<?xml version="1.0" encoding="UTF-8"?>
<rss version="2.0" xmlns:content="http://purl.org/rss/1.0/modules/content/" xmlns:dc="http://purl.org/dc/elements/1.1/">
	<channel>
		<title><![CDATA[Psoriasis Club - Psoriasis And Psoriatic Arthritis Topics ]]></title>
		<link>https://psoriasisclub.org/</link>
		<description><![CDATA[Psoriasis Club - https://psoriasisclub.org]]></description>
		<pubDate>Sun, 19 Apr 2026 13:11:37 +0000</pubDate>
		<generator>MyBB</generator>
		<item>
			<title><![CDATA[PsA and Knee Replacement Surgery]]></title>
			<link>https://psoriasisclub.org/thread-8418.html</link>
			<pubDate>Thu, 05 Feb 2026 07:56:52 -0500</pubDate>
			<dc:creator><![CDATA[<a href="https://psoriasisclub.org/member.php?action=profile&uid=3262">Waine</a>]]></dc:creator>
			<guid isPermaLink="false">https://psoriasisclub.org/thread-8418.html</guid>
			<description><![CDATA[Apologies if this has been covered before but I wasn't able to find anything recent.<br />
<br />
Following recent knee pain my Rheumy refereed me to an Orthopedic Surgeon. X-rays etc later it shows my left knee joint is totally messed up. I had a previous surgery on it in 2007 but now the PsA has done a number on the ACL tendon where it joins the bone, which is almost completely pulled loose and is ripping my meniscus. So I have a total knee replacement scheduled for a couple of weeks from now.<br />
<br />
Does anyone have a real world experience that they can share? Especially on how the recovery period went.]]></description>
			<content:encoded><![CDATA[Apologies if this has been covered before but I wasn't able to find anything recent.<br />
<br />
Following recent knee pain my Rheumy refereed me to an Orthopedic Surgeon. X-rays etc later it shows my left knee joint is totally messed up. I had a previous surgery on it in 2007 but now the PsA has done a number on the ACL tendon where it joins the bone, which is almost completely pulled loose and is ripping my meniscus. So I have a total knee replacement scheduled for a couple of weeks from now.<br />
<br />
Does anyone have a real world experience that they can share? Especially on how the recovery period went.]]></content:encoded>
		</item>
		<item>
			<title><![CDATA[Anger Management and PsA]]></title>
			<link>https://psoriasisclub.org/thread-8413.html</link>
			<pubDate>Sat, 31 Jan 2026 12:29:20 -0500</pubDate>
			<dc:creator><![CDATA[<a href="https://psoriasisclub.org/member.php?action=profile&uid=3262">Waine</a>]]></dc:creator>
			<guid isPermaLink="false">https://psoriasisclub.org/thread-8413.html</guid>
			<description><![CDATA[I'm aware that being quick to anger is a symptom of the inflammation this damn disease causes. Does anyone have suggestions for anything that actually works to keep it under control? I experience it and then am immediately overwhelmed with remorse, to the extent of getting emotions that are difficult to cope with at times. I find myself disassociating more and more for fear of it happening, which is probably the exact opposite of what I need. <br />
<br />
Any suggestions or experience will be helpful.]]></description>
			<content:encoded><![CDATA[I'm aware that being quick to anger is a symptom of the inflammation this damn disease causes. Does anyone have suggestions for anything that actually works to keep it under control? I experience it and then am immediately overwhelmed with remorse, to the extent of getting emotions that are difficult to cope with at times. I find myself disassociating more and more for fear of it happening, which is probably the exact opposite of what I need. <br />
<br />
Any suggestions or experience will be helpful.]]></content:encoded>
		</item>
		<item>
			<title><![CDATA[Injections for psoriasis]]></title>
			<link>https://psoriasisclub.org/thread-8409.html</link>
			<pubDate>Mon, 19 Jan 2026 07:35:01 -0500</pubDate>
			<dc:creator><![CDATA[<a href="https://psoriasisclub.org/member.php?action=profile&uid=2">Fred</a>]]></dc:creator>
