Recent Posts
Topic: RE: VERY cool topical pain med...has changed my life!
WOW I am going to ask my internist about it. I take plaquenil for lupus, but still get joint pain..
Topic: RE: would like some information
ANA is very broad - and can mean nothing, or some other autoimmune illness.
There are antibodies that are far more specific for lupus. One is the anti-Smith antibody.
Renee is right that clinical symptoms must also be considered - non-erosive arthritis (swollen joints), a "butterfly" rash across the face or a discoid rash (if discoid and not systemic lupus),
oral mucosal ulcers (sores in the mouth), severe fatigue, kidney proteinuria (protein in urine) indicating renal problem, and more..
A diagnosis of lupus can be (and usually is) based on a collection of blood tests and clinical symptoms.
There are antibodies that are far more specific for lupus. One is the anti-Smith antibody.
Renee is right that clinical symptoms must also be considered - non-erosive arthritis (swollen joints), a "butterfly" rash across the face or a discoid rash (if discoid and not systemic lupus),
oral mucosal ulcers (sores in the mouth), severe fatigue, kidney proteinuria (protein in urine) indicating renal problem, and more..
A diagnosis of lupus can be (and usually is) based on a collection of blood tests and clinical symptoms.
Topic: RE: VERY cool topical pain med...has changed my life!
I take plaquenil for lupus - still take it. Although my lupus has greatly improved, if I stop taking that, my joints start swelling (esp hands /knuckles and knees) and I really hurt.
My worst pain now is my back - I have osteoarthritis in my back, and I'm sure the weight has not helped. I look forward to the weight loss relieving some of that.
I could not live on narcotics. That would be beyond my ability to tolerate, I think.
My worst pain now is my back - I have osteoarthritis in my back, and I'm sure the weight has not helped. I look forward to the weight loss relieving some of that.
I could not live on narcotics. That would be beyond my ability to tolerate, I think.
Topic: RE: Lupus and chlorophyll (bathroom issue)
Alfalfa sprouts - weird...
I can't even yet think about salads. But one day down the road...
I can't even yet think about salads. But one day down the road...
Maryann G.
on 8/3/09 6:43 pm - East Bridgewater, MA
on 8/3/09 6:43 pm - East Bridgewater, MA
Topic: RE: testing my ticker
me too. I need to delete mine and do a new one. I cannot remember the passcode.
Topic: RE: Lupus and chlorophyll (bathroom issue)
Sorry I don't have an answer to your inquiry.
I am just surprised about the alfalfa sprouts! I have never been told this, but it does make sense. I tend to overload them on salads...never again!!
Thanks a bunch.
Renee
BTW, almost 2 months later, did the chlorophyll work? I'm a pre-op Dser and would love to know just in case for the future.
Thanks again.
I am just surprised about the alfalfa sprouts! I have never been told this, but it does make sense. I tend to overload them on salads...never again!!
Thanks a bunch.
Renee
BTW, almost 2 months later, did the chlorophyll work? I'm a pre-op Dser and would love to know just in case for the future.
Thanks again.
Topic: RE: would like some information
I am curious about this. My mother died at the age of 57 and I just turned 51. Any and all comments are welcome.
Hugs from Baltimore
LoriHi Lori,
Sorry about your mother. Lupus is a treacherous disease and can be quite difficult for physicians to diagnose. Many of the symptoms can mimic other diseases causing much confusion.
I've had lupus for about 24 years. I was diagnosed as a teen.
To my knowledge, depending on the symptoms, one main test is the ANA (anti-nuclear antibody) test, another is a routine CBC, and another is a syphilis test (some with lupus will have a false-positive result thus giving the indication of lupus). Many rheumies use these tests as gages.
Mine used the ANA to diagnose me, plus my symptoms at the time (flushed cheeks, chronic joint pain, blood clotting disorder, joint swelling, hair loss, chronic pain, mucosal ulcers, severely swollen lymph nodes, and a constant low grade fever) pointed to lupus.
My original diagnosis was juvenile rheumatoid arthritis (JRA), but my various symptoms did not fit JRA to the satisfaction of my doc. He was very proactive in seeking the disorder that best fit all of my ongoing issues.
I'm not verse on the inheritability of lupus, but there is a host of information at www.lupus.org.
HTH,
Renee
On July 21, 2009 at 1:02 PM Pacific Time, abuddingrose wrote:
Since this is a lupus forum I have a few questions about lupus. My mother had lupus for 30 yrs before being diagnosed. What kind of testing do they do these days for lupus? What are the chances of inheriting lupus? The last I knew the only way for a true dianosis is made is when an autopsy is done and every thing else is lupus suspect.I am curious about this. My mother died at the age of 57 and I just turned 51. Any and all comments are welcome.
Hugs from Baltimore
Lori
Sorry about your mother. Lupus is a treacherous disease and can be quite difficult for physicians to diagnose. Many of the symptoms can mimic other diseases causing much confusion.
I've had lupus for about 24 years. I was diagnosed as a teen.
To my knowledge, depending on the symptoms, one main test is the ANA (anti-nuclear antibody) test, another is a routine CBC, and another is a syphilis test (some with lupus will have a false-positive result thus giving the indication of lupus). Many rheumies use these tests as gages.
Mine used the ANA to diagnose me, plus my symptoms at the time (flushed cheeks, chronic joint pain, blood clotting disorder, joint swelling, hair loss, chronic pain, mucosal ulcers, severely swollen lymph nodes, and a constant low grade fever) pointed to lupus.
My original diagnosis was juvenile rheumatoid arthritis (JRA), but my various symptoms did not fit JRA to the satisfaction of my doc. He was very proactive in seeking the disorder that best fit all of my ongoing issues.
I'm not verse on the inheritability of lupus, but there is a host of information at www.lupus.org.
HTH,
Renee
Topic: RE: Chronic Illness wls Support Group
Thank you so much for posting this. I was diagnosed with Wegener's Granulomatosis almost 2 years ago and have gained lots of weight due to the medications. I got the VSG about 3 months ago and am so happy! I'm currently down 46 lbs. and feeling much better! Still very tired, but I am able to do a lot more than I did before the surgery.
Thanks again!!!
Thanks again!!!
Topic: RE: RNY and FOBI and LUPUS
Patti Austin is beautiful! I did not know she had bariatric surgery.