Jump to content
This site uses cookies. Continued use is acceptance of our Terms of Use and Privacy Policy. More Info... ×
  • 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

Greetings From Scotland


Evonneda

Recommended Posts

Evonneda Newbie

Hi all

Just thought I'd introduce myself as a new user to this forum and say hello from Bonnie Scotland (although not so bonnie at the moment - it's raining !)

Anyway - I have been diagnosed as Coeliac 3 years in Sept :angry: and I suppose I should be an expert by now but ;) ............... can anyone else help me on gaining some more willpower to maintain a gluten-free diet? I am better and do try to cut out gluten-free foods but if something takes my fancy I will eat it regardless! I find it so hard to stick to gluten-free food as I love all the things that I can't eat and it's the whole wanting something you can't have!

Does anyone have any advice on how they managed to overcome a severe lack of willpower? I am really suffering now with all the horrible symptoms and I do need to get a grip as I do know the complications that come with celiac disease.

Any tips?

Thanks in advance :D


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



Celiac.com Sponsor (A8-M):



Guest gfinnebraska

Hi & Welcome!

I never had any issues with willpower due to one fact: When finding out I had celiac disease, I was told to treat gluten like rat poison. Would you PURPOSELY put rat poison in your body??!! NO, of course not!! So, why would you put gluten in your body when you know it can kill you?? That thought alone has kept me on the straight and narrow!! :D I do not, will not, have never intentionally put gluten in my mouth since that day. No one can "help" you have willpower. That has to come from within and your desire to do what is best for your body. This board is a cornucopia of advice ~ everything you need to live a gluten-free life is here!! Whine, complain, get help, etc. -> we are here for you!!!!

Good luck!! :)

jenvan Collaborator

For me isn't wasn't so hard either--The idea of intestinal cancers with a very slim chance of recovery were enough to make me steer clear. It makes me fearful of accidental or intestinal glutening ! I'm sure some others will have ideas though... I have also found a host of gluten-free foods I love and find it frustrating mostly only when I venture out to restaurants...

tarnalberry Community Regular

There's nothing for it but to practice the willpower. Of course, I would encourage you to get rid of non-gluten-free items in your household if at all possible to reduce your tempation. You know the risks, so I would also encourage you to figure out why you mentally allow yourself to poison yourself. (We all do self-destructive things, the question is why... Often a different answer for each of us.)

I'm certain you have the willpower inside you, and whether it's a matter of exercising it, knocking down any barriers to it, or just locating it, I'm sure you can get there. I know it can be hard, and there are any number of tricks (like avoiding temptation, finding alternatives, diverting your attention onto other activities, etc.) you can use to get you there, but I'm certain you can do it.

Canadian Karen Community Regular

Google up "refractory celiac disease" or "refractory sprue" and read up on it. It certainly was the deciding factor for me to take this disease much more seriously than I was at the beginning......

Oh, by the way, welcome to the board! There's a great bunch of people here for support!

Take care,

Karen

happygirl Collaborator

Whenever I am tempted to eat something (although I think I am starting to forget what wheat tasted like!) I think to myself something along the lines of "Is it more important for me to eat this cake/cookie/bread/pasta/possible gluten food, or is it more important for me to have a happy, healthy life." It puts it in perspective for me real fast! I also have very severe symptoms very quickly, so for me its not the willpower issue, but more of not wanting to feel sick and crappy for days.

cmom Contributor

For me, it was being sick 9 days in a row about 4 summers ago. At that moment, I realized I must take the celiac seriously and commit myself to it. I had suffered problems for several years but it took finally getting sick of being sick to make me strong. I also try to tell myself, "it's just food; don't let it control you." :o


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



Celiac.com Sponsor (A8-M):



Guest zipy

Hmmm...well, for me my reaction to it is so violent and so rapid that I've no desire to eat anything that could cause that reaction. I have put things in the house that I like/want to eat, though...I've stocked up on M&Ms candies, gluten-free icecream, chips and dip, I made gluten-free brownies and intend to make tons of cookies in the next few weeks. That way if I see something that I'd like, I can just pull out my own stuff and eat it instead. Substituting instead of just not eating what you'd like to eat normally. Or try to find what it is you see that you'd like to eat at a store online that sells gluten-free stuff...just keep it around. Don't know if this helps...I'm recently diagnosed, you've known about it for 3 years! I could be singing a different story when my 3 year anniversary comes around!

Good luck!

~zipy

Evonneda Newbie

Hi all

Thanks everyone for their advice and support. :) I am so pleased I have found this forum as I don't know anyone else with celiac disease and feel a bit alone at times when it comes to the diet which is probably why I don't stick to it. :rolleyes: I appreciate your time and posts. I do struggle keeping a gluten-free kitchen though as my partner is not gluten-free and I would find it quite unfair to make him stick to a gluten-free diet. However, enough of the excuses I hear you say and look after yourself, which is what I am going to definately do after hearing about your various experiences. Anyway I will take time to read through the forum as I am sure many of you have posted regarding partner support, recipies, etc. etc.

