Anyone out there with TNBC taking xeloda,I've never seen any posts about xeldoa( I feel like I'm the only one).

Anyone out there with TNBC taking xeloda,I've never seen any posts about xeldoa( I feel like I'm the only one).

A MyBCTeam Member said:

I am TNBC ( now stage 4 ). My cancer spread to lungs & bones a few months after treatments ended. I took Xeloda for 10 months. Hand & foot syndrome was bad, but what ended Xeloda for me was severe non-stop diarrhea. This drug did shrink the tumors while I was taking it.

posted 8 months ago
A MyBCTeam Member said:

Hi - I'm not TNBC, I am ER+, PR+ HER-. I had to take Xeloda for six months after chemo infusions, mastectomy and radiation. I finished Xeloda this past May. If I can answer any questions for you, please let me know.

posted 9 months ago
A MyBCTeam Member said:

I was slotted to take Xeloda had I not gotten pCR. There are a lot of tnbc ladies taking Xeloda on the tnbc foundation website. The side effects appear to be hand and foot disease.

posted 9 months ago
A MyBCTeam Member said:

I just stared xeloda dry mouth fuzzy head stomach ache

posted 4 months ago
A MyBCTeam Member said:

Would you mind telling your story?I was,diagnosed in April with tn multifocal stage 2a,had 6 month of chemo , In nov.I had a single mastectomy with reconstruction( lymph node neg), re-excision surgery in Dec. to get the rest.They put me on 6 to 8 courses of xeloda I guess as a safety measure.Any thoughts or suggestions?How are you doing now?

posted 8 months ago
Browse more questions and answers
Continue with Facebook
Sign up with your email
Already a Member? Log in