			<guid isPermaLink="false">https://psoriasisclub.org/thread-8409.html</guid>
			<description><![CDATA[If you are using injections for psoriasis which type do you prefer, pen type (auto injector) or prefilled syringe ?<br />
<br />
Members and guests can vote in the poll above, and our members are welcome to post in this thread too if they wish.]]></description>
			<content:encoded><![CDATA[If you are using injections for psoriasis which type do you prefer, pen type (auto injector) or prefilled syringe ?<br />
<br />
Members and guests can vote in the poll above, and our members are welcome to post in this thread too if they wish.]]></content:encoded>
		</item>
		<item>
			<title><![CDATA[How it’s got worse]]></title>
			<link>https://psoriasisclub.org/thread-8353.html</link>
			<pubDate>Tue, 21 Oct 2025 13:34:24 -0400</pubDate>
			<dc:creator><![CDATA[<a href="https://psoriasisclub.org/member.php?action=profile&uid=3255">MartinB</a>]]></dc:creator>
			<guid isPermaLink="false">https://psoriasisclub.org/thread-8353.html</guid>
			<description><![CDATA[Hello there. New member and I’m at my wits end. <br />
<br />
Started off with a small scratch on my head around 2007. Within years it spread all over my body but in small, manageable plaques I could treat, initially with Dovobet, then and now with Enstiler. <br />
<br />
The last 12 months it’s changed from plaques and is now all over my body in one big, red rash that I have figured out a cycle of its weekly events. <br />
<br />
Monday it’s at its worse. It now hurts like sun burn. I cover it all with the foam and by Wednesday I can pretty much fill a hoover with the dead skin. Then it’s flat but still very red but no or little dead skin by Wednesday. I then feel like I have even worse sun burn before a couple of days relief but completely red and unsightly. By Sunday night the lumps appear and then it’s rinse and repeat again from Monday. There is no escaping it and it is now at the point where I cannot live a normal or comfortable life, which I could before. I have never been bothered by people looking at me in public and would wear T shirts and shorts. Not anymore. It is ruining my life. <br />
<br />
12 months ago I started smoking and drinking heavily and I know there can be no coincidence, but kicking the two is hard and I use them both as an escape when I look at what the psoriasis is doing to me and how it it how a physical pain as well as a psychological one. <br />
<br />
Why has it changed from manageable plaques to covering my torso as an entirety, and large plaques on my arms and legs? I am only blessed so far it hasn’t affected my face. I am going through 2 cans of foam every 4 weeks, plus tubs and tubs of post shower moisturiser in the form of Adex.]]></description>
			<content:encoded><![CDATA[Hello there. New member and I’m at my wits end. <br />
<br />
Started off with a small scratch on my head around 2007. Within years it spread all over my body but in small, manageable plaques I could treat, initially with Dovobet, then and now with Enstiler. <br />
<br />
The last 12 months it’s changed from plaques and is now all over my body in one big, red rash that I have figured out a cycle of its weekly events. <br />
<br />
Monday it’s at its worse. It now hurts like sun burn. I cover it all with the foam and by Wednesday I can pretty much fill a hoover with the dead skin. Then it’s flat but still very red but no or little dead skin by Wednesday. I then feel like I have even worse sun burn before a couple of days relief but completely red and unsightly. By Sunday night the lumps appear and then it’s rinse and repeat again from Monday. There is no escaping it and it is now at the point where I cannot live a normal or comfortable life, which I could before. I have never been bothered by people looking at me in public and would wear T shirts and shorts. Not anymore. It is ruining my life. <br />
<br />
