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2006-08-31 17:57:13

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2006-08-31 14:02:18

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To Vicki, re liver biopsy

2006-08-31 01:22:10

<!doctype html public "-//w3c//dtd html 4.0 transitional//en"
<html
Vicki,
<br
when you are not even taking the mtx yet!&nbsp; Sorry for my alarm but
I am very concerned.&nbsp; Have you had previous liver problems?&nbsp;
Did you know that everytime you have a liver biopsy it causes damage to
your liver that cannot be restored? I have been told by three different,
independent doctors that liver biopsys are only done when liver functioning
tests are consistently showing problems.&nbsp; And even then you would
be removed for mtx immediately and more blood tests done.&nbsp; If the
blood tests were still showing problems then and only then would a liver
biopsy be done.&nbsp; Please, before you have this procedure, please find
out more.&nbsp; Why go thru something that is not necessary?&nbsp; It seems
to me that some doctors are too quick to run all the tests, when it is
really not necessary, and I have especially noticed this phenomenon with
American doctors.&nbsp; I don't know if you are in the USA, but wow, I
would check further into this before I let them poke around at my liver.&nbsp;
It is too precious an organ to let someone dig around in it for no good
reason.&nbsp; There are blood tests that can be done to determine liver
functioning.&nbsp; That is what the blood works is that you will be taking
every month, to check your liver functioning.
<br
ordering unnecessary tests.
<p
<br
<br
<br
<blockquote TYPE=CITE
recommending mtx and&nbsp; I saw an
<br
a ultra
<br
going into
<br
okay,
<br
says she does a lot
<br
due to
<br
everything's
<br
spend a day
<br
on the mtx, I
<br
<p
<p
<p
<p
<br
cute,
<br
of cards to customize.
<br
href="http://clickme.onelist.com/ad/zing4"
a
"
<p
<br
<br
</html

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2006-08-30 23:24:06

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2006-08-30 16:22:00

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To Lee Ann

2006-08-30 14:53:16

Lee Ann writes:
"Does any one know how much Folic acid a day is safe? I am on 1mg a day
right now. I am wondering if increasing my Folic acid will help with my
cold sores. I will be seeing a RD next week. It was my regular doctor that
put me on the MTX. I will be seeing my moms RD. My doctor gave me this
medication and did not ask to see me again! All he wants to do is get a
blood test every 6 weeks. "
Hi Lee Ann
I'm on 1 mg of folic acid a day and it knocked the mouth sores out right away.
Maybe you need more, I believe you can take up to 5 mg a day.
I wonder, did your Dr. do a full blood work up and chest X-rays before he put
you on MTX. Your doing right by going to see a RD soon. I think that some
Dr.'s don't really know a lot about MTX. Two weeks before I went to see my RD
for the first time I was at a Dermatologist and she wrote me an Rx for MTX and
was just going to send me on my way, when I told her I was going to see a RD she
told me to hold off that the RD would take care of prescribing MTX. Looking
back it concerns me that she would just give me the Rx without any tests.
Good Luck
Shayne

To Oma Marsha

2006-08-30 00:00:40

<!doctype html public "-//w3c//dtd html 4.0 transitional//en"
<html
Actually, it is spelled and pronounced Opa and Oma in Germany, as well.&nbsp;
I have a very close friend who lives in Germany.&nbsp; She lived with my
husband and I for a year here in Canada and we have all grown very close.&nbsp;
I met her family this summer when I visited Germany, and stayed with her
Opa and Oma for some of the time.&nbsp; I have heard other people using
the words Opa and Oma.&nbsp; I think it is a delightful alternative to
Grandma and Grandpa and other words we North Americans use.&nbsp; If I
ever have kids, they will call our parents Opa and Oma.
<p
<br

To Janet

2006-08-29 22:48:25

Hi Janet
I to had very bad foot problems, like you describe, at the beginning of my onset
with PA. It came from the souls of my feet and felt like the pain was shooting
half way up my leg. It was very hard to get out of bed and I also would put a
pillow down for some cushion. I am fortunate to be 6'-4" tall so I would hold
on to the ceiling to keep my balance. I still have some pain in the mornings
but its not as bad as it was. I try to keep my feet stretched out and that
helps. Stretch by pulling your toes toward your knees as if you were stretching
your calf muscle.
Good luck with your classes
Bye for now
Shayne

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2006-08-29 11:20:45

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2006-08-29 06:45:39

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Hello Jayne]

