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

Got My Skin Biopsy!


Crimson

Recommended Posts

Crimson Rookie

Ok. So, had enough of a break out to get the skin biopsy done. Now ten days of waiting. But I'm just sooooo happy to have this part of it done!


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



Celiac.com Sponsor (A8-M):



nasalady Contributor
Ok. So, had enough of a break out to get the skin biopsy done. Now ten days of waiting. But I'm just sooooo happy to have this part of it done!

That's wonderful! Please keep us posted!

JoAnn

Crimson Rookie

Will do!

I'm relieved and ecstatic again today. I made an appointment with a family doctor and they listened to me and requested all the tests. She even gave me a price cut for "doing her job" and coming in with all the info that she needed! *I have no insurance, so I pay out of pocket*

She wants me to get the blood tests and given my reaction to eating gluten, go back to gluten free as soon as the tests are done. *which is tomorrow*

Between the skin biopsy for DH and blood tests, I should have a diagnosis.

I still can't believe that.

I'm in shock. Shocked that the doctor listened to me and understood all that I had to say. She looked up and printed of this 16 page report from the National Institute of Health to help her order tests and such.

I'm just shocked.

The receptionist was great. The student doctor was great and the doctor was great. I'm quite happy to say the least.

I've gotta throw in a thank you to every one here. With out the info found here, this would not have been so easy for me.

Can't wait to get back to Gluten Free!

Cheers!

jerseyangel Proficient

Wow---that's fantastic. Please do keep us posted :)

Crimson Rookie

So. I'm back on the gluten-free diet since Friday.

I feel SO much better! I still have some blisters popping up here and there, random joint pain and my belly is still giving me hell for what I've done to it the past three weeks. But, I am certainly feeling better! Headaches have lessened too. I'm still napping here and there.

BUT I've managed to clean my house and catch up with many things that I've let slip due to feeling so bad for nearly a month. *house work was really piling up on me*

My doctor called to let me know that the blood test for vitamin and blood levels are normal! I was very glad to hear that. So, I've been doing very well for my body in the 16 months of being gluten free. Three weeks of gluten did not disturb my vitamin levels.

Of course, I do take liquid vitamins here and there to make sure that I absorb them properly. So, I'm sure that has a lot to do with that.

I get plenty of sunshine in the summer too. So, my vitamin D is perfect right now. Though, in the winter, I do also supplement vit. D too.

I'm very nervous about the apt. with dermatologist on Fri. I will be getting my results for skin biopsy. So, I'm just trying to keep busy and distracted until then. Then the Celiac blood panel results should be in w/in a week after that. I just hope this goes well. The results come back indicating DH/Celiac. And I can have my diagnosis along with more help on some of my issues that have not yet cleared up on gluten-free diet.

I'm all mania and worry right now. Gluten really seems to put my emotions through the wringer. I'm trying to stay calm. Just ride this out until it's done. Breathe...

  • 3 weeks later...
Crimson Rookie

Ok. So, here's the update...

Frustrating. haha

Biopsy was inconclusive. I suppose I will wait and see if I get anything that can't be misconstrued as anything but DH. I certainly had that with the original blisters. But, they were already opened by the time I got to the derm. So, I paid out a ton of money for them to tell me that I have dermatitis.

I'm a bit frustrated with them.

My vitamin levels and blood work all came back normal.

I was eating gluten for three weeks. Obviously not enough.

Can't. do. it. again.

I simply do not have it in me to eat gluten again.

I'm still working it out of my system. Massive headaches and joint pain.

My skin is going nuts with acne. And I'm all over the place emotionally. Mood swings a bits of depression. *I think I hate that the most* My energy levels are also all over the place. One minute I'm hyper, the next I'm ready for a nap.

I'm still waiting for my stomach to calm down. Pepto bismol gives me heartburn. o_O

I'm still not sure WHY I did this all to myself....

I was looking into the gene thing again. And found that the specific genes that I have DO equate to a predisposition for celiac, just they are a bit more rare.

The DQ2.2 and DQ7 apparently pair together to do exactly what the DQ2.5 does by itself.

At least, that is my understanding.

There's apparently a bit of a link with DQ7 and neurological issues with gluten...? correct me if I'm wrong.

I'm just getting the hang of some of this with the gene analysis.

I'd still like to be tested for other food allergies. But, I think I'll go with the old elimination diet. Much cheaper.

Cheers!

ChemistMama Contributor
Ok. So, here's the update...

