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The New Normal | Living Life With Chronic Disease

Living Life With Chronic Disease

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The New Normal | Living Life With Chronic Disease | creatinganewnormal.wordpress.com Reviews
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Living Life With Chronic Disease
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1 helpful links
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8 chronic illness
9 coping
10 rheumatoid arthritis
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helpful links,the new normal,advertisements,leave a comment,by akajanie,bull;,permalink,chronic illness,coping,rheumatoid arthritis,tagged autoimmune disease,fibromyalgia,parenting,so very tired,8 comments,pain,prednisone,f’ing winter,3 comments,enbrel
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The New Normal | Living Life With Chronic Disease | creatinganewnormal.wordpress.com Reviews

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Living Life With Chronic Disease

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1

So Very Tired | The New Normal

https://creatinganewnormal.wordpress.com/2013/03/19/so-very-tired

Product Reviews and Tips. Living Life With Chronic Disease. I am so tired. I keep saying that to people. At work, at home, at the doctor’s office. I can’t even help myself from saying it sometimes. But here’s the thing I know, and maybe it’s why I keep saying it: I know that none of these people really understand what I mean. I am tired to my core. And I don’t know what to do to get through this. And that I should try increasing my prednisone. And I’m just tired. March 19, 2013. Figuring Out My Life.

2

Being me really pisses me off | The New Normal

https://creatinganewnormal.wordpress.com/2015/05/15/being-me-really-pisses-me-off

Product Reviews and Tips. Living Life With Chronic Disease. Being me really pisses me off. I’m going to tell you the truth: I am really pissed off. I am just pissed. And there’s nothing I can do about it any of it. I know I need to accept who I am and find a way to see the good in myself and my life. But what I really want to do is throw an epic temper tantrum and then hide in my bed under the covers. May 15, 2015. Posted in Auto-immune disease. Posted by akajanie on May 15, 2015. Figuring Out My Life.

3

akajanie | The New Normal

https://creatinganewnormal.wordpress.com/author/akajanie

Product Reviews and Tips. Living Life With Chronic Disease. All posts by akajanie. Being me really pisses me off. I’m going to tell you the truth: I am really pissed off. I am just pissed. And there’s nothing I can do about it any of it. I know I need to accept who I am and find a way to see the good in myself and my life. But what I really want to do is throw an epic temper tantrum and then hide in my bed under the covers. May 15, 2015. Posted in Auto-immune disease. Posted by akajanie on May 15, 2015.

4

Figuring Out My Life | The New Normal

https://creatinganewnormal.wordpress.com/2015/04/30/figuring-out-my-life

Product Reviews and Tips. Living Life With Chronic Disease. Figuring Out My Life. Damn It’s been awhile. I am not even going to try to write about everything that’s happened since I last posted. But here are some highlights:. Started and stopped various medications. Developed tremors and significant memory so added a neurologist to my roster of drs. Had several elevated liver function tests so added a GI specialist to my roster of drs. Got super discouraged and started seeing a counselor. And I am wishin...

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Product Reviews and Tips | The New Normal

https://creatinganewnormal.wordpress.com/product-reviews-and-tips

Product Reviews and Tips. Living Life With Chronic Disease. Product Reviews and Tips. In the last month, I have spent an enormous amount of time on the internet, researching my illnesses, as well as researching ways to make my life easier. Some of these things I have tried, some just remain on my wish list. I thought it might be helpful to me (so I can keep track of what works and what doesn’t! I actually bought these before I was diagnosed, but I have also used them since. I would have to say: I. Mini S...

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I’VE MOVED! | The Progressive Patient

https://theprogressivepatient.wordpress.com/2012/09/15/ive-moved

Is it possible to reverse the effects of an incurable chronic illness? We shall see…. The Progressive Patient has its very own home on the web! To be redirected and please update your bookmarks! When is Enough, Enough? Leave a Reply Cancel reply. Enter your comment here. Fill in your details below or click an icon to log in:. Address never made public). You are commenting using your WordPress.com account. ( Log Out. You are commenting using your Twitter account. ( Log Out. Are you finding my blog helpful?

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Notebook | The Progressive Patient

https://theprogressivepatient.wordpress.com/journey-to-wellness-what-im-doing

Is it possible to reverse the effects of an incurable chronic illness? We shall see…. This page will contain links to blog posts that detail or outline the things I am doing to help my body thrive and to reverse the effects of my chronic illnesses. Basically it will be like a lab book, detailing my experiments and reporting back on the results. Check back regularly for updates! The Steps to Heal Intestinal Permeability. 15 Minute Morning Routine. Leave a Reply Cancel reply. Enter your comment here. After...

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Crazy Train Part 1 | The Progressive Patient

https://theprogressivepatient.wordpress.com/2012/08/18/crazy-train-part-1

Is it possible to reverse the effects of an incurable chronic illness? We shall see…. Crazy Train Part 1. Babs loved a challenge which is why she took on the “difficult” patients. And why she owned three primitive breed dogs that ran out the door at every chance they got and refused to come when called. I probably should have taken a hint from the dogs. This might take a few entries, so grab some popcorn and prepare to go “WTF? 8221; Yeah. It’s one of THOSE. This wasn’t the first time that Dr. ...HELL ye...

