Sorry everyone. I am feeling so frustrated right now. When I think everything is good here comes a reminder that I still have Lupus. On the outside I look (normal) that's what people love to say to me. How do you respond to that. Sometimes I get annoyed then I try to understand that they don;t understand because I am still learning about
this disease. I am often amazed at the responds when they see all of my medicines. They want to know what they are for and why so many? I try to explain based on the information and research
I have done. I feel over whelmed One think goes away only to be replaced with another sympton. I started out hurting all over. I took my medicines and begin to feel better at least I thought so. Then I started to feel nauseated and tired so I sleep most of the day and ate very little. Can any one relate. Some times I think my body tolerates the Cell Cept better than other days. I am not an expert by no means. I have only been taking it for about 6 monthes at this high dosage. can any one relate to my crazy experiences?
Diagnosis Lupus Sle 2006, Fibro 2006, Nephirits 2007, anemia 2005, Hypertension 2006.
Plaquenil 400 mg, Prednisone 15 mg, Cell Cept 3000 mg, Diovan 320, Procardia 120 Mg, Fosonopril 80 mg, Iron supplement, Calcuim W/ Vitamin D, Folic Acid, Tramadol