Polls - Fight MPN | HealthUnlocked

Fight MPN

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Have you watched our ASH 2016 Coverage yet?

Do you know the new NCCN (National Comprehensive Cancer Network) guidelines for MPNs?

Have you advocated for yourself to get better care by seeking a second opinion?

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Are you going to be watch our live broadcast tomorrow (10.22) to get the latest research and treatment news?

Have you watched our replays of this past weekend's event?

How do you cope with your MPN so you know you're not alone?

What symptoms or complications have you had because of your MPN?

Are you attending (in-person or online) our 3-part MPN town meeting series?

What would you like to see come from Patient Power in the upcoming year?

Have you ever had insurance, billing or hospitalization problems ? Let's talk about it in the comments section and through our blog post!

Who is your primary care partner?

What type of MPN do you have?

How can researchers and doctors encourage patients to enroll in more clinical trials?

Have you ever considered or enrolled in a clinical trial?

We've halfway through 2016! What have you done in 2016 to help yourself grow as a "Powerful Patient"?

Pick your top 3 goals that you'd like to achieved through Moonshot.

How does your GP react to your concerns about issues that could be MPN-related? Tick any boxes that may apply & feel free to add further

Do you think pharma companies understand the effect the price of their cancer drugs have on patients and their families?

What was your greatest source of support when you were diagnosed with your MPN?

This Sunday is National Cancer Survivors Day! How do you bring awareness to cancer survivorship?

What topics would you like covered in future Facebook Live Q&A Sessions?

How Do You "Eat Dessert First" aka living fully despite having cancer? Andrew recently blogged his answer here-http://bit.ly/1OpgBtn

What age were you when your MPN was diagnosed? Feel free to leave a comment if you wish to expand your answer

How do you cope with your MPN diagnosis? Feel free to leave a comment to share more about your experience.

What treatments, if any, have you had for your MPN? Feel free to expand by leaving a comment!

How were you diagnosed with your MPN? Feel free to reply to expand on your diagnosis experience.

Would you ever or have you ever participated in a clinical trial? Feel free to reply in order to expand on why you selected that answer.

Have you ever felt confused about the treatment you are receiving, or felt as if your physician was not making the right decision?

Do you feel like your relationships have been impacted since your diagnosis?

Where did you (or your loved one) get the most support after your diagnosis? Feel free to expand or comment any other ways you get support.

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