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Need info

Question:

My aunt was recently diagnosed with lupus and I’m clueless about it…can anyone suggest a good source to find info written in plain English?                                         `-Chris

Response:

Go to Lupus Foundation, Missouri Chapter. they will have EVERYTHING you need to know, if not, as them theyll find it for you!  www.mtio.com/mclfa – Hide quoted text — Show quoted text -Chris wrote in message <3547b63d.10902…@news.mindspring.com>… >My aunt was recently diagnosed with lupus and I’m clueless about >it…can anyone suggest a good source to find info written in plain >English? > `-Chris

Response:

Chris <chand…@mindspring.com> wrote in article <3547b63d.10902…@news.mindspring.com>… > My aunt was recently diagnosed with lupus and I’m clueless about > it…can anyone suggest a good source to find info written in plain > English? >                                    `-Chris

================ The best site is:   http://internet-plaza.net/lupus Be sure to go to the health forums.

Response:

You should visit: http://www.planet-health.com

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Response:

In article <3547b63d.10902…@news.mindspring.com>#1/1,   chand…@mindspring.com wrote: > My aunt was recently diagnosed with lupus and I’m clueless about > it…can anyone suggest a good source to find info written in plain > English? >                                    `-Chris

Chris, Sorry to read about your Aunt.  Probably one of the best Internet sites on Lupus (and non-commercial, better yet!) is the "LUPUS FOUNDATION OF AMERICA" which can be found at:  http://internet-plaza.net/lupus/ They have everything from information to local support groups, to an excellent "Frequently Asked Questions" page, etc. Hope this helps, the Aloe Vera Studies Organization http://www.aloe-vera.org —–== Posted via Deja News, The Leader in Internet Discussion ==—– http://www.dejanews.com/   Now offering spam-free web-based newsreading

Response:

There is also another Lupus site that I think you will find just as usefull and informative, helpful and supportive.  It is called the MCLFA: Missouri Chapter Lupus Foundation of America… http://www.mtio.com/mclfa Good luck and I hope out of the two site you’ve been given you will find some answers. If you need to talk or need any more help….. please feel free to write me anytime. I would be glad to help you any way I can. May the Lord Bless you and keep you safe from all harm. Love and Hugs, and Prayers, Mary in VA

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