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

Am I Being Too Careful?


cdfiance

Recommended Posts

cdfiance Explorer

Since Alex


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



Celiac.com Sponsor (A8-M):



MySuicidalTurtle Enthusiast

I like to avoid things with gluten. It is better safe than sorry especially when it comes to gluten on my hands! Good luck to Alex!

cdfiance Explorer

Sorry, I should have been more specific. Alex is my fiance and she's turning 24. So it would be paints and paintbrushes and not fingerpainting or anything like that.

Sorry for not clarifying that; I can see why it looked like my post should be moved to the kids/babies section -- my bad. :)

Ryan

GeoffCJ Enthusiast
Sorry, I should have been more specific. Alex is my fiance and she's turning 24. So it would be paints and paintbrushes and not fingerpainting or anything like that.

Sorry for not clarifying that; I can see why it looked like my post should be moved to the kids/babies section -- my bad. :)

Ryan

I think you have to pick your battles, and the risks that you can accept. I'd imagine that for an adult, injesting paint is a pretty low risk, but if paint is available gluten-free, then I'd buy it. It might be tough to find ingredient lists.

Hey, How's Alex doing? Is the diabetes diagnosis helping get things settled down for you two? Give Alex our best.

Geoff

darlindeb25 Collaborator

I truly believe we can not be too careful. Once you let up on that carefulness, that's when accidents happen. I think you are doing a wonderful job of supporting Alex--we all should be so lucky. :D

SunnyDyRain Enthusiast

I'd say try to get gluten free, but I agree it might be hard. I'd buy her a box of powder free latex gloves (if she isn't allergic to latex!) for her to mix paints or wash the brushes. I can see that she may not get alot of paint on her hands painting, but it's the set up and clean up it may get under her nails then she could put them in her mouth.

CarlaB Enthusiast

I used to paint paintings... though I might see if gluten-free paints are available, I wouldn't worry about it. I know I never ingested the paint .... and I washed my hands really well to be sure it was all off before I ate.

I paint our walls in our house and never worry about it, though I'm very careful when spackling or sanding drywall because that puts dust in the air ... and yes, drywall does contain gluten.

With all she's been through, I definately think it would be overkill for her to give up her hobby, too, as unlikely as it is that the paint will make it into her mouth. She should just be meticulous in cleaning herself up afterward (I'm thinking paint under fingernails).


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



Celiac.com Sponsor (A8-M):



lovegrov Collaborator

If you can find gluten-free paints, fine, but I do think it would be overkill for a 24-year-old to just never paint again.

richard

cdfiance Explorer

Thanks for the input everyone. I'm still hoping I can find gluten-free paints but if not I do agree that it is probably low risk. The latex gloves sound like a good idea to avoid getting it under her fingernails. I really don't want her to have to give up something she enjoys doing.

Hey, How's Alex doing? Is the diabetes diagnosis helping get things settled down for you two? Give Alex our best.

Actually things have been going pretty well that last week or so. We're starting to get into a good routine with the blood sugar checks and insulin injections and she's getting better all the time at recognizing early when her blood sugar is getting too low or too high. And best of all it seems like her GI tract is finally starting to calm down! She has less pain and fewer bouts of diarrhea a day. Her sleep is much more restful now that she's not up multiple times a night in the bathroom. I'm almost afraid to say it but it looks like we're finally making progress. We even went to see a movie the other day! I know it sounds like nothing but its a big deal considering the doctor's office, the drug store, and the hospital have been pretty much the only places outside our house that Alex has been in the last few months.

Thanks,

Ryan

wowzer Community Regular

I'm glad to hear that Alex is on the mend. I hope that you can find gluten free paint. Good Luck.

GeoffCJ Enthusiast
I'm almost afraid to say it but it looks like we're finally making progress. We even went to see a movie the other day! I know it sounds like nothing but its a big deal considering the doctor's office, the drug store, and the hospital have been pretty much the only places outside our house that Alex has been in the last few months.

