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

Trying To Test My 6 Year Old


mamabear272

Recommended Posts

mamabear272 Explorer

I was just diagnosed 3 weeks ago and want to have my children tested. My two older kids are 19 and 18 and are fine with it. My 6 year old on the other hand threw the biggest fit. I mean kicking, screaming, flailing and everything. I swear I thought that Satan had taken over my baby! :blink: He is asymptomatic for now but I'd really like to know if he has it or not so that if he does I want to get him healing ASAP! Any advice out there to get him to sit for a blood test or should I just let it go for now and maybe try in a year or two?


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



Celiac.com Sponsor (A8-M):



stanleymonkey Explorer

my 2 yr old hates blood tests and usually is pinned down! He may not like the idea, but he'll forget about the test after a while, my daughter gets a small gift afterwards.

he's 6 so he has a good understanding of things. explain that some foods might be hurting his insides, and he might not feel ill now, but he might in the future, and the blood tests will help his doctor work things out.

tell him you dont want him to get sick so would like him to be really brave for a few seconds while they take blood. bribery usually works!!!! even see if he can accompany your older kids to get blood drawn, and get them to make a big deal out of how painless it is.

come dance with me Enthusiast

When I had my 7yo tested I had to sit on the chair with her and have my legs over hers then one arm pinning her arm to her chest to hold her in a way that she wasn't able to throw herself forward and also so she wasn't able to use that arm to attack the nurse with my other arm holding her hand on the arm where the blood was taken from so I could hold her down on the arm of the chair so she couldn't pull away. Oh she screamed! They called in another nurse help out as well so it took 3 of us to hold her an take blood from her. Then she kept screaming even after it was done and cried every time she looked at her arm for the next 24 hours. I never thought to check for it but the new Paediatrician thought she might have it so I tested her for it and yep the Paed is definitely smart! I was tested but don't have it. I want my parents tested now but so far haven't been able to have them checked. My brother's have been. One brother has a brand new baby so I want to know if it's in my side (I have no contact with her father or that part of her family) so they can watch him because I feel terrible about the amount of damage I did to my baby by not knowing she has it. All that bread and cereal and everything else made her sick :(

mamabear272 Explorer

He watched my older son get his done and he even told the 6 yo that it didn't hurt. And I tried telling hims that we wanted to make sure he's not sick. Bit since he doesn't feel sick he was like "but I'm not sick!" I don't know how to argue with his logic. Lol

Mummyto3 Contributor

I was after this advice as I posted lol I'm going to get my 7 and 3 yr old tested but am also worried how they'll be with the blood test.

Jungle Rookie

I spent about a week talking to my 8 and 6 year old before we went. Explaining why, and what it would feel like and that it would only pinch for a minute and then we'd go get a treat. I was not excited about testing my almost 3 year old because she is big and very strong. I decided to wait until she was a bit older so she would understand what we were doing. In the end about 2 weeks after I had the big girls tested with no real problems, my youngest needed blood draw for other reasons so I took a deep breath and took her up to be tested.

My almost 3 year old did amazing. She just sat their and watched and squeezed my hand when they were poking her. I was so shocked. Most adults cause more fuss than she did. So I guess you never know.

A tip from a friend.....there is a numbing cream they can put on the site but it takes about 30 minutes to work.

mamabear272 Explorer

I think I'm going to call my doctor on Monday and see what he suggests. Maybe there's something he can give him for it.


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



Celiac.com Sponsor (A8-M):



October3 Explorer

I think I'm going to call my doctor on Monday and see what he suggests. Maybe there's something he can give him for it.

Ask for EMLA cream. If you put it on his arm with a bandage on it for 30 min before the blood draw he shouldn't feel anything (its a numbing agent). I usually put it on both arms so the phlebotomist can make the decision which to use. If you tell him the cream will make it not hurt hopefully he'll be more willing. Then just cross your fingers that it works. ;)

mamabear272 Explorer

Thanks October!!

stanleymonkey Explorer

make sure a nurse or blood tech i forget what they are called phlebologist i think, draws the blood, docs are useless at blood draws!!!!!!!!!!

mamabear272 Explorer

They don't do them in the office. There's a lab downstairs from the office so we're good there. Plus the doc doesn't do any poking anyway. That way the kids don't relate pain to the doc.

stanleymonkey Explorer

They don't do them in the office. There's a lab downstairs from the office so we're good there. Plus the doc doesn't do any poking anyway. That way the kids don't relate pain to the doc.

thats good our family doc wont even give flu shots to kids for the same reason..just remember a few seconds of pain, a few hours of complaining, for a lifetime of good health is worth it

mamabear272 Explorer

Oh I know that. There was no way the test was happening though the way he was flailing around. My brother works on medical and is bringing me some of the emla cream and we're going to get the test tomorrow.

stanleymonkey Explorer

Oh I know that. There was no way the test was happening though the way he was flailing around. My brother works on medical and is bringing me some of the emla cream and we're going to get the test tomorrow.

good luck, i've got my fingers and toes crossed hoping it is a breeze for your son (and poor mommy too)

mamabear272 Explorer

Didn't make it today cause I had so much to do. Tomorrow for sure.

