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Question:

– Hide quoted text — Show quoted text -> Hi all. > For some 10 years now (I’m 29), I’ve had a sore and flaky scalp, with some > guest appearances in the face (sides of the nose, eyebrows, spots on my > chin), chest and some spots in the "great down under". :-/ > I was initially diagnosed with seborrheic dermatitis, and prescribed a > Diprosalic treatment, which kind of worked, but after each application, > the rash always came back, seemingly a bit stronger than before. > Today, however, my (new) doctor said that it was probably (and > unfortunately) psoriasis, and prescribed me some Diprosalic and Daivonex > (Dovonex in the US?). > I know the symptoms are fairly similar, so I was wondering if there is > any bulletproof way to determine what exactly it is that ails me. And more > importantly, is it vital for a treatment to be successful to know?

A biopsy can be done to determine for sure what it is.  But I don’t know that it’s necessary unless perhaps whatever it is does not respond to treatment.  I have both P and Seb Derm, and am using the same treatment (topical steroids) for both…with the exception of now using something stronger on the P.  The Seb Derm is in my ears, and I don’t think it would be wise to use anything very strong in there. There is no cure for either condition.  Both will come back.  You just have to keep applying the cream.  I have a friend who gets Seb Derm on his face. He said it comes back about every three weeks.  He usually only has to apply the cream once and it takes care of it for a while. — Type 2 http://users.bestweb.net/~jbove/ Julie Bove, posting from new account

Response:

Hi all. For some 10 years now (I’m 29), I’ve had a sore and flaky scalp, with some guest appearances in the face (sides of the nose, eyebrows, spots on my chin), chest and some spots in the "great down under". :-/ I was initially diagnosed with seborrheic dermatitis, and prescribed a Diprosalic treatment, which kind of worked, but after each application, the rash always came back, seemingly a bit stronger than before. Today, however, my (new) doctor said that it was probably (and unfortunately) psoriasis, and prescribed me some Diprosalic and Daivonex (Dovonex in the US?). I know the symptoms are fairly similar, so I was wondering if there is any bulletproof way to determine what exactly it is that ails me. And more importantly, is it vital for a treatment to be successful to know? Vidar

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>I know the symptoms are fairly similar, so I was wondering if there is >any bulletproof way to determine what exactly it is that ails me. And more >importantly, is it vital for a treatment to be successful to know?

Apparently not, to both. If the treatment regimen for either one works better, maybe that proves out the diagnosis! J.

Response:

- Hide quoted text — Show quoted text – > Hi all. > For some 10 years now (I’m 29), I’ve had a sore and flaky scalp, with some > guest appearances in the face (sides of the nose, eyebrows, spots on my > chin), chest and some spots in the "great down under". :-/ > I was initially diagnosed with seborrheic dermatitis, and prescribed a > Diprosalic treatment, which kind of worked, but after each application, > the rash always came back, seemingly a bit stronger than before. > Today, however, my (new) doctor said that it was probably (and > unfortunately) psoriasis, and prescribed me some Diprosalic and Daivonex > (Dovonex in the US?). > I know the symptoms are fairly similar, so I was wondering if there is > any bulletproof way to determine what exactly it is that ails me. And more > importantly, is it vital for a treatment to be successful to know? > Vidar

It sounds as if it is time for you to see a dermatologist. He/She can tell you for sure. — Chuck "If you once forfeit the confidence of your fellow citizens, you can never regain it. It is true that you may fool all of the people some of the time; you can even fool some of the people all of the time; but you can’t fool all of the people all of the time." Abraham Lincoln

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Question:

>Any kind of extra bacterial load may aggravate psoriasis.

True.  When I had my cellulitis infection in the rash from my Enbrel allergic reaction (long story), I flared up in skin psoriasis all over, maybe 90% coverage in one DAY.  Pretty scary I tell you… When I discussed it with the dermatologist, he said it is not uncommon; any kind of bacterial infection can cause a flare in psoriasis. Happily mine was very temporary; once I was put on heavy-duty antibiotics for the infection, my skin calmed down and with the help of some Dovonex ointment, went back to its previous very low coverage of maybe 5 percent or less. LadyAndy Chat live with us at >http://tinyurl.com/4ust < (this is at iVillageHealth – my chats are on Sun evenings at 10 ET) Joint Replacement Board at http://boards.ivillagehealth.com/cgi-bin/boards/bhivhjointreplace

Response:

Now that you mentioned it.  I am also living in pain due to bad teeth.  Now I think maybe there is a connection with p. David

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>Now that you mentioned it.  I am also living in pain due to bad teeth.  Now >I think maybe there is a connection with p. >David

Hey David, whether it is related to the Ps or not, you need to get that taken care of.  If money is the problem, try asking around with some dentists asking if they can help you and offer you payment terms.  You’d be surprised how much some of them will bend over backwards to help out somebody who needs it. You can also post to sci.med.dentistry for some frank replies from several dentists and other dental specialists.  Yeah, there’s some weird stuff there too, but hey, this is Usenet.  :) LadyAndy Chat live with us at >http://tinyurl.com/4ust < (this is at iVillageHealth – my chats are on Sun evenings at 10 ET) Joint Replacement Board at http://boards.ivillagehealth.com/cgi-bin/boards/bhivhjointreplace

Response:

>> Don’t know if the dental problems are a definite link for sure. And if it was, > it could have been the stress from the whole situation, or the infection, or > both. >According to my dermatologist and most things I have read, quite often the first >onset of psoriasis comes about during a time of stress. I would say that two >abscessed teeth would qualify very well.

Any kind of extra bacterial load may aggravate psoriasis. Haven’t they reported a couple of times in recent years that heart disease correlates to arterial inflammation correlates to dental hygiene?  Brush your teeth, protect your heart, and maybe reduce your psoriasis, at least a tad. J.

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- Hide quoted text — Show quoted text – > Yo I can relate to this. > I had 2 abcessing teeth and a couple of cavites for about 18months because I > didn’t have the money to get them fixed with a dentist. about 6 months into the > painful ordeal I got P for the the first time and had it ever since. > Now I just got my teeth fixed (2 root canals, 5 fillings and a deep cleaning > Its been about a week since my last dentist appointment and my P is  a little > better. Which suprised me becasue it should be worse seeing as I havent gone to > the tanning bed in awhile. > Don’t know if the dental problems are a definite link for sure. And if it was, > it could have been the stress from the whole situation, or the infection, or > both.

According to my dermatologist and most things I have read, quite often the first onset of psoriasis comes about during a time of stress. I would say that two abscessed teeth would qualify very well. — Chuck "If you once forfeit the confidence of your fellow citizens, you can never regain it. It is true that you may fool all of the people some of the time; you can even fool some of the people all of the time; but you can’t fool all of the people all of the time." Abraham Lincoln

Response:

I am curious if anyone has had any experience with decaying/impacted/infected wisdom teeth triggering psoriasis.  I had no signs of psoriasis until about two years ago.  My wisdom teeth first popped up four or five years ago.  Now one tooth bothers me on, and off, and I have little doubt that it is infected.  I plan on having all four removed soon.  Any experiences, or guesses would be appreciated. Jeffrey Wilk

Response:

Yo I can relate to this. I had 2 abcessing teeth and a couple of cavites for about 18months because I didn’t have the money to get them fixed with a dentist. about 6 months into the painful ordeal I got P for the the first time and had it ever since. Now I just got my teeth fixed (2 root canals, 5 fillings and a deep cleaning Its been about a week since my last dentist appointment and my P is  a little better. Which suprised me becasue it should be worse seeing as I havent gone to the tanning bed in awhile. Don’t know if the dental problems are a definite link for sure. And if it was, it could have been the stress from the whole situation, or the infection, or both.

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Question:

>      One thing psoriasis teaches you is that you need to have patience. >Maybe that is what I am meant to learn in this life?

Also how to spell stuff like "erythromycin" and what all these biotech terms are that Randall throws our way.  Education is such a pain … :) J.

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I tend to just copy and paste all the hard words!  I don’t think that I have learnt that much patience! ;-)

>      One thing psoriasis teaches you is that you need to have patience. >Maybe that is what I am meant to learn in this life? > Also how to spell stuff like "erythromycin" and what all these biotech > terms are that Randall throws our way.  Education is such a pain … > :) > J.

— Outgoing mail is certified Virus Free. Checked by AVG anti-virus system (http://www.grisoft.com).

