LupusMCTD

Welcome everyone in search of support & information of Lupus & MCTD

Patients who are dedicated to providing information and support to people interested in Lupus and Mixed Connective Tissue Disorders.

Members

  • Kathy
  • myjoy520
  • Suzanne
  • nitebreze
  • Holly P.
  • Kimber
  • Vincy Arredondo
  • Michelle

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Disclaimer~ Information contained in these http://lupusmctd.ning.com/™ pages is not meant to be taken as an endorsement of any medical approach, procedure, or treatment of any kind. If you have symptoms, seek immediate professional medical attention. The topics here are presented solely as potential options to be discussed with your medical professional. If you think you may have a medical emergency, call your doctor or 911 immediately.

www.LupusMCTD.org founded in 2005 as a peer-to-peer endeavor run entirely by volunteers -- patients who are dedicated to providing information and support to people interested in Lupus and Mixed Connective Tissue Disorders.

LupusMCTD Foundation is financially supported solely by individuals who have personally experienced or witnessed through the site what giving can do to make awareness more available to the unknown conditions that are often hidden and called "Invisable Illnesses".

www.LupusMCTD.org does not accept corporate contributions from any industry. None of the people involved in this effort receive a salary or other compensation. The Foundation's mission is to provide information for patients, practitioners and the general public about this important, most often overlooked illnesses.

Page Contents, Layout and Design Copyright© All Graphics Copyrighted by Credited Artists and are Not Public Domain.

Events

 

Latest Activity

(((TESA))))) Richard Pryor made a movie once, he called it "Stir Crazy" And that is what you have!!! Hang in there, remember you have that laptop and can reach out to everyone around the world to help take your mind of of what you are going throug...
4 hours ago
Please feel free to upload your skin conditions that is visable to share with others Kathy~Livedo Reticularis
4 hours ago
Kathy added 2 discussions
4 hours ago
KATHY I AM S0 TIRED OF THIS SHIT I AM READY TO GO HOME GIRLTHAT I DONT NO WHAT TO DO GIRL I JUST WISH I HAD POWERS I WOULD COME AND SEE ALL MY GOOD FREINDS AN GET RID OF ALL OUR PAIN LOL BUT I DONT HAVE POWERS BUT I HAVE PRAYER AN THAT WORKS BETTE...
5 hours ago

Forum

Kathy

Skin Conditions of Many.. 1 Reply

Started by Kathy. Last reply by Kathy 4 hours ago.

myjoy520

STILL IN THE HOSPITAL 1 Reply

Started by myjoy520. Last reply by Kathy 18 hours ago.

Kathy

Merging all LupusMCTD Sites

Started by Kathy 19 hours ago.

Kathy

" Flight of The Hope Bracelet Journey " 3 Replies

Started by Kathy. Last reply by myjoy520 Jun 22.

Kathy

Newsletter ~Update

Started by Kathy Jun 21.

Groups

"Mother Site" www.LupusMCTD.com is closing

www.LupusMCTD.com will be closing within 30 days. Today June 20, 2009 was the last payment made to SMF.

Notes

URL for Forum Address For This Site

http://lupusmctd.ning.com/forum

Created by Kathy Jun 30, 2008 at 11:00am. Last updated by Kathy Jun. 30, 2008.

Last Call For Your Pics For New Videos

Send your pic you want in the summer Lupus video to LupusWebsite@aol.com

Please sign it that I have your permission to use your pic in any form in the LupusMCTD websites & newsletters, but not limited to but will include My Space and You Tube videos as well.

Thank you!

Created by Kathy Jun 17, 2008 at 3:47pm. Last updated by Kathy Jun. 17, 2008.

Videos Added

Two videos were added today June 13, 2008.

The patients video I am trying to gather more pics for the summer viseo I am making, so please send me your picture with your permission to use it to

LupusWebsite@aol.com

Thank you!

Created by Kathy Jun 13, 2008 at 11:48am. Last updated by Kathy Jun. 13, 2008.

 
 

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