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

How Do I Get My Mother To Understand


fujiwabbit

Recommended Posts

fujiwabbit Rookie

Im having a really hard time getting my mother to fully understand how careful one needs to be. About 7yrs ago she was told by a GI that she had an allergy to gluten (with no tests done) and that after her intestine healed she would be able to tolerate some amounts of flour. She eats doughnuts every day.... doesnt watch what she eats and has no reaction, that she's aware of. SO now that ive been diagnosed and she thinks that after awhile i'll be fine and able to tolerate food like her. As well she thinks im being paranoid and that cross contamination isnt a problem (Like frying stuff in the same oil that flour was fryed in) I've tried to explain things to her..and her only responses to me are 'well if u lose anymore weight i'm making you go to the hospital...you have to eat...i have it too, i understand... ure over reacting. ANy suggestions on how i can get her to see that i am different than her (as i can touch flour and get an outbreak on my hands) and that after being off gluten until your body heals doesnt mean that you can start tolerating flour again...?? im at a loss, i've tried to explain things, i've tried directing her to websites, ive tried cutting and pasting basic information and emailing it to her, and i've tried to get her to read on this forum. it has all obviously been a waste of time. she also doesnt hold much faith in the internet and thinks that the info i get off of here is questionable and unless a doctors says it..its not true. (when in truth i think ppl on here kno more than any doctor i've ever seen) Any one else have a mother like this? or any suggests on how get her to understand or jus be able to deal with her inablity to understand??


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



Celiac.com Sponsor (A8-M):



Rusla Enthusiast

An allergy to gluten is NOT Celiac disease. I was told many years ago that I had a wheat allergy (confirmed by tests). I figured as long as it didn't cause me total adverse effects I could live with it then I would continue. When I got diagnosed with this, it was totally different. My sister was the one who impressed upon me to have the tests and told me about what happened to friends of hers.

Maybe if she makes you go to the hospital, one can hope that someone there knows the difference and can drill it into her head. If there is any medication that she is on to sustain life then you need to do what I did with my mother. My mother is on blood thinners Cumodan (sp?). When she declared that "a little bit won't hurt you." I told her that I will have a little bit if she gives up her cumodan for a week. Because if a little bit won't hurt me then being without her meds won't hurt her. She got it and went totally on board especially when it came to Yule dinner. She told me I would have to make the gravy and dressing so I would not get contaminated.

You could also ask your mother if she would drink poison everyday, because she is asking you to kill yourself. If she still doesn't get it you may have to do tough love and tell her that you thought she loved you but what she is trying to do is contrary to that.

jerseyangel Proficient

You know, you can't change someone else--but you can change your response to them. Your mom believes that she is fine now and since she feels well, sees no need to follow the diet. She was never tested--so either she is intolerant or Celiac but has no symptoms, or she isn't. Since you've been Dx, you know how inportant it is to be 100% gluten-free. Do you live with her? Either way, I would prepare my own food and if you share a kitchen, it's up to you to keep a section clean for yourself. It sounds to me like you've done everything you can to convince her--now I would focus on doing what you have to do to keep yourself healthy. Perhaps when she sees your efforts paying off--your skin improving, you feeling better, etc., she will come around. But for now, I don't think she wants to see the truth. :(

Guest nini
You know, you can't change someone else--but you can change your response to them. Your mom believes that she is fine now and since she feels well, sees no need to follow the diet. She was never tested--so either she is intolerant or Celiac but has no symptoms, or she isn't. Since you've been Dx, you know how inportant it is to be 100% gluten-free. Do you live with her? Either way, I would prepare my own food and if you share a kitchen, it's up to you to keep a section clean for yourself. It sounds to me like you've done everything you can to convince her--now I would focus on doing what you have to do to keep yourself healthy. Perhaps when she sees your efforts paying off--your skin improving, you feeling better, etc., she will come around. But for now, I don't think she wants to see the truth. :(

This is EXACTLY what I was going to say!

