chronicallyconstant.wordpress.com
Chronically Constant – Encouragement for the Chronically Ill
Encouragement for the Chronically Ill. Good Days and Bad Days. January 3, 2017. Several weeks ago I celebrated my birthday. As evening fell, multiple people texted and asked me if I had had a good day. I had to think carefully before answering. My initial thought was “No, not really.” My chronic illnesses make no distinction between days and don’t give me a break for holidays or my … More Good Days and Bad Days. Good Days and Bad Days. What I Learned at the Hospital. October 29, 2016. September 26, 2016.
chronicallycontent.com
Chronically Content – Chronically Ill Christian, Challenged to be Content
Chronically Ill Christian, Challenged to be Content. The Search That Never Ends. March 18, 2018. March 16, 2018. Yesterday was my long-awaited rheumatology appointment. Such a high level of anticipation led up to this day. Since I had finally found a diagnosis of Sjogren’s Syndrome, all I needed was for it to be official. Then, I should be able to receive some medical help. Nothing is ever as simple as it seems. After a thorough physical exam and …. CPAP: My New BFF. March 10, 2018. World Kidney Day 2018.
chronicallycool.com
Chronically Cool for kids with chronic illness | Home
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chronicallycourageous.wordpress.com
Chronically courageous | Because life is nothing but a grand adventure, with a few bumps in the road
Because life is nothing but a grand adventure, with a few bumps in the road. A year of falling in love with being alive: the paradox of life and death. 1 year, 12 months, 365 days, 8760 hours, 525,600 minutes, 31,536,00 seconds. Continue reading →. How do these genes make me look? Me attempting to blog for the last few months. Continue reading →. Traveling With Some Extra Baggage. Two steps forward, one step back. Continue reading →. Thankful (a really original title). I am antsy about these kinds of thi...
chronicallycourtney.com
Chronically Courtney - Finding the Funny in Chronic Pain
Check Me Out On Tumblr! December 15, 2016. When I was a teenager I wanted nothing more than to be normal; with my super short, curly, mousy coloured chemo hair I stuck out like a sore thumb. Luckily in high school everyone was so wrapped up in their own lives and drama that people barely gave me so much as a passing glance on their way to English class. And I grew comfortable in my invisibility. I was never the best at anything. I barely scratched the surface of. Most of the time. But I was. I know I hav...
chronicallycrafted.blogspot.com
ChronicallyCrafted
Monday, 2 May 2011. Belated BADD Post: Mobility Scooters and the Posts I Didn't Write. This is a post about mobility scooters, but it's also about the posts I didn't write. Or I'd get scared. See, the things I want to write about are difficult. I want to write about the numerous failings of ATOS medicals. About the demonization of benefit applicants in the media. Instead of helping us, about how stories about ME are covered in the media. I won't be silent, but I have to take small steps. So I decided...
chronicallycrafting.blogspot.com
Chronically Crafting Fibro Fighter
Chronically Crafting Fibro Fighter. I have Fibro and want to be grateful for the things this illness has given me NOT focus on the things it has taken away. It is a battle to remain optimistic but My family and friends, Crafting and the prescription drugs do help! Tuesday, 28 July 2015. Stampotique - background using household objects. The challenge over at Stampotique designers challenge. Is to create your own background using a household object! I mounted it onto kraft card that I inked a stripey patte...
chronicallycrazy.blogspot.com
Chronically Crazy Musings: Life With Chronic Lymphocytic Leukemia
Chronically Crazy Musings: Life With Chronic Lymphocytic Leukemia. Friday, October 5, 2012. Right now I am feeling like CLL is a cake walk. AMAZINGLY, I just want to go back to having plain old CLL. In boring ol' CLL news, my numbers at the oncologists office last week were.the same! In fact there was a slight downward trend. Nothing major, but hey! Tuesday, June 26, 2012. I really just get so exhausted at the thought of going in to the oncologist. Its like a test. Did I pass? Have I exercised enough?
chronicallycrazy.wordpress.com
Chronically Crazy
The Fibro Toybox Part II – All things not Barbie. And on that note: me way-loh koh-koh. Just kidding, no more sleep for me just yet. I’ve got a baby to care for and I need try not to turn into a slinky on the staircase. If anyone has an illness-to-toy comparison to make I’d really love to read them in the comments. This entry was posted on February 2, 2014 and tagged chronic pain. The fibro toybox Part I or Why I’m a Barbie. Me as Teacher Barbie. How does it feel? Her back is a solid length of plastic; s...
chronicallycreative.net
Chronically Creative
Celebrating life and creativity in spite of illness. Dream create. celebrate. Where there is creativity, there is hope." Donna Karan. Friday, March 16, 2018. Picking up My Pen Again. While taking a (forced) break from blogging I've been occupied with trying to get my health back on track. I've been seeking help from an integrative practitioner and trying alternative treatments which I haven't had access to in mainstream medicine. (I posted briefly about it on Instagram. If you're interested.). We didn't ...