Response:

I have finished the week’s worth of erythromycin that the doctor prescribed and have started to apply the Alphosyll HC cream sparing twice a day. I do feel that my psoriasis is gradually calming down. The large patches no longer feel hot to the touch and no longer itch and are smooth with little flaking. This is a slow and sure way of getting rid of it but seems worth persevering with if you have two or three large patches as I do on my elbows and thigh. Another good thing about this cream is that it doesn’t smell and doesn’t stain. This seems to be a quite inexpensive method of treating psoriasis in cases like mine if you can tolerate coal tar. These are the UK details from http://bnf.vhn.net/bnf/documents/bnf.2352.html#BNFID_5961 (The trademarks probably won’t translate properly) Alphosyl HC

Question:

I found this news group over a year ago.  Every day I would come in and read the posts, but I never used to respond.  One day I read a post that tugged at my heart.  It was from a guy that had P and was venting his frustration.  I decided to respond… nothing to exciting, just that I understood exactly what he meant and that if he wanted to talk, I would listen.  He wrote back. I wrote back…and so on and so on…..  It’s been over a year, and i can honestly say, that I have never met anyone with as much fire, passion, sweetness and love. I would have never drempt that responding to a post would be so life changing. You never know…… there is someone, perhaps here in this news group, that would love to give you that hug, and lather you up with lotion, and tell you to stop scratching when you dont even realize that you are, Somone that will  kiss every patch you have, without blinking an eye.  Love is a mysterious thing, it may just be hiding in the next post that you and put up wet (lol sorry!!!), you never know, you just might find someone in here that will be more than willing to help….. I say keep posting, and good Hope

Response:

> bloody hell, I think I could get a trip to the States if this thread > continues!!!

just make sure your passport is up todate..lol > Thanks for the giggles fellas. Much appreciated from a women with > psoriasis all over, yes, even those bits!

your welcome for the giggles – Hide quoted text — Show quoted text -> Here is my unsolicited advice and ramblings. > Don’t forget that women don’t think like men do. That is what always > trips me up. My bloke mates remind me all the time that my body is not > what and who I am. I am female and 50% covered in psoriasis on a good > day. Most of the time much more. > Guys, women are much more understanding than you give us credit for. I > know you haven’t met her yet, but she is there. She is shy and wants to > touch you, but is unsure how to go about it. > There is someone there who will touch you with love. Someone who will > rub cream into  your aching skin. Who will put the hot water bottle > against your sore joints. Someone who will laugh at the amount of > vaccuuming that has to be done. > Someone who will love the bands you are into, the job you do, the footy > team you support. > The tyranny of psoriasis can be overcome. You are not your skin.

I think all I really need is to get the insurence, get to the docotor, and a hug(well not from the doctor…that’s the "cure" treatment that will give me the confidence to ask for the hug..)

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lol shame shame shame…..

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> lol shame shame shame…..

Is this an offer?? lol

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bloody hell, I think I could get a trip to the States if this thread continues!!! Thanks for the giggles fellas. Much appreciated from a women with psoriasis all over, yes, even those bits! Here is my unsolicited advice and ramblings. Don’t forget that women don’t think like men do. That is what always trips me up. My bloke mates remind me all the time that my body is not what and who I am. I am female and 50% covered in psoriasis on a good day. Most of the time much more. Guys, women are much more understanding than you give us credit for. I know you haven’t met her yet, but she is there. She is shy and wants to touch you, but is unsure how to go about it. There is someone there who will touch you with love. Someone who will rub cream into  your aching skin. Who will put the hot water bottle against your sore joints. Someone who will laugh at the amount of vaccuuming that has to be done. Someone who will love the bands you are into, the job you do, the footy team you support. The tyranny of psoriasis can be overcome. You are not your skin. El. – Hide quoted text — Show quoted text -> lol shame shame shame….. > Is this an offer?? > lol

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man or women……just don’t care anymore

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> man or women……just don’t care anymore

Darn too bad your not a woman.. Your more desperate than me it sounds

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How about anyone in philly?  (women please)

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> How about anyone in philly?  (women please)

We’ve started another one of those treads! I’ll go ahead and say I don’t care where you are.. I’ll fly you here…  LOL

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Question:

Perhaps you could feed your baby both baby formula and breast milk.  You can use a breast pump to get whatever breast milk that you can provide, and do so in a more comfortable time frame. Then you can use this milk to supplement the formula feedings. I am told that a mother’s breast milk provides many more things for the baby than just calories, i.e., antigens, and other things to help make a baby healthy. Good luck, Tom – Hide quoted text — Show quoted text – > I want to thank all of you for giving me a response. It’s really > helpfull. Unfortunately I think I have to stop breastfeeding. My baby > is not growing enough. My doctor thinks it might be because of P. The > fact that it hurts gives me stress while feeding so the milk becomes > less. I will try a bit longer with moisturizer and different > positions during feeding but I’m afraid that P. makes it impossible > to feed her the way I want. I don’t have a special lamp and it’s the > midst of winter so there’s no sunlight. He indeed doesn’t want me to > use Daivonex cream, and has no further options for me. > Anyway, thank you all for your tips. You’re great. > This really is a great newsgroup.

Response:

> Maybe someone has experience with breastfeeding and P?

Yup, about a year ago. As a result of our posts to this and other groups, we found we were not alone (others had gone through it), but there were also not many answers. Some had to give up breast feeding – it is *very* painful. My wife managed to persist, but it was really hard at times. The P. eventually reduced at 3-4 mths, but there is still a bit there. A Lanoline cream (eg Lansinoh) was the best answer. Very expensive (in New Zealand at least), but it is safe with baby. Expressing may help. Sunlight/UVB may help, as may sea water. Try crossposting to http://groups.yahoo.com/group/psoriasis_support/ too. — Dave

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>Hallo! >Always be very careful with your medication while breastfeeding, creams >usually are cortisone steroid based.

Often, but I don’t think I’d say usually. Especially as she said that she’s using Dovonex/Daivonex, which is not a corticosteroid. That being said, it’s still probably not a good idea to use it or any other topical while breast feeding both because of the usual issues with the baby picking up the topical from the skin surface while feeding, but also because of possible problems from what gets absorbed in your system. With daivonex, that concern involves getting too much calcium in your system if you go over a certain weekly dose and I would think the baby might be even more sensitive to the effects. Iris – everything I’ve seen says to talk with your doctor about using dovonex/daivonex when breast feeding. They don’t say you can’t use it, but I think there’s concern because they really don’t known enough about how safe it is. It’s probably better to avoid all topical or systemic medicines and switch to a combination of safe moisturizers and UV light treatments while breast feeding if that’s an option and one that would be effective for you. This has been talked about here before, so let me give you a link to prior discussion in case you find any helpful ideas there from others who’ve been through the same thing: http://pinch.com/skinny?skin=psoriasis+AND+%28breastfeed+OR+%22breast… Kim The Psoriasis Newsgroup Resource FAQ can be found at               http://www.psoriasisfaq.com but will also be coming soon (twice a month) to a            newsgroup near you…

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> Then in january 2002 I got pregnant and it all went away. (I’m not suggesting > pregancy is the answer)

I have heard that a woman’s immune system is turned down during pregnancy.  Why?  Because there is a foreign organism growing inside her that should not be attacked by the immune system.  The baby is half the father’s genes.

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>> Then in january 2002 I got pregnant and it all went away. (I’m not > suggesting pregancy is the answer) >I have heard that a woman’s immune system is turned down during >pregnancy.  Why?  Because there is a foreign organism growing inside >her that should not be attacked by the immune system.  The baby is >half the father’s genes.

May be true for many women out there, but not all.  Some largish percentage of psoriatics who get pregnant actually have their psoriasis get worse, instead of better.  And some more experience no change whatsoever.  I forget the exact numbers. – Dave W. http://psorsite.com/

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I want to thank all of you for giving me a response. It’s really helpfull. Unfortunately I think I have to stop breastfeeding. My baby is not growing enough. My doctor thinks it might be because of P. The fact that it hurts gives me stress while feeding so the milk becomes less. I will try a bit longer with moisturizer and different positions during feeding but I’m afraid that P. makes it impossible to feed her the way I want. I don’t have a special lamp and it’s the midst of winter so there’s no sunlight. He indeed doesn’t want me to use Daivonex cream, and has no further options for me. Anyway, thank you all for your tips. You’re great. This really is a great newsgroup.

– Hide quoted text — Show quoted text -> Hallo! > Always be very careful with your medication while breastfeeding, creams > usually are cortisone steroid based. > It is indeed very confusing at times to understand all the drug names in > Enlish. > I have P. for 20 years (I’m 29) and I had all sorts of creams. The tough > part of P. is it sometimes need radical medication to get rid of it. In your > case you can only use mild medication because of your little one. When > you’re done breastfeeding go back to your dermatologist and ask for some > good research on your P. and get some bloodwork done. Sometimes P. appears > because you had a yeast infection, > (schimmel infectie) but there could be many triggers. For me it was a skin > discoloration in my neck that was scrubbed clean, or they tried to anyway, > and that started to irritate. If you have any trouble understanding some of > the names used give me a yell, and if I understand it myself I’ll explain it > to you. If there is something that even I do not understand the people here > are nice enough to try and give you their explantion. > Groetjes, > Misty. > Hai, > I’m Iris from Holland. I’m very confused when I read all the messages > here. > It’s difficult to understand the names of the drugs in english. I hope you > understand what I’m talking about. > My grandfather and mother both suffered from severe psoriasis. I got in > november 2001, it started with little spots all over my body. Then in > january 2002 I got pregnant and it all went away. (I’m not suggesting > pregancy is the answer) In october I delivered and just 3 weeks later it > returned. Unfortunately on my breasts. I’m still breastfeeding so I’m not > sure if I can use the drug I have. It’s called Daivonex creme. That’s the > dutch name. It contains calcipotriol, dinatriumedetate, dinatriumfosfate > dihydrate, liquid parafine, glycerol, cetomacrogol 1000, ceylstearyl > alcohol, chloorallylhexaminium-chloride and water. I hope someone > recognizes > this and can help me. Cause from spots I went to big (??what’s this in > english??) "places". > Maybe someone has experience with breastfeeding and P? > Thanx  Iris

Response:

Hai, I’m Iris from Holland. I’m very confused when I read all the messages here. It’s difficult to understand the names of the drugs in english. I hope you understand what I’m talking about. My grandfather and mother both suffered from severe psoriasis. I got in november 2001, it started with little spots all over my body. Then in january 2002 I got pregnant and it all went away. (I’m not suggesting pregancy is the answer) In october I delivered and just 3 weeks later it returned. Unfortunately on my breasts. I’m still breastfeeding so I’m not sure if I can use the drug I have. It’s called Daivonex creme. That’s the dutch name. It contains calcipotriol, dinatriumedetate, dinatriumfosfate dihydrate, liquid parafine, glycerol, cetomacrogol 1000, ceylstearyl alcohol, chloorallylhexaminium-chloride and water. I hope someone recognizes this and can help me. Cause from spots I went to big (??what’s this in english??) "places". Maybe someone has experience with breastfeeding and P? Thanx  Iris

