I was just diagnosed with RA about a week ago. I have been taking celebrex
and Percocets for the pain and swelling at this point and would really like
to get off of both and onto something that will make me as painfree and
stiffness free as possible. (I'm also wondering if RA can be misdiagnosed
and I may have lupus instead). My primary care doctor has not referred me
yet to a rheumatologist and it took pulling teeth to get a diagnoses out of
him. He has sent me for blood tests a CBC, comprehensive Chem Profile and a
urianalsys. Is there anything else that he should be testing for??? Besides
the Ovious ANA test.
Jennifer
Diane - 01 Jun 2006 20:27 GMT
jennifer,
welcome! sorry you have to be here, though.
insist on a referral to a rheumatologist. that's essential for an
accurate diagnosis and treatment.
diane
DeeTee and Bob Taggart - 01 Jun 2006 20:43 GMT
Yes, what she said. Only a rheumatologist can adequately diagnose and treat
you for this.
On the other hand, welcome to our little group (said with tongue firmly in
cheek). Don't miss a day or you'll have a heck of a time catching up with
all the posts.
DeeTee
> jennifer,
> welcome! sorry you have to be here, though.
[quoted text clipped - 3 lines]
>
> diane
Harvey R. Stone - 01 Jun 2006 21:33 GMT
> jennifer,
> welcome! sorry you have to be here, though.
[quoted text clipped - 3 lines]
>
> diane
Its like Diane said,,,, insist on a referral to an RD. You are in the
right newsgroup for talking about medicines,,, doctors,,,, pain and problems
with having inflam.arth. and we are here to help you do well with having
what we have.
Harv
Thumper - 01 Jun 2006 22:15 GMT
>I was just diagnosed with RA about a week ago. I have been taking celebrex
>and Percocets for the pain and swelling at this point and would really like
[quoted text clipped - 5 lines]
>urianalsys. Is there anything else that he should be testing for??? Besides
>the Ovious ANA test.
If he thinks it might be RA he should be giving you a referral to an
RD and the RD will order any tests you may need with regard to
arthritis. Don't be afraid to ask the RD if it could be Lupus. I
don't know how frequently it happens but I know a woman who was
diagnosed as having Lupus for 15 years. She recently went to another
RD and he diagnosed RA, put her on Enbrel and she feels like a new
woman. Many of the drugs used for Lupus and RA are the same so an
early mis-diagnosis of moderate RA shouldn't be harmful. Some of the
newer nsaids and immunosuppressant drugs are used for RA and not Lupus
so far. Severe RA mis-diagnosed can be very harmful.
Thumper
>Jennifer
yodlrscowgrl@gmail.com - 02 Jun 2006 08:34 GMT
Jennifer I had some problems convincing my PCP that there was something
wrong with my wrist. He thought I had sprained it or something. After
two weeks it kept getting worse so he ordered an MRI on it. Turns out I
have a ganglion cyst (which is non cancerous type of cyst) under a bone
on my wrist and it is putting pressure on the bone and nerves.
Before I got the test results back though I went and made me an
appointment with an orthopedic surgeon because I already knew what the
problem was. My doctor was surprised by that but seemed glad to know
that I'm willing to take the initiative.
Even if your doc refuses to give you a referral maybe you can find one
on your own and schedule an appointment. Don't wait around for some
doctor to decide several months down the road after many expensive
tests.
Jennifer Massey-Howe - 02 Jun 2006 15:11 GMT
Thank you all for you encouraging words, I don't know sometimes whether to
be scared to death of all this or roll with the punches. I have 2 small
children as well to care for which I have not been able to do, I am only 30.
My oldest will be 3 in august and my youngest turns 1 sunday. My mom told
me that my aunt's lupus didn't really trigger til after she had my last
cousin. Then she started having flare-ups about a year later. This is what
makes me think that the primary is mis-diagnosing me. Some days are better
then others, as soon as I wake up in the morning before attempting to even
get out of bed I have to take a percocet to relieve the pain and stiffness
from sleeping. I usually wait til after breakfest before I take the
celebrex, Atentolol (blood pressure meds) and water pill. sometimes I wait
to take the water pill til in the evening seems to work better that way. I
go back to my doc on monday. I do know I have arthritis in my L2 of my back
as well that was diagnosed about 2 weeks ago before all of this started
happening. at the end of March I started to have severe pain in my back and
could not left my son. Still have lots of pain there but not as bad as what
I feel in my ankles and the bottom of my feet when I try to walk. (feels
like I have a million tiny little blisters). As things go along I will let
you all know how I'm feeling and what my doctors are saying.
Thank you all for listening
Jennifer
>I was just diagnosed with RA about a week ago. I have been taking celebrex
>and Percocets for the pain and swelling at this point and would really like
[quoted text clipped - 7 lines]
>
> Jennifer
Nann Bell - 04 Jun 2006 03:21 GMT
Hi Jennifer!
I've been rather quiet here lately - far more to do than I have energy for
doing! Besides, I agree with all the advice given to you already.
Your aunt's history of lupus indicates a genetic susceptibility to
auto-immune illnesses, but doesn't necessarily determine WHICH auto-immune
illness any individual family member will come down with. You may have
lupus, you may have RA, you may (God forbid!) have both - or even something
else all together. You definitely want to get to a rheumatologist. They
have the specific training to sort out all this stuff.
(My family has a genetic predisposition to auto-immune stuff on both sides.
All 5 of us in my nuclear family have/had at least one auto-immune illness.
We all share allergies and my mom and sister are both hypo-thyroid.
Otherwise, we all have different things wrong! In fact, my dad and I managed
to get different types of auto-immune arthritis! sigh........ I've been
known to refer to the "genetic cesspool" in my family. It's given me the
chance to learn about a lot of different things though! LOL)

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Nann
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Simply the thing I am shall make me live --- William Shakespeare
Diane - 04 Jun 2006 19:32 GMT
there's definitely a genetic predispostion to auto immune diseases,
although when i was first diagnosed 12 years ago, they didn't think so.
now they do and are doing lot osf research on it. however, the diseases
can all be different. like nann, my family's an autoimmune train wreck.
i have RA and my three sibs have psoriasis, MS, and autoimmune kidney
disease. my mother had PMR and my grandmother had an RA-type illness.
diane
Charrlygrl1 - 05 Jun 2006 21:23 GMT
Jennifer,
Please get yourself to a rheumatologist right away.
Also, if the Celebrex isn't doing anything for you, call you doc and
ask for something else,. We are all different and especially with
arthritis, what works wonderfully for one person may not do diddly for
the next person.
I would not delay on making an appointment with a rheummy. No matter
what kind, erosive arthritis can sometimes do damage very quickly.
Chronic inflammation is also not good-the sooner it can be brought
down, the better off you are.
Good luck to you, and please let us know what happens,
Char