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

I'm Getting So Frustrated!


Connie R-E

Recommended Posts

Connie R-E Apprentice

My friend's 7 year old boy was just diagonsed with reumetiod arthiritus(where's spell check when you need it?). He can't walk well due to it, has food aversions, takes asthma medications daily. He, and his siblings, have ashen skin and allergy shiners under their eyes...(people are always asking who gave them the black eyes!) and they are so darn skinny!

And, their grandmother was just doctor diagnosed with Celiac!

I have tried and tried to tell her about celiac, and how she could help her family...

I'm getting so frustrated!!! :angry:

The other women in my/our group (Ya-Ya's) agree with me (they always go out of their way to make things gluten free for our weekly get togethers!) And, they actually understand about celiac.

We may just sit her down and try, yet again, to explain that it isn't that much more expensive to go gluten-free(her main argument)--especially when she could save a bunch of money on all the medications her kids have to take in a day! --which I bet would be near unneccesary on a gluten-free diet.

So, is it wrong to have an "intervention" for our friend and her kids/family?

We are all to that point. :blink:

Connie


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



Celiac.com Sponsor (A8-M):



seeking-wholeness Explorer

Oh, Connie, I feel for you! I know a family of four where I think they ALL need to be tested for celiac disease, but I had to bite my tongue with them, or they would close their minds to it forever! I actually did get an opportunity to talk to the the father and mention testing the baby, at least--and I know that my expression was dead serious and not the least bit apologetic, because I was shocked to discover that the baby's belly was distended (which didn't show through heavy winter clothes) and his torso and legs were covered with eczema patches and a pimple-like rash! We'll see what comes of it, but I'm not holding my breath.

It IS so terribly frustrating, and somehow it is especially hard when children are involved! WHY won't their parents advocate for them, since they have NO power to improve their own health? I get the feeling that this woman in your group either doesn't understand the extent of the damage that gluten is doing to her children's bodies or is deathly afraid of accepting the ongoing, unrelenting responsibility of implementing and maintaining the gluten-free diet--or both. It's easier to say, "it's not my fault" and demand a magic pill to fix the situation than it is to make a permanent lifestyle change (especially one that is widely perceived to be extremely restrictive). I would be surprised to hear that the expense of the gluten-free diet is TRULY her primary objection; I think it's more likely to be an excuse to avoid examining the truth of the situation and her own emotions and priorities.

If you and your friends all sit down and explain the facts, calmly but with NO TRACE of apology, you might actually get somewhere--but then, you might not. It depends on how proud this woman is, and whether she is willing to let her guard down around all of you and acknowledge her deep, dark feelings (frustration, fear, deep sadness, inadequacy--to name just a few). It might be a good idea to approach the emotional aspect of being the parent of sick children first. If your friend believes that her feelings are understood and respected, she will probably be more open to listening as you describe the probable necessity of making a major lifestyle change!

I think you and your friends are within your rights to express your deep concern to this woman, as long as you do it in a friendly and mature way. It would probably be a good idea to meet first with your friends to discuss how you will approach the matter with this woman, and to make sure that everyone will be able to remain calm and not lose her temper if the woman is reluctant to listen. Remember, too, that you can lead a horse to water, but you can't make it drink. If she won't consider implementing the gluten-free diet for her children, don't bring it up again. Ultimately, no matter how hard it is to accept, this woman's children are her responsibility, and she has just as much right as anyone else to make a poor decision. Hopefully, if that happens, she will eventually change her mind on her own!

I hope my opinions help you clarify your own position on this matter, and I wish you success if you decide to "intervene"!

wclemens Newbie

Connie, my heart goes out to you! I can almost see those children in my mind's eye, and the suffering they are enduring. Sarah's comments should be so helpful, and I agree, there is every reason to boldly approach the subject with your friend. Is there any way to convince the recently-diagnosed Grandma to add her input? She must care about her family members, and perhaps she would know a strategy that would work. I'll be hoping that your intervention is a success. Welda

