00:00The Italian Association of Multiple Sclerosis has chosen to give life to the Italian Neuromedical Association,
00:10obviously together with people with optical neuromedical disease,
00:14because it is right that there is a reference association for each disease
00:19and there are people who are primarily protagonists of their choices, but also of the defense of their rights.
00:28This means, of course, with the three key words that must always characterize an association,
00:35people, research and rights.
00:38It is important that there are reference centers,
00:43because people must be able to find in their territorial reality
00:48who is able to make an accurate tempestuous diagnosis,
00:53a diagnosis that does not stop as a first step,
00:58because in reality there is a monitoring, a cure that must continue,
01:03up to the evaluations through the center, through the territorial network,
01:09of all those needs that must find answers for the person,
01:14the possibility of living their own life in addition to the disease.
01:17Surely drugs today are a reality, as for other diseases,
01:23they are innovative drugs, they can bring us close to 100% of the block of the evolution of the disease,
01:31which in the past was not possible,
01:34and therefore the right to have these cures is fundamental,
01:38the right to have the possibility to look to the future,
01:42because these drugs can allow to block the evolution of the disease.
01:47www.cdc.gc.ca
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