Patients with autoimmune thyroid disease who are using LDN are invited to participate in a survey on AHSTA. The link is:
http://www.ahsta.com/Features/LDNSurvey/tabid/171/Default.aspx
In addition, the LDN Research Trust in the UK is looking for people who have been using LDN for at least 4 months to participate in their ongoing surveys. There's a separate survey for people with MS and another for people taking LDN for any other reason. The surveys are designed to be taken initially and repeated every 6 months to give a good overview of the response to LDN.
The survey results will be published anonymously in the Research Trust Newsletter after analysis by a third party. Interested subjects need to register to take part in this free survey. The link for MS patients is http://www.ldnresearchtrust.org/survey.asp.
For individuals with other conditions, the survey link is http://forum.ldnresearchtrust.org/ Here you can post your experience under the LDN section according to your specific condition.
The Research Trust would also like to hear from anyone willing to share their LDN story for their newsletter. LDN users can send their stories anonymously or send in their names along with a photo. All stories will be edited for spelling and grammar without changing the meaning in anyway.
Interested parties can email Linda at contact@ldnresearchtrust.org.
UK residents are asked to sign the LDN Petition http://petitions.number10.gov.uk/LowDNaltrexone/ strength is in numbers.