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🌟 July 2026 Radiation Roll Call — Come On In For Support and Info🌟

If radiation therapy is part of your treatment plan this July, we'd love for you to join us here. ☀️

Whether you're preparing for your first session, settling into the daily routine, or counting down your final treatments, this thread is a place to connect with people who understand what you're experiencing.

Radiation often becomes part of everyday life for several weeks, bringing questions, routines, challenges, milestones, and plenty of emotions along the way. Whether you're feeling hopeful, nervous, tired, determined, or somewhere in between, you're welcome here.

✨ Introduce Yourself

Say hello, share your start date, tell us where you are in treatment, or simply post, "I'm here."

Then keep coming back.

Many members find these monthly Radiation Roll Calls become a place to share their journey—from the first planning appointment through the last treatment and into recovery. We'd love for this thread to be a place where you can check in, ask questions, celebrate milestones, and receive support throughout the month.

💬 Check In Throughout Your Journey

This thread isn't just for your first post—we hope you'll return often.

Share updates like:

  • How you're preparing for treatment
  • How your appointments are going
  • Questions about what to expect
  • Skin changes, fatigue, or other side effects you're experiencing
  • Tips, routines, and little discoveries that are helping
  • Milestones along the way
  • Difficult days when you could use some extra encouragement

Even a short update lets everyone know how you're doing and gives others the opportunity to support you.

💛 Every Update Matters

Someone may be reading quietly today, wondering if anyone else is experiencing the same thing.

When you share your story, you help someone else feel less alone. When you reply to another member, you remind them that they have people cheering them on.

This community grows stronger with every question, every update, every milestone, and every kind word.

🌸 Already Started—or Finished Radiation?

We'd love to hear from you, too.

The experiences you've gained—whether practical advice, encouragement, or simply sharing what helped you through the daily routine—can make a meaningful difference to someone just beginning treatment.

Sometimes hearing, "I remember that stage," can bring a great deal of comfort.

✨ Easy Ways to Join In

  • Share your radiation start date or treatment schedule
  • Introduce yourself
  • Post updates as treatment continues
  • Ask questions—no matter how small
  • Share tips that have helped you
  • Encourage another member
  • Stop back in anytime you have news or simply need support

There's no such thing as posting too often—we'd love to hear how you're doing.

🌟 One Session at a Time

We'll take this together—one appointment, one week, one milestone at a time.

We'll be here to celebrate your progress, offer encouragement on the harder days, and cheer you on until you ring that final bell—or reach whatever milestone marks the end of treatment for you.

📌 Helpful Resources

🤝 Looking for More Support?

Our Virtual Support Groups are here before, during, and after treatment.

One Last Thing

You don't need the perfect words—or even a long update—to participate.

If you've been following along and wondering whether to post, consider this your invitation.

Whether you're waiting for your first appointment, halfway through treatment, celebrating your final session, or adjusting to life after radiation, there's a place for you here.

We hope you'll check in often, share your journey as it unfolds, and support others along the way. Together, we'll get through treatment—one session, one week, and one milestone at a time.

🌟

— The Mods

Comments

  • Just finished and rang the bell today! Anyone else have a delayed crying episode after it seems to be all done?

    I find my emotions have gone off the rail tonight. Relief and the what now is a bit ovetwhelming.

  • @jane.e.taylor75 Congratulations! I'm really happy for you - and the crying make sense. I feel like we're all in survival mode, and this is an all-encompassing journey. It probably is quite overwhelming now that you've reached the other side. Hugs to you.

    I'm just starting radiation this month. I have to go in for my initial run through and treatment schedule on the 13th. I'm a bit nervous because I have very sensitive, fair skin and I'm already exhausted. I'm looking forward to the day when I get to ring the bell.

  • l1ttlec
    l1ttlec Posts: 27

    Congratulations Jane.e.taylor75!!

    canijustbemary - I had my appt for the setup and run through but my RO wants me to see my surgeon (July 8) again before actually starting radiation. I saw the PA for my post op. I’m nervous, too, but anxious to get it started. I’m not looking forward to the daily trips to the hospital through downtown traffic. I’ve also been exhausted on and off since the surgery which felt minor at the time-lumpectomy and 4 sentinel nodes and pretty easy, quick healing. I have insomnia so I’m used to being tired but there are days when the exhaustion just feels like I’ve hit a brick wall. If I feel like this now, what’s it going to be like when I actually start treatment?

  • moderators
    moderators Posts: 10,261

    @jane.e.taylor75 congratulations!!!

    @canijustbemary ,

    It's understandable to be feeling nervous while you're waiting to get started. The waiting can be one of the hardest parts.

    Many people are surprised by how much fatigue they feel after a lumpectomy, even when the surgery itself seems relatively minor. Healing takes energy, and it's not unusual for that "brick wall" exhaustion to come and go.

    Hopefully, others who have been through radiation will share how their energy changed during treatment and what helped them manage it. Wishing you all the best for your appointment with your surgeon on July 8. 💗

  • sethsim
    sethsim Posts: 2

    hello. I have hormone positive HER2 negative invasive . I just had a lumpectomy on June 23 and have good clear margins and no lymph node involvement. The doctors are pushing me to do proton radiation. I have a great number of comorbidities and I am not sure that what I will gain is worth the risk of going through the radiation. The minimize the risks because they’re trying to convince me to go forward, but I am very uncomfortable about the notion since I already have 31% working lungs and 31% working hard. The rest are already dead from fibrotic issues. So any radiation will only potentially compromise that. I would love to learn from the women who have already gone through these things. Thank you in advance for sharing your stories.

  • sethsim
    sethsim Posts: 2

    my radiation oncologist says that by doing the radiation I will reduce the recurrence risk of 20% to about 3%. If there is a recurrence risk of 20% following the lumpectomy that means there is an 80% chance of absolutely nothing going wrong. But there is definitely a risk associated with radiation so I don’t know how to calculate whether or not it’s worth it to do the radiation. I think I would rather take the chance and not do it. I’m so confused.

  • l1ttlec
    l1ttlec Posts: 27

    My appt with the surgeon went well and she said everything has healed well. I finally got the call yesterday that radiation will start on Tuesday the 14th. I am ready to get this started and having an actual date has helped.

    The exhaustion definitely comes and goes. I seem to have 2 total exhaustion days followed by maybe 1 or 2 good days. I was able to mow today so I figure the brick wall will hit again tomorrow. I’m still amazed at how this surgery has hit me compared to surgeries I’ve had in the past. It helps to know that it’s not unusual.