Jump to content
This site uses cookies. Continued use is acceptance of our Terms of Use and Privacy Policy. More Info... ×
  • 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

** Help! Waiting On Blood Test Results But Dr Diagnosed Rash As Scabies?!**


Amandal03

Recommended Posts

Amandal03 Newbie

Hi everyone

I am very new here. For the past three months I have struggled with what I thought was small mosquito and gnat bites but in the last 2-3 months the rash got out of control. I was desperate for some answers and made an appt to see my dr. A few days before my appt, I noticed my rash seemed to get worse after I ate so I started researching food allergies. I notices my rash looked alot like DH and decided to cut out gluten to see what happened. Well after only being off it one day it was a huge improvement! My rashes were much less and the bumps on my arms started shrinking. This was 2 days before my dr appt.

Two days gluten free pretty much (I made a few mistakes ingesting some gluten) and I go to the Dr. I tell him how I stopped gluten and saw a huge improvement and how I think I may be celiac. He tells me he has seen some celiac rashes look like that but he thinks its scabies. He than asks one of his colleagues to come look and he says scabies as well. Except he says the ones on my lower back look different. So they prescribe me scabies meds and I decided not to take them til I get my bloodwork back. It hasn't even been a week off gluten and my arms look substantially better but I am still getting new rashes that look like tiny bumps and welts on my fingers, neck and sometimes arms but they are so much less inflamed. I've been so worried this is scabies and how it will affect my family. My husband doesn't think it's scabies ESP since no one in my family has caught it. Has anyone been through something similar? There is no way scabies would get better without meds right? Also is it common for DH to keep having new rashes even after cutting our gluten?

Thank you for your help!


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



Celiac.com Sponsor (A8-M):



Archived

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


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      128,374
    • Most Online (within 30 mins)
      7,748

    jbayer
    Newest Member
    jbayer
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      121.1k
    • Total Posts
      70.8k

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Levi
      I have taken D2 50K oral capsules once weekly for 7 years consecutively due to a dangerously low deficiency level of 17. It took 3 whole years before I reached D level 34, followed by higher D levels up to low 70s. Two or three times throughout the following 4 yrs my labs would show slight high TSH (hypothyroidism). Is it possible that the last 4 of the 7 consecutive years of D2 50K which gradually increased my D levels to 60s & 70s is causing current labs of high TSH, even though for at least the last 4 months I have reduced my D2 50K intake to half dosage, every other week vs. weekly? 
    • Scott Adams
      Untreated celiac disease is associated with arthritis and other autoimmune diseases which can cause such pain. These categories have research articles on this topic: https://www.celiac.com/celiac-disease/celiac-disease-amp-related-diseases-and-disorders/fibromyalgia-and-celiac-disease/ https://www.celiac.com/celiac-disease/celiac-disease-amp-related-diseases-and-disorders/arthritis-and-celiac-disease/
    • Paula Andrews
      Hi! Did anyone experience severe body aches prior to being diagnosed?  Last year I suddenly experienced widespread pain, completely unexplained. After numerous tests with normal results I was diagnosed with fibromyalgia in August and started taking Cymbalta, which helped about 80%. Now other than pain, I did not have any additional fibromyalgia symptoms.    In the following months I started experiencing diarrhea, to the point where it was constant. In January I was diagnosed with celiac disease and microscopic colitis after having an endoscopy/colonoscopy. I've been gluten-free since that day and recently my pain level has dropped to ZERO.  I'm starting to wonder if I even have fibromyalgia, or if all of my symptoms were celiac and colitis.  I've seen several doctors and no one suggested this, but from what I'm reading it sounds possible.  The fact that I was diagnosed with two different diseases within a few months also seems odd. Has anyone else experienced all-over body aches with celiac?  And if so did the pain end after eliminating gluten?  Unfortunately I don't know anyone who has either celiac or fibromyalgia to talk to.
    • Scott Adams
      Understood, and with any positive blood test the usual next step is a biopsy to confirm celiac disease, and this would be true even if the tTg-IgA is negative.
    • Levi
      ADA, if that applies to you, has specific procedures, guidelines, rules, and regulations for employers to accommodate employees with disabilities. Check with your company HR Dpt. As Scott has mentioned this would be a quick fix, with the protection afforded employees with disabilities through ADA there is no need for you to job hunt. Hope this helps.    Ps. Coeliac Disease is now a listed Disability in the U.S.  
×
×
  • Create New...