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Re: Psorisis of the Scalp

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,

Hi! My son and I both use Betamethasone Dipropionate Lotion 0.05%

(prescription) and it works great. It is a clear liquid (in a squeeze bottle)

alcohol

based so you can put it on wet or dry hair and you cannot even tell you have it

in...when the hair dries (if wet). We also use Selsun (Green bottle) sorry

can't remember the name. Actually we haven't had to use Selsun since we have

been using the above RX. The pharmacist has tried to give us the lotion

(cream) in place of the squeeze bottle before so be sure when you pick it up

they

have given you the correct RX (it's happened more than once) and they sometimes

have had to order it but it only takes a day or so to get it in. Good Luck.

P in the scalp/hair is so annoying! (Va.)

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In a message dated 1/5/04 3:35:51 PM Eastern Standard Time,

<<Does anyone have tips or remedies that they find useful for treating

the scalp. Thanks>>

,

Try 's Tea Tree shampoo. It is great!

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Sorry , short of shaving your head and doing PUVA treatments, TGel and

keeping my scalp really clean and dry is the only thing I have ever found that

works, except MTX. I was nearly free of itching while on MTX. I have very thick

coarse red hair and when I get sweaty (which is often these days thanks to the

prednisone induced hot flashes) I know the itch will follow. I try to stay as

cool as possible all the time. There are some prescription things for scalps

you might want to try. I think Dovonex is one but it made my scalp feel greasy

and increased the heated up feeling. I wish you luck......Cheri :-))

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,

What I use is Luxiq foam. It must be prescribed by your doctor but

it works great for me. Not sure of the cost, if you have insurance

then it should not be a problem. It is basicaly like a moose foam

that you just spread on your scalp. I usually only use it on flare

ups and after a few days it goes away. Give it a try.

Dennis

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I have to step in and beg to differ here.

There is one more thing that works just as good as PUVA or MTX. Soriatane. It

has cleared 3/4th of my scalp!!!!!

LeAnn Cayer & Furbrats Blossom & Meriko

Heart Bandits American Eskimo Dog Rescue

Railroad Coordinator www.heartbandits.com

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" prednisone induced hot flashes "

Cheri hi, I did a ten-day tapering dose of prednisone

about a month ago and still am experiencing damn hot

flashes that I've never had before in my life! Is that

what caused it? Does it ever go away? I find it rather

bothersome although I feel warmer than usual in our

near zero temps :-)

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HI -

Now, I don't have p, just the pa, but I have a *very* scaly scalp and

Neutrogena T-Gel shampoo has been a life saver. It is coal tar based,

but, in my opinion, not horrible smelling, and if you use a nice-

smelling conditioner afterwards, you can't smell it on your hair. I

am kinda weird, I like the slight medicinal smell of it. I have been

using T-Gel for about 6 years now and I have had great success with

it--I can wear black again! Sam's Club and Costco carry the big

bottles of this now, and you can also find the jumbo size at Target.

They recommend using it only every other day. I hope this works for

you. T-Gel comes in Extra Strength too, but not in the jumbo bottle

size.

-julie

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I have tried may different shampoos. My best results are obtained by

rubbing a few drops of T-Gel or MG217(Walgreens) in at night on the

affected areas and also rub in Dovonex so I end up with this mixture

on my scalp overnight. I wash it out in the AM. I use nothing during

the day.

> Hi,

>

> Does anyone have tips or remedies that they find useful for

treating

> the scalp. i hate that awful tar shampoo and refuse to use it. I

> don't suffer very badly but I have recently suffered a flare up and

> my scalp is very itchy at the moment.

>

> Thanks

>

>

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Dear ,

Against the itch, nothing works better than tar, in any form. Sure, tar shampoos

smell... and tar ointments smell even worse!

But you can avoid tar. I have gotten good results with calcipotriol (or

calcipotriene, depending on country...). It is sold with the brand name Daivonex

(or Dovonex, again depending on country!). Be sure to get the scalp lotion,

because it also comes as ointment for other parts of the body. Apply twice

daily, lightly, using the application nozzle of the little bottle. I apply it

only to affected areas of the scalp, and try to use as little as possible,

because it's quite expensive (but orders of magnitude less than biologic

treatments!!!).

The stuff comes with an instructions leaflet, stating maximum doses, and so. The

amount I need is about one tenth of the maximum dosage, and in this amounts it's

basically free of secondary effects, a welcome feature.