12 months ago I started smoking and drinking heavily and I know there can be no coincidence, but kicking the two is hard and I use them both as an escape when I look at what the psoriasis is doing to me and how it it how a physical pain as well as a psychological one. <br />
<br />
Why has it changed from manageable plaques to covering my torso as an entirety, and large plaques on my arms and legs? I am only blessed so far it hasn’t affected my face. I am going through 2 cans of foam every 4 weeks, plus tubs and tubs of post shower moisturiser in the form of Adex.]]></content:encoded>
		</item>
		<item>
			<title><![CDATA[Pustular psoriasis advice needed]]></title>
			<link>https://psoriasisclub.org/thread-8243.html</link>
			<pubDate>Wed, 02 Apr 2025 07:51:44 -0400</pubDate>
			<dc:creator><![CDATA[<a href="https://psoriasisclub.org/member.php?action=profile&uid=3237">Alleyes</a>]]></dc:creator>
			<guid isPermaLink="false">https://psoriasisclub.org/thread-8243.html</guid>
			<description><![CDATA[Hi there , I hope you can assist me in some way please with some advice , I have had Pustular psoriasis since 2016 and my latest GPP is ongoing since 23rd January 2025 , I am glad it isn't as bad as it was but at its worst I was sent to hospital twice being told I needed IV but was sent home which surprised me given the state my skin was also had cellulitis in both legs and feet , the antibiotics (3) different types didn't do anything , I started reading about Metformin being a help with all psoriasis types , I have asked my diabetic nurse and she hadn't even heard of pustular psoriasis infact 2 out 3 doctors I have visited hadn't either , this is a concern that there clearly isn't enough of any knowledge on pustular psoriasis and/or GPP , I get that it is rare but that doesn't mean its any less dangerous!<br />
I don't mean any disrespect but because there is such a lack of knowledge from medical professionals I have had to come on to this forum to find people that have knowledge first hand along the lines of what is the best medication available in UK because nobody in medical profession seems to be able to help or even heard know what GPP is ! <br />
I'm in my 10th week and still having outbreaks of new pustules daily on various parts of my body and would appreciate any advice you could offer please .]]></description>
			<content:encoded><![CDATA[Hi there , I hope you can assist me in some way please with some advice , I have had Pustular psoriasis since 2016 and my latest GPP is ongoing since 23rd January 2025 , I am glad it isn't as bad as it was but at its worst I was sent to hospital twice being told I needed IV but was sent home which surprised me given the state my skin was also had cellulitis in both legs and feet , the antibiotics (3) different types didn't do anything , I started reading about Metformin being a help with all psoriasis types , I have asked my diabetic nurse and she hadn't even heard of pustular psoriasis infact 2 out 3 doctors I have visited hadn't either , this is a concern that there clearly isn't enough of any knowledge on pustular psoriasis and/or GPP , I get that it is rare but that doesn't mean its any less dangerous!<br />
I don't mean any disrespect but because there is such a lack of knowledge from medical professionals I have had to come on to this forum to find people that have knowledge first hand along the lines of what is the best medication available in UK because nobody in medical profession seems to be able to help or even heard know what GPP is ! <br />
I'm in my 10th week and still having outbreaks of new pustules daily on various parts of my body and would appreciate any advice you could offer please .]]></content:encoded>
		</item>
		<item>
			<title><![CDATA[Traveling to Japan with psoriasis]]></title>
			<link>https://psoriasisclub.org/thread-8193.html</link>
			<pubDate>Thu, 30 Jan 2025 23:23:28 -0500</pubDate>
			<dc:creator><![CDATA[<a href="https://psoriasisclub.org/member.php?action=profile&uid=3233">IAmNotMySkin</a>]]></dc:creator>
			<guid isPermaLink="false">https://psoriasisclub.org/thread-8193.html</guid>
