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 Need Help


SammieMtz

Recommended Posts

SammieMtz Rookie

Hey all.... ive had celiac for about a year now and my family does absolutely nothing to support me. i really need support its hard doing this alone. almost everynight we have sumthing with gluten in it for dinner. ive tried the gluten-free diet a few times and its been successful for a few weeks but its like my family expects me 2 fail each and everytime. and I do. anyone else feel alone in this..? im scared and im not sure how 2 handle bein a celiac even after a year.


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



Celiac.com Sponsor (A8-M):



Lisa Mentor

I am sorry that you are having so much trouble. How old are you, are you living at home with your family.?

Dealing with Celiac is not always easy, but it will get better in time. Keep reading some of these posts and I am sure that it will be helpful to you.

There are alot of people here that are going through what you are, or have been. Sometimes it hard to get support from people around us, that why we have to be strong withing ourselves. My father, who died along time ago, used to say "What challenges us will make us stronger".

There is always alot of support here. So please stay with us, we all try to get through this disease together....and it just makes it a little easier. :)

Take care, Lisa B.

Lollie Enthusiast

I'm sorry your having such a hard time with your family. I know how it feels for your family to just sit back and hope you fail....my family took bets on how long I would make it at college! :angry: Luckily I won that bet! I finished! My point is that you have to go gluten-free for yourself, not for the family and with or without their support, even though that's hard, you have to think of your health! Do you help out with the shopping or cooking? That would be a great way to incorporate the diet, for you and the family!

This is a great way to get the support you don't get from the family! Just give us the word, we'll help you feel better, or at least try!

Hang in there you are not alone!!!!!!

-Lollie

Guest nini

gee, that is tough... one would hope that your family would be the FIRST in line to be supportive of you, but unfortunately that isn't always the case.

I agree, you have to do this for yourself, be strong within yourself and don't rely on your family to help you. All you can do is present them with as much research and evidence that with your DX you absolutely need to be on this diet and they absolutely should not try to sabotage you. You have to be convinced that you need to be on the diet. With a positive dx, if you do not stay on the diet you increase your risks of certain cancers and many other health issues.

If you are not responsible for any of the shopping or cooking in the house, you should start. Get foods that are naturally gluten free. Fresh fruits and vegetables, lean proteins, whole cheeses (if you can tolerate dairy) and safe carbs like rice and potatoes and corn... There is a whole world of food out there that is not expensive and easy to prepare and you do not have to buy specialty foods to do this. If you would like my collection of files of safe lists and menus and dining out suggestions, feel free to e-mail me at nisla@comcast.net and request my "newbie survival kit" it's a zip file download, so you need an unzip program to open it, but if you want it it's yours.

tiffjake Enthusiast

I am sooo sorry to hear about that. I don't live with my family, but when I am around them for the holidays, they just don't get it. So I do know what thats like. I agree with the above responses. You can control what is right infront of you. If they are having steak and potato for dinner, then you can have that, but what if they are having spaghetti (sp?)? Maybe you could suggest to your family or parents that you have some gluten free frozen dinners, like Amy's Kitchen, in the freezer for the meals that they will be eating without you, like a pasta dish. Or maybe you could make a salad on those nights, or something else that you know you can trust to be gluten free.I wish there was more that I could think of to help....that is a tough situation. But be strong. You are being healthy. And that is really great!! Keep up the great work!!

TCA Contributor

This group is sooo supportive. Everyone here has helped me learn about the diet and implement it with my kids. There are so many lists of things. If I could send you anything, please let me know. The diet is not nearly as hard as you might think once you get going on it. I wish your family were more supportive, but maybe they can be convinced. I'll pray for it!

SammieMtz Rookie

thank you alll very very much! and i am responsible for alot of the cooking/shopping altho i am only 16 and my mom basically says what im 2 prepare that night and alot of the times ill suggest certain things but then everyone else overrules me and then gets offended when i dont have what theyre having. im trying very hard and my boyfriend that im currently dating is very very supportive. and even when i have a sudden craving for sumthin i should not eat he makes sure i dont eat it. certainly this site....all the great pplz on it.. and my bf is what is helpin me thru. thanx all one again. ive tried explaining it to my family several times...they just dont get it. thank you tho... feels great that im not alone!


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



Celiac.com Sponsor (A8-M):



karisox Newbie

I feel so bad for you! Thankfully (i guess that sounds wierd) my mom has celiac too and was diagnosed years before me so it was easy for me to start the diet. Maybe if you take your parents with you to the doctor or explain to them if you don't stay on the diet you can die. Sometimes you need to spell it out for people so they understand how critical it is to stay gluten free. I am sure if you parents understand how important it is they will help more! As for food options, baked potatoes are always a good option. They take about 7 min to cook in the microwave and are quick and easy. I know im sick of them but its better than not eating! Good luck and I hope explaining your situation to your parents will help them be more supportive!

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,855
    • Most Online (within 30 mins)
      7,748

    Tara M
    Newest Member
    Tara M
    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

    • trents
    • 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.
×
×
  • 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.