Guest guest Posted February 7, 2010 Report Share Posted February 7, 2010 My last request a week or so ago asking for help to find the email addresses of the owners of thyroid web sites, thyroid support groups and Internet thyroid support groups, was met with silence, apart from a couple of members who offered help. I sent my request for help to every one of our members individually, plus the top thyroid forums. I also posted on to the American support groups to see whether anybody there would organise a team to find the email addresses of the owners of thyroid web sites or thyroid forums in every State. Nobody responded. I am also trying to find the email addresses of doctors who might prescribe T3 in combination with T4 or who prescribe natural thyroid extract in order that I can write to them and ask them if their secretary would send the link to the Questionnaire to give their patients the opportunity to sign it. Again, little response, but about three of you have already written to give me the names of their endocrinologists and the hospital they work in so many thanks for that. PLEASE, if this Register of Counterexamples is going to work - to show that levothyroxine (T4) doesn't work for everybody, we need to give tens of thousands of sufferers the opportunity to respond, after which time, we need to send it to all the Heads/Deans of Medical Schools, Medical Boards, World Health Organisation, Authors of Guidelines on the diagnosis and management of hypothyroidism and endocrine/thyroid associations throughout the world. It would help me if there is there somebody out there please who will try and find the email addresses of the doctors mentioned here in Australia http://www.thyroid-info.com/topdrs/australia.htm It would also help if somebody in the US would find the email addresses of the American thyroid web sites and forums. I do, of course, have the main ones. Unless help is forthcoming - we might as well give up any idea of creating such a Register, which I, for one, consider to be absolutely vital if ever we are to bring about changes in the treatment of the symptoms of hypothyroidism. It is a physical impossibility to do such a massive job on our own. Also, if your Mother tongue is not English, we want the Questionnaire translating into as many languages as we can. So far, we have German, and French translations, with promises of Italian, Swedish, and Finnish. If you can translate to other languages (and I don't mean by using Google translators) please let me know. Luv - Sheila Quote Link to comment Share on other sites More sharing options...
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