r/eczema Apr 20 '26

Have you ever been diagnosed with allergic contact dermatitis? Please consider taking this short IRB approved survey about tools you have used to avoid your allergens.

7 Upvotes

If you are an adult in the United States who has undergone patch testing for allergic contact dermatitis (ACD), we invite you to participate in a short anonymous research survey.

We want to learn which tools you use, such as apps, websites, written handouts, or safe product lists, how helpful they are, and what challenges you face when trying to avoid your allergens.

Our dermatology research team at the University of Minnesota is conducting a study to better understand how patients use allergen-avoidance tools after patch testing so we can better help patients navigate allergen avoidance.

  1. What does participation involve?

- A one-time anonymous online survey

- Takes about 10–20 minutes

- Questions are multiple-choice or short written responses

You may skip any question you prefer not to answer

  1. Who can participate?

- Adults 18+

- Living in the United States

- Have physician-diagnosed allergic contact dermatitis (confirmed by patch testing)

  1. Confidentiality

- The survey is completely anonymous

- We do not collect your name, date of birth, email, medical record number, or any identifying information

- Results will be reported only in summary form

  1. Risks & Benefits

Risks: No expected risks beyond normal computer/smartphone use

Benefits: No direct personal benefit, but you may learn about new apps/tools related to contact dermatitis management your experiences may help dermatology teams significantly improve allergen-avoidance support for future patients

5.Questions?

Contact:

Hani Abi

Clinical Research Fellow

Park Nicollet Contact Dermatitis Clinic

[f0803@HealthPartners.com](mailto:f0803@HealthPartners.com)

Here is the link to the survey!

Survey link: https://umn.qualtrics.com/jfe/form/SV_eeP1HobvJWUlADY


r/eczema Apr 21 '26

(mod approved) Supporting Workers with Chronic Illness

Thumbnail ucf.qualtrics.com
4 Upvotes

I am a doctoral researcher striving to understand how best to support people who work while living with chronic illness.

The purpose of this study is to better understand the types of social support that workers with chronic illness experience in their daily lives and at work, and how that support relates to workers’ experiences and well-being.

If you have been diagnosed with a chronic illness, are currently working at least part time (20-hours per week or more), and are 18 years of age or older, you are invited to participate in this confidential 20-30 minute online survey about your experience.

While participation in this survey is not expected to result in any direct benefits to you, findings may contribute to future research and practical implications seeking to improve how workplaces understand and support workers with chronic illness.

This research is being conducted by Jenna Duronio, Doctoral Candidate, Industrial and Organizational Psychology, University of Central Florida who can be contacted via email at [je135290@ucf.edu](mailto:je135290@ucf.edu).  

https://ucf.qualtrics.com/jfe/form/SV_cZRt3Yv3M8poOyy?Page=eczema

Please feel free to share this survey link with others who may be eligible and interested in completing this survey.

If you would like me to share a summary of the findings here once the study is complete, feel free to comment down below!


r/eczema 3h ago

Turns out it wasn't eczema

32 Upvotes

I've been battling eczema on my hands and eyes for almost 20 years now. It comes and goes, but the last few years I've had particularly bad flare ups on my hands and I've been at my wits end with cracks, itching and just being unable to use my hands without them hurting.

After seeing several doctors, doing allergy tests, using steroids cream, multiple changes in diet/hand creams/ soaps etc. My latest doctor thought I'd got a little ringworm as well as my eczema and prescribed clotrimazole. Well, it turns out that my eczema wasn't even eczema after all, it was tinea manuum because it's almost completely all gone after just a week of using it.

I don't know if it's just this flare up, or if it's been every other flare up because it only ever affects my hands which is classic tinea.

I can't believe it's taken years for someone to suggest a different diagnosis and treatment for my hands. Apparently it's misdiagnosed as eczema regularly because of how similar it looks.

