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Lupie Life

Saturday, April 26, 2014. I'll jump right into the nitty gritty here. I've been on Methotrexate now for almost a year and a half. For those of you who do not know what Methotrexate is, it is an oral chemotherapy drug used to treat various kinds of cancer and in select moderate to severe autoimmune disorders. Why chemotherapy for Lupus? I think this winter I consumed more chocolate than I ever had in the rest of my life. Dark chocolate of course. Nothing but the best for those steroid cravings. Nope There...

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Lupie Life | lupielife.blogspot.com Reviews
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Saturday, April 26, 2014. I'll jump right into the nitty gritty here. I've been on Methotrexate now for almost a year and a half. For those of you who do not know what Methotrexate is, it is an oral chemotherapy drug used to treat various kinds of cancer and in select moderate to severe autoimmune disorders. Why chemotherapy for Lupus? I think this winter I consumed more chocolate than I ever had in the rest of my life. Dark chocolate of course. Nothing but the best for those steroid cravings. Nope There...
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Lupie Life | lupielife.blogspot.com Reviews

https://lupielife.blogspot.com

Saturday, April 26, 2014. I'll jump right into the nitty gritty here. I've been on Methotrexate now for almost a year and a half. For those of you who do not know what Methotrexate is, it is an oral chemotherapy drug used to treat various kinds of cancer and in select moderate to severe autoimmune disorders. Why chemotherapy for Lupus? I think this winter I consumed more chocolate than I ever had in the rest of my life. Dark chocolate of course. Nothing but the best for those steroid cravings. Nope There...

LINKS TO THIS WEBSITE

corislupusupdates.blogspot.com corislupusupdates.blogspot.com

My Lupus Update: Frustration

http://corislupusupdates.blogspot.com/2012/04/frustration.html

So I am going to put together my own Lupus site. So many people ask what's going on and I'm not sure how much they really want to know. so I am going to keep everyone posted here. I hope that other "Lupies" will find my site and post comments on how they have done things to survive. Wednesday, April 18, 2012. I have been playing with this post in my head for a few weeks now. But this weekend really set off my frustrations. Why do I do this to myself? Why do I think that any drug will make me "normal"?

corislupusupdates.blogspot.com corislupusupdates.blogspot.com

My Lupus Update: Put on Purple for Lupus

http://corislupusupdates.blogspot.com/2012/04/put-on-purple-for-lupus.html

So I am going to put together my own Lupus site. So many people ask what's going on and I'm not sure how much they really want to know. so I am going to keep everyone posted here. I hope that other "Lupies" will find my site and post comments on how they have done things to survive. Wednesday, April 18, 2012. Put on Purple for Lupus. On May 18th the Lupus Foundation of America is hosting a "Put on Purple for Lupus" event. The goal is to get people to wear purple to raise awareness for Lupus.

corislupusupdates.blogspot.com corislupusupdates.blogspot.com

My Lupus Update: What World Lupus day & Lupus Awareness Month mean to me

http://corislupusupdates.blogspot.com/2012/05/what-world-lupus-day-lupus-awareness.html

So I am going to put together my own Lupus site. So many people ask what's going on and I'm not sure how much they really want to know. so I am going to keep everyone posted here. I hope that other "Lupies" will find my site and post comments on how they have done things to survive. Thursday, May 10, 2012. What World Lupus day and Lupus Awareness Month mean to me. No more Dr. House jokes, let's get rid of this once and so no one else has to deal with this! Subscribe to: Post Comments (Atom).

corislupusupdates.blogspot.com corislupusupdates.blogspot.com

My Lupus Update: May 2012

http://corislupusupdates.blogspot.com/2012_05_01_archive.html

So I am going to put together my own Lupus site. So many people ask what's going on and I'm not sure how much they really want to know. so I am going to keep everyone posted here. I hope that other "Lupies" will find my site and post comments on how they have done things to survive. Thursday, May 10, 2012. What World Lupus day and Lupus Awareness Month mean to me. No more Dr. House jokes, let's get rid of this once and so no one else has to deal with this! Subscribe to: Posts (Atom). My Wife has Lupus.

