Thanks, ladies!

2006-09-30 13:34:21

Thank you everyone who responded to my question about monthly cycles
and flares. At least I no longer feel like I was imagining the
worsening. I do plan to go back on the Pill next month and hope to
see relief.
In the meantime, whereas my hands were all that have been swollen for
the past several months, both wrists and elbows are now swollen and
sore as well (this has been in the past month). I am now taking 10mg
Prednisone in addition to the Plaquenil. It has been a week since I
started the Prednisone and I definitely know when each dosage is
about to wear off. However, I am still able to work and get stuff
done around the house so I really can't complain...much. LOL
As for weather, oh yeah, I can already tell Northern Virginia in
winter is going to be...interesting...
Take care, y'all! Thanks again and God bless!
-Millie

Arava and nausea

2006-09-30 12:50:48

Hi,
I'm an Australian male of 42 and I've had RA. for about 7 years. I've
tried a few slow acting drugs and I'm now on Arava. (a fairly new
one). It seems to work fairly well but I get very sick and spend lots
of time in the loo. Does anyone have any good remedies for this?
I'd be very greatful for your help. Thanks.
Jason

New Memeber

2006-09-30 04:50:42

Hi evryone my name is Shawna....I'm 16 years old...And I have RA...I
got it when I was 11...And I still don't know how to deal with
it....The pain gets so pain at times I cant sit....I live in the
florida area....So if you are in my area and around my age i'd love
to talk...Also for everyone else...If you have anything to help I'd
really thank it.....Shawna

New here and to RA!

2006-09-29 23:11:45

Hello~
my name is Delena, I am a 45 year old homemaker, married with 2 grown
sons. I found out 3 weeks ago I have RA. I live in a very small town
in the Ozark Mtns., of Arkansas....aside from my family doctor there
isn't a rheumatologist for miles around! I do have my first appt.,
with one Nov. 21st! That is as soon as i could get an appt! We will
drive 3 1/2 hours to Little Rock to see him. At times the pain and
stiffness is so bad, I can hardly move much less go about my daily
routine.......I am on medication to stop the progression, and
Vioxx....I can't really tell much is happening at all. I have had to
be put on perdnisone twice for inflammation...as soon as the
treatment is completed the pain, inflammation comes back....strong
and very bad!
I was wondering if someone could tell me what to expect at my first
visit to the Rheumatologist and what do you do to help relieve the
pain when you are having your *Flare Ups*......All and any thoughts,
prayers, advice etc., will be so appreciated!! Thanks so much and
God bless......
Delena

Hello, just joined

2006-09-29 21:50:59

Hello, I just joined tonight.
My name is delphina, and was just told today that I have Rheumatoid
Arthritis. I had asked to be checked for Lupus in July, was told to
go for a conference after the results came in, chicken out in making
an appointment, and finally today because I couldn't shake a flu,
husband made me go, :o(
I don't know nothing about this. I was referred to a doctor in
Houston but the earlist I can see him is in Feb.2003. I hope you can
help me with questions, what I am looking for, what kind of
medications are out there. Oh, another thing, I also have
osteoporosis, sever on my left hip. I was diagnose 4 years ago. Does
osteroporosis also cause rheumatoid arthritis? Now I wonder if the
doctor thought I had osterporosis when it was the beginning of R/A.
All I can say, is that I know my immune system is low, I am not as
active on some days, when the weather changes you can say I am in
pain-city big time. If the grandkids have a cold, I get the flu from
them.
I hope you can give me some advice. And I hope you all can walk me
thourgh this. It's hard enough explaining to family and friends my
osteroporsis, they think because they see me some days fine I'm okay.
But then they are not around at night when I can't sleep, or find a
comfortable way to sit down without the pain traveling from my hip
down to my leg. Are why, I have to take a pain pill just to ride in
the van.
I'm sorry for feeling sorry for myself, I went thourgh this when I
first told about my osteroporsis, there was so much the doctor made
me give up..walking (could fall down) dancing, my grandkids climbing
on my lap, or even getting bear hugs, driving, shopping. It seens
like I been living with pain for too long. Now this :o(
Sorry for this being so long, and my first post to sound so pitty.
Really, I'm not like this, I am shy. Guess I just needed to get it
off my chest, so I can relax and be me.
delphina

Plaquinel, Prednisone, Methotrexate together

2006-09-29 14:18:33

Hi there, I'm wondering if anyone is on the above three together? I
cannot take anything like Celebrex due to aspirin alergy and gi
issues. I'm going to start on Methotrexate on Oct 20th (after my
sister's wedding) and I am also wondering if there is basically good
response to it.
Also, I live in Wisconsin, is RA affected by the cold weather?
Tamra
Sero-Negative Rheumatoid
33

I am new to all of this......

2006-09-29 10:04:31

Hi, my name is Delena, I was diagnosed with RA just 2 weeks ago. I
just turned 45 and have not been feeling well for over 6 weeks. I
went to my DR. 3 times for different blood-work before he tested for
RA. I live in a small Ozark communtiy in Arkansas and the closest
Rheumatologist (in our insurance plan) is in Little Rock which is 3
1/2 hours away!!! I couldn't get an appt., until Nov. 21st!
What I would love is if some of you could tell me what to expect in
that first visit to the rheumatologist. I am completely in the dark
and am a bit stressed out.I really have learned alot just reading
your posts and info......I am also a wife and mother of two sons.
Somedays the pain is unbearable, others not so bad.....I paint wood
crafts and cross stitch, I haven't been able to do either for a long
time....do you think I will be able to return to the things I love to
do? The joints affected are my wrists, knuckles (across the tops of
my fingers) and my arm/shoulders joints where they met together.
Somedays my knees hurt too but my shoulders and wrists are the worst.
Also, can you tell me about certain conditons that may make it
worselike weather, stress etc.? ANY info will be appreciated so much!
Thanks and God Bless!
Delena

Question for the women...

2006-09-29 00:37:05

First of all, I'll apologize in advance to the men on this board for
taking the discussion in such a personal direction...
I would love to know if any of the females have noticed an increase
in pain, swelling, or stiffness immediately before thier monthly
cycles? Also, I have read in the literature about how some women
report thier symptoms eased when they were pregnant...has anyone
noticed a difference when on the Pill (which simulates pregnancy)?
I am asking because I have noticed the first and am thinking I may
just be wierd. My dr. didn't seem impressed when I mentioned it to
her. Also, I am taking plaquenil and clinoril (been taking them
since the end of July) and WAS on the Pill. Stopped taking the Pill
at the end of August and the month of September has been hellacious,
despite my continuing to take the plaquienil and clinoril. I am
having to take Tylenol for arthritis mid-day nearly every day in
order to be able to continue to work.
I still do not have an official diagnosis (other than 'joint pain')
and do not like the fact that I may now be written off as 'female
problems'. It seemed like the meds were helping in August, next to
no pain until PMS struck. September on, I have been in pain every
day. Any suggestions? I'm already going to seek another dr for a
second opinion.
Thanks!
Millie
(Sorry so long-winded but this has been bugging me for days...)

pain med

2006-09-28 12:26:49

Does anyone have any experience with the pain med Bextra? I am just starting on
it-5 days already- and don't seem to notice a difference?....does it take a few
wees to build up? thanks, sherri

remicade

2006-09-28 10:16:56

I have been trying without luck to lower my prednisone dose (now at 10 mg)
and have had no luck. I'm also on Neoral, Methotrexate and Plaquenil. My
doctor said to increase the metho to 8 tabs/week and then try tapering the
prednisone. If I still have symptoms after that, then it's onto Remicade.
Anyone taking Remicade? I know it's a fairly new drug (5 years only) and
apparently there's a waiting list of 17,000 for Enbrel. I got the info on
Remicade, but just thought I'd put this out there to see if anyone has any
personal experience with it.
gloria

oint replacement.

2006-09-28 06:51:13

Hi everyone,

My name is Diane.

has any one here had a Joint replaced in the elbow?

The reason I'm asking is, My rhumatolajust sent me to a surgeon because the ra has eaten a way at my right elbow, and medicines aren't helping.

So the orthopedic surgeon recommend this surgery.

Can anyone give me any information?

Thanks for being there,

Diane.

Relief?

2006-09-27 22:20:09

Hi all!!!!!! I just started MTX 15 mg./wk on Tuesday the 17th...much to my
disappointment. (I have been trying to get pregnant, but at 35 yo, the doc says
my RA is severe, and needs to be under control first...) Anyway, does anyone
know how quickly the MTX can work? I am also on 20mg prednisone and am trying to
ween down. Also, does anyone have any experience with the pain med Bextra?
Thanks to one and all!!!!! Sherri

My girlfriend was diagnosed with RA at 18

2006-09-27 21:54:38

Hi. I feel a little odd writing on this board since I do not have
rheumatoid arthritis myself. I just started looking around on this
group and the people who post here seem to be very nice.
I knew that my girlfriend had RA when I started dating her, but she
was in a good spell so I had no idea just how bad she had been
suffering. I recently found out when I went to visit her at school.
She's in Law School in DC and I live in Miami so we have a long
distance relationship. When I went to visit her, her pains were
pretty bad. She had tried getting off of her meds, (methotrexate?)
and some injected medication because she says that although her pain
was better she felt sicker. She had been sort of self-medicating
with Ibuprofren and glusamine/chondritin supplements.
Well, the day I left she couldn't get out of bed to walk me to the
door. I had to pack and leave her there because I would have missed
my flight. I felt so guilty leaving her there. Now that I'm here I
just keep trying to research things to help make her feel better. I
worry so much that she has no one to care for her away, her room-
mates nice, but she's not an old friend or anything. I guess I would
really just like to hear from anyone who is either in my position, or
anyone who has had any success treating their arthritis. Her diet
seems to be a key factor, but even when she has good days, she is
NEVER 100%. Has anyone out there beat this thing into remission?? I
want to help her but I feel so useless. I'm currently pre-med and I
am now planning on going into rheumatology and immunology research, I
need to find something to help. I guess I must be rambling, but it
just hurts to watch your girlfriend, only 21 years old now (diagnosed
at 18) suffer and feel so impotent. Is it possible, can it be beaten?
Thank you so much, and good luck to you all in your challenges...
Roger

STRETCH MARKS

2006-09-27 07:58:25

I AM WONDERING IF ANYONE HAS STRETCH MARKS DUE TO WEIGHT GAIN IN THE
BELLY AREA AND THIGHS. MINE LOOKS LIKE A BUNCH OF DARK PURPLE TIGER
STRIPES! DOES ANYONE HAVE ANY IDEAS ON HOW TO GET RID OF THEM? I
THOUGHT ONLY WOMEN WHO GAVE BIRTH GOT BIRTH MARKS.. BOY WAS I WRONG!
LOL... ANY THOUGHTS?
THANKS,
DAVID
YOU CAN EMAIL ME DIRECT IF YOU WANT.
davidskrepps@...

