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

My Son Has His Frst Post Dx Party Tomorrow. I'm Scared


jsmjboertlein

Recommended Posts

jsmjboertlein Rookie

My son fell ill shortly after weaning from the breast. He almost died at age 3 by bleeding out from his nose and mouth massive quantities of blood. He's been through a barrage of testing through St. Jude and finally got a dx of celiac disease. He is so much better off gluten. He rarely has a bleed and if he does we can always track it back to some minor cross contamination. Well tomorrow he has a "pizzas n pj's" party at his cousin's house. There will be 20 some parents and kids his age and younger there. He is 5. I am bringing his favorite gluten-free pizza in my own pan, my own dedicated pizza cutter, home made gluten-free chocolate chip cookies to share and his own cup. A friend is bringing cupcakes, so I will probably make him a gluten-free one to bring too. So I have that all figured out but I'm so scared another little one might drink from his cup, or touch his mouth after eating gluten. Sadly that's all it takes for my baby. I once kissed him after I ate a muffin and he went into anaphalaxis. This was before we knew he was sick. He doesn't have anaphalaxis anymore but he bleeds so bad when he comes into contact with gluten and there's no way to stop it. He is very very sensitive to gluten. I don't wanna even take him because of all of the risks, but he is looking so foward to it, and we have to regain some sort of normalcy here. Is there anything else you would reccomend to help me relax? I don't want to make him stand out any more than I absoloutely have to. He gets self concious and I look like an overprotective drama queen. Any tips? What do you all do for parties?


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



Celiac.com Sponsor (A8-M):



kareng Grand Master

A Haz-Mat suit? Naw, every kid would want one.

What about each kid has a cup with thier name on it? Would work if they are all old enough to read thier names. Also, lots of different color cups with stickers on them. Hand each kid one and note the sticker. "Joey, your cup had a green star on a yellow cup." Susie, you have a yellow flower on a red cup.

Kid can wash hands before eating and then everyone wash after. This and the cups can be covered up as germ protection and keeping food messes off the furniture.

Otherwise, you will have to take an active role in what he is doing. At 5, they don't mind if you play along. You can play cars with them and try to keep your kid from only playing with the blue truck and the green car. If he lets go, you can grab it before another kid does. I know this is extreme but it sounds like he is very sensitive or maybe allergic, too.

You will become a popular mom. Every grade school parent loves an extra parent at parties.

jsmjboertlein Rookie

Good ideas! I so wish I could put him in a bubble. He is also allergic to wheat. I am excited for him to be with his friends, but scared. O ya I will be hovering!

celiac-mommy Collaborator

Yeah, I think your biggest threat will be the other kids' pizza covered hands and faces and the crumbs from the pizza and cupcakes. From personal experience, especially with kids this age, the crumbs get all over the floor, which get stepped on and thus moved from room to room. It's a tuffy.... I'd be hovering like crazy too ;)

kareng Grand Master

Thought some more. Maybe you can have some kids to your house sometimes or all the time. They could wash hands before coming in, you could serve only gluten-free snacks, play with gluten-free toys, etc. Talk to the parents of his friends. We like to know what to look for or avoid or do special. My kids are teens now but as kids, they had friends with food issues or one in a wheelchair. They always wanted to make arrangements for the kids to have fun. When I was a kid, my brother's little 5 year old friend lost her hair to chemo. She wore a wig. It was a big no-no to touch her wig. Once the kids knew, they avoided it.

Skylark Collaborator

Gosh, I don't have kids or a clue. I'd be wanting to provide all the food and make the party gluten-free, which is as almost as impractical as putting him in a bubble. :blink:

Let us know how it turns out. I am curious and really hoping for you that he has a great time and doesn't get sick.

jsmjboertlein Rookie

Thanks everyone. I just got home from the store after buying all of his gluten-free stuff. I will def let you all know how it goes. I'm a nervous wreck.


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



Celiac.com Sponsor (A8-M):



jsmjboertlein Rookie

Well today's the day. I'll log on later and let you all know how it went

cahill Collaborator

Well today's the day. I'll log on later and let you all know how it went

I hope everything goes well. You and the little guy have a good time and stay safe

jsmjboertlein Rookie

We just arrived home and I would say it went fairly well! There weren't nearly that many kids there and we had one close call. One of the dads handed my son a plate of reg. pizza, but my guy was aware enough to say no thanks that's not my kind. Then I grabbed a plate and gave him his pizza and later saw some of his buddies pizza on his plate. Thankfully I think he was done eating by then and if he got any cross contamination at all, I don't know, but he hasn't acted like he did. He had a great time and the other moms loved his gluten-free cookies! Now I'm excited for the next one! I think you aren't allowed to post links to pics on this site? Is that right? Let me know if I'm mistaken on that, and I will link to some of the party pics!!

psawyer Proficient

I think you aren't allowed to post links to pics on this site? Is that right? Let me know if I'm mistaken on that, and I will link to some of the party pics!!

