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Medical Forum / Diseases and Disorders / Lupus / November 2005

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Brenda - 28 Nov 2005 03:45 GMT
Hello my name is Brenda I did post before the day i finaly found out i
have lupus though a skin biopsy,i have been readind many of the posts
daily, right now i need all the info i can get.My family doctor doesn"t
treat much Lupus he did make me a rhumatoligst appointment and he sent
me for blood work witch i have copies of the results of., the only thing
that bothers me almost all the time is the pain in my knees, the skin
rash i had seems to be gone for now, I Have a question about these blood
test results everything seems to be in the normal range, will i need to
go for more? What is my next step?Thanks for help., Brenda
Shelagh - 28 Nov 2005 04:12 GMT
Hi Brenda, and welcome to our group which is very friendly and supportive.
Re 'what you do next': just go and see your rheumatologist on the appt. day
established by your PCP and he will either start you on treatment for your
knee pain or choose to watch you; also you might like to know that blood lab
values do not always reflect our disease activity and so when they are all
reading in the 'normal range' it doesn't mean a whole lot to us or to the
doctors, at least not to the doctors who understand how lupus works
individually; by the way, lupus is a very individual illness and no two
people are alike in symptoms or treatment but almost all of us have shared
problems with each other and gotten a lot of help and feedback from those
who have been through similar 'flares' with their illness.
Ask away, all of us are ready to answer all and any questions you may want
to put to us and most of us as well are well qualified to answer on a
medical knowledge basis for helping you out whether it be for treatments or
just questions to put to your specialist when you see him.
Good luck~ ----> http://clik.to/lupus <---- this site should help with your
questions.
hugs,
Shelagh

> Hello my name is Brenda I did post before the day i finaly found out i
> have lupus though a skin biopsy,i have been readind many of the posts
[quoted text clipped - 5 lines]
> test results everything seems to be in the normal range, will i need to
> go for more? What is my next step?Thanks for help., Brenda
Brenda - 28 Nov 2005 06:29 GMT
thanks for the web site, i saved it, i wasn"t even told what kind i have
yet my appointment isn't for 3 weeks yet will my

Rheumatologist be able to tell me that? other than the skin lessions ,
i have really bad knee pain, but i do work in a factory standing on a
cement floor for 12 hours a day and i always thought thats why i have
knee pain and also i will be 40 in 2 months, that doesn"t help me either
.
Shelagh - 29 Nov 2005 00:04 GMT
Your rheumy should be able to give you the dx of what he 'thinks' you have
re 'discoid' or 'systemic' lupus..... and to me with your joint involvement
with the knee pains, it sounds like you have systemic lupus with discoid
rashes which is common or possibly discoid lupus which has gone into
systemic involvement which is also very common; whichever one you have it is
treatable and very successfully so! so don't worry about it ahead of
time.... even taking extra aspirin can make a difference to the inflammation
created by lupus.... usually it is treated with anti inflammatory drugs like
aspirin and Non steroidal anti inflammatories like motrin, advil, naproxyn
etc... and then the big guns like steroids ie: prednisone, medrol, decadron
and the immunosuppressives like chemo drugs ie: imuran, cytotoxan,
cyclophosphamide and methotrexate are all available should you need them at
any point in your life with lupus.
Good luck with your appointment and feel free to ask any questions to any of
us here!
Signature

hugs, Shelagh
http://clik.to/lupus

> thanks for the web site, i saved it, i wasn"t even told what kind i have
> yet my appointment isn't for 3 weeks yet will my
[quoted text clipped - 4 lines]
> knee pain and also i will be 40 in 2 months, that doesn"t help me either
> .
KCat - 28 Nov 2005 15:40 GMT
you are now a member of this group!  :)

welcome and post whatever questions you have.  Yes, you should get your labs
done regularly.  depending on your severity of symptoms that could be once a
quarter or once  a year.  O generally go every 6 months but i skipped the
last doctor guantlet because of a ton of turmoil in my life and i was
feeling pretty good at the time.

but especially if you go on any particular meds - you need to monitor blood
counts, and kidney and liver function.  Most docs (assuming they are
rheumatologists or at least familiar with lupus and it's ilk) will have a
standard set of tests they give on an annual or semi-annual basis.*

*because this confuses some people semi-annually means every half-year or 2X
a year.  Biannually means every 2 years.

Signature

KCat

For Pen Talk, Images, Trading and Reviews: The Fountain Pen Network
http://www.fountainpennetwork.com

For Lupus Support and Info
http://www.ghg.net/schwerpt/ASLFAQ/

> Hello my name is Brenda I did post before the day i finaly found out i
> have lupus though a skin biopsy,i have been readind many of the posts
[quoted text clipped - 5 lines]
> test results everything seems to be in the normal range, will i need to
> go for more? What is my next step?Thanks for help., Brenda
Andy - 28 Nov 2005 16:30 GMT
[]

>*because this confuses some people semi-annually means every half-year or 2X
>a year.  Biannually means every 2 years.

Maybe in Texas English (Texish? Tenglish?) ... here "biannual" means
"taking place twice every year" (= every half-year) while "biennial"
with an E is "taking place once every two years".
Signature

Andy Taylor [Chair, N E Lupus Group]
See http://www.northeastlupus.org.uk for more!

J - 29 Nov 2005 10:59 GMT
> you are now a member of this group!  :)
>
[quoted text clipped - 8 lines]
> rheumatologists or at least familiar with lupus and it's ilk) will have a
> standard set of tests they give on an annual or semi-annual basis.*

and eyes, if on plaquenil - type meds.
J
Sherry - 28 Nov 2005 16:23 GMT
Brenda,
Welcome to the group!  Jump in anytime you want and ask whatever you want
and need to ask.  Someone here will either know the answer or try to find
it!  Once again Welcome!

Hugs,
sherry
 
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