Drug side effects

2006-09-27 04:22:03

I've been reading all your posts about being scared of taking Plaquenil,
Methotrexate and Prednisone. I have been on all three for quite a while and
am happy to say that I suffer NO side effects. I know I am extremely lucky in
this - but it is possible. My blood levels are excellent (according to my
doctor), I have only gained about 7 pounds from the prednisone and have also
not suffered any discernable changes in my health. I'm also on Neoral - a
cyclosporine derivative that also can have major side effects. I just want to
say that you do have to be careful of the side effects, but the choice
between trying the drug and continuing to live in severe pain seems like a
clear one to me. You too may be able to withstand these drugs and gain some
relief. Although I hate the idea of being dependent on drugs, I am grateful
for their help and hope that they can help you too.
gloria

can some one help me please

2006-09-26 21:38:38

Hi Julie,
How can we help?
Trish
Florida
http://www.herbals-unlimited.com
trish@...

Sad

2006-09-26 21:25:11

Hi all!!!!! I am pretty much a silent member, but do read the posts and try to
respond as often as I can. I was diagnosed in Nov. 2001, recovering from a knee
replacement. Was on Kineret-didn't work, and now the rheumy wants to put me on
MTX!!!!!! On top of all this...I have been seeing an infertilty doc-'cause life
just needs to be any more rougher- and just found out today that since I have a
pretty severe case of RA-Iam 35- that I will probably not be able to have a
baby. Doc wants to try MTX for a few months and see if it works.....(You can not
get pregnant on this drug) I was really hoping to have a baby before going on
this drug, but that now seems remotely impossible. I am scared of the
Methyltrexate, but do undertand why I need to go on them.....I am an RN....well,
thanks for listening....I need to go and cry this out!!!!!!

new member here

2006-09-26 17:01:19

I cam across this site looking for surport for RA.
I have Ostieprossis in my disk L4 L5 it is to the point that it
has decentared to just a hair hanging on .
also I have it in my hips and that bothers me rally bad.
I jst found out a few weeks ago that I am in the eary
stages of RA. I am 53 now. I have been told off and on that my blood
test has shone the factor for Ra in earler years but they said do'nt
wory about it is not much really low.I have my tisk for a bout 30
years nows stedlly getting worse.My hands got to the point that they
were hurting so much with my wrist that I went back to the doctor and
he sent me to a rheumatoid doctor that comfirmed it.I have only seen
him one and he gave me some meds and told me to get them refiled thru
my reg doctor. he did not like what he gave me so he stoped them said
they would hurt me more then help me.I wish I could find a doctor
here that would work together.I am taking celabrex and have roxilox
for pain when it gets really bad witch I take at night or else I
could not sleep.I try to walk as much as I can and have excercises to
so .My hubby has heart problems so the diet is really good very low
carbs.I know this site will be a great place to get surport and share
with friends
love to you all,
julie

New to this board & to RA

2006-09-26 09:51:25

Hi everyone! Im new to the RA community (unfortunately) and wanted to
share my story with you all, since you all can relate to what Ive
been going through. Im 27 years old and live in Austin, Texas with
my fiance. We're supposed to be getting married next spring, but the
wedding planning is on hold while I try to stabilize my RA.
Here is a little history on my experience with RA:
Last fall my mom and I opened a business (a doll store!) and ever
since the grand opening, my feet would just kill me! They hurt so bad
that the only time they didnt hurt was when I was laying in bed. From
the moment I got out of bed in the morning, til the moment I went
back to bed at night, they would hurt. Every step I took I was aware
of. If the ground wasnt level, it hurt. Going down stairs was next to
impossible, and I live on the 3rd floor! I just kept telling myself
that the floor must be too hard at work or that I was working too
much on my feet. And I just kept going.
Then I started noticing my hands were getting weak. I was having
trouble gripping things, opening soda bottles, was clumsy, etc. I
also started noticing some small nodes in the palm of my hand, which
appeared to be making my fingers curl in slightly, so I couldnt
straighten them out. They, too, ached so badly! I would cry myself to
sleep most nights because of the pain. Another thing I noticed about
my hands was that when my fiance and I went ring shopping, I was
having to try on rings much larger than my normal size because my
knuckles were so swollen.
I started to see a doctor in January of this year, who diagnosed me
incorrectly (but that caused me A LOT of stress) because I was told I
would be deformed and would need surgery after surgery and that there
was nothing else that could be done.
Well, I decided that I needed to see a hand specialist. While I was
waiting to be seen by him, I was put on a whole slew of medications
from Naproxen and Relafen to Vioxx and Celebrex. Nothing was helping.
I felt like I was losing my mind! I also had xrays done, nerve tests,
etc. while waiting to see the specialist.
When I was finally able to see the hand specialist, he confirmed that
I was misdiagnosed and even told me why I didnt have what I was told.
I was impressed! This guy was wonderful! Then he told me that he
thought I had arthritis. And gave me several names of top
Rheumatologists here in town. He even personally called and made my
appointment with the one he thought was best! Needless to say, this
guy was my lifesaver!!!
I saw the Rheumatologist 2 weeks later, did blood tests and had my
exam and was put on Prednisone while we waited to see how the tests
came back. On 8-8-02 was diagnosed with Sero-Negative Rheumatoid
Arthritis, which they suspect was viral-induced from a Strep Virus I
had last fall (right before all this started). But since it had been
soo long since then, they werent able to determine if it is or not.
I started on Plaquenil and exactly 2 weeks later stopped taking it
because I developed an allergic reaction to it and broke out in a
rash. Ugh! I went to see the Rheumatologist again (to confirm this)
and have now doubled my Prednisone til the rash is gone and then will
start on Methotrexate.
Ive done a lot of reading on it and am a little upset about having to
take it because as I said (way above) Im about to be married and this
will mean I will have to wait to have children at least 2 years. But
I know that its in my best interest to get this under control and
into remission.
The Prednisone is helping (and much better now that Im on the double
dose). My fingers are straightening back out and Im able to walk with
a bounce in my step again and I can even go down stairs normally (but
slowly) instead of one-at-a-time. I still cant make a fist and my
hands still ache and are stiff through out the day, but at least Im
functioning on my own!
Anyway, Im sure you'll see me around here plenty. Any advice any of
you may have is always welcome and appreciated! Thanks for listening!!
Meg

RH. ART/and arthriis article link

2006-09-25 20:54:37

Interesting and worthwhile reading...
http://mercola.com/2002/sep/4/arthritis.htm

Ellen

The CARBS are killing us!

www.golowcarb.com

Prednisone

2006-09-25 19:33:35

Hey all... i am a 29 yr old male. was diagnosed with RA back in
1996. Ive been on prednisone for a while now. i have gained weight
in my belly and face. when i try to taper off the steroids i get
really achy and sick. I try to excercise but the littlest bit of
excercise causes me to get very achy. I am to the point where i dont
know what else to do. any ideas on how to help?

can some one help me please

2006-09-25 11:34:08

I would like to talk to some one about my arthritis
thanks julie

special diets

2006-09-25 05:49:44

Hi Ruth,
This is what I do for my Rheumatoid Arthritis.
Drink a gallon of filtered water a day.
Do not eat refined sugar. Including cake mixes and
biscuit mixes. When they say sugar as an ingred. its
refined sugar. (Sugar builds up in your system and
causes pain and swelling)
I eat Raw sugar only and then just as little as
possible.
Do not eat or use bleached flour. Use unbleached
flour and stay away from white bread and white
biscuits because they use bleached flour.
Do not eat nutrasweet of any kind. This also
builds up in your system and can cause many problems.
No Chocolate or Caffiene.....oh my that causes
pain!
Exercise - on alternating days I walk 2 miles.
(when I can)
Exercise - On alternating days I work with lite
hand weights (when I can)
I also take targeted supplements....let me know if you
want that inf. too.
Trish
http://www.herbals-unlimited.com

plaquenil

2006-09-24 19:44:20

hello everyone...hope you all are doing ok...
i just wanted to ask if anyone has had any success with plaquenil...i
started taking them a week ago and i can't believe how fast they are
working....my rheumy prescribed them to me a long time ago, and i
kept putting off taking them...i was in denial because my bloodwork
was negative.. and didn't think i needed anything like that...last
week i got scared because i could hardly walk because my feet were so
tender when they touched the floor and my knees were so swollen...i
decided i didn't want to end up staying in bed so i broke down and
took the plaquenil about 7 days ago..
i'm walking much better and my knees don't seem as swollen..i feel
better except the chronic fatigue still follows me around all day
long and i'd love to wake up one morning feeling rested.
just wondering if plaquenil has helped any of you and if there are
side effects to look out for...
thanks for listening and i really wish you all strength to bear your
pain..
patty

new member

2006-09-24 15:25:17

i am just dignosed with ra and worried

News!

