Basically, when you've used steroids (oral and topical) to suppress eczema, your skin can become addicted. In my case, the lower doses stopped working, so my derm prescribed higher and higher amounts. I used topical steroids on and off for YEARS - everything from OTC hydrocortisone to prednisone oral.
When you stop taking/using the steroids, your skin erupts. Red, hot, burning, oozing, flaky, swollen - everywhere. No matter where you used the steroids. One classic symptom is red skin stopping at your wrists. This pic isn't me, but it's exactly what I look like:
It's awful. It's so itchy, I want to rip my skin off. I'm so gross, I hate being in public. My face isn't too bad (today), but my arms and hands are horrible. My neck is a mess and my lips are swollen. No lotion or cream is enough to help - I went through a tub of raw shea butter in about 1.5 weeks. The only thing that will cure it is time. I have to let this all get out of my system. No clue how long it will be Some people get better in a few months, some take a year +.
I guess I'm sharing this b/c I know a lot of posters have eczema and/or your kids have it, so PLEASE try to avoid the topic steroids. Here is where I'm finding a lot of my support: www.itsan.org/eczemacure.html
Oh, I feel for you just seeing the pic. I never knew that could happen from steroid use. I hope it will start to clear up soon so you can feel some relief.
Poor thing! Would an oatmeal bath, or whatever you do for chicken pox, give some relief?
In my case, the water makes me feel even worse. :-( I feel good when I'm in the tub, but even more dry when I'm out.
I can't do anything to make it go faster, unfortunately. I can use some lotions to help alleviate the flaking/shedding that is constant, but that's about it.
I've become really anti-social since this started b/c I just feel like a freak of nature. I have a lot of presentations/conferences coming up and I am vain enough to be super worried about being there. I'm a bit thankful that it's winter so I can cover my hideous red and flaking legs and arms, but if I still have this when it gets warmer, I don't know what I'll do.
I've become really anti-social since this started b/c I just feel like a freak of nature. I have a lot of presentations/conferences coming up and I am vain enough to be super worried about being there. I'm a bit thankful that it's winter so I can cover my hideous red and flaking legs and arms, but if I still have this when it gets warmer, I don't know what I'll do.
I would just think you had vacationed recently somewhere truly amazing and had gotten some sun, and I would be jealous.
I cannot tell you what a single person who I've seen present at a conference has looked like or worn. Its the content that matters, not what you look like. Promise.
You better not beg out of meeting me in MD because of this. Not a valid excuse!
{{hugs}}
LOL, I have no choice! We posted a position and already have over 50+ people that want to interview at TPE with us!
Post by chickadee77 on Feb 11, 2014 11:19:57 GMT -5
Oh, no, I'm sorry. And ouch.
I used to sometimes use topical steroid on patches on my face, but read about this when I got my first BFP. It scared me into tossing the meds and figuring out alternatives.
We are supposed to do steroids up to twice a day when M flares but I hate using them so try to limit.
But he is SO flared right now I have no other options.
I don't know what to do.
Honestly, I would say do some research with the link I just posted. I can't tell you what to do, but if I had known this is what I would go through, I never would have started using the topical steroids on myself.
Oh man I'm so sorry! I have psoriasis and I have been avoiding cortisone creams unless absolutely necessary. I was given a warning by a doc years ago not to get attached to the creams, for this very reason (well that and the whole liver issue). Anyways, I hope you start feeling some relief! Drink lots of water!
Ugh I'm wriggling thinking of being in your shoes right now
Ugh - I have moderate to severe psoriasis and have been on topical steroids for over 6 years - they don't even clear it up - just make it a little more bearable I guess? I'm also on Humira right now, but will be TTC soon and was hoping I could stave off the worst of it with topicals. Off to research that link - thanks OP and I'm SO sorry you're going through this. Sometimes this skin stuff can be the worst.
Oh man I'm so sorry! I have psoriasis and I have been avoiding cortisone creams unless absolutely necessary. I was given a warning by a doc years ago not to get attached to the creams, for this very reason (well that and the whole liver issue). Anyways, I hope you start feeling some relief! Drink lots of water!
Ugh I'm wriggling thinking of being in your shoes right now
Ugh - I have moderate to severe psoriasis and have been on topical steroids for over 6 years - they don't even clear it up - just make it a little more bearable I guess? I'm also on Humira right now, but will be TTC soon and was hoping I could stave off the worst of it with topicals. Off to research that link - thanks OP and I'm SO sorry you're going through this. Sometimes this skin stuff can be the worst.
Ugh, yeah. It's so hard.
And it makes me really mad at my derm b/c he kept giving me more and more and more steroids. Over and over again. Prednisone, topic ointments, etc. And all he would tell me is to use in moderation b/c it would thin my skin. NOTHING about what other things it would do.
. Glad you found out the problem, and hope it clears quickly.
Eczema sucks. Very interesting about the wrists. They're one of my worst places on my body. I hate getting them wet.
YES
The backs of my hands are soooo bad. I hate washing my hands and giving DS a bath b/c the water makes it worse.
It's like the water can send the itching into overdrive. I wear gloves when I cook, so I can lessen the number of times I have to wash them. I change pairs in between working with certain things like eggs and meat, but it's almost a necessity as much.
Taking a shower doesn't bother me as much as getting them wet when I'm just washing my hands, oddly enough.
That stinks! I"m sorry! I hope it's a short term thing for you!
(also, good to know! Because I have super bad eczema on my hands and I've been debating on getting a prescription for it! I'll stick with my steroid free cream!)
Post by asoctoberfalls on Feb 13, 2014 18:34:13 GMT -5
How do you tell if you have this? I have super severe eczema, mostly on my hands. We are talking constantly flaring, constantly infected and weeping, etc. I stopped using my steroids for 2 weeks and it became even worse. My derm told me to go back on them immediately. I asked her about topical steroid addiction, but she said it's a concern only when the steroids are used on areas with thin skin, like your face.
I've had at least 20 derm appts in the last year. I'm sick of it! I feel your pain!