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706d
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.
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626d
I do the injections. They are very painful.
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704d
Same here! I get my infusions at the hospital too.
@purplewolf how do you feel after getting infusions?
702d
@shannice I’m normally tired for a day after, but then I feel much better: energy boosted and less achy.
Hi I'm shannice, I have lupus and was suggested benlysta! How do you feel after getting infusion? I'm not comfortable with injections.
Hi Carrie my name is Mortisha I have end stage renal failure thx for sharing
@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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