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

Alone In My Struggles


PamelaB

Recommended Posts

PamelaB Newbie

I have been 5 weeks gluten free and it has been a struggle.  I also suffer with IBS-C and anemia due to the celiac but am currently receiving IV iron infusions to increase my levels.  My struggle is my spouse and his inability to grasp the severity of the situation.  Or maybe he has just become desensitized to hearing me say "I don't feel good" for so long that he doesn't get it.  I think he hopes that some time in the future I will be better and no longer have to adhere to a gluten free diet.  I feel like I am constantly debating with him about how I feel and that it is related to what I eat.  He doesn't seem to get that I don't feel well because of what I eat therefore I can't eat certain things anymore.  To be more specific, I am finding the longer I go gluten-free more food intolerances are rearing their ugly heads.  I am already lactose intolerant, have been for numerous years, but now seem to be corn intolerant and he just cannot and will not accept this.  Today I ate a gluten-free English muffin made out of corn flour and I am now down for the count...fatigued, body aches, nauseous.  And I have been noticing trouble with corn products but just wanted to ignore them.  How do I get him to understand that being Celiac can be more then just needing to be gluten free, but a whole host of other things can come into play?  Thinking of going to an allergist to have a blood test for food allergies done because he only seems to believe it if I have medical proof.  How I am feeling does not matter.  Feeling all alone.


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



Celiac.com Sponsor (A8-M):



Celiac Mindwarp Community Regular

Sorry you are having a tough time.

I found a number of other intolerances surfaced once I went gluten-free. I am NCGI, but still need to do gluten-free for life.

I did an elimination diet and kept a food diary to work out the intolerances.

I am wondering why your husband is unhappy for you to be altering your diet, if it keeps you healthier. Is he concerned that you won't prepare for for him, or that it will be harder to eat out?

I am lucky that my family is supportive, but even they get sick of me talking about what I do and don't eat. I now try and quietly get on with sorting my own food out, and come here to talk to people who understand.

I hope we can offer some support. You will be gluten-free for life now, and while the adjustment can be tricky, it starts to become normal in a few months or so.

The biggest convincer for my family was the massive improvement in my health. Maybe that will convince your husband it is all worth it.

Welcome to the board, ask lots of questions, come and vent if you need to :)

notme Experienced

poor baby ;(  so sorry - it sure does suck and i know where you're coming from.  i was so sick of saying, "i'm so sick" that when this finally got diagnosed, he was happy to put a name on it.  then he could fight it.  maybe he would see it from that angle?

 

 i had to skip dairy for awhile (but was able to add it back) and soy is still a problem <boy, if you think gluten is in every dad gum thing! soy is maybe more so lolz)  

 

but here's the kicker:  i am soooooo much better.  i FEEL better, all over, and i am more of myself again.  stick to your (dietary) guns, refine the way you need to eat (and every one is different)  and hopefully he will see the difference.  you're struggling now, no doubt, but it pays off.  good luck and if you hang around here, you are bound to get pointers and whatnot.  at least here it's ok to rant/vent - we have all been there   :blink: welcome to the club you never wanted to join.............. <_<   

IssuesWithLife Newbie

Aw,I'm sorry.It really sucks when other people don't get it.I found out I had celiac when I was 10,so it's been 9 years.I've been having issues with other foods recently and it is quite frustrating!One of the reasons why it is,is cause my mom thinks certain foods are fine for all celiacs and certain ones are not and doesn't like to listen if one of the "bad" foods doesn't make me sick and one of the "good" foods does.

But it's not unusual at all for people with celiac to not be able to handle corn,I have found out.Also soy,dairy and eggs tend to be the big ones,but it can vary wildly from person to person.

Maybe if you can find blogs and articles online where other people are like you and show it to him it would make a difference?

1desperateladysaved Proficient

I experienced the same difficulties just about a year ago.  My weakness caused me and my family great struggles.  I was nearly dying, he was inviting a family of 12 for dinner.  He just didn't get it.

 

Now, he says that clearly I do have a gluten problem.  He has seen profound improvements in the last 9 months.  Things are not perfect, but they are getting better with my energy levels coming up.

