Behaviour Suggestions What to do with gluten moods
#1
Posted 19 November 2009 - 02:47 PM
My 9 year old daughter doesn't have an obvious reaction right after she has been glutened. She will complain of a tummy ache for a couple of days and then the mood swings hit. We can deal with the physical complaints, but the emotional ones are driving me nuts.
She flies into a tantrum at the slightest provacation and it can take over an hour to calm her down. There is no reasoning with her at all. It is like all logic has left her brain.
I know this is a reaction she has to gluten so I try not to punish her too much, but how do I make sure that she understands it isn't ok to be so disrespectful? And how do we manage these episodes with out losing our own sanity.
Any and all suggestions are greatly appreciated.
Thanks!
DD diagnosed with Asthma November 2009 at 8 years old.
#2
Posted 20 November 2009 - 11:20 AM
Rondar2001, on Nov 19 2009, 03:47 PM, said:
My 9 year old daughter doesn't have an obvious reaction right after she has been glutened. She will complain of a tummy ache for a couple of days and then the mood swings hit. We can deal with the physical complaints, but the emotional ones are driving me nuts.
She flies into a tantrum at the slightest provacation and it can take over an hour to calm her down. There is no reasoning with her at all. It is like all logic has left her brain.
I know this is a reaction she has to gluten so I try not to punish her too much, but how do I make sure that she understands it isn't ok to be so disrespectful? And how do we manage these episodes with out losing our own sanity.
Any and all suggestions are greatly appreciated.
Thanks!
You may want to talk to your GI about it. Our hospital has social workers to help with this aspect. Maybe that will help?
#3
Posted 20 November 2009 - 01:19 PM
Our five year old does the same thing. We know we are in trouble and storms a brewing when his outer ears turn red and he boom, get the red rash ring around his mouth. Then, the tantrums begin, bad. Since he only five, he is small enough for myself or my husband to hold tightly (not, "that" tight but enough to restrain him comfortably) in a big hug to help him calm down. I try to deviate his attention with pretty much anything, even if it means packing the whole family outside to play or go to the park. That usually helps although it's not realistic to do, say at ten at night. I also try to give him extra fluids of whatever he will drink. I know that probably doesn't make a difference in getting those darn gluten molecules out of his system but it makes me feel like I'm doing something.
The tantrums are very hard to handle for us, too. Our nine year old gluten-free daughters have more "mood swings" with an attitude and get mean, mouthy and hard to get along with, but they don't physically tantrum like they used too.
Good luck to you!!!!
#4
Posted 20 November 2009 - 02:15 PM
I also try to just lay low if possible...I don't take them anywhere when they are in the thick of it. Any sort of gliche can cause a huge meltdown, and they are too big now for me to carry them back out to the car! I remember calling my mom crying, b/c my 5 year old was just screaming, in a horrible rage, b/c he'd had some milk. There was nothing I could do except wait for it to pass and make sure he didn't hurt himself or anyone else.
Sorry, guess I'm not much help am I???
Age 11 - Psoriasis
Age 8- dx'd Celiac March 2005
Age 6- gluten-free/cf, allergy related seizures
Age 4 - reflux, resolved with gluten-free/cf
#5
Posted 21 November 2009 - 12:38 PM
chiroptera, on Nov 20 2009, 01:19 PM, said:
Our five year old does the same thing. We know we are in trouble and storms a brewing when his outer ears turn red and he boom, get the red rash ring around his mouth. Then, the tantrums begin, bad. Since he only five, he is small enough for myself or my husband to hold tightly (not, "that" tight but enough to restrain him comfortably) in a big hug to help him calm down. I try to deviate his attention with pretty much anything, even if it means packing the whole family outside to play or go to the park. That usually helps although it's not realistic to do, say at ten at night. I also try to give him extra fluids of whatever he will drink. I know that probably doesn't make a difference in getting those darn gluten molecules out of his system but it makes me feel like I'm doing something.
The tantrums are very hard to handle for us, too. Our nine year old gluten-free daughters have more "mood swings" with an attitude and get mean, mouthy and hard to get along with, but they don't physically tantrum like they used too.
Good luck to you!!!!
No, our hospital celiac program has people (dieticians and social workers) specially trained in celiac and behavioral stuff. I don't think a normal social worker would be too helpful. Usually at each appointment the GI asks about physical, social, and emotional adjustments.
http://www.childrenshospital.org/clinicals...ageS2166P0.html
#6
Posted 22 November 2009 - 03:38 AM
#7
Posted 22 November 2009 - 03:38 AM
#8
Posted 22 November 2009 - 06:01 AM
My ds also has "after" affects of the gluten. I don't know how much help I can be because she just cries and cries uncontrollably. She will be cranky and moody but not aggressive towards us or her brother. Just cranky, usually she just stomps off. We remind her gently that it is the gluten talking and to try to control her words a little better. When she does hit the wall and starts the crying binge, we just sit on the sofa and hold her and let her cry it out. The crying is usually the last stage of it and she usually does this at night and basically just cries herself to sleep. It is heartbreaking. Luckily she is getting older and a little more responsible at school so we have only hit that once so far this year.
It is such a hard thing to deal with because even though you know it is the gluten, it doesn't make it any easier to deal with. Maybe if you have another adult at home to help you can trade off dealing with tantrums when they hit so each of you have a break. Good luck and I hope you dd is doing well.
