That's right. Only about 50% of SLE lupus patients get kidney involvement. Many will get the joint pain, fatigue, rashes only. Those are my main symptoms but I've also had pleurisy which could be viewed as some type of organ involvement.
none the wiser.........
Hi All,
Just got back, Like i said none the wiser.
But way more tests, blood, urine, chest xray, xrays on hands & feet, & bone & muscle tests (neurolgist i think).
My family DR did not even send any test results that he or the other Dr had done, she only had the letter of referal, so glad i got the test results.
She did say that she could not give a diagnosis on the ANA & ENA test results alone, because all the other tests done were normal.
Real sense of dread again!!!!!!!
So it's just a waiting game again, i could have to wait upto 6 months for the bone Or the muscle tests.
Sandra......
Just got back, Like i said none the wiser.
But way more tests, blood, urine, chest xray, xrays on hands & feet, & bone & muscle tests (neurolgist i think).
My family DR did not even send any test results that he or the other Dr had done, she only had the letter of referal, so glad i got the test results.
She did say that she could not give a diagnosis on the ANA & ENA test results alone, because all the other tests done were normal.
Real sense of dread again!!!!!!!
So it's just a waiting game again, i could have to wait upto 6 months for the bone Or the muscle tests.
Sandra......
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