 

You do have to look after your own health.  I mean, if you can't eat corn don't eat it.  I have been trying to come to grips with allowing people to look down on me and not fretting.  This is hard to do, but if one can manage it they should be happier, I think.

 

My husband has all of the energy he wants.  How on earth can he understand analyzing carefully how to plan my day, so as not to totally exhaust my self by 9 am?

 

I am not sure if the situation were reversed if I could believe some of the claims I make!

 

D

dilettantesteph Collaborator

I remember feeling like you do.  I think that it made things worse when I went to support group meetings and saw all the other celiacs there with their spouses.  Both parents were there when it was their children.  In our case it was me and our child and still my spouse showed no interest.  Despite the diagnosis being direct from the doctor, my husband wouldn't believe it.  This was especially so when we didn't get all the way better immediately.  

 

In our case it was issues with gluten cross contamination rather than other food intolerances that caused our problems, but it took awhile to figure that out.  The food/symptom journal really helps in either case.  In case it is gluten cc, it is important to keep track of source of the food as well as the ingredients.  6 years later my spouse is more supportive.   Give you husband some more time.  He is probably in denial.  Things will probably get better.

PamelaB Newbie

I can't thank all of you enough for your kind words of support. Like you said as my husband sees me getting better then maybe his support will grow. I have to admit it is still hard for me to wrap my head around the fact that this is for life. Nothing feels in my control anymore. As I gain a sense of control back and a routine to shopping, cooking and eating, I am hoping that things will get better for the household. Right now is an awful learning curve. And yes, getting him to understand the cross contamination issue is huge. Was thinking today that I might give him his own dedicated counter space in the kitchen, since he doesn't clean up after himself. Anyways thank you again for allowing me to just vent and think out loud.


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



Celiac.com Sponsor (A8-M):



Celiac Mindwarp Community Regular

My husband and kids have their own counter space now. We also have separate utensils, so all of mine are purple and easy to spot! I have a purple toaster, breadbin etc. too, and pink dishcloths. We use a lot of foil on the grill, and paper towels for wiping down. If I have to clear breadcrumbs for example, I use a wet paper towel and throw away, then wash my hands.

 

We tend to try and cook 'naturally' gluten-free a lot, so dishes based on potatoes, rice, rice noodles, sweet potaoes for example which helps everyone I think.

 

I know it seems overwhelming at first, but it is surprising how quickly it sinks in. We have some good food ideas (and a lot of chat!!) over on the What's for Dinner thread, if you are looking out for food ideas (and good company ;) ).

 

Keep reading and asking questions, there are loads of good ideas around

 

Mw

notme Experienced

I can't  And yes, getting him to understand the cross contamination issue is huge. Was thinking today that I might give him his own dedicated counter space in the kitchen, since he doesn't clean up after himself. Anyways thank you again for allowing me to just vent and think out loud.

lolz - i have visions of me leaping across the kitchen just as he is about to use the Same Tongs - like i was diving on a grenade.  that was a tough one - i think i ended up explaining it in NCIS abby's lab terms <he loves that show and the guy who plays mike franks has a house nearby)  explaining plastic containers and cc is ridiculously ridiculous - one of my friends is always showing me:  look!  no stainless steel is touching plastic......................  um...................  ok........................?   it'll get easier - even my kids and grandkids are pretty savvy once they understood the concept ^_^  

tommysmommy Newbie

Navigating the whole gluten-free/food intolerance world is hard, getting others to understand it is torture. My suggestion, accept that to him - this whole food thing seemss ridiculous & try not talk about it for a few Weeks. During this time stick to a very simple diet - fresh fruit, vegis, chicken, rice (no corn or dairy)... eat very plain foods but eat lots of them plus gluten-free vitamins & probiotics. Betcha you'll feel different & he'll witness the transformation. Sometimes you have to see it to believe it. My family went gluten-free when my son was dx celiac & in a very short amount of time - we all started changing dramatically. I wouldn't have believed it if I hadn't lived it. Good luck!

