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

Me Again - Sorry - About My Daughter


macocha

Recommended Posts

macocha Contributor

I posted a bit ago and need some more follow up. I was looking at some of the photos and daughter's don't look exactly like. Her rash though is getting worse and no meds are working :( She has it on her eyelids, inner elbows/arm, and neck. The photos are poor quality because of the camera phone, but you get the gist.

On the eyelids - on the left side you can see a small bit in the crease, but tonight it has spread to be even redder (inflamed) and goes beyond the eyelid to the side of her face. (sigh) on the right it is in the upper eyelid and somewhat the crease. These areas burn a great deal and she is suffering :(

On her neck, they are 1 to 2 inch patches. Photos don't catch it all. those don't bother her as much, but they aren't as inflamed.

The ones on her arms (only including one side) are heck-a inflamed. they are horrid and hurt her a great deal too. the photo doesn't show how much it is inflamed, but it is...badly.

Do these even look like any cases you have seen? She doesn't get into the derm for a few weeks, so I am struggling with what to do for her to ease the pain.

leftarm.webp?t=1292571222

leftneck.webp?t=1292571222

eyes.webp?t=1292571222


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



Celiac.com Sponsor (A8-M):



ravenwoodglass Mentor

The lesions on her arm look much like the lesions I had as a child, but mine covered my entire legs and arms and at times my face.

After you see the derm if you are done with testing do try her on the diet.

Nothing topical they ever gave me helped either except for once a year when they would give me prednisone. They wouldn't give it to me more than once a year because of the side effects and of course the lesions would come back after a month or so. I was told as a child that I had 'poison ivy' in my blood stream to explain why I had the lesions all year.

Jestgar Rising Star

Can you remind us what you think it is and what meds she's tried?

macocha Contributor

She has tried:

Elidel - 1% cream

mupirocin - 2%

Hydrocortisone 2.5%

and one other - an ointment her allergist gave her

What do I think it is. I am leaning towards DH. She has fructose malabsorption already. Her brother has celiac. I want to know for sure because if it is this and that makes the FM worse than what it is. This has never fully gone away like sometimes exzema does in diff weather. It has always been a problem.

ravenwoodglass Mentor

I would give her a trial of the diet after testing is done. You never know the FM may be a result of the celiac impact and it might resolve after she has been gluten free for a bit.

tarnalberry Community Regular

Dose anything else go on her skin? Soap (she could try avoiding it)? Shampoo (try baking soda & vinegar, perhaps)? Lotion (try olive oil?)? Detergent from laundry? Is there any other doctor you can get to sooner?

Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      131,796
    • Most Online (within 30 mins)
      7,748

    Raybo
    Newest Member
    Raybo
    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

    • nanny marley
      Oh yes I can understand the tiredness after going threw all that, must be exhausting especially on the mind I have high aniexty so I can understand that , I wish there more easier ways for people to get help , I had a MRI on my spine some years ago without anything it was really quick and no prep , I understand the need for  them to see better with the bowel ,but you think they would use something a little less traumatic  for ibd sufferers on the bowels by now ,I hope your feeling better today 🙏
    • Colleen H
      The previous post did not come through right. I wonder if tingling burning feet are part of it.. I'm not sure if it's the med reaction that people with gluten intolerance get or the food we ate  It's frustrating because a person who did not want to admit to himself I had this condition wanted me to eat this chicken sandwich and now I'm stuck with a variety of symptoms plus now I'm hungry on top of it..  I'm new to this so I forget that "one bite" of the wrong thing can hurt us.😔. Do we stop eating if someone exposed us to gluten ??  My stomach is rumbling but my joints hurt ...  It's weird because I can feel the anxiety coming on.  I get joint problems ,  I don't know if anyone ever got hot flashes?? I suppose if it affects people head to toes you can get that too.   It's weird...hard to decipher what is what.   Also how long do I have to deal with this attack??  Makes me feel like not getting up out of bed.  I get too many symptoms which  horrible.  Thank you for your response..  
    • Colleen H
      Hello  I was glutened by a person that knew it.  I'm having 
    • wellthatsfun
      as my last post stated, i was diagnosed via endoscopy on the 14th of june. i have been eating amazing home cooked meals, luckily, mainly cooked by my boyfriend who is extremely careful about contamination (and is an incredible cook at that). however, i find myself in a mental rut still. being 18, this is the time in my life where i should be exploring things, going out, having fun. yet every corner i turn i'm tortured by the amazing smell of something i can't have anymore. the wonderful sight of such yummy foods. it's near torture. if my boyfriend and his friend who lives with us buy something i can't have, they'll usually eat it outside of the house or the car or wherever we are - which is greatly appreciated - but even seeing a burger or chips or a sausage roll in their hands guts me almost beyond repair. i just wanna have it again too. i miss it. i feel left out and it makes me very sad all the time. it's not their fault. they are allowed to eat whatever they want to, whatever their intestines will allow. it just stings, bad. and i feel so ungrateful given i basically have a private chef who is doubly the love of my life. but it's just so hard. i know i'll adapt. i haven't given up hope.i just wanted to vent. thank you for reading
    • RDLiberty
      Thank you. I must have misinterpreted a study or something. Thank you for the clarification. Much appreciated. Almost three years into my celiac diagnosis and I'm still learning new things. 
×
×
  • 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.