lupusranting.wordpress.com

LupusRanting

30 things about my invisible illness you may not know – 2011. September 12, 2011. 30 THINGS ABOUT MY INVISIBLE ILLNESS YOU MAY NOT KNOW. 1 The illness I live with is: Systemic Lupus Erythematosis, Sjogren’s syndrome and autoimmune hypothyroidism. 2 I was diagnosed with it in the year: 1992. 3 But I had symptoms since: I was 9 years old. 4 The biggest adjustment I’ve had to make is: avoiding UVA/UVB rays. 5 Most people assume: I’m NOT sick because I don’t often look ill. 19 It was really hard to have to g...

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LupusRanting | lupusranting.wordpress.com Reviews

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30 things about my invisible illness you may not know – 2011. September 12, 2011. 30 THINGS ABOUT MY INVISIBLE ILLNESS YOU MAY NOT KNOW. 1 The illness I live with is: Systemic Lupus Erythematosis, Sjogren’s syndrome and autoimmune hypothyroidism. 2 I was diagnosed with it in the year: 1992. 3 But I had symptoms since: I was 9 years old. 4 The biggest adjustment I’ve had to make is: avoiding UVA/UVB rays. 5 Most people assume: I’m NOT sick because I don’t often look ill. 19 It was really hard to have to g...

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LupusRanting | lupusranting.wordpress.com Reviews

https://lupusranting.wordpress.com

30 things about my invisible illness you may not know – 2011. September 12, 2011. 30 THINGS ABOUT MY INVISIBLE ILLNESS YOU MAY NOT KNOW. 1 The illness I live with is: Systemic Lupus Erythematosis, Sjogren’s syndrome and autoimmune hypothyroidism. 2 I was diagnosed with it in the year: 1992. 3 But I had symptoms since: I was 9 years old. 4 The biggest adjustment I’ve had to make is: avoiding UVA/UVB rays. 5 Most people assume: I’m NOT sick because I don’t often look ill. 19 It was really hard to have to g...

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lupusranting.wordpress.com

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one year later …. | LupusRanting

https://lupusranting.wordpress.com/2011/09/03/one-year-later

One year later …. September 3, 2011. My sister once told me that it takes about two years to settle in to a new living environment, new city, new community, new life. That would mean I am halfway through the process. Life is good in Cape. At the same time, I really do miss many aspects of my old life in my hometown. I can’t help it. Obviously, I haven’t written much this year. I was shocked to see my last post was in February. My inner slacker has been running wild. Then again, I’...3 responses ». I move...

2

Subjective Truth | LupusRanting

https://lupusranting.wordpress.com/personal-trivia

Check back, as the list will certainly get longer. 63-I thought I knew the names of all types of precipitation. However, the terms “Freezing Drizzle” and “Freezing Fog” are new. And annoying. 62-I’m not feelin the love when it comes to Christmas shopping. 61-I’m a devout American Idol fan. Simon may piss everybody off, but he’s usually correct. 60-I’m a seriously picky vegetable eater. Don’t even ask me about brussel sprouts. 58-Okra is a furry, slimy excuse of a vegetable. 49-I prefer hardware stores to...

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lfa-inc.blogspot.com

Road to a Lupus Cure: Guest Column: Summer Travel Packing List for Special Diets

http://lfa-inc.blogspot.com/2013/06/guest-column-summer-travel-packing-list.html

Join the Lupus Foundation of America as we continue down the road to finding a cure for lupus. June 17, 2013. Guest Column: Summer Travel Packing List for Special Diets. By Jessica Goldman Foung. But dietary limitations don't have to take the spontaneity or flavor out of adventures. Nor do they have to add stress to your well-deserved R and R. With a little extra effort and the following tips, anyone with any dietary needs can stay full no matter where the journey takes them. First and foremost, carry em...

lfa-inc.blogspot.com

Road to a Lupus Cure: Activists Do Make a Difference

http://lfa-inc.blogspot.com/2013/07/activists-do-make-difference.html

Join the Lupus Foundation of America as we continue down the road to finding a cure for lupus. July 16, 2013. Activists Do Make a Difference. By Kimberly Cantor, Senior Director of Public Policy and Government Relations. 8221; The Advocacy Summit is always an energizing and rewarding event, and 2013 was no exception. And to co-sponsor H.R. 460, the Patients’ Access to Treatments Act (PATA). Which seeks to ensure access to treatments for lupus and other chronic conditions. Bringing the total number of co-...

trishatruly.wordpress.com

that’s stupid |

https://trishatruly.wordpress.com/2009/10/14/thats-stupid

Just the crap in my head trying to get out. Was it something I said? Suck sucky suck suck. According to the magazine. Women rate drinking enough water over having sex. According to the women in the survey their priorities rank in order:. Keeping stress level low. Finding time to relax. Drinking the recommended amount of water. Finding time to exercise. Let’s look at that list again. 8211;Sleep AFTER sex, people! It’s the BEST sleep in the world! Keeping stress level low. 8212; Sex is a stress reliever!

lfa-inc.blogspot.com

Road to a Lupus Cure: Bringing Lupus Advocacy to Capitol Hill and Beyond - National Lupus Advocacy Summit 2013

http://lfa-inc.blogspot.com/2013/07/bringing-lupus-advocacy-to-capitol-hill.html

Join the Lupus Foundation of America as we continue down the road to finding a cure for lupus. July 01, 2013. Bringing Lupus Advocacy to Capitol Hill and Beyond - National Lupus Advocacy Summit 2013. One of the many activists to join us in Washington, DC, to reflect on her advocacy experience, including a meeting at the White House. By Erin Kotecki Vest. From the day I was diagnosed with lupus, I knew I had to do something. As part of the National Lupus Advocacy Summit. My family and I dipped back into m...

whateverbabythinks.wordpress.com

Videos of Me | Whatever Baby Thinks

https://whateverbabythinks.wordpress.com/2009/07/01/videos-of-me

Guess what I did today! The Trials and Tribulations of an 8 Week Old! July 1, 2009 · 10:16 PM. Lilah not being happy. My Noni likes the first one the best. In the second video it only took 1 minute and 18 seconds for Noni to put the camera down and pick me up. Ha! I’ve got her under my tiny thumb! Guess what I did today! The Trials and Tribulations of an 8 Week Old! 8 responses to “. July 2, 2009 at 4:31 AM. Awww lilah. you just got me longing for my own baby too. -. July 2, 2009 at 11:25 AM. Address nev...

chronicchicktalk.com

Chronic Chick Links | Chronic Chick Talk

http://www.chronicchicktalk.com/chronic-chick-links

If you would like me to add your link, let me know in a comment. Please be patient it may take me a week to add you as I have my ups and downs with the lupus. I updated the list on 11/23/08, if I missed adding you kindly let me know. I can’t fit my jeans. Getting Closer To Myself. Lupus Foundation of America. But You Don’t Look SIck. Embracing health for life. Women’s Self esteem Blog. Other Great Blog Reads. A Father’s Life Online. A life in Bloom. Everything Plus the Kitchen Sink. My children n Me.

ruminarispoonie.wordpress.com

Gravity Wars | Me Versus the Pain

https://ruminarispoonie.wordpress.com/2010/02/25/gravity-wars

Me Versus the Pain. Living a life with many diagnoses of chronic pain. I lost a battle with gravity yesterday. Big loss. Gravity wiped the floor with me. Literally. I have a giant bruise on the back of my right thigh (from the handle of the rollator, I think), a sizable bruise on my left shin (from the top bar of the rollator, I think), unhappy wrists and elbows from breaking my fall, and general pain everywhere. Ow… ow… ow…. So I’m happy that I didn’t missing anything. From → arthritis. Ruminari" and ht...

incaseimgone.com

Trying to get my life back on point | in case i'm gone

https://incaseimgone.com/2011/09/13/open-thoughts-image-test-1

Letters to my son. Trying to get my life back on point. By LeighMcG on September 13, 2011. Really girl who went to University, Graduate School and Conservatory? Your day was Costco? I’m starting this blog now to take charge. To begin again and to remind myself that I’m someone worth listening too. Stay at home mom. Its about who you touch. On behalf of all who know you…. We are so touched. October 5, 2011. I love how honest this is. I’m a new mom and feel the same way most of the time.it&#8...You have su...