			<description><![CDATA[Does anyone have experience traveling in Japan with Psoriasis?<br />
<br />
I was thinking of going, but read the Japanese see it as somewhat of a 'stigma.' Especially in the public baths, (not that I was considering that.)<br />
<br />
I am concerned that it will become too much of a problem since I can't possibly cover-up all of it and I don't know just how much of a stigma it would be.<br />
<br />
An feedback would be appreciated.<br />
<br />
Thanks.]]></description>
			<content:encoded><![CDATA[Does anyone have experience traveling in Japan with Psoriasis?<br />
<br />
I was thinking of going, but read the Japanese see it as somewhat of a 'stigma.' Especially in the public baths, (not that I was considering that.)<br />
<br />
I am concerned that it will become too much of a problem since I can't possibly cover-up all of it and I don't know just how much of a stigma it would be.<br />
<br />
An feedback would be appreciated.<br />
<br />
Thanks.]]></content:encoded>
		</item>
		<item>
			<title><![CDATA[Dermatology Appointment Yesterday]]></title>
			<link>https://psoriasisclub.org/thread-8150.html</link>
			<pubDate>Wed, 11 Dec 2024 08:39:35 -0500</pubDate>
			<dc:creator><![CDATA[<a href="https://psoriasisclub.org/member.php?action=profile&uid=3055">Forest Walker</a>]]></dc:creator>
			<guid isPermaLink="false">https://psoriasisclub.org/thread-8150.html</guid>
			<description><![CDATA[I had a dermatology appointment yesterday.  I'm seeing this doctor annually now that I've learned how to manage my psoriasis and am doing okay.  I'm just so grateful to her.  She is thorough and smart and committed to relieving suffering.  This person could have risen to the top in any field, but she chose skin and her dedication to years of medical education and the care she has provided to me have helped me (along with many others, of course).  I am better.  I guess I just want to acknowledge this.<br />
<br />
But as I get older, I think there's gonna be annual biopsies for skin cancer, too.  I have two sore spots now, covered in bandages from yesterday's punch biopsies.  <br />
<br />
Maybe in the long run, having psoriasis lowers my chances of dying from skin cancer since it will be checked for regularly.  I might not have ever seen a dermatologist if I didn't get psoriasis.]]></description>
			<content:encoded><![CDATA[I had a dermatology appointment yesterday.  I'm seeing this doctor annually now that I've learned how to manage my psoriasis and am doing okay.  I'm just so grateful to her.  She is thorough and smart and committed to relieving suffering.  This person could have risen to the top in any field, but she chose skin and her dedication to years of medical education and the care she has provided to me have helped me (along with many others, of course).  I am better.  I guess I just want to acknowledge this.<br />
<br />
But as I get older, I think there's gonna be annual biopsies for skin cancer, too.  I have two sore spots now, covered in bandages from yesterday's punch biopsies.  <br />
<br />
Maybe in the long run, having psoriasis lowers my chances of dying from skin cancer since it will be checked for regularly.  I might not have ever seen a dermatologist if I didn't get psoriasis.]]></content:encoded>
		</item>
		<item>
			<title><![CDATA[Guttate Psoriasis 3 years]]></title>
			<link>https://psoriasisclub.org/thread-8144.html</link>
			<pubDate>Fri, 29 Nov 2024 08:36:19 -0500</pubDate>
			<dc:creator><![CDATA[<a href="https://psoriasisclub.org/member.php?action=profile&uid=3229">paul1961</a>]]></dc:creator>
			<guid isPermaLink="false">https://psoriasisclub.org/thread-8144.html</guid>
			<description><![CDATA[I have had Guttate Psoriasis for almost three years now, after a mild case of COVID (That's a story for another day}.  Guttate typically resolves fairly quickly, mine did not.  I was on Humira for 7 months and got moderate relief.  The Humira quit working for me.  I am now trying to get on Tremfya.  I have had Plaque psoriasis since I was 12 years old, and that is largely in remission.]]></description>