Guest PastorDave

Hi there. I know that this may not of be much help, but I was thinking about the "cost too much" arguement. I am a pastor, and although I am well paid, I didn't get into the ministry to get rich, and it shows. My wife works full time as well, but we live in Missouri, where there are few people who get paid well. Since I had to go gluten-free, we faced it as a challenge. (Fortunatly for my I found out before it got bad, my Mom has it and convinced me to get tested). We actually enjoy finding ways to save money on gluten-free stuff. My wife bought a flour mill (of course you have to buy one new which is expensive) and we grind our own flour, and this has been a big money saver in the long run as you can buy the beans, rice, and other grains alot cheaper at bulk food stores. We found a health food store that has "Super Tuesday" the first Tuesday of every month where the take 10% off everything in the store. We just have fun with it.

When you think of all the awful things that I can get as a result of Celiac, things like cancer (scary), the cost doesn't seem so bad.

I hope this will help. Be encouraged.

God Bless :D

tarnalberry Community Regular

Being someone who's had the "my brother has this and it sounds like what you have, you should get it checked out", I can understand, to a point, where your friend might not welcome the news. (I tried to tell the person, "Nah, I know my asthma pretty well," but he thought I was just being dismissive.) On the other hand, I agree, it can be very very frustrating.

Perhaps a call to the friendship, asking her to listen - for your sake - just once with an open mind. Have your evidence layed out before you and your facts prepared - like a lawyer - but stay away from scaremongering (like "your kid could end up dead from cancer at 40!") because it can sound like a hard-sell from a car salesman. I think it's a fine line to walk.... I think I'd be just about as indecisive as you about the intervention. (Though really, she's just uncreative if she thinks that a gluten-free diet has to be more expensive... It's not like we need bread to survive! :-) )

Connie R-E Apprentice

:) Thanks for all the advice and encouragement!

I've been trying the slow but consistant approach, and I think it will work. I give her a few facts and figures when appropriate... This weekend I gave her Enterolab's brouchure. It seems the doctors now can't decide if her MIL has celiac or what! My vote is still on celiac, knowing it is difficult to diagnose. If her MIL uses Enterolab, or if she does, then maybe something good will come of it. I also suggested that the gluten-free diet could make the medications unnessecary and then the food money could increase (and reminded her that my family is next to dirt poor, and we've eaten gluten-free for 6 years!). We found some books that suggested that her husband's mood swings could be food allergy related--she was interested in that! (His Mom is the celiac.)

Don't be mad at her.... Our friend is a little "mouse" of a woman (depressed, fatigued, skinny, ashen... *celiac*... ;) ), and if I were to say "Boo!" loudly I think she might faint! (Not a Tiger, like me!) I know she is just scared, and feels even more powerless in her life with this new obsticle.

"...it's more likely to be an excuse to avoid examining the truth of the situation and her own emotions and priorities." "...her deep, dark feelings (frustration, fear, deep sadness, inadequacy--to name just a few."--seeking_wholeness

Right on the mark! I think. Do you know her? :lol: LOL!

I know she already has trouble with doing her day-to-day chores...

I'm sure she can't even imagine cooking from scratch!

So, now we've talked to her about her kids, her husband, her MIL, and soon we will talk about how she could feel better, too. Our next project is to see if we can get her to try gluten-free for her whole family for 1 week--and see if it helps anyone. (I bet she will have more energy!) I think I can arrange her current menu to be gluten-free, and even help her shop for a gluten-free week--if she'll let me--but she'll have to cook a bit! ;)

We don't mind helping her at all--it just looks like a long term project!! :P

I guess I'll live up to my name!

Constance

It is difficult to change your diet, I do understand. I've been there myself many times. You don't know what to buy, what to eat, or how to fix it.... (Right now, I have to avoid sugar and high carb foods--I'm still adjusting! :blink: )

Guest TESTinME

I hate to hear stories like this. I don't understand how a parent could neglect to look into these things when there is obvoiusly something wrong. I was very skinny as a kid with shiners too.

I'd print out some articles on celiac desease that talk about different symptoms. What does she say about her kids being skinny and the shiners?

Unlike the other poster, I would resort to scare mongering. Celiac's is serious business and your friend needs to realise that her kids long term health could suffer greatly if they are celiac and not gluten-free (including BIG increase in risk of colon cancer).