Response:

Hallo! Always be very careful with your medication while breastfeeding, creams usually are cortisone steroid based. It is indeed very confusing at times to understand all the drug names in Enlish. I have P. for 20 years (I’m 29) and I had all sorts of creams. The tough part of P. is it sometimes need radical medication to get rid of it. In your case you can only use mild medication because of your little one. When you’re done breastfeeding go back to your dermatologist and ask for some good research on your P. and get some bloodwork done. Sometimes P. appears because you had a yeast infection, (schimmel infectie) but there could be many triggers. For me it was a skin discoloration in my neck that was scrubbed clean, or they tried to anyway, and that started to irritate. If you have any trouble understanding some of the names used give me a yell, and if I understand it myself I’ll explain it to you. If there is something that even I do not understand the people here are nice enough to try and give you their explantion. Groetjes, Misty. – Hide quoted text — Show quoted text -> Hai, > I’m Iris from Holland. I’m very confused when I read all the messages here. > It’s difficult to understand the names of the drugs in english. I hope you > understand what I’m talking about. > My grandfather and mother both suffered from severe psoriasis. I got in > november 2001, it started with little spots all over my body. Then in > january 2002 I got pregnant and it all went away. (I’m not suggesting > pregancy is the answer) In october I delivered and just 3 weeks later it > returned. Unfortunately on my breasts. I’m still breastfeeding so I’m not > sure if I can use the drug I have. It’s called Daivonex creme. That’s the > dutch name. It contains calcipotriol, dinatriumedetate, dinatriumfosfate > dihydrate, liquid parafine, glycerol, cetomacrogol 1000, ceylstearyl > alcohol, chloorallylhexaminium-chloride and water. I hope someone recognizes > this and can help me. Cause from spots I went to big (??what’s this in > english??) "places". > Maybe someone has experience with breastfeeding and P? > Thanx  Iris

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Question:

Thank you for your help.  I looked at some of the sites on P but was a bit overwhelmed.  There is so much information.  You referred to the UVB.  It has been so long I can not remember how we used it.  I think perhaps we just got a UV bulb and put it in a  lamp that would hang directly over the floor.  We would just get him to lay under it for 10-15 min on each side.  Something like that.  Is that the right thing to do?  How many times a day should he do it?   It seems like there was a salve we put on him but it was very messy.  Thanks for your response. – Hide quoted text — Show quoted text ->Hi, there’s a link in my .sig to the group FAQ, which is itself >basically a set of links to other information sources such as you are >looking for. >Strep is a pretty common trigger of a type of psoriasis called guttate >because it comes out in a bunch of not very scaly red droplets. Sounds >like that’s what he’s got and FWIW in that case some of the new things >people are posting about, like Amevive, are not appropriate for that >form. >One of the first things to do to treat it is to try to get rid of the >strep infection that is triggering the outbreak. After that, there has >been a lot of progress in treatments in the 20 years since, but in a >lot of cases they aren’t appropriate unless the case is particularly >severe because of side effect risks. UVB is still a good place to >start, because it can be very effective for that kind and is also very >safe. After that, there are a few different categories of topicals to >use singly or in combination with UVB/each other. These include >different strengths of cortico-steroids, which are probably what he >was given as a kid. Fairly safe to use, but some side effect risks >with high strength long term continual use. Dovonex, a vitamin D >analogue that is slower to work but has less side effect risks. >Steroids and dovonex together are often more effective than either >alone.  Anthralin, another topical that can stain and irritate but is >otherwise very safe and can be quite effective. And on. >Seriously, what you should do is read a bit from some of the places >linked to in the FAQ, like the NPF, to get a bit of basic info about >what your options are, then make an appointment with a good derm to >get treatment that will get it under control ASAP.. >Kim >My son had psoriasis as a child.  It only showed up on two occassions >when he had strep throat at ages 7 and 14.  In both cases we used some >kind of ointment and had him sit under an ultraviolet lamp.  It seemed >like it went away in a month or so.   As a 30 year old adult he >occassionally has minimal shows of the condition that do not last >long.  Recently he had a sore throat and it poped out all over him. >What is the state of the art of treatment for psoriasis now?  Any >recommendations for treatment or advice about how to proceed will be >appreciated.  Also, if there are any good web sites on this, please >let me know.   Thanks >The Psoriasis Newsgroup Resource FAQ can be found at >              http://www.psoriasisfaq.com >but will also be coming soon (twice a month) to a >           newsgroup near you…

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Hi, there’s a link in my .sig to the group FAQ, which is itself basically a set of links to other information sources such as you are looking for. Strep is a pretty common trigger of a type of psoriasis called guttate because it comes out in a bunch of not very scaly red droplets. Sounds like that’s what he’s got and FWIW in that case some of the new things people are posting about, like Amevive, are not appropriate for that form. One of the first things to do to treat it is to try to get rid of the strep infection that is triggering the outbreak. After that, there has been a lot of progress in treatments in the 20 years since, but in a lot of cases they aren’t appropriate unless the case is particularly severe because of side effect risks. UVB is still a good place to start, because it can be very effective for that kind and is also very safe. After that, there are a few different categories of topicals to use singly or in combination with UVB/each other. These include different strengths of cortico-steroids, which are probably what he was given as a kid. Fairly safe to use, but some side effect risks with high strength long term continual use. Dovonex, a vitamin D analogue that is slower to work but has less side effect risks. Steroids and dovonex together are often more effective than either alone.  Anthralin, another topical that can stain and irritate but is otherwise very safe and can be quite effective. And on. Seriously, what you should do is read a bit from some of the places linked to in the FAQ, like the NPF, to get a bit of basic info about what your options are, then make an appointment with a good derm to get treatment that will get it under control ASAP.. Kim >My son had psoriasis as a child.  It only showed up on two occassions >when he had strep throat at ages 7 and 14.  In both cases we used some >kind of ointment and had him sit under an ultraviolet lamp.  It seemed >like it went away in a month or so.   As a 30 year old adult he >occassionally has minimal shows of the condition that do not last >long.  Recently he had a sore throat and it poped out all over him. >What is the state of the art of treatment for psoriasis now?  Any >recommendations for treatment or advice about how to proceed will be >appreciated.  Also, if there are any good web sites on this, please >let me know.   Thanks

The Psoriasis Newsgroup Resource FAQ can be found at               http://www.psoriasisfaq.com but will also be coming soon (twice a month) to a            newsgroup near you…

Response:

> My son had psoriasis as a child.  It only showed up on two occassions > when he had strep throat at ages 7 and 14.  In both cases we used some > kind of ointment and had him sit under an ultraviolet lamp.  It seemed > like it went away in a month or so.   As a 30 year old adult he > occassionally has minimal shows of the condition that do not last > long.  Recently he had a sore throat and it poped out all over him. > What is the state of the art of treatment for psoriasis now?  Any > recommendations for treatment or advice about how to proceed will be > appreciated.  Also, if there are any good web sites on this, please > let me know.   Thanks

Hi, http://www.yourmedicalsource.com/library/psoriasis/PSO_treatment.html Or www.psoriasis.org And/or, he can try a diet like Terrys or relaxation or ssri’s etc. Does he know how to google? You can extract any info out of this psoriasis group with a few choice keywords. Use www.deja.com and enter psorisis into the search box and then click the longer of the two options. (alt.support.skin-diseases.psoriasis) Then click the search this group only option and enter whatever keywords into the search box. Say you want to know what terrys diet is. Enter diet terry. Have a haPPy day. randall

Response:

My son had psoriasis as a child.  It only showed up on two occassions when he had strep throat at ages 7 and 14.  In both cases we used some kind of ointment and had him sit under an ultraviolet lamp.  It seemed like it went away in a month or so.   As a 30 year old adult he occassionally has minimal shows of the condition that do not last long.  Recently he had a sore throat and it poped out all over him. What is the state of the art of treatment for psoriasis now?  Any recommendations for treatment or advice about how to proceed will be appreciated.  Also, if there are any good web sites on this, please let me know.   Thanks

Response:

Question:

>But was it then treatable (manageable), and/or cured to your >satisfaction? >Ralph

Ralph, I don’t know if you haven’t read this yet, but psoriasis is not curable.  It may go into remission, or may be controlled adequately by medication or UVB radiation or any of a number of other variations, but it doesn’t go away completely. Happily in my case the psoriasis of my skin has never been a major disability. At its worst, it was maybe 60 – 70% coverage, but ever since starting treatment for my related psoriatic arthritis (PA), it has been below about 10% coverage and currently is below 5% coverage.  It is something I can easily put out of my mind completely. I do have psoriatic arthritis though, which in my case is the more serious side of the disease.  However, most people with psoriasis do not get the related arthritis, so do not be too concerned about it.  If your mom should begin to get arthritis symptoms, then she may wish to consult a rheumatologist to rule out psoriatic arthritis. LadyAndy Chat live with us at >http://tinyurl.com/4ust < (this is at iVillageHealth – my chats are on Sun evenings at 10 ET) Joint Replacement Board at http://boards.ivillagehealth.com/cgi-bin/boards/bhivhjointreplace

Response:

>Well, I agree, if there is no solution as yet, in her seeing four >dermatologists, she should see another until this is relieved, >if not cured, but one can’t go on forever in that process can they?