2006-09-24 14:02:41

I recently found this in our local paperSTUDY LINKS RA,CARBOHYDRATESShining a
light onto the elusive rootsof RA, Harvard researchers have annonced they have
pinpointed a chiefcause of RA.Biological chemist Julia Ying Yang andDr. M.Roehrl
found that carbo'scommon inhuman tisue may act like magnets for certain immune
cells,concentrating them in the joints and causing inflamm. andstiffness.That
thinking is being used to searchfor treatments that could reverse the course of
RA, rather than treatsymptoms.I have shortened this a tad but theimportant stuff
is there.Hopefully yours, Shirley

new member plz help

2006-09-24 11:00:10

i am 36 and recently diagnosed with ra.my doctor told me to take
methrexate .when i read its side effects i became so worried and i
dont want to take it. iwant to know that if i dont take it with
in how much time i will become disable and if i take it i
know i will have some liver or lungs problem i want to know
the people who took it for more than a year .

Last Reminder Live chat TONITE at 7 p.m. Pacific

2006-09-23 23:02:36

Subject : Live chat, pulsed elect magnetic pain relief
http://papimi.com/chat/indexmain.htm
Unlike the old chat room, this one is easy and user friendly, no
horrific filling in forms and registering, just pick a user ID and
you're in. So do join us tonight, Chuck Wallach, an expert in Pap
Imi, and very knowledgeable of all that came before ( Rife, Clark,
etc ) is our guest speaker.
Pap Imi, a device using pulsed electro magnetic energy is now on
study in
the USA. It has had great success in Europe. After the chat address
is more
info on the device.
The PAP-IMI is really surprising many doctors around the country, as
it
helps so many different problems (usually caused by low energy), and
it
works so fast. We have cases of people who have tried everything they
could
find for years, with no relief; then the PAP-IMI took away the pain
in less
than a week. This is especially true if the diagnosis is not clear,
or it is
a condition that conventional medicine has no answers
Pain Reduction with Pulsed Electro-Magnetic Field Therapy
All cells of the body have a natural electric current flowing through
them.
The current is caused by the electrically charged particles in the
cells
called ions. Ions affect the metabolism, or the work of the cells.
Through
the use of the advanced PAP-IMI device we apply an electro-magnetic
field to
the body, influencing the interaction of the ions and improving the
flow of
nutrients into the cells, which may speed the healing process and
reduce
pain.
This new treatment has been in development for over ten years with
more than
300 devices in use worldwide with documented success. Since the PAP-
IMI
device is still in the development stage, studies are being organized
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Anyone who wants to know more is invited to participate.
Go to papimi.com, on the first page of the site is a link to the chat
or go directly to chat at : http://papimi.com/chat/indexmain.htm
More info from the pap Imi site :
The PAP-IMI is really surprising many doctors around the country, as
it
helps so many different problems (usually caused by low energy), and
it
works so fast. We have cases of people who have tried everything they
could
find for years, with no relief; then the PAP-IMI took away the pain
in less
than a week. This is especially true if the diagnosis is not clear,
or it is
a condition that conventional medicine has no answers
Pain Reduction with Pulsed Electro-Magnetic Field Therapy
All cells of the body have a natural electric current flowing through
them.
The current is caused by the electrically charged particles in the
cells
called ions. Ions affect the metabolism, or the work of the cells.
Through
the use of the advanced PAP-IMI device we apply an electro-magnetic
field to
the body, influencing the interaction of the ions and improving the
flow of
nutrients into the cells, which may speed the healing process and
reduce
pain.
This new treatment has been in development for over ten years with
more than
300 devices in use worldwide with documented success. Since the PAP-
IMI
device is still in the development stage, studies are being organized
to
determine its safety and effectiveness with its intended use.

special diets

2006-09-23 18:22:43

Gloria,
Yes I use a special diet and supplements.....have been
for years and it is working great! Sometimes I faulter
and I know it!
I dont eat refined or bleached sugar or flour.
Very little processed foods.
No Sodas, no artifical sweetners,
I drink plenty of water and excercise when i have the
time. And I take targeted supplements.
I have had no signs of my RA for years now :
Trish
hello_its_trish@...

nodules???

2006-09-23 08:58:29

Hi All,
Just Joined and was happy to see such
an active helpful group. I have lots
of nodules with more forming every day.
Just wondering if anyone else has these,
if so, have you found any way to reduce
the size or number of them? My Rheu.MD
does not know of any way.
I am on Metho.(inj). Bextra, which I
have found to be a wonderful help,
tetracycline, and vitamins. Doing quite
well.
Thanks for any input
Shirley

special diets

2006-09-23 01:40:09

I was wondering if anyone is trying anything special with their diet to try
and control their RA. I have been off wheat, sugar (including fruit) and
dairy (all the good things in life) for a few months now. Things have
improved, but it may just be all the meds and supplements kicking in. I did
try an experiment yesterday - I ate chicken burger with a whole wheat bun,
and some blueberries. Maybe a bite of a cookie. Later that night I noticed a
definite stiffening in my right hand and this morning I felt worse than I
have in a few days.
anyway, thought I would pass that on. I'd be interested to hear if anyone
else is doing anything diet wise to try and control the symptoms.
gloria

Firsit time visit

2006-09-22 21:24:05

Me again. I am going to my first Rheumatologist visit Wednesday 14th. Can anyone suggest anything that I might need to ask of this doctor? I will be bringing my films from my CAT Scan, copies of my blood work showing my Rheumatoid Factor count and my Sed Rate.

Please email me at "my" email address because time is running short and I don't seem to get these messages for a few days.

Thanks,

Judy

Tailbone

2006-09-22 19:10:58

Is anyone having trouble getting these messages? I don't get messages
for 3 or 4 days and than I get several.
I want to thank all you that responded to my message concerning my
tailbone problem. While I hate to hear you all are having problems too,
it's good to know I'm not alone.
To Donna, yes, I had xrays taken Thursday and I'm just waiting on the
results.
To Joy, that's me exactly. If I sit any length of time, I can hardly
move.
To Barbara, my doctor prescribed Ultram in a very low dose. My problem
is that there is very little I can take. I can't take aspirin,
Ibuprophen, etc, because I have Barrett's Esophagus and I can't take
Tylenol because it shoots my liver count through the roof and I wouldn't
be able to go on cholesterol medicine if I'd need to and I'm this close (
) to having to go on it.
Judy

discourgaed :( :(

2006-09-22 14:05:33

Hi All
I read al the posts and I am Grateful to u all who post.. my problem
is in short Does ur blood work have to be abnormal for a Rhumatory dr
to want to keep seeing u
RA/OA by a neurolgist? I had a MRI takin and it showed RA Nodules (
joint effusions) on my wrists and fingers plus deteration in my neck
C6-C7
I have already went to a new rhumy and he dropped me for same
reason
seeing me due to law suit from a car accident i was in
I am so tired of DRs BS and at witts end
sujestions?? please...God Bless Donna

RE:Tailbone

2006-09-22 10:07:59

Hi
I am a silent member I read all the posts
my tailbone
damage also in lower spine which adds to this
ray to see if theres any damage
alone
ice on and off
Message: 1
Date: Mon, 5 Aug 2002 09:19:47 -0400
From: J-J-W@...
Subject: Tailbone
I am having a terrible time with my tailbone - don't laugh :-)
Has anyone had a problem to where they can hardly sit down, or get
back
up from sitting?

Tailbone

2006-09-21 23:53:39

I am having a terrible time with my tailbone - don't laugh :-)
Has anyone had a problem to where they can hardly sit down, or get back
up from sitting? I am even having a bad time trying to sleep because it
hurts so bad. It's right at the end of my tailbone, but I don't have any
outward signs of a problem, but boy it sure does hurt.
Judy - in Florida

naproxen

2006-09-21 14:08:31

Would 1000mg OTC Napoxen be the same as 2 500mg prescription
naproxen? I am pretty sure it is but just wanted to double check.
Rhonda

Newbie with a few questions.......

2006-09-21 12:50:43

Hello, I just joined this group and am curious about a few things.
I've been on metho (along with folic acid, prednisone, & for pain, I
take oxy and vicadin) for three months and have just started
experiencing the side effects. Extreme tiredness and upset stomach.
Does anyone else have these side effects, and if you do, how do you
cope? I take metho once a week and the side effects of taking it on
Monday (3 days ago) are still with me. I feel very weak, even right
now and am so tired. I've also been experiencing heart burn, or acid
reflux and I don't know what I can take, if anything. Does anyone
have any suggestions? Does it sound like it's not 'agreeing with me'
to the point of getting off of metho? I read a few posts and saw
that some of you are on several different pills that I didn't
recognize. Are these pills that are taken in place of metho? I was
reading my book and it said that metho is a cancer drug. In what
sense?? Is it like a very low dose of chemo?? One more question...
I read some posts about antibiotics. What are they being taken for?
Please forgive my 20 questions, this is all so new to me & there is
so much to learn.
Also, I read some posts about Minocycline. My daughter was just
perscribed this for her face. What are the benefits of taking this
for RA?
Thanks for listening & hope you all are doing well.
God Bless,
Sandy

Please help...

