Cortisone reaction

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    I have a diagnosis of CIDP for some 4 years now, and currently have 2 grams of intravenous Cortisone infusions every 2 weeks as treatment (IVIG didn’t work).

    I usually have this on the Monday, however on Thursday I seem to suffer some kind of reaction to the treatment, I feel tired and lacking energy, and my hands and feet become even more numb/insensitive; this lasts about 24 hours, then improves.

    It seems like I suffer some kind of reaction to the cortisone some 3 to 4 days after treatment.

    Does anyone else suffer this?

    The doctors cannot explain it.

    Thank you.

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