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Chronically Ill | My journey through chronic illness as a young adultMy journey through chronic illness as a young adult
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My journey through chronic illness as a young adult
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Chronically Ill | My journey through chronic illness as a young adult | chronically89.wordpress.com Reviews
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My journey through chronic illness as a young adult
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Chronically Ill | My journey through chronic illness as a young adult | Page 2
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My journey through chronic illness as a young adult. September 4, 2015. September 4, 2015. All new posts are only on chronically89.com. From now on. Please come a pay me a visit and follow me and my journey there 🙂. This will be my last post on here. Take care guys! Thanks for the support! September 2, 2015. September 2, 2015. I hope all my old posts and comments have been moved successfully and I apologise if anything has been lost during the moving process! So please follow me on chronically89.com.
April | 2016 | Chronically Ill
https://chronically89.wordpress.com/2016/04
My journey through chronic illness as a young adult. April 27, 2016. My god I feel like I’m dying today. I have been out more so than usual over these last few days (yay! But it has definitely caught up with me now (boo! When I Feel Like Everyone Moved On While I’m Stuck in My Life With Chronic Illness. April 21, 2016. Article from http:/ themighty.com/2016/04/feeling-stuck-in-life-and-left-out-with-chronic-illness/. That u can definitely relate to in many ways. Well, that’s how I’ve been feeling. I don’...
Brain fog | Chronically Ill
https://chronically89.wordpress.com/2016/03/02/brain-fog
My journey through chronic illness as a young adult. March 2, 2016. Utm source=Facebook&utm medium=ChronicIllness Page&utm campaign=ChronicIllness. I definitely know what this feels like and I hate it. Yesterday I referred to an item of clothing as blue about ten times before my mum corrected me to say it was green. Ugh. What chronic fatigue feels like. I miss my life →. 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).
June | 2016 | Chronically Ill
https://chronically89.wordpress.com/2016/06
My journey through chronic illness as a young adult. This pic is definitely my today. June 13, 2016. Ugh what a day today. I slept really bad last night (overthinking is a b*tch! But didn’t feel that bad this morning. After a few minutes at work I just started to feel so low. I haven’t felt this low in a while. I just wanted to burst into tears at any moment! Lots of girls have cried before at work but I have never done it! This pic is definitely my today. What chronic fatigue feels like.
September | 2015 | Chronically Ill
https://chronically89.wordpress.com/2015/09
My journey through chronic illness as a young adult. September 4, 2015. September 4, 2015. All new posts are only on chronically89.com. From now on. Please come a pay me a visit and follow me and my journey there 🙂. This will be my last post on here. Take care guys! Thanks for the support! September 2, 2015. September 2, 2015. I hope all my old posts and comments have been moved successfully and I apologise if anything has been lost during the moving process! So please follow me on chronically89.com.
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How I make myself sick | In The Lupus
https://inthelupus.org/2014/07/18/how-i-make-myself-sick
Staying in the Loop and Living with Lupus. How I make myself sick. July 18, 2014. This about sums it up. Thanks for sharing @livingincurably! What Does a Lupus Flare Feel Like? Three Cheers for Stem Cells… →. Tell me what you're thinking and 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. Build a ...
Letting Life with Lupus Out of the Bag | In The Lupus
https://inthelupus.org/2014/05/30/letting-life-with-lupus-out-of-the-bag
Staying in the Loop and Living with Lupus. Letting Life with Lupus Out of the Bag. May 30, 2014. Here I am, the face of people living life (and doing pretty well) with Lupus. Well folks, I told the whole world that I have Lupus today. New Republic Magazine just posted an article that tells the story of how I was able to start my own business and live a healthy happy life because of Obama Care gave me the option of buying my own insurance coverage. Here is how it all unfolded. January 6, 2014. I knew ther...
Will I ever get home? – Peachy Peonys
https://peachypeonys.wordpress.com/2015/08/29/will-i-ever-get-home
I'm a pretty sick dude. Will I ever get home? Will I ever get home? August 29, 2015. Haven’t settled in too hospital. Today has gone so slow. I woke up at 5am and I’m just waiting for the day to end. I wish they would give me something to just knock me so I could wake up when I’m better. Sadly they can’t do that, I’ve asked…. I’m so desperate to just be better and home. I need to go home…. Takeing tubes down the nose. 2 thoughts on “ Will I ever get home? August 30, 2015 at 2:35 pm. Will I get better?
