looking for WBR survivors

[nvsavin]

Hi there everyone. I just wanted to hear from some of you who've survived WBR. How many years has it been and what side effects are you experiencing. I just would like to hear that it's not hopeless and that many of you are managing your side effects, if any. Basically, the neurosurgeon told my mother, who had WBR over 1 1/2 years ago, that her symptoms now (some memory loss and confusion, etc.) are progressive and that most people who survive the cancer die from the WBR. This can't always be true!