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When is Enough, Enough? | The Progressive Patient

https://theprogressivepatient.wordpress.com/2012/08/28/when-is-enough-enough

Is it possible to reverse the effects of an incurable chronic illness? We shall see…. When is Enough, Enough? One of my best friends lives out of state and struggles with very similar medical issues. Unlike me, she’s lived with some degree of chronic illness since she was a child. We chat on the phone frequently (sometimes multiple times per day! And keep each other updated regarding the different things we’re trying in order to improve functionality and restore wellness. During the years I struggled wit...

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Disclaimer | The Progressive Patient

https://theprogressivepatient.wordpress.com/disclaimer-read-me-first

Is it possible to reverse the effects of an incurable chronic illness? We shall see…. Leave a Reply Cancel reply. Enter your comment here. Fill in your details below or click an icon to log in:. Address never made public). You are commenting using your WordPress.com account. ( Log Out. You are commenting using your Twitter account. ( Log Out. You are commenting using your Facebook account. ( Log Out. You are commenting using your Google account. ( Log Out. Notify me of new comments via email. Yes, I Tweet.

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Fibro Blogger Directory: Directory

http://www.fibrobloggerdirectory.com/p/directory.html

A DIRECTORY OF PEOPLE WHO BLOG ABOUT FIBROMYALGIA. WELCOME TO FIBRO BLOGGERS DIRECTORY. Take a look around and visit some amazing blogs and if you write one yourself go to the SUBMIT page. And we'll have a look at your blog.maybe we will even list it here. An ever growing list of people who blog about fibromyalgia:. Founding member Lee Good in Australia, commenced blog in November 2009. Life with Fibromyalgia, empowered, commenced blog in March 2010. By Julie in Huntsville,. How I deal with life from the...

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Something I rarely do (a vent) | Falling Out of the Fog

https://fallingoutofthefog.wordpress.com/2012/06/05/something-i-rarely-do-a-vent

Skip to main content. Skip to primary sidebar. Skip to secondary sidebar. Falling Out of the Fog. My quest for a diagnosis, and (hopefully) a solution. Larr; The end of Savella, and on to the Bed of Nails. Whoever said “no news is good news” should be shot →. Something I rarely do (a vent). The thing that makes me mad is… there was one girl (I’ll fuzz some details here because I don’t want anyone to ever figure out who I mean). She sings well, reads well… and she should! The concept of “moral suppo...

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Fighting to the surface | Falling Out of the Fog

https://fallingoutofthefog.wordpress.com/2012/07/09/fighting-to-the-surface

Skip to main content. Skip to primary sidebar. Skip to secondary sidebar. Falling Out of the Fog. My quest for a diagnosis, and (hopefully) a solution. Larr; Whoever said “no news is good news” should be shot. Fighting to the surface. Hello, my friends, it’s been awhile, I know. I’ve come to the not-so-shocking conclusion that I am depressed, and that, combined with a boyfriend-free week has been cause for introspection. “What a wonderful time to blog,” you might say, but I didn&#82...If I died three wee...

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A conference on Aboriginal Mental Health and Wellness. What is it that the claim expressed by the current government? Meanwhile, claims to politics and business qualities of the current government has expressed about the same number of respondents (17.1% and 21.8% of the respondents, each of whom gave more than one answer.) Among the http:/ followfy.com. Desirability of accelerating reforms that earlier standard of living was higher and the like, but all – is very uncertain. Power looks like a negative i...

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Wednesday, November 26, 2014. We hope you will get to spend time enjoying the holiday with family and friends. This is the time of year when we begin bracing ourselves for cold weather, crowds and holiday weight gain. It is a common belief among Americans that holiday parties and feasting can result in a weight gain of 5lbs or more. Here are a few tips for weight management during the holiday season. Choose smart sancks to maintain blood glucose and energy levels. Be safe and enjoy! November is American ...

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The New Normal | Living Life With Chronic Disease

Product Reviews and Tips. Living Life With Chronic Disease. Being me really pisses me off. I’m going to tell you the truth: I am really pissed off. I am just pissed. And there’s nothing I can do about it any of it. I know I need to accept who I am and find a way to see the good in myself and my life. But what I really want to do is throw an epic temper tantrum and then hide in my bed under the covers. May 15, 2015. Posted in Auto-immune disease. Posted by akajanie on May 15, 2015. Figuring Out My Life.

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Where do I go from here . Sunday, June 3, 2012. I've realized that . The sites that really intrigued me where the ones that shot non-human subjects and if there is a person in the shoot it's a candid shoot. It started me thinking about the photo's that I take and how I tend to enjoy taking pictures of animals or nature so much more. It's always great getting an awesome picture of my kids as well, but I tend to be more naturally drawn to non human subjects. Today I wanted to go to Barnes and Noble and loo...

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