2006-09-21 05:18:53

Yesterday I went to the doctor. My mother has rheumatoid arthritis
and her hands and feet are disfigured. She is 72. I am 40. I have
had mild symptoms (achiness in my joints) off and on for a couple
years but NOTHING like this! It hurts so bad! And it's my whole
body and it's all the time. This really hit me this hard about three
or four weeks ago. I had been trying for the past month OTC meds
like Ibuprophen, Naproxen, and Tylenol. Nothing touches this pain.
I am really starting to worry that it is something else. Yesterday
I went to my family doctor finally because I could not locate a
rheumatologist close to here. My family doctor said it could be any
number of things (coelic disease, osteoporosis, leukemia, cancer of
the bone, fibromyalgia, or a viral infection of the bone). However,
she said it sounds like rheumatoid arthritis to her and gave me
Celebrex to try until the results come back form my bloodwork. She
said to take one (200mg) a day but I could take two a day if I am
having a bad day. She said I should see results shortly after I take
the first one. I took one at her office yesterday at 11AM.
Throughout the day I noticed no difference and I was still in a LOT
of pain so at 8PM I took a second one but still noticed no
difference. I took another when I got up this morning but my body is
still throbbing. This is so painful I do not know if I can stand
it! My entire body throbs 24 hours a day. This constant non-
relenting pain is really starting to tax me out. I cannot imagine
living another 50 years like this!
A little more info on me (could be related or not): As I've said, my
mom has RA. I am 40. I had three daughters at the ages of 17, 18,
and 23. I have enjoyed good health over the years and always felt
young and spry. In 1999 I gave birth to my first son. The pregnancy
went well but ended in a cesarean section. Three months later I had
emergency gall bladder removal. Three months ago, in April of this
year, I gave birth to my second son. He also was delivered by
cesarean section. In the past three years I have felt increasingly
exhausted and generally not well. I attributed this to the birth of
my sons at a late age but now I am not so sure. Also, I have been
overweight since puberty. I am right now 5'7" and weight 225
pounds.
Any help (especially what to do for this pain) would be MUCH
appreciated!
~*~Rhonda~*~

[rheumatoid_arthritis] daren

2006-09-21 04:28:59

Hey Daren,

I lost your email address and my email has been down at work for 8 weeks. I just got it fixed last week. Please email me again if you are still on this list.

Thanks,

Stephanie

Hi gang, boy have I been busy

2006-09-20 16:27:32

Hello To All,
I think the last time I talked to ya'll" CAN YOU TELL I'M FROM THE
SOUTH" I was helping my mom recover from a mild stroke, she is doing
great thank you. Next came the flood,I live in the New Braunfels TX
area, and I tell you what between helping my mom and some of my
friends clean up, and all this wet weather I'm now in a BIG flare up.
I 've got to tell you about July 4, that is the day the flooding
started, I live on Canyon Lake and every year the north side has a
fireworks batel with the south side,well with all the distress going
on we don't think anyone would be in the mood to celebrate.BOY was I
wrong, I think it was one of the best I've ever seen, It was like
everybody wanted to forget the ugly of the light of day, and enjoy
the child like love of the beauty we get from watching the rockets
red glar. It was great.
I guess it's like liveing with our RA, sometimes between the pain we
can still see who we used to be, and have hope that one day we can go
back to that life.
To all you new folks rember to ask questions of your DR, and if
you don't understand something MAKE them explane it again, also if
you don't like your DR, find another, this is a joint "no pun "
adventuer and there must be good relationship with you and your
doctors at no time should you feel in the dark, and as for as blood
work goes, you tell them what you want, you pay for it not them. It
is your life, your body, and your future.
Well gang it took me 2hrs to type this and my hands are killing me,
but remmber what I always say, hot baths, and sleep are the free
things you can do for yourself.
Keep your chins up
Pamela G

Stress Fractures/Ankle Joint Replacement

2006-09-20 15:34:41

I've had RA for 20 years... dealing with stress fractures and in need
of ankle joint replacements. Has anyone had any experience with
either?

Newbie here...intro

2006-09-20 10:06:12

Hi,
I was (tentatively) diagnosed with RA yesterday. I say tentatively
because all my bloodwork keeps coming back negative, but my
Rhuematologist looked at the ever-increasing swelling in my hands and
said she doesn't know what else it could be. I think I'm still in
denial. I have spent the past 3.5 months going to drs, only to have
every test come back negative. Yesterday's diagnosis wasn't a
surprise as my dr and I had discussed the possibility but were hoping
that something else would come back positive (like a viral
infection). Didn't happen.
This all started when I went to my PCP 3.5 months ago for hand pain.
Initially I was thinking I had CTS as I work on computers all day.
Any way, now I've been on Relafen for 2 months and even had the
dosage increased once but my hands keep on swelling and the pain
keeps increasing. I guess I'm lucky that that's all I have to deal
with at this point.
My dr is sending me for a whole body bone scan before we start
treatment, which presumeably will start with a short-term run of
prednosone. Can anyone tell me what a bone scan is? All I know is
its suppose to identify areas of inflamation.
Thanks in advance for any information you can offer!
-Millie

Rare Disease Support T-Shirts NOW AVAILABLE

2006-09-19 23:15:54

International Rare Disease Support Network (IRDSN)
T-Shirts Now Available
The International Rare Disease Support Network has, in an effort to
promote our community, developed a T-Shirt to be worn by our members.
To view the images on the shirts, click on the following links. You

Rare Disease Support T-shirts NOW AVAILABLE

2006-09-19 12:25:32

International Rare Disease Support Network (IRDSN)

T-Shirts Now Available

The International Rare Disease Support Network has, in an effort to promote our community, developed a T-Shirt to be worn by our members.

Just Joining ... question about Methotrexate

2006-09-19 09:54:33

My dr. put me on Methotrexate and I understand this is a great help
to RA patients. Is Methotrexate a drug that I will stay on or just
when I have flares? (I'm on prednisone also right now and other
drugs due to Fibro and a few minor things)
Thoughts?

plaquenel

2006-09-19 00:29:47

Hi, my rheumy diagnoised me with ra last year...He put me on
plaquenel as he said i'm in the early stages and he hoped the meds
would slow it down..
i had serious side affects fro the medicine...hair started coming out
in clumps, dizzy spells, stomach upset, eye problems, skin rash.
He gave me a three month supply and said come back in 3 months to see
how i was doing..
well, after 2 months i stopped taking the medicine because it's side
effects. now i'm afraid to go back because he's going to want to put
me on prednisone probably.. i don't want to take that drug either.
It's been 6 months since i've seen the rheumy and my ra is
progressing rapidly...
My knees have two large painful lumps (swelling that don't go away)
over them on the left sides of the knees.. (what exactly is the
swelling...is it fluid?? i didn't have this when i saw the
rheumatoligist and my fingers are doing the swanneck thing and some
of them look like sausages...my feet hurt so bad, i can hardly walk
at times..My elbows hurt just carrying a light bag of grocerys and my
wrists are hurting as i type. When i sit in a chair for more than
10min, it's very painfull and slow getting up.
my question is: what else can i take besides the 2 meds i mentioned
because i'm going to see the rheumatolist soon and i can talk to him
about it.
i have extreme fatigue and weakness now and it's causing a lot of
depression...i can't take anti-depression meds because i take maxalt
for migraine and the two can be a deadly mix. I can't give up the
maxalt as i would have to go to emergency for relief. I really
wanted to try the anti-depressants but this stopped me.
thank you for listening.
patti

My new aol IM name

2006-09-18 20:56:52

When my pc crashed, I lost all my necessary info. So I resigned w/AOL IM. My
screen name is Naes2429. Anyone who wants to add me as a buddy is fine & I'd
like to get my buddies back if possible. So send me your IM 1-1 if you have
one. Sometimes I'm not interested in really surfing the web, just enjoy
staying in touch.

my name is Jenn

2006-09-18 18:36:53

I was told amost 3 yrs. ago about my RA and in scared me. I not
scared anymore but I need to talk to poeple or a person who knows
what this feels like everyday. I am only 23 and noone esle I have
meet has had this so young. I guess I am wondering f there are other
people out there like me......

Trans fatty acids

2006-09-18 10:38:35

Just got this off one of my sources - They also neglected to put in this, however, that they are a large part of margarine! USE BUTTER, NEVER MARGARINE!

And the number of things with partially hydrogenated vegetable oil in them are extensive - really frightening.

"TRANS-FATS"
7/11/02

The FDA is moving to get a new item - trans-fatty acids - listed on nutrition labels as soon as next spring. That after a report from the national academy of sciences confirmed that just like saturated fats, trans-fats can increase cholesterol levels, and set the stage for heart disease. Trans-fats are found in processed foods like cookies and crackers. You'll see them listed on ingredients labels as "partially hydrogenated vegetable oil."