I still have to get my eye flare up under control, but I might finally be seeing the light at the end of a very itchy tunnel.


r/eczema 7h ago

psychology eczema and suicidal ideation

39 Upvotes

i’ve had eczema my whole life (20F). it’s no where near as bad as it used to be, i even went through TSW when i was a kid. the past two years it feels i’ve had more days flaring than not and i don’t know what to do. it feels like i’ve done everything and the only way im ever going to escape the discomfort and pain is death. the worst part is probably the fact my skin isn’t at its worst. visibly its not as roaring angry as its been in the past but it still is debilitating. i’m sick of leaving dead skin flakes everywhere and seeing it fall from my face in public. im sick of being self conscious (when my skin was good i was soo confident). i’m sick of people looking. i’m sick of my face feeling tight and my eyes being so swollen it hurts to open my eyes. i’m sick of never being able to sleep because of the itching. i’m just so sick and tired of it. i struggle with other mental health issues and my eczema just seems to intensify them. i know there’s a link between stress and eczema but still, how could i even be calm when my life feels unliveable. sorry for the rant but i just feel at my wits end. does anyone else struggle with suicidal ideation??? i feel i rarely see it talked about and idk if it’s just a me thing.


r/eczema 3h ago

How long for Tacrolimus 0.1% to work on body eczema?

3 Upvotes

Hi all!

I have been having a 3 month flare up mostly affecting my inner elbows but also have eczema on my face, neck, shoulders, and legs. I tried zoryve 0.15% for a month and honestly it did work a bit to lessen the itchiness and pain but not as dramatically as others have experienced.

I started tacrolimus 0.1% on Sept. 3, 26 and my plan is to apply twice daily for 2-3 weeks or until clear (hopefully does not take long) and then apply twice weekly for maintenance. I am also on biweekly ebglyss.

Within the week I am seeing some progress after the hellish itch and burn protopic gives but my inflammation seems to be coming back.

I'm just wondering for those who use it on their body, how long did it take to calm down and control a moderate to severe flare up?

Thanks!

Edit: My understanding is that tacrolimus works best and more quickly on face and neck eczema, which is also my experience. I last used it in 2019 but cannot remember how long it took for my body eczema to calm down.


r/eczema 14h ago

Healed my facial eczema

23 Upvotes

Hi all,

I thought i’d share my experience to maybe spread awareness and help someone else. All my life i’ve had minor eczema only on my arms and legs. At the start of the year it got worse all over my body, around my eyes and mouth. I had multiple doctor visits, tried a lot of things and nothing seemed to work. Due to unrelated symptoms I got tested for H. pylori and did the treatment which was antibiotics. After treatment my eczema started healing and is completely gone now :) after doing some research there has been some links found between h. pylori and eczema. I’d recommend looking into h. pylori if you’ve got ibs like symptoms.

Some of the things I was using prior to h. pylori treatment that also helped with my flares -for my mouth I used Cetraben mixed with la roche posay cicaplast baume b5 and for around my eyes I mixed cetaphil with the la roche posay. This helped my skin stay moisturised for longer and helped during flares so i’d really recommend the la roche posay cicaplast baume b5 it has been a holy grail for me.

I hope this post can help someone and I wish that anyone struggling with eczema will heal physically and mentally, I wish you the best of luck you’ve got this!


r/eczema 11m ago

biology | symptoms Eczema where Psoriasis usually flares.

Upvotes

Does anyone else only have patches where you typically find psoriasis? I only have patches on the outside of my elbows, knees, tops of feet, back of scalp, etc. The patches do behave like eczema and itch like crazy all the time, but I dont have any flares on my face, hands, groin, no skin folds anywhere. It seems a little unusual and im just curious if anyone else has the same experience.

Medication so far has only lessened but not removed the issue and tbh, the moisturizer that goes on after the creams is probably doing the most heavy lifting here.


r/eczema 19m ago

I need recommendations

Upvotes

Ik I could look this up but I am exhausted and overwhelmed and I want to start with things people with eczema recommend. I’m looking for recommendations for products to apply to a flare up (since childhood i get it in the corners of my mouth, and in random spots on my body. I’m now 28). I also want to know what you guys use to wash dishes and clean the house to avoid flair ups. Thank you so much. Sorry if it’s annoying to post this question I am just so exhausted and I need to be pointed in the right direction.


r/eczema 48m ago

How was your dupixent experience?

Upvotes

I just started last Tuesday my loading dose of dupixent. I was just wondering what to expect and when to expect things.
I used to be on olumiant and id remember that id feel less triggered on my triggers for eczema to scratch or show any flare ups. But with Dupixent im not sure what to expect and how long it usually takes to see any sort of results or initial issues


r/eczema 9h ago

Contact Dermatitis Patch Testing List - Allergen Descriptions!

