STIFF PERSON SYNDROME





THIS WEBSITE IS ABOUT THE FOLLOWING:

1. NEW RESEARCH PROJECT ON STIFF PERSON SYNDROME

2. A STUDY OF 33 PEOPLE WITH STIFF PRSON SYNDROME.

3. MY STORY AS WELL AS OTHER PEOPLES STORIES OF HOW THEY DISCOVERED SPS, HOW IT CHANGED THEIR LIFE, AND HOW THEY ARE DEALING WITH SPS TODAY.

4. TO SUBMIT A PERSONAL STORY TO BE PUBLISHED ON THIS SITE OR PARTICIPATE IN THE STUDY TO HELP THE PEOPLE WHO DEAL WITH IT DAILY. CLICK ON THE "SUBMISSIONS" LINK.

5. LINKS TO AQUIRE A DEEPER MORE COMPREHENSIVE UNDERSTANDING OF MEDICAL TERMS, DRUG TREATMENT INFORMATION, AND DRUG INTERACTION.

6. THE PROBLEM OF THE MISDIAGNOSES OF MANY AUTOIMMUNE ILLNESSES


STIFF PERSON (STIFFMAN) SYNDROME AFFECTS APPROXIMATLEY 1 IN EVERY 1 MILLION PEOPLE IN THE UNITE STATES, MY PRAYER IS THIS SITE AND LINKS TO OTHERS WILL HELP OBTAIN A DIAGNOSES EARLIER, HELP PEOPLE UNDERSTAND BETTER WHAT SPS IS ABOUT, AND HOW TO ADJUST TO THE BEST POSSIBLE QUALITY OF LIFE WHILE LIVING WITH SPS.





JohnC Crawford john@stiffpersonsyndrome.net

Copyright 2009-2012


DISCLAIMER

THIS WEB SITE IS NOT AFFILIATED WITH ANY CHARITY NOR ENDORSES ANY MEDICAL FACILITY, PHYSICAN, OR TREATMENT FOR STIFF PERSON (STIFFMAN) SYNDROME.

NOTHING ON THIS WEB SITE SHOULD BE CONSIDERED MEDICAL ADVICE. PLEASE CONTACT YOUR DOCTOR TO SEEK MEDICAL ADVICE OR MEDICAL TREATMENT FOR ANY ILLNESS YOU MAY HAVE. THE INFORMATION ON THIS SITE IS TO GIVE A PERSPECTIVE ON THIS ILLNESS FROM THE POINT OF A PATIENT AND NOT TO BE USED TO DIAGNOSE, TREAT, OR IN ANYWAY TRY TO BE USED FOR MEDICAL PURPOSES.

ALL ARTICLES, STORIES, OR OPINIONS EXPRESSED ON THIS SITE ARE THOSE OF THE AUTHOR OF SAID ARTICLES, STORIES, OR OPINIONS AND NOT THAT OF THE WEB SITE OR ANY OF IT'S EMPLOYEES
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