			<content:encoded><![CDATA[I have had Guttate Psoriasis for almost three years now, after a mild case of COVID (That's a story for another day}.  Guttate typically resolves fairly quickly, mine did not.  I was on Humira for 7 months and got moderate relief.  The Humira quit working for me.  I am now trying to get on Tremfya.  I have had Plaque psoriasis since I was 12 years old, and that is largely in remission.]]></content:encoded>
		</item>
		<item>
			<title><![CDATA[Clothes and psoriasis]]></title>
			<link>https://psoriasisclub.org/thread-8127.html</link>
			<pubDate>Fri, 01 Nov 2024 08:50:08 -0400</pubDate>
			<dc:creator><![CDATA[<a href="https://psoriasisclub.org/member.php?action=profile&uid=2">Fred</a>]]></dc:creator>
			<guid isPermaLink="false">https://psoriasisclub.org/thread-8127.html</guid>
			<description><![CDATA[Does psoriasis effect the clothes you wear ? <br />
<br />
Members and guests can vote in the poll above, and our members are welcome to post in this thread too if they wish.<br />
<br />
More <a href="thread-4060.html">Psoriasis Club Polls</a>]]></description>
			<content:encoded><![CDATA[Does psoriasis effect the clothes you wear ? <br />
<br />
Members and guests can vote in the poll above, and our members are welcome to post in this thread too if they wish.<br />
<br />
More <a href="thread-4060.html">Psoriasis Club Polls</a>]]></content:encoded>
		</item>
		<item>
			<title><![CDATA[Psoriasis Comorbidities]]></title>
			<link>https://psoriasisclub.org/thread-8109.html</link>
			<pubDate>Wed, 02 Oct 2024 08:04:07 -0400</pubDate>
			<dc:creator><![CDATA[<a href="https://psoriasisclub.org/member.php?action=profile&uid=2">Fred</a>]]></dc:creator>
			<guid isPermaLink="false">https://psoriasisclub.org/thread-8109.html</guid>
			<description><![CDATA[Do any of you have/had any comorbidities ? I've added the most common to the poll above, if you have others please let me know. <br />
<br />
Members and guests can vote in the poll above, and our members are welcome to post in this thread too if they wish.<br />
<br />
More <a href="thread-4060.html">Psoriasis Club Polls</a>]]></description>
			<content:encoded><![CDATA[Do any of you have/had any comorbidities ? I've added the most common to the poll above, if you have others please let me know. <br />
<br />
Members and guests can vote in the poll above, and our members are welcome to post in this thread too if they wish.<br />
<br />
More <a href="thread-4060.html">Psoriasis Club Polls</a>]]></content:encoded>
		</item>
		<item>
			<title><![CDATA[Psoriasis and Sinus issues]]></title>
			<link>https://psoriasisclub.org/thread-8049.html</link>
			<pubDate>Tue, 21 May 2024 19:28:20 -0400</pubDate>
			<dc:creator><![CDATA[<a href="https://psoriasisclub.org/member.php?action=profile&uid=3147">BigA1988</a>]]></dc:creator>
			<guid isPermaLink="false">https://psoriasisclub.org/thread-8049.html</guid>
			<description><![CDATA[Just wondered how many of you on here who suffer with psoriasis, also suffer, or<br />
Have suffered, with sinus problems at some point in your life?]]></description>
			<content:encoded><![CDATA[Just wondered how many of you on here who suffer with psoriasis, also suffer, or<br />
Have suffered, with sinus problems at some point in your life?]]></content:encoded>
		</item>
		<item>
			<title><![CDATA[Cutting a lifted toe nail - yes or no?!]]></title>
			<link>https://psoriasisclub.org/thread-7980.html</link>
			<pubDate>Sun, 21 Jan 2024 13:09:02 -0500</pubDate>
			<dc:creator><![CDATA[<a href="https://psoriasisclub.org/member.php?action=profile&uid=2837">Cowsaregreat</a>]]></dc:creator>
			<guid isPermaLink="false">https://psoriasisclub.org/thread-7980.html</guid>