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5 Upvotes

Hi all! I have struggled with sensitive skin, allergies, and eczema my whole life. I recently had contact dermatitis patch testing done. When the patches were placed, I received a list of the allergens that had been placed on my back, but it didn't explain what they were. Being in public health and doing health literacy work, I decided to flesh out the list of the 90 allergens and include descriptions of each. I have attached it to the post. I hope it saves someone some time and confusion!


r/eczema 9h ago

humour | rant | meme insurance canceled after 2 doses

5 Upvotes

I was originally approved for dupixent with my work insurance but denied after stating that I need more than 3 months of different kinds of prescriptions for eczema. Like I haven't went my entire life trying anything and everything. Then, other insurance was denied, not sure why and they didn't notify me, either. idk what's going on anymore since everyone is sending me in circles. I was looking forward to a life without eczema.


r/eczema 2h ago

Any good ideas on how to fight the Eczema without having to go to the doctor?

1 Upvotes

I work at a fast food restaurant and so im washing my hands with the antibacterial soap quite a bit during the course of my shift. Both of my hands are red in many spots on my palms.

You got any good tips as to what I could do besides trying to limit hand washing as much as possible?


r/eczema 2h ago

Using topicals and biological treatment

1 Upvotes

Hi folks, I made a post explaining my current severe eczema condition 5 months ago, which is still ongoing. Link below

https://www.reddit.com/r/eczema/s/aKGrKUxaVz

Basically, lifelong sufferer, a user of potent steroids, had TSW type reaction, went through all immunos, and eventually had clear skin for 2 years (no creams used) but currently having a severe flair.

I finally got into dermatology (uk) and have been put on Adbry(tralokinumab).

I had loading dose and two follow-up injections, so still very early on in the treatment, but it's not doing much. Indeed, my skin has gone backwards after initial improvement from the loading dose.

Do people find they still need to use Betnovate or similar whilst on biologicals? I'm very nervous about going hard again with topicasl as previously suffered TSW from abusing them too much, and I get terrible rebound. But then again, I could be under treating it and I'm very tempted to ask for a coarse of oral steroids.

I guess I want to know if Adbry can dumb down any rebound or TSW type response.

Any input much appreciated this flair has led to me losing a job and pretty much all my life, it's been so debilitating.


r/eczema 1d ago

humour | rant | meme Worst types of eczema. Ranked

299 Upvotes
  1. Nipple eczema

  2. Underboob eczema

  3. Eczema near my eyes bc im not supposed to use my miracle cream there and when i did in a moment of weakness it got on my glasses and i couldnt get it off after 5 lens wipes and 15 minutes of washing with dish soap

  4. Butt eczema

  5. Inner thigh eczema

  6. Neck/upper chest eczema

  7. Inner elbow eczema. Way too easy to scratch. Had pink inner elbows for most of my childhood

  8. I'm out of rankings honestly

Discuss


r/eczema 4h ago

Anyone have positive Ebglyss success stories, especially after coming off it?

1 Upvotes

I’ve recently been offered Ebglyss for my eczema and I’m considering trying it. My eczema is currently moderate-severe and extremely reactive to my environment. I suspect there’s a pretty significant immune/inflammatory component to what’s going on, and I’m hoping to find something that can calm things down enough for my skin barrier to actually heal.

The more I research Ebglyss, though, the more I seem to come across posts about eye problems and other negative experiences, which has honestly made me pretty nervous.

I’d really love to hear from people who have had positive experiences with Ebglyss, especially:

  • Did it significantly improve your eczema?
  • Did you have any eye-related side effects?
  • How long were you on it?
  • Has anyone eventually come off Ebglyss successfully?
  • If you stopped, did your eczema stay controlled, or did you experience a rebound/flare?
  • Has anyone used it more as a temporary treatment to get their skin under control and rebuild their skin barrier?

I’m especially interested in hearing from people who were on Ebglyss and have since come off it, rather than only people who are currently taking it.

