valued Once all the symptoms (like lupus), the rheumatologist prescribed me some pills containing the active era hydroxychloroquine. For years I took the drug but not all my pain was relieved. As happened before, before taking hydroxychloroquine, it is mandatory to pass an eye examination with fundus study, since the drug in question may undesirable effects on vision, it is advisable to review the start of treatment and continue during such periodic inspections and prescription taken. I recently taking hydroxychloroquine, not relieved me of anything besides lupus and again produced some discomfort and nausea, as in previous years. After consulting the rheumatologist withdrew the medication.
As still had stains on the face and burning sensation, the solution was sought to extend the time of injecting the biological. Instead of pricking every 15 days, would be once every 3 weeks, and await the outcome.
After several months of the implementation of the new guideline, the pain increased moderately and some little morning stiffness began to be noticed.
was evident that could not reduce the biological dose Enbrel. I was hoping that by reducing the injection would improve the lupus, unfortunately not, so I went back again to inject my usual dose of an injection of 25 mg every 15 days.
By lengthening the time period of injection and the subsequent increase in pain, it has been shown that even I have spondylitis of the active phase. The rheumatologist explained that with age often comes spondylitis in remission period and comes to rest, that yes, always suffer the consequences that have left the body through joint damage, bone and other reasons.
sitomatología I still have lupus, I have to avoid the sun and any heat source to have photosensitivity (exaggerated response of the skin to sunlight or ultraviolet light). Every time I go out, I must protect arms and face with sunscreen with the highest protection, hat and sunglasses. I hope
lupus remains in this state and no increase in intensity and scope.
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