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  1. WELCOME NEW MEMBERS!

    1. INTRODUCE YOURSELF!

      Please introduce yourself here and then move on to the many other forums!

      43.8k
      posts
  2. STORIES OF SURVIVORSHIP

    1. SHARE YOUR LUNG CANCER STORY

      These are the inspirational and personal stories of the LUNGevity LCSC members.

      2.3k
      posts
  3. DISCUSSION FORUMS

    1. GENERAL

      General discussion about all things lung cancer.

      95.6k
      posts
    2. LC SURVIVORS

      A forum for anyone diagnosed with lung cancer, those in treatment and those who are not, to express the thoughts and issues that are specific to people living with lung cancer.

      9.1k
      posts
    3. NSCLC GROUP

      A forum where general thoughts or issues regarding NSCLC and sub-types of NSCLC can be found. Support is here for anyone facing this diagnosis.

      43.6k
      posts
    4. SCLC GROUP

      A forum for patients and caregivers impacted by Small Cell Lung Cancer. Share latest SCLC news, information and get and give support here.

      16.6k
      posts
    5. US VETERANS

      This is a forum for all US veterans impacted by a lung cancer diagnosis. This forum is moderated by a veteran-survivor.

      51
      posts
    6. NATIONAL HEALTH SYSTEM TREATMENT

      This forum is for patients to discuss the unique challenges of receiving lung cancer treatment in countries who have a National Health System. Navigating diagnosis difficulties and dealing with treatment availability are important topics to members receiving treatment within a National Health Care System.

      4
      posts
    7. CAREGIVER RESOURCE CENTER

      A forum for FAMILY MEMBERS/CAREGIVERS: Air your feelings, get and give support from others who are co-surviving lung cancer. Post and share resources for caregivers here.

      29.6k
      posts
  4. TREATMENT FORUMS

    1. CHEMOTHERAPY

       A forum for patients and caregivers impacted by chemotherapy treatment. Connect here to offer insight, get advice and peer support. Share Information and news about chemotherapy here.

      1.2k
      posts
    2. IMMUNOTHERAPY

      A forum for those on or interested in immunotherapy treatments, latest news and peer support.

      2.2k
      posts
    3. RADIATION

      A forum for patients and caregivers impacted by radiation. Connect here to offer insight, get advice and peer support. Share Information and news about radiation and new radiation therapies here.

      397
      posts
    4. SURGERY

      A forum to discuss lung cancer surgeries, share experiences, get and give support.

      500
      posts
    5. SUPPORTIVE CARE

      A forum about supportive/palliative care. Learn about palliative care for lung cancer survivorship, get advice and support and share your resources here.

      17
      posts
  5. LUNG CANCER NAVIGATOR

    1. LUNG CANCER NAVIGATOR

      Do you have general questions about lung cancer? Post them here! We will reply with links and resources. This forum & site are NOT substitutes for professional medical advice. Please read all site disclaimers and consult your treating doctor about everything you read on the internet.

      751
      posts
  6. NEWS / ADVOCACY

    1. LUNG CANCER IN THE NEWS

      News posted here may not necessarily be endorsed or supported by LUNGevity in anyway, should NOT be taken as medical advice and are for informational purposes only.

      10.8k
      posts
    2. ADVOCACY

      Advocate, raise awareness, participate in events and find volunteer opportunities in this forum.

      3.5k
      posts
  7. LIVING WELL

    1. HEALTHY LIVING / RECIPES

      Nutritional information, exercise, diet and therapies. Links and newstories that may be beneficial to health and survival may be posted here. No advertisements.

      533
      posts
    2. HOPE

      Inspire us with your good news and hopeful articles!

      33.1k
      posts
    3. JUST FOR FUN

      A forum for jokes, word games, and fun postings. "Air" your days events or concerns in the Daily "AIR".
      {Fun Found Here!}

      40.5k
      posts
  8. SUPPORT

    1. SUPPORT RESOURCES

      Suggestions, links, recommendations and tools to help support you during the lung cancer journey

      465
      posts
  9. GRIEF

    1. GRIEF

      A forum for anyone who has lost a loved one to lung cancer. Post general updates, memorial notices and any tributes here. Share resources for those who may be grieving.

      37.9k
      posts
  10. TERMS OF USE

    1. FEATURES AND SUPPORT

      You can create your own blog, chat, and more! Learn the basics and ask site support questions here.

      34
      posts
  • Member Statistics

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    Most Online
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    Newest Member
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  • Forum Statistics

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    422.4k
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  • Recent Discussions

    • Are you joining us in Atlanta May 3-5 for HOPE Summit? Saturday night is looking like lots of fun! From 7:15-9:15pm you'll be able to choose from the following activities: Sip and Paint with The White Ribbon Project: Join founders Heidi and Pierre Onda for a meaningful “Sip and Paint” session. Complete a ribbon for yourself to keep, give to someone else, bring to your community, or make available for someone newly diagnosed. Check your email for the RSVP link for this event. Improv Your Life with Sheryl Katzovitz: Join Sheryl— a medical training coordinator, seasoned theater performer, Atlanta native, and devoted mom and grandma— as she leads you through a series of fun games and exercises to expand your creativity and bring your playful side out of hiding! Zero theater experience required, just a willingness to try something new and be in the moment. Fun Zone with Epic Experience: Hosted by an organization that empowers adult cancer thrivers and survivors to live beyond cancer. Enjoy games such as Rumikub, cornhole, and Umali. Having a difficult time deciding? Don't worry, you'll have enough time to check out all of the activities! Learn more about the HOPE Summit Agenda and register for free by visiting lungevity.org/HopeSummit24
    • Bob, The waiting is one of the worst things about this disease.  Hang in there. Lou
    • Thank you to all the good thoughts. i had the CT on the 1st of April and waited a week for the doctor to call. Nothing, I already saw the results on my Advanced Radiology portal. it Grew to the 8mm as they wanted so i called the doctor's office and they set an appointment for May 29th. Two months after the CT scan and then they may eithe schedule a biopsy or a PET scan. 2 months not knowing what the next action is can drive someone insane. I am looking things up and everything says to get these things as early as possible. That is hard to do with waiting 2 months for a doctor's visit. 
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