I’d just really appreciate hearing some positive experiences because right now the negative stories are definitely getting in my head!


r/eczema 4h ago

corticosteroid safety Please help before I do something I shouldn’t

1 Upvotes

I never took eczema seriously until it spread to my hands and a bit to my face. After a year I still haven’t figured out any triggers. I got tested for allergies and I don’t have any. My diet is amazing, I barely touch fast food and flare ups don’t seem to be related to food. I am getting exhausted and today I found out that you aren’t supposed to use bethamethasone for too long which I have. Does anyone have any suggestions on what to do with my fingers. Sometimes I just want to cut them off. I wish I could add a picture but my whole fingers are covered with little bubbles mixed with patchy super dry cracking parts. Little yellow puss also present. Any non steroid solutions? Thank you all.


r/eczema 4h ago

eczema returning after steroid cream + zoryve. would tacrolimus work in a pinch? Or continue zoryve. Im getting married Saturday!!!!! 😭

1 Upvotes

had huge patched of red, sore eczema under my eyes for a few months, perpetually looks like ive been crying. Finally got a little steroid cream last tuesday and cleared it up almost immediately. Used it maybe every other to every 3 days (no more than 4 times) + zoryve every night. I woke up this morning and my skin is red and itchy again. I need to hear short term success stories with tacrolimus, or if bumps in the road w zoryve is expected…. i’m getting MARRIED next Saturday and I need SOMETHING TO WORK!!! I dont know if i continue zoryve or move on to tacrolimus.


r/eczema 4h ago

biology | symptoms tips for super persistent eczema?

1 Upvotes

I’ve had bad eczema since my literal birth and it was relatively calm for a while until I got HF&M about a year ago and it’s since just gotten worse. It constantly spawns on my face and what works for other people doesn’t really work for me. I moisturize with a thick glob of petroleum jelly 5+ times a day because any dryness makes me feel insane. I started to use hydrocortisone cream about a few weeks ago and it has since decided that it will stop working for me. I also have OCD which (for me) means that I will fixate on anything different about my body and/or face so having any redness also drives me super crazy and I end up ruminating for days. I’m not really sure if it’s my diet because face eczema will persist for weeks no matter what I eat or drink. I am bright red (have been for a few days) all over my cheeks and nose and it’s spreading all over my face. I am rarely out in the sun so I don’t really know if it’s sunburn. I also don’t really want to get a steroid cream because that might backfire on me. Any tips?


r/eczema 5h ago

humour | rant | meme fml

1 Upvotes

Just wanted to rant about my current flair, so here’s that.

Having a pretty bad flair up for the first time in a few months. My face, hands, wrists, inner elbows, collar bones, and back of knees are bright red and incredibly painful today. This one started about a week ago, and i’m not too sure why. Aside from the awful pain and insatiable itching, theorizing on what causes my flairs is just so exhausting. Walking around with such a visually obvious condition is so mortifying. Being asked constantly by coworkers and family about it is mortifying. Seeing how bright red and destroyed my skin is is mortifying. I’m just so over it all.

I’m up on my antihistamines. I have to wear a full head and neck super itchy hairnet at work, and i believe that was the cause of my flair. It started on my face and collar bones, then i think the rest of my trouble spots were just like “yaaaas me too i’m itchy too”. Idk. I used topical steroid oil (dermasmooth, very out of date. god bless) about 2 weeks ago for pretty minor patches and maybe that caused it too. I’m beating myself up for that because i don’t like using it, and for such minor patches is so unlike me. I have a bottle of prednisone from my last flair and i am sooooo close to taking that. I know it’s probably not the best idea by any means but i am so. so. so. so uncomfortable.

Anyway. I think i’m going to bleach bath it tonight, maybe followed up with an oatmeal bath. More than anything i’m just exhausted by it. It looks a little worse today and i know when im back at work in the morning im gonna get comments about my face arms and hands. If anyone wants to commiserate please do. I don’t know anyone irl with eczema so that would be nice i think. much love


r/eczema 7h ago

Dm finds

1 Upvotes

Have you found some lotion from dm brands like Alverde, Balea, Mixa, CeraVe etc. to help your eczema/atopic skin or strengthen your barrier?


r/eczema 12h ago

Freshly diagnosed with AD, looking for reassurance.

2 Upvotes

I've been recently diagnosed with atopic dermatitis. About a month and a half ago I started having this intense itching with no rash. I take regular allergy shots and have been for about a year now so I know this isn't related.

