Welcome to our website!
We are a non-profit corporation whose mission is to raise awareness about the condition of HELLP Syndrome, raise money for research, provide support to families affected by this condition and conduct research on the condition.
We're glad you stopped by! Our membership is growing every day. We have already touched several thousand families from the United States and at least sixteen other countries.
Before you go any further, please be aware that while many of our members have extensive medical experience, we are NOT a substitute for your doctor's care or advice. The information presented here and in our newsletters is as accurate as we can make it, but medical advances or new treatments may arise in between page editings. Also, please be aware that HELLP Syndrome can take many forms. Most women will experience some symptoms, (and a few will experience ALL of them), but the syndrome may take different courses in different women.
| Mission Statement Our mission is to become the premier partner to the world's medical community for the study and eventual cure of HELLP Syndrome, while at the same time, providing families who are affected by this condition with comfort, knowledge and a pathway to recovery from this extremely traumatic condition. |
The HELLP Syndrome Society
is a member of
ISSHP, NASSHP and INTERPREA
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