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Re: PSC Itching

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I've experienced exactly the same symptoms (itching, blotchy after

running) several years before PSC diagnosis. In my case, it was

eczema. If it responds to topical steroids (mine did), it's not PSC.

I wonder if it's somehow related though.

The way most people describe " PSC " itching (pruritis) is as a deep-

seated itch that's not relieved by scratching, primarily on places like

soles of feet, palms of hands, forearms, shins, but can be just about

anywhere.

Arne

How do you know if itching is caused by PSC? I have noticed that when i

come in from the cold i will get itches or when I run on a treadmill...

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My husband does not have PSC, but he says when he jogs and then sweats, if he

doesn't shower off right away, the salt or sodium in his sweat irritates the

nerves under his skin causing itching. so I would say, when something irritates

the nerve endings in the skin, itching can result.

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My husband does not have PSC, but he says when he jogs and then sweats, if he

doesn't shower off right away, the salt or sodium in his sweat irritates the

nerves under his skin causing itching. so I would say, when something irritates

the nerve endings in the skin, itching can result.

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My husband does not have PSC, but he says when he jogs and then sweats, if he

doesn't shower off right away, the salt or sodium in his sweat irritates the

nerves under his skin causing itching. so I would say, when something irritates

the nerve endings in the skin, itching can result.

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My PSC itching is everywhere, in eyeballs, inner ears, in nose, mouth, face,

head, armpits, feet, hands, legs, arms....and every other space and/or

opening....nothing is safe from the pruitis.

When my hands and feet itch, scratching relieves it in the moments when I am

scratching or raking some hard sharp object over the bottom of my feet...I would

describe it as a very compelling obsession to continue scratching that spot

until the point that pain is introduced...then the pain overrides the incredible

urge to continue scratching. when it wakes me during the night, I run cold

water in the tub and stand in their...until my feet are numb from the cold, then

I pat dry and patter back to bed to fall asleep before the next cycle of itching

starts. I keep some sharp implements at myy bedside for those emergency

scratches.

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My PSC itching is everywhere, in eyeballs, inner ears, in nose, mouth, face,

head, armpits, feet, hands, legs, arms....and every other space and/or

opening....nothing is safe from the pruitis.

When my hands and feet itch, scratching relieves it in the moments when I am

scratching or raking some hard sharp object over the bottom of my feet...I would

describe it as a very compelling obsession to continue scratching that spot

until the point that pain is introduced...then the pain overrides the incredible

urge to continue scratching. when it wakes me during the night, I run cold

water in the tub and stand in their...until my feet are numb from the cold, then

I pat dry and patter back to bed to fall asleep before the next cycle of itching

starts. I keep some sharp implements at myy bedside for those emergency

scratches.

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Any changes of body temperature send me into an itchy period. We live in

Ontario and have

had a fairly cold winter this year. Just going from inside to a car drives me

nuts. My husband

will quite often warm the car up for me. Or if we are out somewhere, he'll go

get the car and

pick me up at the door.... he's great.

Then there is the heat factor as well. The only time I can stand being hot or

warm is if I am

out in the sunshine ie. Mexico for a week. The sunshine helps the itching so

much.

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Hello

My husband is the one with psc but has no itching. Mself I have this

itching on my foot and I scratch it with whatever until sometimes it

is raw and still itches. I am not sure what I have but it sounds soo

much like my foot. Nothing I put on it works to stop that feeling and

I really dont want to go to the dr cause of a foot itch sounds to

petty. Ice packs work for a little bit. I don't have psc or anything

close but I got gastritis that doesn't seem to want to go away and if

I think back it was about the same time as my foot itch. Not sure if

related but would love that feeling to go away.

thanks for listening

skomula MN

>

>

> My PSC itching is everywhere, in eyeballs, inner ears, in nose,

mouth, face, head, armpits, feet, hands, legs, arms....and every

other space and/or opening....nothing is safe from the pruitis.

