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Charrellpayton

722d

Hi I'm Carrie! Although I do take Benlysta for Systematic Lupus, I do not do the Injections. I do infusion treatments at the hospital. Infusion was not an option for me to choose when I filled in the medication portion of my profile. If someone were to ask me about my experience with Injections I wouldn't have an answer.

Top reply
    • Wolflady22

      642d

      I do the injections. They are very painful.

    • Wolflady22

      642d

      I do the injections. They are very painful.

    • purplewolf

      720d

      Same here! I get my infusions at the hospital too.

      • shannice

        720d

        @purplewolf how do you feel after getting infusions?

        • purplewolf

          718d

          @shannice I’m normally tired for a day after, but then I feel much better: energy boosted and less achy.

    • shannice

      722d

      Hi I'm shannice, I have lupus and was suggested benlysta! How do you feel after getting infusion? I'm not comfortable with injections.

    • GOLDENGODDESS81

      722d

      Hi Carrie my name is Mortisha I have end stage renal failure thx for sharing

      • Charrellpayton

        722d

        @GOLDENGODDESS81 Hello Mortisha! 👋🏾 Is nice talking with you!

☝ This content is generated by our users and it is not a substitute for professional medical advice. Please consult with your physician before making any medical decision

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