My mother hasn't been dx'ed, but she did really well on the low carb/atkins diet several years ago. As soon as she added gluten back into her diet she gained the weight back and started getting C again... She refuses to consider changing her diet and refuses to be tested. I've done all I can do. Unfortunately my sister (who also has symptoms) also believes my mom's version of things and refuses to get tested.

tiredofdoctors Enthusiast

Can't change them, only you . . . I do the same thing -- make my stuff, then take it wherever I need to take it! I will say, though, my husband is having a really difficult time with this -- with my family and his. Birthdays are BIG at our house -- but since I've been diagnosed, I haven't been able to participate in the cake and ice cream. I had to bake my own brownies one time, and no one would turn the oven on for me (I'm a little "inconvenienced" in the wheelchair). My husband has decided that for MY birthday, we're telling the family that he's taking care of the cake & ice cream. Then, when it comes time for the birthday part, we won't have anything. When they ask where the cake is, we're going to tell them that we're having the cake and ice cream that I have at EVERY birthday -- and so are they. Passive-Aggressive? Definitely. But sometimes you have to stun them before they "get it". . . . Good luck with your mom . . . .Lynne

Guest nini
Can't change them, only you . . . I do the same thing -- make my stuff, then take it wherever I need to take it! I will say, though, my husband is having a really difficult time with this -- with my family and his. Birthdays are BIG at our house -- but since I've been diagnosed, I haven't been able to participate in the cake and ice cream. I had to bake my own brownies one time, and no one would turn the oven on for me (I'm a little "inconvenienced" in the wheelchair). My husband has decided that for MY birthday, we're telling the family that he's taking care of the cake & ice cream. Then, when it comes time for the birthday part, we won't have anything. When they ask where the cake is, we're going to tell them that we're having the cake and ice cream that I have at EVERY birthday -- and so are they. Passive-Aggressive? Definitely. But sometimes you have to stun them before they "get it". . . . Good luck with your mom . . . .Lynne

I hate to say it, but I love that... yes it's passive aggressive, but I agree, sometimes shocking them into a reality check is a good thing.

ianm Apprentice

Some people are just completely incapable of wrapping their brain around a food intolerance. My ex-wife was and still is that way. My life has changed very dramatically since we divorced and I gave up gluten and she still just can't make the connection. You may never be able to get mom to get it but you will have to stand your ground on this one.


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



Celiac.com Sponsor (A8-M):



marciab Enthusiast

So many people assume everyone's symptoms will be the same as theirs. When I hear that, I remind people about that Norwalk virus that hit that cruise ship a couple of years ago. Some people only got slightly nauseas and others had to air lifted off the ship ......

For me, I am happiest when I am calm, so I have learned to do what is right for me and forget about what others are thinking. I used to tell my mom when I was younger and she got in my way "You do things your way and I'll do things mine" . She got indignant, but she also got the point. Years later, she repeated that to me verbatim as she got older and I wanted her to do things my way. We'd just laugh.

Good luck marcia

Guest nini

I was talking to my mom today about this again (why do I bother?) and I'd mention certain foods and she'd say, "oh I don't eat those anyway, they give me symptoms" SYMPTOMS OF WHAT MOTHER????? CELIAC!!!!! Geez! But no, it's not wheat or gluten that's the problem for her... nope...

CMCM Rising Star

The biggest thing I've learned in my life is that you can't convince ANYONE of ANYTHING if they don't want to hear it. Heck, sometimes you can't even convince YOURSELF of something! This is such a wheat-dominated society, and most of our goddies are wheat based, and so much enjoyment comes from eating these addictive wheat foods....it's a real bear to give it up. So unless you get violently ill from eating gluten, you're not going to be realistic about it.

The sad thing is that for some people, they'll put up with the annoying symptoms, and not find out about celiac until they get some kind of lymphoma, or another autoimmine disease. It's like smoking, I guess...people who smoke don't think lung cancer will happen to them.

All you can do, i've learned, is offer the information and it's up to them to take it or leave it. There's not much else you can do! :(

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. - knitty kitty replied to Sarah Grace's topic in Related Issues & Disorders
      21

      Headaches / Migraines and Hypoglycaemia

    2. - Jmartes71 posted a topic in Coping with Celiac Disease
      0

      Related issues

    3. - trents replied to Sarah Grace's topic in Related Issues & Disorders
      21

      Headaches / Migraines and Hypoglycaemia

    4. - Scott Adams replied to jessicafreya's topic in Gluten-Free Foods, Products, Shopping & Medications
      1

      Tamale ingredients

    5. - Wheatwacked replied to Roses8721's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      6

      GI DX celiac despite neg serology and no biopsy


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,145
    • Most Online (within 30 mins)
      7,748