Live Chat, Pap Imi , Pain Reduction w/ Pulsed Electro-Magnetic Field Therapy

2006-09-18 07:00:46

Come to our live chat, to learn more about the pap imi, where any
questions can be answered. scroll below the chatroom instructions
url, for more info on the pap imi.
Thursday, 11th of July at 7 PM at our MSN chat site
go to: http://chat.msn.com/join.msnw
and after the 2 minute download (if connected at 56K ) of MSN chat
in the search bar , please type : pap imi chatroom
or
copy and paste the url below into your address bar:
http://chat.msn.com/chatroom.msnw?
rm1=Pap+Imi+chatroom&cat=HE&lang=1&des1=&welcome1=&prFilter=1&loc=EN-
US&newroom=1&rm=Pap%2520Imi%2520chatroom&des=Electro-magnetic%
2520therapies&welcome=Hello%2520%2526%2520Welcome%2520to%2520the%
2520pap%2520imi%2520chatroom
Pain Reduction with Pulsed Electro-Magnetic Field Therapy
All cells of the body have a natural electric current flowing through
them. The current is caused by the electrically charged particles in
the cells called ions. Ions affect the metabolism, or the work of the
cells. Through the use of the advanced PAP-IMI device we apply an
electro-magnetic field to the body, influencing the interaction of
the ions and improving the flow of nutrients into the cells, which
may speed the healing process and reduce pain.
This new treatment has been in development for over ten years with
more than 300 devices in use worldwide with documented success. Since
the PAP-IMI device is still in the development stage, studies are
being organized to determine its safety and effectiveness with its
intended use.
Only qualified and authorized individuals may participate in the
investigative studies of the PAP-IMI device's effects when used to
treat pain. No one should use the PAP-IMI device without first
consulting with a doctor and only use the PAP-IMI device under the
supervision of qualified personnel
Beyond The Rife machine, The Crane Device,
The Lakhovsky Device, The Priore Device,
The Dotto Ring, The Rapsomanikis Device
& other treatments
The PAP-IMI is really surprising many doctors around the country, as
it helps so many different problems (usually caused by low energy),
and it works so fast. We have cases of people who have tried
everything they could find for years, with no relief; then the PAP-
IMI took away the pain in less than a week. This is especially true
if the diagnosis is not clear, or it is a condition that conventional
medicine has no answers. Our advice to those with aches and pains of
mysterious origins, "If you don't know what you've got, the PAP-IMI
is your best shot!"
The Pap-Imi machine < Pap Ion Magnetic Inductor
powerful & focused.
It is used in Europe to as an aid to healing and for pain reduction.
Currently avail. in the U.S.A. having been approved for a study.
This study has been approved by the IRB (Institution Review Board),
Bio-Med of San Diego. The machine operators undergo full training in
the use of the machine. The current study results will be gathered
and tabulated by an outside authority, and then submitted to the FDA
for final approval
The PAP-IMI Device belongs to the same category as the devices of
Tesla, D'Arsonval, Rife, Becker and others
The modern scientific term for these devices is Pulsed
Electromagnetic Devices
The PAP-IMI was found to surpass corresponding devices by a factor of
one hundred to one thousand times faster and more efficient
The superiority of the PAP-IMI is due to its unique pulses that are
faster and stronger, with far higher instantaneous power (10,000 to
100,000 faster and more powerful).
The PAP-IMI pulses are of smaller duration.
These results to less heat energy to be distributed out, avoiding
thermoplexy and thermal damages, while the phenomenon of biological
synthesis takes place
The Pap-imi machine is becoming available in many states and has been
in use in europe for many years.
( There are several here in S. CA & we can inform you where else The
Pap-Imi Machines are located )
To learn more about the pap imi, join our chat - Thursday, 11th of
July at 7 PMat our MSN chat site
go to: http://chat.msn.com/join.msnw
and after the 2 minute download (if connected at 56K ) of MSN chat
in the search bar , please type : pap imi chatroom
or
copy and paste the url below into tour address bar:
http://chat.msn.com/chatroom.msnw?
rm1=Pap+Imi+chatroom&cat=HE&lang=1&des1=&welcome1=&prFilter=1&loc=EN-
US&newroom=1&rm=Pap%2520Imi%2520chatroom&des=Electro-magnetic%
2520therapies&welcome=Hello%2520%2526%2520Welcome%2520to%2520the%
2520pap%2520imi%2520chatroom

In Denial

2006-09-17 21:23:57

Hi. I just joined this support group. I am a 42 year old female
who hasn't actually been diagnosed with RA. I have been going to a
Rheumatologist since 1997. My illness began with pericarditis. I
thought I was having a heart attack. After having an echo, they
told me I had fluid around my heart and that it is usually a once in
a lifetime occurence. However, I had it repeatedly and was
hospitalized twice. After seing a cardiologist and going through a
series of tests, they turned me over to a Rheumatologist. The
Rheumatoligist would only tell me that I had a connective tissue
disease. For years I have wondered what exactly I have. My
Rheumatologist has recently been stating that I have "apparent" RA.
She never really comes right out and says it is RA. I could not
accept this. I know people with RA and I am nothing like them. I
do suffer with stiff knees and I have pain around my spine at
times. However, my most severe pain is in my chest. It actually
hurts to breath! I have been taking prednisone since I was first
diagnosed in 1997. It has been a miracle drug for me. I know it
has some really bad side effects. But, when I have a flare up, I
can take the predinisone and after a few hours, I am good as new!
No Pain!
I know RA has different symptoms. I just would like to know if
there is anyone out there who has had similar symptoms. Is this
really RA? Please help!

hi diagnoised with RA today

2006-09-17 12:27:02

Hi
I have been diagnoised with RA today before it wa thought I had
psorisic arthritis. Anyhoooooo my finger joints are really bad at
the moment, but if I can help it I would like to stay away from
prescribed drugs for the time being, I have been taking naproxen etc
but they didn't work so i would like to give alternative therapys a
try and just wondered if anyone has tried anything or have some help
and advice for me :O)
Thankyou
Ruth

Rheumatoid

2006-09-17 08:24:00

I'm 53 y o and have had RA for 36 years. I've had 4 hip replacements
and 3 knee replacements, Surgeries on both hands and wrists (tendon
transfers). I'm married and have 2 grown girls. I continue to work
full time although it is getting to be a real struggle. I've asked my
doctor why after working full time for 37 years, I haven't seen one
other person struggling in the workplace like I am. He tells me they
are out there but you would think I would recognize someone with the
familiar sway or maybe a cane which I often must use. I'm looking for
someone who I can relate to, someone who has had RA for many years
with multiple joint replacements. Someone who might be dealing with
some of the same issues as myself. Please, if anyone would like to
share ideas or information, please contact me.
Thank you so

PLEDGE BANNED! (Forward To Friends!)

2006-09-17 06:49:49

U R G E N T U P D A T E
PLEDGE OF ALLEGIANCE BANNED FROM SCHOOLS
BY U.S. FEDERAL COURT!
CLICK BELOW TO TAKE A STAND IN SUPPORT OF
THE PLEDGE:
http://www.pledge-of-allegiance.org/pledge.asp?PID=2452321&P=1
7/1/02
Dear friend,
We are RUSHING you this update because the Ninth Circuit
Court of Appeals just ruled the Pledge Of Allegiance
unconstitutional in our public schools!
The judges ruled that the phrase "under God" is a violation
of the U.S. Constitution because it creates an "establishment"
of religion.
THIS IS OUTRAGEOUS!!! WE MUST TAKE ACTION!
Grassfire.net has just launched a nationwide petition to rally
hundreds of thousands of Americans as quickly as possible who
will stand up and say, "I Support The Pledge In Our Schools".
* * * * * ACTION ITEM
CLICK BELOW TO TAKE A STAND IN SUPPORT OF THE
PLEDGE IN OUR SCHOOLS:
http://www.pledge-of-allegiance.org/pledge.asp?PID=2452321&P=1
Grassfire.net wants to deliver 1,000,000 petitions as soon as
possible directly to the Ninth Circuit Court of Appeals, as
well as the U. S. Supreme Court, leaders in Congress and
President Bush.
WE NEED YOUR HELP!!!
PLEASE SIGN THE PETITION IN SUPPORT OF THE PLEDGE.
THEN, ALERT YOUR FRIENDS.
THANK YOU FOR YOUR HELP!!!
Grassfire.net
P.S. If you haven't yet read what these judges said in their
ruling, be sure to click the link below. YOU WILL BE SHOCKED
to read how they have made a mockery of the Pledge! We must
respond quickly. Please sign. Then, rally your friends.
P.P.S. We are also rallying 1 MILLION people to pause at
High Noon this July 4th and recite the Pledge with family
and friends. Click below for details.
+ + + + + + + + + + + + + + + + + + + + + + + + +
CLICK BELOW TO TAKE A STAND AND SAY
"I SUPPORT THE PLEDGE IN OUR SCHOOLS!"
http://www.pledge-of-allegiance.org/pledge.asp?PID=2452321&P=1
This petition is sponsored by:
Grassfire.net

Pain meds

2006-09-16 21:27:23

Hi Everyone:
I was diagnosed a few months ago and am on the usual meds: Prednisone (5 mg),
Methotrexate, Plaquenil and Neoral (cyclosporine). I take Darvocet everyday,
but I still have terrific pain. I've tried Vicodin and Ultram, both of which
don't really help the pain, but do put me to sleep. Has anyone tried anything
else they can recommend?
Thanks
gloria

New member..need guidance..update

2006-09-16 16:57:13

hello

Thanks for the two people who replied and others who read my first post. I would like to give

an update to the group. My brother has been diagnosed to have "psoriatic arthritis". I just now

saw a post titled "there are 130 forms of PA"..have not read it completely. He has been prescribed

sulfasalazine by his rheumatologist. I would like to know, whether, anybody has any experience with

this drug. The doc has not prescribed Methotrexate yet. Is the drug sulfasalazine better than methotrexate ?

Would appreciate replies.

Warm regards and thanks for the wishes that members conveyed. Surely helps.

Sanjay

welshwarrior73030 <welshwarrior73030@...

Hi...I'm new here but have so much to reply to!!!

