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In a message dated 15/10/01 14:35:27 GMT Daylight Time,

nct-coffee writes:

<< you tell everyone what's wrong with you and explain that

it's not infectious (it's genetic). But at its height, last time, I had

people shooing their children away from me, taking wide detours round me,

and even, at the supermarket, had people " ewwww " ing >>

Huge sympathies - my DS1 suffers from psoriasis in various forms and we have

had to endure reactions like this, too. When he was 7-ish it was particularly

bad, with his scalp and feet the worst affected although I had to wrap his

whole body in tar bandages and cling-film every night. His feet would be

bleeding so badly by lunchtime that he couldn't walk and you could literally

lift his hairline away from his scalp because it was one big scab. His saving

grace was when his father (DH1) was made redundant and was able to afford the

time and money to take him to the Dead Sea for treatment there. Quite

honestly has never looked back although he does have flare-ups now and

again (and I have been warned that with his GCSEs this summer he may well

have a massive flare-up) and still suffers from psoriac arthritis (sp?) in

his toes... means he needs to pop an anti-inflamitory before he plays rugby :)

Does bathing in dead sea salt help the itching? says it does but

depends on the water temp being just right.

ann SAHM to (15/1/86), Kirsty (5/6//87) and Ben (11/7/98) DS3 due March

2002. Editor Cambridge newsletter

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Ann wrote:

> Huge sympathies - my DS1 suffers from psoriasis in various forms

and we have

> had to endure reactions like this, too. <snip>

(and I have been warned that with his GCSEs this summer he may well

> have a massive flare-up) <snip>

My friend with Psoriasis that suffers with it on her nipples also had

it when she did her GCSE's (actually that is when it first started)

then again after the birth of each of her children. So she thinks it

is stress related.

Trisha

SAHM to 3 boys

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Salt bathing does help with the itching, provided there aren't too many

open sores at the time :) DH talked about sending me to the Dead Sea last

time, as it was pretty bloody, but we really couldn't afford it. TBH now

I've had the diagnosis confirmed, and have a referral to the derm. under

way I'm not so bothered: there are worse things! And it's early days yet,

so may not affect much more than it's already on (where it's still nice and

faint!)

I get arthritis in my big toes and one little finger - painful stuff, but

I'm putting off the treatments until I think I really need the big

guns. There are some really good drugs now, and if your DS1 feels a need

for support and information, the National Psoriasis Foundation

(http://www.npf.com, I think) - an American group needless to say - is

brilliant!!

And take heart: it's not necessarily the case that stress causes flare-ups

- it does for some, but not for others!

The only thing that makes mine go completely is pregnancy!!

Vicki

>Does bathing in dead sea salt help the itching? says it does but

>depends on the water temp being just right.

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Oh bad luck Vicki - I do hope it doesn't get any worse and does get

better...

Just a thought, have just noticed DS's ezcema has returned in little

patches and I was rather hoping he'd grown out of it having been

pretty clear all summer - I'm really really wondering whether central

heating has made the ezcema reerupt. Could there be any correlation

with the psoriasis? Or does it not have much to do with dryness?

<<<hugs>>>

Caro

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I don't know - Joshi's eczema does seem to get worse with the central

heating. TBH, though, I slather so much axle grease over myself on a

permanent basis, I don't think my skin knows much about the seasons :))

Vicki

I'm really really wondering whether central

>heating has made the ezcema reerupt. Could there be any correlation

>with the psoriasis? Or does it not have much to do with dryness?

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> I'm really really wondering whether central

> >heating has made the ezcema reerupt. Could there be any

correlation

> >with the psoriasis? Or does it not have much to do with dryness?

>>>>>>>>>>>

Is it the heating or the fact that the air is not getting to the

relevant parts of the body?

My elbows always play up in winter but I am not sure if that is

because I have long sleeves on or because of the heating. I am sure

that the sunshine helps.

Trisha

SAHM to 3 boys

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I think it is a bit of both. Fran has very bad eczema on elbows - inside and

out across her shoulders and tops of ears - her legs have cleared up. It is

getting much better but flares when her immune system is under attack or if she

is stressed and tired. It is worse in winter so she wears short sleeved shirts

at school and a skirt - not a dress and sits away from windows and radiators.

She has stopped her homeopathic treatment and we seem to be managing it ok. Her

dirty protest had helped it so she only baths and washes her hair once a week.

Caroline

Jersey

>

> > I'm really really wondering whether central

> > >heating has made the ezcema reerupt. Could there be any

> correlation

> > >with the psoriasis? Or does it not have much to do with dryness?

> >>>>>>>>>>>

>

>

> Is it the heating or the fact that the air is not getting to the

> relevant parts of the body?

> Trisha

> SAHM to 3 boys

Germain

Jersey

British Channel Islands

49º11'30 " N

02º06'12 " W

WGS84

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Trisha you could test this by putting four or five t-shirts on at a

time to keep warm ... but with arms exposed ? and report back!

Caro

;-))

-

> My elbows always play up in winter but I am not sure if that is

> because I have long sleeves on or because of the heating. I am sure

> that the sunshine helps.

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Caro wrote:

> Trisha you could test this by putting four or five t-shirts on at a

> time to keep warm ... but with arms exposed ? and report back!

> Caro

> ;-))

>>>>>>>>>>>>>>>

How do I say this Caroline - in one word - NO! my arms are always

freezing in winter and I would not be seen dead with no sleeves or

socks!

At the moment I do have a t-shirt on (and I would not go outside liek

this I need my fleece on as well) but it is lovely and sunny today

(and the heating is on) but I still have my socks on and a pair of

sheepskin slippers!

and anyway the 10lbs I have put on are really showing and I need thin

clothes not layers! :)

Trisha

SAHM to 3 boys

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Anyway, everybody's psoriasis is different - mine is better in humid

sunshine than dry sunshine, and even exposed to the air in this weather

will likely continue to deteriorate because it's so dry. Other people do

better in dry than humid :)

I've been involved in a research group at one of the local hospitals, where

the dermatology team are doing lots of psoriasis research - I keep hoping

to get a drug trial, but so far no luck :) But psoriasis is a bizarre

condition because it can't be replicated on animals - even primates don't

get it - so the only way to study it is on humans. So far this year, I've

given 5 skin biopsies to a study looking at the cell differences between

psoriatic and normal skin. Side discovery of this is that psoriasis won't

grow on a deep wound which has actually damaged nerves below the skin, but

it does (in me) grow on spots/scratches/grazes. So, if you're going to cut

me, make it serious please :) I've also been injected with stress hormones

to see if that makes me worse (it didn't make my skin worse, but made

living with me difficult, apparently!) And answered several questionnaires

about how it affects the daily quality of my life (hardly at all except

insofar as it strongly influences what I wear - few short sleeves and no

mini skirts). The human genome project has, apparently, come up with 8

genes which produce psoriasis in different combinations. And there's a

vaccination under development in Oz which will need testers over here

shortly, which is supposed to be brilliant (which is why I keep letting

them have my skin!!)

Vicki

> > My elbows always play up in winter but I am not sure if that is

> > because I have long sleeves on or because of the heating. I am sure

> > that the sunshine helps.

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