2006-08-29 02:30:13

Hello Kelly, Yes that was me, the "dinner issue". My meds only consist
of Naproxen and tylenol.. Not the hard stuff but the stomach stuff. I
wish it meant that if you have a bad stomach you have a flat
stomach!!! I take 375 mg of Naproxen, 3 x's a day, and tylenol in
between. If the Naproxen stops working, I either go back to
indomethcian which works well but gives me serious migraines. My appt
is 9/9, so he might make me change to something else..I'll let you know.
I got my life insurance before I got this so that was good. The more
aliments you have the higher the policy I think. My son, woke up at 4am
with some stomach virus, which is not good, school starts Thurs
here...hopefully 24/hr bug. I am sure it will then make its way around
the house...mom gets it last. Looking foward to talking some more,
Jayne

To Lee Ann

2006-08-28 23:34:32

Thanks for your words of wisdom. I enjoy reading these everyday. I am
no longer the scared person who was handed a diagnosis of something I
had never heard of. Everyones input has been so encouraging. Thanks
to you and everyone!! Jayne
P.S. Lee Ann, what a wonderful mother you must be!.

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2006-08-28 20:14:02

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2006-08-28 15:40:51

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2006-08-28 02:09:21

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2006-08-27 22:31:40

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Valtrex

2006-08-27 15:58:02

Hello,
Has anyone had to take Valtrex? I had to start today. I have
had 3 very painful cold sores in the past 4 weeks. All since I
started MTX. I have a history of these sores but never one right
after the other in a short period of time.
Lee Ann Walter
Wife of Steve;
Mom to: Stephanie 15; Krystle 14;
Caleb 2; Katie 2; Joshua 10 mo.

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2006-08-27 15:40:49

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2006-08-27 08:46:36

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2006-08-26 23:37:25

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turned foot

2006-08-26 11:05:57

Annettte,
How did your foot turn? Did it gradually turn over the years or a sharp tendon
attack or what?
Pat B

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2006-08-26 10:01:59

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2006-08-26 09:14:37

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2006-08-25 16:48:48

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The Jaw thing again

2006-08-25 10:19:30

I couldn't resist! My husband is from Syracuse New York. His family goes to
Cape Cod every year around this time and they send us this fantastic salt
water taffy. It is totally scrumptious! But needless to say... pretty hard
on the jaw! But I couldn't resist!!
yummmmmmmmmmm
Danielle

Tell Me About Meth. Side Effects

2006-08-25 09:42:53

My rheumatologist is trying to decide whether to switch me from sulfasalazine
to methotrexate. I have a mild case of PA (or it's in early stages, can't
tell yet). I also have fibromyalgia and chronic fatigue syndrome, so I'm
very disfunctional from my health problems. It's difficult to know how much
of the muscle and joint pain I have is arthritis or fibro or who knows what,
so I don't know how much benefit I would get from methotrexate.
I mostly hear good things about the medication on this list, so I'm asking if
people would tell me the bad stuff. What kind of side effects did you get,
and how bad are they? When you say you are nauseous for a few hours after
the shot, do you mean feeling queasy, or do you mean vomiting and vertigo?
When you say it causes stomach discomfort, what level of discomfort are we
talking about?
Thanks,
Dwanna

Trauma

2006-08-25 08:45:50

Purtnear -
I have never really thought about when I got PA and what was happening in my
life, but now that you mention it, I was under a lot of stress. Moved out of
my parents house for the first time in 27 years, got into a long term
relationship for the first time, moved in with him, then got married. Moved
5 hours away from all my friends. Left a very secure job with no foreseeable
prospects.
Makes me wonder if that is what triggered it.
Danielle

Tremors/spastic stuff

2006-08-24 22:02:53

Hello
I have a question of you out there, since you have helped me so greatly with
all the other garbage I am living with.......
Does anyone have any "tremmoring" (shaking) in their hands. Or a finger or
hand moving by its self, just kind of wiggling around on its own, moving. I
know to some of you this might sound so damn funny its like a hand with its
own mind. I have had this mildly but it is growing worse....... my typing is
getting slower and fingers not doing what they are told to do. Also my
fingers "get stuck sometimes" very bizzarreeeeeeeee!!
I talked to my Rheumy about this and she just sort of shrugged it off saying
its probably just my nerves playing tricks on me............ well, if this is
a trick where are my treats?!?!?!?
Any info out there?
Thanks bunches,
Sari