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. - Mari replied to tiffanygosci's topic in Coping with Celiac Disease
      10

      New Celiac Mama in My 30s

    2. - tiffanygosci posted a topic in Gluten-Free Foods, Products, Shopping & Medications
      0

      Aldi Pueblo Lindo Yellow Corn Tortillas

    3. - tiffanygosci replied to tiffanygosci's topic in Coping with Celiac Disease
      10

      New Celiac Mama in My 30s

    4. - trents replied to tiffanygosci's topic in Coping with Celiac Disease
      10

      New Celiac Mama in My 30s

    5. - Mari replied to tiffanygosci's topic in Coping with Celiac Disease
      10

      New Celiac Mama in My 30s


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,978
    • Most Online (within 30 mins)
      7,748

    Beverley Blanchard
    Newest Member
    Beverley Blanchard
    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

    • Mari
      There is much helpful 'truth' posted on this forum. Truths about Celiac Disease are based on scientific research and people's experience. Celiac disease is inherited. There are 2 main Celiac 'genes' but they are variations of one gene called HLa - DQ What is inherited when a person inherits one or both of the DQ2 or the DQ8 is a predisposition to develop celiac disease after exposure to a environmental trigger. These 2 versions of the DQ gene are useful in diagnosing  celiac disease but there are about 25 other genes that are known to influence celiac disease so this food intolerance is a multigenic autoimmune disease. So with so many genes involved and each person inheriting a different array of these other genes one person's symptoms may be different than another's symptoms.  so many of these other genes.  I don't think that much research on these other genes as yet. So first I wrote something that seem to tie together celiac disease and migraines.  Then you posted that you had migraines and since you went gluten free they only come back when you are glutened. Then Scott showed an article that reported no connection between migraines and celiac disease, Then Trents wrote that it was possible that celiacs had more migraines  and some believed there was a causal effect. You are each telling the truth as you know it or experienced it.   
    • tiffanygosci
      Another annoying thing about trying to figure this Celiac life out is reading all of the labels and considering every choice. I shop at Aldi every week and have been for years. I was just officially diagnosed Celiac a couple weeks ago this October after my endoscopy. I've been encouraged by my local Aldi in that they have a lot of gluten free products and clearly labeled foods. I usually buy Milagro corn tortillas because they are cheap and are certified. However, I bought a package of Aldi's Pueblo Lindo Yellow Corn Tortillas without looking too closely (I was assuming they were fine... assuming never gets us anywhere good lol) it doesn't list any wheat products and doesn't say it was processed in a facility with wheat. It has a label that it's lactose free (hello, what?? When has dairy ever been in a tortilla?) Just, ugh. If they can add that label then why can't they just say something is gluten free or not? I did eat some of the tortillas and didn't notice any symptoms but I'm just not sure if it's safe. So I'll probably have to let my family eat them and stick with Milagro. There is way too much uncertainty with this but I guess you just have to stick with the clearly labeled products? I am still learning!
    • tiffanygosci
      Thank you all for sharing your experiences! And I am very thankful for that Thanksgiving article, Scott! I will look into it more as I plan my little dinner to bring with on the Holiday I'm also glad a lot of research has been done for Celiac. There's still a lot to learn and discover. And everyone has different symptoms. For me, I get a bad headache right away after eating gluten. Reoccurring migraines and visual disturbances were actually what got my PCP to order a Celiac Panel. I'm glad he did! I feel like when the inflammation hits my body it targets my head, gut, and lower back. I'm still figuring things out but that's what I've noticed after eating gluten! I have been eating gluten-free for almost two months now and haven't had such severe symptoms. I ate a couple accidents along the way but I'm doing a lot better
    • trents
      @Mari, did you read that second article that Scott linked? It is the most recently date one. "Researchers comparing rates of headaches, including migraines, among celiac patients and a healthy control group showed that celiac subjects experienced higher rates of headaches than control subjects, with the greatest rates of migraines found in celiac women.  Additionally, celiacs had higher rates of migraine than control subjects, especially in women. In fact, four out of five women with celiac disease suffered from migraines, and without aura nearly three-quarters of the time."
    • Mari
      As far as I know and I have made severalonline searches, celiac disease disease has not been recognized as a cause of migraines or any eye problems. What I wrote must have been confusing.
×
×
  • 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.