Out of curiosity, has anyone from this forum published anything about their experience of adding T3 to their medication? There's obviously a lot of us on here unhappy about T3 not being prescribed easily on the NHS. A lot of you are undoubtedly very knowledgeable about the subject and give some great advices. I don't know what I would have done without this group. Other than petitions, I was wondering if there's been any other kind of research or publication by group members. I haven't looked through the old posts, so if this has been asked before, please forgive me for asking.