>

> When my hands and feet itch, scratching relieves it in the moments

when I am scratching or raking some hard sharp object over the bottom

of my feet...I would describe it as a very compelling obsession to

continue scratching that spot until the point that pain is

introduced...then the pain overrides the incredible urge to continue

scratching. when it wakes me during the night, I run cold water in

the tub and stand in their...until my feet are numb from the cold,

then I pat dry and patter back to bed to fall asleep before the next

cycle of itching starts. I keep some sharp implements at myy bedside

for those emergency scratches.

>

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Thank you all for all your insight, most appreciated. After assuming my

PSC and cholangitis attacks were heartburn I know better than to

diagnose myself but from what I am reading it seems like it is not from

PSC, especially since my levels have been decent and the itching stops

after a very short time and seems to start exactly when i come out of

the cold or do vigorous activity.

On a sidenote, any medical breakthroughs on the way for PSC? I can't

make the conference due to a charitable event I am helping host.

Excited to hear the results!

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Thank you all for all your insight, most appreciated. After assuming my

PSC and cholangitis attacks were heartburn I know better than to

diagnose myself but from what I am reading it seems like it is not from

PSC, especially since my levels have been decent and the itching stops

after a very short time and seems to start exactly when i come out of

the cold or do vigorous activity.

On a sidenote, any medical breakthroughs on the way for PSC? I can't

make the conference due to a charitable event I am helping host.

Excited to hear the results!

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Thank you all for all your insight, most appreciated. After assuming my

PSC and cholangitis attacks were heartburn I know better than to

diagnose myself but from what I am reading it seems like it is not from

PSC, especially since my levels have been decent and the itching stops

after a very short time and seems to start exactly when i come out of

the cold or do vigorous activity.

On a sidenote, any medical breakthroughs on the way for PSC? I can't

make the conference due to a charitable event I am helping host.

Excited to hear the results!

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cooler temperatures allows my itching to subside a tiny bit. I do know that

when I run a fever (anything over 98.0 for me), my itching comes to a screeching

halt! So when my temp goes up, although that sucks, I get itching relief....but

when my temp returns to normal - itching goes into over-drive.

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Pruitis: itching so bad you can't sleep, think, or reason. You would and often

do scratch your skin off because burning and stinging is preferrable to itching.

Often focused on the palm of hands and soles of feet. Often accompanied by sores

that are similar to sores that meth addicts get. In a bad itching flare it will

last for weeks or months. When you have it, you know it. It is worse than hives

(which I've had also). Hope you never have to suffer through it. Cheryl ID

PSC Itching

> How do you know if itching is caused by PSC? I have noticed that when i

> come in from the cold i will get itches or when I run on a treadmill.

> These are all body temperature changes and i have heard that sweat can

> also do it. Is there a defining characteristic?

>

> Any insight is appreciated.

>

> Cheers,

>

>

> dx PSC 08/07

>

>

>

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Suzanne just had an itching "attack"; it lasted a little over 24 hours. She takes Atarax for it, but this totally knocks her out so if she is working or doing something else she can't take it. We have not found anything really that relieves it.LINDA(Mom of Suzanne, 19, IBD & PSC) Re: Re: PSC Itching

cooler temperatures allows my itching to subside a tiny bit. I do know that when I run a fever (anything over 98.0 for me), my itching comes to a screeching halt! So when my temp goes up, although that sucks, I get itching relief....but when my temp returns to normal - itching goes into over-drive.

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I used to tell people that the best way to get a good idea of what PSC

itching is like would be to sprinkle your bed liberally with fiberglass

insulation every night before bed! Luckily I only suffered with itching

that bad a couple times....

athan

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Atarax did nothing for me, but I did find that if I get enough sleep at night, then I can tolerate more itching during the day. How do I do that? Ambien CR. My Hep prescribes it for me so at least I know at bedtime I will be knocked out of the conscious itching nightmare.

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Atarax did nothing for me, but I did find that if I get enough sleep at night, then I can tolerate more itching during the day. How do I do that? Ambien CR. My Hep prescribes it for me so at least I know at bedtime I will be knocked out of the conscious itching nightmare.

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Ah, athan -- just the right description. During the day, though,

there are times when it's like my socks or other pieces of clothing

are lined with bits of fiberglass. Hands are like I just removed

gloves filled with tiny bits of fiberglass.

