Hi, all. I received an email recently from a researcher who is involved in a project regarding endometriosis and treatment options. I thought I would post their message here for anyone that would like to participate.
In other news, I finally feel as though the Lupron is out of my body in terms of my energy levels. I walk a mile a day. I did read some disturbing stats regarding neuropathy-like effects from Lupron and I am wondering if their is connection.
Message below:
Dear Reader, Neurocrine Biosciences (a San Diego biotechnology company) is conducting an endometriosis patient research survey as a part of our ongoing efforts to understand the disease of endometriosis and the needs of women suffering from its debilitating symptoms. The first 50 qualified participants will receive a $25 honoraria for participating. The survey should take approximately 30 minutes to complete. The information you provide will develop our understanding of the symptoms of endometriosis, the process leading to your diagnosis, and the available treatment options. At the same time, this information will guide decisions on the clinical development of an investigational drug having the potential to treat the symptoms of endometriosis. Your responses are completely confidential, and all results will be used at the aggregate level and only for research purposes. If you are interested in participating, please send an e-mail to endosurvey@neurocrine.com, and we will contact you directly to fill out a screener to determine your eligibility. We appreciate your willingness to share your experience and the important guidance you will provide to our efforts to develop a better treatment alternative. Kind Regards from Neurocrine Biosciences.
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