I was started on 60 mg Cymbalta a year ago after having a full bi-lateral mastectomy and TRAM reconstruction (cutting stomach muscles to reform breasts). I was having nerve pain from the feeling returning to the severed muscles and my oncologist put me on Cymbalta. It definitely worked to control the pain, but around the same time I began chemotherapy so I had no idea what was causing what feelings or sensations. I have been done with chemo for 6 months now.
The brain flashes continued periodically and when I spoke to my oncologist about it she wanted to do an MRI "just to make sure." Well, I have been weaning off of Cymbalta for 6 weeks now and the flashes were increasing, but I never put the two together until today. I finished my last 20 mg dose 2 days ago and the electrical flashes are almost constant, I'm having a hard time focusing, I cry easily and my stomach has been very nauseated with increased acid reflux. It was not until I started talking it out with another cancer survivor here in the office who said she had not heard of anyone having that as a side effect from chemo before when I realized it could be the Cymbalta. My first Google popped up this site and I feel sane again!!
I thought the weight gain was from chemo, but it has not decreased. I’m excited to see what it will be like when the drug is completely out of my system so I can feel a little more “back to normal.” A feeling I have desired for a year now!
Is there an average time most people seem to feel these symptoms once completely off of Cymbalta? Has anyone else tried the counteracting drugs?
Thanks again for all your posts!!

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