These Dangerous Drugs

2006-08-24 18:46:57

I agree that if someone isn't getting any relief, they should talk to their
doctor about stopping. Doctors don't know everything, but then neither do
we, even though we do like to feel in control. If we don't like their
opinions, we can go for a second opinion or change doctors completely, but I
don't think we should assume that they're just out to get us all drugged up.
Surely most of them want what's best for us, if only they knew how to do it?
PA might not kill you, but given the option of another 40 years in pain
which stopped me doing all the things I want to do, or another 10 years
where I could still have a decent quality of life, I'd have the drugs. I'm
lucky at the moment - I can still live a reasonable life without too much
medication, but if I don't fight this disease aggressively, I might not be
able to say that in a few years time.
Yes, there are a lot of messages about drugs. That shows that people are
worried about what they're taking, and want to have as much information as
possible. That way we can make informed choices, not just believe
everything the doctors tell us. Of course we'd all love to take no
medication and keep the PA under control without it, but surely it's better
to stop it getting any worse (or at least reduce the rate at which it's
getting worse) than let it get on with it, in the supposed knowledge that we
know how to deal with it, so it doesn't matter if it gets worse.
Hope I don't sound like I'm having a go at you. We all make choices, and
most people on this list have chosen to go with the drugs. But we still
want to hear about alternatives, or ways to make life a bit easier. I got
lots of helpful hints last week when I was worried about coping with driving
and being at a computer all day (thanks all of you!)
Ali

Weather

2006-08-24 08:44:43

Hey Vicki!
I agree with you about the weather. I live in Louisiana where it is SO
HUMID! When I went up to New York for Thanksgiving it was a total change. I
LOVED IT! Of course I love Louisiana also!
I did go to Arizona a few years ago. That had no effect. The pain was still
very REAL!
My husband has severe allergies. So basically the best place for both of us
to live is not anywhere near Louisiana!
Danielle

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2006-08-24 01:23:42

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Thyroid and PA

2006-08-23 22:38:39

Hello,
It has been suggested to me that I go see a Dr. who specializes
in the Thyroid. I am wondering if any of you know if there is a
connection between PA and Thyroid?
Lee Ann Walter
Wife of Steve;
Mom to: Stephanie 15; Krystle 14;
Caleb 2; Katie 2; Joshua 10 mo.

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to betty

2006-08-23 06:45:37

<!doctype html public "-//w3c//dtd html 4.0 transitional//en"
<html
Betty,
<p
but like I said, I get bored with it.&nbsp; I do watch TV sometimes while
I am on it, and that seems to make the time go faster, too.&nbsp; I try
for 20-30 minutes a few times a week.
<p
<p
diabetics.&nbsp;
It burns carbs at a faster rate and also has an effect on the desire to
eat.&nbsp; My appetite is pretty minimal and sometimes I eat just because
I know I have not had enough to eat in one day.
<p
<br
<br

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2006-08-22 18:08:07

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2006-08-22 14:05:37

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Understanding by others

2006-08-22 06:54:55

I first thought that if they couldn't see it they would say it didn't
exist.
Now I have discovered that the "popping" can drive them up the wall and
they understand based upon hearing. LOL
If a close relative or friend can't understand let them hold your wrist
or ankle and slowly rotate it so they can feel the joint moving
incorrecty.
I have been very fortunate in my family, friends and workplace in that
they believe. That is over half the battle. IMHO
I have yet to meet someone who will trade off their job for my PA.
It is still depressing to take vacation and have the PA come along. Oh
well.
Pat B

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2006-08-21 18:11:28

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To Kathy

2006-08-21 13:22:30

I'll jump on the bandwagon too, asking for information about the "naturals".
None of your posts ever offended me in the least; I found them quite open
minded and informative.
Patty

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2006-08-21 12:59:28

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This is WONDERFUL!

