My daughter started taking Tecfidera on Wednesday and she has now lost her sense of taste. She has numbness down one side of her face also. She’s also had flushing but this is common so not overly worried about this. Could the loss of taste be due to the medication or is it a new MS symptom, and how do you tell! She is going to email the MS nurse on Monday. Just wondered if anyone else has suffered the same.
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