Yes, one can.  But… >I mean it would be quite discouraging for me to continue to >do that.

…this makes sense, too. >Thats why it makes sense to me to have a biopsy, (if she >hasn’t, I don’t know yet), and look to other possible diseases >or "skin conditions," as a possible source of her condition.

A biopsy might rule _out_ psoriasis, or it might help ID the condition as psoriasis, but it’s not going to limit the condition to just a single disease. Any information you can gather might help a doctor make a good diagnosis, but you’ll have to find a doctor who’s willing to listen to your opinions. >Tell me, are all forms of "P" considered to be "infections?"

NO forms of psoriasis are considered to be infections.  None.  Every form of psoriasis might be _triggered_ by an infection (guttate in particular often follows a bout of strep throat), but once psoriasis starts, it can be self-sustaining, and remain long after a triggering infection has been eliminated by the immune system with or without the help of drugs.  But there are lots of other possible triggers besides infection, too. >Well, that could be presumably arrogant and shortsighted if in fact >there are so many different kinds of P, some caused by infection, >some caused by emotional distress, and some caused by other >things, wouldn’t you say?

Well, not really.  Psoriasis may be affected by lots of things (stress in many people, but not in others; diet in some, but not in others; etc.), but that doesn’t mean that these different people necessarily have different diseases, or even different ‘forms’ of the same disease, or even the same disease caused by different things.  80-something percent of people with psoriasis get good results from using potent topical steroids, but that doesn’t mean that the other 20% or so have a different kind of psoriasis, it just means that the drug didn’t work, for any number of reasons. As for the "caused by" phrases, above, we can be pretty darned sure that psoriasis symptoms are caused by an inappropriate immune system response within the skin, in 100% of cases.  What causes that inappropriate response can often be traced to genetics, but the jury is still out on the question of which genes and why.  And it may not be the same set of genes in all cases, but the mechanisms for creating the symptoms in the skin itself are remarkably similar. The classic signs of psoriasis, which I outlined for you, will "catch" a large number of psoriasis patients without need of a biopsy – _if_ the diagnosing doctor knows to look for them.  The derm who said that anyone who relies on a biopsy to diagnose psoriasis doesn’t know psoriasis, was simply saying that much.  If a doctor’s first impulse is to do an invasive procedure (even if only slightly invasive, like a punch biopsy of skin), he/she would actually be a better doctor to refer the patient to someone more knowledgable. >It is certainly well defined, but not by inflamation as much as, (in >the case of her legs anyway), it is by color.  I take inflamation to >mean a rise in elevation of the skin in transition from >the other surrounding skin.

No.  For the purposes of our discussion here, inflammation equals redness.  Red as in "on fire," or "inflamed." If by "elevation" you mean "thickness," that’s covered by the "raised skin" part of the diagnostic checklist. >These are not.

Not which?  Dry or moist?  Sorry, I sometimes have pronoun troubles.  :) >This is the case in some of her smaller patches, but not the large >ones, as those on her legs.  I’m wondering though if thats because >there is a thin-ness of skin and lack of flesh in that area, being near >the "schin" (sp) bone, and by repeated scarring.

Shin skin is pretty thin skin, in general, but my shin plaques, when they’ve occured, have always been raised compared to the surrounding skin. I take it you haven’t been witness to Auspitz’ Sign in your mother’s condition? >Thats encouraging.  I want to ad something here, that may be helpful >for some others, and possibley relates to this. [snip] >I finally went to her primary care physician with her, and described my >mother’s dislike for that heart doctor "for her."  She hadn’t the courage >herself.

[snip] First off, I’m glad that part of the story has a happy ending.  Secondly, it shouldn’t take any more courage to "fire" one of your doctors and find another than it does to "fire" the guy who rips you off when working on your car, and find another auto mechanic.  By paying the doctor, your mother was hiring that doctor to do a job for her.  If she wasn’t satisfied with the service, she should say so, and/or hire someone else.  She shouldn’t act as if the doctor was doing her a _favor_ by seeing her. And I say it _shouldn’t_ take courage to do this, but I’m well aware that some people see doctors as somehow god-like (and some doctors see themselves this way, too), which is why I didn’t say that it _doesn’t_ take courage to do it. In this day-and-age, though, when many people have many doctors available to them within an acceptable distance, your mother probably needs to realize that it’s _her_ health, and she’s got choices.  It’s been a long time since most towns had just the one doctor, and you didn’t want to annoy him by saying anything bad about him because the next-closest doctor was half a day away by ox-cart. This is, of course, true for just about any medical condition, not just heart problems or psoriasis. Hope all this helps. – Dave W. http://psorsite.com/

Response:

– Hide quoted text — Show quoted text -> Did you have a biopsy to determine that you in fact have psoriasis? > I am finding it interesting in my reading tonight to see that > sometimes this is difficult to diagnose, and sometimes requires this > to get an accurate diagnosis. > I’ve read alot about scales having a silvery look.  My mothers scales > aren’t silvery, but I’ve not seen it mentioned that they can also be > yellowish.  Yellowish is definately not silvery is it? > Could it be some other disease like tinea versicolor, a fungal > infection of the skin?  Instead of "P" ? > I don’t know. I do know where you can find an image. > Thanks > Ralph > Why don’t you look at some pictures (google images) and > let us know what you think.

http://images.google.com/images?q=psoriasis&hl=en&lr=&ie=UTF-8&sa=N&ta b=wi – Hide quoted text — Show quoted text -> There are over 4500 images to browse. You may even find > a name to attach to your moms rash. And it may not > fall under the p umbrella. I can think of enough names to > keep you busy for weeks. You may even find something > that looks silvery. > Or you could take davew’s advice and find a few > doctors to confirm the actual condition. > Whether you go home with some gooP for it is > uP to you. > So, lets say you have a name for it and its P. > What do you really know now? > A heck of a lot more then yesterday, for sure. > What do you and her do then? How much time do you > want to expend on the newsgroup cure for it? > Is she really covered or just some mild areas? > I did notice one post on selsun blue with robin > in another thread. Maybe i should have read the > whole thread to make a real diagnosis. > Then i could have told you to get her into > a garage and up on the rack. You only get one > mom and you don’t want to blow it, now do you? > randall… time to call mom and tell her i love  her

Thank you, I can tell you that this is definately not it: http://images.google.com/imgres?imgurl=www.antisense.com.au/images/sta tic/Psoriasis.jpg&imgrefurl=http://www.antisense.com.au/current_atl110 1_whatis.asp&h=152&w=260&prev=/images%3Fq%3Dpsoriasis%26svnum%3D10%26h l%3Den%26lr%3D%26ie%3DUTF-8%26sa%3DN You gave me an idea.  I have a fairly decent digital camera that will take a photograph clearly inside 18" so I will get a picture of my mothers condition, (legs), if she doesn’t mind, and post it to alt.binaries.misc or some such group. Thanks, Ralph

Response:

[snip] – Hide quoted text — Show quoted text -> Excellent clinical definition, DaveW.  Describes my psoriatic plaque lesions to > a "t".  Of course it doesn’t take into account the other forms of psoriasis. > Like you said, best choice is a dermatologist who has an interest in and sees a > lot of psoriasis in his or her practice. > As to the original question, my psoriasis was never biopsied; I guess mine is > typical enough never to have been in question. > LadyAndy > Chat live with us at >http://tinyurl.com/4ust < (this is at iVillageHealth – my > chats are on Sun evenings at 10 ET) > Joint Replacement Board at > http://boards.ivillagehealth.com/cgi-bin/boards/bhivhjointreplace

But was it then treatable (manageable), and/or cured to your satisfaction? Ralph

Response:

Excellent clinical definition, DaveW.  Describes my psoriatic plaque lesions to a "t".  Of course it doesn’t take into account the other forms of psoriasis. Like you said, best choice is a dermatologist who has an interest in and sees a lot of psoriasis in his or her practice. As to the original question, my psoriasis was never biopsied; I guess mine is typical enough never to have been in question. – Hide quoted text — Show quoted text ->Be that as it may, from memory (from a non-medically trained person, too), >here >are a bunch of bits of psoriasis diagnosis: >- Well-defined inflammation.  If the redness "fades" into the normal, >surrounding skin color, it probably isn’t psoriasis.  Psoriasis patches >usually >have very definite "lines" between inflamed skin and normal skin. >- Dry.  Undamaged psoriasis plaques don’t ooze, and they aren’t "moist." >- Raised.  Psoriasis patches are usually "taller" than normal, surrounding >skin, even when they don’t have scale built up on top of them. >- Auspitz Sign.  Because of the changes to the underlying dermis in a >psoriasis >plaque, if you remove a scale which isn’t already "loose," you’ll see lots of >pin-point bleeding.  Lots of little tiny dots of blood will appear where the >scale was well-attached to the dermis.

LadyAndy Chat live with us at >http://tinyurl.com/4ust < (this is at iVillageHealth – my chats are on Sun evenings at 10 ET) Joint Replacement Board at http://boards.ivillagehealth.com/cgi-bin/boards/bhivhjointreplace

Response:

> Did you have a biopsy to determine that you in fact have psoriasis? > I am finding it interesting in my reading tonight to see that > sometimes this is difficult to diagnose, and sometimes requires this > to get an accurate diagnosis. > I’ve read alot about scales having a silvery look.  My mothers scales > aren’t silvery, but I’ve not seen it mentioned that they can also be > yellowish.  Yellowish is definately not silvery is it? > Could it be some other disease like tinea versicolor, a fungal > infection of the skin?  Instead of "P" ?

