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
mamabear272
Posted

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
stanleymonkey
Posted

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
come dance with me
Posted

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
mamabear272
Posted
  • Author

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
Mummyto3
Posted

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
Jungle
Posted

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
mamabear272
Posted
  • Author

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
October3
Posted

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
mamabear272
Posted
  • Author

Thanks October!!

stanleymonkey Explorer
stanleymonkey
Posted

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
mamabear272
Posted
  • Author

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
stanleymonkey
Posted

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
mamabear272
Posted
  • Author

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
stanleymonkey
Posted

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
mamabear272
Posted
  • Author

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

Darn210 Enthusiast
Darn210
Posted

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
Mummyto3
Posted

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
mamabear272
Posted
  • Author

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
mamabear272
Posted
  • Author

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.

Go to topic listing

  • Get Celiac.com Updates:
    Support Celiac.com:
    Join eNewsletter
    Donate
  • Celiac.com Sponsor (A17):
    Celiac.com Sponsor (A17):



    Celiac.com Sponsors (A17-M):



  • Recent Activity

    1. cristiana
      - cristiana replied to sha1091a's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      2

      Issues before diagnosis

      I agree, it so often overlooked! I live in the UK and I have often wondered why doctors are so reluctant to at least exclude it - my thoughts are perhaps the particular tests are expensive for the NHS, so therefore saved for people with 'obvious' symptoms. I was diagnosed in 2013 and was told immediately that my parents, sibling and children should...
    2. chrisinpa
      - chrisinpa commented on Scott Adams's article in Skin Problems and Celiac Disease
      2

      Celiac Disease and Skin Disorders: Exploring a Genetic Connection

      Maybe they can attribute certain skin conditions to either being susceptible to getting Celiac......or the other way around....but I have to ask if certain people are prone to Celiac because of genetics and some people aren't. It's kind of the same thing as what came first.....the chicken or the egg.?
    3. knitty kitty
      - knitty kitty replied to xxnonamexx's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      3

      My journey is it gluten or fiber?

      @xxnonamexx, There's labeling on those Trubar gluten free high fiber protein bars that say: "Manufactured in a facility that also processes peanuts, milk, soy, fish, WHEAT, sesame, and other tree nuts." You may want to avoid products made in shared facilities. If you are trying to add more fiber to your diet to ease constipation, considering...
    4. trents
      - trents replied to sha1091a's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      2

      Issues before diagnosis

      Welcome to celiac.com @sha1091a! Your experience is a very common one. Celiac disease is one the most underdiagnosed and misdiagnosed medical conditions out there. The reasons are numerous. One key one is that its symptoms mimic so many other diseases. Another is ignorance on the part of the medical community with regard to the range of symptoms that celiac...
    5. trents
      - trents commented on Jefferson Adams's article in Other Diseases and Disorders Associated with Celiac Disease
      6

      Celiac Disease Patients Face Higher Risk of Systemic Lupus

      What kind of practitioner did the blood test? Was this a medical doctor, a naturopathic doctor, a GI doc? I would certainly follow up with them and ask why they advised you not to eat red meat. I mean, it could be something like they, themselves, are a vegetarian and give that advice to everyone. Have you had an endoscopy with biopsy of the small bowel...
  • Celiac.com Sponsor (A19):

  • Member Statistics

    • Total Members
      132,692
    • Most Online (within 30 mins)
      7,748
    Ali Zaib
    Newest Member
    Ali Zaib
    Joined
  • Celiac.com Sponsor (A20):
  • Celiac.com Sponsor (A22):

  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):