Frustrating. haha

Biopsy was inconclusive. I suppose I will wait and see if I get anything that can't be misconstrued as anything but DH. I certainly had that with the original blisters. But, they were already opened by the time I got to the derm. So, I paid out a ton of money for them to tell me that I have dermatitis.

I'm a bit frustrated with them.

Crimson, my biopsies were negative, too. I had three done, two near lesions and one of a lesion. Did they make sure to get skin near a lesion? You're not supposed to get the sample from an active lesion.

Open Original Shared Link

Did you try the iodine test yet? The old fashioned way to test for DH was to soak a bandaid with iodine and put it against your skin for several hours to overnight. If you have DH, the skin exposed to the iodine will itch like crazy and eventually blister. I tried it myself and hooo boy was it itchy!!

GOod luck!


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



Celiac.com Sponsor (A8-M):



Crimson Rookie

Thank you for that link! I appreciate it. The biopsy that they did was ON the lesion and not beside it. I don't know of any other dermatologists in the area though.

This one is a 45 min drive.

Anyway, iodine patch test done and the pics are in my other post. You can see them and the patch test that I did on my husband as well. Same amount of time, TOTALLY different outcome.

nasalady Contributor
Thank you for that link! I appreciate it. The biopsy that they did was ON the lesion and not beside it. I don't know of any other dermatologists in the area though.

This one is a 45 min drive.

Anyway, iodine patch test done and the pics are in my other post. You can see them and the patch test that I did on my husband as well. Same amount of time, TOTALLY different outcome.

Crimson, I can understand your frustration and disappointment! But your iodine patch test was absolutely convincing to me....and that used to be the standard test! So I think you do have your answer....

Also, you're correct about DQ7 and DQ2.2 working together to make a DQ2.5; here's a link to a thread from about a year ago which has that information:

https://www.celiac.com/gluten-free/index.php?showtopic=52131

In any case, I'm glad you're not going back on gluten!

Take care,

JoAnn

Crimson Rookie

The patch test is what made me get the appointment for the dermatologist.

Unfortunately, he called it a chemical burn. oi... just oi....

It's all good. I have a few articles printed off just in case I do get an opportunity to try try again. Not sure if I'd do it. But it's nice to know they're there.

Thank you very much for yet another link.

I've been all over the web trying to deepen my understanding of all of this.

I appreciate all the links and extra information you and others have given me access too.

I think it takes time for all of this to settle in to the brain for me.

I'm pretty glad that I won't be going on gluten again too!

Cheers!

Crimson Rookie

Ok, Blood tests: Finally got a copy... sheesh

IgA <1.2 Range : 0.0-10.0

IgG <1.2 Range : 0.0-10.0

She didn't run the total IgA

My LYMPH are low

WBC high

MCH high *not sure what the hay this one is supposed to be for*

If I'm not mistaken, IgA and IgG ARE lymphocytes the LMPH that are low.

I'm guessing this would indicate and IgA deficiency.

I have an appointment in the morning. I'll see if she'll look into it a bit further.

Archived

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

  • 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. - Scott Adams replied to Roses8721's topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      1

      gluten-free Oatmeal

    2. - knitty kitty replied to Jmartes71's topic in Related Issues & Disorders
      22

      My only proof

    3. - knitty kitty replied to Ginger38's topic in Related Issues & Disorders
      10

      Shingles - Could It Be Related to Gluten/ Celiac


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      132,561
    • Most Online (within 30 mins)
      7,748

    Valentino
    Newest Member
    Valentino
    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