I don’t know. I do know where you can find an image. > Thanks > Ralph

Why don’t you look at some pictures (google images) and let us know what you think. http://images.google.com/images?q=psoriasis&hl=en&lr=&ie=UTF-8&sa=N&t… There are over 4500 images to browse. You may even find a name to attach to your moms rash. And it may not fall under the p umbrella. I can think of enough names to keep you busy for weeks. You may even find something that looks silvery. Or you could take davew’s advice and find a few doctors to confirm the actual condition. Whether you go home with some gooP for it is uP to you. So, lets say you have a name for it and its P. What do you really know now? A heck of a lot more then yesterday, for sure. What do you and her do then? How much time do you want to expend on the newsgroup cure for it? Is she really covered or just some mild areas? I did notice one post on selsun blue with robin in another thread. Maybe i should have read the whole thread to make a real diagnosis. Then i could have told you to get her into a garage and up on the rack. You only get one mom and you don’t want to blow it, now do you? randall… time to call mom and tell her i love  her

Response:

>Did you have a biopsy to determine that you in fact have psoriasis? [snip] >Could it be some other disease like tinea versicolor, a fungal >infection of the skin?  Instead of "P" ?

It could be a lot of things, Ralph.  What really needs to happen is that your mom go to as many dermatologists as necessary, to get as many diagnoses as necessary and/or as many treatments as necessary to get real help. A dermatologist who used to post here once said that any derm who relies on a biopsy to diagnose psoriasis doesn’t know psoriasis.  It’s difficult to diagnose without a bioposy if the person attempting diagnosis isn’t familiar with psoriasis.  And it’ll be even more difficult for people who aren’t medically trained (like most of us here). Be that as it may, from memory (from a non-medically trained person, too), here are a bunch of bits of psoriasis diagnosis: – Well-defined inflammation.  If the redness "fades" into the normal, surrounding skin color, it probably isn’t psoriasis.  Psoriasis patches usually have very definite "lines" between inflamed skin and normal skin. – Dry.  Undamaged psoriasis plaques don’t ooze, and they aren’t "moist." – Raised.  Psoriasis patches are usually "taller" than normal, surrounding skin, even when they don’t have scale built up on top of them. – Auspitz Sign.  Because of the changes to the underlying dermis in a psoriasis plaque, if you remove a scale which isn’t already "loose," you’ll see lots of pin-point bleeding.  Lots of little tiny dots of blood will appear where the scale was well-attached to the dermis. None of the above is a marker for "that’s absolutely psoriasis," however, as other skin conditions can have a "psoriaform" appearance.  There’s no shortage of case histories in the medical literature which basically say, "well, this person was being treated for psoriasis, but none of the normal stuff worked, and then he/she came to us, and we saw this symptom that had been overlooked, and that enabled us to make the diagnosis of [insert something other than psoriasis here], which, with proper treatment, was managed/healed/cured easily." If there’s one in your area, take your mom to the dermatology department of a teaching hospital.  From what I’ve been told, they find "borderline" cases where the diagnosis isn’t cut-and-dried to be interesting for the medical students, so it might be more likely that whatever is plauging her will be diagnosed correctly.  Hopefully. And conversely, it’s highly unlikely that "Internet diagnosis" is going to work wonders.  There’s a reason that doctors are legally obligated to actually _see_ their patients before diagnosing them with any particular disease.  And the photos on the Web tend to be of low quality – more than once have I thought I saw psoriasis in a photo online, only to find out by reading the text that I was _way_ off. – Dave W. http://psorsite.com/

Response:

>Did you have a biopsy to determine that you in fact have psoriasis? > [snip] >Could it be some other disease like tinea versicolor, a fungal >infection of the skin?  Instead of "P" ? > It could be a lot of things, Ralph.  What really needs to happen is that your > mom go to as many dermatologists as necessary, to get as many diagnoses as > necessary and/or as many treatments as necessary to get real help.

Well, I agree, if there is no solution as yet, in her seeing four dermatologists, she should see another until this is relieved, if not cured, but one can’t go on forever in that process can they?  I mean it would be quite discouraging for me to continue to do that.  Thats why it makes sense to me to have a biopsy, (if she hasn’t, I don’t know yet), and look to other possible diseases or "skin conditions," as a possible source of her condition. Tell me, are all forms of "P" considered to be "infections?" > A dermatologist who used to post here once said that any derm who relies on a > biopsy to diagnose psoriasis doesn’t know psoriasis.

Well, that could be presumably arrogant and shortsighted if in fact there are so many different kinds of P, some caused by infection, some caused by emotional distress, and some caused by other things, wouldn’t you say? > It’s difficult to > diagnose without a bioposy if the person attempting diagnosis isn’t familiar > with psoriasis.  And it’ll be even more difficult for people who aren’t > medically trained (like most of us here).

Yes, I might suppose so. > Be that as it may, from memory (from a non-medically trained person, too), here > are a bunch of bits of psoriasis diagnosis: > – Well-defined inflammation.  If the redness "fades" into the normal, > surrounding skin color, it probably isn’t psoriasis.  Psoriasis patches usually > have very definite "lines" between inflamed skin and normal skin.

It is certainly well defined, but not by inflamation as much as, (in the case of her legs anyway), it is by color.  I take inflamation to mean a rise in elevation of the skin in transition from the other surrounding skin. > – Dry.  Undamaged psoriasis plaques don’t ooze, and they aren’t

"moist." These are not. > – Raised.  Psoriasis patches are usually "taller" than normal, surrounding > skin, even when they don’t have scale built up on top of them.

This is the case in some of her smaller patches, but not the large ones, as those on her legs.  I’m wondering though if thats because there is a thin-ness of skin and lack of flesh in that area, being near the "schin" (sp) bone, and by repeated scarring. – Hide quoted text — Show quoted text -> – Auspitz Sign.  Because of the changes to the underlying dermis in a psoriasis > plaque, if you remove a scale which isn’t already "loose," you’ll see lots of > pin-point bleeding.  Lots of little tiny dots of blood will appear where the > scale was well-attached to the dermis. > None of the above is a marker for "that’s absolutely psoriasis," however, as > other skin conditions can have a "psoriaform" appearance.  There’s no shortage > of case histories in the medical literature which basically say, "well, this > person was being treated for psoriasis, but none of the normal stuff worked, > and then he/she came to us, and we saw this symptom that had been overlooked, > and that enabled us to make the diagnosis of [insert something other than > psoriasis here], which, with proper treatment, was

managed/healed/cured > easily."

Thats encouraging.  I want to ad something here, that may be helpful for some others, and possibley relates to this.  My mother has also had an arythmic heart for years. For the past six years the steadily declining lack of oxygen to her heart incapacitated her gradually to the point to where walking a few yards, exhausted her.  She expressed to me a dislike of her heart doctor.  She claimed he would not talk to her, acted as if she were a thing, instead of a person.  Sort of as if she weren’t present.  My mother had inquired the possibility early on whether a pacemaker might help her condition and she was told repeatedly by this doctor that that was not an option for her.  I finally went to her primary care physician with her, and described my mother’s dislike for that heart doctor "for her."  She hadn’t the courage herself.  That doctor switched her to a doctor in her group of associates, and in less than 3 months time, after applying shock to the heart in a couple of success attempt to establish a rythm for the heart, which soon reverted, she indeed was fitted with a pacemaker and she is a new woman!  Able to excersize, do her housework, and socialize to the degree she was accoustomed. > If there’s one in your area, take your mom to the dermatology department of a > teaching hospital.  From what I’ve been told, they find "borderline" cases > where the diagnosis isn’t cut-and-dried to be interesting for the medical > students, so it might be more likely that whatever is plauging her will be > diagnosed correctly.  Hopefully.

That is a good idea. > And conversely, it’s highly unlikely that "Internet diagnosis" is going to work > wonders.  There’s a reason that doctors are legally obligated to actually _see_ > their patients before diagnosing them with any particular disease. And the > photos on the Web tend to be of low quality – more than once have I thought I > saw psoriasis in a photo online, only to find out by reading the text that I > was _way_ off. > – Dave W. > http://psorsite.com/

I understand.  Thank you for your post. Ralph

Response:

Did you have a biopsy to determine that you in fact have psoriasis? I am finding it interesting in my reading tonight to see that sometimes this is difficult to diagnose, and sometimes requires this to get an accurate diagnosis. I’ve read alot about scales having a silvery look.  My mothers scales aren’t silvery, but I’ve not seen it mentioned that they can also be yellowish.  Yellowish is definately not silvery is it? Could it be some other disease like tinea versicolor, a fungal infection of the skin?  Instead of "P" ? Thanks Ralph

Response:

Question:

> FDA Approves Biogen Psoriasis Drug > .c The Associated Press > CAMBRIDGE, Mass. (AP) – Biogen, Inc. said Friday that the Food and Drug > Administration had approved its drug Amevive, used to treat moderate and severe > cases of the skin disorder psoriasis.

[snip] Thank you — JDShine

Response:

>Biogen, Inc. said Friday that the Food and Drug >Administration had approved its drug Amevive, used to treat moderate and severe >cases of the skin disorder psoriasis.

thanks for the info I sent it on to a friend.  What have you heard about amevive from the clinical trials? How effective is it?   Is it anti-tnf. — MZ Visit my website: http://www.mzuschlag.com

Response:

>thanks for the info I sent it on to a friend.  What have you heard >about amevive from the clinical trials? How effective is it?   Is it >anti-tnf. — MZ

If you post questions in alt.support.skin-diseases.psoriasis, there are several participants in the trials who post there.  Sounds equally as impressive for psoriasis as the biologics have been around here for various forms of arthritis. The company website has just been set up and is just about complete now (wasn’t just a week ago :) ).  Try:  http://www.amevive.com/ Here is an excerpt from the website about the action of this biologic fusion protein: <<AMEVIVE

Question:

>And compel >them to do more research for a more satisfying solution to the >disease.

