Showing posts with label blog. Show all posts
Showing posts with label blog. Show all posts

Thursday, April 11, 2013

WEGO challenge Day #11 -- social media, what, who, when, wow!

Today's prompt. 

Write about your favorite social network. Do you love Twitter? Facebook? Pinterest? Why?

I love the internet. I can not imagine what life would have been like in High School or college(the first time) with the 24/7 connection to the world. 

Those who know me, know I love them all. Facebook can be oh so annoying, but the positives of what I have gotten from it, make me hang in there. I have reconnected with people who I lost touch with. I get to see where their lives have gone, see their beautiful kids, faces that bring back great memories, and it's effortless to connect and share pics and info with many people at once. Plus, I have a built in IBD network of so many wonderful people that I have never met, and may never meet, who get it and understand and have been in my shoes and me in their's. My facebook IBD groups made me feel less scared and isolated and singular. It allowed me to own my struggle with IBD. It's brilliant!

I also love Twitter. I love getting all my news headlines, traffic issues, funny tidbits, my IBD community exchanges blurbs about their shitty days or their successes. I love the simplicity of the retweet. I love seeing the randomness that celebrities come up with on their accounts. 

On my old macbook. I'm sure my smartphone was with me too.
I'm much newer to Pinterest but I do enjoy it. It is unreal the ideas and recipes and home decor and outfits and picture scenarios can be in one place. It really seems endless and could take up an entire day. I like that everything is on it's own little boards and it becomes it's own little way of passing ideas and stories. 

I use all three to share my blog and share my journey and pass along details and stories of people that I admire or connect with and feel others should read about. 

I love it. I love that you can find out virtually anything in a matter of seconds. I love video chatting and think there should be more of that. I remember dial up with a phone cord stretched into the spare room of my parents house. I remember when AOL disks came in the mail every other day. Amazing how much has changed. I still write thank you cards though. You know, the ones you put a stamp on and mail?! =)


Monday, April 1, 2013

Health Activist Writer's challenge #1- Writing about UC

Hello out there everyone. This is my first attempt at participating in the #HAWMC! I am going to give it my best shot despite being busy with school and kids yadda yadda yadda....
I am not a newbie to WEGO health. My blog was so awesomely nominated as Rookie of the Year for 2012. WEGO is a great community of people who write about health issues.
I know with me I had wanted to start my blog when I first got sick but just didn't have it in me. I was lucky to be barely functioning as a mom while constantly being in a UC flare. Somehow I was dragging my diseased ass to work 40 hours and trying my damnedest to lead a normal life. Hello! Crazy person!! I shouldn't have been driving half the days I did. I was so weak and light headed. Anemic constantly. Malnourished constantly. I should have had a chauffer. So needless to say I was not  up to adding one more thing on my plate by blogging. Once I was scheduled for surgery last year I realized even more how I wish I had chronicled my journey. I had already forgotten details. I mixed up what happened in which hospitalization(like it really matters!) and I wish I had more pictures of what the disease had done to me physically. Hubs refers to me at my worst as Skeletor. Those of you old enough to remember He-Man know what I'm talking about. I have some random pics here and there but I kick myself for not documenting my journey on a bigger scale.
So in early 2012, with my surgery scheduled for May, I figured I would start so that way I could at least tell my story of surgery and recovery. I know a lot of people are so afraid of surgery they'd rather suffer for years and have their body destroyed by meds, so I wanted to make it real. I knew there would be dreadful days, but I also knew there would be many victories. I had the mindset that I would kick some ass in recovery and wanted to put a happy ending of sorts out into the IBD community. I wanted to write about how my health and surgery and recovery impacted my life, good and bad. So that's where I am today. I am closing in on having my blog one year and in that time have had almost 7,500 visitors to my little page. That is amazing to me since for the most part my blog was a little bit of therapy so to be that well received is a bonus.
Worst IV location EVER!!

I'm glad I did it. My story isn't the prettiest, my pictures are kinda gross and shocking, but I don't plan on stopping. I know my story is helping someone out there and I love it.
Until tomorrow, everyone!! Have a great night. XO