young adult cancer Archives - Page 5 of 39

Dude, Where’s My Life?: Dating in Retrospect

The silhouette of a man facing a horizon with a pink sky.

This blog is the first in a series we call “Dude, Where’s My Life?” featuring writing and thoughts from the guys in our community.

YA Cancer Gabfest 2022: Registration Is Open!

Registration for YA Cancer Gabfest 2022 is now open! Throughout the week of December 5th, we invite you to share, explore, and learn as we socialize and engage with each other.

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Research Roundup!

Here at Cactus Cancer Society, we’re always interested in amplifying the voices and experiences of young adults facing cancer, and making sure this population is represented in research. Check out these research opportunities focused on YAs with cancer!

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Our Next Book Club Pick: The Martian

A view of five books stacked on each other, only the white pages visible.

One of the first programs we started here at Cactus Cancer was our book club. September’s choice is The Martian by Andy Weir.

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Looking for Help With Clinical Trials?

Finding a clinical trial can be overwhelming. Patients are often left to search for trials on their own, leaving them with more questions than answers. Fortunately, our friends at The Leukemia & Lymphoma Society provide a free service to take this burden off patients and their families!

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Dating and Cancer History: To Disclose or Not to Disclose?

Cancer is my heaviest baggage. It’s my crazy ex-girlfriend that tried to kill me, and I would hate it if she ever came back, but she’s crazy, so she might. And I feel that I have to tell you at some point, so when’s the right time?

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Write Now With Jean Rowe: Choice

It’s Summer and connecting with one another is more open because we can comfortably meet up outside. How we experience any of these aspects of the season is up to us. Choice bubbles to the surface.

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Progress with Prozac

After Facing Testicular Cancer, I Realized I Was Feeling Depressed – So I Asked For Antidepressants

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You Are Not Alone. I Repeat: You Are Not Alone.

I wish that I had the awareness that this was a common feeling for AYAs when I was first diagnosed and undergoing treatment, because, although I had so much support from my family and friends, I still felt isolated and misunderstood.

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