Making demands of a derm who sees patients will rarely get beyond the derm. Most of them are not involved in research. – Dave W. http://psorsite.com/

Response:

>> >First, steroids do not tackle the root of the > >problem it only suppress symptoms, and while the immune system may be > >locally suppressed the human body through the HPA axis upregulates the > >immune system systemically which results in worse disease in other > >parts of the body. > If you know about the HPA axis stuff, you should know the fairly-strict > definition of "rebound" that Kim is referring to. >Just because I know about the HPA axis I should be able to read minds >as well? >I am waiting for Kim to define her definition of rebound.  

Sorry I didn’t jump to heel fast enough. Guess I didn’t read minds fast enough either, as I only just checked back to see your call. It’s not my personal definition. although it is laid out pretty fully in the FAQ, which I did draft, had you looked (honestly, that’s a good idea with any newsgroup). While Psorsite provides a more technical explanation involving the HPA axis stuff, which is why Dave made the above comment http://psorsite.com/docs/stereffects.html My layman’s version is that a psoriasis rebound is when the treatment itself, once you stop using it or it becomes ineffective, causes the psoriais to abruptly worsen and spread beyond where it was prior to using the med. This is different from a regular flare occuring because the psoriasis isn’t being sufficiently controlled or is being otherwise triggered when you stop using a given treatment, which is the reality behind most of what people mistakenly call rebounds. Flares are a general part of the facts of psoriatic life for most people.  Rebounds are a very specific subset of them. Kim The Psoriasis Newsgroup Resource FAQ can be found at               http://www.psoriasisfaq.com but will also be coming soon (twice a month) to a            newsgroup near you…

Response:

>If you are indeed an exception than great for you.  Do you mean that >you can use steroids whenever you want and your psoriasis just gets >better with each use and now you are psoriasis free?

No, not at all.  I used some steroids back in the early days of my psoriasis, the psoriasis went away a bunch, and when I stopped using the steroids it came back some – but not to its original levels.  Fast forward two _years_, and I got some new patches on completely different limbs. >Maybe you can >share with others your personal experience with steroids, i.e. the >kinds of steroids you used and frequency and duration of use.  Maybe >the vast numbers of people who have problems with steroids have been >using it wrong and can learn something from you.

Please provide evidence supporting your assertion that there are "vast numbers" of people who have problems with steroids.  I can’t answer the implied question when the premise assumes facts not in evidence. >Would be interested to know your personal experience with psoriasis, >age of onset, type, triggers, response, treatment.

Age: 27 (now 36) Type: vulgaris Triggers: beats the heck out of me. Response: what do you mean, response? Treatment: Steroids, early on, coal tar keeps it in check enough for me now. >Exactly, steroids work by suppressing the immune system. However, >there is a distinction that must be made:  Immune suppression on a >systemic level, i.e. HPA axis; but also on a local level where the HPA >axis is not involved.  You assume that only large doses of strong >steroids suppress the immune system.

No, I assume that large doses of strong steroids (or lower dosages for long times) suppresses the HPA axis, which does not equal the immune system.  In fact, when the HPA axis is suppressed, the immune system can run rampant if there’s nothing else going on (like big doses of topical or oral steroids). >Small amounts of nonpotent >steroids used for brief periods of time usually have no effect on the >HPA axis.

Right. >However, because they work as you yourself know, they must >have suppressed the immune system at a local level and it’s this >effect that is worrisome and causes psoriasis to return worse than >before regardless of rebound.  Again, this is local upregulation of >cytokine production from T-cells and does not involve the HPA axis.

There you go again, using absolutes.  Provide evidence that cytokine production is higher after low-dose steroid usage than it was before. >"A few people"  hmmm, I wonder what "evidence" you have to support >your claim that only a few people have bad experience with steroids

You somehow think that every one of the millions of psoriatics in the world read this newsgroup?  The experiences related here are from a very small minority of the people with this disease. >Conversely, what evidence do you have for saying that "millions of >psoriatics" don’t get worse with steroid use.  If you have evidence, >please share it with me.

Actually, I’d much rather you support your claim first.  Your assertion, that is, that anyone who uses steroids for psoriasis "invariably" gets a worse case of psoriasis afterwards.  This is a statement which I’ve never encountered before, while I can say that I’ve read, from the NPF, about how the vast majority of psoriatics have only mild cases of the disease.  You are claiming that all of those people will, indeed, get worse psoriasis after the steroids they tend to use do their nasty work. >I don’t think I have to provide any evidence.

Yes, you do.  You made the claim, now back it up with data or appropriate citations… >Just think back on how your psoriasis first developed and spread.

…and not anecdotal evidence.  Because you’ll be surprised by me, again. Those extra spots that popped up two years after my steroid use?  They’re in places where it’s hard to get topicals to stay put, and so I haven’t been treating them, except for the occassional soak (twice a year, maybe).  But guess what?  They’re going away, anyway. >If psoriasis were a >self-limited disease, you probably wouldn’t have to use any steroids >and you wouldn’t be in a newsgroup trying to find solutions and argue >with me.

You’re making a ton of assumptions.  How much coverage do you think I have? And why didn’t you ask for that piece of data above? >You have yet to provide any convincing arguments or evidence to >counter what I have said in the first post.

I thought it was pretty clear that you provided your own best argument against using absolute terms the way you do.  You spoke of the massive variability of psoriasis.  Claiming that steroids _always_ make the disease worse at some later time disagrees with what you said, and also isn’t discussed in any of the medical literature.  You’re the one who’s making the big positive claims here, you need to back them up. >Which part of my post was >pseudo-medical nonsense, please be more specific.

Any place you used a term which signified certainty about these claims of yours which haven’t, apparently, been tested. >Experiential-I suggest that you look up the word experiential in a >dictionary and then reply.

I apologize.  I mis-read your word.  No need to get dictionary-snippy. >Again, I don’t think many people who are psoriasis sufferers would >agree with you.

Well, that’s one of the problems with your average person, now isn’t it? That’s why testimonials work so well in advertising.  They are not evidence, but billions of people think they are.  Facts, however, aren’t found by popularity contests, and some facts are downright unpopular.  It saddens me that millions of psoriasis sufferers (and billions of others) believe that testimonials are good evidence for medical claims, and I do my best to spread the "testimonials are not evidence" word. – Dave W. http://psorsite.com/

Response:

- Hide quoted text — Show quoted text ->Also, what is your definition of a rebound and how do you distinguish >it from a worsening especially when the disease has been stable over >time and worsened after steriod use? > Steve, I haven’t had the (awful) experience myself, but from all > accounts the "rebound" effect is completely obvious, if someone with > psoriasis goes cold-turkey after getting some relief from steroids. > It gets a lot worse, really fast. >  Also, there are lots of things >which may cause disease progression and steriod use is one of them, >regardless of duration and dosage of use. > That just isn’t clear.  It may well be true, but as you said further > along in your message, there’s a lot of variability in psoriasis, so > it may be a lot more true for some people than for others.  For people > with mild psoriasis, using modest amounts of steroids, there are > apparently a lot of people who manage to use them and get some relief > without major problems.

Steroids as a class of drugs is a double edged sword.  It provides relief but at the real risk of making the disease worse.  As many psoriasis sufferers know, the state of medical care for psoriasis is woefully inadequate.  Granted, medical knowledge has come a long way from the times of blood-letting and leeching(there are actually some indications for leeches).  It still has a long way to go.  I imagine that physicians who will be trained 20 years from now will laugh at our "state of the art medicine".  I urge people to be more sceptical of their M.D. and ask more questions.  I think they will find that the derms just can’t answer many of the basic questions they have. – Hide quoted text — Show quoted text -> I gather you’re not one of them, and neither am I.  In fact, I know > that I am, and perhaps you are, one of those from the other side, for > whom steroids quickly cause more problems than they fix.  I am > completely with you on the anger and disgust at the first > dermatologist I went to who prescribed the stuff, and should have seen > quickly that it wasn’t doing much good and was in fact probably > causing things to worsen.  However, I’m even angrier at the medical > profession as a whole, that has apparently not recognized that there > are people like me (and others who pop up on this newsgroup from time > to time) for whom even modest amounts of common steroid topicals are > downright hazardous. > That said, once I realized this, I found that with careful and > occassional use, I can get some temporary relief from steroids without > any apparent longer-term effects.  I seldom bother, frankly, as it > interferes with other treatments.  Only so much skin, so much time.   > Also, Kim knows all this stuff, too, and her post was reasonable and > informative and I endorse it entirely, fwiw.  If you want to rant at > some of us who’ve been here for a while, you can at least be sure > you’re preaching to the converted on pretty much all the facts that > you cite, and where you wander into some overstatements, as we all may > do when we get up a good head of steam, well, that usually gets > something of a sympathetic reading, plus or minus a little discussion > for any newbies who happen to wander in.