2006-09-16 16:34:09

Oh my gosh! Where to start???!!! I have just been reading some
previous posts and I don't know why I visit here sooner!!
I have had RA for the past 11 years...I noticed symptoms right before
I gave birth to twins (who will turn 11 yrs. old next month). The
most curious thing I have noticed from all the previous posts is that
MOST OF US HAVE MORE THAN ONE ILLNESS. I believe that my arthritis
started out as LYMES DISEASE...but I also had a mild case of psorisis
too and from reading past messages someone else was told that their
RA stemmed from this....so maybe that had something to do with it
(???).
I didn't know anything about LYMES DISEASE until 4 years into my
symptoms and not being diagnosed. I was talking to my brother (who I
used to live with in Oklahoma) and he was telling me about his bout
with Lymes disease and all of his symptoms were identical to mine.
They were arthritis like symptoms but also included fatigue and
itching...also if the surface of the skin was scratched (even
slightly) it would make a red welt appear. In fact, when my brother
went to the doctor, the way the doctor tested to see if my brother
had Lymes disease was by scratching my brother's arm with his
fingernail...in a few minutes the scratch welted up and became red.
My brother was treated right away with the antibiotic Doxicycline and
the illness went away and he was fine. But I went 4 years without
being treated...I would simply take ibuprofen to ease my symptoms.
After learning this info from my brother I was able to convince a
doctor to prescribe me Doxicycline and my symptoms were non-existent,
but unfortunately he only gave me a weeks supply and according to my
brother he was required to take it for 30 days straight. I wasn't
able to get any other doctor to give me anymore. I think this
mutated my Lymes disease and caused me to develop RA...but I could be
wrong. A person can have Lymes disease for years and not know it
becuz it can be dormant, but when your body becomes fatigued or your
immune system is over worked (like during a pregnancy) then the
disease becomes active and your symptoms show up.
DOES THIS SOUND FAMILIAR TO ANYONE? I live in AZ and Lymes disease
isn't common here due to the arrid climate but if you live back East
or where there is alot of vegetation then you could have contracted
this disease and not even know it. My brother is unaware how he
contracted it, but he did. Someone posted a question about itchiness
and burning...maybe this is related?
Gosh...I have so much to reply to...um...I was told by my
rheumatologist that it would not be good for me to have another
pregnancy...and that was years ago. I haven't become pregnant but
becuz I have wanted more children I didn't end up going on the
Methotrexate. The side affects were too risky and the waiver I was
required to sign stated that even if I take the drug theres no
guarantee that it will actually help me. So I decided it wouldn't be
worth the chance of not being able to have children...someone else
previously posted that they had a hysterectomy due to damage done by
Methotrexate.
Although I have much more to say about this illness and how it has
drastically hindered my life and those around me I would like to end
this post with a few questions:
HOW DOES EVERYONE HERE COPE FINANCIALLY? HAS THIS DISEASE KEPT
ANYONE FROM WORKING? HAS ANYONE HERE QUALIFIED FOR DISABILITY BASED
ON RA? DOES ANYONE HERE HAVE RA ONLY AND NO OTHER ILLNESS? AND
LASTLY WHAT DO YOU ALL THINK ABOUT THE NOTION THAT A VEGETARIAN DIET
WILL SIGNIFICANTLY IMPROVE OUR PAIN AND SYMPTOMS?
I'm so glad to be here!! I understand and experience constant
pain...REAL PAIN that just won't stop or go away. Even with taking a
buncha painkillers it's still there!!! It's enuff to make a person
suicidal sometimes...I can relate to the post about feeling like a
burden to everyone around you. When my pain is unbearable it takes
so much mental concentration to deal with it that everything else is
a distraction...and that's not good when you have kids. I wish I
could be the healthy, active mother my twins deserve. Someone said
that sometimes all they're able to do is sleep....I heard that!! I
used to be an athlete and now I can't even manage to hold a job.
Sometimes I have to hop on one foot to the bathroom cuz my other foot
is so stiff. I can't dress myself...I can't brush my hair..simple
things that I used to take for granted. Life with RA is so hard and
I'm so glad I found people who know what I'm talking about.

Fibromyalgia pain isn't all in patients' heads, new brain study finds

2006-09-16 07:49:42

Dear Friends,
I know that this article is about Fibro (I suffer from that
too), but I thought the subject matter is applicable to RA/OA as well.
~~Julie
Fibromyalgia pain isn't all in patients' heads, new brain study finds
(Posted June 7, 2002)
A new brain-scan study confirms scientifically what fibromyalgia
patients have been telling a skeptical medical community for years:
They're really in pain. In fact, the study finds, people with
fibromyalgia say they feel severe pain, and have measurable pain
signals
in their brains, from a gentle finger squeeze that barely feels
unpleasant to people without the disease. The squeeze's force must be
doubled to cause healthy people to feel the same level of pain - and
their pain signals show up in different brain areas.
Lead authors Richard Gracely, Ph.D., and Dr. Daniel Clauw did the
study
at Georgetown University Medical Center and the National Institutes of
Health, but are now continuing the work at the University of Michigan
Health System (UMHS). The results, published in the current issue of
Arthritis & Rheumatism, the journal of the American College of
Rheumatology, may offer the proof of fibromyalgia's physical roots
that
many doubtful physicians have sought. It may also open doors for
further
research on the still-unknown causes of the disease, which affects
more
than 2 percent of Americans, mainly women.
To correlate subjective pain sensation with objective views of brain
signals, the researchers used a super-fast form of MRI brain imaging,
called functional MRI or fMRI, on 16 fibromyalgia patients and 16
people
without the disease. As a result, they say, the study offers the first
objective method for corroborating what fibromyalgia patients report
they feel, and what's going on in their brains at the precise moment
they feel it. And, it gives researchers a road map of the areas of the
brain that are most - and least - active when patients feel pain.
"The fMRI technology gave us a unique opportunity to look at the
neurobiology underlying tenderness, which is a hallmark of
fibromyalgia," says Clauw. "These results, combined with other work
done
by our group and others, have convinced us that some pathologic
process
is making these patients more sensitive. For some reason, still
unknown,
there's a neurobiological amplification of their pain signals."
In the study, fibromyalgia patients and healthy control subjects had
their brains scanned for more than 10 minutes while a small,
piston-controlled device applied precisely calibrated, rapidly pulsing
pressure to the base of their left thumbnail. The pressures were
varied
over time, using painful and non-painful levels that had been set for
each patient prior to the scan. The study's design gave two
opportunities to compare patients and controls: the pressure levels at
which the pain rating given by patients and control subjects was the
same, and the rating that the two different types of participants gave
when the same level of pressure was applied. The researchers found
that
it only took a mild pressure to produce self-reported feelings of pain
in the fibromyalgia patients, while the control subjects tolerated the
same pressure with little pain.
"In the patients, that same mild pressure also produced measurable
brain
responses in areas that process the sensation of pain," says
Clauw. "But
the same kind of brain responses weren't seen in control subjects
until
the pressure on their thumb was more than doubled." In all, the
fibromyalgia patients' brains had both some areas that were activated
in
them but not in controls, and some areas that stayed "quiet" in them
but
became active in the brains of controls feeling the same level of
pain.
This response suggests that patients have enhanced response to pain in
some brain regions, and a diminished response in others, Clauw says.

Women suffer more pain than men but are treated less

2006-09-16 04:18:36

Women suffer more pain than men but are treated less
BY SUSAN FERRARO
New York Daily News
NEW YORK Women are not wusses. They are designed to carry and
deliver babies; the latter stage of the process is often thought to
generate the worst kind of pain. And, in most cases, they are hardy
enough to survive the ordeal and nurture their infants to adulthood.
And yet nature makes it doubly hard for women when it comes to pain:
They not only endure a lot of it, they actually feel pain more
acutely than men do.
It's not "all in their heads," as doctors have been known to tell
women who don't get better on schedule. Women notice and complain
about pain sooner than their male counterparts.
They even react to treatments differently, benefiting more than men
from morphine-like opiates but responding less to common painkillers
like ibuprofen.
And when they do receive treatment, they're often given short-shrift.
Doctors and nurses have long tended to undertreat pain, perhaps
because some of the drugs used are addictive. But in a study of
cancer patients, women got less medication than men, says Dr. Norman
Marcus, who has a private practice at the Norman Marcus Pain
Institute in New York City.
Despite all this, women in pain cope admirably, other research shows.
That makes them heroes, not hypochondriacs or hysterics, says Dr.
Mark Allen Young, author of "Women and Pain: Why It Hurts and What
You Can Do" (Hyperion, $24.95).
Consider Maria Ramos, 48, a wife, mother and baby-sitter in the
Bronx, N.Y. For years, she complained of head, back and neck pain
that eventually spread to a knee. Her doctor blamed sinus problems
and migraines. "But I don't have that, none of the sinus," Ramos
says. "So I keep complaining. I feel bad, because I have all this
pain, and he doesn't do something." Eventually, she got a referral.
Pain specialist Dr. Paru Pandya focused on a herniated disk Ramos
had. The first medication didn't help, but a second approach
numbing muscle injections did. "The pain goes away in the arms, the
knee and the neck," sighs Ramos.
"Sometimes the doctors don't refer people in time," says Pandya. "We
see a lot of women with fibromyalgia, which is muscle aches all over.
It's horrible. The sad part is that they are not believed, not given
medication, and by the time they get to us it has affected
everything."
That's because one pain can lead to another, as a person favoring a
knee, for example, throws a hip out. Or, says Pandya, "They start to
be depressed. Then they have two problems, which might have been
prevented."
Often dismissed as a mere symptom, pain is in fact a $100 billion-a-
year public-health problem, counting treatments, doctor visits and
lost productivity. "In my opinion, chronic pain is a women's health
issue," says Roger Fillingim, a clinical psychologist and leading
women's pain researcher at the University of Florida's College of
Dentistry.
Yet pain itself remains mysterious. It is necessary to life, an early
warning when the body needs help: for burns, broken arms, sore
throats, tumors. But it's also exhausting.
"Persistent pain is garbage in the brain," Marcus says. "It inhibits
healing."
Our tough-it-out American ethic complicates the problem. "Society
assumes that the more pain you can take, the healthier you are,"
Fillingim says. But in some disorders, like bulimia, patients have
less pain perception. Sexual stereotyping also plays a role.
"Men are supposed to be tough, stoic and not expressive, to suck it
up and deal, but it is more socially acceptable for women to be more
expressive," says Dr. Allen Lebovits at the New York University Pain
Management Center.
That means their complaints may not be taken as seriously as men's.
And women have lots of pain: more headaches, arthritis and autoimmune
disease; more knee problems, even as young women, and more intestinal
trouble. They get fibromyalgia more than men and suffer more of
certain injuries. There are also female-only pains: cramps, breast
tenderness and PMS.
Then there's the estrogen factor. Experts blame hormones for a lot of
pain complaints: For example, migraines seem to strike when estrogen
is high. Making matters worse, the normal fluctuation in women's
hormones has hindered research on the subject.
"I wouldn't say... evil male scientists have maliciously ignored
women over the years," Fillingim says. "It is just easier to study
men because (researchers) don't want to mess with hormone changes."
Women may also be more vulnerable because they seem more susceptible
to stress, which undermines the immune system and natural,
painkilling brain chemicals.
Fortunately, nature has ways for women to cope. Sexual stimulation
raises women's pain threshold, but not men's, which means pain women
experience can be helped by sexual activity. " ' I have a headache'
is not a good excuse for (women) not having sex," Fillingim says.
"The bottom line is that women are built differently," says Young,
who uses alternative and conventional therapies. "Doctors need to
realize that women have different pain thermostats, that women are
not small men."