Speak to you all soon :D

Bonnie Explorer

Hi Evonneda,

I am SCOTTISH too although I am living in South Africa at the moment! Got all excited to see another Scottish person with my problems.

I also don't know a single person with celiac disease.

It must be really difficult for you over there as the eating habits in Scotland are incredibly unhealthy. I struggled to eat healthily at all when I was there last.

But you really have to persevere as you cannot possibly feel as well as you should until you give up gluten completely.

Good luck - you are making me homesick!!

Yvonne

Guest nini

Whenever I am tempted by anything, I just repeat a mantra over and over in my head "this is poison for my body, I will not eat it, this is poison for my body I will not eat it" After all, none of us willingly put poison into our mouths, you just have to get the same mindset when it comes to gluten containing foods. That and having a good support network (this board :D ) will get you through!

Evonneda Newbie

Thanks Yvonne - two E/Yvonnes' and both from Scotland with Coeliac Disease !

We are very unhealthy us Scots and it is difficult but I am sure we all find it difficult at times no matter where we are. I feel so much positive about my illness having discovered this forum so thanks again to all. :D

Evonne

Hi Evonneda,

I am SCOTTISH too although I am living in South Africa at the moment!  Got all excited to see another Scottish person with my problems.

I also don't know a single person with celiac disease.

It must be really difficult for you over there as the eating habits in Scotland are incredibly unhealthy.  I struggled to eat healthily at all when I was there last.

But you really have to persevere as you cannot possibly feel as well as you should until you give up gluten completely.

Good luck - you are making me homesick!!

Yvonne

<{POST_SNAPBACK}>

Guest BellyTimber

Hello from a Sassenach!

For me grappling with this same situation after almost 3 years is a matter of experience.

I have an intellectualmemory,a motor memory, sensory memory & so on and they are gradually being educated to get in stepwith each other.

"I will survive"

"Every day, and in every way, I am getting better, and better, and better"

My home computer broke down & they all thought I was caught upin the explosions & sent upa great wall of good wishes & prayers and I have been helped in this very area, of learning how to practice my diet right, during this period and also I have an OT coming soon to help me with the practicalities of that.

Also make sure you don't miss the "International" section of the forum for issues that are UK specific like shopping, restaurants etc etc!

tarnalberry Community Regular
I do struggle keeping a gluten-free kitchen though as my partner is not gluten-free and I would find it quite unfair to make him stick to a gluten-free diet. 

<{POST_SNAPBACK}>

There's a compromise in the middle, where the food that you share (breakfasts/lunchs/dinners you have together) are gluten-free - no need to cook separate meals and be tempted by foods you can't have WHILE you're eating at home (which, above all others, should be a safe place). Foods you'd eat separately, snacks and times when you might eat meals not at the same time, can be a mix. In our house, my husband has his wheaty bread, crackers, and cereal, but it's a smaller portion of what's in the house, and kept in it's own place, so I don't have to search through a bunch of things I'd like to eat, but can't, to find things I can eat, but might not want to as much. Of course, it helps to keep the food to a more simple set of whole foods that are naturally gluten-free - lots of fresh/frozen veggies/produce and meats (and dairy if you can have it). (As always, this is just a way that I find easy, there are so many approaches to dealing with the diet, we all have to find what works best for us. In your case, it seems that what you're doing isn't working, so it's a matter of finding which *other* way works for you. Good luck!! :-) )

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,184
    • Most Online (within 30 mins)
      7,748

    Valerie Mink
    Newest Member
    Valerie Mink
    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