    • Scott Adams
      Oats naturally contain a protein called avenin, which is similar to the gluten proteins found in wheat, barley, and rye. While avenin is generally considered safe for most people with celiac disease, some individuals, around 5-10% of celiacs, may also have sensitivity to avenin, leading to symptoms similar to gluten exposure. You may fall into this category, and eliminating them is the best way to figure this out. Some people substitute gluten-free quinoa flakes for oats if they want a hot cereal substitute. If you are interested in summaries of scientific publications on the topic of oats and celiac disease, we have an entire category dedicated to it which is here: https://www.celiac.com/celiac-disease/oats-and-celiac-disease-are-they-gluten-free/   
    • knitty kitty
    • knitty kitty
      Hi, @Ginger38, I've had shingles in the past.  I understand how miserable you're feeling.   Not only do i have the chickenpox virus lurking about, I also have the cold sore virus that occasionally flares with a huge cold sore on my lip when stressed or exposed to gluten.  The virus lives dormant in the nerves on the left side of my face.  It causes Bell's Palsy (resulting in drooling).  The cold sore virus is also in my eye.  My eye swells up and my vision is diminished permanently whenever I have a flare, so it's of the utmost importance to keep flares away and treat them immediately if they do happen so I don't lose any more vision.   I take the amino acid supplement L-Lysine.  Lysine messes with the replication of viruses, which helps the body fight them off.   I haven't had an outbreak for several years until this year when exceptionally stressed and contaminated, it flared up again. Lysine has been shown to be beneficial in suppression of viruses like the cold sore virus (a herpetic virus), the chickenpox virus (also a herpetic virus), as well as the HIV virus, and even the Covid virus.   I also take additional Thiamine in the form TTFD (tetrahydrofurfuryl disulfide) because Thiamine has antiviral properties as well.   For pain, a combination of Thiamine (like TTFD or Benfotiamine or Thiamine Hydrochloride), with B12 Cobalamine, and Pyridoxine B6 have been shown to have analgesic properties which relieve pain and neuropathy.    The combination of Thiamine B1, Pyridoxine B6 and Cobalamine B12 really does work to relieve pain.  I take it for back pain from crushed vertebrae in my back.  This combination also works on other pain and neuropathy.   I usually buy a supplement that combines all three and also Riboflavin B2 called EXPLUS online.  However, it's made in Japan and the price with the tariffs added makes it really expensive now.  But the combination of Thiamine B1, Pyridoxine B6 and B12 Cobalamine (and Riboflavin B2) still work even if taken separately.   I can't take Tylenol or ibuprofen because of stomach upsets.  But I can take the vitamin combination without side effects.  However, you can take the three vitamins at the same time as other pain relievers for added benefit.  The vitamins help other pain relievers work better. I hope you will try it.  Hopeful you'll feel better quickly. Interesting Reading: Thiamine, cobalamin, locally injected alone or combination for herpetic itching: a single-center randomized controlled trial https://pubmed.ncbi.nlm.nih.gov/23887347/ Mechanisms of action of vitamin B1 (thiamine), B6 (pyridoxine), and B12 (cobalamin) in pain: a narrative review https://pubmed.ncbi.nlm.nih.gov/35156556/ Analgesic and analgesia-potentiating action of B vitamins https://pubmed.ncbi.nlm.nih.gov/12799982/ A Narrative Review of Alternative Symptomatic Treatments for Herpes Simplex Virus https://pmc.ncbi.nlm.nih.gov/articles/PMC10301284/
    • Mari
      I think, after reading this, that you areso traumatized by not being able yo understand what your medical advisors have been  what medical conditions are that you would like to find a group of people who also feel traumatized who would agree with you and also support you. You are on a crusade much as the way the US Cabinet  official, the Health Director of our nation is in trying to change what he considers outdated and incorrect health advisories. He does not have the education, background or experience to be in the position he occupies and is not making beneficial decisions. That man suffered a terrible trauma early in his life when his father was assonated. We see now how he developed and worked himself into a powerful position.  Unless you are willing to take some advice or  are willing to use a few of the known methods of starting on a path to better health then not many of us on this Celiac Forum will be able to join you in a continuing series of complaints about medical advisors.    I am almost 90 years old. I am strictly gluten free. I use 2 herbs to help me stay as clear minded as possible. You are not wrong in complaining about medical practitioners. You might be more effective with a clearer mind, less anger and a more comfortable life if you would just try some of the suggestions offered by our fellow celiac volunteers.  
    • Jmartes71
      Thus has got to STOP , medical bit believing us! I literally went through 31 years thinking it was just a food allergy as its downplayed by medical if THEY weren't the ones who diagnosed us! Im positive for HLA-DQ2 which is first celiac patient per Iran and Turkey. Here in the States especially in Cali its why do you feel that way? Why do you think your celiac? Your not eating gluten so its something else.Medical caused me depression. I thought I was safe with my former pcp for 25 years considering i thought everything I went through and going through will be available when I get fired again for health. Health not write-ups my health always come back when you're better.Im not and being tossed away at no fault to my own other than shitty genes.I was denied disability because person said he didn't know how to classify me! I said Im celiac, i have ibs, hernia, sciatica, high blood pressure, in constant pain have skin and eye issues and menopause intensified everything. With that my celiac nightmare began to reprove my disregarded disease to a bunch of clowns who think they are my careteam when they said I didn't have...I feel Im still breathing so I can fight this so no body else has to deal with this nightmare. Starting over with " new care team" and waisting more time on why I think I am when diagnosed in 1994 before food eliminated from my diet. P.s everything i went through I did write to medical board, so pretty sure I will continue to have a hard time.
×
×
  • 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.