Hello and welcome to the low dose naltrexone (LDN) survey!
I am a CFS patient with training and experience in the biomedical sciences. I find that gathering information about patients' experiences as we currently do through discussion forums is quite inadequate. I would like to explore gathering information through surveys as a better way to obtain and share information on our experiences with treatments, doctors, etc.
All information gathered in this survey is entirely confidential and will only be used to report back to the CFS community our experiences with this drug. The results of this survey will be posted once a reasonable number of responses have been obtained. There are 15 mostly multiple choice questions in the survey. You do not have to answer all of them, but the more information you give, the more your fellow patients will receive.
Any comments are much appreciated! Thank you very much for participating.