daughters know that they can't put anything into the containers that mom can't have but I still end up getting sick from cross contamination. I could easily be a food Nazi given my own kitchen but I don't know what to do short of moving out and I can't afford that.

norahsmommy Enthusiast

your aunt and my grandma are very similar! My grandma brought candy for my kids. My youngest is gluten intolerant and she wanted to give her a kit kat bar. I said no because they have gluten in them. She said, "no its cookie" and I said, "yes but cookies are made of wheat flour and that has gluten in it" and she said, "Oh, how about a twix bar instead?'' I said "no, that has cookie too." Then she offered her a meatball, made with bread. I said no. It just went on and on from there =). She understands more now. But she still tries to give her stuff she can't have.

beefree11 Newbie

I have also had that sort of conversation....I remember my dad getting into it with me and saying something like "the label says MAY contain gluten, not that the product DOES contain gluten" and he was suggesting that I should give it a go! lol. I finally said, "Dad, I'll pass. I'm happy with my lettuce wraps right now"

In the end I appreciate that he just doesn't get it. I mean, there is some sort of huge block for him. He is a smart guy, but this 'gluten free thing' just doesn't jive with him for whatever reason. No big deal. I simply REFUSE to engage in any conversation with him on it. If I am at his house, I bring my own food, cutlery, dishware, microwavable container, etc and if he asks "would you like this or that...do you think it contains gluten" i don't even bother trying to educate him. I just say "no thanks, Dad. I'm good"

At the end of the day, he is not going to ever appreciate the nature of celiac disease and that is okay. I know he loves me and now that I've given up trying to educate him, there's no more of those idiotic stress-filled conversations. phew.

KDawg

Hello K-Dawg...I am new. I stumbled upon this site in a panic state with my gluten intolerant daughter having a severe reaction at 430 am this morning. Her father brushes off the diagnosis of her being gluten sensitive although she IS hashimoto's, hypothyroid (she is on cytomel and synthroid since 05) AND pcos and was being treated for parasites and hey she is still young!! lol (that was more of a sarcastic laugh).

I am wondering do you live with your father? Does he at least acknowledge there is a dietary issue causing you discomfort? My husband doesn't really care. In fact he just recently purchased three diff brands of gluteny cookies, muffins, bagels, breads, cereals, croutons, bread sticks, pretzels and crackers. I have since gathered them up in a BIG basket and stored them in his work room. Fine. He can have them....just not in the kitchen.

I find myself rising earlier than my daughter to clean kitchen counters, cabinets, handles, light switches, floors, etc for the kitchen is usually contaminated. I have gone gluten free along with her. It just makes sense. I don't know if her father is suffering from some other issue for this behavior of his borders on cruelty toward his own daughter.

My focus is her safety and her health right now - not his over consumption of gluten/wheat products which arent doing him any GOOD.

Is there contamination issues with you and your family? Thank you.

  • 2 weeks later...
Brookesmom Newbie

I am wondering do you live with your father? Does he at least acknowledge there is a dietary issue causing you discomfort? My husband doesn't really care. In fact he just recently purchased three diff brands of gluteny cookies, muffins, bagels, breads, cereals, croutons, bread sticks, pretzels and crackers. I have since gathered them up in a BIG basket and stored them in his work room. Fine. He can have them....just not in the kitchen.

I find myself rising earlier than my daughter to clean kitchen counters, cabinets, handles, light switches, floors, etc for the kitchen is usually contaminated. I have gone gluten free along with her. It just makes sense. I don't know if her father is suffering from some other issue for this behavior of his borders on cruelty toward his own daughter.

My focus is her safety and her health right now - not his over consumption of gluten/wheat products which arent doing him any GOOD.

Is there contamination issues with you and your family? Thank you.

