Cyclophosphamide : Anyone else having... - LUPUS UK

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Cyclophosphamide

Cara_H profile image
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Anyone else having cyclophosphamide infusions?or have had them, how did you feel afterwards.

Cara x

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Cara_H
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Ccupcakes profile image
Ccupcakes

Good Morning Cara. Yes I am having them.

Isme profile image
Isme

I had cyclophosphamide and methylprednisolone infusions for Nephritis, they really kicked my body back into shape and I felt better than I had for a few years. X

Akerfoot profile image
Akerfoot

I did 8 months of cyclophosphamide 4 years ago for nephritis and have been in remission since. I didn't feel great for about 36-48 hours after each infusion but on reflection it was worth it. Good luck and feel well! 😀

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