The statement that "steroids make psoriasis worse" can seem plain wrong at first glance.  However, as you know from experience, it is more true than not. All I am trying to convey across is that psoriasis sufferers need to demand from their derms alternatives, even if there are none.  By demanding for medicines that actually help rather than harm the disease you are simply exercising your right as a patient.  And compel them to do more research for a more satisfying solution to the disease. Or you can simply let the derms know that the frontline drug they offer will work in the short term but eventually will make things worse. – Hide quoted text — Show quoted text -> On the Elidel (pimecrolimus) cream, I haven’t tried it (probably > should), but, well, as Kim said, there are some vague reports of at > least quick worsening after Raptiva (nee Xanelim) usage, but certainly > not from Amevive, another biologic, with Enbrel sort of in-between > (and Remicade seems to have reports of longer-lasting relief).  So, > for the biologics overall, it seems the likelihood of actual rebound, > where things quickly get worse than before, is rather small.  At > least, I don’t recall any reports of it on this newsgroup. > On the positive side, there have been several reports on this group of > people using Elidel on psoriasis and getting good response, where the > psoriasis is on thin skin or is otherwise thin and accessible to > topicals.  I’ve seen no reports of it working on thick plaque > psoriasis.  However, I did see one report of trials of elidel as some > kind of systemic treatment, but never saw any trial results. > J.

Response:

Novartis says no rebound (for eczema anyway) http://www.elidel.com/hcp/mechanism.jsp J.

Response:

>    I used elidel for gential inverse P, and it worked initially fairly well >for about a week or so, now I don’t use it, it burns more than protopic, and >doesn’t work at all it seems anymore.. I do use Protopic with quite a bit of >success now, i use the .03% instead of 10% to minimize stinging etc..  I >much prefer the action and application of the Protopic over the Elidel for >The inverse on the Genitals, for those who need to know.

Appreciate the info from someone who’s tried both! Also, Protopic has a more informative and amusing web site, great slide shows and animations (scratch, scratch): http://www.protopic.com/professional/science/moa.php?page=science&sub… J.

Response:

> >Again, I must say that I believe any use of a steroid results in worse >disease than before starting steroids. > If testimonials are accepted as evidence, as you appear to indicate, then I am > the exception to that belief.

If you are indeed an exception than great for you.  Do you mean that you can use steroids whenever you want and your psoriasis just gets better with each use and now you are psoriasis free?  Maybe you can share with others your personal experience with steroids, i.e. the kinds of steroids you used and frequency and duration of use.  Maybe the vast numbers of people who have problems with steroids have been using it wrong and can learn something from you. >It’s just a matter of degree of how much worse. > "Negatively worse" is the answer in my case.

Would be interested to know your personal experience with psoriasis, age of onset, type, triggers, response, treatment. >First, steroids do not tackle the root of the >problem it only suppress symptoms, and while the immune system may be >locally suppressed the human body through the HPA axis upregulates the >immune system systemically which results in worse disease in other >parts of the body. > If you know about the HPA axis stuff, you should know the fairly-strict > definition of "rebound" that Kim is referring to.

Just because I know about the HPA axis I should be able to read minds as well? I am waiting for Kim to define her definition of rebound.   > On the other hand, when a person uses lots of steroids, the HPA axis actually > _down_ regulates the body’s own production of steroids.  Stop applying the > steroids, and the body has a massive debt of them, since it takes several days > for the HPA axis to ramp production of them back up.  During that time, > inflammation can run rampant, and _pow_, a rebound!

Exactly, steroids work by suppressing the immune system. However, there is a distinction that must be made:  Immune suppression on a systemic level, i.e. HPA axis; but also on a local level where the HPA axis is not involved.  You assume that only large doses of strong steroids suppress the immune system.  Small amounts of nonpotent steroids used for brief periods of time usually have no effect on the HPA axis.  However, because they work as you yourself know, they must have suppressed the immune system at a local level and it’s this effect that is worrisome and causes psoriasis to return worse than before regardless of rebound.  Again, this is local upregulation of cytokine production from T-cells and does not involve the HPA axis. >Even if the steroid is tapered slowly and symptoms >seem stable or even improved, the next time psoriasis is triggered >through whatever mechanism it is invariably worse than if no steroids >were used.  The experience of yourself and many others in this group >is ample evidence of my supposition. > A few peoples’ experiences from a newsgroup is no evidence at all.  There are

"A few people"  hmmm, I wonder what "evidence" you have to support your claim that only a few people have bad experience with steroids > millions of psoriatics who use steroids who do _not_ "invariably" get worse > psoriasis symptoms.

Conversely, what evidence do you have for saying that "millions of psoriatics" don’t get worse with steroid use.  If you have evidence, please share it with me. >Steroids only acclerates what >time does to psoriasis-makes it worse faster even if it may offer some >temporary relief. > You’ve got funny ideas about psoriasis.  Where is there evidence that psoriasis > gets worse over time, even if untreated?

I don’t think I have to provide any evidence.  Just think back on how your psoriasis first developed and spread.  If psoriasis were a self-limited disease, you probably wouldn’t have to use any steroids and you wouldn’t be in a newsgroup trying to find solutions and argue with me. >Yes, long term use will certainly result in more noticeable harm but >short term use will also result in rebound albeit they may not be >recognized immediately.  No, these are not potential risks, they are >real but may not be as noticeable. > Your use of absolutes turns what you write into pseudo-medical nonsense, as you

You have yet to provide any convincing arguments or evidence to counter what I have said in the first post.  Which part of my post was pseudo-medical nonsense, please be more specific. > probably know since you also wrote, "The variability of psoriasis is > tremendous, from genetics to disease severity, from disease triggers to > response to treatment." >However, my >belief that steroids will cause disease progression is combined a >priori and experiential. > What?  How can your belief be based on experiments when you go on to _propose_ > an experiment which hasn’t yet been done to test your belief?

Experiential-I suggest that you look up the word experiential in a dictionary and then reply. >The experience of many psoriasis sufferers as posted on this group >will testify to my claim. > Testimonials are worthless as evidence for your claim.

Again, I don’t think many people who are psoriasis sufferers would agree with you. – Hide quoted text — Show quoted text -> – Dave W. > http://psorsite.com/

Response:

> First, have you used Elidel yourself? if not, how do you know that > there is no rebound? I have done some search on this topic and it > seems that Elidel does not improve psoriasis dramatically and of those > who addressed the use of Elidel they did not mention any rebound but I > would like to hear from people who have experience using Elidel. > Also, what is your definition of a rebound and how do you distinguish > it from a worsening especially when the disease has been stable over > time and worsened after steriod use?   Also, there are lots of things > which may cause disease progression and steriod use is one of them, > regardless of duration and dosage of use.

    I used elidel for gential inverse P, and it worked initially fairly well for about a week or so, now I don’t use it, it burns more than protopic, and doesn’t work at all it seems anymore.. I do use Protopic with quite a bit of success now, i use the .03% instead of 10% to minimize stinging etc..  I much prefer the action and application of the Protopic over the Elidel for The inverse on the Genitals, for those who need to know. Dan

Response:

>Again, I must say that I believe any use of a steroid results in worse >disease than before starting steroids.

If testimonials are accepted as evidence, as you appear to indicate, then I am the exception to that belief. >It’s just a matter of degree of how much worse.

"Negatively worse" is the answer in my case. >First, steroids do not tackle the root of the >problem it only suppress symptoms, and while the immune system may be >locally suppressed the human body through the HPA axis upregulates the >immune system systemically which results in worse disease in other >parts of the body.

If you know about the HPA axis stuff, you should know the fairly-strict definition of "rebound" that Kim is referring to. On the other hand, when a person uses lots of steroids, the HPA axis actually _down_ regulates the body’s own production of steroids.  Stop applying the steroids, and the body has a massive debt of them, since it takes several days for the HPA axis to ramp production of them back up.  During that time, inflammation can run rampant, and _pow_, a rebound! >Even if the steroid is tapered slowly and symptoms >seem stable or even improved, the next time psoriasis is triggered >through whatever mechanism it is invariably worse than if no steroids >were used.  The experience of yourself and many others in this group >is ample evidence of my supposition.

A few peoples’ experiences from a newsgroup is no evidence at all.  There are millions of psoriatics who use steroids who do _not_ "invariably" get worse psoriasis symptoms. >Steroids only acclerates what >time does to psoriasis-makes it worse faster even if it may offer some >temporary relief.

You’ve got funny ideas about psoriasis.  Where is there evidence that psoriasis gets worse over time, even if untreated? >Yes, long term use will certainly result in more noticeable harm but >short term use will also result in rebound albeit they may not be >recognized immediately.  No, these are not potential risks, they are >real but may not be as noticeable.

Your use of absolutes turns what you write into pseudo-medical nonsense, as you probably know since you also wrote, "The variability of psoriasis is tremendous, from genetics to disease severity, from disease triggers to response to treatment." >However, my >belief that steroids will cause disease progression is combined a >priori and experiential.

What?  How can your belief be based on experiments when you go on to _propose_ an experiment which hasn’t yet been done to test your belief? >The experience of many psoriasis sufferers as posted on this group >will testify to my claim.

Testimonials are worthless as evidence for your claim. – Dave W. http://psorsite.com/

Response:

>Also, what is your definition of a rebound and how do you distinguish >it from a worsening especially when the disease has been stable over >time and worsened after steriod use?

Steve, I haven’t had the (awful) experience myself, but from all accounts the "rebound" effect is completely obvious, if someone with psoriasis goes cold-turkey after getting some relief from steroids. It gets a lot worse, really fast. >  Also, there are lots of things >which may cause disease progression and steriod use is one of them, >regardless of duration and dosage of use.