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



Celiac.com Sponsor (A8-M):



seeking-wholeness Explorer
Don't be mad at her.... Our friend is a little "mouse" of a woman (depressed, fatigued, skinny, ashen... *celiac*...  ), and if I were to say "Boo!" loudly I think she might faint! (Not a Tiger, like me!) I know she is just scared, and feels even more powerless in her life with this new obsticle.

"...it's more likely to be an excuse to avoid examining the truth of the situation and her own emotions and priorities." "...her deep, dark feelings (frustration, fear, deep sadness, inadequacy--to name just a few."--seeking_wholeness

Right on the mark! I think. Do you know her?  LOL!

I know she already has trouble with doing her day-to-day chores...

I'm sure she can't even imagine cooking from scratch!

Connie, I'm not actually mad at your friend, just sharing in your frustration! Your friend sounds almost like I used to be--except that since I am an Aries, and born in the year of the Dragon, I have always known that deep down inside I am very strong. I used to prefer the victim mentality, though, and I had a hard time even accessing my inner strength because my celiac disease symptoms (severe depression, especially) got in the way. Now that I feel so much better, I have to restrain myself from swinging too far the other way and becoming callous and dismissive when other people act like I used to! (Somebody let me know--gently, please--if I ever come across that way!)

I'm glad that you've found an approach that may work for your friend, and I'm glad you have the "Constance" to treat the situation as a long-term project. :D Your friend is fortunate to have a Tiger to look out for her! I wish you both the best of luck!

Connie R-E Apprentice

Don't worry, Sarah, I know you're not mad at her! :D

Some of the others have sent personal emails that were not as understanding towards her! (But, I understand why they were upset--and they included some great ideas!)

I used to be rather "mousey" myself--until I just got tired of it and let loose my tiger!

Have a great day! :lol:

Connie

Connie R-E Apprentice

Hey! PastorDave,

About that grinder.... What kind of grain-to-flour ratio do you get?

If you grind 1 cup of rice, how much flour would it make?

I've been curious for a while (we live in Arkansas--not a high-income state either! :D )

Thanks,

Connie

  • 3 weeks later...
alexa11219 Newbie

Well, it's called "Welcome to the club". I'm 54. For the whole my life, I've been having stomack/intestinal problems and a whole bunch of other ones. Recently was diagnosed with gluten intolerance. My Father and both grandfathers died of stomach cancer. My daughter is a smart, intelligent, serious girl of 24, studies alternative medicine. Her daughter is 4, extremely skinny, weighing just 29 pounds, her hight is less than average. The skin on her little legs and arms is covered with pimple-like rash (someone mentioned it - is it also a simptom of celiac disease?) since the moment she came to this world. My daughter takes a good care of me and my diet including all the precausions, when I visit them and stay there for a week or so, she is a good cook, she knows all the stores around them with gluten-free foods. They are not rich, they are not poor either. My daughter doesn't want to here about being tested for celiac disease or getting the little one tested though she also knows it's hereditary. She knows everything, all the consequencies. And she does not want to really know about it though she is quite aware of how much I suffered. It's like she is scared to have to face the problem and deal with it. I don't know what to do with her.

This section of the board hasn't been visited for about 3 weeks. Where are you people? Any advice?

Connie R-E Apprentice

Yeah... Welcome to the club, Alexa. :(

It's much worse when it is your own family who won't do anything. With such a family history, it must be really frustrating for you. :angry:

Since I'm not doctor diagnosed, my family acts like it's not real.... I know a gluten-free diet would help them, too. I don't know what to do with them! I just keep trying to be heard...

Since your daughter can make gluten-free food for you, maybe you could visit more often? It does sound like she's scared (just changing one's diet is scary enough--besides all the other things associated with celiac disease to be worried about), but with repeated exposure of how she CAN cook gluten-free, maybe she'll gain confidence and at least get over some of her diet-changing fear? Then maybe the rest will fall into place. (Turn the big obsticles into smaller ones that can be acheived?)

I don't know...

I hope all the best for you.

