Guest guest Posted June 26, 2004 Report Share Posted June 26, 2004 , I am sorry to hear of your struggle. Bless your heart. I also know it is so sad to lose someone you care about and I am sorry for the loss of your Lupies friend. Ok - on to the shakes, I also get shakes and tremors in my hands. WHen a flare up is bad, I can hardly write, or type, or function. Yes it can be embarassing I know. I have had a siezure in the Brain scan did not show anything but swelling. It is known as lupus cerebritits. It caused me a great deal of problems. It caused me complete memory loss and I was driving on a trip. Lost all memory for 4 days. I also have to visit the ER often. It seems my flare ups do not " slow down " unless I have a big, bolus dose of Solumedrol. You mentioned pain....Oh my friend. I do not know what else to do either. Pain meds are bad for our liver and kidneys which mine do NOT need any help getting worse. But there has to be some other things. I do have spinal epidural shots routinely to help with pain and they do help. Have you ever looked into that? I am thinking of you. Let me know how you are doing. You are needed here...don't think of closing those eyes and getting your wings yet! hugs - Quote Link to comment Share on other sites More sharing options...
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