Sorry guys...this is just for the ladies!!

2006-09-15 14:55:05

Here you go gals!! ~~love, Julie
http://www.nhjewelry.com/beautiful_women.htm

websites for prescription assistance

2006-09-15 14:54:34

Dear Friends,
Here are some websites for prescription assistance.
Hope it might help someone! ~Julie~
MED SITES
===================
http://www.freemeds.com (drug companies /
patient assistant programs)
http://members.tripod.com/Catnip100/FreeMeds.html (drug companies /
patient assistant programs)
http://www.themedicineprogram.com/ (drug companies / patient
assistant programs)
www.needymeds.com (drug companies / patient assistant programs)

Pregnancy and RA

2006-09-15 06:41:00

I have had RA for about a year and I am 35, I am taking Azulfadine
right now and Prednisone 10mg. daily and I am doing fine but I want to
have another child but I am afraid, It might have something wrong with
it or when I quit the prednisone I will hurt so much I will want to
die, also I won't be able to take any pain meds when I have bad flare
ups,,, so can anybody tell me if they have had a baby and what they
took and if they know of anyone who has had it, or anything,,, let me know
sincerely,
wendy

Women suffer more pain than men but are treated less

2006-09-14 18:27:22

Thought you might find this article interesting. Feel good today!
~~Julie
Women suffer more pain than men but are treated less
BY SUSAN FERRARO
New York Daily News
NEW YORK Women are not wusses. They are designed to carry and
deliver babies; the latter stage of the process is often thought to
generate the worst kind of pain. And, in most cases, they are hardy
enough to survive the ordeal and nurture their infants to adulthood.
And yet nature makes it doubly hard for women when it comes to pain:
They not only endure a lot of it, they actually feel pain more
acutely than men do.
It's not "all in their heads," as doctors have been known to tell
women who don't get better on schedule. Women notice and complain
about pain sooner than their male counterparts.
They even react to treatments differently, benefiting more than men
from morphine-like opiates but responding less to common painkillers
like ibuprofen.
And when they do receive treatment, they're often given short-shrift.
Doctors and nurses have long tended to undertreat pain, perhaps
because some of the drugs used are addictive. But in a study of
cancer patients, women got less medication than men, says Dr. Norman
Marcus, who has a private practice at the Norman Marcus Pain
Institute in New York City.
Despite all this, women in pain cope admirably, other research shows.
That makes them heroes, not hypochondriacs or hysterics, says Dr.
Mark Allen Young, author of "Women and Pain: Why It Hurts and What
You Can Do" (Hyperion, $24.95).
Consider Maria Ramos, 48, a wife, mother and baby-sitter in the
Bronx, N.Y. For years, she complained of head, back and neck pain
that eventually spread to a knee. Her doctor blamed sinus problems
and migraines. "But I don't have that, none of the sinus," Ramos
says. "So I keep complaining. I feel bad, because I have all this
pain, and he doesn't do something." Eventually, she got a referral.
Pain specialist Dr. Paru Pandya focused on a herniated disk Ramos
had. The first medication didn't help, but a second approach
numbing muscle injections did. "The pain goes away in the arms, the
knee and the neck," sighs Ramos.
"Sometimes the doctors don't refer people in time," says Pandya. "We
see a lot of women with fibromyalgia, which is muscle aches all over.
It's horrible. The sad part is that they are not believed, not given
medication, and by the time they get to us it has affected
everything."
That's because one pain can lead to another, as a person favoring a
knee, for example, throws a hip out. Or, says Pandya, "They start to
be depressed. Then they have two problems, which might have been
prevented."
Often dismissed as a mere symptom, pain is in fact a $100 billion-a-
year public-health problem, counting treatments, doctor visits and
lost productivity. "In my opinion, chronic pain is a women's health
issue," says Roger Fillingim, a clinical psychologist and leading
women's pain researcher at the University of Florida's College of
Dentistry.
Yet pain itself remains mysterious. It is necessary to life, an early
warning when the body needs help: for burns, broken arms, sore
throats, tumors. But it's also exhausting.
"Persistent pain is garbage in the brain," Marcus says. "It inhibits
healing."
Our tough-it-out American ethic complicates the problem. "Society
assumes that the more pain you can take, the healthier you are,"
Fillingim says. But in some disorders, like bulimia, patients have
less pain perception. Sexual stereotyping also plays a role.
"Men are supposed to be tough, stoic and not expressive, to suck it
up and deal, but it is more socially acceptable for women to be more
expressive," says Dr. Allen Lebovits at the New York University Pain
Management Center.
That means their complaints may not be taken as seriously as men's.
And women have lots of pain: more headaches, arthritis and autoimmune
disease; more knee problems, even as young women, and more intestinal
trouble. They get fibromyalgia more than men and suffer more of
certain injuries. There are also female-only pains: cramps, breast
tenderness and PMS.
Then there's the estrogen factor. Experts blame hormones for a lot of
pain complaints: For example, migraines seem to strike when estrogen
is high. Making matters worse, the normal fluctuation in women's
hormones has hindered research on the subject.
"I wouldn't say... evil male scientists have maliciously ignored
women over the years," Fillingim says. "It is just easier to study
men because (researchers) don't want to mess with hormone changes."
Women may also be more vulnerable because they seem more susceptible
to stress, which undermines the immune system and natural,
painkilling brain chemicals.
Fortunately, nature has ways for women to cope. Sexual stimulation
raises women's pain threshold, but not men's, which means pain women
experience can be helped by sexual activity. " ' I have a headache'
is not a good excuse for (women) not having sex," Fillingim says.
"The bottom line is that women are built differently," says Young,
who uses alternative and conventional therapies. "Doctors need to
realize that women have different pain thermostats, that women are
not small men."

Special Thanks

2006-09-14 16:27:27

Hi I been reading the posts and I am Grateful to hear that there are
others as clueless as I am. Only being dignoised not to long ago with
RA I have not yet got me a Rhumatoligist Dr. I had a Neurolgist and
then saw A Special Rhumatoligist, but then I got in a Car accident
and damaged my jaw and more discs in my spine. So I am in a law suit
and fed up with all the drs they have me running to. BUT After my
burst of anger at my physical therpist and then the lawyer the other
day I am aloud to go see a Rhumatoligist. MY question to anyone who
can answer is this...After being stressed do you get the feeling of
bad fatigue and flu like feeling? and does the humidity affect you?
and over excerting one self also does that make u have that flu like
feeling/hung over feeling? If anyone could give me some insight i
would be more then tickled, as IT is no fun feelin like crap,..
KNowing I am not alone helps me alot..and I know I will be ok..I am a
fighter and I have a great outlook...been sick alot as a kid growing
up and been dealing with this for years!!!!!!!!( just couldn,t get
anyone to diganoise me) and drs..... SO Have a Great day all stay in
a Happy Place and don,t over do it . God Bless Donna