			<description><![CDATA[I have psoriasis under 2 finger nails. Luckily for me 1 has cleared up (mostly) but my thumb nail is tough as old boots and I keep it short so I don’t catch it. I now have psoriasis under one toe nail. It’s lifting off and I’m unsure whether to cut it right down as far as possible as it sometimes catches on my sock. It’s only lifting on the left side but it’s nearly down to the bottom and I’m concerned it’ll get ripped off and that’ll hurt! Can anyone advise please.]]></description>
			<content:encoded><![CDATA[I have psoriasis under 2 finger nails. Luckily for me 1 has cleared up (mostly) but my thumb nail is tough as old boots and I keep it short so I don’t catch it. I now have psoriasis under one toe nail. It’s lifting off and I’m unsure whether to cut it right down as far as possible as it sometimes catches on my sock. It’s only lifting on the left side but it’s nearly down to the bottom and I’m concerned it’ll get ripped off and that’ll hurt! Can anyone advise please.]]></content:encoded>
		</item>
		<item>
			<title><![CDATA[Psoriasis and Chronic diseases]]></title>
			<link>https://psoriasisclub.org/thread-7971.html</link>
			<pubDate>Sat, 06 Jan 2024 19:42:47 -0500</pubDate>
			<dc:creator><![CDATA[<a href="https://psoriasisclub.org/member.php?action=profile&uid=846">Kat</a>]]></dc:creator>
			<guid isPermaLink="false">https://psoriasisclub.org/thread-7971.html</guid>
			<description><![CDATA[I started seeing a new dermatologist.  As we were going over medical history stuff, I mentioned that I had been diagnosed with NAFLD (nonalcoholic fatty liver disease) and she replied that was common for people with psoriasis.  Which surprised me a bit as I hadn't heard that before, nor had it been mentioned to me so I did a little looking up on the internet to see what I could find.  I found the following information which seemed to explain it best:<br />
<br />
<span style="font-style: italic;" class="mycode_i">Although many people think of psoriasis primarily as a skin disease, it is a systemic condition that affects other organs as well. People with psoriasis have increased inflammation throughout the body, which increases the risk of developing comorbid conditions (more than one chronic disease at the same time). For example, people with psoriasis have a higher prevalence of fatty liver disease compared to the general population.<br />
<br />
Psoriasis is associated with a higher risk for developing obesity (high body mass index), insulin resistance, and metabolic syndrome — factors that can also increase the risk of NAFLD. A person may be diagnosed with metabolic syndrome if they have three of the following:<br />
<br />
Abdominal obesity<br />
High triglyceride levels<br />
Low HDL cholesterol levels<br />
High glucose levels<br />
Hypertension (high blood pressure)<br />
People with metabolic syndrome and severe psoriasis are at a higher risk of developing NAFLD.</span><br />
<br />
I tick quite a few of those.  Also with inflammation being mentioned it has made me wonder about other things going on with me and how it all ties in together.  Of course having arthritis is a factor for the inflammation as well.<br />
<br />
So now I'm really hopeful to see how Skyrizi will work out for me (calling them next week to have them ship to me).  Maybe if my psoriasis is calmed down so might some other stuff?  It would be nice if it works that way!]]></description>
			<content:encoded><![CDATA[I started seeing a new dermatologist.  As we were going over medical history stuff, I mentioned that I had been diagnosed with NAFLD (nonalcoholic fatty liver disease) and she replied that was common for people with psoriasis.  Which surprised me a bit as I hadn't heard that before, nor had it been mentioned to me so I did a little looking up on the internet to see what I could find.  I found the following information which seemed to explain it best:<br />
<br />
<span style="font-style: italic;" class="mycode_i">Although many people think of psoriasis primarily as a skin disease, it is a systemic condition that affects other organs as well. People with psoriasis have increased inflammation throughout the body, which increases the risk of developing comorbid conditions (more than one chronic disease at the same time). For example, people with psoriasis have a higher prevalence of fatty liver disease compared to the general population.<br />
