CUTIS LAXA INTERNATIONALE
We are starting a great story..............................All together.
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The very life of our association is linked to Media. Without Cecile appearing on the screens during Telethon 2000, each one of us would still remain alone, Cutis Laxa Internationale would not exist.
WHY USING MEDIA ?
Since “Reports” has been broadcasted on the French Channel TF1, on Saturday 18th October 2003, the visits on our website have “exploded” and our email box has been “overloaded”.
In this report Cecile explained what Cutis Laxa has brought in her day to day life, especially the others’gaze.
Here is the “outcome” of what this broadcast brought us. It proves that communicating is an essential work if we want to help Rare Disorders to come out of the shadow :
And we don’t forget Megane who received more than 3000 messages. Megane suffers from Progeria. The second part of the report was about Megane. Cecile and Megane know each other very well . This is how we will “change the gazes”…….
Since December 2000, many articles, broadcasts, reports, helped us get Cutis Laxa better known. Each time, it has been the occasion for new sufferers to join us. You will find all the articles, as well as the mention of all the broadcasts we took part in, classified according to year. There may be others we didn’t know of. Many articles are in French. It was impossible for us to translate them all, so we just indicate the title and subject in brackets. Please accept our apology. You can have a look at some of them by clicking on the links. Go and see what happened in 2017, 2016, 2015, 2014, 2013,