You can post pictures or links to pictures, as long as the content is consistent with our rules.

If the pictures are on a sharing site, such as Flickr or PhotoBucket, then you can share them.

You can post a link:

[url=http://www.wherever.com/picture]Click here.[/url]
or you can hot link the picture so it shows up in your post:
[img=http://www.wherever.com/picture]

jsmjboertlein Rookie

You can post pictures or links to pictures, as long as the content is consistent with our rules.

If the pictures are on a sharing site, such as Flickr or PhotoBucket, then you can share them.

You can post a link:

[url=http://www.wherever.com/picture]Click here.[/url]
or you can hot link the picture so it shows up in your post:
[img=http://www.wherever.com/picture]

Awsome thanks so much!

jsmjboertlein Rookie

Hmm I tried to put a pic up from flickr but it wont let me do it. O well.

psawyer Proficient

Here is an example of an image link, from my photobucket:

[img=http://i42.photobucket.com/albums/e339/tortoiseshell2002/Psillies/Martini1-1.webp]

Produces

Martini1-1.webp

Cheers!

jsmjboertlein Rookie

Here is an example of an image link, from my photobucket:

[img=http://i42.photobucket.com/albums/e339/tortoiseshell2002/Psillies/Martini1-1.webp]

Produces

Martini1-1.webp

Cheers!

MM. I'll take ten! LOL, sorry, got sidetracked. I will try again tomorrow. I'm beat! Thanks for your help!

domesticactivist Collaborator

I was thinking of you and your little guy but didn't get a chance to respond. It sounds like it went really well! I'm happy for you and I'm sure your son will get to enjoy many parties from here on out!

Skylark Collaborator

That's great news! I'm so glad he had a good time and didn't get sick.

jsmjboertlein Rookie

Thanks you guys! I'm thrilled with how it went. I think I am going to have a kid party too. He has some party catchin up to 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. - trents replied to catsrlife's topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      1

      Patiently Waiting to See Results

    2. - trents replied to Leeloff's topic in Gluten-Free Foods, Products, Shopping & Medications
      75

      How Come Gluten Didnt Bother Me In Italy

    3. - Gigi2025 replied to Leeloff's topic in Gluten-Free Foods, Products, Shopping & Medications
      75

      How Come Gluten Didnt Bother Me In Italy

    4. - Rejoicephd replied to JulieRe's topic in Related Issues & Disorders
      7

      Oral thrush question

    5. - catsrlife posted a topic in Celiac Disease Pre-Diagnosis, Testing & Symptoms
      1

      Patiently Waiting to See Results


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,897
    • Most Online (within 30 mins)
      7,748

    Sgp
    Newest Member
    Sgp
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.4k
    • Total Posts
      1m

  • Celiac.com Sponsor (A22):




  • Who's Online (See full list)


