Top 12 Posts of 2012

chroniccurve:

Based on Google Analytics, the top 12 most visited posts of 2012:

image

  1. Painkiller Paranoia: The Stigma of Opioid Use Among Chronically Ill Patients


  2. Fighting the Fog From Pain With Narcotic Medication? New Study Reveals What We Already Know

     
  3. 15 Tips for Your First Visit to a New Rheumatologist
     
     
  4. The Human Pin Cushion: Tips for Making Self Injections Easier
     
     
  5. It’s My (Pity) Party and I’ll Cry if I Want To
     
     
  6. Doctor Disclosure: What to Do After a Terrible Experience
     
     
  7. Download Your Free Chronic Illness Health Information Sheet!
     
     
  8. Chronic Illness & Dwindling Friendships: Finding a Balance and How to Handle Negative or Changing Relationships
     
     
  9. College and Chronic Illness: 19 Tips to Study Strong & Fight the Brain Fog
     
     
  10. The Arthritis Name Game: Five Reasons to Stop Using the “A” Word
     
     
  11. Love Yourself More Chronic Illness Challenge
     
     
  12. Hope: The Thing With Feathers

A huge thank you to the new and old readers here on Chronic Curve for your kind words, your comments  your likes and reblogs, your shares, and your interest. As of today, there are just under 20k of you subscribed to Chronic Curve and it just blows my mind and humbles me each time I see more people reading these posts, learning about these diseases, learning about our lives as chronically ill patients.

What a gift that is. Cannot wait to see what 2013 has in store for us all.

As always, thank you for reading.

Love & spoons,

Emily


*You can find the artist of this lovely painting here.

6 January 2013 ·

bunnyears:

To all my MS, Fibro, Lupus, RA, Pancreatitis, and chronic pain friends. Please try your best to have a wonderful Christmas. I know this time of year is exceptionally hard as we are pushing ourselves and trying to appear normal around friends and family. Trying not to show our pain so we won’t make them feel “uncomfortable”. But tonight, I received a huge reality check as to what my body can and cannot do. 
My face feels like acid has been poured on it. The muscle in my left arm is protruding and so tight and exceptionally painful. My leg muscles are so tight that walking hurts like heck and when staying still it still hurts like heck. Headache escalating quickly.
Doing my best to not let it steal my holiday spirit. It’s easy to say but hard to ensure that is doesn’t. 

bunnyears:

To all my MS, Fibro, Lupus, RA, Pancreatitis, and chronic pain friends. Please try your best to have a wonderful Christmas. I know this time of year is exceptionally hard as we are pushing ourselves and trying to appear normal around friends and family. Trying not to show our pain so we won’t make them feel “uncomfortable”. But tonight, I received a huge reality check as to what my body can and cannot do. 

My face feels like acid has been poured on it. The muscle in my left arm is protruding and so tight and exceptionally painful. My leg muscles are so tight that walking hurts like heck and when staying still it still hurts like heck. Headache escalating quickly.

Doing my best to not let it steal my holiday spirit. It’s easy to say but hard to ensure that is doesn’t. 

image

25 December 2012 ·

"The unwell and disabled life asks nothing more than constant bravery."

~ (via sickgirldiary)

(via sickgirldiary)

4 December 2012 ·

Having new symptoms with no answers is almost more frustrating than not having answers for your other symptoms!

(Source: sickgirldiary, via sickgirldiary)

1 December 2012 ·

For my brain flowers:: National Health Blog Post Month (Melody's Schedule): Why I Write About My Health

signsofmelody:

I started this blog soon after I was officially diagnosed with Rheumatoid Arthritis. Before then, I lived almost a year with debilitating symptoms and no idea what I was to do to help myself. I had no insurance (until later), and very little support from friends and family because many thought…

5 November 2012 ·

Dear Rheumatoid Arthritis

balexan-der:

I hate you. K. Thanks. Bye.

31 March 2012 ·

My doctor put me back on prednisone

F#(*$()$ steroids. can’t live with em (or fit in your clothes/interact with other humans) but can’t live without em. 

wisheezy:

AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA

AAAAAAAAAAAAAAAAAAAAAAAAAAHHHHHHHHHHHHHHHHHHHHHH

HHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHH

HHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHHH!!!!!!!!!!!!!!!!!

!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!

i don’t wanna

:(

15 January 2012 ·

6
  • Me: Prednisone, why are you ruining my life?
  • Prednisone: I'd never do that, I'm here to help. Check out your joints!
  • Me: Ummmm, they are all red and puffy and stiff, AND they hurt like hell!!!
  • Prednisone: I do my job, what are you trying to say? How'd I ruin your life? I want examples!
  • Me: Well, I'm a raging bitch, I gained an amount of weight I can't say out loud without crying, but let's just say you can't tell the difference between me and a woman that is in the beginning of her second trimester of pregnancy, I can't stop eating, my blood sugar is all over the damn place, I have acne, my vision is all strange, AND my head hurts!!!
  • Prednisone: Wasn't me.

23 November 2011 ·

About Me

Thoughts, ramblings, and unsolicited advice about life with Multiple Sclerosis / Chronic Illness, by me and other people on the internet.

Because sometimes it feels good to be able to say "oh man I can relate".


My background. Brief history of how the shit hit the fan, when the shit hit the fan. Written then from that POV. Lets call this link some context to this blog

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