Darn210 Enthusiast

Ask for EMLA cream. If you put it on his arm with a bandage on it for 30 min before the blood draw he shouldn't feel anything (its a numbing agent). I usually put it on both arms so the phlebotomist can make the decision which to use. If you tell him the cream will make it not hurt hopefully he'll be more willing. Then just cross your fingers that it works. ;)

Your pediatrician can prescribe this ahead of time so you can start the process at home and not have to wait in the lab waiting room. Also, I don't think the lab has it on hand (needs to be prescribed by a doctor). . . at least this is how it was in my son's case. Now, my son still did not do that well . . . try to get them to look at something other than the needle. Also, ask for a butterfly needle (they may be using one anyway) because it's a pretty small needle.

My son is now 12 and still does not do that well with blood draws or shots but the last time we went, we used an ice pack on his arm instead of the EMLA cream and he thought it was actually better than the cream.

Good Luck.

Mummyto3 Contributor

Our dr prescribed EMLA cream for my boys. I put it on them this morning for their blood test today. They didn't even flinch when blood was drawn. They did really well, so I would highly recommend it.

mamabear272 Explorer

My brother-in-law brought me some and we put it on both arms so he could choose when he got there. It was still an ordeal (I don't even want to go into detail, just know it involved me and 2 techs) but it got done and after the one tech told him the needle was already in he calmed down. He ended up being fine and all the testing got done. He's cool now cause he realized it didn't hurt. Hopefully, we get results soon and that he doesn't have it. I'm not as much worried about him having it as my 18 year old. He's more symptomatic in the GI dept and he also has headaches, depression, anxiety and Asperger's.

  • 3 weeks later...
mamabear272 Explorer

Good news! Neither of my sons tested positive! Praise the Lord! I know what a time I had adjusting. I'm glad they don't have to, too.

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. - AlwaysLearning replied to Colleen H's topic in Coping with Celiac Disease
      3

      Gluten related ??

    2. - Colleen H replied to Colleen H's topic in Coping with Celiac Disease
      3

      Gluten related ??

    3. - Jmartes71 replied to Jmartes71's topic in Coping with Celiac Disease
      4

      My only proof

    4. - AlwaysLearning replied to Jmartes71's topic in Coping with Celiac Disease
      4

      My only proof


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,089
    • Most Online (within 30 mins)
      7,748

    Clare Durham
    Newest Member
    Clare Durham
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • AlwaysLearning
      Get tested for vitamin deficiencies.  Though neuropathy can be a symptom of celiac, it can also be caused by deficiencies due to poor digestion caused by celiac and could be easier to treat.
    • Colleen H
      Thank you so much for your response  Yes it seems as though things get very painful as time goes on.  I'm not eating gluten as far as I know.  However, I'm not sure of cross contamination.  My system seems to weaken to hidden spices and other possibilities. ???  if cross contamination is possible...I am in a super sensitive mode of celiac disease.. Neuropathy from head to toes
    • Jmartes71
      EXACTLY! I was asked yesterday on my LAST video call with Standford and I stated exactly yes absolutely this is why I need the name! One, get proper care, two, not get worse.Im falling apart, stressed out, in pain and just opened email from Stanford stating I was rude ect.I want that video reviewed by higher ups and see if that women still has a job or not.Im saying this because I've been medically screwed and asking for help because bills don't pay itself. This could be malpratice siit but im not good at finding lawyers
    • AlwaysLearning
      We feel your pain. It took me 20+ years of regularly going to doctors desperate for answers only to be told there was nothing wrong with me … when I was 20 pounds underweight, suffering from severe nutritional deficiencies, and in a great deal of pain. I had to figure it out for myself. If you're in the U.S., not having an official diagnosis does mean you can't claim a tax deduction for the extra expense of gluten-free foods. But it can also be a good thing. Pre-existing conditions might be a reason why a health insurance company might reject your application or charge you more money. No official diagnosis means you don't have a pre-existing condition. I really hope you don't live in the U.S. and don't have these challenges. Do you need an official diagnosis for a specific reason? Else, I wouldn't worry about it. As long as you're diligent in remaining gluten free, your body should be healing as much as possible so there isn't much else you could do anyway. And there are plenty of us out here who never got that official diagnosis because we couldn't eat enough gluten to get tested. Now that the IL-2 test is available, I suppose I could take it, but I don't feel the need. Someone else not believing me really isn't my problem as long as I can stay in control of my own food.
    • AlwaysLearning
      If you're just starting out in being gluten free, I would expect it to take months before you learned enough about hidden sources of gluten before you stopped making major mistakes. Ice cream? Not safe unless they say it is gluten free. Spaghetti sauce? Not safe unless is says gluten-free. Natural ingredients? Who knows what's in there. You pretty much need to cook with whole ingredients yourself to avoid it completely. Most gluten-free products should be safe, but while you're in the hypersensitive phase right after going gluten free, you may notice that when something like a microwave meal seems to not be gluten-free … then you find out that it is produced in a shared facility where it can become contaminated. My reactions were much-more severe after going gluten free. The analogy that I use is that you had a whole army of soldiers waiting for some gluten to attack, and now that you took away their target, when the stragglers from the gluten army accidentally wander onto the battlefield, you still have your entire army going out and attacking them. Expect it to take two years before all of the training facilities that were producing your soldiers have fallen into disrepair and are no longer producing soldiers. But that is two years after you stop accidentally glutening yourself. Every time you do eat gluten, another training facility can be built and more soldiers will be waiting to attack. Good luck figuring things out.   
×
×
  • 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.