It’s a delicate balance

When I was first diagnosed with Granulosa Cell Tumor in 2019, I did a fair amount of research on the subject, but I did not seek out community with others with the same condition.

However, when I was diagnosed with a recurrence in February of 2023, I immediately began searching out a support system, wanting to gather all the information I could before moving forward in making crucial decisions. I found a group of women on Facebook who have been a great support system, a wealth of information.

On the one hand, I am so thankful to hear the stories of others, to read about their experiences, to understand how they came to the decisions they have about their own care.

On the other hand, some days it gets to be a little heavy, hearing how difficult things are for some of my GCT sisters, wondering if my life will be like that in the days ahead.

It’s in those moments, when my mind goes to the “what ifs” I know I need to step back, to stop reading, to give myself room to breathe and remember every person’s story is unique. Though each of us is living with GCT, we’re each on our own unique path.

There's a delicate balance between being informed and being discouraged.