Fibromyalgia pain isn't all in patients' heads, new brain study finds

2006-09-14 13:44:42

Dear Friends,
Although this group is for arthritis, I think there are members
here, who, like me, also suffer from FM. This is a wonderfully
validating article.
~~Julie~~
Fibromyalgia pain isn't all in patients' heads, new brain study finds
(Posted June 7, 2002)
A new brain-scan study confirms scientifically what fibromyalgia
patients have been telling a skeptical medical community for years:
They're really in pain. In fact, the study finds, people with
fibromyalgia say they feel severe pain, and have measurable pain
signals
in their brains, from a gentle finger squeeze that barely feels
unpleasant to people without the disease. The squeeze's force must be
doubled to cause healthy people to feel the same level of pain - and
their pain signals show up in different brain areas.
Lead authors Richard Gracely, Ph.D., and Dr. Daniel Clauw did the
study
at Georgetown University Medical Center and the National Institutes of
Health, but are now continuing the work at the University of Michigan
Health System (UMHS). The results, published in the current issue of
Arthritis & Rheumatism, the journal of the American College of
Rheumatology, may offer the proof of fibromyalgia's physical roots
that
many doubtful physicians have sought. It may also open doors for
further
research on the still-unknown causes of the disease, which affects
more
than 2 percent of Americans, mainly women.
To correlate subjective pain sensation with objective views of brain
signals, the researchers used a super-fast form of MRI brain imaging,
called functional MRI or fMRI, on 16 fibromyalgia patients and 16
people
without the disease. As a result, they say, the study offers the first
objective method for corroborating what fibromyalgia patients report
they feel, and what's going on in their brains at the precise moment
they feel it. And, it gives researchers a road map of the areas of the
brain that are most - and least - active when patients feel pain.
"The fMRI technology gave us a unique opportunity to look at the
neurobiology underlying tenderness, which is a hallmark of
fibromyalgia," says Clauw. "These results, combined with other work
done
by our group and others, have convinced us that some pathologic
process
is making these patients more sensitive. For some reason, still
unknown,
there's a neurobiological amplification of their pain signals."
In the study, fibromyalgia patients and healthy control subjects had
their brains scanned for more than 10 minutes while a small,
piston-controlled device applied precisely calibrated, rapidly pulsing
pressure to the base of their left thumbnail. The pressures were
varied
over time, using painful and non-painful levels that had been set for
each patient prior to the scan. The study's design gave two
opportunities to compare patients and controls: the pressure levels at
which the pain rating given by patients and control subjects was the
same, and the rating that the two different types of participants gave
when the same level of pressure was applied. The researchers found
that
it only took a mild pressure to produce self-reported feelings of pain
in the fibromyalgia patients, while the control subjects tolerated the
same pressure with little pain.
"In the patients, that same mild pressure also produced measurable
brain
responses in areas that process the sensation of pain," says
Clauw. "But
the same kind of brain responses weren't seen in control subjects
until
the pressure on their thumb was more than doubled." In all, the
fibromyalgia patients' brains had both some areas that were activated
in
them but not in controls, and some areas that stayed "quiet" in them
but
became active in the brains of controls feeling the same level of
pain.
This response suggests that patients have enhanced response to pain in
some brain regions, and a diminished response in others, Clauw says.

Neoral

2006-09-14 04:47:48

I was wondering if anyone is taking Neoral. My rheumatologist has me on
methotrexate, plaquenil and has just added Neoral which is a form of
cyclosporine. He said this is the trio they prescribe before moving onto
Remicade or Enbril (sp?) injections. The idea is that small amounts of
different powerful drugs instead of large amounts of one drug, act in concert
to put the disease into remission. Has anyone had any experience with this?
Any luck with this?
I really hate adding more drugs into the mix. My personal philosophy has
always been to handle things naturally. My hope is that after going into
remission, I can switch over to natural supplements and control the disease
through diet. Anyone read the New Arthritis Relief Diet by James Scala?
I have confidence that my RA will go into remission. I suffered from severe
ulcerative colitis which now has been in complete remission for 4 years. I
think combining the best of Western medicine with natural healing and diet,
not to mention a good attitude, has helped me in the past and I hope will
help me with this disease, too.
I know there are a lot of people in a lot of pain and it is good to be able
to use a board like this to express oneself. I would love to hear from those
of you who have had success with their disease and hear your experiences of
how you were able to beat or control your RA. I think we could all use some
positive and hopeful stories.
gloria

Blessed

2006-09-14 00:08:09

I'm not sure anyone here really knows just how wonderful the members of this list really are. Here as well asmy personal e-mail account I read some heart warming letters of faith to advice which I am in the middle of looking into. I have an appointment with my new primary this coming Wed. Maybe fresh blood (no pun intended) would help. All I know is lastnight I was about one degree away from having my daughter call 911 for me. In a 3 hours time frame I consumed 4 percocet, 2 oxycontin, a flexeril and a soma to just get past the pain. It was brutal, I actually broke 3 fingernails from clinching a fist that tight. I apoligize if I took up to much time here, I didn't mean to. Writing and knowing someone cares really makes it easier to get by so for that alone thank you everyone and God bless each and everyone of you.
Fondly
Anne

New member..need guidance

2006-09-13 17:58:21

Greetings and best wishes to all !

My younger brother (29 yrs, married), has been diagnosed with sero -ve RA.
The rheumatologist whome he consulted, said, the possible cause
is psorasis. Though, psorasis was limited only to a small part on
his scalp, and was treated and cured, within weeks, this
condition (sero -ve RA) has been attributed to it.

He has following symptoms
1. Morning stiffness
2. Pain and stiffness of finger joints, ankle joints and back

Would like to request members of this wonderful group, to revert
with whether, there are any more tests that, can confirm this
condition, and also, what typically, is the treatment given
There are a lot of questions brimming in my head
1. Is it completely curable ?
2. How long does it take to cure ?
3. Would he be able to lead a normal life (he is a compute software
professional)
4. If the couple decide to have children, would this be passed
on through the genes ?
5. Can it relapse ?

Can I kindly request the group to respond ASAP..

really worried

Sanjay

Friendship Poem

2006-09-13 09:27:35

Are you tired of all those mushy Friendship Poems that always
sound good but never actually come close to reality? Well, here is a
Friendship Poem that really speaks to true friendship and truth
itself!
My Friend,
When you are sad, ..... I will get you drunk and help you plot
revenge against the sorry bastard who made you sad.
When you are blue, ..... I'll try to dislodge whatever is choking
you.
When you smile, ..... I'll know you finally got laid.
When you are scared....I will rag you about it every chance I get.
When you are worried, ..... I will tell you horrible stories about
how much worse it could be and to quit whining.
When you are confused, ...... I will use little words to explain it
to your dumb ass.
When you are sick, ..... stay away from me until you're well again.
I don't want whatever you have.
When you fall, ..... I will point and laugh at your clumsy ass.
This is my oath, ..... I pledge 'til the end. Why you may ask?
Because you're my friend!
Send this poem to ten of your closest friends and get depressed
because you realize you only have 2 friends, and one of them is not
speaking to you right now anyway.
A FRIEND will listen to you bitch.
A GOOD FRIEND willhelp you hide the bodies.

THINGS TO NEVER SAY TO A COP...

2006-09-13 09:06:00

THINGS TO NEVER SAY TO A COP...
1. I can't reach my license unless you hold my beer.
(OK in Texas)
2. Sorry, Officer, I didn't realize my radar detector wasn't plugged
in.
3.Aren't you the guy from the Village People?
4. Hey, you must've been doin' about 125 mph to keep up with me. Good
job!
5. Are You Andy or Barney?
6. I thought you had to be in relatively good physical condition to
be a police officer.
7. You're not gonna check the trunk, are you?
8. I pay your salary!
9. Gee, Officer! That's terrific. The last officer only gave me a
warning, too!
10. Do you know why you pulled me over? Okay, just so one of us does.
11. I was trying to keep up with traffic. Yes, I know there are no
other cars around. That's how far ahead of me they are.
12. When the Officer says "Gee Son....Your eyes look red, have you
been drinking?" You probably shouldn't respond with,"Gee Officer your
eyes look glazed, have you been eating doughnuts?"

You are an internet addict when...

2006-09-12 17:54:46

You are an internet addict when...
1. You refer to going to the bathroom as downloading.
2. You step out of your room and realize that your parents have moved
and you don't have a clue as to when it happened.
3. Your bookmark takes 15 minutes to go from top to bottom.
4. Your nightmares are in HTML and GIFS.
5. You turn off your modem and get this awful empty feeling, like you
just pulled the plug on a loved one.
6. You start introducing yourself as "Jim at net dot com"
7. Your heart races faster and beats irregularly each time you see a
new WWW site address on TV.
8. You turn on your intercom when leaving the room so you can hear if
new e-mail arrives.
9. Your wife drapes a blond wig over your monitor to remind you of
what she looks like.
10. All of your friends have an @ in their names.
11. When looking at a web page full of someone else's links, you
notice all of them are already highlighted in purple.
12. Your dog has its own home page.
13. You can't call your mother... She doesn't have a modem.
14. You check your mail. It says "no new messages." So you check it
again.
15. Your phone bill is as heavy as a brick.
16. You write your homework in HTML and give your instructor the URL.
17. You don't know the sex of three of your closest friends, because
they have neutral nicknames and you never bothered to ask.
18. Your husband tells you that he has had the beard for 2 months.
19. You wake up at 3 a.m. to go to the bathroom and stop and check
your e-mail on the way back to bed.
20. You tell the kids they can't use the computer because "Daddy's
got work to do" -- even though you don't have a job.
21. You buy a Captain Kirk chair with a built-in keyboard and mouse.
22. Your wife makes a new rule: "The computer cannot come to bed."
23. You get a tattoo that says "This body best viewed with Netscape
3.0 or higher."
24. You never have to deal with busy signals when calling your ISP...
because you never log off.
25. The last girl you picked up was only a GIF.
26. You ask a plumber how much it would cost to replace the chair in
front of your computer with a toilet.
27. Your wife says communication is important in a marriage... so you
buy another computer and install a second phone line so the two of
you can chat.
28. As your car crashes through the guardrail on a mountain road,
your first instinct is to search for the "back" button.

WE ARE ON THE MOVE FINALLY.!!!!!!

2006-09-12 17:43:00

Announcing

DEB & DANNY ARE ON THE MOVE.

Just a quick note to let everyone know that as of the 22nd June I am moving to Queensland.

I will not be on this e-mail address as of the 19th June but I will be e-mailing everyone as soon

as I have a new server up there. I hope to hear from you all as soon as I am back on line and

contacted you so save all your good dirty & clean jokes and messages.

The e-mail address I will be leaving is dcampbell@... and those of you that are in

QLD could you please advise me of a good server to go with up there around Kallangur

just north of Brisbane by about 30 klm's.