Connie

  • 1 month later...
Guest Margawitty

My celiac girlfriend has an identical twin sister (split zygote) and her twin absolutely REFUSES to get tested for Celiacs. She goes through periods when shes fine and then through phases where she'll be calling Andrea (my girlfriend) early every morning saying her stomach hurts so bad and swears she'll try gluten-free but that only lasts like one day. Andrea and her family are constantly trying to sway Jennifer (the twin) to get gluten free but I think she just doesnt want to accept it. She has seen how much better Andrea is now but I think she is afraid to "know" that she has celiacs.

She has the same symptoms that Andrea used to have, they are not as severe but they are bad enough! I think that with some continued gentel pushing that at some point she'll try gluten free long enough to realize how much better she feels, at least that is what we all hope! We know we can't force her to do it!

debmidge Rising Star

I told my sister in law last week that I think she has celiac (her brother, my husband has it) and she told me that she'd rather be dead than have to eat gluten free. She's not denying she has it, she just doesn't want to have the bother of the special diet.

Maybe you can suggest to that mother that next time the baby gets a blood test??? they add the "gluten" test to it too just for safety's sake?

  • 6 months later...
lilliexx Contributor

give her some info, but then leave it at that!! you can not force anyone to do anything they do not want to do!!

i have two people in my life that i believe have celiac. One is my mother, and the other is a friend. i brought it up with my mom first and she just said " oh no...i dont have that trust me, i know" and then i talked to my friend. " he seemed the same way, but a few days ago he called me to say he had been gluten free since our conversation and was wanting some more info.

I believe if you are too pushy it will just make her mad. let her know what you think and that you will be there for support if she does decide to go gluten-free.

darlindeb25 Collaborator
;) we humans are so stubborn--i was telling a girl at work that her mom should get tested for celiacs--the mom has fibermyalgia and the daughter talks about how her mom has trouble with her meds and such, so i told her about celiacs--she went straight to her mom and told her--mom said, "could be true, but, i will live with the fibermyalgia before i will give up my food!" :rolleyes: yet, this same woman called her sister, who suffers also, and told her that she should get tested for celiacs--SOOOO, she believes me, but thinks gluten-free is too big a sacrifice <_< ---my own daughter is just as bad--she tells me she will never give up her pizza or chicken fingers and i tell her, she doesnt have too, she just has to learn to make them gluten-free------i would love to see a follow up on this mom and her kids at the beginning of this thread--i know as a mother, sometimes i feel so guilty for sharing diseases with my children :( , even though it is not my fault to begin with :unsure:

Archived

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

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

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





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - tiffanygosci replied to tiffanygosci's topic in Introduce Yourself / Share Stuff
      1

      Celiac support is hard to find

    2. - trents replied to mamaof7's topic in Parents, Friends and Loved Ones of Celiacs
      1

      Help understand results

    3. - mamaof7 posted a topic in Parents, Friends and Loved Ones of Celiacs
      1

      Help understand results

    4. - Dizzyma replied to Dizzyma's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      3

      Newly diagnosed mam to coeliac 11 year old

    5. - tiffanygosci posted a topic in Introduce Yourself / Share Stuff
      1

      Celiac support is hard to find

  • Celiac.com Sponsor (A19):
  • Member Statistics

    • Total Members
      132,955
    • Most Online (within 30 mins)
      7,748

    JodyBledsoe
    Newest Member
    JodyBledsoe
    Joined
  • Celiac.com Sponsor (A20):
  • Celiac.com Sponsor (A22):
  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Upcoming Events

