Jump to content
RemedySpot.com

Re: and now.......................

Rate this topic


Guest guest

Recommended Posts

Guest guest

Liz, I am sorry to hear has yet another JRA related issue but I know

being the strong gal she is, will endure!

Hang Tight, Hang Tough

Donna

Link to comment
Share on other sites

Guest guest

That is interesting because we are waiting on a dermatology appointment the last

week of this month to rule out psoriasis. My daughters ocular immunologist is

patiently waiting to find out what is said. I just assumed that if it is

psoriasis that another med would be added. Or at the very least, a higher dose

of what she is already on. Let me know what your doc says. Where is her

psoriasis? Does she have nail pitting? My daughter has had a rash on her neck

since January. I didn't think too much about it until about two months ago. It

looks awful.

Thanks for any info,

', a 10 year JIA/Uveitis

liz smith <liz_smith@...> wrote:

Nearly 12 years since onset of arthritis we now have a diagnosis of

psoriasis. I don't know that it actually changes anything, except perhaps a

classification from poly to psoriatic. But it does add to what I need to

know. Because is already on methotrexate and Remicade and the

psoriasis is currently limited to a small area she will only use a topical

ointment to treat it.

She definitely keeps us on our toes.

Liz

Link to comment
Share on other sites

Guest guest

That is interesting because we are waiting on a dermatology appointment the last

week of this month to rule out psoriasis. My daughters ocular immunologist is

patiently waiting to find out what is said. I just assumed that if it is

psoriasis that another med would be added. Or at the very least, a higher dose

of what she is already on. Let me know what your doc says. Where is her

psoriasis? Does she have nail pitting? My daughter has had a rash on her neck

since January. I didn't think too much about it until about two months ago. It

looks awful.

Thanks for any info,

', a 10 year JIA/Uveitis

liz smith <liz_smith@...> wrote:

Nearly 12 years since onset of arthritis we now have a diagnosis of

psoriasis. I don't know that it actually changes anything, except perhaps a

classification from poly to psoriatic. But it does add to what I need to

know. Because is already on methotrexate and Remicade and the

psoriasis is currently limited to a small area she will only use a topical

ointment to treat it.

She definitely keeps us on our toes.

Liz

Link to comment
Share on other sites

Guest guest

Wow Liz,

Thats a shocker, you would think after 12 years nothing would change

so much. I have no idea whats all involved with psoriatic. I guess

you will be doing a lot of reading.

I hope this doesn't cause too many additional problems. How is

she taking the news.

I have to ask, do you think that had anything to do with the hair

loss??? I must admit it was the 1st thing that came to my mind.

Hugs to you all as you venture down a new path.

hugs Helen and (8,systemic)

>

> Nearly 12 years since onset of arthritis we now have a diagnosis of

> psoriasis. I don't know that it actually changes anything, except

perhaps a

> classification from poly to psoriatic. But it does add to what I

need to

> know. Because is already on methotrexate and Remicade and the

> psoriasis is currently limited to a small area she will only use a

topical

> ointment to treat it.

>

>

>

> She definitely keeps us on our toes.

>

>

>

> Liz

>

>

>

>

Link to comment
Share on other sites

Guest guest

Liz,

Our other daughter has psoriasis. We use a topical cream called

protopic. It works great, and clears it up quickly. Although I believe

it is a steroid cream, it works great. Unfortunately we have an awful

history of psorsis in both my husband and my side of the family. Nerves

are a great contributor to the control of psorasis. I have a cousin

that has been hospitalized for her disease several times. When she was

in High School she was in the Mayo Clinic at least 6 weeks every year.

I hope the methotrexate and Remicaid can keep it to a minimum.

My thoughts are with you!

________________________________

From: [mailto: ] On

Behalf Of liz smith

Sent: Thursday, May 11, 2006 6:20 PM

Subject: and now.......................

Nearly 12 years since onset of arthritis we now have a diagnosis of

psoriasis. I don't know that it actually changes anything, except

perhaps a

classification from poly to psoriatic. But it does add to what I need to

know. Because is already on methotrexate and Remicade and the

psoriasis is currently limited to a small area she will only use a

topical

ointment to treat it.

