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.


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,544
    • Most Online (within 30 mins)
      7,748

    Jem68
    Newest Member
    Jem68
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.4k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Beverage
      I had a very rough month after diagnosis. No exaggeration, lost so much inflammatory weight, I looked like a bag of bones, underneath i had been literally starving to death. I did start feeling noticeably better after a month of very strict control of my kitchen and home. What are you eating for breakfast and lunch? I ignored my doc and ate oats, yes they were gluten free, but some brands are at the higher end of gluten free. Lots of celics can eat Bob's Red Mill gluten-free oats, but not me. I can now eat them, but they have to be grown and processed according to the "purity protocol" methods. I mail order them, Montana Gluten-Free brand. A food and symptoms and activities log can be helpful in tracking down issues. You might be totally aware, but I have to mention about the risk of airborne gluten. As the doc that diagnosed me warned . . Remember eyes, ears, nose, and mouth all lead to your stomach and intestines.  Are you getting any cross contamination? Airborne gluten? Any pets eating gluten (they eat it, lick themselves, you pet them...)? Any house remodeling? We live in an older home, always fixing something. I've gotten glutened from the dust from cutting into plaster walls, possibly also plywood (glues). The suggestions by many here on vitamin supplements also really helped me. I had some lingering allergies and asthma, which are now 99% gone. I was taking Albuterol inhaler every hour just to breathe, but thiamine in form of benfotiamine kicked that down to 1-2 times a day within a few days of starting it. Also, since cutting out inflammatory seed oils (canola, sunflower, grapeseed, etc) and cooking with real olive oil, avocado oil, ghee, and coconut oil, I have noticed even greater improvement overall and haven't used the inhaler in months! It takes time to weed out everything in your life that contains gluten, and it takes awhile to heal and rebuild your health. At first it's mentally exhausting, overwhelming, even obsessive, but it gets better and second nature.
    • Jsingh
      Hi,  I care for my seven year old daughter with Celiac. After watching her for months, I have figured out that she has problem with two kinds of fats- animal fat and cooking oils. It basically makes her intestine sore enough that she feels spasms when she is upset. It only happens on days when she has eaten more fat than her usual every day diet. (Her usual diet has chia seeds, flaxseeds, and avocado/ pumpkin seeds for fat and an occasional chicken breast.) I stopped using cooking oils last year, and when I reintroduced eggs and dairy, both of which I had held off for a few months thinking it was an issue of the protein like some Celiac patients habe mentioned to be the case, she has reacted in the same fashion as she does with excess fats. So now I wonder if her reaction to dairy and eggs is not really because of protein but fat.   I don't really have a question, just wondering if anyone finds this familiar and if it gets better with time.  Thank you. 
    • Chanda Richard
      Hello, My name is Chanda and you are not the only one that gose through the same things. I have found that what's easiest for me is finding a few meals each week that last. I have such severe reactions to gluten that it shuts my entire body down. I struggle everyday with i can't eat enough it feels like, when I eat more I lose more weight. Make sure that you look at medication, vitamins and shampoo and conditioner also. They have different things that are less expensive at Walmart. 
    • petitojou
      Thank you so much! I saw some tips around the forum to make a food diary and now that I know that the community also struggles with corn, egg and soy, the puzzle pieces came together! Just yesterday I tried eating eggs and yes, he’s guilty and charged. Those there are my 3 combo nausea troublemakers. I’m going to adjust my diet ☺️ Also thank you for the information about MCAS! I’m from South America and little it’s talked about it in here. It’s honestly such a game changer now for treatment and recovery. I know I’m free from SIBO and Candida since I’ve been tested for it, but I’m still going to make a endoscopy to test for H. Pylori and Eosinophilic esophagitis (EoE). Thank you again!! Have a blessed weekend 🤍
    • knitty kitty
      Yes, I, too, have osteoporosis from years of malabsorption, too.  Thiamine and magnesium are what keep the calcium in place in the bones.  If one is low in magnesium, boron, selenium, zinc, copper, and other trace minerals, ones bone heath can suffer.  We need more than just calcium and Vitamin D for strong bones.  Riboflavin B 2, Folate B 9 and Pyridoxine B 6 also contribute to bone formation and strength.   Have you had your thyroid checked?  The thyroid is important to bone health as well.  The thyroid uses lots of thiamine, so a poorly functioning thyroid will affect bone heath.  
×
×
  • 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.