BT5K season is here! Join the community and walk or run to make strides against brain tumors!
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This year, the brain tumor community can count on the ABTA returning to in-person BT5K’s in several U.S. cities; educational and supportive virtual programs; and more ways for you to get informed and involved.
Brain cancer survivor and patient advocate Wendy Santana shares four ways she’s learned to handle the highs and lows of settling into a new year.
New and updated resources from the ABTA can help you navigate brain tumor treatment and care decisions and receive personalized support.
In his own words, Rick Franzo shares his brain tumor experience at the ABTA National Conference. Learn why Rick’s greatest takeaway from his journey is hope.
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When you think of being a newlywed, what comes to mind? Laughter, love, spending forever with your partner—these are just a few things Amanda thought of. Cancer never crossed her mind.
Steve Archibald, father, blogger, brain tumor survivor, and ABTA patient mentor, reveals the mental health challenges he experienced after treatment.
Meet Wendy. She started a blog when she lost her voice after brain tumor surgery to remove an oligodendroglioma. And now, two years later, she’s using her blog to empower the brain tumor community.
What drives us to share our journey with a brain tumor diagnosis? The answer includes the physical and emotional benefits, and beyond. Dive deeper into this topic with the ABTA Patient Services Team and Steve, a nine-year brain tumor survivor.
The ABTA along with Co-Chair, Erin Dunbar, MD, Piedmont Brain Tumor Center, has designed a meeting to empower and equip newly diagnosed patients and caregivers with information and resources to make informed decisions throughout treatment and care.
Always free for patients & caregivers