Thanks,

Ryan

Ryan,

That's great to hear! It was certainly sounding scary there for a while, so any return to something closer to normal is great.

It's great that you are there for her too. My wife and I are newlyweds (just over a year, I think we still count). I actually started to figure out my Celiac disease after our delayed honeymoon. I haven't had nearly the difficulties Alex has, and I can still say that having a supportive partner is a godsend.

When my wife's mom got sick, and my wife was upset, it was killing me to not be able to "fix" it. As men, we, stereotypically and I think it's true a lot, don't see problems as things to be dealt with, or worked around, but things that should be fixed. Disease can be tough mentally, because often you can't fix it. There are "solutions" in the form of avoiding gluten (and in Alex's case, blood sugar controls) but it's not really fixing it. I was talking to my wife the other day, and mentioned how frustrated I was that there isn't a cure for Celiacs, and we ended up talking about Diabetes too. She was suggesting that there was a cure, avoiding gluten and insulin. I was arguing that those are patches, not cures. My analogy was that it was like driving with one of those little donut spare tires. It might get you home, but it was limiting. A cure would be like getting a new tire. And it got me thinking about how I approach problems, and I think I am the stereotypical guy. I see every problem as something that needs to be fixed, and I get very frustrated when I can't. Especially when it's hurting or affecting the people I love. Have you been having the same reactions?

Anyway, that's just my thoughts. I feel bad for Alex, but it seems like you're doing everything you can, and that's great.

Geoff

CarlaB Enthusiast

Geoff, I think you're right! That is how guys are! Sometimes women will come to their man with a complaint ... we're just looking for a shoulder ... men think we want it fixed ... all we want is someone to say they understand our frustration!

It seems that for women, many things can be "fixed" with a hug ... our idea of fixed is a little different than yours.

Funny observation.

Congratulations to both of you ... I've been married for 22 years.

cdfiance Explorer
I see every problem as something that needs to be fixed, and I get very frustrated when I can't. Especially when it's hurting or affecting the people I love. Have you been having the same reactions?

Yeah, you

aikiducky Apprentice

Ryan and Geoff, I just wanted to say that it's really helpful to read about your frustration because it helps me understand my husband better! I hope other women on the board will read this too. It's not uncommon here to read about a newly diagnosed celiac wondering about why their partner is reacting so seemingly unsupportively, I think it's very good to keep in mind how hard it can be for a guy to be in this situation!

You guys in turn might keep in mind that just like Carla said, women often don't really long for a solution as much as they long for someone to validate their feelings. You know, women (probably even more than men) have often had the experience of being told it's in our head, we're just being hysterical...whatever you do, don't try to downplay problems in hopes it'll make her feel better, because it won't! So if your loved ones are complaining about something, remember the first thing to do is to say something supportive and give them a hug. It really is a kind of a fix even though it might not feel like it to you. :)

I hope you won't mind the slight ranting... I'm hoping this might help someone out eventually, if not, just ignore me. :P:lol:

Pauliina

kbtoyssni Contributor

Although it's extremely unlikely that she'll get glutened off the paint, if you can get gluten-free paint I'd do it. The world is a risky place for celiacs; I prefer to eliminate as many situations with the potential for CC as I can. That way I can engage in other "risky" behavior like going out to eat more frequently.

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,192
    • Most Online (within 30 mins)
      7,748

    teresa1955
    Newest Member
    teresa1955
    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

    • Ginger38
      So I recently had allergy testing for IGE antibodies in response to foods. My test results came back positive to corn, white potatoes, egg whites. Tomatoes, almonds and peanuts to name a few.  I have had obvious reactions to a few of these - particularly tomatoes and corn- both GI issues. I don’t really understand all this allergy versus celiac stuff. If the food allergies are mild do I have to avoid these foods entirely? I don’t know what I will eat if I can’t  have corn based gluten free products 
    • 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.
×
×
  • Create New...