Going up. – Peachy Peonys
https://peachypeonys.wordpress.com/2015/09/03/going-up
I'm a pretty sick dude. September 3, 2015. I finally put on some weight. Thank Jesus. I don’t know how long exactly they want the tube in me because they said they just want to fatten me up so that I can have a buffer for when I get sent home and it isn’t critical or anything if I lose weight. So putting on weight is a plus! Do they mean like 60kg? Like I have no clue. Thus, no clue in when I’m going home. Nup Bloody trigger her PTSD and tell her to eat with the tube. She’ll be right 😉. Liked by 1 person.
Back in hell – Peachy Peonys
https://peachypeonys.wordpress.com/2015/08/28/back-in-hell
I'm a pretty sick dude. August 28, 2015. August 28, 2015. I’m back in hell. I can’t deal with it my mind has left the building. I’ve been the biggest bitch to everyone but I do that cause I feel like people are more likely to listen to someone who shocked them compared to a laid back person. Will I ever get home? 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). Notify me of new comments via email. Will I get better?
What Does a Lupus Flare Feel Like? | In The Lupus
https://inthelupus.org/2014/07/14/what-does-a-lupus-flare-feel-like
Staying in the Loop and Living with Lupus. What Does a Lupus Flare Feel Like? July 14, 2014. July 18, 2014. Someone just asked what a Lupus Flare feels like and I answered:. Here is what the tiny. What does it feel like for you? Post a comment or follow on Facebook. And talk to me there! Keeping an Eye on Plaquenil. How I make myself sick →. 2 thoughts on “ What Does a Lupus Flare Feel Like? July 15, 2014 at 5:17 pm. July 15, 2014 at 7:09 pm. Tell me what you're thinking and leave a reply Cancel reply.
Doctor Patient Relations | In The Lupus
https://inthelupus.org/category/doctor-patient-relations
Staying in the Loop and Living with Lupus. Pancreas and Spleen Unremarkable: Knowing Yourself Inside and Out. February 3, 2015. February 3, 2015. Ladies and Gents do you what it feels like when you know something is off? You can’t put your finger on exactly what is going awry, but you know something (other than your normal lupus symptoms) just isn’t right? I have been feeling like that lately and not to sound like an armchair rheumatologist, but I think it is my thyroid. Annals of the Rheumatic Diseases.
Events | In The Lupus
https://inthelupus.org/category/events
Staying in the Loop and Living with Lupus. The Walk to End Lupus in Your Area. March 31, 2014. March 31, 2014. Looking for a walk in your neck of the woods? Here is link to all the information you need:. Http:/ www.lupus.org/action/walk-to-end-lupus-now? Welcome to a place to stay in the loop of living with Lupus. Follow Blog via Email. Enter your email address to follow this blog and receive notifications of new posts by email. Join 268 other followers. Follow In The Lupus on WordPress.com.
Medicine | In The Lupus
https://inthelupus.org/category/uncategorized/medicine
Staying in the Loop and Living with Lupus. More Than the Sum of our Parts. August 21, 2015. August 21, 2015. Results of a study about how we think of Lupus and why it matters. Doctors and researchers. They are the ones to make all of the difference. The study comes to this rational, logical conclusion (if scientists come to conclusions, I am never sure on that):. From: Nature Reviews Rheumatology, 11, 385 386, (2015) doi:10.1038/nrrheum.2015.61, Published online, 05 May 2015. February 3, 2015. I brought ...
Flares | In The Lupus
https://inthelupus.org/category/flares
Staying in the Loop and Living with Lupus. Tracking Lupus from Both Sides of the Stethoscope. November 26, 2014. I was surfing Facebook this morning and I came upon a posted video from Lupus Foundation of America (LFA) called:. LFA-Real(tm) System is First-of-its-Kind Tool to Monitor Disease Activity. This caught my attention because this is more than a tool for physicians. The system has two parts:. A doctor’s assessment of a patient’s lupus disease activity. And by the way, it is free. Other than massi...
