Hi Staceymommy,
Here is a link that has some good info regarding APS (Hughes). I wish the medical community would stop calling it Hughes Syndrome when this antibody is present in those of us with lupus. I think it creates more confusion when it's being called two different names! I hope you got some relief when that hematoma was drained. That just sounds awful. Let me know if you need any more info about APS. Your rheumy should be very knowledgeable about it. http://www.medicinenet.com/antiphospholipid_syndrome/article.htm
Hi Mom7,
Thank you for your input on the dizzies! Yes, I agree that during my flare ups, my balance is the craps. I'm through my flare now and tapering back down on the prednisone. I haven't had any balance issues for about 2 weeks now. So that really confirmed to me that my lupus is the culprit. Thanks for the support!
Hi Barbara!
Yes, it is much better now. Pretty much gone! I just explained to Mom7 above that it was from my lupus flare. Sometimes though, if I'm on too much prednisone I'll notice a balance issue too. Hard to differentiate sometimes isn't it. How are you doing? I want you to know that you are in my thoughts and prayers too. We gotta stick together through this. Love ya!
Ginny
Oh, I posted to all three of you in one go because the "spam filter" makes me wait about 5 minutes between each post! S L O W!