2006-08-21 01:46:20

Patricia Bias referred me to this list and I am so grateful to her for
doing so! Even though I have not read any postings yet, I am sure I
will get something positive from this. I have been dx with PA for 6
years and have had some very difficult periods with it. It has been a
life altering and humbling affliction for me. I currenly am taking
12.5mg of methotrexate once a week and .5mg of folic acid 5 days a
week. This px works well for me and I have not had to deal with any of
the common side effects that I understand many people deal with. I was
only 26 when I was dx and it has been difficult to get people's
understanding, as most seem to think it is an elders affliction. I only
know of one other person with PA and I have not spoken to her in 2
years. It is wonderful to know there are other people out there who I
can finally talk to about PA. It seems that RA and OA have the market
on publicity and people do not understand when you tell them you have a
different type - it's as if they do not want to hear about it...anyway,
I digress. I look forward to being a part of this list and I hope I can
share some valuable info with you folks!
Janet

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2006-08-21 01:19:37

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2006-08-20 16:26:52

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URL

2006-08-20 05:18:15

try www.americasdoctor.com
it has a doctor on line for you to ask questions etc....
Pat B

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2006-08-20 05:16:04

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2006-08-19 23:47:25

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To Larita

2006-08-19 13:25:30

Well, I must tell you , you have just settled something within me that has been
bothering me for a long time. I take tonnes of meds, too many to list,that most
of them have a potential to affect my kidneys or liver. I dwell on this on a
daily basis, worry about it ALL the time and often put off taking the PRN meds
for fear. Well, what you said in your note about living for today and not
bearing myself down with the " what-ifs" brought it all home. You are so right.
I just never thought about it that way before. I will not die tomorrow or next
week or probably not even next year from the complications, but I will live with
my husband of 12 yrs, my 9 yr old son, my 7 yr old daughter and my family and
friends with as much joy as I can have.
Thank you so much for this thoughtful insight. It has helped me today.
Angela

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2006-08-19 10:59:47

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2006-08-19 03:02:41

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2006-08-18 20:06:04

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2006-08-18 01:04:02

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various replies

2006-08-17 21:18:55

Taking the lead from Pat, here's a bit of feedback on all the
wonderful thoughts on this board....
From: Bcleary2@...
Subject: Re: Sciatica, Hip Pain
It is strange, when someone asks me how are you, I just
automatically say fine thank you.
Whereas on this forum we can say we feel like You know who and
we all understand.
I no longer say, "fine" I try to say something like "I'm ok" or I'm
hanging in there" Usually with a smile however small. I feel more
honest and it opens the door for the few people who REALLY want
to know how I am doing.
My husband is one in a million. We've been married 42yrs and it's
just better every yr.
I'm so glad for you both, Betty. I have been married 18 yrs and it's
wonderful. You make me feel like I can keep looking forward to a
rewarding life together in spite of multi-challenges.

Welcome <a href="/group/PsoriaticArthritis/post?postID=PCp-61gmjcw8UpvZ48BxaiDqD__i5fZZ5xw4i9vijBx3Xm933X-F-D1YPvt9MBHv07KI0bZuJmiHKuZ8RQ">deb_429@...</a>!

2006-08-17 19:27:10

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Teaching Family and Friends

2006-08-17 04:56:46

Does anyone else have a problem getting friends and family to understand when
one minute they seem fine and the next they don't feel able to do anything?
How do you get people to understand without them thinking you're a burden or
just feeling sorry for you and making you wish you hadn't mentioned it?
*****
I haven't had much problem with this. I have approached it as an educational
process. My husband is actually overprotective of me, since I am a "get up
and go, push it to the limit" kind of chick. He'll say "dont' do that you'll
hurt yourself", to which I reply, "would you kindly allow me to judge when
I've had enough?" smilingly, of course.
Anyone who knows me well knows that I'm not a slow moving person. I never
napped until I got PA. So when I started needing a lot more sleep, and being
very frank about it, people seemed to "get it".
In the beginning I put a lot of guilt on myself, thinking I can't be how I
used to be and how is everyone else going to deal with my limitations.
Finally I figured out I can't control how everyone else deals with my ups and
downs. It's not my responsibility, it's theirs. I can educate them about
how this disease works, and fight for the best life I can have. Beyond that,
someone else's reaction is their own.
Patty

Weight

2006-08-17 02:22:54

It seems to me that many people have shared that they are overweight. Is
this pretty true of everyone? If so, is this an area we should explore as
one we all have in common? Also, it seems to me that most of us are
overacheivers, is that true too? Amy
I'm not "overweight" technically, but I am working on losing a few pounds to
optimize my health. And yes, I am definitely an overachiever.
Patty