She definitely keeps us on our toes.

Liz

Link to comment
Share on other sites

Guest guest

I am sorry to hear that Liz. I am glad it is only on a small area....Terri

and now.......................

Nearly 12 years since onset of arthritis we now have a diagnosis of

psoriasis. I don't know that it actually changes anything, except perhaps a

classification from poly to psoriatic. But it does add to what I need to

know. Because is already on methotrexate and Remicade and the

psoriasis is currently limited to a small area she will only use a topical

ointment to treat it.

She definitely keeps us on our toes.

Liz

Link to comment
Share on other sites

Guest guest

’,

’s only affected area right now is right around her eyes. It’s

interesting~~ many years ago her rheumatologist in Houston (we had moved, so

this wasn’t her diagnosing rheumy) said to be aware that we may someday see

psoriasis, based on a sausage shaped finger at diagnosis. After this many

years, though, we didn’t expect it. And I certainly never thought about

having a first round of it while on methotrexate and Remicade! does

not have any nail pitting. I don’t know if that’s just pure luck or if it is

because she’s been on meds for so many years.

She has been started on protopic, an ointment used for psoriasis. Hopefully

that will clear it up quickly. As for adding any other systemic meds, I

really don’t want to go there. And unless the psoriasis gets bad I don’t

think that will even be an issue.

’s next rheumatology appointment/ Remicade infusion is on June 6th.

I’ll let you know if he suggests any changes. Let us know what a’s

dermatologist has to say.

Liz

_____

From: [mailto: ] On Behalf

Of ' Taunton

Sent: Thursday, May 11, 2006 7:42 PM

Subject: Re: and now.......................

That is interesting because we are waiting on a dermatology appointment the

last week of this month to rule out psoriasis. My daughters ocular

immunologist is patiently waiting to find out what is said. I just assumed

that if it is psoriasis that another med would be added. Or at the very

least, a higher dose of what she is already on. Let me know what your doc

says. Where is her psoriasis? Does she have nail pitting? My daughter

has had a rash on her neck since January. I didn't think too much about it

until about two months ago. It looks awful.

Thanks for any info,

', a 10 year JIA/Uveitis

liz smith <liz_smith@...> wrote:

Nearly 12 years since onset of arthritis we now have a diagnosis of

psoriasis. I don't know that it actually changes anything, except perhaps a

classification from poly to psoriatic. But it does add to what I need to

know. Because is already on methotrexate and Remicade and the

psoriasis is currently limited to a small area she will only use a topical

ointment to treat it.

She definitely keeps us on our toes.

Liz

Link to comment
Share on other sites

Guest guest

Helen,

I don't know that anything different will be involved with this, other than

keeping an eye on the skin. I guess I'll learn as I go.

was fine with the news. She has such a great sense of humor! Her only

comment was, " Well, just think how many conversation starters I have! "

As for the hair loss and a possible tie to the psoriasis, I didn't even ask

the dermatologist. If I can find any info online I'll call and ask. The

nurse there is a neighbor of mine and I'm sure would ask for me.

Good luck with Nick's infusion. It's tomorrow, isn't it? I hope things go

smoothly. Hopefully there will be no more grouchy days for a while!

Liz

_____

From: [mailto: ] On Behalf

Of hburger64

Sent: Thursday, May 11, 2006 7:51 PM

Subject: Re: and now.......................

Wow Liz,

Thats a shocker, you would think after 12 years nothing would change

so much. I have no idea whats all involved with psoriatic. I guess

you will be doing a lot of reading.

I hope this doesn't cause too many additional problems. How is

she taking the news.

I have to ask, do you think that had anything to do with the hair

loss??? I must admit it was the 1st thing that came to my mind.

Hugs to you all as you venture down a new path.

hugs Helen and (8,systemic)

>

> Nearly 12 years since onset of arthritis we now have a diagnosis of

> psoriasis. I don't know that it actually changes anything, except

perhaps a

> classification from poly to psoriatic. But it does add to what I

need to

> know. Because is already on methotrexate and Remicade and the

> psoriasis is currently limited to a small area she will only use a

topical

> ointment to treat it.