That just isn’t clear.  It may well be true, but as you said further along in your message, there’s a lot of variability in psoriasis, so it may be a lot more true for some people than for others.  For people with mild psoriasis, using modest amounts of steroids, there are apparently a lot of people who manage to use them and get some relief without major problems. I gather you’re not one of them, and neither am I.  In fact, I know that I am, and perhaps you are, one of those from the other side, for whom steroids quickly cause more problems than they fix.  I am completely with you on the anger and disgust at the first dermatologist I went to who prescribed the stuff, and should have seen quickly that it wasn’t doing much good and was in fact probably causing things to worsen.  However, I’m even angrier at the medical profession as a whole, that has apparently not recognized that there are people like me (and others who pop up on this newsgroup from time to time) for whom even modest amounts of common steroid topicals are downright hazardous. That said, once I realized this, I found that with careful and occassional use, I can get some temporary relief from steroids without any apparent longer-term effects.  I seldom bother, frankly, as it interferes with other treatments.  Only so much skin, so much time.   Also, Kim knows all this stuff, too, and her post was reasonable and informative and I endorse it entirely, fwiw.  If you want to rant at some of us who’ve been here for a while, you can at least be sure you’re preaching to the converted on pretty much all the facts that you cite, and where you wander into some overstatements, as we all may do when we get up a good head of steam, well, that usually gets something of a sympathetic reading, plus or minus a little discussion for any newbies who happen to wander in. On the Elidel (pimecrolimus) cream, I haven’t tried it (probably should), but, well, as Kim said, there are some vague reports of at least quick worsening after Raptiva (nee Xanelim) usage, but certainly not from Amevive, another biologic, with Enbrel sort of in-between (and Remicade seems to have reports of longer-lasting relief).  So, for the biologics overall, it seems the likelihood of actual rebound, where things quickly get worse than before, is rather small.  At least, I don’t recall any reports of it on this newsgroup. On the positive side, there have been several reports on this group of people using Elidel on psoriasis and getting good response, where the psoriasis is on thin skin or is otherwise thin and accessible to topicals.  I’ve seen no reports of it working on thick plaque psoriasis.  However, I did see one report of trials of elidel as some kind of systemic treatment, but never saw any trial results. J.

Response:

> Not at all. The only meds that cause an actual rebound are steroids > and methotrexate (and I believe Xanelim may as well, among the new > biologics being tested, although not sure it that’s official). It’s a > common error – calling any worsening a rebound, when rebound means > something very sepcific and of limited application.

First, have you used Elidel yourself? if not, how do you know that there is no rebound? I have done some search on this topic and it seems that Elidel does not improve psoriasis dramatically and of those who addressed the use of Elidel they did not mention any rebound but I would like to hear from people who have experience using Elidel. Also, what is your definition of a rebound and how do you distinguish it from a worsening especially when the disease has been stable over time and worsened after steriod use?   Also, there are lots of things which may cause disease progression and steriod use is one of them, regardless of duration and dosage of use. >Also, I would like to urge all readers to avoid the use of steriod >creams whenever possible.   > I understand the sentiment behind this, and don’t use them myself, but > you are unnecessarily scaring people with this warning based upon a > mistaken assumption that the results of mis-use/abuse of steroids are > inherent in any use of them.

Again, I must say that I believe any use of a steroid results in worse disease than before starting steroids.  It’s just a matter of degree of how much worse.  First, steroids do not tackle the root of the problem it only suppress symptoms, and while the immune system may be locally suppressed the human body through the HPA axis upregulates the immune system systemically which results in worse disease in other parts of the body.  Even if the steroid is tapered slowly and symptoms seem stable or even improved, the next time psoriasis is triggered through whatever mechanism it is invariably worse than if no steroids were used.  The experience of yourself and many others in this group is ample evidence of my supposition.  Steroids only acclerates what time does to psoriasis-makes it worse faster even if it may offer some temporary relief. > Many derms *are* too quick to prescribe them and keep prescribing them > for too long with insufficient supervision about the results. But > that’s misuse of them.

There is an active search for other meds which may be able to offer relief like steroids but avoid the rebound/suppression effect.   However, meds that suppress the immune system as indiscriminately as many if not all steroids do will invariably result in worse disease. The human body is clever and stubborn and doesn’t like to be told what to do certainly not by steroids.  Again, the fact that you avoid steroids supports my claim if only anecdotally. > The risks of using them come primarily with long term continual use > (with some variation by person on how long qualifies as long term > continual) of higher strengths, and are still only potential risks

Yes, long term use will certainly result in more noticeable harm but short term use will also result in rebound albeit they may not be recognized immediately.  No, these are not potential risks, they are real but may not be as noticeable. > NOTguaranteed problems. They can also be reduced significantly by > using steroids sparingly as part of a combination therapy rather than > over using the streoids alone. > While most people with psoriasis have very mild, stable cases where > proper occasional use of fairly mild steroids is pretty appropriate > and safe, except for individual idiosyncratic reactions.

The variability of psoriasis is tremendous, from genetics to disease severity, from disease triggers to response to treatment.  However, my belief that steroids will cause disease progression is combined a priori and experiential. The experience of many psoriasis sufferers as posted on this group will testify to my claim.  I think that if you add up all the miles that P. sufferers travel back to derms for ever stronger steroid creams you can get enough frequent flier miles to go to the moon. I think that our disagreement can be settled simply with experiments with mice.  Apply steroids to mice with psoriasis for varying amount of times and have control mice who are left alone.  Withdraw the steroid cream from the 1st set of mice however you like provided that they are given ample time for the washout of the steroid from the mice’s system.   I believe that in the end, the mice who are left alone will have less psoriasis. steve

Response:

>I know that there is a nonsteroidal cream out on the market for >eczema.  Have any of the people on this board tried using this cream >for psoriasis or seb. derm.  What results have you obtain using this >cream.  If you have used this cream, Elidel, have you experienced any >rebound effect with Elidel that is certain to happen with steriod >creams.

Check the ng archives, where it has certianly been discussed before: http://pinch.com/skinny?skin=psoriasis+elidel >I suppose that theoretically the dreaded rebound effect is just as >likely with Elidel as with steroid creams.

Not at all. The only meds that cause an actual rebound are steroids and methotrexate (and I believe Xanelim may as well, among the new biologics being tested, although not sure it that’s official). It’s a common error – calling any worsening a rebound, when rebound means something very sepcific and of limited application. >Also, I would like to urge all readers to avoid the use of steriod >creams whenever possible.  

I understand the sentiment behind this, and don’t use them myself, but you are unnecessarily scaring people with this warning based upon a mistaken assumption that the results of mis-use/abuse of steroids are inherent in any use of them. Many derms *are* too quick to prescribe them and keep prescribing them for too long with insufficient supervision about the results. But that’s misuse of them. The risks of using them come primarily with long term continual use (with some variation by person on how long qualifies as long term continual) of higher strengths, and are still only potential risks NOTguaranteed problems. They can also be reduced significantly by using steroids sparingly as part of a combination therapy rather than over using the streoids alone. While most people with psoriasis have very mild, stable cases where proper occasional use of fairly mild steroids is pretty appropriate and safe, except for individual idiosyncratic reactions. Kim The Psoriasis Newsgroup Resource FAQ can be found at               http://www.psoriasisfaq.com but will also be coming soon (twice a month) to a            newsgroup near you…

Response:

I know that there is a nonsteroidal cream out on the market for eczema.  Have any of the people on this board tried using this cream for psoriasis or seb. derm.  What results have you obtain using this cream.  If you have used this cream, Elidel, have you experienced any rebound effect with Elidel that is certain to happen with steriod creams. I suppose that theoretically the dreaded rebound effect is just as likely with Elidel as with steroid creams.  However, since Elidel works in a entirely different manner to all steriod creams it may be able to avoid the rebound effect which results in worse psoriasis than before initiating steriod creams. Also, I would like to urge all readers to avoid the use of steriod creams whenever possible.  Dermatologists tend to prescribe steriod creams in increasing strengths to control psoriasis, however, it results in a vicious cycle as I am sure many people have experienced first hand.  Despite the temporary relief that steriod creams are able to offer, it invariably results in worse psoriasis.  However, I realize that until scientists and clinicians are able to come up with a solution that begins to target the root of the problem, p. sufferers are left with drugs that do more harm to good.

Response:

Question:

I have Psoriasis on a circumcision scar in the groin area (penis). Since I do have some abrasion with underpants from time to time  - seems to heal and then re-appears again — have tried various creams — this spot with psoriasis can become quite painful at times — any suggestions. Sonny

Response:

> I have Psoriasis on a circumcision scar in the groin area (penis). Since I > do have some abrasion with underpants from time to time  - seems to heal and > then re-appears again — have tried various creams — this spot with > psoriasis can become quite painful at times — any suggestions. > Sonny

My derm prescribes Desowen cream for me to use in those sensitive areas. That usually clears it up within a day or two at the most. My other suggestion is do not wear underwear; at least when you have a flare up. This time of year because of the cold I do wear flannel boxers, but I cannot wear my briefs more than two days without getting a bad flare up of inverse psoriasis in the creases between my groin and thighs. Best of luck to you.

Response:

> I have Psoriasis on a circumcision scar in the groin area (penis). Since I > do have some abrasion with underpants from time to time  - seems to heal and > then re-appears again — have tried various creams — this spot with > psoriasis can become quite painful at times — any suggestions. > Sonny

    I use MTX which is about the only thing that helps long term. Protopic and Desowen cream are used on and off, once in a while I will zap it with some Triamcinolone, but I make sure to only use it no more than 2 times a month or so at the most.  Oh and I do know what your feeling in regards to the pain. Dan

Response: