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Redefining Myself... with Lupus and MS

Welcome to Redefining Myself! While living with NP-SLE, RRMS and CIDP. And their overlapping accessories. Slapping the face of many things demyelinating. Sunday, August 11, 2013. Links to this post. This weeks Sound of Crickets Award goes to:. Okay, let me get this straight. My illness is causing you hardship? SickChickPMA #CNSGrrrl #SickChickHumor #SoundofCricketsAward #RedefiningMyself. Take Time for Reflection. Text and image ©2013 Brian Goslow. Saturday, August 10, 2013. I Do Not Need Your Help!

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Redefining Myself... with Lupus and MS | redefiningmyself.com Reviews
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Welcome to Redefining Myself! While living with NP-SLE, RRMS and CIDP. And their overlapping accessories. Slapping the face of many things demyelinating. Sunday, August 11, 2013. Links to this post. This weeks Sound of Crickets Award goes to:. Okay, let me get this straight. My illness is causing you hardship? SickChickPMA #CNSGrrrl #SickChickHumor #SoundofCricketsAward #RedefiningMyself. Take Time for Reflection. Text and image ©2013 Brian Goslow. Saturday, August 10, 2013. I Do Not Need Your Help!
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Redefining Myself... with Lupus and MS | redefiningmyself.com Reviews

https://redefiningmyself.com

Welcome to Redefining Myself! While living with NP-SLE, RRMS and CIDP. And their overlapping accessories. Slapping the face of many things demyelinating. Sunday, August 11, 2013. Links to this post. This weeks Sound of Crickets Award goes to:. Okay, let me get this straight. My illness is causing you hardship? SickChickPMA #CNSGrrrl #SickChickHumor #SoundofCricketsAward #RedefiningMyself. Take Time for Reflection. Text and image ©2013 Brian Goslow. Saturday, August 10, 2013. I Do Not Need Your Help!

INTERNAL PAGES

redefiningmyself.com redefiningmyself.com
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Redefining Myself... with Lupus and MS: Links to Other Sites

http://www.redefiningmyself.com/p/links-to-other-sites.html

Welcome to Redefining Myself! While living with NP-SLE, RRMS and CIDP. And their overlapping accessories. Slapping the face of many things demyelinating. Links to Other Sites. Page last modified on September 18, 2010. Patient Run Friendly Sites and Forums:. Lupus MCTD Foundation of America. Wide World of Lupus. My Life Works Today! Ardent Cerebrations: Musings of a Lupus Survivor. APS Foundation of America. All About Multiple Sclerosis. University California of San Francisco MS Center. Could I Have Lupus?

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Redefining Myself... with Lupus and MS: November 2011

http://www.redefiningmyself.com/2011_11_01_archive.html

Welcome to Redefining Myself! While living with NP-SLE, RRMS and CIDP. And their overlapping accessories. Slapping the face of many things demyelinating. Thursday, November 24, 2011. The Person that I am Becoming. That is one of the finest spiritual paradoxes I've experienced. Oh hell, I assure you that my journey can not be done in isolation! I haven't been able to weather this thing called alone! Most of the people in this world do not suffer from character disorders and are not evil, living against Sp...

3

Redefining Myself... with Lupus and MS: Bio

http://www.redefiningmyself.com/p/bio.html

Welcome to Redefining Myself! While living with NP-SLE, RRMS and CIDP. And their overlapping accessories. Slapping the face of many things demyelinating. I do not know whether I was then a man dreaming I was a butterfly or whether I am now a butterfly dreaming I am a man." Chang-tzu. I'm a NP-SLE and MS patient advocate. That networks with other Lupus and MS patient advocates with the commonality of raising public awareness and most importantly, to inspire, educate and empower other patients. I am the mo...

4

Redefining Myself... with Lupus and MS: August 2013

http://www.redefiningmyself.com/2013_08_01_archive.html

Welcome to Redefining Myself! While living with NP-SLE, RRMS and CIDP. And their overlapping accessories. Slapping the face of many things demyelinating. Sunday, August 11, 2013. This weeks Sound of Crickets Award goes to:. Okay, let me get this straight. My illness is causing you hardship? SickChickPMA #CNSGrrrl #SickChickHumor #SoundofCricketsAward #RedefiningMyself. Take Time for Reflection. Text and image ©2013 Brian Goslow. Links to this post. Saturday, August 10, 2013. I Do Not Need Your Help!

5

Redefining Myself... with Lupus and MS: January 2013

http://www.redefiningmyself.com/2013_01_01_archive.html

Welcome to Redefining Myself! While living with NP-SLE, RRMS and CIDP. And their overlapping accessories. Slapping the face of many things demyelinating. Wednesday, January 23, 2013. Beware of the pity-pot. I've explained to my baby preteen girl, that even though by American standards that we are living at the poverty level, we are still so blessed to have a roof over our heads (even though it is a fight to keep it over our heads, which I'm sure a few of you can relate to). One Ukrainian neurologist expl...

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lupusmagazine.blogspot.com 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 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...

kristelgoodspeedcorrea.wordpress.com kristelgoodspeedcorrea.wordpress.com

Goodbye to the Lupus Magazine (April 2010 – December 2011) – | Lupus & RA~ A lil of this and that

https://kristelgoodspeedcorrea.wordpress.com/2011/12/08/goodbye-to-the-lupus-magazine-april-2010-december-2011

Favorite Lupus Awareness Videos. My old Internet Archived Poems. The dark side My Rashes/Bruises/etc. My List of the Monsters of Autoimmunity. Lupus and RA A lil of this and that. Goodbye to the Lupus Magazine (April 2010 – December 2011) –. Published December 8, 2011. You are an amazing individual and I hope that some of your awesomeness has rubbed off on me too😉 lol I wish you all the best, Geoff and will always be proud of you. Love you xxooxx. Leave a Reply Cancel reply. Enter your comment here.

debrafreemanhighberger.blogspot.com debrafreemanhighberger.blogspot.com

Debra Freeman Highberger: December 2011

http://debrafreemanhighberger.blogspot.com/2011_12_01_archive.html

Thursday, December 1, 2011. During the entire month of November, I heard people expressing how much they were thankful for. Every day they posted what that day’s worth was. They described the usual: family, friends, and in some instances health or fractions of good health which is often the case for a lupus patient. I read each one of these acclamations and wondered, “Is everyone really internalizing these thoughts? Are they mere lists that one feels obligated to write? At the age of 25 I owned a photogr...

debrafreemanhighberger.blogspot.com debrafreemanhighberger.blogspot.com

Debra Freeman Highberger: January 2012

http://debrafreemanhighberger.blogspot.com/2012_01_01_archive.html

Monday, January 30, 2012. A GLIMPSE INTO A WORLD I ONCE WALKED. February brings to mind many things in my life. There is of course, Valentine’s Day and a time to reflect on love. But I want to talk about something more primitive then love. I want to talk about the power of touch. Then four months later I got my answer. I turned to the feel of a tiny tap on my shoulder. Links to this post. Sunday, January 1, 2012. So it begins, a. Some may call these New Year’s resolutions. I have never liked th...Glance ...

debrafreemanhighberger.blogspot.com debrafreemanhighberger.blogspot.com

Debra Freeman Highberger: Desire: The Root of my Existence

http://debrafreemanhighberger.blogspot.com/2011/08/desire-root-of-my-existence.html

Wednesday, August 24, 2011. Desire: The Root of my Existence. We are all born with it. Some use it to its full potential …others not so much. For some poor souls they lose it later in life. I am talking about the feeling of desire. Desire and succeeding takes on a whole new meaning, it is mixed in the soup of the desires we are born with. Have you fulfilled all that you want or are there areas in your life that have been left undone? November 12, 2015 at 9:05 PM. Subscribe to: Post Comments (Atom). Have ...

debrafreemanhighberger.blogspot.com debrafreemanhighberger.blogspot.com

Debra Freeman Highberger: IT TAKES A SPECIAL MAN TO LOVE A LUPUS LADY

http://debrafreemanhighberger.blogspot.com/2011/07/it-takes-special-man-to-love-lupus-lady.html

Saturday, July 23, 2011. IT TAKES A SPECIAL MAN TO LOVE A LUPUS LADY. What are the qualities of man that has the desire to take care of a woman with an illness? Certainly there are some men that find themselves in the position where their loved one comes down with this long after they met. But what about the man that falls in love with a woman who has lupus? Is it a way one looks or perhaps acts? And in the process change me completely” But did he? Certainly there is always their “fantasy woman&#82...

debrafreemanhighberger.blogspot.com debrafreemanhighberger.blogspot.com

Debra Freeman Highberger: Benlysta

http://debrafreemanhighberger.blogspot.com/2011/11/benlysta.html

Wednesday, November 2, 2011. It is 9 am November1, 2011. I am at the Brigham. And Women’s Hospital in Boston. I am getting my monthly Benlysta infusion. Benlysta is the first lupus drug approved in over 50 years. I am one of the fortunate patients that is getting it. I am grateful for this drug because of how much it has given back to me. I had noticed the positive effects of it almost from the start. The first infusion I had was a few days after July 4. Five years later, what this new drug has done for ...

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redefiningmysanity

Wednesday, December 18, 2013. Quick Survey - For the UK folks, and others. Quick survey . mostly for the UK folks but if you live in the US, Australia, Canada, etc. where some version of our American My Plate/Food Pyramid is recommended you can participate too (just identify please ;-) ). Your government counsels limiting fats in general and saturated fats in particular. Can you list 3-5 foods that you would limit in order to limit sat fats? Labels: Oh to heck with labels. Monday, December 16, 2013.

redefiningmyself.com redefiningmyself.com

Redefining Myself... with Lupus and MS

Welcome to Redefining Myself! While living with NP-SLE, RRMS and CIDP. And their overlapping accessories. Slapping the face of many things demyelinating. Sunday, August 11, 2013. Links to this post. This weeks Sound of Crickets Award goes to:. Okay, let me get this straight. My illness is causing you hardship? SickChickPMA #CNSGrrrl #SickChickHumor #SoundofCricketsAward #RedefiningMyself. Take Time for Reflection. Text and image ©2013 Brian Goslow. Saturday, August 10, 2013. I Do Not Need Your Help!

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Redefining Myself - Life with Cancer and Parkinson's  - Blog

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