Six Months of BCRN Blogging

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My first Blood Clot Recovery Network post was on May 1 of this year – that’s just about six months ago. As many of you know, I have actually been blogging for a few years over at Words to Run By, but decided to begin this venture after suffering from a DVT turned PE in June of last 2012 that nearly claimed my life and left my world as I knew it then in devastation. Six months ago I started this blog to share with others about the signs, dangers and effects of blood clots as a result of my own experience and to spread a message of hope for healing from the physical, mental and emotional trauma of such an injury to the body. I was unsure, at the time, if I was making the right move in beginning a second blog still, I felt compelled to share with others what had happened to me for the above reasons. When I was discharged from the hospital after my PE, I felt alone, uncertain and terrified of not only what did happen, but of what would happen. I didn’t want even one other person to feel that way and not have a resource to turn to. I can’t believe it is six months of BCRN blogging since then!

As many of you also know, I am also the grateful recipient of Blog Genie’s Blog School Scholarship, which began this week. If you’re a blogger and not familiar with Blog Genie, head on over to the site to sign up for free emails, which include some awesome tutorials and blogging advice. While I am primarily enrolling Words to Run By in blog school for the time being, I plan to apply the same lessons to BCRN to continue to improve this blog and make it the best it can be for you, my readers.

One of the things I [re]discovered last night as I was learning to read stats in Google Analytics, is how to determine just how many people do read this blog. And I was shocked at what you have made BCRN this far.

Here’s a rundown for you:

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While this blog is very different from my personal blog, it is not entirely an accident on my part. I wanted to create a blog that was very specific in content (recovering from a blood clot), but didn’t want to lose my personal voice in doing so. In a way, this blog has been easier to create (but not always write!) because I have already made mistakes and with BCRN, I have had the opportunity to start fresh, avoiding some of the “rookie” blogging mistakes (not that I don’t have a long way to go, thank you Blog School). It’s been fun for me to [try to] do the things I wish I would have “done from the beginning.”

One of the things that jumped out at me in terms of stats (and no, stats are not everything, but they give a blogger a good idea of what’s happening behind the scenes), was the length of time readers spend on my site. One hour and 49 minutes here (this month) compared to 54 seconds on Words to Run By. That’s pretty significant.

After reading this I mentioned in passing to my husband, “Wow. Someone must just open my site and leave their browser open for an hour!” I mean, who hasn’t done that, right?

He replied, “Uh, no. Probably not actually. You know what it is instead? They’re scared. Think of how you were when you first got out of the hospital. What was the first thing you did?”

Then, it hit me like a wrecking ball.

The first thing I did when I was out of the hospital (and able to stay awake for more than 30 minutes at a time) was scour the internet for information. I was like a sponge and I could not soak up enough information. I searched for information about blood clots, DVT, PE, APS, diagnosis, treatment, prognosis, but mostly I searched for other people who had experienced the same thing. People like me. Stories were hard to find, few and far between. Stories combined with good, tangible, relevant information were even harder to find. No information was too insignificant, no resource left unturned yet, something was missing – a face to blood clots; a story I, as a person living in the real world with real experiences and real fears, could relate to.

I set out to change that.

And six months later, here we are. The support, encouragement, love, hope and yes healing, I have received has been invaluable to me, not only as a writer, but as a survivor. Thank you for that BCRN. Thank you for helping to make these past six months even better than I ever dreamed they would be.

As a thank you, I would like to give away a Special Red Ribbon Survivor Bracelet to one of you. Please enter below and spread the word among your networks (unless you don’t really want to share).

a Rafflecopter giveaway

Here’s to six more months and hopefully many, many more after that!

* Please note, the winner has until October 11th to claim his/her prize or I will select a new winner and post it here.

There is hope for healing and you are not alone,

0-BLOG SIGNATURE SARA

Comments

  1. First, YAY!!!!!!!!!!! The average time on the site is great! I know I’ve spent my fair share hopping around from post to post. 🙂

    Second, I’d enter, but I already have a survivor bracelet. No sense in stealing odds from someone else. After all, if there’s one thing we as survivors know more than just about anyone else, it’s odds. And beating them.

    • Trysh, thank you so much for being with BCRN from the beginning and for being the first to share your story with my site! I appreciate that so very much as you have helped to make t what it is today.

      I totally agree with what you said about the odds of course, but if you want to enter as a gift for a family member or friend, please don’t hesitate! 😉

    • Lisa Marie Wells says

      I’m so proud of you Miss Sara <3 You've come so far in such a short amount of . .time. I'm so happy that I got to be in on this with you from almost the beginning. You were the first site that I ever did go to after I was diagnosed and you directed me to other places which brought me to where I am ….now…<3 thank you!

      • What do you mean ‘almost’!? You have been with me since the beginning and I thank you for that! What you have/are creating is pretty amazing too. Surviving a Silent Killer is by far my favorite FB support group. Thank you for cultivating a place where we can be comfortable to share our thoughts and feelings.

      • Lisa Marie Wells says

        With the way my mind is nowadays, I just couldn’t remember! 😉 & thank you !sweetie!

  2. linda anglebrandt says

    Surviving our son means I feelan obligation to him to spread awareness & try to help others live!

  3. Sara. How wonderful. How far you have come as you recover your health and your confidence. Truly, dear Sara, you are an inspiration and yes, the number do tell part of that tale. The bracelet is beautiful. I hope it goes to someone who will treasure it and wear it proudly, or bestow it as a loving gift to a dear friend or family member.

    • Thank you so much, Elle! I appreciate your support here and elsewhere, as you know! You have been with me on this from the beginning and that means a lot to me. As you know, I was so nervous about starting a new site, but I am very glad I did. Thanks for this and for your friendship. 🙂

  4. There is a teacher at my school who I just recently found out was a survivor. I’d love to give the bracelet to her if I win! 🙂 I also gave her this blog, so you’ve just earned a new reader! 😀 Keep doing what you’re doing- You are amazing! <3

  5. I am a survivor, it’s almost 4 years since I was diagnosed. My sister also had bllod clots and sadly she is deceased because of them, I would love to have a bracelet not only for me but in memory of my sister. Thanks

    • Thank you, Regina! Please make sure you register with the widget above (email) and then select that you left a blog post comment). Thank you so much!

  6. I had a PE on July 17th of this year. I’m still trying to process it and don’t know if I’ll ever come to grips with it. But, being a survivor means I can continue to be a mom and wife, sister, friend, co-worker. I’m forever changed and thankful for more time!

    • Thank you, Sue! Please make sure you register with the widget above (email) and then select that you left a blog post comment). We’re so glad to have you here and a part of this community. Thinking of you.

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