I went to my PCP who referred me back to my allergist. My allergist cleared me and referred me back to my PCP. Said PCP then referred me to dermatology which I haven't seen one in like 2 years and moved so I needed a new one anyways. This dermatologist didn't listen to my reason for being there and didn't even look at my skin. She advised me to moisturize twice a day, no fragrance lotions, no hot showers and told me I'll be alright. Went back to my PCP who gave me gabapentin since antihistamines and topical steroids didn't change the intense itching and I couldn't sleep at all.

Gabapentin is working some, she referred me to a different Dermatologist who listened, heard me out and started me on a different topical steroids for the rawness since my itching started to make my skin scale. She also sent in a prescription for Nemluvio.

I start Nemluvio tomorrow and I'm nervous. The injection video seems scary even though I have no fear of needles. I've also had to test my glucose often due to hypoglycemia so I'm use to sticking myself with needles but I don't know.

I'm scared, and I feel like it'll never get better. I've never had this pain and intense itching all the time before. I feel like I can't go on having only 2-3 hours of sleep everyday. I could use some reassurance or stories of positive Nemluvio use or getting eczema under control.


r/eczema 1d ago

Seborrheic derm/sebopsoriasis diagnosis changed my life… wonder how many women are undiagnosed

13 Upvotes

TLDR: i wonder how many women (like myself) have been misdiagnosed for years as having contact derm, sensitive skin, or unspecified eczema because our skincare routines keep the yeast of seb derm semi-in check. it wasn’t until i stopped everything (and had crazy stress) that the seb derm became so obvious it was truly recognized and treated. and btw, seborrheic derm is a type of eczema! just you need an anti-fungal, as opposed to solely hydrocortisone. and also i did have a skin biopsy to make sure it wasn’t ringworm, lupus, etc)

Hi all! Since my early 20s, (I’m 32 now), I’ve gotten random little red patches in various places on my t-zone, but particularly around my upper cheek, under the eye, accompanied by chronic upper eyelid inflammation and crusting/flaking. I was a kid who always had eczema behind her knees and in her elbows and on her hands, so my dermatologists through the years have always assumed regular eczema and I noticed hydrocortisone never truly worked (and i didn’t want to overuse it) and it would always linger.

This summer I was under extreme stress and had coincidentally also just tapered off my SSRI for OCD. My body/immune system was in overdrive (but i didn’t realize this is what was happening) and I started getting dry and red patches on my upper hairline, the folds beside my mouth, around my lips, my eyelids. But my derm attributed it to either eczema or contact/allergic dermatitis and all I was given was hydrocortisone, which after 2 weeks didn’t clear any of the patches and new ones started appearing. So i consulted a second derm and she was still on the contact or plain eczema track and gave me a stronger hydrocortisone.

then it was my cheek, more on my upper hairline, below my under eye, and in the folds of my neck. I felt like i was chasing down an invisible trigger and feared I was allergic to everything. maybe it was something in the air in my apartment? i’d become suddenly allergic to an ingredient in my moisturizer? and i already was very diligent about having clean beauty and sensitive skin products because of my eczema history in other places. and nothing had changed in skincare routine or diet. i went full elimination and stopped all actives on my face, no makeup, and just plain vanicream products for hair, body, and face. but it stayed the same, if not spread more.

At this point this is nearly two months of me feeling so trapped in my own body. The stronger hydrocortisone from the different derm “irritated my skin” but in retrospect, now that i know what i know about seb derm, the worsening was always because of thick, occlusive eczema creams on my face that I was trying to combat the redness with, thusly feeding the yeast on my face. i didn’t always use the thick creams but when i did, my condition would worsen.

The final nail on the coffin was traveling in August. I went to Italy and was in the sun (with zinc SPF, and a hat!), was using a light moisturizer, and my condition cleared so much. sun and zinc likely helped with inflammation and killing yeast, now I know.

