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What Do You Want to Read on The Daily Headache?

Two years into blogging, I’ve learned that sharing isn’t complaining, writing about myself isn’t necessarily self-centered, and that many people read blogs for the personal connection they feel with the blogger. I’ve also found that I certainly have enough to say without whining and moaning. (I’ve also gotten e-mails asking me to write more about my experiences.)

So, I want to know what you think. Should I write more about what I go through? Essentially, I want to know what keeps you reading The Daily Headache. Here’s a poll to make it easy, but I’d love for you to leave a comment with your thoughts.

8 thoughts on “What Do You Want to Read on The Daily Headache?”

  1. I didn’t answer the poll – how can I decide? I’ve learned so much from your posts – all of them – since I discovered you a few weeks ago. You richly deserve that HealthCentral “Best of” award.

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    Thanks!

    Kerrie

  2. This is a hard little quiz. I actually REALLY enjoy everything that you post. The news is great. I often reserach further so I am educated when I go to the doctor. The educational stuff is great because I am a nerd and love to learn more- I keep a lawyer’s style file folder on migraine info. And your personal stories are encouraging to me- more than you know. So please keep on with whatever you want to post.

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    Thanks for the kind words. It’s always great to hear that someone wants me to do whatever I want!

    Kerrie

  3. I must say that I enjoy the mix you’ve had of different types of posts, but I probably learn the most from reading about your personal experiences.

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    Thanks!

  4. I like reading the info about scientific discoveries. I feel like if I just learn enough physiology, I’ll figure out the cure to these headaches!!! LOL. I’m just kidding, sort of. Thanks for your web site. I love reading it all actually. Lynn

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    Thanks for the kind words, Lynn. While learning the workings of the brain may not be the most direct route :), I think patients do play a huge role in working toward better treatment. Our experiences help drive research.

    Take care,
    Kerrie

  5. Kerrie,

    I will always read it because I am so inspired by you and fascinated at your blog, this impressive repertoire of medical facts and scientific theories! But my very favorite thing is when you weave all this knowledge in with your personal experiences.

    That’s my vote!

    AM

  6. I’m laughing right now because the person that Jamie refers to as her pen pal is me! Funny that both of us have been reading your blog! It’s been wonderful talking to you as well, Jamie!

    Anyway, I echo her comments.. You were the first person I found who had CDH and that alone made me feel connected to you. Hearing what you’re going through makes me feel like I’m not alone in this, which is often how I feel.

    I’d love to hear more about your personal experiences, but I also like the news and education materials posts too. Perhaps more polls like the one you just posted would be interesting too!

    *******
    That’s great! I’m so glad that you two have gotten in touch.

    Thanks for your input. Like I told Erin, I’ll eventually figure out how to mix it all in.

    Take care,
    Kerrie

  7. Kerrie, I wish you’d let us pick more than one topic!!!
    Primarily, I like hearing about your personal experiences. I see that as the primary function of blogging.
    However, I also see this site as a good resource of current, cutting-edge migraine information. I hope that just because many people say they want to read your personal experiences, you don’t stop providing up-to-date information.

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    Thanks for your input. I’ll figure out how to cover all the information still. The responses to this poll will guide me in figuring out how I do it.

    I couldn’t find a poll that would let you rank your choices, but I tried!

    Take care,
    Kerrie

  8. Hey Kerrie. I totally agree with what you said about the personal connection (not to sound too creepy ha ha!). You were the first person I ever found that struggles with CDH and talking with you and reading about your day to day life made me feel that I was not all alone. I know it sounds cliche and dumb, but it was very important to me (and still is!). I have recently been paired with a pen pal through the Headache Foundation who also has CDH (the only other person I have ever found) and it is wonderful to be able to talk to her as well.

    Hope all is well with you!

    Jamie

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    Thanks, Jamie. It’s a cliche, but you’re certainly not alone. I’m so glad your pen pal is helpful.

    I think of you often and hope you are doing well.

    Kerrie

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