>

>

>

> She definitely keeps us on our toes.

>

>

>

> Liz

>

>

>

>

Link to comment
Share on other sites

Guest guest

,

The dermatologist said that protopic is not a steroid cream, which is why we

(the derm and I) chose that over the other one he offered. I'm glad to hear

that it works so well. 's psoriasis is currently limited to the area

around her eyes, but because of the location is easily noticed, so she wants

it cleared up as quickly as possible.

I'm sorry that so many in your family deal with it. How does your daughter

handle it?

Liz

_____

From: [mailto: ] On Behalf

Of Ray

Sent: Thursday, May 11, 2006 7:57 PM

Subject: RE: and now.......................

Liz,

Our other daughter has psoriasis. We use a topical cream called

protopic. It works great, and clears it up quickly. Although I believe

it is a steroid cream, it works great. Unfortunately we have an awful

history of psorsis in both my husband and my side of the family. Nerves

are a great contributor to the control of psorasis. I have a cousin

that has been hospitalized for her disease several times. When she was

in High School she was in the Mayo Clinic at least 6 weeks every year.

I hope the methotrexate and Remicaid can keep it to a minimum.

My thoughts are with you!

________________________________

From: [mailto: ] On

Behalf Of liz smith

Sent: Thursday, May 11, 2006 6:20 PM

Subject: and now.......................

Nearly 12 years since onset of arthritis we now have a diagnosis of

psoriasis. I don't know that it actually changes anything, except

perhaps a

classification from poly to psoriatic. But it does add to what I need to

know. Because is already on methotrexate and Remicade and the

psoriasis is currently limited to a small area she will only use a

topical

ointment to treat it.

She definitely keeps us on our toes.

Liz

Link to comment
Share on other sites

Guest guest

Liz,

Luckily it is in her scalp, and you can't see it. But it can get to be

the size of a " silver dollar pancake " sometimes. It is itches and

bleeds. So it isn't pretty. But she does quite well with it. The

summer sun helps a lot. Just one more thing on the agenda to deal with,

but she seems to do ok with it!

I lover your daughter's attitude! Keep up the great spirit.

________________________________

From: [mailto: ] On

Behalf Of liz smith

Sent: Thursday, May 11, 2006 7:47 PM

Subject: RE: and now.......................

,

The dermatologist said that protopic is not a steroid cream, which is

why we

(the derm and I) chose that over the other one he offered. I'm glad to

hear

that it works so well. 's psoriasis is currently limited to the

area

around her eyes, but because of the location is easily noticed, so she

wants

it cleared up as quickly as possible.

I'm sorry that so many in your family deal with it. How does your

daughter

handle it?

Liz

_____

From: [mailto: ] On

Behalf

Of Ray

Sent: Thursday, May 11, 2006 7:57 PM

Subject: RE: and now.......................

Liz,

Our other daughter has psoriasis. We use a topical cream called

protopic. It works great, and clears it up quickly. Although I believe

it is a steroid cream, it works great. Unfortunately we have an awful

history of psorsis in both my husband and my side of the family. Nerves

are a great contributor to the control of psorasis. I have a cousin

that has been hospitalized for her disease several times. When she was

in High School she was in the Mayo Clinic at least 6 weeks every year.

I hope the methotrexate and Remicaid can keep it to a minimum.

My thoughts are with you!

________________________________

From: [mailto: ] On

Behalf Of liz smith

Sent: Thursday, May 11, 2006 6:20 PM

Subject: and now.......................

Nearly 12 years since onset of arthritis we now have a diagnosis of

psoriasis. I don't know that it actually changes anything, except

perhaps a

classification from poly to psoriatic. But it does add to what I need to

know. Because is already on methotrexate and Remicade and the

psoriasis is currently limited to a small area she will only use a

topical

ointment to treat it.

She definitely keeps us on our toes.