alupussurvivorresource.blogspot.com

Webliography & Resources: 11.2009

http://alupussurvivorresource.blogspot.com/2009_11_01_archive.html

FDA Alert: Information on Suicidality and Antiepileptic Drugs. Actavis Recalls Certain Fentanyl Patches in the US as Precaution. FDA Issues Warning Letters to Ranbaxy Laboratories Ltd., and an Import Alert for Drugs from Two Ranbaxy Plants in India: Actions affect over 30 different generic drugs;. Banners, Badges, Books and Videos. Would you'd like to ". Email your html code for banners, badges, videos or links. Subject to approval. Audo Message: Seeking Lupus Survivors Stories. Subscribe to: Posts (Atom).

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We are dedicated to. Raising awareness of Lupus. Welcome to Lupus Racing Team. We are a Professional UCI continental racing team that is dedicated to raising awareness and funding in search of a cure for this autoimmune disease. Click here to see the latest LRT news. And please visit our great sponsors page. For more information about this disease that affects approximately 1.5 million people in the USA go to www.lupus.org. Learn More About Lupus. March 3 - 8. March 27 - 29. April 8 - 12. Bull; Learn More.

lupusranting.wordpress.com

LupusRanting

30 things about my invisible illness you may not know – 2011. September 12, 2011. 30 THINGS ABOUT MY INVISIBLE ILLNESS YOU MAY NOT KNOW. 1 The illness I live with is: Systemic Lupus Erythematosis, Sjogren’s syndrome and autoimmune hypothyroidism. 2 I was diagnosed with it in the year: 1992. 3 But I had symptoms since: I was 9 years old. 4 The biggest adjustment I’ve had to make is: avoiding UVA/UVB rays. 5 Most people assume: I’m NOT sick because I don’t often look ill. 19 It was really hard to have to g...

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lupusreallysucks.wordpress.com

Lupus Really Sucks!

Post 18: Feeling Overwhelmed and Need Feedback. I ended up in the emergency again a couple of weeks ago, primarily because my legs didn’t want to work right. They kept me there all day and ran a zillion tests including 2 MRIs and 2 different sets of blood tests (among other things). Here is the list of things they diagnosed me with:. Final: OTHER MALAISE AND FATIGUE. Final: SYSTEMIC LUPUS ERYTHEMATOSUS. Final: PAIN IN JOINT INVOLVING PELVIC REGION AND THIGH. Final: Chronic kidney disease, unspecified.

lupusrecovery.com

Lupus Diet: Natural Treatment for Systemic and Discoid Lupus Disease

The Lupus Recovery Diet. An insider shortcut guide to getting rid of lupus so that you can live a normal life again, pain free, without dangerous drugs by simple and inexpensive diet changes, not expensive supplements or products. Click here to Order the Book. You may reading this letter because you, or someone you care about, has lupus. Or maybe you're struggling to get a diagnosis, and have been told that you have a lupus like condition. This letter contains the help you've been desperately looking for.

lupusrecoverydiet.com

The Lupus Recovery Diet

The Lupus Recovery Diet. Do You Want to Get Rid of Lupus. And Live a Normal Life Again? What if you could do it with simple and inexpensive diet changes? Click here to Order the Book. You may reading this letter because you, or someone you care about, has lupus. Or maybe you’re struggling to get a diagnosis, and have been told that you have a lupus like condition. This letter contains the help you’ve been desperately looking for. I know. I’ve been where you are today. By changing the foods I eat. I under...

lupusrecoveryjourney.blogspot.com

Kedra's Journey to Health & Happiness

Kedras Journey to Health and Happiness. Wednesday, November 9, 2011. Water weight is starting to come off! Seriously it's just flying off the last few days. I have been constantly peeing. it's like someone is squeezing me like a sponge. This is great, I will be back to normal soon. sigh. Thank God! I took some before pics/weekly progress pics and will be posting them next month to show a significant difference. I'm still not taking any medications at all to help me get back to normal. Jesse is really hap...