Tylenol and MTX

2006-08-17 00:57:01

Lee Ann -
A little pain relief works great for me - I take MTX, and also Neoral. My
Rheumy currently has me on Naproxen Sodium (Naprelan). I'd suggest that you
try and get a prescription NSAID for a couple reasons. First, insurance will
pay for it. Second, after a while they can start ulcers and lose efficacy.
The Doc will probably swap meds occasionally to move the point in your
digestive tract where the NSAID disburses, hence reducing the chance of
ulcers, and also keeping the med effective.
I ate Ibuprofen like popcorn for a while - it works but there are better ways.
happy trails - Rob Glover
<<
Hello,
Can I take a pain killer like Tylenol with MTX? I would like to
know if anyone knows exactly what the MTX does. I did not think
to really ask my Dr. because the news of all of this was a bit
overwhelming at the time.
Thanks,
Lee Ann

Various responses / getting others to understand / stress / diet

2006-08-16 13:43:11

Sorry for the length of this email and the number of topics - I got a bit
carried away!
Various responses to messages from the last few days
1. I too have lots of pain around mid cycle, but my RD said that was quite
unusual and most people have worse pain at the time of their period (partly
because they tend to feel bad anyway). I think I'm therefore quite lucky, as at
least I don't have period pain and bad PA at the same time.
2. Where can I get Aquaphor? Or does anyone have an easy to get alternative?
(I'm in the UK, so a lot of the stuff I see mentioned here doesn't seem to be
available.)
3. I'm so relieved to hear someone else say they have a terrible time holding
their arms in the air, eg folding sheets. My PA isn't bad, but I can be in
agony if I have to hold my arms up for more than about 10 seconds. It makes me
feel so stupid when I can't do the simplest things!
Getting others to understand
I feel like a bit of a fraud at the moment. Have just spent a couple of days up
in Yorkshire. Went walking over the moors, played tennis, went swimming. Hurt
a bit but certainly not in agony. Had to drive most of the way home (250+
miles) as my boyfriend didn't feel too good and I was then really hurting. By
the time I got home, my hands and my right leg were quite painful and I just had
to lie down. I guess all the exercise over the weekend just built up on me, but
I find it difficult to make anyone understand that I can do all those things and
then a simple non-strenuous thing like driving can be just too much for me.
Does anyone else have a problem getting friends and family to understand when
one minute they seem fine and the next they don't feel able to do anything? How
do you get people to understand without them thinking you're a burden or just
feeling sorry for you and making you wish you hadn't mentioned it?
Stress
Unlike so many of you with families to care for, I live on my own. I can't
think how I'd cope if I had to worry about looking after children rather than
just myself. At least I can just let the housework go or live on takeaways when
things aren't good. But part of the problem is that, because I don't have to
worry about getting home for other people, I work too hard, which means lots of
stress, and I'm sure that can't help.
Diet
There seems to have been lots of talk about diet etc. Different people seem to
have tried different things, and I guess that what works for one may not work
for another. Does anyone know of any actual research? If not, I guess I just
have to try cutting things out of my diet or adding them back in and see what
happens. But how quickly should I expect a reaction? If I have to try
something for three months, say, at a time this could take forever to identify
what does and doesn't help!

this to will pass

2006-08-16 11:28:34

i keep telling my self this disease will be over. but some times it gets worse.
it hard for me to type because of my carpal tunnel after i go for the two knees
to be done then i am going for my hands and wrist. they are hurt real bad .
bunnylane@...

Tylenol and MTX

2006-08-16 08:49:24

Hello,
Can I take a pain killer like Tylenol with MTX? I would like to
know if anyone knows exactly what the MTX does. I did not think
to really ask my Dr. because the news of all of this was a bit
overwhelming at the time.
Thanks,
Lee Ann

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2006-08-15 22:39:56

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2006-08-15 07:39:09

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what do you use on your face?

2006-08-15 03:17:55

I am wondering what people have found helpful for areas of flaking on the
face and on the eyelids. every commercial preparation I have found says to
avoid the area around the eyes or to avoid the face entirely. The
cortosine perscription cream I have came with an avoid on face warning.
I have been using petrolium jelly to help on my eyelids, but the flakes
still stick to my eyelids and my glasses lenses. Any advise??
Phyllis
........................................................................
mailto:wo286@... http://www.victoria.tc.ca/~wo286/

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2006-08-14 22:27:45

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Thank You

2006-08-14 21:39:31

I just wanted to say thanks to all of you for your thoughts on the Enbrel and
folic acid questions, as well as listening to my awful story about an *ex*
friend. It means a lot to have people to listen and care, and give
feedback.....it's the reason I joined this great list, and I'm happy that
someone finally understands!
Thanks for listening--
Kim

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Welcome <a href="/group/PsoriaticArthritis/post?postID=MlE2YEE8_-TxvRa1MNcTVuw4h6IPoaUsrB4BhSlfJfxj8mOsFuF2X0IoWcjYaRejsvOGd1WCP65hKYr4z1KfPZwu">scenicroute@...</a>!