    • Kris2093u4
      Geography makes a difference.  I'm in the West and Trader Joe's gluten-free bread tastes great and is a better price than most gluten-free breads sold elsewhere in my area.  
    • JForman
      We have four children (7-14 yo), and our 7 year old was diagnosed with NCGS (though all Celiac labs were positive, her scope at 4 years old was negative so docs in the US won't call it celiac). We have started her on a Gluten Free diet after 3 years of major digestive issues and ruling out just about everything under the sun. Our home and kitchen and myself are all gluten-free. But I have not asked my husband/her dad or her other siblings to go completely gluten-free with us. They are at home, but not out of the home. This has led to situations when we are eating out where she has to consistently see others eating things she can't have and she has begun to say "Well, I can't have <fill in the blank>...stupid gluten."  How have you supported your gluten-free kiddos in the mental health space of this journey, especially young ones like her. I know it's hard for me as an adult sometimes to miss out, so I can't imagine being 7 and dealing with it! Any tips or ideas to help with this? 
    • Jane878
      By the time I was 5 I had my first auto0immune disorder, Migraine headaches, with auras to blind me, and vomiting, sensitivity to light and sound. I was 5 years old, and my stepfather would have pizza night, milling his own flour, making thick cheesy gluten pizza, that I would eat and the next day, I would have serious migraines, and my mother & stepfather did nothing about my medical problems. When I was 17 in my first year at college, I was diagnosed with my 2nd known auto-immune disorder, Meniere's disease. I was a elite athlete, a swimmer, and soccer player. And once again my parents didn't think anything of understanding why I had a disorder only older people get. Now after my mother passed from Alzheimer's disease she also suffered with living with gluten. She had a rash for 30 years that nobody could diagnose. She was itchy for 45 years total. My brother had a encapsulated virus explodes in his spleen and when this happened his entire intestines were covered with adhesions, scar tissue and he almost lost his life. He has 5 daughters, and when I finally was diagnosed after being pregnant and my body went into a cytokine storm, I lost my chance to have children, I ended up having Hashimoto's disease, Degenerative Disc disease, and my body started to shut down during my first trimester. I am 6ft tall and got down to 119lbs. My husband and I went to a special immunologist in Terrace, California. They took 17 vials of blood as we flew there for a day and returned home that evening. In 3 weeks, we had the answer, I have Celiac disease. Once this was known, only my father and husband made efforts to change their way of feeding me. At the family cabin, my stepfather & mother were more worried that I would ruin Thanksgiving Dinner. It wasn't until one of my cousins was diagnosed with Celiac disease. They finally looked into getting Gluten Free flour and taking measures to limit "gluten" in meals. He did nothing but ask for me to pay for my own food and wi-fi when I came to the cabin to stay after our house burned down. When he informed my mother, they proceeding to get into a physical fight and she ended up with a black eye. The is just more trauma for me. Sam had no interest in telling the truth about what he wanted. He lied to my mother that he had asked my husband if I could pay for "food" when he asked Geoffrey if I had money to pay for my wi-fi. My mother hates when he spends so much time on the computer so he lied and said I could pay for my own food. I will remind you I weighed 119lbs at this time. (At 6ft) that is a very sick looking person. Neither parent was worried about my weight, they just fought about how cheap my stepfather was. As my mother was diagnosed with Alzheimer's disease in 2014. He had her sign over the will to a trust and added his children. He had no testimonial capacity at the time, so she signed without proper papers. Making this Trust null and void. When I gave my brother my childhood home, my mother stated I would be getting an equal part of inheritance to the house on Race. It currently worth 2.0 million $. I got nothing, and my stepfather has since disowned me b/c of my claim and he knows that my mother would never have left it uneven between my biological brother and myself. She sat me and my husband down, as we lived at the Race Street house and treated and took care of it as our own. My brother took over b/c he was going through a horrific divorce and needed a home so he could get a better custody deal with his soon to be ex-wife who was a Assist DA for Denver. She used the girls against him, and he & I were the primary caregivers. We, Judd and I spent the most time with them pre the divorce. Once Judd moved into the house, he threw all of my mother, grandmother and my family heirlooms out to the Goodwill. Nobody told my mother about this as she was going through cancer treatment and had Alzheimer's disease in her mother and her sister. My stepfather and biological brother took advantage of this matter, as I called a "family council" that my brother just never could make it to at the last moment. All of the furnishing, kitchen ware, everything was in the house my brother just moved into. He had had 2 weddings, I chose to elope b/c my stepfather ruined my brother's first wedding by talking about his relationship with my brother in front of my dad and his entire family, insulting him and having my grandfather leave the ceremony. It was a disaster. My stepfather just plays dumb and blames my father for the slight. I was the only child not to have a wedding. So, my mother and stepfather never had to pay for a thing. My mother had had an agreement with my father he'd pay for college and all medical issues with their kids, myself and Judd. So truly my mother never had to pay for anything big for me in her entire life. I am looking for anyone that has had a similar story, where they grew up in a household that had a baker that regularly milled flour and ate gluten. What happened to you? DId you suffer from different auto-immune diseases b/c of living with a baker using "gluten" Please let me know. I have been looking into legal ways to get my stepfather to give me what my mother had promised, and he erased. Thank you for listening to my story. Jane Donnelly  
    • trents
      Possibly gluten withdrawal. Lot's of info on the internet about it. Somewhat controversial but apparently gluten plugs into the same neuro sensors as opiates do and some people get a similar type withdrawal as they do when quitting opiates. Another issue is that gluten-free facsimile flours are not fortified with vitamins and minerals as is wheat flour (in the U.S. at least) so when the switch is made to gluten-free facsimile foods, especially if a lot of processed gluten-free foods are being used as substitutes, vitamin and mineral deficiencies can result. There is also the possibility that she has picked up a virus or some but that is totally unrelated to going gluten-free.
    • Sheila mellors
      I asked about the new fruit and nut one and the Dietician said yes I could eat it safely. Hooe this helps
×
×
  • Create New...