    Kundrey
    Newest Member
    Kundrey
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Who's Online (See full list)

    • There are no registered users currently online
  • Upcoming Events

  • Posts

    • knitty kitty
      @Sarah Grace,  Thank you for the update!  It's so good to hear from you!  I'm glad Thiamine, B Complex and magnesium have helped you.  Yes, it's important to take all three together.    I had to quit eating cheese and nuts a long time ago because they triggered migraines in me, too.  They are high in tyrosine, an amino acid, found also in fermented foods like sauerkraut and red wine.   I found taking Tryptophan very helpful with migraines.  Tryptophan is a precursor of serotonin and people with migraines are often low in serotonin.  (Don't take tryptophan if you're taking an SSRI.)     This recent study shows tryptophan really helps. The association between dietary tryptophan intake and migraine https://pubmed.ncbi.nlm.nih.gov/31254181/   For immediate respite from a migraine, try smiling REALLY BIG, mouth closed, tongue pressed against roof of mouth, and crinkle up your eyes like you just heard or saw the funniest thing...  This causes an endorphin release in the brain.  Usually it's the funny event, then the endorphin release and then the smile.  Smiling first makes the endorphin center think it missed something and it catches up quickly by releasing endorphins after the big crinkle eyed smile.  Must make crinkly eyes with smile or it won't work.  If you do this too frequently within a short time frame (several hours), you can deplete your endorphins, but you'll make more in a couple of hours, so no worries. Get your thyroid checked, too.  Migraines are also seen in low thyroid function (Hashimoto's or hypothyroidism).  Celiac and thyroid problems go hand in hand.   Vitamin D helps, too.  Low Vitamin D is found in migraine.   I'm so glad you're doing better.  
    • Jmartes71
      Its been a complete nightmare dealing with all these health issues one thing after another and being told many different things.I am looking for a new primary care physician considering when I told my past doctor of 25 years I was diagnosed before any foods eliminated from my diet and now this year at age 54 no longer able to push considering Im always exhausted, leg pain , stomach,skin and eye issues,high blood pressure to name a few all worsen because I was a  school bus driver and few years until my immune system went to hell and was fired because of it.Im still struggling now, Im sibo positive and been told im not celiac and that I am.I have a hernia and dealing with menopause. Its exhausting and is causing depression because of non medical help. Today I saw another gastrointestinalist and he said everything im feeling doesn't add up to celiac disease since my ITg levels are normal so celiac disease is under control and it's something else. I for got I had Barrett's esophagus diagnosed in 2007 because recent doctors down played it just like my celiac disease. Im currently looking for a pcp in my area because it is affecting me personally and professionally. Im told since celiac looks under control it's IBS and I need to see a therapist to control it. Gastrointestinalist around here think only food consumption and if ITG looks normal its bit celiac disease it's something else. Is this right? This is what im being told. I want medical help but told its IBS.Im feel lost by " medical team "
    • trents
      My migraines generally have their onset during the early morning hours as well. Presently, I am under siege with them, having headaches all but two days so far this month. I have looked at all the things reported to be common triggers (foods, sleep patterns, weather patterns, stress, etc.). Every time I think I start to see a pattern it proves not to pan out in the long run. I'm not sure it's any one thing but may, instead, be a combination of things that coalesce at certain times. It's very frustrating. The medication (sumatriptan or "Imatrix") is effective and is the only thing that will quell the pain. NSAIDs, Tylenol, even hydrocodone doesn't touch it. But they only give you 9 does of sumatriptan a month. And it doesn't help that medical science doesn't really know what causes migraines. They know some things about it but the root cause is still a mystery.
    • Scott Adams
      These are labeled gluten-free: https://www.amazon.com/Corn-Husks-Tamales-Authentic-Flavorful/dp/B01MDSHUTM/
    • Wheatwacked
      Just a gluten free diet is not enough.  Now you have to identify and replenish your malnutrition.  Celiac disease is co-morbid with malabsorption syndrome.  Low vitamin D, Low Thiamine caused Gastointeston Beriberi, low choline, low iodine are common the general population, and in newly diagnosed Celiacs in the western culture its is more likely.  It takes time to heal and you need to focus on vitamins and minerals.  Gluten free foods are not fortified like regular processed foods.  
×
×
  • 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.