Home » Who Is Janet Freeman-Daily?

20 thoughts on “Who Is Janet Freeman-Daily?

  1. Pingback: [events|travel] In Seattle for the Locus Awards | jlake.com

  2. Hi, Janet. I came to your blog via Sandra Nachlinger. I have just been diagnosed with lung cancer and am blogging my journey. Sandra read it and referred me to your blog. I am looking forward to reading your journey.

    Blessings.

    Like

    • Good luck with your lung cancer journey, Ruth. I hope you get good treatment news once all the workups are complete. Please feel free to email me if you want to chat. Sandra can give you my email address (I don’t want to publish it on a blog).

      Like

    • Hey Gordon! Thanks for reading. I didn’t realize we were in Cambridge, MA, during the same era. Please help me figure out how we’re related — my chemo brain isn’t making the connection.

      Like

  3. Pingback: #JACR Chat 6/26: Patient Perspective on Lung Cancer Screening (#LCSM cohosts) | #LCSM

  4. Pingback: #JACR Chat 6/26: Patient Perspective on Lung Cancer Screening (#LCSM cohosts) | Gray Connections

  5. Pingback: #JACR Chat 6/26: Patient Perspective on Lung Cancer Screening (#LCSM cohosts) | CancerGeek

  6. Pingback: Go Ahead (and ask me if I smoked) … Make My Day

  7. Pingback: Tweeting Up Ideas | HIMSS Blog

  8. Hello,
    My name is Dr. Dana Hansen and I am faculty at Kent State University, College of Nursing. You may view my faculty website page at http://www.kent.edu/nursing/facstaff/bio/~dhansen1/ .
    We are contacting you because you are listed as the contact person of the blog. My research team and I are interested in learning about the family caregiver’s experience with reading their loved one’s illness blog.
    Therefore, we are conducting a research study and are inviting you to participate. Below are details of the study. You can also find out more by going to our study website: (will be added once website developed).
    If you are not the family caregiver of the person with a serious illness, please forward this information to someone who is.
    Family caregivers are eligible to participate in the study if:
    • Both you and your loved one are 18 years or older
    • The blogger/ill person must have a diagnosis of cancer, congestive heart failure (CHF), chronic obstructive lung disease (COPD), or human immunodeficiency virus (HIV)/acquired immunodeficiency syndrome (AIDS)
    • The blogs must be written in English with a minimum of 1 posting per month
    • The family caregiver must participate in the blog by responding to the blog or reading the blog

    Procedure and Time Commitment:
    The family caregiver should go to our website where they can click on an icon labeled “participate in study”. The family caregiver will be asked to read and agree to a consent form. If they choose not to participate after reading the consent form, they click on the icon labeled “I disagree”.
    If the family caregiver agrees to participate, they will complete a form asking their name and how to contact them. Then a member of our research team will contact them to schedule a time to conduct a 1-2 hour interview where we will ask questions about their experience as a caregiver interacting with their loved one on an illness blog. A nominal onetime payment of $50.00 will be sent to the participant once the interview is complete.
    Participation is voluntary, refusal to take part in the study involves no penalty or loss of benefits to which participants are otherwise entitled, and participants may withdraw from the study at any time without penalty or loss of benefits to which they are otherwise entitled.
    Thank you for your time and consideration,
    Dr. Dana Hansen
    Dana Hansen RN, PhD
    Assistant Professor
    Kent State University, College of Nursing
    113 Henderson Hall, P. O. Box 5190, Kent, OH 44242

    Like

  9. Hi Janet! I just discovered your blog and story and it gives me hope. Would love to connect by email. I have stage 4 lung cancer diagnosed 20+ months ago. I only learned about genetic testing by getting a third opinion on treatment options. First two docs didn’t even mention it. I have been in an out of state trial since Jan for a met mutation. So far so good but not NED or expecting that. Send me an email when you have time! Good luck and hugs, Diann

    Like

  10. Pingback: MSL on the Road: Boston Open Vis + GET Conference | Mozilla Science Lab

  11. Pingback: #LCSM Chat topic 11/17– FB Live Q&A with NCI on Immunotherapy and Clinical Trials | #LCSM

Leave a Reply

Fill in your details below or click an icon to log in:

WordPress.com Logo

You are commenting using your WordPress.com account. Log Out / Change )

Twitter picture

You are commenting using your Twitter account. Log Out / Change )

Facebook photo

You are commenting using your Facebook account. Log Out / Change )

Google+ photo

You are commenting using your Google+ account. Log Out / Change )

Connecting to %s