Oh BeeFree, I just saw this. I had to go gluten free 100% a year ago after positive results, and my daughter a month ago after *her* positive results. At first my husband didn't take me seriously but he's getting better educated and keeping junk out of the kitchen now that it's my daughter too. However, for the past year, especially before my daughter's tests, he bought a multipack of whole wheat pasta! from Costco, giant boxes of Triscuits and most recently a giant box of wheat thins. Are there no gluten free snacks? The most annoying was Costco sized Shredded Wheat. Talk about crumbs. I got really pissed I must say and forbid him from making bread in the breadmaker with flour or cooking pasta in my pots. He has a dedicated wheat pan, but has decided it's mostly too much work and eats gluten free at home. He *has* to have his bags of supermarket bagels in the car for the ride to work though. I think he's kinda addicted to wheat because it's either wheat snacks or beer. Grr...

I think you need to take charge of your kitchen! Give them a pan or two and cook gluten free for them. Let them have a gluten snack in their backpack or work bag if they must. Forbid flour or crumbs at the table. They can eat it when they're at work/school if it's so darn important! Try showing them studies about antibodies not going down from cross contamination and how continued exposure increases risk of lymphomas and other cancers. Hang in there!

  • 1 month later...
nmthommy Rookie

There is a great test that you can do from home. Never need to see a doctor!!! no I don't work there but I had all my tests done with them and tested positive for gluten sensitivity after testing negative with blood tests.

EnteroLab www.enterolab.com

they send everything you need to your home and then send you the results in 3 - 4 weeks. They can also do DNA testing for sensitivities.

I'm having my children tested too since it is inherited.

nmthommy Rookie

That's funny.

I told my brother that I am alergic to gluten and he said that I should try eating organic.

OMG reading these posts made me laugh and cringe at the same time. I'm new to this so 'that gluten thing again' seems to be a topic of conversation with just about everyone I eat with. Last week eating dinner with a friend: "All your having is a salad?", my response "Yes, I like salad". But they have so many good things here at this 'SANDWICH' restaurant" I try to explain for the 100th time that I can't eat the bread to no avail so I outright asked the manager if they had gluten free bread for their lovely sandwiches and she said oh no we don't. End of conversation or so I thought. I get my salad and friend says to me 'you forgot your croutons, I'll get them for you"... heavy sigh and want to escape through the bathroom window!

Another friend via email that I love dearly and we laughed about this later when I called her on it.. I said I tried the gluten free frozen waffles and the texture of them was a little strange once I put the syrup on them they seemed to melt on my plate. Lovely friend replies "You should try the whole wheat one's in the health food section at the store they are really good"... I stop, I reread this again and then I ask her if she's gone mad.... she says why zo I explain to her again that wheat has gluten... she feels dumb and says omg I must have been tired when I wrote that, I know that.. Note to self never eat at her house in case she's tired when she's cooking... LOL (I told her that too)

Trying to keep my sense of humor in tact above all else as I venture into the gluten free world that to others seems to be a dark and evil place! :P It's not so dark and evil so far, it's a wee bit texture challenged but I'll get used to it (I hope)

T.H. Community Regular

That's funny.

I told my brother that I am alergic to gluten and he said that I should try eating organic.

It's surprising how often people think that's the answer, isn't it? My favorite was an acquaintance who thought all my troubles with gluten would be solved if I went on a macrobiotic diet...the one where grains are the main source of nutrition. Then proceeded to give me all these whole wheat and barley recipes. :rolleyes:

  • 2 weeks later...
catsmeow Contributor

It's surprising how often people think that's the answer, isn't it? My favorite was an acquaintance who thought all my troubles with gluten would be solved if I went on a macrobiotic diet...the one where grains are the main source of nutrition. Then proceeded to give me all these whole wheat and barley recipes. :rolleyes:

OY!!!!!!!!! My friend thinks I can solve a wheat allergy if I fix what she thinks is a leaky gut........I'm sorry, but a leaky gut DOES not cause a major histamine response. She thinks if I follow this fix and take pro-biotics, I will be fixed, and able to eat wheat again...I can't convince her otherwise. It's so frusterating...

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    • 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 .
    • Francis M
      Thanks. Since the back and forth and promises of review and general stalling went on for more than six months, the credit company will no longer investigate. They have a cutoff of maybe six months.
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