  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • trents
      Welcome to the forum, @catsrlife! Celiac disease can be diagnosed without committing to a full-blown "gluten challenge" if you get a skin biopsy done during an active outbreak of dermatitis herpetiformis, assuming that is what is causing the rash. There is no other known cause for dermatitis herpetiformis so it is definitive for celiac disease. You would need to find a dermatologist who is familiar with doing the biopsy correctly, however. The samples need to be taken next to the pustules, not on them . . . a mistake many dermatologists make when biopsying for dermatitis herpetiformis. 
    • trents
      You state in an earlier post that you don't have celiac disease. Here in this post you state you will "be doing another test". What will this test be looking for? What kind of celiac disease testing have you had done? If you have used a Entero Labs it sounds like you have had stool testing done for celiac disease which is not widely accepted as a valid celiac disease diagnostic testing method. Have you had blood antibody testing for celiac disease done and do you realize that for antibody testing to be valid you must have been eating generous amounts of gluten for a period of weeks/months? 
    • Gigi2025
      No, I've not been diagnosed as celiac.  Despite Entero Labs being relocated to Switzerland/Greece, I'll be doing another test. After eating wheat products in Greece for 4 weeks, there wasn't any reaction.  However, avoiding it here in the states.   Thanks everyone for your responses.  
    • Rejoicephd
      Thank you @JulieRe so much for sharing this extra information. I'm so glad to hear you're feeling better and I hope it keeps moving in that direction. I feel I'm having so many lightbulb moments on this forum just interacting with others who have this condition. I also was diagnosed with gastric reflux maybe about 10 years ago. I was prescribed ranitidine for it several years back, which was working to reduce my gastric reflux symptoms but then the FDA took ranitidine off the shelves so I stopped taking it. I had a lot of ups and downs healthwise in and around that time (I suddenly gained 20 pounds, blood pressure went up, depression got worse, and I was diagnosed with OSA). At the time I attributed my change in symptoms to me taking on a new stressful job and didn't think much else about it. They did give me a replacement gastric reflux drug since ranitidine was off the shelves, but when I went on the CPAP for my OSA, the CPAP seemed to correct the gastric reflux problem so I haven't been on any gastric reflux drug treatment for years although I still do have to use a CPAP for my OSA. Anyway that's a long story but just to say… I always feel like I've had a sensitive stomach and had migraines my whole life (which I'm now attributing to having celiac and not knowing it) but I feel my health took a turn for much worse around 2019-2020 (and this decline started before I caught covid for the first time). So I am now wondering based on what you said, if that ranitidine i took could have contributed to the yeast overgrowth, and that the problem has just been worsening ever since. I have distinctly felt that I am dealing with something more than just stress and battling a more fundamental disease process here. I've basically been in and out of different doctor specialties for the past 5 years trying to figure out what's wrong with me. Finally being diagnosed with celiac one year ago, I thought I finally had THE answer but now as I'm still sick, I think it's one of a few answers and that maybe yeast overgrowth is another answer. For me as well, my vitamin deficiencies have persisted even after I went gluten-free (and my TTG antibody levels came down to measurably below the detectable limit on my last blood test). So this issue of not absorbing vitamins well is also something our cases have in common. I'm now working with a nutritionist and taking lots of vitamins and supplements to try and remedy that issue. I hope that you continue to see improvements in working with your naturopath on this. Keep us posted!
    • catsrlife
      Back at the end of July I got this rash on both of my forearms. It started on my right and continued to the left. It was on the top and side. The rash has bumps that would pop with clear liquid if scratched. They would almost crystalize and scab up. They reminded me of chicken pox. They would scab for weeks and not heal much at all except for the blood clotting. If the scab was scratched off, it would bleed and bleed until it scabbed up again. The skin has lost its pigment where the scabs are. I figured it was probably either the plant I had trimmed around the 15th or some reaction to the magnesium complex I was taking or an allergic reaction to the asthma meds I was on. I stopped the asthma meds and the magnesium. The rash seemed to get better but when I took the asthma meds it flared up again so I went to the urgent care as my doctor was unavailable. The UC doctor said it probably wasn't the meds and asked about my diet. I said I was strict keto. I usually am, but there is a story around this. I feel amazing on keto. When I eat sugar, wheat, and starchy veggies I feel horrible. Blood sugar goes up, IBS type symptoms, brain fog, etc. But I have a horrible addiction to carbs so I blow it sometimes and after Mom died in 2023, I fell off the wagon. No rashes, just weight gain. I finally went back on keto and then around that time had a piece of pizza (or so, it's hard to stop the carb rush.) So I was strict keto, off and on. She ignored that and prescribed some allergy meds. It didn't go away.  What was happening by then was that the rash was now on my upper elbows, both of them, on the back of my arms. It starts with a very itchy bump, spreads around it and sometimes just burns like crazy and other times just itches. Then it started on the sides of my knees on the oustide, a little bit down the sides of the calves. It's not as bad there as it is on my arms even though it comes and goes (and so does wheat in my diet.) I then got three tiny blisters on each hand, 3 on the insdie of my index finger on the right hand and 3 on the inside of middle finger of my left hand. There is still a little scab there even though it was two weeks ago. No more have appeared on the fingers. But right now the back of the arms above my elbows are starting to itch. At some point I started to think mites from the possum that was sneaking into our house but it's been 3 months and they would be dead already. It wouldn't be from humans because I don't go near any humans although I did take an Uber to the doctor and the bus back. Plus, it's symmetrical. It starts on one side and is almost identical on the other.  I did my DNA with Ancestry and MyHeritage. I don't have the HLA-DQ2 or HLA-DQ8. I do have HLA-DQ2.2. I took the blood test but it was negative. Then again, I don't eat wheat every day. I rarely eat it except for lately when I've been preparing for the blood test if I have to take it again. I don't like to. It makes my joints hurt, gives me brain fog, stomach problems, I sleep in the middle of the day, etc. I have a doctor appointment tomorrow. I hope that she will be more serious about this than the UC doctor was.  So I have no idea. With my luck they'll magically disappear before the doctor appointment. That's what happens with everything.
×
×
  • 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.