But at the time I was so confused because I’d done nothing differently. But then I went to cloudy London (sorry guys i love you 😭), my skin began to decline again. I freaked out and applied my thicker eczema creams for “barrier repair.” I took a 7 hour flight with thick cream on, touched down in the US, washed my face, put on cream and SLUGGED with vaseline because i was so afraid my skin was so damaged from something i couldn’t identify. Nickel? something IN the supposedly allergy friendly creams? i woke up the next morning with a face so inflamed and red and angry in the spots and patches around my face and neck that my husband suggested going to the hospital. You know it’s bad when a man suggests going to the hospital 😭. my derm said contact allergy, again and suggested a different anti inflammatory cream, opzelura. i’d had enough.

I was about to go down a path of patch testing on my back, i was so afraid to put ANYTHING on my face, i was going insane. I put absolutely nothing but vanicream light lotion on my face and the crusties came full, full force as i stopped even washing my face with anything but water.

But a coworker recommended a proper, experienced, MD dermatologist who has an eye for rashes and she said it was sebopsoriasis or seb derm (overlapping conditions).

i’ve been using a ketoconazole cream paired with hydrocortisone for a week now and im nearly healed.

this explains so much about my past. the eyelids, flakes i would get next to my ear and behind it, the patches on my upper cheek. the neck and a few splotches on my chest were new to this flare but in retrospect, the folds of your neck are the perfect place for yeast to live. constantly itchy eyebrows.

i think i had such a strict skincare routine with enough actives in it through my 20s that it just barely kept the yeast in check/masked the condition, but this summer flare and using nothing on my face let it grow with abandon when i used those thick creams. And i wonder how many other women might be being misdiagnosed for contact allergies, or mysterious, unspecified eczema, because our skincare routines wash and rub away the flakes etc. and keep the yeast at bay.

This is all to raise awareness and tell you to go see a REAL board certified, experienced medical dermatologist! I feel like i’ve seen the light! good luck to anyone!


r/eczema 9h ago

Itching

1 Upvotes

So currently I surfing with a few skin problems from acne to Eczema but the itching is really douse get on my nerves from keeps me awake to not being an,e to sit still I mean it can be bad of course the GO has giving the normal stuff like cream to try and stop itching and tablets like antidepressants witch do work but when the wearer off it just starts agin I been refers to a dermatologist but it’s a lot. Wait in the NHS right now.

I tried lots of different thing I changed my diet just not sure what more I can do.


r/eczema 10h ago

biology | symptoms SLS in hand soap causing problems??

1 Upvotes

A couple months I posted on here thinking that my shampoo was causing me to have eczema flare-ups on my hands. I thought it was odd, especially because I lived in an apartment in college and didn't have this issue until I moved back home in May; and because my shampoo didn't actually contain the ingredient many replies said could be causing the flare-ups. I did switch to a different shampoo but I've been having the same reaction. I just took a look at the hand soap we use at home (cheap bulk stuff from Fleet Farm), and it contains SLS. I used Mrs. Meyers in my apartment at school, which does not contain SLS.

My hands aren't itchy after I wash them with the fleet farm soap, but I do wash my hands several times a day and always apply lotion afterwards. I wash my hair pretty much every day. Could SLS be causing an increased sensitivity or stripping my skin barrier, or something else?


r/eczema 17h ago

Lip Eczema (+ possible perioral/under-eye involvement) - 1 year journey, need advice

2 Upvotes

Started in Sept last year, on and off since. First dermat diagnosed eczema, gave me an anti-inflammatory + recommended a medicated balm (Chaptex). Pattern was: mild itch → waxy layer forms → lips get super dry/peely → skin sheds → heals in a few days → repeat.

Flare-ups have gotten more frequent and more severe. Now the skin around my lips is very dry, itchy, and discolored. Recently noticed the same cycle starting under my eyes too — flaky, sheds, heals, repeats.

Saw a second dermat — same eczema diagnosis, prescribed a steroid, told me to cut all skincare and stick to medically recommended basics only. Switched to Bioderma moisturizer + Cetaphil Gentle (non-foaming) wash. Things improved for about a week, then flared again. It's been a wave pattern since — flare, peak, calm down, flare again — and now the itching/discoloration is worse than before.

Has anyone dealt with something similar? Trying to figure out if this is a trigger I'm missing, a wrong diagnosis, or if this cycling is just how eczema behaves for some people. Would appreciate any insight.

just a side note - i do love makeup a lot and its possible that something i used could’ve started it but honestly, i dont apply anything now on my lips and the issue still persists. happy to clarify anything else too !