2006-08-13 16:55:20

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Michelle
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Welcome <a href="/group/PsoriaticArthritis/post?postID=OivzIL_tuuDFxk-OW0_neRWBsLJn6G4yBzQIOhSNKkFl6gokk1H31iSXMrlKR0ImBkj39xMAHrp5Qg">xxmarchxx@...</a>!

2006-08-13 11:44:35

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Michelle
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2006-08-13 05:55:34

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Michelle
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2006-08-13 02:53:00

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Michelle
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2006-08-12 20:37:01

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Michelle
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2006-08-12 05:16:43

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Michelle
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2006-08-12 04:42:37

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What's in DermaNail Nail Conditioner?

2006-08-12 03:02:15

In a message dated 7/19/99 4:46:18 AM Central Daylight Time,
PsoriaticArthritis@onelist.com writes:
do you know what its ingredients are?

To Pat:re urine and blood tests

2006-08-11 12:21:15

For the metho, I get my bloods done once a month, but since starting gold
injections I have a urinalysis and a CBC done once a week, the day before the
injection. The CBC is to check the white blood cells ( leukocytes), red blood
cells ( hemoglobin) and clotting factors ( platlets). Gold can affect the white
blood cells, causing them to be lower, making me more apt to get infections,
illnesses, ect. The platlets can go up or down, which affects the blood clotting
mechanism in the body. The urinalysis is mainly for protein in the urine. Gold
can cause kidney problems( some quite severe) so the protein needs to be
watched. Normal is 0, and I have had 0.3 for the last two weeks, so my dosage of
gold will be decreased this week.
So, to answer your question, no you cannot avoid the blood tests by going to
gold, just the opposite, you will need more. One other thing they look for in
the urine is blood. I was positive once, they did a c&s urine, but all was OK.

Welcome <a href="/group/PsoriaticArthritis/post?postID=S-PnukHN4dfdiWn8NLZaZ5k-ZKKRB5RkXDN___8F1dJL0woWNYdNrDuMcnSMqQ17Jv36I9t2GfE">pjalge@...</a>!

2006-08-11 11:17:03

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2006-08-11 02:34:30

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Michelle
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2006-08-10 22:04:07

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Michelle
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2006-08-10 10:58:16

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Michelle
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2006-08-10 10:10:51

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Michelle
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2006-08-10 08:37:48

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Michelle
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2006-08-09 20:09:02

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Michelle
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2006-08-09 17:40:16

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Thursday Chat on About.com

2006-08-09 14:54:25

Hi LaRita --
Thanks for reminding me about this -- I will forward
the same note to the whole list.
The Thursday PA chat is on About.com at 8 EST. When I
go to the chat logon page the URL is:
http://arthritis.about.com/mpchat.htm?pid=2750&cob=home
copy and paste this into your browser. If this does
not work go to
http://arthritis.about.com/mbody.htm?cob=&pid=
And click on "Chat." Unlike the Wednesday chat (on
drkoop.com) you do not have to register -- just fill
in a logon name and click "connect."
Please let me know if you need anything.
Robert, Wayne NJ
raharris@...

To say hello,

2006-08-09 05:13:54

Hi all,
I just wanted to pop in and give a quick hello. I have been away alot this
summere so far and got a new PC so it had to be re-set up and I just got my
e-mail set up tonight. I had 50 messages waiting for me!! ANyway, I am doing OK.
Better since I stopped working. I still have a fair amount of pain, but I don't
let myself get to the point where I can't move anymore. The gold may or may not
be working ( it's too soon to tell), but we have to decrease the dose a bit as I
have had 0.3 of protein in my urine the last two weeks. I wonder if anyone else
has had this happen...what happened.
Angela

Welcome <a href="/group/PsoriaticArthritis/post?postID=mq6ST83I8ytYlWJhzRMtXUFiC3_1qDr3jkSPGRWxXYsJZRUMIRcW1uhL-JpMEw0jYFQ3ZOOvYTBRlCyt">ljacobs@...</a>!

2006-08-09 01:12:50

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2006-08-08 21:32:32

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