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chronically (Emma Krijnen) | DeviantArt
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chronically in a sentence | simple examples
In A Sentence .org. The best little site that helps you understand word usage with examples. Chronically in a sentence. EARECKSON TADA: Well, Im what they call chronically disabled. Denying other educational options to children stuck in chronically failing schools is legalized cruelty. Nutritional status assessment in chronically ill children. Both Clinton and Gates have pushed for more funding for what they call a chronically underfunded State Department. Use extramarital in a sentence. The study was co...
chronically20something.wordpress.com
Chronically Twenty Something | The adventures of a chronically ill twenty something year old woman. #spoonie
The adventures of a chronically ill twenty something year old woman. #spoonie. 10 Quotes That Helped Me Fight Chronic Illness. January 7, 2017. I have often throughout my battle found comfort, hope or strength in literature. These words have carried me through the darkest of times, and I feelcthat most people will be able to find strength in them. May they bless you, as they have blessed me. 8220;Some women are lost in the fire. Some women are built from it.” – Michelle K. 8220;Whatever you are physicall...
Chronically 3D - 3D Printing for the Cannabis Community
Chronically 3D - 3D Printing for the Cannabis Community
Chronically Ill | My journey through chronic illness as a young adult
My journey through chronic illness as a young adult. This pic is definitely my today. June 13, 2016. Ugh what a day today. I slept really bad last night (overthinking is a b*tch! But didn’t feel that bad this morning. After a few minutes at work I just started to feel so low. I haven’t felt this low in a while. I just wanted to burst into tears at any moment! Lots of girls have cried before at work but I have never done it! April 27, 2016. But it has definitely caught up with me now (boo! April 21, 2016.
chronicallyabsent.deviantart.com
chronicallyAbsent - DeviantArt
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chronicallyacademic.blogspot.com
Chronically Academic
Saturday, 10 December 2016. Ten Ways to Make Conferences Accessible to People with Disabilities. Written by Debra Guckenheimer. Debra kindly gave us permission to re-post this article from medium.com. The original can be found here:. Attending workshops, lectures, symposium, conferences, and other events are difficult or even impossible for some people with disabilities. Rarely have I seen disability given much thought in conference planning, even when the topic is diversity and inclusion. Include a stat...
chronicallyadorninggrace.wordpress.com
Chronically Adorning Grace | My "adventures" through the pain infiltration…
My adventures through the pain infiltration…. January 1, 2013. Another New Year…. I’m sitting here thinking about what 2013 will be like and I can’t shake off the feelings of anxiety that come with it. I know, I know, I over analyze everything and bring this all upon myself. However, I don’t think I’m the only one who feels this way. Especially, if you’re a chronic pain sufferer. I never make resolutions for the new year. Why you ask? A simple act of kindness goes a long way. Hold a door open for som...
chronicallyaskew
Bacardí Limón (pre-iPod). Hey Hey My My. CARE for Sandy (branding). CARE for Sandy (before/after). Poster postcard interactive flash banner. Crossword puzzles for Visual Arts Press. Consumer print OOH (copy art). Whole in the Wall. Helenbeck Gallery, Paris and NYC). DIRECTV NFL Flying Toy Promo. Sweepstakes insert as seen in Sports Illustrated and ESPN. Branded print OOH packaging galore. Global photo restoration charity (Founder). Unusual POP paper engineering. DIRECTV NFL Sunday Ticket.
The Chronically Awesome Foundation ⋆ Supporting the needs of the chronically awesome through peer support and artistic expression
What is Chronically Awesome? Chronically Awesome Featured Partners. DrugRehab.com: 2017 Featured Partner. Real Talk with Miss Florida 2017 Sara Zeng. Chronic Chronicles Podcast: Addiction Awareness. April Is Alcohol Awareness Month. Addiction Isn’t a Choice. The Stigma Surrounding Addiction. The Mesothelioma Center: Our 2016 Featured Partner. Tips to Being Chronically Awesome. News You Can Use. Fibromyalgia Resources and Support. Bipolar: Resources, Support & Information. Individual and Group Support.