Diagnosed Fibromyalgia March 2007
Mom to Katharine, 5 years old diagnosed Celiac Disease Sept 2006
Peanut allergy
Michael 3 years old diagnosed infant reflux at 6 weeks
Dairy Soy allergy until 22 months
Neg blood tests and biopsy Feb 2008
Positive gluten-free dietary response
[size=2]You may have to fight a battle more than once to win it.
Margaret Thatcher
Fall down seven times stand up eight.
"I've decided that after air, water, and dirt, the next most common substance on the planet must be gluten!"
Toni Nolte, Overland Park, Kansas
#9
Posted 23 November 2009 - 01:32 PM
I think it helps just to know we are not the only ones going through this. Now to get the hubby to understand that she isn't meaning to act this way; at least he ususally just gets frustrated and hides out in the garage.
DD diagnosed with Asthma November 2009 at 8 years old.
#10
Posted 23 November 2009 - 02:11 PM
#11
Posted 18 December 2009 - 06:34 AM
chiroptera, on Nov 20 2009, 01:19 PM, said:
Don't associate 'social worker' with Children Services - it's a common misconception.
Even if a social worker isn't familiar with celiac's, the social worker may be able to at least help with behavior modification, stress management for the parent, etc. Once the mood swing is set in motion, what started the mood swing (gluten or casien or whatever) doesn't necessarily determine what you do to soothe the child or help the parent cope - and those types of things are what the social worker may know.
And, if the social worker isn't familiar with celiac's, educate him or her.
#12
Posted 21 December 2009 - 11:25 AM
#13
Posted 22 December 2009 - 09:48 AM
What I wanted to teach him - what we all have to learn as we move into adulthood - is that emotion are not bad. It's all in how we channel them. Small children may not be able to grasp this, but over time, as they get older, they find a safe way to have their emotions, and then they do not fear them or try to suppress them - neither of which is healthy. Just a thought, and again, I can't directly relate because as far as I know, they do not have gluten issues. But all kids have emotions, and this is what has worked in our house.
Best of luck, and hang in there. Too soon they're grown up and you wonder what happened!
Peanut and dairy free: Dec. 2009
Rediscovered dairy: March 2010 (in small quantities)
Peanuts added back: June 2010 (in small quantities)
#14
Posted 31 December 2009 - 11:03 PM
If you can go to a support group (if you're not near Boston), they may be able to help point you in a better direction. Right now we just try to grin and bear it while where protective gear!
#15
Posted 02 January 2010 - 12:14 AM
Daughter is 11 now and no longer does this. BTW she does not have celiac, but food allergies.
She used to have fits like this far more often before we learned of the food allergies at age 6. I do not know if the fits she had after were related to allergies or not. We do eat out a lot and it is possible she ate something she shouldn't have. I recently found out that the enchilada sauce she had at one place had peanut butter in it and at another place had peanut butter, wheat and dairy! She seemed to have no reactions to these foods, so I don't know.
I do know that when she got very upset like this, there was nothing anyone could do to help her. You can not use the phrase "time out" to her even now. I think this stems from a very bad experience at a neighbor's house. I wasn't there so don't know exactly what happened. The neighbor put her in a time out in their small bathroom after she hit their puppy with a stick. She was about 2 or 3 then. Can't remember the exact age.
The only other time out she had ever gotten was by me where I made her sit quietly on the couch for 2 minutes. That didn't go well. She was not quiet and had to be restrained. That time it was for running out the door and crossing two streets by herself at about 18 months.
Anyway, when I got to the neighbor's house, she was screaming like a banshee and trying to beat the door down. Since then that is what she has done when we've tried to put her in a time out. Her arms would be bruised from the pounding and she would also either vomit or pee on the floor. It was NOT good so I tried not to use this as a form of discipline. Luckily she doesn't do too many bad things so doesn't much need discipline.
My husband however would not tolerate her screaming, angry fits and would try to shut her in her room. This only made things worse.
What I learned to do was try to get her in another room. It did not work to tell her to go to her room. That only made her more hysterical. She does not sleep in her room, but sleeps in mine on a separate bed. If I could get her to that bed, it did help slightly to calm her down. I would get her to lay down and perhaps I would lay there for a little while. If she could calm down slightly, I would let her cry or whatever she needed to do. But if she was hurting me by hitting or kicking, I would leave. If she was screaming at me, I would leave.
If I could not get her into another room, I would either go into another room myself or at least get away from her. And then I would not pay any attention to her. I have a rule and that is, if she can not speak to me quietly and rationally, she can not speak to me at all. I will not tolerate screaming, name calling, or telling me what to do.
In her case it seemed to take a good hour of hysteria. By then she was just exhausted and only then would she calm down. She did tell me once before we knew of her allergies that she "wished God had not maked me". I have to wonder if it is not because she felt so sick all the time. I have food allergies myself and was not diagnosed until a few years ago. I just thought everyone felt sick to their stomachs all the time. I used to get angry with people smiling. I would think... How can they smile when they feel so bad? But it was only after I felt better that I realized how bad I really had felt.
Her behavior in school is different now too. They used to think she had ADD. She would sometimes act spaced out and would not pay attention. That's all over now. I do think we are much better with the diet now, especially since she can read food labels for herself. My husband used to feed her allergens such as Teriyaki because he doesn't believe in food allergies. She will no longer go out to eat with him unless it's at a restaurant where they know her and make special food for her. She has also admitted to sneaking the allergens at a younger age, thinking that it wouldn't matter. So who knows? She may have had bread or something on those occasions where she acted out. I do keep it in the house, but away from her food.
I also think being older helps her to better explain to me when she is in pain or having other medical issues.
IgG, daughter: Wheat, spelt, lentils, peas, peanuts, almonds

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