<br />
Psoriasis is associated with a higher risk for developing obesity (high body mass index), insulin resistance, and metabolic syndrome — factors that can also increase the risk of NAFLD. A person may be diagnosed with metabolic syndrome if they have three of the following:<br />
<br />
Abdominal obesity<br />
High triglyceride levels<br />
Low HDL cholesterol levels<br />
High glucose levels<br />
Hypertension (high blood pressure)<br />
People with metabolic syndrome and severe psoriasis are at a higher risk of developing NAFLD.</span><br />
<br />
I tick quite a few of those.  Also with inflammation being mentioned it has made me wonder about other things going on with me and how it all ties in together.  Of course having arthritis is a factor for the inflammation as well.<br />
<br />
So now I'm really hopeful to see how Skyrizi will work out for me (calling them next week to have them ship to me).  Maybe if my psoriasis is calmed down so might some other stuff?  It would be nice if it works that way!]]></content:encoded>
		</item>
		<item>
			<title><![CDATA[Psoriasis on eyebrow]]></title>
			<link>https://psoriasisclub.org/thread-7962.html</link>
			<pubDate>Wed, 27 Dec 2023 16:16:05 -0500</pubDate>
			<dc:creator><![CDATA[<a href="https://psoriasisclub.org/member.php?action=profile&uid=2">Fred</a>]]></dc:creator>
			<guid isPermaLink="false">https://psoriasisclub.org/thread-7962.html</guid>
			<description><![CDATA[Had my cataracts done recently and got some psoriasis on one eyebrow, I think the sticky tape to keep the eye shield in place has made it flare though it didn't in the first one. <br />
<br />
Obviously I can't use anything near the eye at the moment so I'm trying the good old substitute of coconut oil, I'll see how it goes.]]></description>
			<content:encoded><![CDATA[Had my cataracts done recently and got some psoriasis on one eyebrow, I think the sticky tape to keep the eye shield in place has made it flare though it didn't in the first one. <br />
<br />
Obviously I can't use anything near the eye at the moment so I'm trying the good old substitute of coconut oil, I'll see how it goes.]]></content:encoded>
		</item>
		<item>
			<title><![CDATA[Holiday Itch]]></title>
			<link>https://psoriasisclub.org/thread-7953.html</link>
			<pubDate>Fri, 22 Dec 2023 08:57:39 -0500</pubDate>
			<dc:creator><![CDATA[<a href="https://psoriasisclub.org/member.php?action=profile&uid=3055">Forest Walker</a>]]></dc:creator>
			<guid isPermaLink="false">https://psoriasisclub.org/thread-7953.html</guid>
			<description><![CDATA[I'm suddenly getting itchy patches in many places, all at once.  I think it's the happy anticipation of adult children coming to stay with us for a couple of nights, trying to make everything ready combined with colder air outside and drier air inside from the furnace.  Whatever the cause, it's irritating.  <br />
<br />
It'll soon be like living in a snow globe, all these little flakes falling to the floor or on the backs of chairs.<br />
<br />
I believe stress, whether positive or negative, affects my skin.  <br />
<br />
Does anyone else feel that way?]]></description>
			<content:encoded><![CDATA[I'm suddenly getting itchy patches in many places, all at once.  I think it's the happy anticipation of adult children coming to stay with us for a couple of nights, trying to make everything ready combined with colder air outside and drier air inside from the furnace.  Whatever the cause, it's irritating.  <br />
<br />
It'll soon be like living in a snow globe, all these little flakes falling to the floor or on the backs of chairs.<br />
<br />
I believe stress, whether positive or negative, affects my skin.  <br />
<br />
Does anyone else feel that way?]]></content:encoded>
		</item>
	</channel>
</rss>