lupusmagazine.blogspot.com
Shoyea- Gaye Grant's Articles ~ The Lupus Magazine: August 2011
http://lupusmagazine.blogspot.com/2011_08_01_archive.html
Shoyea- Gaye Grant's Articles The Lupus Magazine. Ƹ̵Ӝ̵̨̄Ʒ Lil. Miss. Butterfly Ƹ̵Ӝ̵̨̄Ʒ. Every day I fight Lupus, and it doesn't get easier. . . but giving up is not an option. Most days I smile through the pain because I refuse to allow Lupus to limit or define me . I absolutely ENJOY dancing in the rain and singing in my shower (even though I can do neither very well! View my complete profile. Sunday, 21 August 2011. The relationship between friends:. The relationship with family:. It has reached and it...
lupusmagazine.blogspot.com
Shoyea- Gaye Grant's Articles ~ The Lupus Magazine: You are not Alone
http://lupusmagazine.blogspot.com/2011/11/you-are-not-alone.html
Shoyea- Gaye Grant's Articles The Lupus Magazine. Ƹ̵Ӝ̵̨̄Ʒ Lil. Miss. Butterfly Ƹ̵Ӝ̵̨̄Ʒ. Every day I fight Lupus, and it doesn't get easier. . . but giving up is not an option. Most days I smile through the pain because I refuse to allow Lupus to limit or define me . I absolutely ENJOY dancing in the rain and singing in my shower (even though I can do neither very well! View my complete profile. Thursday, 24 November 2011. You are not Alone. You are a teen,. Your future should look bright. Society dictate...
notyouraveragelupussite.blogspot.com
Living with Lupus: September 2012
http://notyouraveragelupussite.blogspot.com/2012_09_01_archive.html
Every day struggles with helpful tips and positive inspiration. Friday, September 14, 2012. I still hurt. In a new way now. The body is funny. Just when you think you're feeling better, BAM! On a good note, I have a date for the first Lupus support group meeting in Columbia! October 4th is the big day and I can't wait. I'm putting a flyer together and I'll get them out ASAP! Well, for now this is all I can do in my condition! Links to this post. Friday, September 7, 2012. I want to scream! It gives me ti...
notyouraveragelupussite.blogspot.com
Living with Lupus: Dizzy
http://notyouraveragelupussite.blogspot.com/2013/11/dizzy.html
Every day struggles with helpful tips and positive inspiration. Monday, November 18, 2013. Getting dizzier by the moment. That can be taken two ways! Well I'm still sitting up. Still dizzy, but not nauseas. Is that a good sign of getting better or I still need the blood patch? Time to get some answers. Subscribe to: Post Comments (Atom). Lupus-What's up with that? Lupus Foundation of America. View my complete profile. The Lupus Magazine Archive. Battle Realms Winter Of The Wolf Game. On the Road to a Cure.
notyouraveragelupussite.blogspot.com
Living with Lupus: October 2012
http://notyouraveragelupussite.blogspot.com/2012_10_01_archive.html
Every day struggles with helpful tips and positive inspiration. Wednesday, October 31, 2012. Being true to myself. Lol) So, I'm taking it to social media! I have to figure out how to set up a facebook page. I know things aren't easy. I don't want easy. I like a challenge. I don't want it to feel hopeless. I need to feel like I'm making a difference and I don't anymore. (again outside of my family). My kids are making things work on their own. Which is fantastic! Live Laugh.Love.Enjoy! Links to this post.
notyouraveragelupussite.blogspot.com
Living with Lupus: December 2011
http://notyouraveragelupussite.blogspot.com/2011_12_01_archive.html
Every day struggles with helpful tips and positive inspiration. Saturday, December 17, 2011. Just when I think I have it under control, bam! Because I don't call my doctors twice a day to tell them of the pain I'm in (they don't do much if anything about the pain other than what I'm already on), I wear makeup and take care of my skin so I don't look like the living dead, I stopped seeing my therapist because I wouldn't afford her, and I try to alway have a sunny disposition- I'm fine! Links to this post.
notyouraveragelupussite.blogspot.com
Living with Lupus: April 2013
http://notyouraveragelupussite.blogspot.com/2013_04_01_archive.html
Every day struggles with helpful tips and positive inspiration. Sunday, April 7, 2013. Well I'm back in CT with the whole family. I'm actually thrilled to be back. You don't realize how good things are until you live somewhere else. CT isn't so bad. SC is a beautiful place to visit with very charming people. I look forward to visiting next year! I drove 15 hrs straight and I'm paying for it. I'm in PT and on Valium. What the f# *! This too shall pass. Good to be home! Links to this post.
notyouraveragelupussite.blogspot.com
Living with Lupus: For today
http://notyouraveragelupussite.blogspot.com/2014/07/for-today.html
Every day struggles with helpful tips and positive inspiration. Monday, July 7, 2014. Every day is a silent struggle. I know it will get better. Subscribe to: Post Comments (Atom). Lupus-What's up with that? Lupus Foundation of America. View my complete profile. The Lupus Magazine Archive. Battle Realms Winter Of The Wolf Game. On the Road to a Cure. Guest Blog: Climbing Kilimanjaro for Lupus Awareness. Lupus- What's up with that? Travel template. Powered by Blogger.
lupusmagazine.blogspot.com
Shoyea- Gaye Grant's Articles ~ The Lupus Magazine: September 2011
http://lupusmagazine.blogspot.com/2011_09_01_archive.html
Shoyea- Gaye Grant's Articles The Lupus Magazine. Ƹ̵Ӝ̵̨̄Ʒ Lil. Miss. Butterfly Ƹ̵Ӝ̵̨̄Ʒ. Every day I fight Lupus, and it doesn't get easier. . . but giving up is not an option. Most days I smile through the pain because I refuse to allow Lupus to limit or define me . I absolutely ENJOY dancing in the rain and singing in my shower (even though I can do neither very well! View my complete profile. Friday, 16 September 2011. Ƹ̵Ӝ̵̨̄Ʒ. Ƹ̵Ӝ̵̨̄Ʒ. I was in a relationship. A few years ago when I got diagnosed, wit...
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