corislupusupdates.blogspot.com corislupusupdates.blogspot.com

My Lupus Update: October 2011

http://corislupusupdates.blogspot.com/2011_10_01_archive.html

So I am going to put together my own Lupus site. So many people ask what's going on and I'm not sure how much they really want to know. so I am going to keep everyone posted here. I hope that other "Lupies" will find my site and post comments on how they have done things to survive. Wednesday, October 26, 2011. Now my infusions are monthly, so I guess time will tell. Tuesday, October 18, 2011. Benlysta and Other feelings. So far other than the two days after each infusion I feel my normal. It's just inte...

corislupusupdates.blogspot.com corislupusupdates.blogspot.com

My Lupus Update: July 2012

http://corislupusupdates.blogspot.com/2012_07_01_archive.html

So I am going to put together my own Lupus site. So many people ask what's going on and I'm not sure how much they really want to know. so I am going to keep everyone posted here. I hope that other "Lupies" will find my site and post comments on how they have done things to survive. Thursday, July 5, 2012. A brief background for you before I get into the real motivation for this post. A feeling I haven't really felt this strongly in several months. Today I was studying Ruth for a weekly bible study I am ...

corislupusupdates.blogspot.com corislupusupdates.blogspot.com

My Lupus Update: April 2012

http://corislupusupdates.blogspot.com/2012_04_01_archive.html

So I am going to put together my own Lupus site. So many people ask what's going on and I'm not sure how much they really want to know. so I am going to keep everyone posted here. I hope that other "Lupies" will find my site and post comments on how they have done things to survive. Wednesday, April 18, 2012. Put on Purple for Lupus. On May 18th the Lupus Foundation of America is hosting a "Put on Purple for Lupus" event. The goal is to get people to wear purple to raise awareness for Lupus. I had made p...

corislupusupdates.blogspot.com corislupusupdates.blogspot.com

My Lupus Update: July 2012

http://corislupusupdates.blogspot.com/2012/07/july-2012.html

So I am going to put together my own Lupus site. So many people ask what's going on and I'm not sure how much they really want to know. so I am going to keep everyone posted here. I hope that other "Lupies" will find my site and post comments on how they have done things to survive. Thursday, July 5, 2012. A brief background for you before I get into the real motivation for this post. A feeling I haven't really felt this strongly in several months. Today I was studying Ruth for a weekly bible study I am ...

corislupusupdates.blogspot.com corislupusupdates.blogspot.com

My Lupus Update: Update

http://corislupusupdates.blogspot.com/2012/03/update.html

So I am going to put together my own Lupus site. So many people ask what's going on and I'm not sure how much they really want to know. so I am going to keep everyone posted here. I hope that other "Lupies" will find my site and post comments on how they have done things to survive. Tuesday, March 27, 2012. Not much new to update on my end. Wait, I take that back. I have been putting off posting for so long I haven't give you the latest update. so here goes. Subscribe to: Post Comments (Atom).

corislupusupdates.blogspot.com corislupusupdates.blogspot.com

My Lupus Update

http://corislupusupdates.blogspot.com/2012/06/like-last-year-i-will-be-giving-away.html

So I am going to put together my own Lupus site. So many people ask what's going on and I'm not sure how much they really want to know. so I am going to keep everyone posted here. I hope that other "Lupies" will find my site and post comments on how they have done things to survive. Friday, June 22, 2012. Like last year I will be giving away a Disney gift basket that will include 2 one day park hopper passes to a Disney park*. Pictures will be posted next couple of weeks. Join our team HERE.

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Livin' La Vida Lupie. Living, loving and laughing with lupus. Skip to primary content. Skip to secondary content. It’s All About Perspective. July 23, 2012. Picture this: a fat, 49-year-old on roller skates, dressed in full body armor (or so it seems, with all the head-to-toe protective gear), using walking poles for balance, creeping along, trying not to fall too often or too hard. 8221; His mom replied, “That’s roller skating.”. As long as I’m still impressing them, I’ll be okay. 😉. The Gift of Joy.

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Purple Healers, Inc.

