← Return to Cognitive changes after chemo
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Replies to "Baeph, Your story opened my eyes as none have before. I had to look up Ampullary..."
Another type A here. I’m 4 years out from my mastectomy and still working to rid myself of the chemo side effects. My oncologist told me I had more side effects than any other patient he’s ever seen. One is “brain fog’. I take Prevagen and ginkgo biloba. They work differently, hence my taking both. Prevagen is expensive, but my recovery didn’t pick up speed until I started with it. Some patients seem to eventually no longer need anything. I’m not so lucky. I’m better, but at 69 age can become a factor. It’s hard, because my brain is how I made my living and the key to my former career in Technology. But I’ve adapted, lots of sticky notes. As I have said for decades, you cannot control what happens in your life, only your attitude about it. Hope your recovery goes well.
@bcwarrior God Bless you!!! I was diagnosed two years ago and I still can’t grasp the fact that I have breast cancer or should I say HAD! I really don’t know what to say because I don’t know if I’m cancer free I go for a mammogram every six months and all I get is I’ll see you in six months. They never tell me if the cancer is gone if I still have it.????? I guess if I had it, they would be doing some kind of treatment on me still but I would just like to hear the words it’s gone! I feel like my life will never be the same. It just seems like after this chemo and radiation. It’s just one thing after another after another. I never feel like me anymore. I’m gonna try hard harder. I want my life back.!!!!
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Such a helpful post, @bcwarrior
@baeph, I hope you saw the post above from BCwarrior. You might also be interested in the helpful posts that members offered in this discussion:
- Trying to understand my friend's chemo brain: How can I help? https://connect.mayoclinic.org/discussion/chemo-brain-or-fog/