  • Posts

    • tiffanygosci
      EDIT: I did find a monthly Zoom meeting for Celiacs through the Celiac Disease Foundation, so I'll be able to talk with some other people on January 15. And I also found a Celiac Living podcast on Spotify made by a celiac. I feel a little bit better now and I am still hoping I will find some more personal connections in my area.
    • trents
      Welcome to the celiac.com community, @mamaof7! It means for the one celiac disease antibody test that was ordered, she tested negative. However, other tests should have been ordered, especially for someone so young who would have an immature immune system where there would be a high probability of being IGA deficient.  The one test that was ordered was an IGA-based antibody test. It is not the only IGA antibody test for celiac disease that can be run. The most common one ordered by physicians is the TTG-IGA. Whenever IGA antibody tests are ordered, a "total IGA" test should be included to check for IGA deficiency. In the case of IGA deficiency, all other IGA tests results will be inaccurate. There is another category of celiac disease antibody tests that can be used in the case of IGA deficiency. They are known as IGG tests. I will attach an article that gives an overview of celiac disease antibody tests. All this to say, I would not trust the results of the testing you have had done and I would not rule out your daughter having celiac disease. I would seek further testing at some point but it would require your daughter to have been eating normal amounts of gluten for weeks/months in order for the testing to be valid. It is also possible she does not have celiac disease (aka, "gluten intolerance") but that she has NCGS (Non Celiac Gluten Sensitivity, or just "gluten sensitivity" for short) which is more common. The difference is that celiac disease is an autoimmune disorder that damages the lining of the small bowel whereas NCGS does not autoimmune in nature and does not damage the lining of the small bowel, though the two conditions share many of the same symptoms. We have testing to diagnose celiac disease but there are no tests for NCGS. To arrive at a diagnosis of NCGS, celiac disease must first be ruled out. A gluten free diet is the solution to both maladies.   
    • mamaof7
      For reference, daughter is 18 mths old. Was having painful severe constipation with pale stool and blood also bloating (tight extended belly.) Liver and gallbladder are normal. Ultrasound was normal. Dr ordered celiac blood test. We took her off gluten after blood draw. She is sleeping better, no longer bloated and stools are still off color but not painful.    "GLIADIN (DEAMID) AB, IGA FLU Value  0.84 Reference Range: 0.00-4.99 No further celiac disease serology testing to be performed. INTERPRETIVE INFORMATION: Deamidated Gliadin Peptide (DGP) Ab, IgA A positive deamidated gliadin (DGP) IgA antibody result is associated with celiac disease but is not to be used as an initial screening test due to its low specificity and only occasional positivity in celiac disease patients who are negative for tissue transglutaminase (tTG) IgA antibody."   Anyone know what in the world this means. She isn't scheduled to see GI until late April. 
    • Dizzyma
      Hi Trent and Cristiana, thank you so much for taking the time out to reply to me.  My daughters GP requested bloods, they came back as showing a possibility of celiac disease, she advised me to continue feeding gluten as normal and wait on a hospital appointment. When we got that the doctor was quite annoyed that the gp hadn’t advised to go gluten free immediately as she explained that her numbers were so high that celiac disease was fairly evident. That doctor advised to switch to a gluten-free diet immediately which we did but she also got her bloods taken again that day as it made sense to double check considering she was maintaining a normal diet and they came back with a result of 128. The hospital doctor was so confident of celiac disease that she didn’t bother with any further testing. Cristiana, thank you for the information on the coeliac UK site however I am in the Rrpublic of Ireland so I’ll have to try to link in with supports there. I appreciate your replies I guess I’ll figure things as we go I just feel so bad for her, her skin is so sore around her mouth  and it looks bad at an age when looks are becoming important. Also her anxiety is affecting her sleep so I may have to look into some kind of therapy to help as I don’t think I am enough to help. thanks once again, it’s great to be able to reach out xx   
    • tiffanygosci
      I have been feeling so lonely in this celiac disease journey (which I've only been on for over 4 months). I have one friend who is celiac, and she has been a great help to me. I got diagnosed at the beginning of October 2025, so I got hit with all the major food holidays. I think I navigated them well, but I did make a couple mistakes along the way regarding CC. I have been Googling "celiac support groups" for the last couple days and there is nothing in the Northern Illinois area. I might reach out to my GI and dietician, who are through NW Medicine, to see if there are any groups near me. I cannot join any social media groups because I deleted my FB and IG last year and I have no desire to have them back (although I almost made a FB because I'm desperate to connect with more celiacs). I'm glad I have this forum. I am praying God will lead me to more people to relate to. In my opinion, celiac disease is like the only food- related autoimmune disease and it's so isolating. Thanks for walking alongside of me! I'm glad I know how to help my body but it's still not easy to deal with.
×
×
  • 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.