I am posting the above leaflet in the hope that more people than just me who are on this forum will be able to attend. It would be good to have some back-up and to be able to ask questions about Levothyroxine (T4) and Liiothyronine (T3). I attended such a meeting in 2013 in Braintree and many people were complaining about the use of generic medicines, noteably people from the Parkinsons Society. Nothing has changed since then, other than T3 has been taken away. Please contact me by PM if you want to make yourself known to me.