  • Upcoming Events

  • Posts

    • cristiana
      Issues before diagnosis

      By cristiana · Posted

      I agree, it so often overlooked! I live in the UK and I have often wondered why doctors are so reluctant to at least exclude it - my thoughts are perhaps the particular tests are expensive for the NHS, so therefore saved for people with 'obvious' symptoms.  I was diagnosed in 2013 and was told immediately that my parents, sibling and children should be checked.  My parents' GP to this day has not put forward my father for testing, and my mother was never tested in her lifetime, despite the fact that they both have some interesting symptoms/family history that reflect they might have coeliac disease (Dad - extreme bloating, and his Mum clearly had autoimmune issues, albeit undiagnosed as such; Mum - osteoporosis, anxiety).  I am now my father' legal guardian and suspecting my parents may have forgotten to ask their GP for a test (which is entirely possible!) I put it to his last GP that he ought to be tested.  He looked at Dad's blood results and purely because he was not anemic said he wasn't a coeliac. (This was the same GP who said Dad didn't have dementia, when months before one of his colleagues suspected it and told me Dad must be diagnosed).  Hopefully as the awareness of Coeliac Disease spreads among the general public, people will be able to advocate for themselves.  It is hard because in the UK the NHS is very stretched, but the fallout from not being diagnosed in a timely fashion will only cost the NHS more money. Interestingly, a complete aside, I met someone recently whose son was diagnosed (I think she said he was 8).  At a recent birthday party with 8 guests, 4 boys out of the 8 had received diagnosis of Coeliac Disease, which is an astounding statistic  As far as I know, though, they had all had obvious gastric symptoms leading to their NHS diagnosis.  In my own case I had  acute onset anxiety, hypnopompic hallucinations (vivid hallucinations upon waking),  odd liver function, anxiety, headaches, ulcers and low iron but it wasn't until the gastric symptoms hit me that a GP thought to do coeliac testing, and my numbers were through the roof.  As @trents says, by the grace of God I was diagnosed, and the diet has pretty much dealt with most of those symptoms.  I have much to be grateful for. Cristiana
    • knitty kitty
      My journey is it gluten or fiber?

      By knitty kitty · Posted

      @xxnonamexx, There's labeling on those Trubar gluten free high fiber protein bars that say: "Manufactured in a facility that also processes peanuts, milk, soy, fish, WHEAT, sesame, and other tree nuts." You may want to avoid products made in shared facilities.   If you are trying to add more fiber to your diet to ease constipation, considering eating more leafy green vegetables and cruciferous vegetables.  Not only are these high in fiber, they also are good sources of magnesium.  Many newly diagnosed are low in magnesium and B vitamins and suffer with constipation.  Thiamine Vitamin B1 and magnesium work together.  Thiamine in the form Benfotiamine has been shown to improve intestinal health.  Thiamine and magnesium are important to gastrointestinal health and function.  
    • trents
      Issues before diagnosis

      By trents · Posted

      Welcome to celiac.com @sha1091a! Your experience is a very common one. Celiac disease is one the most underdiagnosed and misdiagnosed medical conditions out there. The reasons are numerous. One key one is that its symptoms mimic so many other diseases. Another is ignorance on the part of the medical community with regard to the range of symptoms that celiac disease can produce. Clinicians often are only looking for classic GI symptoms and are unaware of the many other subsystems in the body that can be damaged before classic GI symptoms manifest, if ever they do. Many celiacs are of the "silent" variety and have few if any GI symptoms while all along, damage is being done to their bodies. In my case, the original symptoms were elevated liver enzymes which I endured for 13 years before I was diagnosed with celiac disease. By the grace of God my liver was not destroyed. It is common for the onset of the disease to happen 10 years before you ever get a diagnosis. Thankfully, that is slowly changing as there has developed more awareness on the part of both the medical community and the public in the past 20 years or so. Blessings!
    • knitty kitty
      Dizziness after eating green beans?

      By knitty kitty · Posted

      @EndlessSummer, You said you had an allergy to trees.  People with Birch Allergy can react to green beans (in the legume family) and other vegetables, as well as some fruits.  Look into Oral Allergy Syndrome which can occur at a higher rate in Celiac Disease.   Switching to a low histamine diet for a while can give your body time to rid itself of the extra histamine the body makes with Celiac disease and histamine consumed in the diet.   Vitamin C and the eight B vitamins are needed to help the body clear histamine.   Have you been checked for nutritional deficiencies?
    • sha1091a
      Issues before diagnosis

      By sha1091a · Posted

      I found out the age of 68 that I am a celiac. When I was 16, I had my gallbladder removed when I was 24 I was put on a medication because I was told I had fibromyalgia.   going to Doctor’s over many years, not one of them thought to check me out for celiac disease. I am aware that it only started being tested by bloodwork I believe in the late 90s, but still I’m kind of confused why my gallbladder my joint pain flatulent that I complained of constantly was totally ignored. Is it not something that is taught to our medical system? It wasn’t a Doctor Who asked for the test to be done. I asked for it because of something I had read and my test came back positive. My number was quite high.Are there other people out here that had this kind of problems and they were ignored? 
×
×
  • 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.