Be patient. Calcipotriol starts working after about 2 weeks, and reaches full

effect only after about one month.

> Does anyone have tips or remedies that they find useful for treating

> the scalp.

NEVER, absolutely never, scrape the lesions! That makes them flare more than

anything! If you don't use a tar shampoo, use a neutral one, as free as possible

from scenting substances.

Should I add the usual stuff about consulting your dermatologist? I guess we

can obviate that recommendation by now! Everyone should know that that's the

official, correct, legal, recommended, politically correct thing to do! :-)

Good luck!

Manfred (with scalp psoriasis for 12 years - and still alive!)

--------------------------

Visit my hobby homepage!

http://www.qsl.net/xq2fod

--------------------------

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Jane, this is a first for me too. i had a hystorectomy and tapered off hormone

replacement therapy and never had a single hot flash but the prednisone really

stirs them up. I get so sweaty all over and it happens instantly! My hair is

thick and feels like a soggy mop when the sweat hits. If I stick to 10 mg I'm

okay, minor melt downs, but some days I am so stiff that I take 20 mg and then

the hot flashes are horrible. My new doc suggested Effexor as a new approach to

dealing with the hot flashes but not only did it have very little effect it

changed my personality so much that I will not take it again, even if I melt

down into a big puddle. I hope yours go away soon. Cheri :-))

" prednisone induced hot flashes "

Cheri hi, I did a ten-day tapering dose of prednisone

about a month ago and still am experiencing damn hot

flashes that I've never had before in my life! Is that

what caused it? Does it ever go away? I find it rather

bothersome although I feel warmer than usual in our

near zero temps :-)

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Cheri, I had a hysterectomy in Sept 01 but they never

suggested any hormone replacement therapy. Is that

something that would stop the annoying fire that burns

within me? (My fiance can't comprehend how I could be

burning up when my skin feels like ice) Jane

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Jane, I had hormone replacement therapy because they took my ovaries, if you

still have one or both of yours it may be that you are beginning menopause but I

would blame the prednisone if it started when you began to take it. Cheri

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Cheri,

I have had psorisis of the scalp for about 35 years.

No other problems. Then when I had a complete

hysterectomy (dr took my ovaries out) & put me on

estrogen. Because my mother had breast cancer, I went

off the estrogen and that's when all heck broke loose.

I began having major flushes all the time with

sweating! Not sleeping well and then the leg

stiffness began. Now pain in knee and hard to

straiten the knees after sitting. Also at that same

time began having eye problems, watering eyes, then

red eyeballs, etc. I am now putting eye drops to

moisture my eyes due to what I'm told is blepharitis.

Did you have any of these problems or are you still on

hormones?

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, My mom had breast cancer too and that is when I started thinking about

quitting the HRT. I didn't have a single hot flash since quitting estradial in

June but as soon as I started taking prednisone in November, wham! it hit like a

ton of bricks. I do suffer from heat though, but it is different than the hot

flashes. I am going to explore Erythromelalgia as a possible cause. It seems

that all my life I have had scalp involvment but by comparison to a lot of the

contributors on this site my P is pretty mild. I have more spots now but not

too bad........hands, feet, nails, under one breast, top of the crack of my

butt and one small spot on my hip. My journey into PA began with a really bad

fall 2 1/2 years ago. My journey with autoimmune disease, in particular

allergies, began about 10 years ago after a 5 month bout with mononucleosis. So

I don't know how we compare. I've just about given up on trying to figure out

which came first, the chicken or the egg. I try not to blame everything on PA

but it is difficult to separate symptoms because it all seems to come back to

autoimmunie disease. Clear as muc????? Sorry, I feel like I am ranbling.

Cheri :-))

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Thanks much Cheri,

I am new to this group and appreciate your help. When

I went off hormones, that when the PA began in my

body. Actually it may even have been after the

hysterectomy, hard to tell but the estrogen may have

subdued it.

Again, thanks!

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Betamethasone Valerate lotion USP, 0.1% works for mine. It is a liquid in a

bottle with

an eye dropper top. I tried all the " shampoos " and none worked.

Tom

> Hi,

>

> Does anyone have tips or remedies that they find useful for treating

> the scalp. i hate that awful tar shampoo and refuse to use it. I

> don't suffer very badly but I have recently suffered a flare up and

> my scalp is very itchy at the moment.

>

> Thanks

>

>

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