Liz

Link to comment
Share on other sites

Guest guest

Liz,

You said that her only area affected is around her eye. What does it look

like? has had several places where her skin turns brown and flakes off

and is raw for a bit. Her Ped. tells us it is JRA related the rheumy said maybe

JRA related? We put a cream on it and it goes away so I don't worry too much

about it.

Veri & Jaye 12 poly

Link to comment
Share on other sites

Guest guest

Hi Liz,

Sorry to hear about this new complication. Hope the protopic works quickly.

Take care. (and Ezra, 10 year old systemic)

On 5/11/06 8:38 PM, " liz smith " <liz_smith@...> wrote:

> ¹,

>

> ¹s only affected area right now is right around her eyes. It¹s

> interesting~~ many years ago her rheumatologist in Houston (we had moved, so

> this wasn¹t her diagnosing rheumy) said to be aware that we may someday see

> psoriasis, based on a sausage shaped finger at diagnosis. After this many

> years, though, we didn¹t expect it. And I certainly never thought about

> having a first round of it while on methotrexate and Remicade! does

> not have any nail pitting. I don¹t know if that¹s just pure luck or if it is

> because she¹s been on meds for so many years.

>

> She has been started on protopic, an ointment used for psoriasis. Hopefully

> that will clear it up quickly. As for adding any other systemic meds, I

> really don¹t want to go there. And unless the psoriasis gets bad I don¹t

> think that will even be an issue.

>

> ¹s next rheumatology appointment/ Remicade infusion is on June 6th.

> I¹ll let you know if he suggests any changes. Let us know what a¹s

> dermatologist has to say.

>

> Liz

>

>

>

> _____

>

> From: [mailto: ] On Behalf

> Of ' Taunton

> Sent: Thursday, May 11, 2006 7:42 PM

>

> Subject: Re: and now.......................

>

>

>

> That is interesting because we are waiting on a dermatology appointment the

> last week of this month to rule out psoriasis. My daughters ocular

> immunologist is patiently waiting to find out what is said. I just assumed

> that if it is psoriasis that another med would be added. Or at the very

> least, a higher dose of what she is already on. Let me know what your doc

> says. Where is her psoriasis? Does she have nail pitting? My daughter

> has had a rash on her neck since January. I didn't think too much about it

> until about two months ago. It looks awful.

>

>

> Thanks for any info,

> ', a 10 year JIA/Uveitis

>

>

> liz smith <liz_smith@...> wrote:

> Nearly 12 years since onset of arthritis we now have a diagnosis of

> psoriasis. I don't know that it actually changes anything, except perhaps a

> classification from poly to psoriatic. But it does add to what I need to

> know. Because is already on methotrexate and Remicade and the

> psoriasis is currently limited to a small area she will only use a topical

> ointment to treat it.

>

>

>

> She definitely keeps us on our toes.

>

>

>

> Liz

>

>

>

>

Link to comment
Share on other sites

Guest guest

Veri,

's affected areas had sort of red raised bumps which then became scaly.

The skin never turned brown. I'd suggest consulting a dermatologist if it

continues. They're the experts when it comes to the skin. I honestly don't

know enough about it to give any good info. It was one of those things I

didn't think I needed to know!! I guess that has changed now.

Hope you've had a good Mother's Day,

Liz

From: [mailto: ] On Behalf

Of veristroud@...

Sent: Friday, May 12, 2006 8:00 AM

Subject: Re: and now.......................

Liz,

You said that her only area affected is around her eye. What does it look

like? has had several places where her skin turns brown and flakes

off

and is raw for a bit. Her Ped. tells us it is JRA related the rheumy said

maybe

JRA related? We put a cream on it and it goes away so I don't worry too much

about it.

Veri & Jaye 12 poly

_____

Link to comment
Share on other sites

Join the conversation

You are posting as a guest. If you have an account, sign in now to post with your account.
Note: Your post will require moderator approval before it will be visible.

Guest
Reply to this topic...

×   Pasted as rich text.   Paste as plain text instead

  Only 75 emoji are allowed.

×   Your link has been automatically embedded.   Display as a link instead

×   Your previous content has been restored.   Clear editor

×   You cannot paste images directly. Upload or insert images from URL.

Loading...
×
×
  • Create New...