Couple o' wonderings about itching -- I have had bouts in the past of

the continual itching but now it's more come and go, with periods of

a few hours when it will be particularly bad (scratching myself raw)

but there will be long stretches some days when there will be no

problem. I get really hopeful that it is fading away and then I'll

have another couple hours of torture (I should say mild torture,

really -- it's not as bad as it's been at times; I only have about 3

patches on my legs where I've broken skin from scratching). Is this

typical for others?

Also, I'm switching from zoloft to rifampin. Started taking the

rifampin a week ago and increased the dose over the week until

yesterday when I was up to 150mg TID. I haven't taken this in years

and I can't recall how quickly it takes effect if it's going to help.

Anybody have an idea? I thought it was working yesterday but when I

woke up this morning, it's back...

Philip

35, married, 3 kids; PSC 94, UC 2008, DMII 2009

>

> I used to tell people that the best way to get a good idea of what

PSC

> itching is like would be to sprinkle your bed liberally with

fiberglass

> insulation every night before bed! Luckily I only suffered with

itching

> that bad a couple times....

>

> athan

>

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Ah, athan -- just the right description. During the day, though,

there are times when it's like my socks or other pieces of clothing

are lined with bits of fiberglass. Hands are like I just removed

gloves filled with tiny bits of fiberglass.

Couple o' wonderings about itching -- I have had bouts in the past of

the continual itching but now it's more come and go, with periods of

a few hours when it will be particularly bad (scratching myself raw)

but there will be long stretches some days when there will be no

problem. I get really hopeful that it is fading away and then I'll

have another couple hours of torture (I should say mild torture,

really -- it's not as bad as it's been at times; I only have about 3

patches on my legs where I've broken skin from scratching). Is this

typical for others?

Also, I'm switching from zoloft to rifampin. Started taking the

rifampin a week ago and increased the dose over the week until

yesterday when I was up to 150mg TID. I haven't taken this in years

and I can't recall how quickly it takes effect if it's going to help.

Anybody have an idea? I thought it was working yesterday but when I

woke up this morning, it's back...

Philip

35, married, 3 kids; PSC 94, UC 2008, DMII 2009

>

> I used to tell people that the best way to get a good idea of what

PSC

> itching is like would be to sprinkle your bed liberally with

fiberglass

> insulation every night before bed! Luckily I only suffered with

itching

> that bad a couple times....

>

> athan

>

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Ah, athan -- just the right description. During the day, though,

there are times when it's like my socks or other pieces of clothing

are lined with bits of fiberglass. Hands are like I just removed

gloves filled with tiny bits of fiberglass.

Couple o' wonderings about itching -- I have had bouts in the past of

the continual itching but now it's more come and go, with periods of

a few hours when it will be particularly bad (scratching myself raw)

but there will be long stretches some days when there will be no

problem. I get really hopeful that it is fading away and then I'll

have another couple hours of torture (I should say mild torture,

really -- it's not as bad as it's been at times; I only have about 3

patches on my legs where I've broken skin from scratching). Is this

typical for others?

Also, I'm switching from zoloft to rifampin. Started taking the

rifampin a week ago and increased the dose over the week until

yesterday when I was up to 150mg TID. I haven't taken this in years

and I can't recall how quickly it takes effect if it's going to help.

Anybody have an idea? I thought it was working yesterday but when I

woke up this morning, it's back...

Philip

35, married, 3 kids; PSC 94, UC 2008, DMII 2009

>

> I used to tell people that the best way to get a good idea of what

PSC

> itching is like would be to sprinkle your bed liberally with

fiberglass

> insulation every night before bed! Luckily I only suffered with

itching

> that bad a couple times....

>

> athan

>

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Hi Karyn

Yep ... Aurora is not that far away. My hepatologist is here in

Hamilton. Dr. Witt-Sulivan. She also cross-specializes in

gastroenterology so I see her for my UC as well. Kinda nice that way

insofar as I don't have to see someone separate for that.

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Hi Karyn

Yep ... Aurora is not that far away. My hepatologist is here in

Hamilton. Dr. Witt-Sulivan. She also cross-specializes in

gastroenterology so I see her for my UC as well. Kinda nice that way

insofar as I don't have to see someone separate for that.

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