Purple Healers, Inc. Saturday, December 19, 2009. Purple Healers, Inc. Purple Healers was the name of Kesha’s lupus walk team when she participated in her first Walk for Lupus Now walk in Oklahoma City, OK at the zoo in 2007 and Kesha chose that as the name of her organization too. Her “Purple Healers” dream became more than she ever thought that it would be. Labels: A Non-Profit Organization. Subscribe to: Posts (Atom). Purple Healers, Inc. I am a lupus fighter and survivor! I am the President of Purple...

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Lupie Hugs - Blankets for Lupus - Lupie Wrap

Purple Healers, Inc. 4 Lupus. Links to Partners websites. Thank you for visiting the Lupie Hugs website! Please look through the pages of our site and contact us with any questions. Thank you for visiting www.lupiehugs.com! Be sure to visit our donations page to show your support and aid in Lupus research. Links to Partners websites. A Fighter and Lupus Warrior. Smiling Everyday, CO. 169; 2018 Purple Healers, Inc. 4Lupus. This site built at www.EchoFireSites.com.

lupielady.com lupielady.com

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lupielife.blogspot.com lupielife.blogspot.com

Lupie Life

Saturday, April 26, 2014. I'll jump right into the nitty gritty here. I've been on Methotrexate now for almost a year and a half. For those of you who do not know what Methotrexate is, it is an oral chemotherapy drug used to treat various kinds of cancer and in select moderate to severe autoimmune disorders. Why chemotherapy for Lupus? I think this winter I consumed more chocolate than I ever had in the rest of my life. Dark chocolate of course. Nothing but the best for those steroid cravings. Nope There...

lupieliving.blogspot.com lupieliving.blogspot.com

Living Life as a Lupie

Living Life as a Lupie. Lawyer. Photographer. Wife. Mother. Daughter. Sister. Friend. And a Lupie. I moved: please follow me on www.lupieliving.com. Thank you for following me. I moved to www.lupieliving.com. You can also follow me on Instagram @lindalupie. Sunday, October 26, 2014. It's the best kind of cancer". Hmmmm . . . the problem with this reasoning is that it's still cancer. CANCER. So as my surgery date for the total removal of my thyroid gland approaches, I have to muse about how I'm feeling.

lupieliving.com lupieliving.com

Lupieliving | living with lupus, day by day, moment by moment

Living with lupus, day by day, moment by moment. The Affordable Care Act in Danger. November 10, 2016. It was a dark day for many Hillary supporters today. And some nonchalantly dismissed the potential harm of having Trump as our president-elect with a “how much damage can he possibly do? 8221; It remains to be seen if he follows through with his promise of racist and misogynistic policies. I hope not. October 22, 2016. And so why do I keep going? With my body being what it is, I am thankful that I can e...

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Lupie Loops

CLICK HERE FOR FREE BLOGGER TEMPLATES, LINK BUTTONS AND MORE! My life with Lupus. God only gives exceptional people Lupus; the ordinary ones can't handle it. -Dynamo. Saturday, February 26, 2011. We have 3 girls that can all be very sweet and very NOT! Lately we have been dealing with a Bi-polar child and that in itself is difficult, throw in a 6yr old sassy pants and a 16yr old drama queen and you can just imagine our house! Maybe I need to make an appointment with the doc and see about changing my depr...

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Lupieloop Chronicles | My journey living with a chronic illness and other observations.

My journey living with a chronic illness and other observations. 8220;Little Becomes Much”. November 23, 2014. Http:/ www.npr.org/2014/11/21/365433685/if-we-left-they-wouldnt-have-nobody. If you haven’t, please listen to the story above. I am so grateful for these young men. No, there wasn’t one of my family members in the facility, but it could have been. Isn’t it something how GOD can use something in your past that the devil meant for evil, to help someone else! He used a cook and a janitor who helped...

lupieloveandlaughter.blogspot.com lupieloveandlaughter.blogspot.com

Lupie Love and Laughter

Lupie Love and Laughter. I created my own blog as an outlet to convey my daily feelings of frustration, anger, and acceptance in dealing with a connective tissue disease (lupus). Maybe by telling my story, I will help others who are going through a similar situation or shed some light on a condition that often does not get the exposure it deserves. View my complete profile. Sunday, August 21, 2011. Thursday, August 11, 2011. Insanity Day 13 and going Strong. That's all I can say. In one week I can se...